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Education and the moderating roles of age, sex, ethnicity and apolipoprotein epsilon 4 on the risk of cognitive impairment
- Source :
- Zaguán. Repositorio Digital de la Universidad de Zaragoza, instname, Archives of Gerontology and Geriatrics, Archives of Gerontology and Geriatrics, Elsevier, 2020, 91, pp.104112. ⟨10.1016/j.archger.2020.104112⟩, Arch Gerontol Geriatr
- Publication Year :
- 2020
-
Abstract
- International audience; Background: We examined how the relationship between education and latelife cognitive impairment (defined as a Mini Mental State Examination score below 24) is influenced by age, sex, ethnicity, and Apolipoprotein E epsilon 4 (APOE*4).Methods: Participants were 30,785 dementia-free individuals aged 55-103 years, from 18 longitudinal cohort studies, with an average follow-up ranging between 2 and 10 years. Pooled hazard ratios were obtained from multilevel parametric survival analyses predicting cognitive impairment (CI) from education and its interactions with baseline age, sex, APOE*4 and ethnicity. In separate models, education was treated as continuous (years) and categorical, with participants assigned to one of four education completion levels: Incomplete Elementary; Elementary; Middle; and High School.Results: Compared to Elementary, Middle (HR = 0.645, P = 0.004) and High School (HR = 0.472, P < 0.001) education were related to reduced CI risk. The decreased risk of CI associated with Middle education weakened with older baseline age (HR = 1.029, P = 0.056) and was stronger in women than men (HR = 1.309, P = 0.001). The association between High School and lowered CI risk, however, was not moderated by sex or baseline age, but was stronger in Asians than Whites (HR = 1.047, P = 0.044), and significant among Asian (HR = 0.34, P < 0.001) and Black (HR = 0.382, P = 0.016), but not White, APOE*4 carriers.Conclusion: High School completion may reduce risk of CI associated with advancing age and APOE*4. The observed ethnoregional differences in this effect are potentially due to variations in social, economic, and political outcomes associated with educational attainment, in combination with neurobiological and genetic differences, and warrant further study.
- Subjects :
- Apolipoprotein E
Male
Aging
Health (social science)
Apolipoprotein B
[SDV]Life Sciences [q-bio]
Apolipoprotein E4
Ethnic group
Cognitive decline
MESH: Cognitive Dysfunction
0302 clinical medicine
MESH: Aged, 80 and over
MESH: Risk Factors
Risk Factors
80 and over
Ethnicity
Medicine
030212 general & internal medicine
Longitudinal Studies
MESH: Apolipoprotein E4
Cognitive impairment
MESH: Longitudinal Studies
Aged, 80 and over
MESH: Aged
biology
Hazard ratio
Educational Status
MESH: Ethnic Groups
Female
Sex
Clinical Sciences
Article
Education
03 medical and health sciences
Age
Clinical Research
Acquired Cognitive Impairment
Humans
Cognitive Dysfunction
Aged
MESH: Humans
030214 geriatrics
business.industry
Prevention
Neurosciences
Educational attainment
MESH: Male
Brain Disorders
Quality Education
Ageing
for Cohort Studies of Memory in an International Consortium
Geriatrics
biology.protein
Dementia
Geriatrics and Gerontology
business
MESH: Educational Status
Gerontology
MESH: Female
Demography
Subjects
Details
- ISSN :
- 01674943
- Database :
- OpenAIRE
- Journal :
- Zaguán. Repositorio Digital de la Universidad de Zaragoza, instname, Archives of Gerontology and Geriatrics, Archives of Gerontology and Geriatrics, Elsevier, 2020, 91, pp.104112. ⟨10.1016/j.archger.2020.104112⟩, Arch Gerontol Geriatr
- Accession number :
- edsair.doi.dedup.....2a378f5f859c3ebd72248353567523bc
- Full Text :
- https://doi.org/10.1016/j.archger.2020.104112⟩