Increased risk for fetal loss in carriers of the factor V Leiden mutation

Citation
Jr. Meinardi et al., Increased risk for fetal loss in carriers of the factor V Leiden mutation, ANN INT MED, 130(9), 1999, pp. 736-739
Citations number
17
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
ANNALS OF INTERNAL MEDICINE
ISSN journal
00034819 → ACNP
Volume
130
Issue
9
Year of publication
1999
Pages
736 - 739
Database
ISI
SICI code
0003-4819(19990504)130:9<736:IRFFLI>2.0.ZU;2-9
Abstract
Background: An increased risk for fetal loss caused by placental thrombosis is probable in carriers of the factor V Leiden mutation but has not been d emonstrated consistently in previous studies. Objective: To determine the overall risk for fetal loss and the separate ri sks for miscarriage and stillbirth in carriers of the factor V Leiden mutat ion. Design: Retrospective cohort study. Setting: Three university hospitals. Participants: 228 carriers of the factor V Leiden mutation (77 propositi, 1 51 relatives) and 121 noncarrier relatives (controls). All participants had been pregnant at least once. Measurements: Risks for fetal loss, miscarriage (defined as fetal loss with in 20 weeks of gestation),and stillbirth (defined as fetal loss after >20 w eeks of gestation) in women and in pregnancies were estimated and compared in carriers and noncarriers. Adjusted odds ratios were calculated by using multiple regression analysis. A random-effects model was used for compariso ns of pregnancies. Results: Fetal loss occurred in 31.6% of carriers and 22.3% of noncarriers, miscarriage occurred in 29.4% of carriers and 17.4% of noncarriers. and st illbirth occurred in 5.7% of carriers and 5.0% of noncarriers. Fetal loss r ecurred in 10.1% of carriers and 4.1% of noncarriers (odds ratio, 2.60 [95% CI, 0.96 to 7.03]). Adjusted odds ratios were 2.12 (CI, 1.35 to 3.33) for fetal loss, 2.08 (CI, 1.33 to 3.25) for miscarriage, and 1.60 (CI, 0.58 to 4.43) for stillbirth when pregnancies in carriers and noncarriers were comp ared. Homozygous carriers had a greater risk for fetal loss (odds ratio; 2. 01 [CI, 0.94 to 4.32]) and stillbirth (odds ratio, 4.85 [CI, 0.82 to 25.58] ) than heterozygous carriers. Conclusions: Carriers of the factor V Leiden mutation have a greater risk f or fetal loss (particularly miscarriage) than noncarriers. These data furth er suggest a greater risk for recurrence of fetal loss in carriers than in noncarriers and a greater risk for fetal loss and stillbirth in homozygous carriers than in heterozygous carriers.