27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial

Author:

Sandebring-Matton AnnaORCID,Goikolea Julen,Björkhem Ingemar,Paternain Laura,Kemppainen Nina,Laatikainen Tiina,Ngandu Tiia,Rinne Juha,Soininen Hilkka,Cedazo-Minguez Angel,Solomon Alina,Kivipelto Miia

Abstract

Abstract Background 27-Hydroxycholesterol (27-OH), the main circulating oxysterol in humans and the potential missing link between peripheral hypercholesterolemia and Alzheimer’s disease (AD), has not been investigated previously in relation to cognition and neuroimaging markers in the context of preventive interventions. Methods The 2-year Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER) included older individuals (60–77 years) at increased risk for dementia but without dementia or substantial cognitive impairment from the general population. Participants were randomized to a multidomain intervention (diet, exercise, cognitive training, and vascular risk management) or control group (general health advice) in a 1:1 ratio. Outcome assessors were masked to group allocation. This FINGER exploratory sub-study included 47 participants with measures of 27-OH, cognition, brain MRI, brain FDG-PET, and PiB-PET. Linear regression models were used to assess the cross-sectional and longitudinal associations between 27-OH, cognition, and neuroimaging markers, considering several potential confounders/intervention effect modifiers. Results 27-OH reduction during the intervention was associated with improvement in cognition (especially memory). This was not observed in the control group. The intervention reduced 27-OH particularly in individuals with the highest 27-OH levels and younger age. No associations were found between changes in 27-OH levels and neuroimaging markers. However, at baseline, a higher 27-OH was associated with lower total gray matter and hippocampal volume, and lower cognitive scores. These associations were unaffected by total cholesterol levels. While sex seemed to influence associations at baseline, it did not affect longitudinal associations. Conclusion 27-OH appears to be a marker not only for dementia/AD risk, but also for monitoring the effects of preventive interventions on cholesterol metabolism. Trial registration ClinicalTrials.gov, NCT01041989. Registered on 4 January 2010

Funder

Vetenskapsrådet

Center for Innovative Medicine, SLL

Margareta af Ugglas foundation

Alzheimerfonden

Knut och Alice Wallenbergs Stiftelse

Stiftelsen Stockholms sjukhem

Konung Gustaf V:s och Drottning Victorias Frimurarestiftelse

Gun och Bertil Stohnes Stiftelse

Karolinska Institutet fund for geriatric research

Stiftelsen för Gamla Tjänarinnor

Alzheimer's Research & Prevention Foundation

Academy of Finland

Finnish Social Insurance Institution

Finnish Ministry of Education and Culture

Juho Vainion Säätiö

Joint Program of Neurodegenerative Disorders – prevention

European Research Council

Yrjö Jahnsson Foundation

Finnish Cultural Foundation

Region Stockholm ALF

EVO grant Turku University Hospital

EVO/VTR funding from Kuopio University Hospital

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Clinical Neurology,Neurology

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