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The association between single nucleotide polymorphism in interleukin-27 gene and recurrent pregnancy loss in Iranian women. 伊朗妇女白介素-27基因单核苷酸多态性与复发性流产的关系
Zeinab Nematollahi, Hossein Hadinedoushan, Abbas Aflatoonian, Gilda Eslami, Nasrin Ghasemi

Background: Recurrent pregnancy loss (RPL) has been defined as two or more miscarriages before 20(th) week of gestation. It seems that IL-27 may reduce inflammatory responses and affect the survival of the embryo during human pregnancy. IL-27 polymorphisms may influence RPL by altering the levels or the activity of gene product.

Objective: We studied for the first time the association of IL-27 -964 A>G single nucleotide polymorphism (SNP) with RPL in Iranian women.

Materials and methods: A case-controlled study was performed on two groups consisting of 150 healthy women with at least one delivery (control group) and 150 women with two or more primary RPLs history (RPL group). The -964 A>G SNP in IL-27 gene was determined by PCR-RFLP technique. Genotype and allele frequencies were compared using (2) tests between two groups.

Results: There was no difference between the two groups regarding age of women (29±4.4 [control] vs. 30.84±5.2 years [case]). In the RPL group, the genotype frequencies of -964 A>G polymorphism were AG (49.3%), AA (40%), and GG (10.7%), and in the control group, they were AG (43.3%), AA (48.7%), and GG (8%). There was no significant difference between the genotypes of AA, AG, and GG in two groups (p=0.23). As the frequency of allele A was 64.7% in the RPL group and 70.3% in the control group, the difference in frequency of allele A in -964 A>G between two groups was not significant (p=0.19).

Conclusion: Our findings indicate that SNP of -964 A>G in IL-27 gene is not a risk factor for RPL in Iranian women.

背景:复发性妊娠丢失(RPL)被定义为妊娠20周前两次或两次以上流产。IL-27可能会减少妊娠期间的炎症反应并影响胚胎的存活。IL-27多态性可能通过改变基因产物的水平或活性来影响RPL。目的:首次研究伊朗女性IL-27 - 964a >G单核苷酸多态性(SNP)与RPL的关系。材料和方法:病例对照研究分为两组,包括150名至少有一次分娩的健康妇女(对照组)和150名有两次或两次以上原发性RPL史的妇女(RPL组)。采用PCR-RFLP技术检测IL-27基因- 964a >G SNP。采用(2)试验比较两组间基因型和等位基因频率。结果:两组女性年龄无差异(对照组29±4.4岁,病例30.84±5.2岁)。RPL组-964 A>G多态性基因型频率为AG(49.3%)、AA(40%)和GG(10.7%),对照组为AG(43.3%)、AA(48.7%)和GG(8%)。两组患者AA、AG、GG基因型差异无统计学意义(p=0.23)。RPL组A等位基因频率为64.7%,对照组为70.3%,两组间-964 A>G中A等位基因频率差异无统计学意义(p=0.19)。结论:IL-27基因-964 A>G的SNP不是伊朗女性RPL的危险因素。
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引用次数: 0
SULF 1 gene polymorphism, rs6990375 is in significant association with fetus failure in IVF technique. sulf1基因多态性rs6990375与体外受精胎儿失败有显著相关性。
Eskandar Taghizadeh, Seyed Mehdi Kalantar, Reza Mahdian, Mohammad Hasan Sheikhha, Ehsan Farashahi-Yazd, Saeed Ghasemi, Zahra Shahbazi

Background: Sulfatase 1 (SULF1) function is to remove the 6-O-sulphate group from heparan sulfate. This action changes the binding sites of extracellular growth factors. SULF1 expression has been reported to be changed in angiogenesis. We hypothesized that single nucleotide polymorphisms (SNPs) of SULF1 would impact clinicopathologic characteristics.

Objective: Study of SULF1 gene polymorphism with fetus failure in in vitro fertilization (IVF) technique.

