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Gene-environment interactions between methylenetetrahydrofolate reductase (MTHFR) 677C>T and metabolic syndrome for the prevalence of ischemic stroke in Koreans

  • Ok Joon Kim
  • , Seung Ho Hong
  • , Young Joo Jeon
  • , Seung Hun Oh
  • , Hyun Sook Kim
  • , Young Seok Park
  • , Eo Jin Kim
  • , Nam Keun Kim
  • CHA University
  • Jeju National University
  • Chung-Ang University

Research output: Contribution to journalArticlepeer-review

Abstract

Although metabolic syndrome (MS) is recognized as a risk factor for ischemic stroke, little is known about genetic variants that confer susceptibility to ischemic stroke among individuals with or without MS. This study was completed to investigate whether the methylenetetrahydrofolate reductase (MTHFR) 677C>T polymorphism is associated with MS as a risk factor for ischemic stroke in the Korean population. The prevalence of MS was significantly higher in ischemic stroke patients than controls (adjusted odds ratio [AOR]. = 1.420; 95% confidence interval [CI] = 1.017-1.982, P= 0.040). MS prevalence was also significantly different between patients with subtypes of small-artery occlusion (AOR = 1.707; 95% CI = 1.081-2.695, P= 0.022) and large-artery occlusion (AOR = 1.661; 95% CI = 1.089-2.534, P= 0.019) versus controls. The frequencies of the MTHFR 677 TT genotype (AOR = 3.001; 95% CI = 1.487-6.057, P= 0.002) and CT genotype (AOR = 1.772; 95% CI = 1.053-2.983, P= 0.031) of the MS group, and for the CC genotype in those without MS were significantly different between the ischemic stroke patients and controls. The MTHFR 677C>T polymorphism was associated with a higher risk of MS among ischemic stroke patients in the Korean population.

Original languageEnglish
Pages (from-to)11-16
Number of pages6
JournalNeuroscience Letters
Volume533
Issue number1
DOIs
StatePublished - 15 Jan 2013
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Metabolic syndrome (MS)
  • Methylenetetrahydrofolate reductase (MTHFR)
  • Polymorphism
  • Risk factor
  • Stroke

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