首页 > 最新文献

Human reproduction最新文献

英文 中文
Pretreatment with luteal estradiol for programming antagonist cycles compared to no pretreatment in advanced age women stimulated with corifollitropin alfa: a non-inferiority randomized controlled trial. 使用黄体雌二醇对高龄妇女进行编程拮抗剂周期预处理与不进行预处理的比较:非劣效随机对照试验。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae167
Isabelle Cédrin-Durnerin, Isis Carton, Nathalie Massin, Nicolas Chevalier, Sophie Dubourdieu, Bettina Bstandig, Xénia Michelson, Seydou Goro, Camille Jung, Anne Guivarc'h-Lévêque
<p><strong>Study question: </strong>Does luteal estradiol (E2) pretreatment give a similar number of retrieved oocytes compared to no-pretreatment in advanced-aged women stimulated with corifollitropin alfa in an antagonist protocol?</p><p><strong>Summary answer: </strong>Programming antagonist cycles with luteal E2 gave similar number of retrieved oocytes compared to no-pretreatment in women aged 38-42 years.</p><p><strong>What is known already: </strong>Programming antagonist cycles with luteal E2 pretreatment is a valuable tool to organize the IVF procedure better and is safe without any known impact on cycle outcome. However, variable effects were observed on the number of retrieved oocytes depending on the treated population. In advanced-age women, recruitable follicles tend to decrease in number and to be more heterogeneous in size but it remains unclear if estradiol pretreatment could change the oocyte yield through its negative feed-back effect on FSH intercycle rise.</p><p><strong>Study design, size, duration: </strong>This non-blinded randomized controlled non-inferiority trial was conducted between 2016 and 2022 with centrally computerized randomization and concealed allocation. Participants were 324 women aged 38-42 years undergoing IVF treatment. The primary endpoint was the total number of retrieved oocytes. Statistical analysis was performed with one-sided alpha risk of 2.5% and 95% confidence interval (CI) with the non-inferiority of E2 pretreatment proved by a P value <0.025 and a lower delta margin of the CI within two oocytes compared to no pretreatment. Secondary endpoints were duration and total dosage of recombinant FSH, cancellation rate, percentage of oocyte pick-up (OPU) on working days, total number of metaphase II oocytes and obtained embryos, fresh transfer live birth rate, and cumulative live birth rate.</p><p><strong>Participants/materials, setting, methods: </strong>This multicentric study enrolled women with regular cycles, weight >50 kg and body mass index <32, IVF cycle 1-2. According to randomization, micronized estradiol 2 mg twice a day was started on days 20-24 and continued until Wednesday beyond the onset of menses followed by administration of corifollitropin alfa on Friday, i.e. stimulation (S)1 or from D1-3 of a natural cycle in unpretreated patients. GnRH antagonist was started at S6 and additional FSH at S8.</p><p><strong>Main results and the role of chance: </strong>Basal characteristics were similar in patients randomized in E2 pretreated (n = 164) and non-pretreated (n = 160) groups (intended to treat (ITT) population). A total of 291 patients started treatment (per protocol (PP) population), 147 in E2 pretreated group with a mean number [SD] of pre-treatment days 9.8 [2.6] and 144 in the non-pretreated group. Despite advanced age, oocyte yields ranged from 0 to 29 in both groups with a median number of 6 retrieved oocytes in accordance with a mean anti-Müllerian hormone (AMH) level above 1.2 ng/ml.
研究问题黄体雌二醇(E2)预处理与不预处理相比,在拮抗剂方案中使用促花粉素α刺激的高龄妇女是否能获得相似数量的卵母细胞?在38-42岁的妇女中,使用黄体E2进行拮抗剂周期方案与不进行前处理相比,获得的卵母细胞数量相似:黄体 E2 预处理拮抗剂周期是更好地组织试管婴儿程序的重要工具,而且安全,对周期结果没有任何已知影响。然而,根据治疗人群的不同,拮抗剂对取回卵母细胞数量的影响也不尽相同。在高龄女性中,可募集卵泡的数量往往会减少,大小也更不均匀,但雌二醇预处理是否会通过其对FSH周期间上升的负反馈效应而改变卵母细胞产量,目前仍不清楚:这项非盲随机对照非劣效性试验于2016年至2022年期间进行,采用中央电脑随机化和隐蔽分配。参与者为324名接受试管婴儿治疗的38-42岁女性。主要终点是取回的卵母细胞总数。统计分析采用单侧α风险2.5%和95%置信区间(CI),以P值证明E2预处理的非劣效性:这项多中心研究招募了周期规律、体重大于 50 千克且体重指数正常的女性:随机分入 E2 预处理组(164 人)和非预处理组(160 人)(意向治疗(ITT)人群)的患者基础特征相似。共有 291 名患者开始治疗(按方案(PP)人群),其中 E2 预处理组 147 人,平均治疗前天数 [SD] 为 9.8 [2.6],非预处理组 144 人。尽管年龄偏大,但两组的卵母细胞产量从 0 到 29 个不等,中位数为 6 个,抗缪勒氏管激素(AMH)平均水平高于 1.2 ng/ml。我们证明了 E2 预处理的非劣效性,在 PP 组中,平均差异为-0.1 个卵母细胞 95% CI [-1.5; 1.3] P = 0.004;在 ITT 组中,平均差异为-0.44 个卵母细胞 [-1.84; 0.97] P = 0.014。E2 预处理患者更常在工作日取卵(91.9% 对 74.2%,P 限制,谨慎原因):年龄超过 38 岁的受刺激妇女获得的卵母细胞采集范围很广,这表明两组妇女的卵巢衰老阶段截然不同。在卵巢衰老阶段,E2 预处理更有可能增加卵母细胞产量,而卵巢衰老的特点是卵泡群减少的不同步。另一个限制因素是AMH患者亚组分析的样本量:对高龄女性来说,在黄体E2预处理的情况下安排拮抗剂周期似乎是一种有用的工具,可以更好地安排在工作日取卵。然而,采集卵母细胞数量的潜在益处仍有待在更大的人群中证实,这些人群显示出波塞冬分类中卵巢储备功能下降的特征:法国 Organon 公司 (MSD) 的研究基金。I.C.、S.D.、B.B.、X.M.、S.G.和 C.J. 与本研究无利益冲突。I.C.D. 申报了默克集团、Gedeon Richter、MSD (Organon, France)、Ferring、Theramex 和 IBSA 的演讲酬金,以及默克集团顾问委员会的参与酬金。I.C.D. 还申报了默克公司的咨询费、差旅费和会议支持。N.M. 申报了其所在机构从 MSD (Organon, France) 获得的资助;从 MSD (Organon, France)、Ferring 和 Merck KGaA 获得的咨询费;从 Merck KGaA、General Electrics、Genevrier (IBSA Pharma) 和 Theramex 获得的酬金;从 Theramex、Merck KGaG 和 Gedeon Richter 获得的差旅和会议支持;以及从 Goodlife Pharma 向其所在机构支付的设备费。N.C. 申报了 IBSA Pharma、Merck KGaG、Ferring 和 Gedeon Richter 的资助;IBSA Pharma、Merck KGaG、MSD (Organon, France)、Gedeon Richter 和 Theramex 的差旅和会议支持;以及 Merck KGaA 咨询委员会的参与。A.G.L.申报了默克集团、Gedeon Richter、MSD(法国 Organon)、Ferring、Theramex 和 IBSA 的演讲费:ClinicalTrials.gov NCT02884245.试验注册日期:2016年8月29日.首例患者入组日期:2016年11月4日:首例患者入组日期:2016 年 11 月 4 日。
{"title":"Pretreatment with luteal estradiol for programming antagonist cycles compared to no pretreatment in advanced age women stimulated with corifollitropin alfa: a non-inferiority randomized controlled trial.","authors":"Isabelle Cédrin-Durnerin, Isis Carton, Nathalie Massin, Nicolas Chevalier, Sophie Dubourdieu, Bettina Bstandig, Xénia Michelson, Seydou Goro, Camille Jung, Anne Guivarc'h-Lévêque","doi":"10.1093/humrep/deae167","DOIUrl":"10.1093/humrep/deae167","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;Does luteal estradiol (E2) pretreatment give a similar number of retrieved oocytes compared to no-pretreatment in advanced-aged women stimulated with corifollitropin alfa in an antagonist protocol?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;Programming antagonist cycles with luteal E2 gave similar number of retrieved oocytes compared to no-pretreatment in women aged 38-42 years.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;Programming antagonist cycles with luteal E2 pretreatment is a valuable tool to organize the IVF procedure better and is safe without any known impact on cycle outcome. However, variable effects were observed on the number of retrieved oocytes depending on the treated population. In advanced-age women, recruitable follicles tend to decrease in number and to be more heterogeneous in size but it remains unclear if estradiol pretreatment could change the oocyte yield through its negative feed-back effect on FSH intercycle rise.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;This non-blinded randomized controlled non-inferiority trial was conducted between 2016 and 2022 with centrally computerized randomization and concealed allocation. Participants were 324 women aged 38-42 years undergoing IVF treatment. The primary endpoint was the total number of retrieved oocytes. Statistical analysis was performed with one-sided alpha risk of 2.5% and 95% confidence interval (CI) with the non-inferiority of E2 pretreatment proved by a P value &lt;0.025 and a lower delta margin of the CI within two oocytes compared to no pretreatment. Secondary endpoints were duration and total dosage of recombinant FSH, cancellation rate, percentage of oocyte pick-up (OPU) on working days, total number of metaphase II oocytes and obtained embryos, fresh transfer live birth rate, and cumulative live birth rate.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, setting, methods: &lt;/strong&gt;This multicentric study enrolled women with regular cycles, weight &gt;50 kg and body mass index &lt;32, IVF cycle 1-2. According to randomization, micronized estradiol 2 mg twice a day was started on days 20-24 and continued until Wednesday beyond the onset of menses followed by administration of corifollitropin alfa on Friday, i.e. stimulation (S)1 or from D1-3 of a natural cycle in unpretreated patients. GnRH antagonist was started at S6 and additional FSH at S8.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;Basal characteristics were similar in patients randomized in E2 pretreated (n = 164) and non-pretreated (n = 160) groups (intended to treat (ITT) population). A total of 291 patients started treatment (per protocol (PP) population), 147 in E2 pretreated group with a mean number [SD] of pre-treatment days 9.8 [2.6] and 144 in the non-pretreated group. Despite advanced age, oocyte yields ranged from 0 to 29 in both groups with a median number of 6 retrieved oocytes in accordance with a mean anti-Müllerian hormone (AMH) level above 1.2 ng/ml.","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141619867","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transgender persons' view on previous fertility decision-making and current infertility: a qualitative study. 变性人对以往生育决策和当前不孕症的看法:一项定性研究。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae155
J D Asseler, I de Nie, F B van Rooij, T D Steensma, D Mosterd, M O Verhoeven, M Goddijn, J A F Huirne, N M van Mello

