Literature DB >> 25528068

Prothrombin G20210A mutation is associated with recurrent pregnancy loss: a systematic review and meta-analysis update.

Hui Gao1, Fang-biao Tao2.   

Abstract

BACKGROUND: Thrombophilia is reported to be a candidate etiology of recurrent pregnancy loss (RPL). No conclusive results on the association between prothrombin G20210A mutation and RPL have been reported.
METHODS: We undertook a systematic review and meta-analysis of 37 case-control studies using a comprehensive electronic search on papers published by May 2014. We studied 5400 cases and 4640 controls to investigate the potential association between G20210A and RPL. In this review, we define RPL as more than 2 miscarriages.
RESULTS: A significant association was found between G20210A and RPL, with a combined odds ratio (OR) of 1.81 (95% confidence interval [CI]: 1.26-2.60). However, the risks differed in the subgroup analyses, categorized by study sites, maternal age, and type of miscarriages. The pooled OR remained significant in European studies (OR: 1.80, 95% CI: 1.35-2.41), whereas in the Middle-Eastern studies, it was not significant (OR: 2.39, 95% CI: 0.96-5.92). The risk of RPL was significantly higher in women older than 29 years (OR: 1.91, 95% CI: 1.61-6.11), and a positive relationship was only observed between prothrombin G20210A mutation and fetal loss, but not embryonic loss. There was no evidence of publication bias in any of the analyses. The sensitivity analyses showed that the findings were quite stable.
CONCLUSION: This meta-analysis suggests that the G20210A prothrombin mutation increases the risk of RPL (fetal loss, primary RPL, or secondary RPL), particularly in Europeans and women older than 29 years. We recommend further screening in more specific groups among women.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  G20210A; Meta-analysis; Polymorphism; Recurrent pregnancy loss; Thrombophilia

Mesh:

Substances:

Year:  2014        PMID: 25528068     DOI: 10.1016/j.thromres.2014.12.001

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  7 in total

Review 1.  Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.

Authors:  Luis Alejandro Arias-Sosa; Iván Darío Acosta; Elkin Lucena-Quevedo; Harold Moreno-Ortiz; Clara Esteban-Pérez; Maribel Forero-Castro
Journal:  J Assist Reprod Genet       Date:  2018-01-09       Impact factor: 3.412

2.  Association between Thrombophilic Genes Polymorphisms and Recurrent Pregnancy Loss Susceptibility in the Iranian Population: a Systematic Review and Meta-Analysis

Authors:  Mahdieh Kamali; Sedigheh Hantoushzadeh; Sedigheh Borna; Hossein Neamatzadeh; Mahta Mazaheri; Mahmood Noori-Shadkam; Fatemeh Haghighi
Journal:  Iran Biomed J       Date:  2017-07-23

3.  Risk factors and role of low molecular weight heparin in obstetric complications among women with inherited thrombophilia - a cohort study.

Authors:  María Manuela Clavijo; Carolina Valeria Mahuad; María de Los Angeles Vicente Reparaz; María Florencia Aizpurua; Adriana Ventura; Claudia Erica Casali
Journal:  Hematol Transfus Cell Ther       Date:  2019-06-20

4.  Association of Inherited Thrombophilia with Recurrent Pregnancy Loss in A Population of Lebanese Women: A Case Control Study.

Authors:  Sara Khalife; Regina Geitani
Journal:  Int J Fertil Steril       Date:  2022-08-21

5.  Pregnancy complications in G20210A mutation carriers associated with high prothrombin activity.

Authors:  M G Nikolaeva; A P Momot; M S Zainulina; N N Yasafova; I A Taranenko
Journal:  Thromb J       Date:  2021-06-05

6.  Etiologic characteristics and index pregnancy outcomes of recurrent pregnancy losses in Korean women.

Authors:  Gi Su Lee; Joon Cheol Park; Jeong Ho Rhee; Jong In Kim
Journal:  Obstet Gynecol Sci       Date:  2016-09-13

7.  Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues.

Authors:  Mert Ulaş Barut; Murat Bozkurt; Mehmet Kahraman; Engin Yıldırım; Necat Imirzalioğlu; Ayhan Kubar; Sibel Sak; Elif Ağaçayak; Tarık Aksu; Hakan Çoksüer
Journal:  Med Sci Monit       Date:  2018-06-22
  7 in total

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