Association of the MTHFR 677C>T and 1298A>C polymorphisms and male infertility risk: a meta-analysis

Fereshteh Aliakbari1, Farkhondeh Pouresmaeili2, Nahal Eshghifar1,3

  • 1Men's Health & Reproductive Health Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Abstract

Insights

Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms, specifically 677C>T, are linked to increased male infertility risk. Further research is needed to confirm these findings and explore gene-environment interactions in male infertility.

Area of Science:

  • Genetics and Reproductive Medicine
  • Molecular Epidemiology
  • Human Genetics

Background:

  • Polymorphisms in the Methylenetetrahydrofolate reductase (MTHFR) gene are potential risk factors for male sterility.
  • Previous epidemiological studies have yielded inconsistent results regarding the association between MTHFR polymorphisms and male infertility risk.

Purpose of the Study:

  • To conduct a meta-analysis of published case-control studies.
  • To re-examine the controversial association between MTHFR gene polymorphisms and the risk of male infertility.

Main Methods:

  • Comprehensive electronic searches of major databases (Cochrane, EMBASE, Google Scholar, PubMed) were performed.
  • Eligible high-quality case-control studies published up to May 2019 were included based on predefined criteria.
  • Crude odds ratios (OR) with 95% confidence intervals (CI) were calculated to assess the risk.

Main Results:

  • The meta-analysis included 34 studies (9662 cases, 9154 controls) for MTHFR 677C/T and 22 studies (5893 cases, 6303 controls) for MTHFR 1298A/C.
  • Both MTHFR 677C/T and 1298A/C polymorphisms showed significant associations with male infertility risk.
  • Significant associations were observed in Asian and Caucasian populations for 677C/T, and in Asians for 1298A/C.

Conclusions:

  • The MTHFR 677C>T polymorphism is associated with an elevated risk of male infertility.
  • Further analytical studies are recommended to confirm these findings and elucidate gene-environment interactions contributing to male infertility.

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