4.6 Article

Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study

Journal

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
Volume 12, Issue 4, Pages 469-478

Publisher

WILEY-BLACKWELL
DOI: 10.1111/jth.12509

Keywords

meta-analysis; genetics; pregnancy; risk factors; cohort study

Funding

  1. Canadian Institutes of Health Research (CIHR) [MOP 64461, MOP 82802, MOP 53188]
  2. Heart and Stroke Foundation of Ontario (HSFO) [NA 5178]
  3. Heart and Stroke Foundation
  4. University of Ottawa Faculty of Medicine Research Chair Awards
  5. University of Ottawa Department of Medicine Research Salary Award
  6. Ontario Women's Health Council-Institute of Gender and Health of Canadian Institutes of Health Research (CIHR) Mid Career Award

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Background Case control studies suggest that genetic thrombophilias increase the risk of placenta-mediated pregnancy complications (pregnancy loss, small for gestational age (SGA), preeclampsia and/or placental abruption). Cohort studies have not supported this association but were underpowered to detect small effects. Objective To determine if factor V Leiden (FVL) or the prothrombin gene mutation (PGM) were associated with placenta-mediated pregnancy complications. Patients/Methods A prospective cohort of unselected, consenting pregnant women at three Canadian tertiary care hospitals had blood drawn in the early second trimester and were genotyped for FVL and PGM after delivery. The main outcome measure was a composite of pregnancy loss, SGA <10th percentile, preeclampsia or placental abruption. Results Complete primary outcome and genetic data were available for 7343 women. Most were Caucasian (77.7%, n=5707), mean age was 30.4 (+/- 5.1) years, and half were nulliparous. There were 507 (6.9%) women with FVL and/or PGM; 11.64% had a placenta-mediated pregnancy complication. Of the remaining 6836 women, 11.23% experienced a complication. FVL and/or PGM was associated with a relative risk of 1.04 (95% CI, 0.81-1.33) for the composite outcome, with similar results after adjustment for important covariates. Conclusions Carriers of FVL or PGM are not at significantly increased risk of these pregnancy complications.

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