Apolipoproteins and HDL cholesterol do not associate with the risk of future dementia and Alzheimer’s disease: the National Finnish population study (FINRISK)

• Published in: AGE 2016-12, Vol.38 (5-6), p.465-473
• Main Authors: Tynkkynen, Juho, Hernesniemi, Jussi A., Laatikainen, Tiina, Havulinna, Aki S., Sundvall, Jouko, Leiviskä, Jaana, Salo, Perttu, Salomaa, Veikko
• Format: Article
• Language: English
• Subjects: Accuracy; Adult; Aged; Alzheimer Disease - blood; Alzheimer Disease - epidemiology; Alzheimer's disease; Apolipoprotein A-I - blood; Apolipoproteins; Apolipoproteins B - blood; Bayesian analysis; Biomarkers - blood; Biomedical and Life Sciences; Blood pressure; Cell Biology; Cholesterol; Cholesterol, HDL - blood; Cohort Studies; Dementia; Disease; Ethics; Ethnicity; European Continental Ancestry Group; Female; Finland - epidemiology; Geriatrics/Gerontology; Health care; High density lipoprotein; Hospitals; Humans; Incidence; Laboratories; Life Sciences; Male; Middle Aged; Molecular Medicine; Monte Carlo simulation; Original; Original Article; Peptides; Population; Proportional Hazards Models; Prospective Studies; Proteins; Public health; Regression analysis; Risk Factors; Statistical analysis; Time Factors; White people
• ISSN: 0161-9152; 2509-2715; 1574-4647; 2509-2723
• DOI: 10.1007/s11357-016-9950-x

Data on associations of apolipoproteins A-I and B (apo A-I, apo B) and HDL cholesterol (HDL-C) with dementia and Alzheimer’s disease (AD) are conflicting. Our aim was to examine, whether apo B, apoA-I, their ratio, or HDL-C are significant, independent predictors of incident dementia and AD in the general population free of dementia at baseline. We analyzed the results from two Finnish prospective population-based cohort studies in a total of 13,275 subjects aged 25 to 74 years with mainly Caucasian ethnicity. The follow-up time for both cohorts was 10 years. We used Cox proportional hazards regression to evaluate hazard ratios (HR) for incident dementia (including AD) ( n  = 220) and for AD ( n  = 154). Cumulative incidence function (CIF) analysis was also performed to adjust the results for competing risks of death. Adjusted for multiple dementia and AD risk factors, log-transformed apo A-I, log HDL-C, log apo B, and log apo B/A-I ratio were not associated with incident dementia or AD. HDL-C was inversely associated with AD risk when adjusted for competing risks but no other statistically significant associations were observed in the CIF analyses. Apo A-I, HDL-C, apo B, or apo B/A-I ratio were not associated with future dementia or AD. HDL-C was inversely associated with incident AD risk when adjusted for competing risks of death, but the finding is unlikely to be of clinical relevance. Our study does not support the use of these risk markers to predict incident dementia or AD.