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Meta-analysis of the efficacy of different blue light therapy methods for neonatal jaundice. 不同蓝光疗法对新生儿黄疸疗效的 Meta 分析。
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-01 Epub Date: 2024-11-25 DOI: 10.1080/14767058.2024.2430649
Ruoya Wu, Lingling Wen

Objective: To analyze and evaluate the efficacy of different blue light therapy methods and provide evidence-based recommendations for their selection in clinical practice.

Methods: Clinical randomized controlled trials (RCTs) evaluating the efficacy of various blue light therapy methods for neonatal jaundice were retrieved from both domestic and international databases. The search period covered the inception of each database until November 2023. After screening, the quality of the included studies was assessed using the Cochrane Risk of Bias tool. Literature management was conducted with NoteExpress 3.2, while data collection and extraction were performed using Excel 2003. Statistical analysis was carried out using RevMan 5.4.1. Heterogeneity was assessed using the Q test (p value), and the OR value of the combined effect was calculated using either a fixed-effects or random effects model, depending on the presence of heterogeneity. A forest plot was generated to visualize the results. Sensitivity analysis was performed by excluding the largest-weighted study, and the potential for bias in outcome indicators was assessed using a funnel plot.

Results: A total of 652 articles were retrieved, with 16 clinical RCTs meeting the inclusion criteria. The meta-analysis results indicated that, compared to continuous blue light therapy in the control group, intermittent blue light therapy achieved a higher total effective rate (OR = 1.82, 95%CI (1.25-2.64), p = .002), significantly lower serum bilirubin levels post-treatment (OR = -14.59, 95%CI (-26.11 to -3.08), p = .01), and a shorter time to jaundice resolution (OR = -2.35, 95%CI (-3.83 to -0.87), p = .002). Additionally, the incidence of adverse reactions was lower in the intermittent therapy group compared to the control group (OR = 0.27, 95%CI (0.19-0.36), p < .00001). Sensitivity analysis confirmed that the combined effect size was stable and reliable (OR (95%CI) = -16.23 (-28.67 to -3.79), p = .01). The funnel plot suggested potential publication bias.

Conclusions: Intermittent blue light therapy is effective and demonstrates significant clinical benefits, making it a valuable treatment option for neonatal jaundice in clinical practice.

目的分析和评估不同蓝光治疗方法的疗效,并为临床实践中选择这些方法提供循证建议:从国内外数据库中检索评估各种蓝光疗法对新生儿黄疸疗效的临床随机对照试验(RCT)。检索时间从各数据库建立之初至 2023 年 11 月。筛选后,使用 Cochrane 偏倚风险工具评估了纳入研究的质量。文献管理使用 NoteExpress 3.2,数据收集和提取使用 Excel 2003。统计分析使用 RevMan 5.4.1 进行。使用 Q 检验(P 值)评估异质性,并根据是否存在异质性,使用固定效应或随机效应模型计算综合效应的 OR 值。生成森林图以直观显示结果。通过排除权重最大的研究进行敏感性分析,并使用漏斗图评估结果指标偏倚的可能性:结果:共检索到 652 篇文章,其中 16 项临床研究符合纳入标准。荟萃分析结果表明,与对照组的持续蓝光疗法相比,间歇蓝光疗法的总有效率更高(OR = 1.82,95%CI (1.25-2. 64),P = .002)。64),p = .002),治疗后血清胆红素水平显著降低(OR = -14.59,95%CI (-26.11 to -3.08),p = .01),黄疸消退时间更短(OR = -2.35,95%CI (-3.83 to -0.87),p = .002)。此外,与对照组相比,间歇治疗组的不良反应发生率较低(OR = 0.27,95%CI (0.19-0.36),P = .01)。漏斗图显示可能存在发表偏差:间歇性蓝光疗法有效,临床疗效显著,是临床上治疗新生儿黄疸的重要选择。
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引用次数: 0
Association of pre-/early pregnancy high blood pressure and pregnancy outcomes: a systemic review and meta-analysis. 孕前/孕早期高血压与妊娠结局的关系:系统回顾和荟萃分析。
IF 1.8 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2023-12-27 DOI: 10.1080/14767058.2023.2296366
Ming Jin, Xiaowen Liu, Xiaojing Liu, Yaxian Wu, Yali Zhang, Le Zhang, Zhiwen Li, Rongwei Ye, Nan Li

Background: Maternal high blood pressure (BP) was associated with adverse pregnancy outcomes. This study aimed to synthesize evidence on the association between high BP prior to or in early pregnancy with maternal and fetal complications.

Methods: We searched the cohort studies assessing the effect of high BP in the Medline, Embase, Web of Science and China National Knowledge Internet databases. A random-effects model was used to estimate the pooled odds ratios (ORs) with 95% confidence intervals (CIs). The protocol was registered in PROSPERRO (CRD 42023414945).

Results: 23 eligible studies were identified. High BP prior to or in early pregnancy was associated with higher odds of hypertensive disorders of pregnancy (OR 2.90, 95% CI 1.91-3.89), gestational hypertension (2.56, 2.01-3.12), preeclampsia (3.20, 2.66-3.74), gestational diabetes mellitus (1.71, 1.36-2.06), preterm birth (1.66, 1.39-1.93), stillbirth (2.01, 1.45-2.58) and neonatal intensive care unit admission (1.22, 1.08-1.37). Subgroup analyses indicated that pre-hypertension could significantly increase the odds of these outcomes except for stillbirth, though the odds were lower than hypertension.

Conclusions: High BP prior to or in early pregnancy was associated with adverse pregnancy outcomes and this association increased with hypertension severity. The findings emphasized an urgent need for heightened surveillance for maternal BP, especially pre-hypertensive status.

背景:孕产妇高血压(BP)与不良妊娠结局有关。本研究旨在总结孕前或孕早期高血压与母体和胎儿并发症之间关系的证据:我们在 Medline、Embase、Web of Science 和中国知网数据库中检索了评估高血压影响的队列研究。采用随机效应模型估算出合并的几率比(ORs)及 95% 的置信区间(CIs)。研究方案已在 PROSPERRO(CRD 42023414945)上注册。孕前或孕早期血压高与妊娠高血压疾病(OR 2.90,95% CI 1.91-3.89)、妊娠高血压(2.56,2.01-3.12)、子痫前期(3.20,2.66-3.74)、妊娠糖尿病(1.71,1.36-2.06)、早产(1.66,1.39-1.93)、死胎(2.01,1.45-2.58)和新生儿重症监护室入院(1.22,1.08-1.37)。亚组分析表明,除死胎外,高血压前期可显著增加上述结果的几率,但几率低于高血压:结论:孕前或孕早期血压偏高与不良妊娠结局有关,且这种关联随着高血压严重程度的增加而增加。研究结果强调,迫切需要加强对孕产妇血压的监测,尤其是高血压前期状态。
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引用次数: 0
Fetal congenital talipes equinovarus: genomic abnormalities and obstetric follow-up results. 胎儿先天性马蹄内翻足:基因组异常和产科随访结果。
IF 1.8 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2023-12-27 DOI: 10.1080/14767058.2023.2299113
Meiying Cai, Jiansong Lin, Yanting Que, Liangpu Xu, Na Lin, Hailong Huang

Objective: The etiology of congenital talipes equinovarus (CTEV) is unknown, and the relationship between chromosome microdeletion/microduplication and fetal CTEV is rarely reported. In this study, we retrospectively analyzed fetal CTEV to explore the relationship among the CTEV phenotype, chromosome microdeletion/microduplication, and obstetric outcomes.

Methods: Chromosome karyotype analysis and single nucleotide polymorphism (SNP) array were performed for the 68 fetuses with CTEV.

Results: An SNP array was performed for 68 fetuses with CTEV; pathogenic copy number variations (CNVs) were detected in eight cases (11.8%, 8/68). In addition to one case consistent with karyotype analysis, the SNP array revealed seven additional pathogenic CNVs, including three with 22q11.21 microdeletions, two with 17p12p11.2 microduplications, one with 15q11.2 microdeletions, and one with 7q11.23 microduplications. Of the seven cases carrying pathogenic CNVs, three were tested for family genetics; of these, one was de novo, and two were inherited from either the father or mother. In total, 68 fetuses with CTEV were initially identified, of which 66 cases successfully followed-up. Of these, 9 were terminated, 2 died in utero, and 55 were live births. In 9 cases, no clinical manifestations of CTEV were found at birth; the false-positive rate of prenatal ultrasound CTEVdiagnosis was thus 13.6% (9/66).

Conclusion: CTEV was associated with chromosome microdeletion/microduplication, the most common of which was 22q11.21 microdeletion, followed by 17p12p11.2 microduplication. Thus, further genomic detection is recommended for fetuses with CTEV showing no abnormalities on conventional karyotype analysis.

目的:先天性马蹄内翻足(CTEV)的病因不明,染色体微缺失/微重复与胎儿CTEV之间的关系也鲜有报道。在这项研究中,我们对胎儿CTEV进行了回顾性分析,以探讨CTEV表型、染色体微缺失/微重复与产科结局之间的关系:方法:对68名CTEV胎儿进行染色体核型分析和单核苷酸多态性(SNP)阵列分析:结果:对 68 例 CTEV 胎儿进行了 SNP 阵列分析,其中 8 例(11.8%,8/68)检测到致病性拷贝数变异(CNV)。除了一例与核型分析一致的病例外,SNP 阵列还发现了另外七例致病性 CNV,包括三例 22q11.21 微缺失、两例 17p12p11.2 微重复、一例 15q11.2 微缺失和一例 7q11.23 微重复。在 7 例携带致病性 CNV 的病例中,有 3 例进行了家族遗传学检测;其中 1 例为新发病例,2 例为父亲或母亲的遗传病例。共初步鉴定出 68 例患有 CTEV 的胎儿,其中 66 例成功进行了随访。其中 9 例终止妊娠,2 例死于宫内,55 例为活产。有 9 例在出生时未发现 CTEV 的临床表现;因此,产前超声 CTEV 诊断的假阳性率为 13.6%(9/66):结论:CTEV 与染色体微缺失/微重复有关,其中最常见的是 22q11.21 微缺失,其次是 17p12p11.2 微重复。因此,建议对常规核型分析未显示异常的 CTEV 胎儿进行进一步的基因组检测。
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引用次数: 0
Fibrinogen as a potential diagnostic marker for prediction and evaluation of postpartum hemorrhage: a retrospective study. 纤维蛋白原作为预测和评估产后出血的潜在诊断标志物:一项回顾性研究。
IF 1.8 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-01-07 DOI: 10.1080/14767058.2023.2300418
Yanke Zou, Yixiao Jiang, Dawei Zhu, Ling Liu, Xiuhui Zheng, Xing Gu, Changxiao Huang, Li Li

Objective: To investigate whether prenatal fibrinogen (FIB) or other related factors could be utilized to evaluate the risk of postpartum hemorrhage (PPH).