Materials and methods: We studied one common (minor allele frequency >0.05) regulatory SNP, rs6990375, with polymerase chain reaction and restriction fragment length polymorphism method, in 53 infertile women with fetus failure in IVF technique and 53 women with at least one healthy child as controls.

Results: We found that rs6990375 is significantly associated with an early failure in IVF and frequency of G allele is high in women with fetus failure in IVF technique (p<0.001).

Conclusion: These findings suggest that SULF1genetic variations may play a role in IVF technique fetus failure. Further studies with large sample sizes on SULF1 SNPs may be useful in support of this claim.

背景:磺化酶1 (SULF1)的功能是去除硫酸肝素中的6- o -硫酸盐基团。这一作用改变了细胞外生长因子的结合位点。据报道,SULF1的表达在血管生成中发生改变。我们假设SULF1的单核苷酸多态性(snp)会影响临床病理特征。目的:探讨体外受精(IVF)技术中SULF1基因多态性与胎儿失败的关系。材料与方法:采用聚合酶链反应和限制性片段长度多态性方法,对53例IVF技术胎儿失败的不孕妇女和53例至少有一个健康孩子的妇女进行了rs6990375共同(次要等位基因频率>0.05)调控SNP的研究。结果:我们发现rs6990375与体外受精早期失败显著相关,G等位基因在体外受精胎儿失败女性中出现频率高(p)。结论:这些发现提示suls1基因变异可能在体外受精胎儿失败中起作用。进一步的大样本量SULF1 snp研究可能有助于支持这一说法。
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引用次数: 0
Granulocyte colony-stimulating factor and reproductive medicine: A review. 粒细胞集落刺激因子与生殖医学研究进展。
Marcelo Borges Cavalcante, Fabrício DA Silva Costa, Ricardo Barini, E Araujo Júnior

Background: Recently, the use of granulocyte colony-stimulating factor (G-CSF) has been proposed to improve pregnancy outcomes in reproductive medicine.

Objective: A systematic review of the current use of G-CSF in patients who have difficulty conceiving and maintaining pregnancy was performed.

Materials and methods: Two electronic databases (PubMed/ Medline and Scopus) were searched. Study selection, data extraction and quality assessment were performed in duplicate. The subject codes used were granulocyte colony-stimulating factor, G-CSF, recurrent miscarriage, IVF failure, and endometrium.

Results: The search of electronic databases resulted in 215 citations (PubMed/ Medline: 139 and Scopus: 76), of which 38 were present in both databases. Of the remaining 177 publications, seven studies were included in the present review.

Conclusion: Treatment with G-CSF is a novel proposal for immune therapy in patients with recurrent miscarriage and implantation failure following cycles of IVF. However, a larger number of well-designed studies are required for this treatment to be established.

背景:近年来,粒细胞集落刺激因子(G-CSF)在生殖医学中被提出用于改善妊娠结局。目的:系统回顾目前在妊娠和维持妊娠困难患者中使用G-CSF的情况。材料与方法:检索PubMed/ Medline和Scopus两个电子数据库。研究选择、数据提取和质量评估一式两份。使用的受试者代码是粒细胞集落刺激因子、G-CSF、复发性流产、IVF失败和子宫内膜。结果:在电子数据库中检索到215篇引文(PubMed/ Medline: 139篇,Scopus: 76篇),其中38篇在两个数据库中均存在。在其余177份出版物中,本综述包括了7份研究报告。结论:G-CSF治疗是体外受精周期后复发性流产和着床失败患者的一种新的免疫治疗方案。然而,要建立这种治疗方法,还需要大量精心设计的研究。
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引用次数: 0
Comparison of serum 25-hydroxy vitamin D levels between mothers with small for gestational age and appropriate for gestational age newborns in Kerman. 克尔曼地区小胎龄与适宜胎龄新生儿母亲血清25-羟基维生素D水平的比较
Fatemeh Mirzaei, Tayebeh Amiri Moghadam, Peyman Arasteh

Background: Vitamin D deficiency during pregnancy is associated with some adverse pregnancy outcomes but its relationship with fetal growth is unknown.

