Cited by 34Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsLipoproteins and Cardiovascular Health

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Statin Initiation and Risk of Incident Alzheimer Disease and Cognitive Decline in Genetically Susceptible Older Adults

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Abstract

Background and Objectives The association of statin initiation with incident Alzheimer disease (AD) dementia and cognitive decline by the APOE ε4 allele is unknown. Our objective was to examine whether the association of statin initiation with incident AD dementia and cognitive decline differs by the APOE ε4 allele. Methods This population-based longitudinal cohort study was conducted in 4 urban communities in Chicago, IL, United States, consisting of 4,807 participants. Statin initiation is based on the inspection of medications during home assessments. Clinical diagnosis for incident AD used the NINCDS-ADRDA criteria, and longitudinal measurements of global cognition consisted of episodic memory, perceptual speed, and the Mini-Mental State Examination tests. Results The study participants had a mean age of 72 years, consisting of 63% female individuals and 61% non-Hispanic Black individuals. During the study period, 1,470 (31%) participants reported statin initiation. In a covariate-adjusted competing risk model, statin initiation was associated with a reduced risk of incident clinical AD [hazard ratio (HR) 0.81 (95% CI 0.70–0.94)] compared with nonusers. This association was statistically significantly lower ( p interaction = 0.015) among participants with the APOE ε4 allele [HR 0.60 (95% CI 0.49–0.74)] compared with those without the APOE ε4 allele [HR 0.96 (95% CI 0.82–1.12)]. The annual decline in global cognition (β = 0.021, 95% CI 0.007–0.034) and episodic memory (β = 0.020, 95% CI 0.007–0.033) was also substantially slower among participants with the APOE ε4 allele after statin initiation compared with nonusers. However, the association of statin initiation with cognitive decline was not significant among those without the APOE ε4 allele. Discussion Our findings suggest that statins might be associated with a lower risk of incident AD among individuals with the APOE ε4 allele. The benefits of statin therapy need further consideration in randomized clinical trials, especially among those with the APOE ε4 allele. Classification of Evidence This study provides Class II evidence that among those aged 65 years or older, statin initiation was associated with a reduced risk of Alzheimer disease, especially in the presence of an APOE -e4 allele.

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Metadata

Authors
Rajan, K. B., Mcaninch, E. A., Wilson, R. S., Dhana, A., Evans-Lacko, S., & Evans, D. A.
Affiliations
Rush University Medical Center (US)
Venue
Neurology
Published
2024-04-09
Volume
102
Issue
7
Pages
e209168-e209168
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W4392529943
Cited by
34
References
8
Citations by year
2026: 12 · 2025: 14 · 2024: 8
FWCI
9.99
Type
journal article
Language
en
Open access
Locations
  • Neurology (publishedVersion)
  • PubMed Central (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed (publishedVersion)
  • London School of Economics and Political Science Research Online (London School of Economics and Political Science) (submittedVersion)
  • London School of Economics and Political Science Theses Online (London School of Economics and Political Science) (submittedVersion)
Funders
  • National Institutes of Health
  • National Institute on Aging (R01AG058679, UH2AG083289, R01AG073627)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
Keywords
statins, Alzheimer's disease, cognitive decline, APOE ε4, genetic susceptibility, older adults, episodic memory, perceptual speed, Mini-Mental State Examination
MeSH terms
Aged, Alzheimer Disease, Cognition, Female, Humans, Longitudinal Studies, Male, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Genetic Predisposition to Disease, Apolipoprotein E4, Cognitive Dysfunction

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