Methods: A retrospective study was conducted in a database from January 2015 to December 2019. A total of 128 patients were enrolled and evaluated with FIB, in which 55 patients were assigned to low FIB and 73 in normal FIB.

Results: According to the volume of blood loss, the mean of the low FIB group (<4 g/L) was markedly higher than that of the normal FIB group (≥4 g/L). Prenatal FIB was negatively correlated with PPH volume. The receiver operating characteristic (ROC) curve results indicated that the value of prenatal FIB was 0.701 to predict refractory PPH.

Conclusions: Prenatal FIB was significantly related to thrombin time (TT), which may be an independent factor to predict the coagulation state of prenatal pregnancy.

目的研究是否可以利用产前纤维蛋白原(FIB)或其他相关因素来评估产后出血(PPH)的风险:在2015年1月至2019年12月的数据库中进行了一项回顾性研究。共有128名患者入选并接受了FIB评估,其中55名患者被分配到低FIB,73名患者被分配到正常FIB:根据失血量,低FIB组的平均值(结论:产前 FIB 与凝血酶时间(TT)明显相关,这可能是预测产前妊娠凝血状态的一个独立因素。
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引用次数: 0
The predictive value of transvaginal cervical length and cervical angle ultrasonography in term delivery outcomes: a cohort study. 经阴道宫颈长度和宫颈角超声波检查对足月分娩结果的预测价值:一项队列研究。
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-19 DOI: 10.1080/14767058.2024.2406344
Ghazal Tajeran, Roya Derakhshan, Fatemeh Jayervand, Maryam Rahimi, Parisa Hajari, Neda Hashemi

Background: Various techniques have been proposed to predict and evaluate the timing and conditions of childbirth in pregnant women at different stages of pregnancy. Providing precise methods for forecasting childbirth status can reduce the burden on the healthcare system. This study aimed to evaluate the predictive value of transvaginal sonography of cervical length (CL) and cervical angle (CA) on full-term delivery outcomes.

Methods: This cohort study analyzed 151 pregnant women between 37 and 42 weeks of gestational age who were treated at Rasoul Akram Hospital affiliated with Iran University of Medical Sciences from June 2023 to January 2024. All Participants received transvaginal examinations. This study evaluated the accuracy of CL and CA by transvaginal sonography in predicting outcomes like vaginal delivery, cesarean section, necessity for labor induction, and the rate of Premature Rupture of Membranes (PROM). The study used the Receiver Operating Characteristic (ROC) curve to determine the optimal cutoff for predicting birth outcomes.

Results: The mean age of the pregnant women was 28.9 ± 4.22 years, while the average duration of pregnancy was 39.8 ± 2.11 weeks. Cesarean delivery was performed on 45 individuals (29.8%) and 106 (70.1%) underwent vaginal delivery. The mean CL overall stood at 21.2 ± 6.4 mm. PROM was observed in 41 cases (27.1%) among full-term pregnancies. A significant difference was noted in mean CL between the cesarean and vaginal delivery groups (24.2 ± 2.4 vs. 20.1 ± 2.1 mm, p = 0.001). The predictive value of a CL measuring 21 mm for cesarean delivery was 72.2% sensitive and 79.1% specific. Similarly, a CL of 22 mm showed 66.6% sensitivity and 80.2% specificity for labor induction. Regarding PROM in full-term pregnancies, a CL assessment demonstrated 59.8% sensitivity and 69.1% specificity. Finally, a CA of 115.2° exhibited 70.3% sensitivity and 78.4% specificity in predicting vaginal delivery.

Conclusion: The present study showed that evaluating CL and CA via transvaginal sonography demonstrated adequate diagnostic accuracy in predicting spontaneous birth, need for labor induction, cesarean delivery, and incidence of PROM in full-term pregnant women. This method is suggested to be an accurate and appropriate way to predict delivery results.