Objective: We compared the 25-hydroxy vitamin D levels between mothers and their small for gestational age (SGA) newborns with mothers and their appropriate for gestational age (AGA) newborns.

Materials and methods: The study population included pregnant women that referred to Afzalipour Hospital in Kerman from 2012 to 2013. The case and control group consisted of 40 pregnant mothers with SGA and AGA newborns, respectively. The maternal and infants 25-hydroxy vitamin D levels were measured in the two groups.

Results: 25-hydroxy vitamin D deficiency (<20 ng/ml) was statistically higher in women with SGA newborns in comparison to women with AGA newborns (p=0.003).Vitamin D deficiency was higher among the SGA newborns in comparison to AGA newborns (25% vs. 17.5%), although this finding was not statistically meaningful (p=0.379). The relationship of vitamin D deficiency levels between mothers and infants in both the SGA group and the AGA group was significant.

Conclusion: Our study reveals a high prevalence of vitamin D deficiency in women with SGA infants in comparison to women with AGA children. In addition, maternal vitamin D deficiency is associated with its deficiency in newborns.

背景:妊娠期维生素D缺乏与一些不良妊娠结局有关,但其与胎儿生长的关系尚不清楚。目的:比较母亲及其小胎龄(SGA)新生儿与母亲及其适宜胎龄(AGA)新生儿的25羟基维生素D水平。材料和方法:研究人群包括2012年至2013年在克尔曼Afzalipour医院转诊的孕妇。病例组和对照组分别由40名患有SGA和AGA新生儿的孕妇组成。测定两组产妇和婴儿的25-羟基维生素D水平。结论:我们的研究表明,与AGA儿童相比,SGA婴儿中维生素D缺乏症的发生率较高。此外,母亲缺乏维生素D与新生儿缺乏维生素D有关。
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引用次数: 0
Assessment of the relationship of basal serum anti-mullerian hormone levels with oocyte quality and pregnancy outcomes in patients undergoing ICSI. 评估ICSI患者基础血清抗苗勒管激素水平与卵母细胞质量和妊娠结局的关系。
Gültekin Adanaş Aydın, Arzu Yavuz, Hasan Terzi, Tayfun Kutlu

Background: Anti-Mullerian hormone (AMH) is constantly secreted during menstrual cycles and may offer several advantages over traditional biomarkers of ovarian reserve.

Objective: To assess the relationship of anti-Mullerian hormone (AMH) values, which are used to evaluate ovary reserves, with oocyte and embryo quality and with ART outcomes in patients undergoing intra-cytoplasmic sperm injection (ICSI).

Materials and methods: This cross sectional study was performed using 50 women undergoing ICSI in IVF center of Zeynep Kamil Women's and Children's Hospital, İstanbul, Turkey. All patients received the long protocol. Follicle-stimulating hormone, luteinizing hormone, estradiol, and AMH levels were measured and antral follicle counts were obtained on the 3(rd) day of menstruation. A cut-off value based on the number of oocytes was determined for AMH, and women were evaluated after being divided into two groups as bad responders and good responders, according to their AMH levels.

Results: Twelve (27.3%) women were in bad responders group and 32 (72.7%) women were in good responders group. AMH measurements were statistically significantly different between the two groups (p<0.01). Based on this significance, the researchers used ROC analysis to estimate a cut-off point for AMH. The researchers detected the good responders with an AMH level 1.90 or above, with 87.50% sensitivity, 66.67% specificity, 87.50% positive prediction, and 66.67% negative prediction (AUC=0.777, p<0.01).

Conclusion: Basal AMH levels can be used as an indicator to determine the ovarian response in women undergoing ICSI. AMH can be used to predict the number of mature oocytes that can be collected during treatment and the number of oocytes that can be fertilized. However, AMH is not a valuable tool to evaluate oocyte quality, the development of high-quality embryos, or pregnancy conception.

