妊娠障碍与新生儿黄疸的因果关系:一项双样本孟德尔随机化研究。

IF 1.5 4区 医学 Q2 PEDIATRICS
Translational pediatrics Pub Date : 2024-12-31 Epub Date: 2024-12-27 DOI:10.21037/tp-24-335
Yingying Wang, Shanshan Li, Jiajin Lu, Tianming Yuan
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引用次数: 0

摘要

背景:一些研究提示妊娠期并发症,如先兆子痫、妊娠期平滑肌瘤、催产素诱导、分娩方式等可能是新生儿黄疸的危险因素。在此,我们应用孟德尔随机化(MR)分析来调查妊娠障碍和新生儿黄疸之间的因果关系。方法:新生儿黄疸和妊娠疾病(包括先兆子痫或子痫、妊娠糖尿病和妊娠水肿)的相关数据来自FinnGen Consortium和综合流行病学单位(IEU)数据库。采用反方差加权(IVW)作为数据分析的主要方法,采用MR-Egger、加权中位数(WM)和加权模态方法验证结果的稳健性。采用MR-Egger回归方法探讨水平多效性的存在。采用MR多效性残差和异常值法(MR- presso)检测潜在异常值。采用Cochran’s Q检验评估工具变量间的异质性;留一分析(LOO)用于评估优势IVs的存在。结果:IVW方法显示,先兆子痫或子痫{比值比(or)[95%可信区间(CI)]: 0.86 (0.36-2.07), P=0.73},妊娠期水肿和蛋白尿[or (95% CI): 1.04 (0.62-1.74), P=0.87],妊娠期糖尿病[or (95% CI): 0.95 (0.60-1.49), P=0.81]与新生儿黄疸无关。MR-Egger回归结果显示,水平多效性不影响暴露因素与结果之间的关系。此外,没有观察到异质性。MR-PRESSO分析没有显示异常值,证实了这些数据是可靠的。结论:我们的数据显示子痫前期或子痫、妊娠水肿、蛋白尿、妊娠糖尿病和新生儿黄疸之间没有遗传因果关系。然而,需要进一步的研究来确定这些结果是否适用于其他种族。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Causal association between pregnancy disorders and neonatal jaundice: a two-sample Mendelian randomization study.

Background: Some studies have suggested that complications during pregnancy, such as preeclampsia, leiomyoma during pregnancy, oxytocin induction, and mode of delivery, may be risk factors for neonatal jaundice. Herein, we applied Mendelian randomization (MR) analysis to investigate a causal association between pregnancy disorders and neonatal jaundice.

Methods: Data related to neonatal jaundice and pregnancy disorders (including pre-eclampsia or eclampsia, gestational diabetes, and gestational edema) were sourced from the FinnGen Consortium and Integrated Epidemiology Unit (IEU) databases. Inverse-variance weighted (IVW) was used as a main approach for data analysis, while MR-Egger, weighted median (WM), and weighted mode methods were used to validate the robustness of the results. MR-Egger regression method was applied to explore the presence of horizontal pleiotropy. MR pleiotropy residual sum and outlier (MR-PRESSO) method was used to detect potential outliers. Cochran's Q test was used to assess heterogeneity among instrumental variables (IVs); leave-one-out (LOO) analyses were used to evaluate the presence of predominant IVs.

Results: The IVW approach showed that pre-eclampsia or eclampsia {odds ratio (OR) [95% confidence interval (CI)]: 0.86 (0.36-2.07), P=0.73}, gestational edema and proteinuria [OR (95% CI): 1.04 (0.62-1.74), P=0.87], and gestational diabetes mellitus [OR (95% CI): 0.95 (0.60-1.49), P=0.81] were not associated with neonatal jaundice. The MR-Egger regression results showed that horizontal pleiotropy did not affect the relationship between exposure factors and outcomes. Also, no heterogeneity was observed. The MR-PRESSO analysis showed no outliers, confirming that these data were robust.

Conclusions: Our data suggested no genetic causal association between pre-eclampsia or eclampsia, gestational edema, proteinuria, gestational diabetes mellitus, and neonatal jaundice. However, further research is needed to determine if these results apply to other races.

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来源期刊
Translational pediatrics
Translational pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.50
自引率
5.00%
发文量
108
期刊介绍: Information not localized
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