背景:人们提出了各种技术来预测和评估孕妇在不同孕期的分娩时间和条件。提供预测分娩状况的精确方法可减轻医疗系统的负担。本研究旨在评估经阴道超声检查宫颈长度(CL)和宫颈角度(CA)对足月分娩结果的预测价值:这项队列研究分析了 2023 年 6 月至 2024 年 1 月期间在伊朗医科大学附属拉苏尔-阿克拉姆医院接受治疗的 151 名孕龄介于 37 周和 42 周之间的孕妇。所有参与者均接受了经阴道检查。本研究评估了经阴道超声检查的 CL 和 CA 在预测阴道分娩、剖宫产、引产必要性和胎膜早破(PROM)率等结果方面的准确性。研究采用接收者操作特征曲线(ROC)来确定预测分娩结果的最佳临界值:孕妇的平均年龄为(28.9±4.22)岁,平均怀孕时间为(39.8±2.11)周。45人(29.8%)进行了剖宫产,106人(70.1%)进行了阴道分娩。平均CL值为(21.2 ± 6.4)毫米。在足月妊娠中,有 41 例(27.1%)观察到 PROM。剖宫产组和阴道分娩组的平均CL有明显差异(24.2 ± 2.4 vs. 20.1 ± 2.1 mm,p = 0.001)。21毫米的CL对剖宫产的预测价值为72.2%的敏感性和79.1%的特异性。同样,22 毫米的 CL 对引产的敏感性为 66.6%,特异性为 80.2%。关于足月妊娠的 PROM,CL 评估的敏感性为 59.8%,特异性为 69.1%。最后,CA 115.2°在预测阴道分娩方面的敏感性为 70.3%,特异性为 78.4%:本研究表明,通过经阴道超声波检查评估CL和CA,在预测足月孕妇的自然分娩、引产需求、剖宫产和PROM发生率方面具有足够的诊断准确性。这种方法被认为是预测分娩结果的准确而恰当的方法。
{"title":"The predictive value of transvaginal cervical length and cervical angle ultrasonography in term delivery outcomes: a cohort study.","authors":"Ghazal Tajeran, Roya Derakhshan, Fatemeh Jayervand, Maryam Rahimi, Parisa Hajari, Neda Hashemi","doi":"10.1080/14767058.2024.2406344","DOIUrl":"https://doi.org/10.1080/14767058.2024.2406344","url":null,"abstract":"<p><strong>Background: </strong>Various techniques have been proposed to predict and evaluate the timing and conditions of childbirth in pregnant women at different stages of pregnancy. Providing precise methods for forecasting childbirth status can reduce the burden on the healthcare system. This study aimed to evaluate the predictive value of transvaginal sonography of cervical length (CL) and cervical angle (CA) on full-term delivery outcomes.</p><p><strong>Methods: </strong>This cohort study analyzed 151 pregnant women between 37 and 42 weeks of gestational age who were treated at Rasoul Akram Hospital affiliated with Iran University of Medical Sciences from June 2023 to January 2024. All Participants received transvaginal examinations. This study evaluated the accuracy of CL and CA by transvaginal sonography in predicting outcomes like vaginal delivery, cesarean section, necessity for labor induction, and the rate of Premature Rupture of Membranes (PROM). The study used the Receiver Operating Characteristic (ROC) curve to determine the optimal cutoff for predicting birth outcomes.</p><p><strong>Results: </strong>The mean age of the pregnant women was 28.9 ± 4.22 years, while the average duration of pregnancy was 39.8 ± 2.11 weeks. Cesarean delivery was performed on 45 individuals (29.8%) and 106 (70.1%) underwent vaginal delivery. The mean CL overall stood at 21.2 ± 6.4 mm. PROM was observed in 41 cases (27.1%) among full-term pregnancies. A significant difference was noted in mean CL between the cesarean and vaginal delivery groups (24.2 ± 2.4 vs. 20.1 ± 2.1 mm, <i>p</i> = 0.001). The predictive value of a CL measuring 21 mm for cesarean delivery was 72.2% sensitive and 79.1% specific. Similarly, a CL of 22 mm showed 66.6% sensitivity and 80.2% specificity for labor induction. Regarding PROM in full-term pregnancies, a CL assessment demonstrated 59.8% sensitivity and 69.1% specificity. Finally, a CA of 115.2° exhibited 70.3% sensitivity and 78.4% specificity in predicting vaginal delivery.</p><p><strong>Conclusion: </strong>The present study showed that evaluating CL and CA via transvaginal sonography demonstrated adequate diagnostic accuracy in predicting spontaneous birth, need for labor induction, cesarean delivery, and incidence of PROM in full-term pregnant women. This method is suggested to be an accurate and appropriate way to predict delivery results.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"37 1","pages":"2406344"},"PeriodicalIF":1.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142299823","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Dried blood spots-based metabolomic analysis in preterm infants with necrotizing enterocolitis. 基于干血斑的早产儿坏死性小肠结肠炎代谢组学分析
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-20 DOI: 10.1080/14767058.2024.2416610
Tiantian Zhang, Shimin Yang, Ruotong Li, Ruiqian Dong, Hui Zou

Objective: Necrotizing enterocolitis (NEC) is the leading cause of death among premature infants, and there is a lack of specific early diagnostic markers. Blood sampling is expected to better reflect pathophysiological and metabolic changes in systematic illness, but there is a risk of iatrogenic anemia, especially in premature infants. Dried blood spots technique seems to have important advantages compared to whole blood sampling as it requires only 12-15 μL as sample volume. This study aimed to investigate the special metabolomics of preterm neonates at high risk of NEC using dried blood spots.

Methods: Cases and controls were strictly matched 1:1. Dried blood spots (n = 32, 16 cases-16 controls) from newborn screening were subjected to LC-MS/MS. Metabolomic data were analyzed by orthogonal partial least squares-discriminant analysis (OPLS-DA) and univariate/multivariate statistical analysis.

Results: Compared to the control group, the NEC group had a significant reduction in seven amino acids (glycine, alanine, threonine, proline, ornithine, lysine, and asparagine).

Conclusions: The metabolic profile of neonates with NEC differs significantly from that of controls, making possible their separation with the use of targeted (LC-MS/MS) dried blood spots-based metabolomic analysis. Seven specific markers were identified for early detection and intervention.

