MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis

Background: Published research findings regarding the relationship between the methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism and the risk of preeclampsia (PE) have generated conflicting results. A meta-analysis was conducted to investigate whether the MTHFR A1298C polymorphism is a...

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Main Authors: Yong Hu, Ao Wang, Ke Yi
Format: Article
Language:English
Published: IMR Press 2023-12-01
Series:Clinical and Experimental Obstetrics & Gynecology
Subjects:
Online Access:https://www.imrpress.com/journal/CEOG/50/12/10.31083/j.ceog5012266
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author Yong Hu
Ao Wang
Ke Yi
author_facet Yong Hu
Ao Wang
Ke Yi
author_sort Yong Hu
collection DOAJ
description Background: Published research findings regarding the relationship between the methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism and the risk of preeclampsia (PE) have generated conflicting results. A meta-analysis was conducted to investigate whether the MTHFR A1298C polymorphism is associated with preeclampsia. Methods: We conducted a systematic search across several databases, including PubMed, Embase, Web of science, China National Knowledge Infrastructure, and Chinese Biomedicine Databases, to identify relevant studies. We then calculated pooled odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) to assess the association between the MTHFR A1298C polymorphism and preeclampsia (PE) risk. Results: A total of 11 studies were enrolled in this meta-analysis. The pooled analyses revealed that MTHFR A1298C polymorphism significantly decreased the risk of PE (allele contrast (A (alanine) vs. C (glutamate) ): OR, 0.81; 95% CI, 0.71–0.93, p = 0.207; homozygote (AA vs. CC): OR, 0.57; 95% CI, 0.40–0.79, p = 0.056; heterozygote (AC vs. CC): OR, 0.62; 95% CI, 0.45–0.87, p = 0.010; dominant model (AA + AC vs. CC): OR, 0.59; 95% CI, 0.43–0.81, p = 0.031; recessive model (AA vs. AC + CC): OR, 0.83; 95% CI, 0.70–0.98), p = 0.817. Conclusion: Present meta-analysis reveals that MTHFR A1298C variant may serve as genetic biomarkers of PE. The study was registered on PROSPERO (https://www.crd.york.ac.uk/prospero/), registration number: CRD42023459681.
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spelling doaj.art-34a9b4836a3d4c539150cbb9454931062024-01-05T07:27:09ZengIMR PressClinical and Experimental Obstetrics & Gynecology0390-66632023-12-01501226610.31083/j.ceog5012266S0390-6663(23)02234-0MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-AnalysisYong Hu0Ao Wang1Ke Yi2Department of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children of the Ministry of Education, West China Second University Hospital, Sichuan University, 610041 Chengdu, Sichuan, ChinaKey Laboratory of Obstetrics & Gynecologic and Pediatric Diseases and Birth Defects of the Ministry of Education, West China Second University Hospital, Sichuan University, 610041 Chengdu, Sichuan, ChinaKey Laboratory of Obstetrics & Gynecologic and Pediatric Diseases and Birth Defects of the Ministry of Education, West China Second University Hospital, Sichuan University, 610041 Chengdu, Sichuan, ChinaBackground: Published research findings regarding the relationship between the methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism and the risk of preeclampsia (PE) have generated conflicting results. A meta-analysis was conducted to investigate whether the MTHFR A1298C polymorphism is associated with preeclampsia. Methods: We conducted a systematic search across several databases, including PubMed, Embase, Web of science, China National Knowledge Infrastructure, and Chinese Biomedicine Databases, to identify relevant studies. We then calculated pooled odds ratios (ORs) and their corresponding 95% confidence intervals (CIs) to assess the association between the MTHFR A1298C polymorphism and preeclampsia (PE) risk. Results: A total of 11 studies were enrolled in this meta-analysis. The pooled analyses revealed that MTHFR A1298C polymorphism significantly decreased the risk of PE (allele contrast (A (alanine) vs. C (glutamate) ): OR, 0.81; 95% CI, 0.71–0.93, p = 0.207; homozygote (AA vs. CC): OR, 0.57; 95% CI, 0.40–0.79, p = 0.056; heterozygote (AC vs. CC): OR, 0.62; 95% CI, 0.45–0.87, p = 0.010; dominant model (AA + AC vs. CC): OR, 0.59; 95% CI, 0.43–0.81, p = 0.031; recessive model (AA vs. AC + CC): OR, 0.83; 95% CI, 0.70–0.98), p = 0.817. Conclusion: Present meta-analysis reveals that MTHFR A1298C variant may serve as genetic biomarkers of PE. The study was registered on PROSPERO (https://www.crd.york.ac.uk/prospero/), registration number: CRD42023459681.https://www.imrpress.com/journal/CEOG/50/12/10.31083/j.ceog5012266mthfrpolymorphismspreeclampsiameta-analysis
spellingShingle Yong Hu
Ao Wang
Ke Yi
MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
Clinical and Experimental Obstetrics & Gynecology
mthfr
polymorphisms
preeclampsia
meta-analysis
title MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
title_full MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
title_fullStr MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
title_full_unstemmed MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
title_short MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
title_sort mthfr a1298c polymorphism and risk of preeclampsia a meta analysis
topic mthfr
polymorphisms
preeclampsia
meta-analysis
url https://www.imrpress.com/journal/CEOG/50/12/10.31083/j.ceog5012266
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