Study question: How do adult transgender and gender diverse (TGD) people, who are infertile due to prior gender-affirming treatment, view their current infertility and their reproductive decisions made in the past?

Summary answer: In a time where sterilization was mandatory, transgender adolescents prioritized gender-affirming treatment over their future fertility and would make the same choice today despite emotional challenges related to infertility experienced by some.

What is known already: Under transgender law in the Netherlands, sterilization was required for legal gender recognition until 2014, resulting in permanent infertility. The long-term consequences of this iatrogenic infertility in transgender adolescents who have now reached adulthood remain underexplored.

Study design, size, duration: Qualitative study design based on 21 in-depth one-on-one semi-structured interviews.

Participants/materials, setting, methods: TGD people in a stage of life where family planning may be a current topic were eligible for participation. They all received gender-affirming treatment in adolescence prior to the legislation change in 2014. A purposeful sampling technique was used from participants of another ongoing study. Eleven people assigned female at birth and ten people assigned male at birth were included. Interview transcripts were thematically analysed using a modified version of Braun and Clarke's six steps theory.

Main results and the role of chance: Six main themes were generated: (i) personal considerations regarding fertility and fertility preservation in the past; (ii) external considerations regarding fertility and fertility preservation in the past; (iii) current vision on past considerations and decisions; (iv) Current experiences and coping with infertility; (v) future family building; (vi) advice regarding fertility and fertility preservation decision-making.

Limitations, reasons for caution: Selection, recall, and choice supportive bias may play a role in interpreting our results.

Wider implications of the findings: This study highlights the importance of tailored counselling and comprehensive information on fertility preservation for transgender individuals, especially adolescents, undergoing gender-affirming treatment.

Study funding/competing interest(s): N/A.

Trial registration number: N/A.

