Is KIBRA polymorphism associated with memory performance and cognitive impairment in Alzheimer's disease?

J Alzheimers Dis. 2024 Nov;102(1):218-227. doi: 10.1177/13872877241284313. Epub 2024 Oct 15.

Abstract

Background: Genetic variations in a common single nucleotide polymorphism in the ninth intron of the KIBRA gene have been linked to memory performance and risk of Alzheimer's disease (AD).

Objective: We examined the risk of AD related to presence of KIBRA T allele (versus CC homozygote) and to memory performance. The role of established genetic risk factors APOE ε4 and BDNF Met was also considered.

Methods: Participants were cognitively healthy individuals (n = 19), participants with amnestic mild cognitive impairment (aMCI) due to AD (n = 99) and AD dementia (n = 37) from the Czech Brain Aging Study. Binary and multinomial logistic regressions compared odds of belonging to a certain diagnostic category and multivariate linear regressions assessed associations with memory.

Results: KIBRA T allele was associated with increased AD dementia risk (odds ratio [OR] = 5.98, p = 0.012) compared to KIBRA CC genotype. In APOE ε4 negative individuals, KIBRA T allele was associated with a greater risk of both aMCI due to AD (OR = 6.68, p = 0.038) and AD dementia (OR = 15.75, p = 0.009). In BDNF Met positive individuals, the KIBRA T allele was associated with a greater risk of AD dementia (OR = 10.98, p = 0.050). In AD dementia, the association between KIBRA T allele and better memory performance approached significance (β = 0.42; p = 0.062). The link between possessing the KIBRA T allele and better memory reached statistical significance only among BDNF Met carriers (β = 1.21, p = 0.027).

Conclusions: Findings suggest that KIBRA T allele may not fully protect against AD dementia but could potentially delay progression of post-diagnosis cognitive deficits.

Keywords: Alzheimer's disease; ApoE; BDNF; KIBRA; cognitive impairments; memory.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alleles
  • Alzheimer Disease* / genetics
  • Apolipoprotein E4 / genetics
  • Brain-Derived Neurotrophic Factor / genetics
  • Cognitive Dysfunction* / genetics
  • Female
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Male
  • Memory / physiology
  • Neuropsychological Tests
  • Polymorphism, Single Nucleotide* / genetics

Substances

  • WWC1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Brain-Derived Neurotrophic Factor
  • Apolipoprotein E4