Association between neurotrophin-3 polymorphisms and executive function in Japanese patients with amnestic mild cognitive impairment and mild Alzheimer disease

Dement Geriatr Cogn Disord. 2012;34(3-4):190-7. doi: 10.1159/000343075. Epub 2012 Oct 15.

Abstract

Background: We investigated whether neurotrophin (NT)-3 polymorphisms influenced the executive function of patients with 2 separate disease stages with similar dementia conditions: amnestic mild cognitive impairment (A-MCI) or mild Alzheimer disease (AD).

Methods: Among 215 outpatients with dementia and MCI, 155 with mild AD (n = 108) or A-MCI (n = 47) were recruited and divided into three genotypic groups based on the representative NT-3 functional polymorphisms rs6332 and rs6489630. Next, we compared the frontal assessment battery (FAB) total and subtest scores between the three genotypic groups.

Results: The total FAB score was not significantly associated with the rs6332 and rs6489630 genotypes; however, the conflicting instructions score among the 6 subtests was significantly associated with the rs6332 genotype (p < 0.05). Moreover, in patients with mild AD, the conflicting instructions score differed significantly among the three genotypic groups of rs6332 (p < 0.05) (G/G < A/A: p = 0.042 and G/A < A/A: p = 0.041). No significant differences in any other demographic variables were observed among the three genotypes of rs6332 and rs6489630.

Conclusion: These results suggested that an NT-3 polymorphism, rs6332, may significantly influence executive function, reflecting interference performances among patients with mild-stage AD.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / complications
  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / genetics*
  • Analysis of Variance
  • Asian People
  • Cognitive Dysfunction / complications
  • Cognitive Dysfunction / diagnosis
  • Cognitive Dysfunction / genetics*
  • Dementia / complications
  • Dementia / diagnosis
  • Dementia / genetics*
  • Executive Function*
  • Female
  • Genotype
  • Humans
  • Male
  • Memory Disorders / etiology
  • Memory Disorders / genetics*
  • Neuropsychological Tests
  • Neurotrophin 3 / genetics*
  • Polymorphism, Single Nucleotide*
  • Severity of Illness Index

Substances

  • Neurotrophin 3