SLE患者不良母婴结局的危险因素:一项系统回顾和荟萃分析。

IF 3.1 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Frontiers in Medicine Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.3389/fmed.2025.1573573
Hang Liu, Meifei Li, Meijiao Wang, Minzhe Ren, Jiaying Fu, Ying Cai, Zhiyu Li, Ting Zhao, Jing Sun, Zhijun Xie
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引用次数: 0

摘要

背景:系统性红斑狼疮(SLE)是一种多系统自身免疫性疾病,SLE妊娠会增加母体和胎儿不良结局的风险。识别潜在的危险因素可以加强SLE妊娠的孕前风险评估,从而减轻SLE患者的妊娠负担。目的:本荟萃分析的目的是通过对文献和荟萃分析的系统回顾,确定SLE妊娠中不利的母胎结局的危险因素。方法:使用固定效应模型或随机效应模型估计比值比(ORs)和相关的95%置信区间(ci)。I2统计量用于评估异质性。同时进行敏感性分析、Egger检验、Newcastle-Ottawa质量评估量表(NOS)和分级建议评估、发展和评价(GRADE)系统。结果:在筛选的2467篇引用中,荟萃分析了11篇涉及1790名怀孕SLE患者的论文。荟萃分析的结果表明,SLE的发病与早产风险增加相关(OR: 2.85; 95% CI: 2.04, 3.99)。高血压与复合妊娠结局(OR: 4.56; 95% CI: 2.42, 8.53)、早产(OR: 2.20; 95% CI: 1.53, 3.17)和先兆子痫(OR: 10.11; 95% CI: 1.83, 55.89)的风险增加相关。肾脏受累与复合妊娠结局(OR: 3.09; 95% CI: 1.66, 5.72)和早产(OR: 1.65; 95% CI: 1.22, 2.23)的风险增加相关。抗dsdna与早产风险增加(OR: 1.83; 95% CI: 1.13, 2.92)和妊娠丢失(OR: 2.64; 95% CI: 1.09, 6.40)相关。药物治疗与复合妊娠结局(OR: 0.51; 95% CI: 0.31, 0.85)、早产(OR: 0.66; 95% CI: 0.48, 0.89)和妊娠丢失(OR: 0.42; 95% CI: 0.21, 0.84)的风险降低相关。敏感性分析表明我们的结果是可靠的。埃格的检验没有发现明显的发表偏倚。结论:SLE的发病、高血压、肾脏受累、药物治疗和血清学因素对SLE妊娠不良母胎结局的发生具有预测作用。加强SLE患者的孕前风险评估对降低妊娠风险,提高妊娠期生活质量具有重要作用。系统评价注册:https://www.crd.york.ac.uk/prospero/#recordDetails,标识符:CRD42024564190。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk factors for adverse maternal and fetal outcomes in SLE patients: a systematic review and meta-analysis.

Background: Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease that increases the risk of adverse maternal and fetal outcomes in SLE pregnancies. Identifying potential risk factors can enhance preconception risk assessment for SLE pregnancies, thereby reducing the burden of pregnancy for SLE patients.

Objective: The goal of this meta-analysis is to designate the risk factors for unfavorable maternal and fetal outcomes in SLE pregnancies by means of a systematic review of the literature and meta-analysis.

Methods: The odds ratios (ORs) and associated 95% confidence intervals (CIs) were estimated using either a fixed-effects model or a random-effects model. The I2 statistic was used to assess heterogeneity. Sensitivity analysis, Egger's test, the Newcastle-Ottawa Quality Assessment Scale (NOS), and the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) system were also performed.

Results: Eleven papers with 1,790 SLE patients who were pregnant were examined in the meta-analysis out of 2,467 citations that were screened. The meta-analysis's findings indicated that the onset of SLE is associated with an increased risk of preterm birth (OR: 2.85; 95% CI: 2.04, 3.99). Hypertension is associated with an increased risk of composite pregnancy outcomes (OR: 4.56; 95% CI: 2.42, 8.53), preterm birth (OR: 2.20; 95% CI: 1.53, 3.17) and preeclampsia (OR: 10.11; 95% CI: 1.83, 55.89). Renal involvement is associated with an increased risk of composite pregnancy outcomes (OR: 3.09; 95% CI: 1.66, 5.72) and preterm birth (OR: 1.65; 95% CI: 1.22, 2.23). Anti-dsDNA is associated with an increased risk of preterm birth (OR: 1.83; 95% CI: 1.13, 2.92) and pregnancy loss (OR: 2.64; 95% CI: 1.09, 6.40). Drug therapy is associated with a decreased risk of composite pregnancy outcomes (OR: 0.51; 95% CI: 0.31, 0.85), preterm birth (OR: 0.66; 95% CI: 0.48, 0.89) and pregnancy loss (OR: 0.42; 95% CI: 0.21, 0.84). Sensitivity analysis demonstrated how solid our results are. Egger's test revealed no discernible publication bias.

Conclusion: The onset of SLE, hypertension, renal involvement, drug therapy, and serological factors have a predictive effect on the occurrence of adverse maternal and fetal outcomes in SLE pregnancies. Strengthening preconception risk assessment for SLE patients plays an important role in reducing pregnancy risks and improving the quality of life during pregnancy.

Systematic review registration: https://www.crd.york.ac.uk/prospero/#recordDetails, identifier: CRD42024564190.

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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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