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Association Between APOE Alleles and Change of Neuropsychological Tests in the Long Life Family Study.
Du, Mengtian; Andersen, Stacy L; Schupf, Nicole; Feitosa, Mary F; Barker, Megan S; Perls, Thomas T; Sebastiani, Paola.
Afiliación
  • Du M; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Andersen SL; Geriatrics Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
  • Schupf N; Department of Neurology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, and the Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA.
  • Feitosa MF; Department of Epidemiology, Columbia University Mailman School of Public Health, Sergievsky Center, New York, NY, USA.
  • Barker MS; Division of Statistical Genomics, Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Perls TT; Department of Neurology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, and the Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA.
  • Sebastiani P; Geriatrics Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
J Alzheimers Dis ; 79(1): 117-125, 2021.
Article en En | MEDLINE | ID: mdl-33216038
ABSTRACT

BACKGROUND:

The Long Life Family Study (LLFS) is a family based, prospective study of healthy aging and familial longevity. The study includes two assessments of cognitive function that were administered approximately 8 years apart.

OBJECTIVE:

To test whether APOE genotype is associated with change of cognitive function in older adults.

METHODS:

We used Bayesian hierarchical models to test the association between APOE alleles and change of cognitive function. Six longitudinally collected neuropsychological test scores were modelled as a function of age at enrollment, follow-up time, gender, education, field center, birth cohort indicator (≤1935, or >1935), and the number of copies of ɛ2 or ɛ4 alleles.

RESULTS:

Out of 4,587 eligible participants, 2,064 were male (45.0%), and age at enrollment ranged from 25 to 110 years, with mean of 70.85 years (SD 15.75). We detected a significant cross-sectional effect of the APOEɛ4 allele on Logical Memory. Participants carrying at least one copy of the ɛ4 allele had lower scores in both immediate (-0.31 points, 95% CI -0.57, -0.05) and delayed (-0.37 points, 95% CI -0.64, -0.10) recall comparing to non-ɛ4 allele carriers. We did not detect any significant longitudinal effect of the ɛ4 allele. There was no cross-sectional or longitudinal effect of the ɛ2 allele.

CONCLUSION:

The APOEɛ4 allele was identified as a risk factor for poorer episodic memory in older adults, while the APOEɛ2 allele was not significantly associated with any of the cognitive test scores.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Atención / Cognición / Apolipoproteína E2 / Apolipoproteína E3 / Apolipoproteína E4 / Envejecimiento Cognitivo / Memoria Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Atención / Cognición / Apolipoproteína E2 / Apolipoproteína E3 / Apolipoproteína E4 / Envejecimiento Cognitivo / Memoria Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Alzheimers Dis Asunto de la revista: GERIATRIA / NEUROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos