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TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes.

Publication ,  Journal Article
Watts, A; Haneline, S; Welsh-Bohmer, KA; Wu, J; Alexander, R; Swerdlow, RH; Burns, DK; Saunders, AM
Published in: J Alzheimers Dis
2023

BACKGROUND: TOMM40 '523 has been associated with cognitive performance and risk for developing Alzheimer's disease independent of the effect of APOE genotype. Few studies have considered the longitudinal effect of this genotype on change in cognition over time. OBJECTIVE: Our objective was to evaluate the relationship between TOMM40 genotype status and change in cognitive performance in the TOMMORROW study, which was designed to prospectively evaluate an algorithm that includes TOMM40 '523 for genetic risk for conversion to mild cognitive impairment. METHODS: We used latent growth curve models to estimate the effect of TOMM40 allele carrier (short, very long) status on the intercept and slope of change in cognitive performance in four broad cognitive domains (attention, memory, executive function, and language) and a combined overall cognitive score over 30 months. RESULTS: TOMM40 very long allele carriers had significantly lower baseline performance for the combined overall cognitive function score (B = -0.088, p = 0.034) and for the executive function domain score (B = -0.143, p = 0.013). Slopes for TOMM40 very long carriers had significantly greater increases over time for the executive function domain score only. In sensitivity analyses, the results for executive function were observed in participants who remained clinically stable, but not in those who progressed clinically over the study duration. CONCLUSIONS: Our results add to the growing body of evidence that TOMM40, in the absence of APOEɛ4, may contribute to cognitive changes with aging and dementia and support the view that mitochondrial function is an important contributor to Alzheimer's disease risk.

Duke Scholars

Published In

J Alzheimers Dis

DOI

EISSN

1875-8908

Publication Date

2023

Volume

95

Issue

4

Start / End Page

1697 / 1707

Location

United States

Related Subject Headings

  • Neurology & Neurosurgery
  • Mitochondrial Precursor Protein Import Complex Proteins
  • Humans
  • Homozygote
  • Genotype
  • Executive Function
  • Cognitive Dysfunction
  • Cognition
  • Apolipoproteins E
  • Alzheimer Disease
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Watts, A., Haneline, S., Welsh-Bohmer, K. A., Wu, J., Alexander, R., Swerdlow, R. H., … Saunders, A. M. (2023). TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes. J Alzheimers Dis, 95(4), 1697–1707. https://doi.org/10.3233/JAD-230066
Watts, Amber, Stephen Haneline, Kathleen A. Welsh-Bohmer, Jingtao Wu, Robert Alexander, Russell H. Swerdlow, Daniel K. Burns, and Ann M. Saunders. “TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes.J Alzheimers Dis 95, no. 4 (2023): 1697–1707. https://doi.org/10.3233/JAD-230066.
Watts A, Haneline S, Welsh-Bohmer KA, Wu J, Alexander R, Swerdlow RH, et al. TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes. J Alzheimers Dis. 2023;95(4):1697–707.
Watts, Amber, et al. “TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes.J Alzheimers Dis, vol. 95, no. 4, 2023, pp. 1697–707. Pubmed, doi:10.3233/JAD-230066.
Watts A, Haneline S, Welsh-Bohmer KA, Wu J, Alexander R, Swerdlow RH, Burns DK, Saunders AM. TOMM40 '523 Genotype Distinguishes Patterns of Cognitive Improvement for Executive Function in APOEɛ3 Homozygotes. J Alzheimers Dis. 2023;95(4):1697–1707.

Published In

J Alzheimers Dis

DOI

EISSN

1875-8908

Publication Date

2023

Volume

95

Issue

4

Start / End Page

1697 / 1707

Location

United States

Related Subject Headings

  • Neurology & Neurosurgery
  • Mitochondrial Precursor Protein Import Complex Proteins
  • Humans
  • Homozygote
  • Genotype
  • Executive Function
  • Cognitive Dysfunction
  • Cognition
  • Apolipoproteins E
  • Alzheimer Disease