研究问题:成年变性人和性别多元化(TGD)人因之前接受过性别确认治疗而不育,他们如何看待自己目前的不育症和过去做出的生育决定?在强制绝育的时代,变性青少年优先考虑的是性别确认治疗,而不是他们未来的生育能力,尽管有些人经历了与不孕不育有关的情感挑战,他们今天也会做出同样的选择:根据荷兰的变性法律,直到 2014 年,合法的性别认可都要求进行绝育手术,这导致了永久性不孕。研究设计、规模、持续时间:研究设计、规模、持续时间:基于 21 次一对一半结构式深度访谈的定性研究设计:研究对象/材料、环境、方法:处于计划生育可能是当前主题的人生阶段的 TGD 人符合参与条件。他们都在 2014 年立法修改之前的青春期接受过性别确认治疗。从另一项正在进行的研究的参与者中采用了有目的的抽样技术。其中包括 11 名出生时被分配为女性的人和 10 名出生时被分配为男性的人。采用布劳恩和克拉克的六步骤理论的改进版对访谈记录进行了主题分析:产生了六大主题:(i) 过去对生育和生育保护的个人考虑;(ii) 过去对生育和生育保护的外部考虑;(iii) 目前对过去考虑和决定的看法;(iv) 目前的经历和应对不孕不育;(v) 未来的家庭建设;(vi) 对生育和生育保护决策的建议:研究结果的广泛意义:这项研究强调了为接受性别确认治疗的变性人(尤其是青少年)提供量身定制的咨询和有关生育力保存的全面信息的重要性:不详。试验注册号:不详:不适用。
{"title":"Transgender persons' view on previous fertility decision-making and current infertility: a qualitative study.","authors":"J D Asseler, I de Nie, F B van Rooij, T D Steensma, D Mosterd, M O Verhoeven, M Goddijn, J A F Huirne, N M van Mello","doi":"10.1093/humrep/deae155","DOIUrl":"10.1093/humrep/deae155","url":null,"abstract":"<p><strong>Study question: </strong>How do adult transgender and gender diverse (TGD) people, who are infertile due to prior gender-affirming treatment, view their current infertility and their reproductive decisions made in the past?</p><p><strong>Summary answer: </strong>In a time where sterilization was mandatory, transgender adolescents prioritized gender-affirming treatment over their future fertility and would make the same choice today despite emotional challenges related to infertility experienced by some.</p><p><strong>What is known already: </strong>Under transgender law in the Netherlands, sterilization was required for legal gender recognition until 2014, resulting in permanent infertility. The long-term consequences of this iatrogenic infertility in transgender adolescents who have now reached adulthood remain underexplored.</p><p><strong>Study design, size, duration: </strong>Qualitative study design based on 21 in-depth one-on-one semi-structured interviews.</p><p><strong>Participants/materials, setting, methods: </strong>TGD people in a stage of life where family planning may be a current topic were eligible for participation. They all received gender-affirming treatment in adolescence prior to the legislation change in 2014. A purposeful sampling technique was used from participants of another ongoing study. Eleven people assigned female at birth and ten people assigned male at birth were included. Interview transcripts were thematically analysed using a modified version of Braun and Clarke's six steps theory.</p><p><strong>Main results and the role of chance: </strong>Six main themes were generated: (i) personal considerations regarding fertility and fertility preservation in the past; (ii) external considerations regarding fertility and fertility preservation in the past; (iii) current vision on past considerations and decisions; (iv) Current experiences and coping with infertility; (v) future family building; (vi) advice regarding fertility and fertility preservation decision-making.</p><p><strong>Limitations, reasons for caution: </strong>Selection, recall, and choice supportive bias may play a role in interpreting our results.</p><p><strong>Wider implications of the findings: </strong>This study highlights the importance of tailored counselling and comprehensive information on fertility preservation for transgender individuals, especially adolescents, undergoing gender-affirming treatment.</p><p><strong>Study funding/competing interest(s): </strong>N/A.</p><p><strong>Trial registration number: </strong>N/A.</p>","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11373325/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141619869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Infertility treatments and cyanotic congenital heart defects among livebirths in the USA: findings from a contemporary cohort. 美国活产婴儿中的不孕症治疗与紫绀型先天性心脏缺陷:当代队列研究结果。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae161
Duke Appiah, Julie Sang, Olumakinwa E Olayemi, Eric K Broni, Buse Baykoca-Arslan, Imo A Ebong, Catherine Kim
<p><strong>Study question: </strong>Is there an elevated risk of cyanotic congenital heart defects (CCHD) among livebirths following infertility treatments?</p><p><strong>Summary answer: </strong>In this population-based study of single livebirths, infertility treatment (either ART or non-ART) was associated with a higher prevalence of CCHD among livebirths.</p><p><strong>What is known already: </strong>The use of infertility treatment has been on the rise over the past few decades. However, there are limited studies assessing the risk of major cardiac defects following infertility treatments.</p><p><strong>Study design, size, duration: </strong>A retrospective cohort study of livebirth data from the National Vital Statistics System (NVSS) was conducted, comprising of 9.6 million singleton livebirths among first-time mothers aged 15-49 years from 2016 to 2022.</p><p><strong>Participants/materials, setting, methods: </strong>Information on infertility treatment use and CCHD was obtained from the health and medical information section of birth certificates, which was completed by healthcare staff after reviewing medical records. Logistic regression models were used to estimate odds ratios (OR) and 95% CI. Entropy balancing weighting analysis and probabilistic bias analysis were also performed.</p><p><strong>Main results and the role of chance: </strong>The proportion of births following infertility treatment increased from 1.9% (27 116) to 3.1% (43 510) during the study period. Overall, there were 5287 cases of CCHD resulting in a prevalence of 0.6 per 1000 livebirths. The prevalence was 1.2 per 1000 live births among infertility treatment users (ART: 1.1 per 1000 livebirths; non-ART: 1.3 per 1000 livebirths) while that for naturally conceived births was 0.5 per 1000 livebirths. Compared to naturally conceived births, the use of any infertility treatment (OR: 2.06, 95% CI: 1.82-2.33), either ART (OR: 2.02, 95% CI: 1.73-2.36) or other infertility treatments (OR: 2.12, 95% CI: 1.74-2.33), was associated with higher odds of CCHD after adjusting for maternal and paternal age, race and ethnicity, and education, as well as maternal nativity, marital status, source of payment, smoking status, and pre-pregnancy measures of BMI, hypertension and diabetes. This association did not differ by the type of infertility treatment (ART versus other infertility treatments) (OR: 1.04, 95% CI: 0.82-1.33, P = 0.712), and was robust to the presence of exposure and outcome misclassification bias and residual confounding.</p><p><strong>Limitations, reasons for caution: </strong>The findings are only limited to livebirths. We did not have the capacity to examine termination data, but differential termination by mode of conception has not been supported by previous studies designed to consider it. Infertility treatment use was self-reported, leading to the potential for selection bias and misclassification for infertility treatment and CCHD. However, the association persist
研究问题:不孕症治疗后的活产婴儿发生紫绀型先天性心脏缺陷(CCHD)的风险是否升高?在这项针对单胎活产婴儿的人群研究中,不孕症治疗(抗逆转录病毒疗法或非抗逆转录病毒疗法)与活产婴儿先天性心脏畸形(CCHD)发病率较高有关:过去几十年来,不孕不育治疗的使用呈上升趋势。研究设计、规模、持续时间:一项回顾性队列研究:研究对来自全国人口动态统计系统(NVSS)的活产儿数据进行了回顾性队列研究,包括2016年至2022年期间年龄在15-49岁的初产妇中960万例单胎活产:不孕不育治疗和慢性儿童疾病的信息来自出生证明的健康和医疗信息部分,由医护人员在查看医疗记录后填写。采用逻辑回归模型估算几率比(OR)和 95% CI。此外,还进行了熵平衡加权分析和概率偏差分析:在研究期间,不孕症治疗后生育的比例从 1.9%(27 116 例)增至 3.1%(43 510 例)。总体而言,共有 5287 例儿童先天性心脏病,患病率为每 1000 例活产中 0.6 例。不孕症治疗者的发病率为每 1000 例活产 1.2 例(抗逆转录病毒疗法:每 1000 例活产 1.1 例;非抗逆转录病毒疗法:每 1000 例活产 1.3 例),而自然受孕者的发病率为每 1000 例活产 0.5 例。与自然受孕分娩相比,使用任何不孕不育治疗方法(OR:2.06,95% CI:1.82-2.33),无论是 ART(OR:2.02,95% CI:1.73-2.36)还是其他不孕不育治疗方法(OR:2.12,95% CI:1.74-2.33),都与较高的几率有关。33),在调整了母亲和父亲的年龄、种族和民族、教育程度以及母亲的出生地、婚姻状况、支付来源、吸烟状况和孕前体重指数、高血压和糖尿病测量值后,与较高的儿童先天性心脏病几率相关。这种关联在不孕症治疗类型(抗逆转录病毒疗法与其他不孕症治疗)上没有差异(OR:1.04,95% CI:0.82-1.33,P = 0.712),并且在存在暴露和结果分类偏差及残余混杂的情况下也是稳健的:研究结果仅限于活产婴儿。我们没有能力检查终止妊娠的数据,但以往旨在考虑终止妊娠的研究并未支持按受孕方式区分终止妊娠。不孕不育治疗的使用情况是自我报告的,这可能会导致选择偏差以及不孕不育治疗和慢性儿童疾病的错误分类。但是,如果在分析中考虑到系统性偏差以及暴露和结果分类偏差,则两者之间的联系仍然存在。研究结果的广泛意义:鉴于美国和其他国家使用不孕不育治疗的趋势日益明显,本研究的发现对育龄人群的临床和公共健康具有重要意义。数据显示,使用不孕不育治疗可能会增加后代患严重先天性心脏缺陷(如本研究中的 CCHD)的几率。这些研究结果不能作因果关系解释。我们的研究结果有助于为通过抗逆转录病毒疗法或其他不孕不育治疗方法受孕的孕妇提供孕前咨询和产前护理,同时也支持目前的一些建议,即通过不孕不育治疗方法受孕的孕妇应接受胎儿超声心动图筛查:本研究未寻求任何资助。作者声明不存在利益冲突:不详。
{"title":"Infertility treatments and cyanotic congenital heart defects among livebirths in the USA: findings from a contemporary cohort.","authors":"Duke Appiah, Julie Sang, Olumakinwa E Olayemi, Eric K Broni, Buse Baykoca-Arslan, Imo A Ebong, Catherine Kim","doi":"10.1093/humrep/deae161","DOIUrl":"10.1093/humrep/deae161","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;Is there an elevated risk of cyanotic congenital heart defects (CCHD) among livebirths following infertility treatments?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;In this population-based study of single livebirths, infertility treatment (either ART or non-ART) was associated with a higher prevalence of CCHD among livebirths.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;The use of infertility treatment has been on the rise over the past few decades. However, there are limited studies assessing the risk of major cardiac defects following infertility treatments.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;A retrospective cohort study of livebirth data from the National Vital Statistics System (NVSS) was conducted, comprising of 9.6 million singleton livebirths among first-time mothers aged 15-49 years from 2016 to 2022.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, setting, methods: &lt;/strong&gt;Information on infertility treatment use and CCHD was obtained from the health and medical information section of birth certificates, which was completed by healthcare staff after reviewing medical records. Logistic regression models were used to estimate odds ratios (OR) and 95% CI. Entropy balancing weighting analysis and probabilistic bias analysis were also performed.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;The proportion of births following infertility treatment increased from 1.9% (27 116) to 3.1% (43 510) during the study period. Overall, there were 5287 cases of CCHD resulting in a prevalence of 0.6 per 1000 livebirths. The prevalence was 1.2 per 1000 live births among infertility treatment users (ART: 1.1 per 1000 livebirths; non-ART: 1.3 per 1000 livebirths) while that for naturally conceived births was 0.5 per 1000 livebirths. Compared to naturally conceived births, the use of any infertility treatment (OR: 2.06, 95% CI: 1.82-2.33), either ART (OR: 2.02, 95% CI: 1.73-2.36) or other infertility treatments (OR: 2.12, 95% CI: 1.74-2.33), was associated with higher odds of CCHD after adjusting for maternal and paternal age, race and ethnicity, and education, as well as maternal nativity, marital status, source of payment, smoking status, and pre-pregnancy measures of BMI, hypertension and diabetes. This association did not differ by the type of infertility treatment (ART versus other infertility treatments) (OR: 1.04, 95% CI: 0.82-1.33, P = 0.712), and was robust to the presence of exposure and outcome misclassification bias and residual confounding.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Limitations, reasons for caution: &lt;/strong&gt;The findings are only limited to livebirths. We did not have the capacity to examine termination data, but differential termination by mode of conception has not been supported by previous studies designed to consider it. Infertility treatment use was self-reported, leading to the potential for selection bias and misclassification for infertility treatment and CCHD. However, the association persist","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141619865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A modified flexible GnRH antagonist protocol using antagonist early cessation and a gonadotropin step-down approach improves live birth rates in fresh cycles: a randomized controlled trial. 采用拮抗剂提前停用和促性腺激素逐步减少方法的改良灵活 GnRH 拮抗剂方案可提高新鲜周期的活产率:随机对照试验。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae145
Bei Xu, Dirk Geerts, Jiaying Yuan, Mengting Wang, Zhou Li, Qiaohong Lai, Yu Zheng, Si Liu, Shulin Yang, Guijin Zhu, Lei Jin
<p><strong>Study question: </strong>Can pregnancy outcomes following fresh elective single embryo transfer (eSET) in gonadotropin-releasing hormone (GnRH) antagonist protocols increase using a gonadotropin (Gn) step-down approach with cessation of GnRH antagonist on the day of hCG administration (hCG day) in patients with normal ovarian response?</p><p><strong>Summary answer: </strong>The modified GnRH antagonist protocol using the Gn step-down approach and cessation of GnRH antagonist on the hCG day is effective in improving live birth rates (LBRs) per fresh eSET cycle.</p><p><strong>What is known already: </strong>Currently, there is no consensus on optimal GnRH antagonist regimens. Studies have shown that fresh GnRH antagonist cycles result in poorer pregnancy outcomes than the long GnRH agonist (GnRHa) protocol. Endometrial receptivity is a key factor that contributes to this phenomenon.</p><p><strong>Study design, size, duration: </strong>An open label randomized controlled trial (RCT) was performed between November 2021 and August 2022. There were 546 patients allocated to either the modified GnRH antagonist or the conventional antagonist protocol at a 1:1 ratio.</p><p><strong>Participants/materials, setting, methods: </strong>Both IVF and ICSI cycles were included, and the sperm samples used were either fresh or frozen from the partner, or from frozen donor ejaculates. The primary outcome was the LBRs per fresh SET cycle. Secondary outcomes included rates of implantation, clinical and ongoing pregnancy, miscarriage, and ovarian hyperstimulation syndrome (OHSS), as well as clinical outcomes of ovarian stimulation.</p><p><strong>Main results and the role of chance: </strong>Baseline demographic features were not significantly different between the two ovarian stimulation groups. However, in the intention-to-treat (ITT) population, the LBRs in the modified antagonist group were significantly higher than in the conventional group (38.1% [104/273] vs. 27.5% [75/273], relative risk 1.39 [95% CI, 1.09-1.77], P = 0.008). Using a per-protocol (PP) analysis which included all the patients who received an embryo transfer, the LBRs in the modified antagonist group were also significantly higher than in the conventional group (48.6% [103/212] vs. 36.8% [74/201], relative risk 1.32 [95% CI, 1.05-1.66], P = 0.016). The modified antagonist group achieved significantly higher implantation rates, and clinical and ongoing pregnancy rates than the conventional group in both the ITT and PP analyses (P < 0.05). The two groups did not show significant differences between the number of oocytes retrieved or mature oocytes, two-pronuclear zygote (2PN) rates, the number of embryos obtained, blastocyst progression and good-quality embryo rates, early miscarriage rates, or OHSS incidence rates (P > 0.05).</p><p><strong>Limitations, reasons for caution: </strong>A limitation of our study was that the subjects were not blinded to the treatment allocation in the RCT tria