目的:坏死性小肠结肠炎(NEC)是早产儿死亡的主要原因:坏死性小肠结肠炎(NEC)是早产儿死亡的主要原因,目前还缺乏特异性的早期诊断指标。血液采样有望更好地反映系统性疾病的病理生理和代谢变化,但存在先天性贫血的风险,尤其是早产儿。与全血采样相比,干血点技术似乎具有重要的优势,因为它只需要 12-15 μL 的样本量。本研究旨在利用干血斑技术研究NEC高风险早产儿的特殊代谢组学:方法:病例和对照组严格按 1:1 配对。对新生儿筛查中的干血斑(n = 32,16 例-16 例对照)进行 LC-MS/MS。代谢组数据通过正交偏最小二乘判别分析(OPLS-DA)和单变量/多变量统计分析进行分析:结果:与对照组相比,NEC 组的七种氨基酸(甘氨酸、丙氨酸、苏氨酸、脯氨酸、鸟氨酸、赖氨酸和天冬酰胺)显著减少:结论:患有 NEC 的新生儿的代谢特征与对照组有很大不同,因此可以利用基于干血斑的定向(LC-MS/MS)代谢组学分析将其分离出来。研究发现了七种可用于早期检测和干预的特异性标记物。
{"title":"Dried blood spots-based metabolomic analysis in preterm infants with necrotizing enterocolitis.","authors":"Tiantian Zhang, Shimin Yang, Ruotong Li, Ruiqian Dong, Hui Zou","doi":"10.1080/14767058.2024.2416610","DOIUrl":"https://doi.org/10.1080/14767058.2024.2416610","url":null,"abstract":"<p><strong>Objective: </strong>Necrotizing enterocolitis (NEC) is the leading cause of death among premature infants, and there is a lack of specific early diagnostic markers. Blood sampling is expected to better reflect pathophysiological and metabolic changes in systematic illness, but there is a risk of iatrogenic anemia, especially in premature infants. Dried blood spots technique seems to have important advantages compared to whole blood sampling as it requires only 12-15 μL as sample volume. This study aimed to investigate the special metabolomics of preterm neonates at high risk of NEC using dried blood spots.</p><p><strong>Methods: </strong>Cases and controls were strictly matched 1:1. Dried blood spots (<i>n</i> = 32, 16 cases-16 controls) from newborn screening were subjected to LC-MS/MS. Metabolomic data were analyzed by orthogonal partial least squares-discriminant analysis (OPLS-DA) and univariate/multivariate statistical analysis.</p><p><strong>Results: </strong>Compared to the control group, the NEC group had a significant reduction in seven amino acids (glycine, alanine, threonine, proline, ornithine, lysine, and asparagine).</p><p><strong>Conclusions: </strong>The metabolic profile of neonates with NEC differs significantly from that of controls, making possible their separation with the use of targeted (LC-MS/MS) dried blood spots-based metabolomic analysis. Seven specific markers were identified for early detection and intervention.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"37 1","pages":"2416610"},"PeriodicalIF":1.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142479414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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 mitochondrial regulator protein, MNRR1, is elevated in the maternal blood of women with preeclampsia. 子痫前期妇女的母体血液中线粒体调节蛋白 MNRR1 升高。
IF 1.8 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-01-14 DOI: 10.1080/14767058.2023.2297158
Manaphat Suksai, Roberto Romero, Mariachiara Bosco, Francesca Gotsch, Eunjung Jung, Piya Chaemsaithong, Adi L Tarca, Dereje W Gudicha, Nardhy Gomez-Lopez, Marcia Arenas-Hernandez, Arun Meyyazhagan, Lawrence I Grossman, Siddhesh Aras, Tinnakorn Chaiworapongsa
<p><strong>Objective: </strong>Preeclampsia, one of the most serious obstetric complications, is a heterogenous disorder resulting from different pathologic processes. However, placental oxidative stress and an anti-angiogenic state play a crucial role. Mitochondria are a major source of cellular reactive oxygen species. Abnormalities in mitochondrial structures, proteins, and functions have been observed in the placentae of patients with preeclampsia, thus mitochondrial dysfunction has been implicated in the mechanism of the disease. Mitochondrial nuclear retrograde regulator 1 (MNRR1) is a newly characterized bi-organellar protein with pleiotropic functions. In the mitochondria, this protein regulates cytochrome <i>c</i> oxidase activity and reactive oxygen species production, whereas in the nucleus, it regulates the transcription of a number of genes including response to tissue hypoxia and inflammatory signals. Since MNRR1 expression changes in response to hypoxia and to an inflammatory signal, MNRR1 could be a part of mitochondrial dysfunction and involved in the pathologic process of preeclampsia. This study aimed to determine whether the plasma MNRR1 concentration of women with preeclampsia differed from that of normal pregnant women.</p><p><strong>Methods: </strong>This retrospective case-control study included 97 women with preeclampsia, stratified by gestational age at delivery into early (<34 weeks, <i>n</i> = 40) and late (≥34 weeks, <i>n</i> = 57) preeclampsia and by the presence or absence of placental lesions consistent with maternal vascular malperfusion (MVM), the histologic counterpart of an anti-angiogenic state. Women with an uncomplicated pregnancy at various gestational ages who delivered at term served as controls (<i>n</i> = 80) and were further stratified into early (<i>n</i> = 25) and late (<i>n</i> = 55) controls according to gestational age at venipuncture. Maternal plasma MNRR1 concentrations were determined by an enzyme-linked immunosorbent assay.</p><p><strong>Results: </strong>1) Women with preeclampsia at the time of diagnosis (either early or late disease) had a significantly higher median (interquartile range, IQR) plasma MNRR1 concentration than the controls [early preeclampsia: 1632 (924-2926) pg/mL vs. 630 (448-4002) pg/mL, <i>p</i> = .026, and late preeclampsia: 1833 (1441-5534) pg/mL vs. 910 (526-6178) pg/mL, <i>p</i> = .021]. Among women with early preeclampsia, those with MVM lesions in the placenta had the highest median (IQR) plasma MNRR1 concentration among the three groups [with MVM: 2066 (1070-3188) pg/mL vs. without MVM: 888 (812-1781) pg/mL, <i>p</i> = .03; and with MVM vs. control: 630 (448-4002) pg/mL, <i>p</i> = .04]. There was no significant difference in the median plasma MNRR1 concentration between women with early preeclampsia without MVM lesions and those with an uncomplicated pregnancy (<i>p</i> = .3). By contrast, women with late preeclampsia, regardless of MVM lesions, had a significantl
目的:子痫前期是最严重的产科并发症之一,是一种由不同病理过程导致的异质性疾病。然而,胎盘氧化应激和抗血管生成状态起着至关重要的作用。线粒体是细胞活性氧的主要来源。在子痫前期患者的胎盘中已观察到线粒体结构、蛋白质和功能的异常,因此线粒体功能障碍已被认为与该病的发病机制有关。线粒体核逆行调节因子 1(MNRR1)是一种新发现的具有多种功能的双细胞器蛋白。在线粒体中,该蛋白调节细胞色素 c 氧化酶的活性和活性氧的产生,而在细胞核中,它调节一些基因的转录,包括对组织缺氧和炎症信号的反应。由于 MNRR1 的表达会随着缺氧和炎症信号而改变,因此 MNRR1 可能是线粒体功能障碍的一部分,并参与子痫前期的病理过程。本研究旨在确定子痫前期妇女的血浆 MNRR1 浓度与正常孕妇是否存在差异:这项回顾性病例对照研究纳入了97名子痫前期妇女,按分娩时的胎龄分为早期(40人)和晚期(≥34周,57人)子痫前期,并按是否存在与母体血管灌注不良(MVM)一致的胎盘病变(抗血管生成状态的组织学对应物)进行分层。不同孕龄、足月分娩的无并发症妊娠妇女作为对照组(n = 80),并根据静脉穿刺时的孕龄进一步分为早期对照组(n = 25)和晚期对照组(n = 55)。母体血浆中 MNRR1 的浓度通过酶联免疫吸附试验进行测定:1)诊断时患有子痫前期(早期或晚期)的妇女血浆 MNRR1 浓度的中位数(四分位数间距,IQR)明显高于对照组[早期子痫前期:1632 (924-2926) pg/mL vs. 630 (448-4002) pg/mL,p = .026;晚期子痫前期:1833 (1441-5534) pg/mL vs. 910 (526-6178) pg/mL,p = .021]。在早期子痫前期的妇女中,胎盘有MVM病变的妇女的血浆MNRR1浓度中位数(IQR)在三组中最高[有MVM:2066 (1070-3188) pg/mL vs. 无MVM:888 (812-1781) pg/mL,p = .03;有MVM vs. 对照组:630 (448-4002) pg/mL,p = .04]。无MVM病变的早期子痫前期妇女与无并发症妊娠妇女的血浆MNRR1浓度中位数无明显差异(p = .3)。相比之下,患有晚期子痫前期的妇女,无论是否有MVM病变,其血浆MNRR1浓度中位数(IQR)明显高于对照组妇女[有MVM:1609 (1392-3135) pg/mL,对照组:910 (526-6178),p = .045;无MVM:2023 (1578-8936) pg/mL,对照组:2023 (1578-8936) pg/mL,p = .01]:结论:MNRR1 是一种线粒体调节蛋白,在诊断子痫前期(早期和晚期)妇女的母体血浆中均有升高。这些发现可能在一定程度上反映了线粒体功能障碍、血管内炎症或其他未知病理过程,而这些正是这种产科综合征的特征。
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引用次数: 0
The association of assisted reproductive technology with fetal malpresentation: a systematic review and meta-analysis. 辅助生殖技术与胎儿畸形的关系:系统回顾和荟萃分析。
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-02-05 DOI: 10.1080/14767058.2024.2313143
Konstantinos Stavridis, Maria Pisimisi, Olga Triantafyllidou, Theodoros Kalampokas, Nikolaos Vlahos, Stavroula L Kastora