背景:抗苗勒管激素(AMH)在月经周期中不断分泌,与传统的卵巢储备生物标志物相比,它可能具有许多优势。目的:探讨行胞浆内精子注射(ICSI)患者抗苗勒管激素(AMH)值与卵母细胞和胚胎质量及抗逆转录病毒治疗效果的关系。材料和方法:本横断面研究是在土耳其Zeynep Kamil妇女儿童医院(İstanbul) IVF中心进行的50名接受ICSI的妇女。所有患者都接受了长方案。在月经第3天测定促卵泡激素、黄体生成素、雌二醇和AMH水平,并测定窦腔卵泡计数。根据AMH的卵母细胞数量确定一个临界值,并根据她们的AMH水平将妇女分为两组,分别为不良反应者和良好反应者。结果:不良反应组12例(27.3%),良好反应组32例(72.7%)。结论:基础AMH水平可作为判断ICSI患者卵巢反应的一个指标。AMH可以用来预测在治疗过程中可以收集到的成熟卵母细胞的数量和可以受精的卵母细胞的数量。然而,AMH并不是评估卵母细胞质量、高质量胚胎发育或妊娠的有价值的工具。
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引用次数: 0
Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders. 缺乏DRD3和CNR1多态性与经前焦虑症的关联。
Mesut Yıldız, Mehmet Vural, Mehmet Emin Erdal, Özlem İzci Ay, Şenay Görücü Yılmaz, İbrahim Fatih Karababa, Salih Selek

Background: Premenstrual dysphoric disorder (PMDD) is a mood disorder characterized with physical and affective symptoms during the luteal phase of susceptible women.

Objective: The aim of this study was to investigate the association of Dopamine D3 receptor (DRD3) polymorphism, and Cannabinoid receptor Type 1 (CNR1) polymorphism with PMDD.

Materials and methods: Fifty one participants with documented PMDD according to the DSM IV criteria and 51 healthy controls were included in this cross sectional study. Symptom severity was measured with daily self-rating, monthly premenstrual assessment forms and psychiatric interviews. The genotyping of DRD3 receptor and Cannabinoid type 1 receptors were performed using Taqmanfluorogenic assay method.

Results: Distribution of DRD3 and CNR1 polymorphism was not different between patients and controls.

Conclusion: These findings do not support a major role of DRD3, and CNR1 polymorphisms in contributing to susceptibility to premenstrual dysphoric disorder.

背景:经前烦躁不安障碍(PMDD)是一种情绪障碍,其特征是易受影响的女性在黄体期出现身体和情感症状。目的:探讨多巴胺D3受体(DRD3)多态性和大麻素受体1型(CNR1)多态性与PMDD的关系。材料和方法:本横断面研究包括51名符合DSM IV标准的经前不悦症患者和51名健康对照者。通过每日自评、每月经前评估表和精神病学访谈来测量症状严重程度。采用Taqmanfluorogenic assay法对DRD3受体和大麻素1型受体进行基因分型。结果:DRD3和CNR1多态性在患者和对照组之间的分布无明显差异。结论:这些发现不支持DRD3和CNR1多态性在促进经前焦虑症易感性中的主要作用。
{"title":"Lack of association of DRD3 and CNR1 polymorphisms with premenstrual dysphoric disorders.","authors":"Mesut Yıldız,&nbsp;Mehmet Vural,&nbsp;Mehmet Emin Erdal,&nbsp;Özlem İzci Ay,&nbsp;Şenay Görücü Yılmaz,&nbsp;İbrahim Fatih Karababa,&nbsp;Salih Selek","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Premenstrual dysphoric disorder (PMDD) is a mood disorder characterized with physical and affective symptoms during the luteal phase of susceptible women.</p><p><strong>Objective: </strong>The aim of this study was to investigate the association of Dopamine D3 receptor (DRD3) polymorphism, and Cannabinoid receptor Type 1 (CNR1) polymorphism with PMDD.</p><p><strong>Materials and methods: </strong>Fifty one participants with documented PMDD according to the DSM IV criteria and 51 healthy controls were included in this cross sectional study. Symptom severity was measured with daily self-rating, monthly premenstrual assessment forms and psychiatric interviews. The genotyping of DRD3 receptor and Cannabinoid type 1 receptors were performed using Taqmanfluorogenic assay method.</p><p><strong>Results: </strong>Distribution of DRD3 and CNR1 polymorphism was not different between patients and controls.</p><p><strong>Conclusion: </strong>These findings do not support a major role of DRD3, and CNR1 polymorphisms in contributing to susceptibility to premenstrual dysphoric disorder.</p>","PeriodicalId":14673,"journal":{"name":"Iranian Journal of Reproductive Medicine","volume":"13 4","pages":"221-6"},"PeriodicalIF":0.0,"publicationDate":"2015-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475771/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33868441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anti-mullerian hormon level and polycystic ovarian syndrome diagnosis. 抗苗勒管激素水平与多囊卵巢综合征的诊断。
Shahrzad Zadehmodarres, Zahra Heidar, Zahra Razzaghi, Leili Ebrahimi, Kaveh Soltanzadeh, Farhang Abed

