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The influence of APOE status on rate of cognitive decline.
Morrison, Cassandra; Oliver, Michael D; Berry, Virginia; Kamal, Farooq; Dadar, Mahsa.
Afiliação
  • Morrison C; Department of Psychology, Carleton University, Ontario, K1S 5B6, Canada. cassandramorrison@cunet.carleton.ca.
  • Oliver MD; Department of Psychological Science and Neuroscience, Belmont University, Nashville, TN, 37212, USA.
  • Berry V; Belmont Data Collaborative, Belmont University, Nashville, TN, 37212, USA.
  • Kamal F; Department of Psychological Science and Neuroscience, Belmont University, Nashville, TN, 37212, USA.
  • Dadar M; Department of Psychiatry, McGill University, Montreal, QC, H3A 1A1, Canada.
Geroscience ; 46(3): 3263-3274, 2024 06.
Article em En | MEDLINE | ID: mdl-38253819
ABSTRACT

BACKGROUND:

Apolipoprotein (APOE) ɛ4 positivity and subjective cognitive decline (SCD) both increase risk of Alzheimer's disease (AD) development. However, few studies have examined the relationship between SCD and APOE status, especially using longitudinal data. The current study examined whether APOE is associated with the rate of cognitive change in SCD and mild cognitive impairment (MCI).

METHODS:

A sample of 3494 older adults (1990 normal controls, NC, 775 SCD, and 729 MCI) with a mean follow-up of 9.09 years were included from the Rush Alzheimer's Disease Center Research Sharing Hub. Linear mixed effects models examined the relationship between APOE status and cognitive change in older adults with SCD normal controls, and people with MCI.

RESULTS:

The presence of at least one ɛ2 allele in SCD and MCI results in cognitive change rates similar to a NC with the ɛ3ɛ3 genotype. Older adult SCD-ɛ4 individuals exhibited increased rate of cognitive decline compared to all groups, including NC-ɛ4 and MCI-ɛ4.

CONCLUSION:

People with SCD with at least one ɛ4 allele experience increased rates of cognitive decline compared to cognitively healthy older adults and people with MCI. These findings have important implications for treatments and interventions and can improve future research and clinical trials by targeting people in the preclinical AD phase (i.e., SCD) who also possess at least one APOE ɛ4 allele.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Prognostic_studies Limite: Aged / Humans Idioma: En Revista: Geroscience Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Prognostic_studies Limite: Aged / Humans Idioma: En Revista: Geroscience Ano de publicação: 2024 Tipo de documento: Article