研究问题:在促性腺激素释放激素(GnRH)拮抗剂方案中使用促性腺激素(Gn)降阶法,并在卵巢反应正常的患者施用 hCG 当日(hCG 日)停止使用 GnRH 拮抗剂,能否提高新鲜选择性单胚胎移植(eSET)后的妊娠结局?使用 Gn 降阶梯方法和在 hCG 日停止 GnRH 拮抗剂的改良 GnRH 拮抗剂方案可有效提高每个新鲜 eSET 周期的活产率(LBR):目前,关于最佳的 GnRH 拮抗剂方案尚未达成共识。研究表明,与长GnRH激动剂(GnRHa)方案相比,新鲜GnRH拮抗剂周期的妊娠结局较差。子宫内膜接受能力是导致这一现象的关键因素:2021年11月至2022年8月期间进行了一项开放标签随机对照试验(RCT)。共有546名患者按1:1的比例被分配到改良GnRH拮抗剂或传统拮抗剂方案中:试管婴儿和卵胞浆内单精子显微注射周期均包括在内,所使用的精子样本为来自伴侣的新鲜或冷冻精子,或来自冷冻捐献者射精的精子。主要结果是每个新鲜 SET 周期的 LBRs。次要结果包括植入率、临床和持续妊娠率、流产率、卵巢过度刺激综合征(OHSS)以及卵巢刺激的临床结果:两个卵巢刺激组的基线人口学特征无明显差异。然而,在意向治疗(ITT)人群中,改良拮抗剂组的LBR显著高于常规组(38.1% [104/273] vs. 27.5% [75/273],相对风险1.39 [95% CI, 1.09-1.77],P = 0.008)。按方案(PP)分析包括所有接受胚胎移植的患者,改良拮抗剂组的 LBR 也明显高于常规组(48.6% [103/212] vs. 36.8% [74/201],相对风险 1.32 [95% CI, 1.05-1.66],P = 0.016)。在ITT和PP分析中,改良拮抗剂组的植入率、临床妊娠率和持续妊娠率均显著高于常规组(P 0.05):我们研究的一个局限性是,在 RCT 试验中,受试者对治疗分配没有盲法。只有预后良好的 40 岁以下女性被纳入分析。因此,在卵巢储备功能低下的老年患者中使用改良拮抗剂方案仍有待研究。此外,第 5 天选择性 SET 的样本量较小,因此需要更大规模的试验来加强这些研究结果:研究经费/竞争权益:采用Gn阶梯式下降方法和在hCG日停止使用GnRH拮抗剂的改良GnRH拮抗剂方案提高了正常反应者每个新鲜eSET周期的LBRs:本项目由国家重点研发计划项目 2022YFC2702503 和北京健康促进会项目 2021140 资助。作者声明无利益冲突:该 RCT 已在中国临床试验注册中心注册;研究编号:ChiCTR2100053453:ChiCTR2100053453.试验注册日期:2021年11月21日.首例患者入组日期:2021年11月23日.
{"title":"A modified flexible GnRH antagonist protocol using antagonist early cessation and a gonadotropin step-down approach improves live birth rates in fresh cycles: a randomized controlled trial.","authors":"Bei Xu, Dirk Geerts, Jiaying Yuan, Mengting Wang, Zhou Li, Qiaohong Lai, Yu Zheng, Si Liu, Shulin Yang, Guijin Zhu, Lei Jin","doi":"10.1093/humrep/deae145","DOIUrl":"10.1093/humrep/deae145","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;Can pregnancy outcomes following fresh elective single embryo transfer (eSET) in gonadotropin-releasing hormone (GnRH) antagonist protocols increase using a gonadotropin (Gn) step-down approach with cessation of GnRH antagonist on the day of hCG administration (hCG day) in patients with normal ovarian response?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;The modified GnRH antagonist protocol using the Gn step-down approach and cessation of GnRH antagonist on the hCG day is effective in improving live birth rates (LBRs) per fresh eSET cycle.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;Currently, there is no consensus on optimal GnRH antagonist regimens. Studies have shown that fresh GnRH antagonist cycles result in poorer pregnancy outcomes than the long GnRH agonist (GnRHa) protocol. Endometrial receptivity is a key factor that contributes to this phenomenon.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;An open label randomized controlled trial (RCT) was performed between November 2021 and August 2022. There were 546 patients allocated to either the modified GnRH antagonist or the conventional antagonist protocol at a 1:1 ratio.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, setting, methods: &lt;/strong&gt;Both IVF and ICSI cycles were included, and the sperm samples used were either fresh or frozen from the partner, or from frozen donor ejaculates. The primary outcome was the LBRs per fresh SET cycle. Secondary outcomes included rates of implantation, clinical and ongoing pregnancy, miscarriage, and ovarian hyperstimulation syndrome (OHSS), as well as clinical outcomes of ovarian stimulation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;Baseline demographic features were not significantly different between the two ovarian stimulation groups. However, in the intention-to-treat (ITT) population, the LBRs in the modified antagonist group were significantly higher than in the conventional group (38.1% [104/273] vs. 27.5% [75/273], relative risk 1.39 [95% CI, 1.09-1.77], P = 0.008). Using a per-protocol (PP) analysis which included all the patients who received an embryo transfer, the LBRs in the modified antagonist group were also significantly higher than in the conventional group (48.6% [103/212] vs. 36.8% [74/201], relative risk 1.32 [95% CI, 1.05-1.66], P = 0.016). The modified antagonist group achieved significantly higher implantation rates, and clinical and ongoing pregnancy rates than the conventional group in both the ITT and PP analyses (P &lt; 0.05). The two groups did not show significant differences between the number of oocytes retrieved or mature oocytes, two-pronuclear zygote (2PN) rates, the number of embryos obtained, blastocyst progression and good-quality embryo rates, early miscarriage rates, or OHSS incidence rates (P &gt; 0.05).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Limitations, reasons for caution: &lt;/strong&gt;A limitation of our study was that the subjects were not blinded to the treatment allocation in the RCT tria","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141467613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The impact of type 2 diabetes on polycystic ovary syndrome in patients undergoing sleeve gastrectomy. 2 型糖尿病对袖状胃切除术患者多囊卵巢综合征的影响。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae159
Tao Zhu, Yian Zhao, Xiaocheng Bi, Peikai Zhao, Teng Liu, Yuxuan Li, Shumin Li, Shigang Zhao, Shaozhuang Liu, Xin Huang
<p><strong>Study question: </strong>Does the concurrent type 2 diabetes mellitus (T2DM) aggravate the features and prognosis of PCOS in patients undergoing sleeve gastrectomy (SG)?</p><p><strong>Summary answer: </strong>For patients undergoing SG with obesity, concurrent T2DM is associated with aggravated metabolic but milder reproductive features of PCOS and did not attenuate the resumption of regular menstruation for up to 1 year after surgery.</p><p><strong>What is known already: </strong>Women with T2DM have an increased risk of PCOS. However, whether concurrent T2DM further increases the disease burden and treatment difficulty of PCOS in patients with obesity requires further investigation.</p><p><strong>Study design, size, duration: </strong>This was a single-center, two-arm, prospective, cohort study enrolling a total of 329 women with PCOS and scheduled for SG because of obesity at an university-affiliated hospital between January 2020 and August 2023, with a 1-year follow-up after surgery.</p><p><strong>Participants/materials, setting, methods: </strong>Comparisons were made between patients with T2DM (PCOS+T2DM) and without (PCOS) to examine the impact of T2DM on the metabolic, reproductive, and psychological features of PCOS. The follow-up data of weight loss and menstruation were analyzed to determine the impact of T2DM on PCOS prognosis for up to 1 year after SG.</p><p><strong>Main results and the role of chance: </strong>After controlling for confounders, patients in the PCOS+T2DM group (n = 98) showed more severe insulin resistance, glucose intolerance, dyslipidemia, and non-alcoholic fatty liver disease (NAFLD) (NAFLD activity score 4.31 ± 1.15 versus 3.52 ± 1.42, P < 0.001) than those in the PCOS group (n = 149). In addition, the PCOS+T2DM group had a lower level of total testosterone (1.63 ± 0.69 versus 1.82 ± 0.76, P = 0.045), a lower ratio between luteinizing hormone and follicle-stimulating hormone (median 1.48 versus 1.68, P = 0.030), and a lower proportion of patients with polycystic ovarian morphology (88% versus 96%, P = 0.022) than the PCOS group. As a result, the two groups differed significantly in terms of the Rotterdam classification of PCOS (P = 0.009). No significant difference was detected by group in the psychological features of PCOS except a lower degree of emotional eating in the PCOS+T2DM group (P = 0.001). Although the PCOS+T2DM group took longer to resume regular menstruation after SG (P = 0.037), the two groups had similar proportions of patients with regular menstruation (85% versus 87%, P = 0.758) 1 year after SG, which was further confirmed by subgroup analyses by body mass index.</p><p><strong>Limitations, reasons for caution: </strong>The prognosis of PCOS after SG mainly focused on the results of menstruation rather than a complete evaluation of the remission of the disease.</p><p><strong>Wider implications of the findings: </strong>Our study showed that, for patients with obesity, concurrent T2DM is
研究问题:在接受袖带胃切除术(SG)的患者中,并发2型糖尿病(T2DM)是否会加重多囊卵巢综合征的特征和预后?对于接受袖带胃切除术的肥胖患者来说,并发 T2DM 与多囊卵巢综合征的代谢特征加重有关,但生殖特征较轻,而且在术后长达 1 年的时间里,T2DM 并不影响正常月经的恢复:已知信息:患有 T2DM 的女性患 PCOS 的风险更高。然而,并发 T2DM 是否会进一步增加肥胖患者多囊卵巢综合征的疾病负担和治疗难度,还需要进一步研究:这是一项单中心、双臂、前瞻性、队列研究,在 2020 年 1 月至 2023 年 8 月期间,在一所大学附属医院共纳入 329 名因肥胖而计划接受 SG 治疗的 PCOS 女性患者,术后随访 1 年:对患有 T2DM(多囊卵巢综合征+T2DM)和未患有 T2DM(多囊卵巢综合征)的患者进行比较,以研究 T2DM 对多囊卵巢综合征的代谢、生殖和心理特征的影响。对体重减轻和月经情况的随访数据进行了分析,以确定 T2DM 对多囊卵巢综合征预后的影响,最长可达 SG 后 1 年:在控制了混杂因素后,PCOS+T2DM组(n = 98)的患者表现出更严重的胰岛素抵抗、葡萄糖不耐受、血脂异常和非酒精性脂肪肝(NAFLD)(NAFLD活动评分为4.31 ± 1.15对3.52 ± 1.42,P 局限性,需谨慎的原因):SG治疗后多囊卵巢综合征的预后主要集中在月经结果上,而不是对疾病缓解情况的全面评估:我们的研究表明,对于肥胖症患者而言,并发 T2DM 与多囊卵巢综合征的代谢特征加重但生殖特征较轻有关,而且在术后长达 1 年的时间里,T2DM 并不影响正常月经的恢复。我们的研究还强调,需要进行高质量的研究,更全面地评估T2DM对SG术后多囊卵巢综合征患者预后的影响:本研究由国家自然科学基金(82100853)、山东省自然科学基金(ZR2021QH028)和山东大学临床研究项目(2020SDUCRCC024)资助。作者无利益冲突:中国临床试验注册中心,注册号:ChiCTR1900026845。
{"title":"The impact of type 2 diabetes on polycystic ovary syndrome in patients undergoing sleeve gastrectomy.","authors":"Tao Zhu, Yian Zhao, Xiaocheng Bi, Peikai Zhao, Teng Liu, Yuxuan Li, Shumin Li, Shigang Zhao, Shaozhuang Liu, Xin Huang","doi":"10.1093/humrep/deae159","DOIUrl":"10.1093/humrep/deae159","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;Does the concurrent type 2 diabetes mellitus (T2DM) aggravate the features and prognosis of PCOS in patients undergoing sleeve gastrectomy (SG)?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;For patients undergoing SG with obesity, concurrent T2DM is associated with aggravated metabolic but milder reproductive features of PCOS and did not attenuate the resumption of regular menstruation for up to 1 year after surgery.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;Women with T2DM have an increased risk of PCOS. However, whether concurrent T2DM further increases the disease burden and treatment difficulty of PCOS in patients with obesity requires further investigation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;This was a single-center, two-arm, prospective, cohort study enrolling a total of 329 women with PCOS and scheduled for SG because of obesity at an university-affiliated hospital between January 2020 and August 2023, with a 1-year follow-up after surgery.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, setting, methods: &lt;/strong&gt;Comparisons were made between patients with T2DM (PCOS+T2DM) and without (PCOS) to examine the impact of T2DM on the metabolic, reproductive, and psychological features of PCOS. The follow-up data of weight loss and menstruation were analyzed to determine the impact of T2DM on PCOS prognosis for up to 1 year after SG.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;After controlling for confounders, patients in the PCOS+T2DM group (n = 98) showed more severe insulin resistance, glucose intolerance, dyslipidemia, and non-alcoholic fatty liver disease (NAFLD) (NAFLD activity score 4.31 ± 1.15 versus 3.52 ± 1.42, P &lt; 0.001) than those in the PCOS group (n = 149). In addition, the PCOS+T2DM group had a lower level of total testosterone (1.63 ± 0.69 versus 1.82 ± 0.76, P = 0.045), a lower ratio between luteinizing hormone and follicle-stimulating hormone (median 1.48 versus 1.68, P = 0.030), and a lower proportion of patients with polycystic ovarian morphology (88% versus 96%, P = 0.022) than the PCOS group. As a result, the two groups differed significantly in terms of the Rotterdam classification of PCOS (P = 0.009). No significant difference was detected by group in the psychological features of PCOS except a lower degree of emotional eating in the PCOS+T2DM group (P = 0.001). Although the PCOS+T2DM group took longer to resume regular menstruation after SG (P = 0.037), the two groups had similar proportions of patients with regular menstruation (85% versus 87%, P = 0.758) 1 year after SG, which was further confirmed by subgroup analyses by body mass index.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Limitations, reasons for caution: &lt;/strong&gt;The prognosis of PCOS after SG mainly focused on the results of menstruation rather than a complete evaluation of the remission of the disease.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Wider implications of the findings: &lt;/strong&gt;Our study showed that, for patients with obesity, concurrent T2DM is","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141619868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Moonshot. Long shot. Or sure shot. What needs to happen to realize the full potential of AI in the fertility sector? 登月。长镜头。还是万无一失?要充分发挥人工智能在生育领域的潜力,需要做些什么?
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae144
Gerard Letterie

