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Genetic risk score for Alzheimer's disease predicts brain volume differences in mid and late life in UK biobank participants.
Buto, Peter T; Wang, Jingxuan; La Joie, Renaud; Zimmerman, Scott C; Glymour, M Maria; Ackley, Sarah F; Hoffmann, Thomas J; Yaffe, Kristine; Zeki Al Hazzouri, Adina; Brenowitz, Willa D.
Afiliación
  • Buto PT; Department of Epidemiology & Biostatistics, University of California, San Francisco, California, USA.
  • Wang J; Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.
  • La Joie R; Department of Epidemiology & Biostatistics, University of California, San Francisco, California, USA.
  • Zimmerman SC; Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Glymour MM; Memory and Aging Center, University of California, San Francisco, California, USA.
  • Ackley SF; Department of Epidemiology & Biostatistics, University of California, San Francisco, California, USA.
  • Hoffmann TJ; Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Yaffe K; Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Zeki Al Hazzouri A; Department of Epidemiology & Biostatistics, University of California, San Francisco, California, USA.
  • Brenowitz WD; Department of Epidemiology & Biostatistics, University of California, San Francisco, California, USA.
Alzheimers Dement ; 20(3): 1978-1987, 2024 03.
Article en En | MEDLINE | ID: mdl-38183377
ABSTRACT

INTRODUCTION:

We estimated the ages when associations between Alzheimer's disease (AD) genes and brain volumes begin among middle-aged and older adults.

METHODS:

Among 45,616 dementia-free participants aged 45-80, linear regressions tested whether genetic risk score for AD (AD-GRS) had age-dependent associations with 38 regional brain magnetic resonance imaging volumes. Models were adjusted for sex, assessment center, genetic ancestry, and intracranial volume.

RESULTS:

AD-GRS modified the estimated effect of age (per decade) on the amygdala (-0.41 mm3 [-0.42, -0.40]); hippocampus (-0.45 mm3 [-0.45, -0.44]), nucleus accumbens (-0.55 mm3 [-0.56, -0.54]), thalamus (-0.38 mm3 [-0.39, -0.37]), and medial orbitofrontal cortex (-0.23 mm3 [-0.24, -0.22]). Trends began by age 45 for the nucleus accumbens and thalamus, 48 for the hippocampus, 51 for the amygdala, and 53 for the medial orbitofrontal cortex. An AD-GRS excluding apolipoprotein E (APOE) was additionally associated with entorhinal and middle temporal cortices.

DISCUSSION:

APOE and other genes that increase AD risk predict lower hippocampal and other brain volumes by middle age.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos