Methylene tetrahydrofolate reductase and methionine synthase gene polymorphisms as genetic determinants of

V O Osunkalu1, I A Taiwo2, C C Makwe3

  • 1Department of Haematology and Blood Transfusion, College of Medicine, University of Lagos, Nigeria.

Insights

Genetic variations in methylene tetrahydrofolate reductase (MTHFR) and methionine synthase (MTR) genes are linked to pre-eclampsia in Nigerian women. These MTHFR C677T and MTR A2756G polymorphisms may increase pre-eclampsia risk.

Area of Science:

  • Genetics
  • Obstetrics
  • Molecular Biology

Background:

  • Pre-eclampsia (PE) is a significant cause of maternal and neonatal mortality in Africa.
  • PE is influenced by genetic, metabolic, and environmental factors.
  • MTHFR and MTR gene polymorphisms have been inconsistently linked to PE in various populations.

Purpose of the Study:

  • To investigate the prevalence of MTHFR C677T and MTR A2756G polymorphisms in a Nigerian population.
  • To assess the association between these polymorphisms and the occurrence of pre-eclampsia.
  • To examine potential links to homocysteine metabolic derangement.

Main Methods:

  • Hospital-based study in Lagos, Nigeria, involving 200 pre-eclamptic and 200 control pregnant women.
  • Genotyping of MTHFR C677T and MTR A2756G using PCR-RFLP.
  • Statistical analysis including logistic regression and Hardy-Weinberg equilibrium testing.

Main Results:

  • Pre-eclampsia occurrence was significantly associated with the T allele of MTHFR (OR=1.855) and the G allele of MTR (OR=1.269).
  • Homozygosity for the TG haplotype notably increased pre-eclampsia risk (OR=2.252).
  • Plasma homocysteine levels were not significantly influenced by MTHFR/MTR haplotypes.

Conclusions:

  • MTHFR C677T and MTR A2756G polymorphisms are associated with pre-eclampsia in Nigerian pregnant women.
  • These genetic variations may contribute to PE susceptibility in this population.
Abstract

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