Background: Since its introduction, assisted reproductive technology (ART) has developed into a common clinical practice around the world; yet it still raises a lot of questions. Throughout time, many researchers have investigated its association with several obstetric incidences and its consequences on perinatal outcomes. The aim of the current meta-analysis was to estimate the correlation between ART procedures and malpresentation of the fetus in singleton pregnancies.

Methods: The study was conducted according to the Preferred Reporting Items of Systematic Reviews and Meta-analyses (PRISMA) guidelines and prospectively registered under the PROSPERO database (CRD42023458084). Five databases (Embase, MEDLINE®, APA PsycInfo, Global Health, Health Management Information Consortium (HMIC)) and two additional sources were searched from inception to 31 May 2023. Quality of the included studies was assessed using the ROBINS-1 scale, whilst quality of evidence by the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) framework. Summative and subgroup data as well as heterogeneity were generated by the Cochrane platform RevMan Web.

Results: Overall, 11 studies were included in the study with a total of 3,360,134 deliveries. Results indicate a higher risk of malpresentation at delivery in fetuses conceived through ART than those conceived naturally (RR: 1.50, (95% confidence interval (CI):1.30, 1.73)). This risk decreased when adjustments for potential confounders were applied (RR = 1.12, 95% CI 1.02, 1.23).

