Department of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, the Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, Sichuan, China.
West China School of Medicine, Sichuan University, Chengdu, Sichuan, China.
Acta Obstet Gynecol Scand. 2019 Dec;98(12):1523-1533. doi: 10.1111/aogs.13665. Epub 2019 Jun 19.
Antiphospholipid syndrome is a chronic autoimmune disease with a high prevalence in females. Published data have identified that antiphospholipid antibodies (APLA) of antiphospholipid syndrome are risk factors for poor pregnancy outcomes, such as recurrent spontaneous abortion, intrauterine growth restriction and preeclampsia. However, the association between APLA and late fetal loss is not fully understood and remains controversial. The aim of this study is to identify and analyze the recent publications to better understand the association between APLA and late fetal loss.
The literature was searched on 31 January 2019 using Ovid, Medline, EMBASE and the Cochrane Central Register of Controlled Trials (CENTRAL) to evaluate the association between APLA and late fetal loss, with articles published before January 2019, according to the PRISMA statement. Without imposing regional restrictions, referenced articles were selected. Quality assessment was conducted independently by two reviewers, based on the Newcastle-Ottawa scale. For the meta-analysis, we used odds ratios (random effects model). The between-study heterogeneity was assessed by Q test. Publication bias was assessed by funnel plots.
Nineteen studies (with 10 265 cases) were included in the final analysis. The odds ratio (OR) for the late fetal loss with lupus anticoagulant was 5.02 (95% confidence interval [CI] 2.14-7.89). Seven included studies reported that lupus anticoagulant had a statistically significant association with late fetal loss. The results did not show a statistically significant association between anticardiolipin antibodies and late fetal loss. The pooled odds ratio for the association of anticardiolipin antibodies with late fetal loss was 3.47 (95% CI 0.68-6.26). However, we did find the relation between anticardiolipin antibodies and late fetal loss among cohort studies (OR 2.27, 95% CI 1.20-3.44). Anti-beta2 glycoprotein 1 antibodies (β2GP1) showed a significant association with late fetal loss (OR 3.13, 95% CI 0.75-5.50).
Lupus anticoagulant is strongly associated with late fetal loss in antiphospholipid syndrome patients. However, the association between anticardiolipin antibodies and late fetal loss is inconsistent. There are currently insufficient data to support a significant relation between β2GP1 and late fetal loss.
抗磷脂综合征是一种慢性自身免疫性疾病,在女性中的发病率较高。已有研究表明,抗磷脂综合征患者的抗磷脂抗体(APLA)是不良妊娠结局(如复发性自然流产、宫内生长受限和子痫前期)的危险因素。然而,APLA 与晚期胎儿丢失之间的关联尚未完全阐明,且仍存在争议。本研究旨在通过识别和分析现有文献,更好地了解 APLA 与晚期胎儿丢失之间的关系。
本研究于 2019 年 1 月 31 日在 Ovid、Medline、EMBASE 和 Cochrane 中央对照试验注册中心(CENTRAL)上进行文献检索,根据 PRISMA 声明评估了 APLA 与晚期胎儿丢失之间的关联。检索时间截至 2019 年 1 月之前发表的文章,不设地域限制,筛选参考文献。两名评审员独立进行质量评估,基于 Newcastle-Ottawa 量表。对于荟萃分析,我们使用比值比(随机效应模型)。采用 Q 检验评估组间异质性。采用漏斗图评估发表偏倚。
最终分析纳入了 19 项研究(共 10265 例病例)。狼疮抗凝物与晚期胎儿丢失的比值比(OR)为 5.02(95%置信区间 [CI] 2.14-7.89)。7 项纳入的研究报告称狼疮抗凝物与晚期胎儿丢失具有统计学显著相关性。结果并未显示抗心磷脂抗体与晚期胎儿丢失之间存在统计学显著相关性。抗心磷脂抗体与晚期胎儿丢失关联的汇总 OR 为 3.47(95% CI 0.68-6.26)。然而,我们确实在队列研究中发现了抗心磷脂抗体与晚期胎儿丢失之间的关系(OR 2.27,95% CI 1.20-3.44)。抗β2 糖蛋白 1 抗体(β2GP1)与晚期胎儿丢失有显著关联(OR 3.13,95% CI 0.75-5.50)。
狼疮抗凝物与抗磷脂综合征患者的晚期胎儿丢失密切相关。然而,抗心磷脂抗体与晚期胎儿丢失之间的关系并不一致。目前尚无足够的数据支持β2GP1 与晚期胎儿丢失之间存在显著关联。