Quality healthcare requires two critical components: patients' best interests and best decisions to achieve that goal. The first goal is the lodestar, unchanged and unchanging over time. The second component is a more dynamic and rapidly changing paradigm in healthcare. Clinical decision-making has transitioned from an opinion-based paradigm to an evidence-based and data-driven process. A realization that technology and artificial intelligence can bring value adds a third component to the decision process. And the fertility sector is not exempt. The debate about AI is front and centre in reproductive technologies. Launching the transition from a conventional provider-driven decision paradigm to a software-enhanced system requires a roadmap to enable effective and safe implementation. A key nodal point in the ascending arc of AI in the fertility sector is how and when to bring these innovations into the ART routine to improve workflow, outcomes, and bottom-line performance. The evolution of AI in other segments of clinical care would suggest that caution is needed as widespread adoption is urged from several fronts. But the lure and magnitude for the change that these tech tools hold for fertility care remain deeply engaging. Exploring factors that could enhance thoughtful implementation and progress towards a tipping point (or perhaps not) should be at the forefront of any 'next steps' strategy. The objective of this Opinion is to discuss four critical areas (among many) considered essential to successful uptake of any new technology. These four areas include value proposition, innovative disruption, clinical agency, and responsible computing.

优质医疗服务需要两个关键要素:患者的最佳利益和实现这一目标的最佳决策。第一个目标是长期不变的标准。第二个要素则是医疗保健中更动态、更快速变化的范式。临床决策已从基于意见的模式过渡到基于证据和数据的流程。人们认识到技术和人工智能可以为决策过程带来价值,这为决策过程增添了第三个组成部分。生育领域也不例外。关于人工智能的讨论是生殖技术领域的焦点。要从传统的由医疗服务提供者驱动的决策模式过渡到软件增强型系统,需要制定一个路线图,以便有效、安全地实施。人工智能在生育领域的上升弧线中的一个关键节点是,如何以及何时将这些创新引入 ART 常规,以改善工作流程、结果和底线绩效。人工智能在其他临床护理领域的发展表明,在多方面敦促广泛采用人工智能的同时,还需要谨慎行事。但是,这些技术工具对生育保健的诱惑和变革的幅度仍然令人深感兴趣。在任何 "下一步 "战略中,最重要的是探索能促进深思熟虑的实施和迈向临界点(或许不会)的因素。本《意见书》旨在讨论被认为对任何新技术的成功应用都至关重要的四个关键领域(在众多领域中)。这四个方面包括价值主张、创新颠覆、临床代理和负责任的计算。
{"title":"Moonshot. Long shot. Or sure shot. What needs to happen to realize the full potential of AI in the fertility sector?","authors":"Gerard Letterie","doi":"10.1093/humrep/deae144","DOIUrl":"10.1093/humrep/deae144","url":null,"abstract":"<p><p>Quality healthcare requires two critical components: patients' best interests and best decisions to achieve that goal. The first goal is the lodestar, unchanged and unchanging over time. The second component is a more dynamic and rapidly changing paradigm in healthcare. Clinical decision-making has transitioned from an opinion-based paradigm to an evidence-based and data-driven process. A realization that technology and artificial intelligence can bring value adds a third component to the decision process. And the fertility sector is not exempt. The debate about AI is front and centre in reproductive technologies. Launching the transition from a conventional provider-driven decision paradigm to a software-enhanced system requires a roadmap to enable effective and safe implementation. A key nodal point in the ascending arc of AI in the fertility sector is how and when to bring these innovations into the ART routine to improve workflow, outcomes, and bottom-line performance. The evolution of AI in other segments of clinical care would suggest that caution is needed as widespread adoption is urged from several fronts. But the lure and magnitude for the change that these tech tools hold for fertility care remain deeply engaging. Exploring factors that could enhance thoughtful implementation and progress towards a tipping point (or perhaps not) should be at the forefront of any 'next steps' strategy. The objective of this Opinion is to discuss four critical areas (among many) considered essential to successful uptake of any new technology. These four areas include value proposition, innovative disruption, clinical agency, and responsible computing.</p>","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141534319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction: Placental structural adaptation to maternal physical activity and sedentary behavior: findings of the DALI lifestyle study. 更正:胎盘结构对母体运动和久坐行为的适应性:DALI 生活方式研究的结果。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae173
{"title":"Correction: Placental structural adaptation to maternal physical activity and sedentary behavior: findings of the DALI lifestyle study.","authors":"","doi":"10.1093/humrep/deae173","DOIUrl":"10.1093/humrep/deae173","url":null,"abstract":"","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11373336/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141792334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Survey on ART and IUI: legislation, regulation, funding, and registries in European countries-an update. 抗逆转录病毒疗法和人工授精调查:欧洲国家的立法、法规、资金和登记--最新情况。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae163
C Calhaz-Jorge, J Smeenk, C Wyns, D De Neubourg, D P Baldani, C Bergh, I Cuevas-Saiz, Ch De Geyter, M S Kupka, K Rezabek, A Tandler-Schneider, V Goossens
<p><strong>Study question: </strong>How are ART and IUI regulated, funded, and registered in European countries, and how has the situation changed since 2018?</p><p><strong>Summary answer: </strong>Of the 43 countries performing ART and IUI in Europe, and participating in the survey, specific legislation exists in only 39 countries, public funding varies across and sometimes within countries (and is lacking or minimal in four countries), and national registries are in place in 33 countries; only a small number of changes were identified, most of them in the direction of improving accessibility, through increased public financial support and/or opening access to additional subgroups.</p><p><strong>What is known already: </strong>The annual reports of the European IVF-Monitoring Consortium (EIM) clearly show the existence of different approaches across Europe regarding accessibility to and efficacy of ART and IUI treatments. In a previous survey, some coherent information was gathered about how those techniques were regulated, funded, and registered in European countries, showing that diversity is the paradigm in this medical field.</p><p><strong>Study design, size, duration: </strong>A survey was designed using the SurveyMonkey tool consisting of 90 questions covering several domains (legal, funding, and registry) and considering specific details on the situation of third-party donations. New questions widened the scope of the previous survey. Answers refer to the situation of countries on 31 December 2022.</p><p><strong>Participants/materials, settings, methods: </strong>All members of the EIM were invited to participate. The received answers were checked and initial responders were asked to address unclear answers and to provide any additional information considered relevant. Tables resulting from the consolidated data were then sent to members of the Committee of National Representatives of ESHRE, requesting a second check. Conflicting information was clarified by direct contact.</p><p><strong>Main results and the role of chance: </strong>Information was received from 43 out of the 45 European countries where ART and IUI are performed. There were 39 countries with specific legislation on ART, and artificial insemination was considered an ART technique in 33 of them. Accessibility is limited to infertile couples only in 8 of the 43 countries. In 5 countries, ART and IUI are permitted also for treatments of single women and all same sex couples, while a total of 33 offer treatment to single women and 19 offer treatment to female couples. Use of donated sperm is allowed in all except 2 countries, oocyte donation is allowed in 38, simultaneous donation of sperm and oocyte is allowed in 32, and embryo donation is allowed in 29 countries. Preimplantation genetic testing (PGT)-M/SR (for monogenetic disorders, structural rearrangements) is not allowed in 3 countries and PGT-A (for aneuploidy) is not allowed in 10; surrogacy is accepted in 15 countries.
研究问题:欧洲国家对 ART 和 IUI 的监管、资助和注册情况如何,2018 年以来情况有何变化?在欧洲开展 ART 和 IUI 并参与调查的 43 个国家中,仅有 39 个国家制定了具体立法,公共资金在各国之间不尽相同,有时在国家内部也不尽相同(有 4 个国家缺乏公共资金或资金极少),有 33 个国家建立了国家注册机构;仅发现了少量变化,其中大多数变化是通过增加公共资金支持和/或向更多亚群体开放获取途径来改善可及性:欧洲试管婴儿监测联合会(EIM)的年度报告清楚地表明,欧洲各国在抗逆转录病毒疗法和人工授精疗法的可及性和疗效方面存在着不同的做法。在之前的一项调查中,我们收集到了一些有关欧洲国家如何监管、资助和注册这些技术的连贯信息,这表明在这一医疗领域存在着多样性:使用 SurveyMonkey 工具设计了一项调查,包括 90 个问题,涉及多个领域(法律、资金和注册),并考虑了第三方捐赠情况的具体细节。新的问题扩大了上次调查的范围。参与者/材料、设置、方法:邀请 EIM 的所有成员参与。对收到的答案进行了核对,并要求初步答复者对不明确的答案进行解释,并提供任何相关的补充信息。然后,将综合数据形成的表格发送给 ESHRE 国家代表委员会成员,要求进行第二次核对。主要结果和偶然性的作用:在进行抗逆转录病毒疗法和人工授精的 45 个欧洲国家中,有 43 个国家提供了相关信息。有 39 个国家制定了有关 ART 的专门法律,其中 33 个国家将人工授精视为 ART 技术。在这 43 个国家中,只有 8 个国家的不育夫妇可以获得人工授精。在 5 个国家, ART 和人工授精也被允许用于治疗单身女性和所有同性夫妇,而总共有 33 个国家为单身女性提供治疗,19 个国家为女性夫妇提供治疗。除 2 个国家外,其他所有国家都允许使用捐献的精子,38 个国家允许捐献卵细胞,32 个国家允许同时捐献精子和卵细胞,29 个国家允许捐献胚胎。3 个国家不允许进行植入前基因检测(PGT)-M/SR(检测单基因遗传疾病、结构重排),10 个国家不允许进行植入前基因检测-A(检测非整倍体);15 个国家接受代孕。除婚姻/性状况外,女性年龄是最常报告的限制合法接受抗逆转录病毒疗法的标准:最小年龄通常定为 18 岁,最大年龄从 42 岁到 54 岁不等,有些国家没有使用数字定义。只有极少数国家规定了男性的最高年龄。在允许第三方捐赠的国家,年龄往往是一个限制性标准(男性最高年龄从 35 岁到 50 岁不等;女性最高年龄从 30 岁到 37 岁不等)。第三方捐献的其他法律限制是同一捐献者所生子女的数量(或在某些国家,同一捐献者所生子女的家庭数量),在 12 个国家,卵细胞捐献数量有上限。各国处理匿名问题的方式多种多样:严格匿名、仅对受捐者匿名(对达到法定成年年龄的儿童不匿名)、混合制度(匿名和非匿名捐献)以及严格的非匿名。对捐献者基因筛查的调查显示,大多数国家都实施了强制性建议或科学建议,将最普遍的遗传疾病排除在外,但也存在明显的多样性。欧洲有 30 多个国家实行报销/补偿制度,其中约有 10 个国家明确规定了可接受的最高金额。公共资助制度的差异极大。有一个国家不向 ART/IUI 患者提供经济援助,有三个国家只提供最低限度的支持。其他国家则规定了提供资助的限制条件,如年龄(女性的最高年龄是最常用的)、是否生育过子女、体重指数、公共资助的最多治疗次数以及无权获得资助的技术。在少数国家,报销与临床政策挂钩。对试管婴儿/卵胞浆内单精子显微注射周期内的费用类型、最高限额以及患者自付费用比例的定义也极为不同。在参与调查的 43 个国家中,有 33 个国家建立了国家抗逆转录病毒疗法登记册,其中 19 个国家建立了捐献者登记册。
