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P3‐142: Cholesterol in mild cognitive impairment and Alzheimer's disease in a prospective population‐based study in Germany
Author(s) -
Schröder Johannes,
Sattler Christine,
Schönknecht Peter,
Toro Pablo
Publication year - 2009
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2009.04.1117
Subject(s) - apolipoprotein e , disease , risk factor , epidemiology , medicine , cholesterol , population , cognitive impairment , longitudinal study , prospective cohort study , cohort , alzheimer's disease , psychology , gerontology , pathology , environmental health
Background: Animal research and epidemiological studies identified cholesterol as a risk factor for mild cognitive impairment (MCI) and Alzheimer’s disease (AD). We therefore investigated the potential impact of plasma total cholesterol (TC) on the development of MCI and AD in a longitudinal study of a representative birth cohort born between 1930 and 1932. Methods: 500 participants of the Interdisciplinary Longitudinal Study on Adult Development and Aging (ILSE) were examined in 1993/94 (t1), 1997/98 (t2) and 2005/07 (t3). Results: Prevalence of MCI increased from 13% to 23% and 29% over time; in addition, 7% of the participants had developed AD at t3. At t1 and t2 MCI patients showed the highest TC level and control subjects the lowest with AD patients occupying an intermediate position. When compared to control subjects, patients with MCI or AD showed a significant decrease of TC levels between t1 and t3. In all examination waves APOE4 carriers showed higher TC levels in comparison to the non-APOE4 carriers. Analyses of variance yielded significant (p<0.05) main effects for diagnosis, presence of an APOE4 allele and time. The interactions time*diagnose and time*diagnose*APOE also reached significance. Conclusions: Our findings confirm the hypotheses that high midlife serum TC constitutes a risk factor for the development of MCI and AD and demonstrate that this effect particularly strikes at the APOE4 carriers. The reduction of TC among the patients could explained by a disease effect.