Conclusions: Based on observational studies, this meta-analysis indicated that singleton pregnancies conceived through ART are associated with higher risk of malpresentation than those conceived naturally, albeit the difference was lower when potential confounders were examined. Thus, future large studies are required to better understand possible reversible and irreversible factors of this relationship.

背景:辅助生殖技术(ART)自问世以来,已发展成为全球普遍的临床实践,但仍引发了许多问题。一直以来,许多研究人员都在调查辅助生殖技术与几种产科疾病的关联及其对围产期结果的影响。本次荟萃分析的目的是估算抗逆转录病毒疗法与单胎妊娠胎儿畸形之间的相关性:本研究根据系统综述和荟萃分析首选报告项目(PRISMA)指南进行,并在 PROSPERO 数据库(CRD42023458084)中进行了前瞻性注册。研究人员检索了五个数据库(Embase、MEDLINE®、APA PsycInfo、Global Health、Health Management Information Consortium (HMIC))和两个其他来源,检索时间从开始至 2023 年 5 月 31 日。纳入研究的质量采用 ROBINS-1 量表进行评估,证据质量则采用建议、评估、发展和评价分级(GRADE)框架进行评估。总和数据、亚组数据以及异质性数据由 Cochrane 平台 RevMan Web 生成:研究共纳入了 11 项研究,总计 3,360,134 例分娩。结果表明,与自然受孕的胎儿相比,通过抗逆转录病毒疗法受孕的胎儿在分娩时出现胎位不正的风险更高(RR:1.50,(95% 置信区间(CI):1.30,1.73))。在对潜在混杂因素进行调整后,这一风险有所降低(RR = 1.12,95% 置信区间:1.02, 1.23):基于观察性研究,该荟萃分析表明,通过抗逆转录病毒疗法受孕的单胎妊娠比自然受孕的单胎妊娠发生胎位不正的风险更高,尽管在对潜在的混杂因素进行检查后,差异有所降低。因此,今后需要开展大型研究,以更好地了解这种关系中可能存在的可逆和不可逆因素。
{"title":"The association of assisted reproductive technology with fetal malpresentation: a systematic review and meta-analysis.","authors":"Konstantinos Stavridis, Maria Pisimisi, Olga Triantafyllidou, Theodoros Kalampokas, Nikolaos Vlahos, Stavroula L Kastora","doi":"10.1080/14767058.2024.2313143","DOIUrl":"10.1080/14767058.2024.2313143","url":null,"abstract":"<p><strong>Background: </strong>Since its introduction, assisted reproductive technology (ART) has developed into a common clinical practice around the world; yet it still raises a lot of questions. Throughout time, many researchers have investigated its association with several obstetric incidences and its consequences on perinatal outcomes. The aim of the current meta-analysis was to estimate the correlation between ART procedures and malpresentation of the fetus in singleton pregnancies.</p><p><strong>Methods: </strong>The study was conducted according to the Preferred Reporting Items of Systematic Reviews and Meta-analyses (PRISMA) guidelines and prospectively registered under the PROSPERO database (CRD42023458084). Five databases (Embase, MEDLINE<sup>®</sup>, APA PsycInfo, Global Health, Health Management Information Consortium (HMIC)) and two additional sources were searched from inception to 31 May 2023. Quality of the included studies was assessed using the ROBINS-1 scale, whilst quality of evidence by the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) framework. Summative and subgroup data as well as heterogeneity were generated by the Cochrane platform RevMan Web.</p><p><strong>Results: </strong>Overall, 11 studies were included in the study with a total of 3,360,134 deliveries. Results indicate a higher risk of malpresentation at delivery in fetuses conceived through ART than those conceived naturally (RR: 1.50, (95% confidence interval (CI):1.30, 1.73)). This risk decreased when adjustments for potential confounders were applied (RR = 1.12, 95% CI 1.02, 1.23).</p><p><strong>Conclusions: </strong>Based on observational studies, this meta-analysis indicated that singleton pregnancies conceived through ART are associated with higher risk of malpresentation than those conceived naturally, albeit the difference was lower when potential confounders were examined. Thus, future large studies are required to better understand possible reversible and irreversible factors of this relationship.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"37 1","pages":"2313143"},"PeriodicalIF":1.7,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139693383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Pregnancy outcomes of cerclage in twin gestations: a multicenter retrospective cohort study. 双胎妊娠环扎术的妊娠结局:一项多中心回顾性队列研究。
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-06-16 DOI: 10.1080/14767058.2024.2355495
Jee Yoon Park, Kyong-No Lee, Hyeon Ji Kim, Kiroong Choe, Aeri Cho, Bohyoung Kim, Jinwook Seo, Hayan Kwon, Jong Woon Kim, Jin-Gon Bae, Ji-Hee Sung, Se Jin Lee, Young Mi Jung, You Jung Han, Subeen Hong, Jin-Hoon Chung, Hye-Sung Won, Jong Kwan Jun

Objectives: To determine the effects of cerclage on twin pregnancies.

Methods: A multicenter, retrospective, cohort study was conducted at 10 tertiary centers using a web-based data collection platform. The study population included twin pregnancies delivered after 20 weeks of gestation. Patients with one or two fetal deaths before 20 weeks of gestation were excluded. Maternal characteristics, including prenatal cervical length (CL) and obstetric outcomes, were retrieved from the electronic medical records.