Background: Polycystic ovarian syndrome (PCOS) is a common endocrinopathy that accompanied with long term complications. The early diagnosis of this syndrome can prevent it.

Objective: The aim was to determine the role of anti-mullerian hormon (AMH) in PCOS diagnosis and to find cut off level of it.

Materials and methods: In this cross sectional study, 117 women between 20-40 years old were participated in two groups: 60 PCOS women (based on Rotterdam criteria consensus) as the case group and 57 normal ovulatory women as the control group. In day 2-4 of cycle, transvaginal sonography was performed and serum hormonal level of AMH, luteinizing hormone (LH), follicle stimulating hormone (FSH), estradiol (E2), testosterone, fasting blood sugar (FBS), thyroid stimulating hormone (TSH), and prolactin (PRL) were measured in all of participants. For all of them score of hirsutism (base on Freeman-Galloway scoring) was determined.

Results: There were statistically significant in irregular pattern of menstruation, AMH and FSH level, and presence of hirsutism between two groups. But regarding mean of age, body mass index, plasma level of PRL, TSH, LH, Testosterone, FBS, and E2 differences were not significant. Construction by ROC curve present 3.15 ng/ml as AMH cut off with 70.37% sensitivity and 77.36% specificity in order to PCOS diagnosis.

Conclusion: AMH with cut off level of 3.15 ng/ml with sensitivity 70.37% and specificity 77.36% could use for early diagnosis of PCOS patients.