{"title":"Survey on ART and IUI: legislation, regulation, funding, and registries in European countries-an update.","authors":"C Calhaz-Jorge, J Smeenk, C Wyns, D De Neubourg, D P Baldani, C Bergh, I Cuevas-Saiz, Ch De Geyter, M S Kupka, K Rezabek, A Tandler-Schneider, V Goossens","doi":"10.1093/humrep/deae163","DOIUrl":"10.1093/humrep/deae163","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;How are ART and IUI regulated, funded, and registered in European countries, and how has the situation changed since 2018?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;Of the 43 countries performing ART and IUI in Europe, and participating in the survey, specific legislation exists in only 39 countries, public funding varies across and sometimes within countries (and is lacking or minimal in four countries), and national registries are in place in 33 countries; only a small number of changes were identified, most of them in the direction of improving accessibility, through increased public financial support and/or opening access to additional subgroups.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;The annual reports of the European IVF-Monitoring Consortium (EIM) clearly show the existence of different approaches across Europe regarding accessibility to and efficacy of ART and IUI treatments. In a previous survey, some coherent information was gathered about how those techniques were regulated, funded, and registered in European countries, showing that diversity is the paradigm in this medical field.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;A survey was designed using the SurveyMonkey tool consisting of 90 questions covering several domains (legal, funding, and registry) and considering specific details on the situation of third-party donations. New questions widened the scope of the previous survey. Answers refer to the situation of countries on 31 December 2022.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, settings, methods: &lt;/strong&gt;All members of the EIM were invited to participate. The received answers were checked and initial responders were asked to address unclear answers and to provide any additional information considered relevant. Tables resulting from the consolidated data were then sent to members of the Committee of National Representatives of ESHRE, requesting a second check. Conflicting information was clarified by direct contact.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;Information was received from 43 out of the 45 European countries where ART and IUI are performed. There were 39 countries with specific legislation on ART, and artificial insemination was considered an ART technique in 33 of them. Accessibility is limited to infertile couples only in 8 of the 43 countries. In 5 countries, ART and IUI are permitted also for treatments of single women and all same sex couples, while a total of 33 offer treatment to single women and 19 offer treatment to female couples. Use of donated sperm is allowed in all except 2 countries, oocyte donation is allowed in 38, simultaneous donation of sperm and oocyte is allowed in 32, and embryo donation is allowed in 29 countries. Preimplantation genetic testing (PGT)-M/SR (for monogenetic disorders, structural rearrangements) is not allowed in 3 countries and PGT-A (for aneuploidy) is not allowed in 10; surrogacy is accepted in 15 countries.","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11373472/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141751542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unexplained infertility and age-related infertility: indistinguishable diagnostic entities but different IVF prognosis. 原因不明的不孕症和年龄相关性不孕症:诊断实体无法区分,但试管婴儿预后不同。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae140
Giulia Mattei, Marco Reschini, Letizia Li Piani, Gianfranco Fornelli, Paola Vigano, Ludovico Muzii, Paolo Vercellini, Edgardo Somigliana
<p><strong>Study question: </strong>Is IVF indicated for couples with age-related infertility?</p><p><strong>Summary answer: </strong>IVF may be of doubtful utility for age-related infertility.</p><p><strong>What is known already: </strong>A diagnosis of unexplained infertility is drawn when the diagnostic work-up fails to identify any patent cause. Although typically managed uniformly, unexplained infertility is likely to comprise a wide range of conditions, including age-related infertility (at least in older women). Unfortunately, no validated tests for the identification of age-related infertility exist and these women are typically treated as unexplained cases. However, homologous ART may be less effective for these women because these techniques may be unable to treat the detrimental effects of ageing on oocyte competence.</p><p><strong>Study design, size, duration: </strong>Women aged 18-42 years who underwent IVF procedures between January 2014 and December 2021 were selected retrospectively. In the first part of the study, we aimed to assess whether the proportion of women with unexplained infertility (i.e. without patent causes of infertility) increased with age. In the second part of the study, women with unexplained infertility were matched 1:1 by age, study period, and duration of infertility, to those with a patent cause of infertility. If our hypothesis is valid, the first part of the study should highlight an increase in the proportion of unexplained infertility with age. Moreover, in the second part of the study, one should observe a sharper decrease in the rate of IVF success of the procedure with age in women with an unremarkable work-up compared to those with a definite cause of infertility.</p><p><strong>Participants/materials, setting, methods: </strong>Women were included if: they had been trying to conceive for more than 2 years, they had retrieved more than three oocytes, and had not undergone previous IVF attempts. We exclude couples with severe male factor (criptozoospermia), chronic anovulation, untreated hydrosalpinx, or intracavitary diseases. The first part of the study aimed at investigating the relative proportion of unexplained infertility with age. The outcome of the second part was the distribution of the live births between unexplained versus explained infertility, in women younger or older than 35 years. Only the results of the first IVF cycle were considered (including both fresh and frozen cycles). The live birth rate corresponded to the cumulative chance of a live birth per oocyte retrieval.</p><p><strong>Main results and the role of chance: </strong>One thousand five hundred and thirty-five women were selected for the first part of the study; 742 of them had unexplained infertility (48%). The frequency of this diagnosis was lower among women aged <35 years (40%) compared to those ≥35 years (52%) (P < 0.001). A clear gradient emerged when considering smaller intervals of age (P < 0.001). A total of 1134 wo
研究问题:试管婴儿是否适用于老年性不孕症夫妇?试管婴儿对高龄相关性不孕症的作用值得怀疑:当诊断工作未能找到任何明确的原因时,就会诊断为原因不明的不孕症。虽然不明原因的不孕症通常是统一管理的,但它可能包含多种情况,包括与年龄相关的不孕症(至少在老年妇女中)。遗憾的是,目前还没有有效的检测方法来识别与年龄相关的不孕症,因此这些妇女通常被视为不明原因的病例。然而,同源抗逆转录病毒疗法对这些女性的效果可能较差,因为这些技术可能无法治疗衰老对卵母细胞能力的不利影响:研究设计、规模和持续时间:回顾性选取了2014年1月至2021年12月期间接受试管婴儿手术的18-42岁女性。在研究的第一部分,我们旨在评估不明原因不孕(即无明确不孕原因)的女性比例是否会随着年龄的增长而增加。在研究的第二部分,根据年龄、研究时间和不孕持续时间,将不明原因不孕的妇女与有明确不孕原因的妇女进行1:1配对。如果我们的假设成立,那么研究的第一部分应突出显示,随着年龄的增长,不明原因不孕症的比例会增加。此外,在研究的第二部分,我们应该观察到,与有明确不孕原因的妇女相比,检查结果无异常的妇女的试管婴儿成功率会随着年龄的增长而急剧下降:如果妇女尝试怀孕的时间超过 2 年,取回的卵母细胞超过 3 个,且之前未尝试过试管婴儿,则将其纳入研究范围。我们排除了患有严重男性因素(无精子症)、慢性无排卵、未治疗的鞘膜积液或腔内疾病的夫妇。研究的第一部分旨在调查不明原因不孕症随年龄增长的相对比例。第二部分的研究结果是,在 35 岁以下或 35 岁以上的妇女中,原因不明的不孕症与原因不明的不孕症之间的活产分布情况。研究只考虑了第一个试管婴儿周期的结果(包括新鲜周期和冷冻周期)。活产率与每次取卵的活产累积几率相对应:第一部分研究选取了 1535 名妇女,其中 742 人(48%)患有原因不明的不孕症。在年龄较大的妇女中,这一诊断的频率较低:我们推测,原因不明组的试管婴儿成功率随着年龄的增长而下降,这可能与年龄相关性不孕症妇女比例的增加有关。然而,即使这在理论上是符合逻辑的,但由于缺乏诊断高龄相关性不孕症的有效工具,我们的推断也是推测性的。我们不能排除其他不明原因的不孕症的发病率也会随着年龄的增长而增加,而这些原因也无法通过试管婴儿有效克服:我们的研究结果表明,试管婴儿对于治疗与年龄有关的不孕症可能有一定的作用。对于不孕症检查结果无异常的高龄妇女,是否提供这种治疗可能会受到质疑。然而,年龄相关性不孕症的诊断仍具有挑战性,因此确定一种能可靠诊断年龄相关性不孕症的生物标志物是当务之急:该研究部分由意大利卫生部--当前研究IRCCS资助,并由Ferring提供专项资助。ES 声明从 IBSA 和 Gedeon-Richter 处获得会议演讲酬金,他还从 Ferring、IBSA、Theramex 和 Gedeon-Richter 处获得私人研究基金。所有其他作者均无任何利益冲突需要声明:不适用。
{"title":"Unexplained infertility and age-related infertility: indistinguishable diagnostic entities but different IVF prognosis.","authors":"Giulia Mattei, Marco Reschini, Letizia Li Piani, Gianfranco Fornelli, Paola Vigano, Ludovico Muzii, Paolo Vercellini, Edgardo Somigliana","doi":"10.1093/humrep/deae140","DOIUrl":"10.1093/humrep/deae140","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Study question: &lt;/strong&gt;Is IVF indicated for couples with age-related infertility?&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Summary answer: &lt;/strong&gt;IVF may be of doubtful utility for age-related infertility.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;What is known already: &lt;/strong&gt;A diagnosis of unexplained infertility is drawn when the diagnostic work-up fails to identify any patent cause. Although typically managed uniformly, unexplained infertility is likely to comprise a wide range of conditions, including age-related infertility (at least in older women). Unfortunately, no validated tests for the identification of age-related infertility exist and these women are typically treated as unexplained cases. However, homologous ART may be less effective for these women because these techniques may be unable to treat the detrimental effects of ageing on oocyte competence.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study design, size, duration: &lt;/strong&gt;Women aged 18-42 years who underwent IVF procedures between January 2014 and December 2021 were selected retrospectively. In the first part of the study, we aimed to assess whether the proportion of women with unexplained infertility (i.e. without patent causes of infertility) increased with age. In the second part of the study, women with unexplained infertility were matched 1:1 by age, study period, and duration of infertility, to those with a patent cause of infertility. If our hypothesis is valid, the first part of the study should highlight an increase in the proportion of unexplained infertility with age. Moreover, in the second part of the study, one should observe a sharper decrease in the rate of IVF success of the procedure with age in women with an unremarkable work-up compared to those with a definite cause of infertility.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Participants/materials, setting, methods: &lt;/strong&gt;Women were included if: they had been trying to conceive for more than 2 years, they had retrieved more than three oocytes, and had not undergone previous IVF attempts. We exclude couples with severe male factor (criptozoospermia), chronic anovulation, untreated hydrosalpinx, or intracavitary diseases. The first part of the study aimed at investigating the relative proportion of unexplained infertility with age. The outcome of the second part was the distribution of the live births between unexplained versus explained infertility, in women younger or older than 35 years. Only the results of the first IVF cycle were considered (including both fresh and frozen cycles). The live birth rate corresponded to the cumulative chance of a live birth per oocyte retrieval.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main results and the role of chance: &lt;/strong&gt;One thousand five hundred and thirty-five women were selected for the first part of the study; 742 of them had unexplained infertility (48%). The frequency of this diagnosis was lower among women aged &lt;35 years (40%) compared to those ≥35 years (52%) (P &lt; 0.001). A clear gradient emerged when considering smaller intervals of age (P &lt; 0.001). A total of 1134 wo","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141436778","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An expert opinion on rescuing atypically pronucleated human zygotes by molecular genetic fertilization checks in IVF. 关于在试管婴儿中通过分子遗传受精检查挽救非典型去核人类合子的专家意见。
IF 6 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2024-09-01 DOI: 10.1093/humrep/deae157
Antonio Capalbo, Danilo Cimadomo, Giovanni Coticchio, Christian Simon Ottolini