Results: A total of 1,473 patients had available data regarding the CL measured before 24 weeks of gestation. Seven patients without CL data obtained prior to cerclage were excluded from the analysis. The study population was divided into two groups according to the CL measured during the mid-trimester: the CL ≤2.5 cm group (n = 127) and the CL >2.5 cm group (n = 1,339). A total of 127 patients (8.7%) were included in the CL ≤2.5 cm group, including 41.7% (53/127) who received cerclage. Patients in the CL >2.5 cm group who received cerclage had significantly lower gestational age at delivery than the control group (hazard ratio (HR): 1.8; 95% confidence interval (CI): 1.11-2.87; p = .016). Patients in the CL ≤2.5 cm group who received cerclage had a significantly higher gestational age at delivery than the control group (HR: 0.5; 95% CI: 0.30-0.82; p value = .006).

Conclusions: In twin pregnancies with a CL ≤2.5 cm, cerclage significantly prolongs gestation. However, unnecessary cerclage in women with a CL >2.5 cm may result in a higher risk of preterm labor and histologic chorioamnionitis although this study has a limitation originated from retrospective design.

目的:确定环扎术对双胎妊娠的影响:确定环扎术对双胎妊娠的影响:利用网络数据收集平台,在 10 个三级医疗中心开展了一项多中心、回顾性、队列研究。研究对象包括妊娠 20 周后分娩的双胎妊娠。在妊娠 20 周前有一个或两个胎儿死亡的患者被排除在外。产妇特征,包括产前宫颈长度(CL)和产科结果,均从电子病历中获取:结果:共有 1,473 名患者提供了妊娠 24 周前测量的宫颈长度数据。分析中排除了 7 名在宫颈环扎术前未获得 CL 数据的患者。根据妊娠中期测量的CL值将研究对象分为两组:CL≤2.5厘米组(n = 127)和CL>2.5厘米组(n = 1,339)。CL≤2.5厘米组共有127名患者(8.7%),其中41.7%(53/127)的患者接受了环扎术。接受环扎术的 CL >2.5 厘米组患者的分娩胎龄明显低于对照组(危险比 (HR):1.8;95% 置信区间 (CI):1.11-2.87;P = .016)。接受环扎术的CL≤2.5厘米组患者的分娩时胎龄明显高于对照组(HR:0.5;95% CI:0.30-0.82;P = .006):结论:在CL≤2.5厘米的双胎妊娠中,环扎术可显著延长妊娠期。结论:在CL≤2.5厘米的双胎妊娠中,环扎术可明显延长妊娠期,但在CL>2.5厘米的产妇中,不必要的环扎术可能会导致较高的早产风险和组织学上的绒毛膜羊膜炎,尽管该研究存在回顾性设计的局限性。
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引用次数: 0
Nomogram for fetal limb bones in Chinese ethnicity. 华裔胎儿肢骨的提名图。
IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2024-12-01 Epub Date: 2024-07-25 DOI: 10.1080/14767058.2024.2380726
Ho Yin Diana Lee, Wendy Shu, Kwok Yiu Choi, Lin Wai Chan

Objective: To construct fetal limb bone nomograms in the Chinese ethnic population.

Methods: This was a prospective cross-sectional study on singleton pregnancies between 12 and 37 weeks of gestation. Femur, tibia, fibula, humerus, ulna, radius, and foot length were measured in a standardized manner by one of the three sonographers. Each fetus's measurements were only included once and those who developed maternal or fetal complications were excluded. Fractional polynomial regression model was used to obtain the 3rd, 10th, 50th, 90th, and 97th centiles for each of the limb measurement. Z-score for the 50th centile of each fetal limb measurement was then compared with published nomograms derived from other populations.

Results: Of the 843 scans performed, 775 were included in analysis after excluding conditions such as pre-eclampsia, chromosomal abnormalities, single umbilical artery and skeletal dysplasia. Comparison with other populations showed that Chinese had shorter fetal limb bone lengths than the Caucasian and Afro-Caribbean populations.

Conclusion: This study established nomograms for all the fetal limb bones in the Chinese ethnic population, which showed lengths comparatively shorter than Caucasian and Afro-Caribbean nomograms. This would reduce the false alarm of short fetal limb bone lengths and its consequent anxiety and intervention.

目的方法:这是一项前瞻性横断面研究,对象是妊娠 12 至 37 周的单胎孕妇:这是一项前瞻性横断面研究,对象为妊娠 12 至 37 周的单胎孕妇。由三位超声技师中的一位以标准化方式测量股骨、胫骨、腓骨、肱骨、尺骨、桡骨和足长。每个胎儿的测量结果只纳入一次,那些出现母体或胎儿并发症的胎儿将被排除在外。采用分数多项式回归模型得出每个肢体测量值的第 3、10、50、90 和 97 百分位数。然后将每个胎儿肢体测量值第 50 百分位数的 Z 值与其他人群中已发表的提名图进行比较:在进行的 843 次扫描中,有 775 次在排除子痫前期、染色体异常、单脐动脉和骨骼发育不良等情况后纳入分析。与其他人群的比较显示,中国人的胎儿肢骨长度短于高加索人和非洲-加勒比人:结论:这项研究为华裔胎儿的所有肢骨建立了提名图,显示其长度相对短于高加索人和非洲-加勒比人的提名图。这将减少因胎儿肢骨长度过短而引起的误报,以及由此导致的焦虑和干预。
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引用次数: 0
期刊
Journal of Maternal-Fetal & Neonatal Medicine
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