背景:多囊卵巢综合征(PCOS)是一种常见的内分泌疾病,长期伴有并发症。这种综合征的早期诊断可以预防它。目的:探讨抗苗勒管激素(AMH)在多囊卵巢综合征(PCOS)诊断中的作用,并寻找其临界值。材料与方法:本横断面研究选取年龄在20-40岁的117名女性,分为两组:60名PCOS女性(基于鹿特丹标准共识)为病例组,57名正常排卵女性为对照组。在月经周期第2-4天行阴道超声检查,测定所有受试者血清AMH、促黄体生成素(LH)、促卵泡激素(FSH)、雌二醇(E2)、睾酮、空腹血糖(FBS)、促甲状腺激素(TSH)、催乳素(PRL)水平。以Freeman-Galloway评分法测定多毛症评分。结果:两组患者月经不规律、AMH、FSH水平及多毛现象比较,差异均有统计学意义。但在平均年龄、体质指数、血浆PRL、TSH、LH、睾酮、FBS、E2水平方面差异无统计学意义。ROC曲线构建为3.15 ng/ml, AMH诊断PCOS的敏感性为70.37%,特异性为77.36%。结论:AMH截断水平为3.15 ng/ml,敏感性为70.37%,特异性为77.36%,可用于PCOS患者的早期诊断。
{"title":"Anti-mullerian hormon level and polycystic ovarian syndrome diagnosis.","authors":"Shahrzad Zadehmodarres,&nbsp;Zahra Heidar,&nbsp;Zahra Razzaghi,&nbsp;Leili Ebrahimi,&nbsp;Kaveh Soltanzadeh,&nbsp;Farhang Abed","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Polycystic ovarian syndrome (PCOS) is a common endocrinopathy that accompanied with long term complications. The early diagnosis of this syndrome can prevent it.</p><p><strong>Objective: </strong>The aim was to determine the role of anti-mullerian hormon (AMH) in PCOS diagnosis and to find cut off level of it.</p><p><strong>Materials and methods: </strong>In this cross sectional study, 117 women between 20-40 years old were participated in two groups: 60 PCOS women (based on Rotterdam criteria consensus) as the case group and 57 normal ovulatory women as the control group. In day 2-4 of cycle, transvaginal sonography was performed and serum hormonal level of AMH, luteinizing hormone (LH), follicle stimulating hormone (FSH), estradiol (E2), testosterone, fasting blood sugar (FBS), thyroid stimulating hormone (TSH), and prolactin (PRL) were measured in all of participants. For all of them score of hirsutism (base on Freeman-Galloway scoring) was determined.</p><p><strong>Results: </strong>There were statistically significant in irregular pattern of menstruation, AMH and FSH level, and presence of hirsutism between two groups. But regarding mean of age, body mass index, plasma level of PRL, TSH, LH, Testosterone, FBS, and E2 differences were not significant. Construction by ROC curve present 3.15 ng/ml as AMH cut off with 70.37% sensitivity and 77.36% specificity in order to PCOS diagnosis.</p><p><strong>Conclusion: </strong>AMH with cut off level of 3.15 ng/ml with sensitivity 70.37% and specificity 77.36% could use for early diagnosis of PCOS patients.</p>","PeriodicalId":14673,"journal":{"name":"Iranian Journal of Reproductive Medicine","volume":"13 4","pages":"227-30"},"PeriodicalIF":0.0,"publicationDate":"2015-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475772/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34248844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Types of reproductive disorders in underweight and overweight young females and correlations of respective hormonal changes with BMI. 体重过轻和超重年轻女性生殖障碍类型及各自激素变化与BMI的相关性。
Nutsa Aladashvili-Chikvaidze, Jenara Kristesashvili, Manana Gegechkori

Background: Higher risks of reproductive problems have been found in underweight and overweight women with rapid weight gain or loss but evidence is inconsistent especially in relation to the effect of age of body weight changes.

Objective: The aim of our study was to detect the peculiarities of menstrual function, prevalence of different types of reproductive disorders and correlations of respective hormonal changes with body mass index (BMI) in young female patients with thinness or obesity since childhood.

Materials and methods: In this prospective cross-sectional study 48 underweight and 55 overweight/obese young women with different reproductive problems underwent complete clinical and hormonal analyses. All 103 patients had weight problems since childhood.

Results: Polycystic ovarian syndrome and metabolic syndrome was the most frequent in overweight and obese women, whilst non-classical congenital adrenal hyperplasia and ovarian dysfunction prevailed in underweight women (p˂0.001). No difference was determined according to the age of menarche (p=0.885) and types of menstrual disturbances (p=0.34) between the study groups. Hypogonadotropic hypogonadism was not found in young women who were lean since childhood. Follicle-stimulating hormone (FSH) (p=0.013) and sex hormone binging globulin (SHBG) (p˂0.001) levels were higher in women with low BMI, whilst free testosterone (FT) (p=0.019) and total testosterone (TT) (p=0.003) levels were higher in high BMI participants. BMI negatively correlated with FSH (p=0.009) and SHBG (p=0.001); and positively correlated with FT (p=0.001) and TT (p=0.002).

Conclusion: Peculiarities of menstrual function and hormonal changes in young women with thinness or obesity since childhood are related to the types of reproductive disorders and their childhood BMI.

