Maternal IVS1-401 T allele of the estrogen receptor alpha is an independent predictor of late fetal loss

To investigate whether sequence variants in the gene encoding for estrogen receptor alpha (ER-alpha) are risk determinants for fetal loss. Case-control study. University medical center. One hundred four women with a history of fetal loss and 277 healthy women with at least one previous pregnancy and...

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Published in:Fertility and sterility Vol. 86; no. 2; p. 448
Main Authors: Gerhardt, Andrea, Scharf, Rüdiger E, Mikat-Drozdzynski, Barbara, Krüssel, Jan S, Bender, Hans-Georg, Zotz, Rainer B
Format: Journal Article
Language:English
Published: United States 01-08-2006
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Summary:To investigate whether sequence variants in the gene encoding for estrogen receptor alpha (ER-alpha) are risk determinants for fetal loss. Case-control study. University medical center. One hundred four women with a history of fetal loss and 277 healthy women with at least one previous pregnancy and no previous fetal loss. None. The IVS1-401C/T polymorphism of the human ER-alpha, the G1691A mutation of the factor V gene (factor V Leiden), the G20210A mutation of the prothrombin gene, and the C677T polymorphism of the methylenetetrahydrofolate-reductase (MTHFR) gene were determined by polymerase chain reaction. In the subgroup analysis of women with at least one late miscarriage (n = 70), the prevalences of the ER-alpha IVS1-401 T allele (T/T vs. C/C, odds ratio [OR]: 2.85, P=.018; T/T + C/T vs. C/C, OR: 2.28, P=.043) and of heterozygous factor V Leiden (OR, 3.2; P=.002) were significantly higher among women with late fetal loss than among healthy women. Carriers of both risk determinants have an at-least additive increase in risk for late abortions (OR, 7.0; P=.0004). The population of all late abortions that would be attributable to the genetic variants (population attributable risk) was 13.9% for factor V Leiden and 49.2% for the ER-alpha IVS1-401 T allele. Women with the IVS1-401 T allele of the ER-alpha and/or factor V Leiden are at increased risk for late fetal loss.
ISSN:1556-5653
DOI:10.1016/j.fertnstert.2005.12.051