IVF laboratories routinely adopt morphological pronuclear assessment at the zygote stage to identify abnormally fertilized embryos deemed unsuitable for clinical use. In essence, this is a pseudo-genetic test for ploidy motivated by the notion that biparental diploidy is required for normal human life and abnormal ploidy will lead to either failed implantation, miscarriage, or significant pregnancy complications, including molar pregnancy and chorionic carcinoma. Here, we review the literature associated with ploidy assessment of human embryos derived from zygotes displaying a pronuclear configuration other than the canonical two, and the related pregnancy outcome following transfer. We highlight that pronuclear assessment, although associated with aberrant ploidy outcomes, has a low specificity in the prediction of abnormal ploidy status in the developing embryo, while embryos deemed abnormally fertilized can yield healthy pregnancies. Therefore, this universal strategy of pronuclear assessment invariably leads to incorrect classification of over 50% of blastocysts derived from atypically pronucleated zygotes, and the systematic disposal of potentially viable embryos in IVF. To overcome this limitation of current practice, we discuss the new preimplantation genetic testing technologies that enable accurate identification of the ploidy status of preimplantation embryos and suggest a progress from morphology-based checks to molecular fertilization check as the new gold standard. This alternative molecular fertilization checking represents a possible non-incremental and controversy-free improvement to live birth rates in IVF as it adds to the pool of viable embryos available for transfer. This is especially important for the purposes of 'family building' or for poor-prognosis IVF patients where embryo numbers are often limited.

