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The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature

BACKGROUND: The true relationship between methylenetetrahydrofolate reductase C677T homozygosity and risk of recurrent spontaneous abortion is unknown, and it is unclear if women with these mutations should be anticoagulated during pregnancy. OBJECTIVES: We report a series of 8 patients with this is...

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Autores principales: Altomare, Ivy, Adler, Alan, Aledort, Louis M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098747/
https://www.ncbi.nlm.nih.gov/pubmed/17941987
http://dx.doi.org/10.1186/1477-9560-5-17
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author Altomare, Ivy
Adler, Alan
Aledort, Louis M
author_facet Altomare, Ivy
Adler, Alan
Aledort, Louis M
author_sort Altomare, Ivy
collection PubMed
description BACKGROUND: The true relationship between methylenetetrahydrofolate reductase C677T homozygosity and risk of recurrent spontaneous abortion is unknown, and it is unclear if women with these mutations should be anticoagulated during pregnancy. OBJECTIVES: We report a series of 8 patients with this issue and review the current literature. METHODS: 8 patients (3 of whom were actively pregnant) were referred with histories of spontaneous fetal loss; hypercoaguability work-ups revealed each were homozygous for the MTHFR C677T mutation without other thrombophilias. RESULTS: In the 3 women who have conceived, treatment with LMW heparin during pregnancy led to two full-term births and one additional pregnancy without complication. For the 5 who have not, we recommended treatment with LMW heparin upon conception. CONCLUSION: We provide evidence to support the relationship between MTHFR C677T mutations and recurrent fetal loss, and to suggest that anticoagulation of these patients during pregnancy can lead to a successful pregnancy outcome.
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spelling pubmed-20987472007-11-29 The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature Altomare, Ivy Adler, Alan Aledort, Louis M Thromb J Original Clinical Investigation BACKGROUND: The true relationship between methylenetetrahydrofolate reductase C677T homozygosity and risk of recurrent spontaneous abortion is unknown, and it is unclear if women with these mutations should be anticoagulated during pregnancy. OBJECTIVES: We report a series of 8 patients with this issue and review the current literature. METHODS: 8 patients (3 of whom were actively pregnant) were referred with histories of spontaneous fetal loss; hypercoaguability work-ups revealed each were homozygous for the MTHFR C677T mutation without other thrombophilias. RESULTS: In the 3 women who have conceived, treatment with LMW heparin during pregnancy led to two full-term births and one additional pregnancy without complication. For the 5 who have not, we recommended treatment with LMW heparin upon conception. CONCLUSION: We provide evidence to support the relationship between MTHFR C677T mutations and recurrent fetal loss, and to suggest that anticoagulation of these patients during pregnancy can lead to a successful pregnancy outcome. BioMed Central 2007-10-17 /pmc/articles/PMC2098747/ /pubmed/17941987 http://dx.doi.org/10.1186/1477-9560-5-17 Text en Copyright © 2007 Altomare et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Clinical Investigation
Altomare, Ivy
Adler, Alan
Aledort, Louis M
The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title_full The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title_fullStr The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title_full_unstemmed The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title_short The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature
title_sort 5, 10 methylenetetrahydrofolate reductase c677t mutation and risk of fetal loss: a case series and review of the literature
topic Original Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098747/
https://www.ncbi.nlm.nih.gov/pubmed/17941987
http://dx.doi.org/10.1186/1477-9560-5-17
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