系统性红斑狼疮妊娠期疾病爆发的风险和保护因素:一项系统综述和荟萃分析

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-03-01 Epub Date: 2025-01-27 DOI:10.1007/s10067-025-07341-y
Yudi Yang, Yangzhong Zhou, Xueyang Zhang, Can Huang, Lingshan Liu, Jiuliang Zhao, Xinping Tian, Mengtao Li, Xiaofeng Zeng, Yan Zhao, Yijun Song
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引用次数: 0

摘要

为了综合妊娠期系统性红斑狼疮(SLE)发作相关预测因素的现有证据,我们系统地检索了MEDLINE、Embase和Cochrane图书馆,检索了截至2024年1月的妊娠期系统性红斑狼疮发作风险和保护因素的观察性研究。使用优势比(OR)和平均差异(MD)及其95%置信区间(CI)来量化效应大小。我们采用基于异质性评估的固定效应或随机效应模型(I2统计)。采用留一法进行敏感性分析,通过Egger检验评估发表偏倚。meta分析纳入了32项研究。与妊娠期发作高风险相关的显著基线SLE特征被确定为:血小板减少(OR [95%CI], 2.29[1.14-4.58])、低补体血症(1.70[1.28-2.27])、抗dsdna阳性(1.43[1.16-1.77])和狼疮肾炎史(2.34[1.70-3.21])。保护因素包括妊娠前缓解(0.32[0.20-0.49])和基线抗疟药物使用(0.71[0.55-0.92])和妊娠期间(0.44[0.33-0.58])。其他危险因素包括基线糖皮质激素使用(1.51[1.17-1.94])、妊娠期间糖皮质激素使用(3.39[1.90-6.06])、基线时使用其他免疫抑制药物(1.46[1.00-2.12])和高血压(2.16[1.45-3.23])。此外,与非耀斑组相比,耀斑组的个体更年轻,基线疾病活动性更高,C3/C4水平更低。本研究强调了妊娠前控制SLE疾病活动的关键作用,以尽量减少耀斑风险,并确定了与耀斑相关的重要风险和保护因素。这些证据有助于制定更好的SLE孕妇临床管理策略。•综合与妊娠期SLE发作相关的风险和保护因素的现有证据。•强调在怀孕前有效管理疾病活动的极端重要性。•为SLE患者妊娠的风险分层和管理策略提供见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk and protective factors of disease flare during pregnancy in systemic lupus erythematosus: a systematic review and meta-analysis.

To synthesize available evidence on predictive factors associated with systemic lupus erythematosus (SLE) flares during pregnancy, we systematically searched MEDLINE, Embase, and the Cochrane Library through January 2024 for observational studies on risk and protective factors of SLE flares during pregnancy. Odds ratios (OR) and mean differences (MD), as well as their 95% confidence intervals (CI) were used to quantify effect sizes. We employed fixed-effect or random-effect models based on heterogeneity assessments (I2 statistics). Sensitivity analyses were performed using the leave-one-out method, and publication bias was assessed through Egger's test. Thirty-two studies were included in the meta-analysis. Significant baseline SLE characteristics associated with higher risks for flares during pregnancy were identified: thrombocytopenia (with OR [95%CI], 2.29 [1.14-4.58]), hypocomplementemia (1.70 [1.28-2.27]), anti-dsDNA positivity (1.43 [1.16-1.77]), and a history of lupus nephritis (2.34 [1.70-3.21]). Protective factors included achieving remission before pregnancy (0.32 [0.20-0.49]) and antimalarial use at baseline (0.71 [0.55-0.92]) and during pregnancy (0.44 [0.33-0.58]). Additional risk factors included baseline glucocorticoid usage (1.51 [1.17-1.94]), glucocorticoid administration during pregnancy (3.39 [1.90-6.06]), use of other immunosuppressive drugs at baseline (1.46 [1.00-2.12]), and hypertension (2.16 [1.45-3.23]). Furthermore, individuals in the flare group were younger, had higher baseline disease activity, and lower C3/C4 levels compared to the non-flare group. This study highlighted the critical role of managing SLE disease activity prior to pregnancy to minimize flare risks, and identified significant risk and protective factors associated with flares. These evidences facilitate better clinical management strategies for pregnant women with SLE. Key Points • Synthesizes existing evidence on the risk and protective factors associated with SLE flares during pregnancy. • Highlights the critical importance of effectively managing disease activity prior to conception. • Provides insights to enhance risk stratification and management strategies for pregnancies in patients with SLE.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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