试管婴儿实验室通常会在胚胎阶段进行形态学原核评估,以识别被认为不适合临床使用的异常受精胚胎。从本质上讲,这是一种假遗传学的倍性检测,其动机是双亲二倍体是正常人类生命的必需条件,而异常倍性将导致植入失败、流产或重大妊娠并发症,包括臼齿妊娠和绒毛膜癌。在此,我们回顾了有关人类胚胎倍性评估的文献,这些胚胎来自于显示非标准双核构型的子代胚胎,以及移植后的相关妊娠结果。我们强调,尽管代核评估与异常倍性结果有关,但在预测发育中胚胎的异常倍性状态方面特异性较低,而被视为异常受精的胚胎可产生健康的妊娠。因此,这种通用的前核评估策略必然会导致 50%以上来自非典型前核合子的囊胚被错误分类,并在体外受精中系统地处理潜在的可行胚胎。为了克服当前做法的这一局限性,我们讨论了能准确鉴定植入前胚胎倍性状态的植入前基因检测新技术,并建议从基于形态学的检查发展到分子受精检查作为新的黄金标准。这种可供选择的分子受精检查可增加可供移植的存活胚胎数量,从而提高试管婴儿的活产率,而且不会增加费用,也不会引起争议。这对于 "建立家庭 "或预后不良的试管婴儿患者尤为重要,因为胚胎数量往往有限。
{"title":"An expert opinion on rescuing atypically pronucleated human zygotes by molecular genetic fertilization checks in IVF.","authors":"Antonio Capalbo, Danilo Cimadomo, Giovanni Coticchio, Christian Simon Ottolini","doi":"10.1093/humrep/deae157","DOIUrl":"10.1093/humrep/deae157","url":null,"abstract":"<p><p>IVF laboratories routinely adopt morphological pronuclear assessment at the zygote stage to identify abnormally fertilized embryos deemed unsuitable for clinical use. In essence, this is a pseudo-genetic test for ploidy motivated by the notion that biparental diploidy is required for normal human life and abnormal ploidy will lead to either failed implantation, miscarriage, or significant pregnancy complications, including molar pregnancy and chorionic carcinoma. Here, we review the literature associated with ploidy assessment of human embryos derived from zygotes displaying a pronuclear configuration other than the canonical two, and the related pregnancy outcome following transfer. We highlight that pronuclear assessment, although associated with aberrant ploidy outcomes, has a low specificity in the prediction of abnormal ploidy status in the developing embryo, while embryos deemed abnormally fertilized can yield healthy pregnancies. Therefore, this universal strategy of pronuclear assessment invariably leads to incorrect classification of over 50% of blastocysts derived from atypically pronucleated zygotes, and the systematic disposal of potentially viable embryos in IVF. To overcome this limitation of current practice, we discuss the new preimplantation genetic testing technologies that enable accurate identification of the ploidy status of preimplantation embryos and suggest a progress from morphology-based checks to molecular fertilization check as the new gold standard. This alternative molecular fertilization checking represents a possible non-incremental and controversy-free improvement to live birth rates in IVF as it adds to the pool of viable embryos available for transfer. This is especially important for the purposes of 'family building' or for poor-prognosis IVF patients where embryo numbers are often limited.</p>","PeriodicalId":13003,"journal":{"name":"Human reproduction","volume":null,"pages":null},"PeriodicalIF":6.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141751541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Human reproduction
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1