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

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...

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Autores principales: Sandebring-Matton, Anna, Goikolea, Julen, Björkhem, Ingemar, Paternain, Laura, Kemppainen, Nina, Laatikainen, Tiina, Ngandu, Tiia, Rinne, Juha, Soininen, Hilkka, Cedazo-Minguez, Angel, Solomon, Alina, Kivipelto, Miia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937194/
https://www.ncbi.nlm.nih.gov/pubmed/33676572
http://dx.doi.org/10.1186/s13195-021-00790-y
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author Sandebring-Matton, Anna
Goikolea, Julen
Björkhem, Ingemar
Paternain, Laura
Kemppainen, Nina
Laatikainen, Tiina
Ngandu, Tiia
Rinne, Juha
Soininen, Hilkka
Cedazo-Minguez, Angel
Solomon, Alina
Kivipelto, Miia
author_facet Sandebring-Matton, Anna
Goikolea, Julen
Björkhem, Ingemar
Paternain, Laura
Kemppainen, Nina
Laatikainen, Tiina
Ngandu, Tiia
Rinne, Juha
Soininen, Hilkka
Cedazo-Minguez, Angel
Solomon, Alina
Kivipelto, Miia
author_sort Sandebring-Matton, Anna
collection PubMed
description 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
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spelling pubmed-79371942021-03-09 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial Sandebring-Matton, Anna Goikolea, Julen Björkhem, Ingemar Paternain, Laura Kemppainen, Nina Laatikainen, Tiina Ngandu, Tiia Rinne, Juha Soininen, Hilkka Cedazo-Minguez, Angel Solomon, Alina Kivipelto, Miia Alzheimers Res Ther Research 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 BioMed Central 2021-03-06 /pmc/articles/PMC7937194/ /pubmed/33676572 http://dx.doi.org/10.1186/s13195-021-00790-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sandebring-Matton, Anna
Goikolea, Julen
Björkhem, Ingemar
Paternain, Laura
Kemppainen, Nina
Laatikainen, Tiina
Ngandu, Tiia
Rinne, Juha
Soininen, Hilkka
Cedazo-Minguez, Angel
Solomon, Alina
Kivipelto, Miia
27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title_full 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title_fullStr 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title_full_unstemmed 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title_short 27-Hydroxycholesterol, cognition, and brain imaging markers in the FINGER randomized controlled trial
title_sort 27-hydroxycholesterol, cognition, and brain imaging markers in the finger randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937194/
https://www.ncbi.nlm.nih.gov/pubmed/33676572
http://dx.doi.org/10.1186/s13195-021-00790-y
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