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Early age-related macular degeneration, cognitive function, and dementia: the Cardiovascular Health Study.

TitleEarly age-related macular degeneration, cognitive function, and dementia: the Cardiovascular Health Study.
Publication TypeJournal Article
Year of Publication2009
AuthorsBaker, ML, Wang, JJin, Rogers, S, Klein, R, Kuller, LH, Larsen, EK, Wong, TYin
JournalArch Ophthalmol
Volume127
Issue5
Pagination667-73
Date Published2009 May
ISSN1538-3601
KeywordsAged, Aged, 80 and over, Cardiovascular Diseases, Cognition Disorders, Dementia, Female, Humans, Intelligence Tests, Macular Degeneration, Male, Neuropsychological Tests, Odds Ratio, Prospective Studies, Risk Factors, United States
Abstract<p><b>OBJECTIVE: </b>To describe the association of cognitive function and dementia with early age-related macular degeneration (AMD) in older individuals.</p><p><b>METHODS: </b>This population-based study included 2,088 persons aged 69 to 97 years who participated in the Cardiovascular Health Study. The AMD was assessed from retinal photographs based on a modified Wisconsin AMD grading system. Cognitive function was assessed using the Digit Symbol Substitution Test (DSST) and the Modified Mini-Mental State Examination. Participants were also evaluated for dementia using detailed neuropsychological testing.</p><p><b>RESULTS: </b>After controlling for age, sex, race, and study center, persons with low DSST scores (lowest quartile of scores, < or =30) were more likely to have early AMD (odds ratio, 1.38; 95% confidence interval, 1.03-1.85) than were persons with higher DSST scores. In analyses further controlling for education, systolic blood pressure, total cholesterol level, diabetes mellitus, smoking status, and apolipoprotein E genotype, this association was stronger (odds ratio, 2.00; 95% confidence interval, 1.29-3.10). There was no association of low Modified Mini-Mental State Examination scores, dementia, or Alzheimer disease with early AMD.</p><p><b>CONCLUSIONS: </b>In this older population, cognitive impairment may share common age-related pathogenesis and risk factors with early AMD.</p>
DOI10.1001/archophthalmol.2009.30
Alternate JournalArch. Ophthalmol.
PubMed ID19433718
PubMed Central IDPMC3001290
Grant ListN01 HC085086 / HC / NHLBI NIH HHS / United States
N01 HC085083 / HC / WHI NIH HHS / United States
N01 HC085081 / HC / NHLBI NIH HHS / United States
U01 HL080295-04 / HL / NHLBI NIH HHS / United States
U01 HL080295 / HL / NHLBI NIH HHS / United States
N01 HC075150 / HC / NHLBI NIH HHS / United States
N01 HC015103 / HC / NHLBI NIH HHS / United States
N01 HC085083 / HC / NHLBI NIH HHS / United States
R21-HL077166 / HL / NHLBI NIH HHS / United States
N01 HC085085 / HC / NHLBI NIH HHS / United States
N01HC55222 / HL / NHLBI NIH HHS / United States
N01-HC-85086 / HC / NHLBI NIH HHS / United States
N01HC85086 / HL / NHLBI NIH HHS / United States
N01 HC085082 / HC / NHLBI NIH HHS / United States
N01 HC085080 / HC / NHLBI NIH HHS / United States
N01 HC-55222 / HC / NHLBI NIH HHS / United States
N01 HC055222 / HC / NHLBI NIH HHS / United States
N01-HC-75150 / HC / NHLBI NIH HHS / United States
N01 HC085079 / HC / WHI NIH HHS / United States
N01 HC085081 / HC / WHI NIH HHS / United States
N01 HC045133 / HC / WHI NIH HHS / United States
N01 HC085084 / HC / NHLBI NIH HHS / United States
N01HC75150 / HL / NHLBI NIH HHS / United States
R21 HL077166 / HL / NHLBI NIH HHS / United States
N01-HC-85079 / HC / NHLBI NIH HHS / United States
N01HC85079 / HL / NHLBI NIH HHS / United States
N01 HC085079 / HC / NHLBI NIH HHS / United States
N01 HC045133 / HC / NHLBI NIH HHS / United States
N01 HC035129 / HC / NHLBI NIH HHS / United States
R21 HL077166-02 / HL / NHLBI NIH HHS / United States