Literature DB >> 31322569

TOMM40 '523 Associations with Baseline and Longitudinal Cognition in APOE ɛ3 Homozygotes.

Amber Watts1,2, Heather M Wilkins1, Elias Michaelis1,3, Russell H Swerdlow1,4,5,6.   

Abstract

TOMM40 '523 is associated with Alzheimer's disease (AD), but APOE linkage disequilibrium confounds this association. In 170 APOE ɛ3 homozygotes, we evaluated relationships between short and very long TOMM40 alleles and longitudinal declines in three cognitive domains (attention, verbal memory, and executive function). We used factor analysis to create composite scores from 10 individual cognitive tests, and latent growth curve modeling adjusting for clinical status (normal, amnestic mild cognitive impairment, or AD) to summarize initial performance and change over three years. Relative to individuals with two very long TOMM40 alleles, APOEɛ3 homozygotes with one or two short alleles showed lower baseline cognitive performance regardless of clinical status. The number of short or very long TOMM40 alleles was not associated with longitudinal cognitive changes. In APOEɛ3 homozygotes from the University of Kansas Alzheimer's Disease Center cohort, an association between TOMM40 '523 and cognition is consistent with the possibility that TOMM40 influences cognition independent of APOE.

Entities:  

Keywords:  APOE; TOMM40; cognition; factor analysis; longitudinal

Year:  2019        PMID: 31322569      PMCID: PMC7206989          DOI: 10.3233/JAD-190293

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  25 in total

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4.  TOMM40'523 variant and cognitive decline in older persons with APOE ε3/3 genotype.

Authors:  Lei Yu; Michael W Lutz; Robert S Wilson; Daniel K Burns; Allen D Roses; Ann M Saunders; Chris Gaiteri; Philip L De Jager; Lisa L Barnes; David A Bennett
Journal:  Neurology       Date:  2017-01-20       Impact factor: 9.910

Review 5.  Mitochondria and cell bioenergetics: increasingly recognized components and a possible etiologic cause of Alzheimer's disease.

Authors:  Russell H Swerdlow
Journal:  Antioxid Redox Signal       Date:  2011-09-15       Impact factor: 8.401

6.  The effect of TOMM40 poly-T length on gray matter volume and cognition in middle-aged persons with APOE ε3/ε3 genotype.

Authors:  Sterling C Johnson; Asenath La Rue; Bruce P Hermann; Guofan Xu; Rebecca L Koscik; Erin M Jonaitis; Barbara B Bendlin; Kirk J Hogan; Allen D Roses; Ann M Saunders; Michael W Lutz; Sanjay Asthana; Robert C Green; Mark A Sager
Journal:  Alzheimers Dement       Date:  2011-07       Impact factor: 21.566

7.  A homopolymer polymorphism in the TOMM40 gene contributes to cognitive performance in aging.

Authors:  Kathleen M Hayden; Jill M McEvoy; Colton Linnertz; Deborah Attix; Maragatha Kuchibhatla; Ann M Saunders; Michael W Lutz; Kathleen A Welsh-Bohmer; Allen D Roses; Ornit Chiba-Falek
Journal:  Alzheimers Dement       Date:  2012-08-03       Impact factor: 21.566

Review 8.  Alzheimer's disease risk genes and mechanisms of disease pathogenesis.

Authors:  Celeste M Karch; Alison M Goate
Journal:  Biol Psychiatry       Date:  2014-05-17       Impact factor: 13.382

9.  Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE.

Authors:  Lynn M Bekris; Franziska Lutz; Chang-En Yu
Journal:  J Hum Genet       Date:  2011-11-17       Impact factor: 3.172

10.  Age-related decline in brain resources modulates genetic effects on cognitive functioning.

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