背景:在体重迅速增加或减少的体重过轻和超重妇女中发现生殖问题的风险较高,但证据不一致,特别是在年龄对体重变化的影响方面。目的:探讨自幼偏瘦或肥胖的年轻女性患者月经功能的特点、不同类型生殖障碍的患病率以及各自激素变化与体重指数(BMI)的相关性。材料和方法:在这项前瞻性横断面研究中,48名体重不足和55名超重/肥胖的年轻女性患有不同的生殖问题,对她们进行了完整的临床和激素分析。所有103例患者从小就有体重问题。结果:多囊卵巢综合征和代谢综合征在超重和肥胖女性中最常见,而非典典性先天性肾上腺增生和卵巢功能障碍在体重不足的女性中最常见(p小于0.001)。根据月经初潮年龄(p=0.885)和月经紊乱类型(p=0.34),各组间无差异。从小就瘦的年轻女性没有发现促性腺激素减退症。低BMI的女性卵泡刺激素(FSH) (p=0.013)和性激素暴球蛋白(SHBG) (p小于0.001)水平较高,而高BMI的女性游离睾酮(FT) (p=0.019)和总睾酮(TT) (p=0.003)水平较高。BMI与FSH (p=0.009)、SHBG (p=0.001)呈负相关;与FT (p=0.001)、TT (p=0.002)呈正相关。结论:从小开始偏瘦或偏胖的年轻女性月经功能及激素变化的特殊性与生殖障碍类型及儿童期BMI有关。
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引用次数: 0
Association of assisted reproductive technology with adverse pregnancy outcomes. 辅助生殖技术与不良妊娠结局的关系。
Zhang Jie, Ding Yiling, Yu Ling

Background: More and more infertile patients have accepted the assisted reproductive technique (ART) therapy. Concerns have been raised over an increased risk of adverse maternal outcomes in ART populations as compared with natural conception (NC).

Objective: The aim was to improve the ART in clinicial work and to reduce the incidence of pregnancy complications in ART group according to analyzing the reasons of high incidence of pregnancy complications in ART group, comparing the incidence of pregnancy complications in different controlled ovarian hyperstimulation (COH) programs and evaluating the effects of ART which attribute to adverse pregnancy outcomes.

Materials and methods: In this prospective population-based cohort study,3216 pregnant women with gestational age ≤12 weeks, regular antenatal examination,and ultrasound identification of intrauterine pregnancy were enrolled from January 2010 to June 2013. According to having ART history, the participantswere divided into two groups: ART group (contains fresh embryo transfer group or frozen-thawed embryo transfer group) and NC group. We compared the incidence of pregnancy complications between different groups and evaluated the factors which could affect the occurrence of these complications.

Results: When compared to NC group, significantly increased rates of gestational diabetes mellitus (GDM) (p<0.01), preeclampsia (PE) (p<0.01) and intrahepatic cholestasis of pregnancy (ICP) (p˂0.01) were observed in ART group. There was no significant difference in the incidence of birth defect between the two groups (p=0.07). Multiple pregnancies and Gonadotropin (Gn) were risk factors in GDM, PE, and ICP. The exogenous progesterone treatment had no effect on GDM, PE or ICP.

Conclusion: ART increases the risk of adverse maternal complications such as GDM, PE and ICP. The dosages of Gn should be reduced to an extent and the number of embryo implantation should be controlled. Exogenous progesterone treatment is safe.

