The 894G > T (Glu298Asp) variant in the endothelial NOS gene and MTHFR polymorphisms influence homocysteine levels in patients with cognitive decline

Demetrio Caccamo, Paolo Maria Rossini, N Ferlazzo, G Gorgone, M Currò, S Condello, Francesca Pisani, F Vernieri, R. Ientile

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

The presence and severity of cerebrovascular pathological findings have been shown to increase the risk and stage of cognitive decline observed in Alzheimer's disease and vascular dementia. Thus, the modification of vascular risk factors seems useful to reduce the risk of dementia regardless of type. Hyperhomocysteinemia has long been known as a major independent risk factor for vascular dysfunction. In this study, we evaluated the relationships between plasma homocysteine levels and genetic risk factors for hyperhomocysteinemia, i.e., the presence of gene variants for methylenetetrahydrofolate reductase (MTHFR) and endothelial nitric oxide synthase (eNOS) in patients with cognitive impairment. Genotyping for MTHFR C677T and eNOS 894G > T polymorphisms was carried out in 69 patients with probable diagnosis of AD and anamnestic mild cognitive impairment, matched for age and gender with 69 healthy volunteers. Patients with MTHFR TT677 genotype showed higher plasma Hcy levels than controls, even after adjustment for folate levels (P < 0.05). Moreover, Hcy plasma levels were higher in cases than controls for any given eNOS genotype. In particular, the presence of eNOS TT894 genotype in patients with cognitive decline resulted significantly associated with increased plasma Hcy levels when compared with controls having the same genotype or patients having other eNOS genotypes (P = 0.02). These data suggest that both MTHFR C677T and eNOS G894T variants should be regarded as genetic risk factors for hyperhomocysteinemia in patients with cognitive decline.
Original languageEnglish
Pages (from-to)167-174
Number of pages8
JournalNeuroMolecular Medicine
Volume13
DOIs
Publication statusPublished - 2011

Keywords

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease
  • Cognition Disorders
  • Female
  • Genotype
  • Humans
  • Hyperhomocysteinemia
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Nitric Oxide Synthase Type III
  • Polymorphism, Genetic
  • Risk Factors

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