Thrombosis Program, Division of Hematology, Departments of Medicine, Obstetrics and Gynecology and Epidemiology/Community Medicine, University of Ottawa, Ottawa, Ontario, Canada.
PLoS Med. 2010 Jun 15;7(6):e1000292. doi: 10.1371/journal.pmed.1000292.
Factor V Leiden (FVL) and prothrombin gene mutation (PGM) are common inherited thrombophilias. Retrospective studies variably suggest a link between maternal FVL/PGM and placenta-mediated pregnancy complications including pregnancy loss, small for gestational age, pre-eclampsia and placental abruption. Prospective cohort studies provide a superior methodologic design but require larger sample sizes to detect important effects. We undertook a systematic review and a meta-analysis of prospective cohort studies to estimate the association of maternal FVL or PGM carrier status and placenta-mediated pregnancy complications.
A comprehensive search strategy was run in Medline and Embase. Inclusion criteria were: (1) prospective cohort design; (2) clearly defined outcomes including one of the following: pregnancy loss, small for gestational age, pre-eclampsia or placental abruption; (3) maternal FVL or PGM carrier status; (4) sufficient data for calculation of odds ratios (ORs). We identified 322 titles, reviewed 30 articles for inclusion and exclusion criteria, and included ten studies in the meta-analysis. The odds of pregnancy loss in women with FVL (absolute risk 4.2%) was 52% higher (OR = 1.52, 95% confidence interval [CI] 1.06-2.19) as compared with women without FVL (absolute risk 3.2%). There was no significant association between FVL and pre-eclampsia (OR = 1.23, 95% CI 0.89-1.70) or between FVL and SGA (OR = 1.0, 95% CI 0.80-1.25). PGM was not associated with pre-eclampsia (OR = 1.25, 95% CI 0.79-1.99) or SGA (OR 1.25, 95% CI 0.92-1.70).
Women with FVL appear to be at a small absolute increased risk of late pregnancy loss. Women with FVL and PGM appear not to be at increased risk of pre-eclampsia or birth of SGA infants. Please see later in the article for the Editors' Summary.
因子 V 莱顿(FVL)和凝血酶原基因突变(PGM)是常见的遗传性血栓形成倾向。回顾性研究表明,母体 FVL/PGM 与胎盘介导的妊娠并发症之间存在关联,包括妊娠丢失、小于胎龄儿、子痫前期和胎盘早剥。前瞻性队列研究提供了一种优越的方法学设计,但需要更大的样本量来检测重要的影响。我们进行了一项系统评价和前瞻性队列研究的荟萃分析,以评估母体 FVL 或 PGM 携带状态与胎盘介导的妊娠并发症之间的关联。
我们在 Medline 和 Embase 中运行了全面的搜索策略。纳入标准为:(1)前瞻性队列设计;(2)明确界定的结局,包括以下之一:妊娠丢失、小于胎龄儿、子痫前期或胎盘早剥;(3)母体 FVL 或 PGM 携带状态;(4)有足够的数据计算比值比(ORs)。我们确定了 322 个标题,对 30 篇文章进行了纳入和排除标准的审查,并将 10 项研究纳入荟萃分析。FVL 女性(绝对风险 4.2%)妊娠丢失的几率高出 52%(OR=1.52,95%置信区间[CI]1.06-2.19),而非 FVL 女性(绝对风险 3.2%)。FVL 与子痫前期(OR=1.23,95%CI0.89-1.70)或 FVL 与 SGA(OR=1.0,95%CI0.80-1.25)之间无显著关联。PGM 与子痫前期(OR=1.25,95%CI0.79-1.99)或 SGA(OR1.25,95%CI0.92-1.70)之间也没有关联。
FVL 女性似乎处于妊娠晚期丢失的绝对风险略有增加的状态。FVL 和 PGM 的女性似乎没有增加子痫前期或 SGA 婴儿出生的风险。请在文章后面查看编辑摘要。