背景:越来越多的不孕患者接受了辅助生殖技术(ART)治疗。与自然受孕(NC)相比,ART人群中孕产妇不良结局的风险增加,这引起了人们的关注:目的:通过分析 ART 组妊娠并发症高发的原因,比较不同控制性卵巢过度刺激(COH)方案的妊娠并发症发生率,评估导致不良妊娠结局的 ART 的影响,从而改进 ART 的临床工作,降低 ART 组妊娠并发症的发生率:在这项基于人群的前瞻性队列研究中,2010年1月至2013年6月期间,3216名孕龄≤12周、定期进行产前检查并经超声检查发现宫内妊娠的孕妇被纳入研究。根据有无 ART 史,将参与者分为两组:ART组(包含新鲜胚胎移植组或冷冻解冻胚胎移植组)和NC组。我们比较了不同组间妊娠并发症的发生率,并评估了可能影响这些并发症发生的因素:结果:与 NC 组相比,妊娠期糖尿病(GDM)的发生率明显增加(p):抗逆转录病毒疗法会增加孕产妇出现不良并发症的风险,如 GDM、PE 和 ICP。应在一定程度上减少 Gn 的用量,并控制胚胎植入的数量。外源性黄体酮治疗是安全的。
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引用次数: 0
Intrauterine synechiae after myomectomy; laparotomy versus laparoscopy: Non-randomized interventional trial. 子宫肌瘤切除术后宫内粘连;剖腹手术与腹腔镜手术:非随机介入试验。
Zahra Asgari, Leili Hafizi, Rayhaneh Hosseini, Atiyeh Javaheri, Hathis Rastad

Background: Leiomyomata is the most frequent gynecological neoplasm. One of the major complications of myomectomy is intrauterine adhesion (synechiae).

Objective: To evaluate and compare the rate and severity of synechiae formation after myomectomy by laparotomy and laparoscopy.

Materials and methods: In this non-randomized interventional trial, hysteroscopy was performed in all married fertile women who had undergone myomectomy (type 3-6 interamural and subserosal fibroids) via laparotomy and laparoscopy in Tehran's Arash Hospital from 2010 to 2013. Three months after the operation, the occurrence rate and severity of intrauterine synechiae, and its relationship with type, number and location of myomas were investigated and compared in both groups.

Results: Forty patients (19 laparoscopy and 21 laparotomy cases) were studied. Both groups were similar regarding the size, type (subserosal or intramural), number and location of myoma. The occurrence rate of synechiae in the laparoscopy and laparotomy group was 21% and 19%, respectively; showing no significant difference (p=0.99). Among all patients, no significant relationship was found between the endometrial opening (p=0.92), location (p=0.14) and type of myoma (p=0.08) with the occurrence rate of synechiae. However, a significant relationship was observed between myoma's size (p=0.01) and the location of the largest myoma with the occurrence of synechiae (p=0.02).

Conclusion: With favorable suturing methods, the outcome of intrauterine synechiae formation after myomectomy, either performed by laparotomy or laparoscopy, is similar. In all cases of myomectomy in reproductive-aged women, postoperative hysteroscopy is highly recommended to better screen intrauterine synechiae.

背景:平滑肌瘤是最常见的妇科肿瘤。子宫肌瘤切除术的主要并发症之一是子宫内粘连(粘连)。目的:比较剖腹和腹腔镜子宫肌瘤切除术后粘连的发生率和严重程度。材料和方法:在这项非随机介入性试验中,2010年至2013年在德黑兰Arash医院通过剖腹和腹腔镜进行子宫肌瘤切除术(3-6型壁间和浆膜下肌瘤)的所有已婚育龄妇女均行宫腔镜检查。术后3个月,比较两组患者宫内粘连发生率、严重程度及其与肌瘤类型、数量、部位的关系。结果:40例患者中腹腔镜19例,开腹21例。两组肌瘤的大小、类型(浆膜下或膜内)、数量和位置相似。腹腔镜组和开腹组的粘连发生率分别为21%和19%;无统计学差异(p=0.99)。在所有患者中,子宫内膜开口(p=0.92)、位置(p=0.14)和肌瘤类型(p=0.08)与粘连发生率无显著关系。然而,肌瘤的大小(p=0.01)和最大肌瘤的位置与粘连的发生有显著关系(p=0.02)。结论:在良好的缝合方法下,子宫肌瘤切除术后宫内粘连形成的结果,无论是剖腹手术还是腹腔镜手术,都是相似的。在所有育龄妇女子宫肌瘤切除术的病例中,强烈建议术后宫腔镜检查以更好地筛查宫内粘连。
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Iranian Journal of Reproductive Medicine
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