Aβ misfolding in blood plasma is inversely associated with body mass index even in middle adulthood.


Journal

Alzheimer's research & therapy
ISSN: 1758-9193
Titre abrégé: Alzheimers Res Ther
Pays: England
ID NLM: 101511643

Informations de publication

Date de publication:
30 08 2021
Historique:
received: 17 02 2021
accepted: 13 08 2021
entrez: 31 8 2021
pubmed: 1 9 2021
medline: 14 9 2021
Statut: epublish

Résumé

To understand the potential for early intervention and prevention measures in Alzheimer's disease, the association between risk factors and early pathological change needs to be assessed. Hence, the aim of this study was to determine whether risk factors of Alzheimer's clinical syndrome (clinical AD), such as body mass index (BMI), are associated with Aβ misfolding in blood, a strong risk marker for AD among older adults. Information on risk factors and blood samples were collected at baseline in the ESTHER study, a population-based cohort study of older adults (age 50-75 years) in Germany. Aβ misfolding in blood plasma was analyzed using an immuno-infrared-sensor in a total of 872 participants in a nested case-control design among incident dementia cases and matched controls. Associations between risk factors and Aβ misfolding were assessed by multiple logistic regression. For comparison, the association between the risk factors and AD incidence during 17 years of follow-up was investigated in parallel among 5987 cohort participants. An inverse association with Aβ misfolding was seen for BMI at age 50 based on reported weight history (aOR 0.64, 95% CI 0.43-0.96, p = 0.03). Similar but not statistically significant associations were seen for BMI at baseline (i.e., mean age 68) and at age 40. No statistically significant associations with Aβ misfolding were found for other risk factors, such as diabetes, smoking, and physical activity. On the other hand, low physical activity was associated with a significantly reduced risk of developing clinical AD compared to physical inactivity. Our results support that AD pathology may be detectable and associated with reduced weight even in middle adulthood, many years before clinical diagnosis of AD. Physical activity might reduce the risk of onset of AD symptoms.

Sections du résumé

BACKGROUND
To understand the potential for early intervention and prevention measures in Alzheimer's disease, the association between risk factors and early pathological change needs to be assessed. Hence, the aim of this study was to determine whether risk factors of Alzheimer's clinical syndrome (clinical AD), such as body mass index (BMI), are associated with Aβ misfolding in blood, a strong risk marker for AD among older adults.
METHODS
Information on risk factors and blood samples were collected at baseline in the ESTHER study, a population-based cohort study of older adults (age 50-75 years) in Germany. Aβ misfolding in blood plasma was analyzed using an immuno-infrared-sensor in a total of 872 participants in a nested case-control design among incident dementia cases and matched controls. Associations between risk factors and Aβ misfolding were assessed by multiple logistic regression. For comparison, the association between the risk factors and AD incidence during 17 years of follow-up was investigated in parallel among 5987 cohort participants.
RESULTS
An inverse association with Aβ misfolding was seen for BMI at age 50 based on reported weight history (aOR 0.64, 95% CI 0.43-0.96, p = 0.03). Similar but not statistically significant associations were seen for BMI at baseline (i.e., mean age 68) and at age 40. No statistically significant associations with Aβ misfolding were found for other risk factors, such as diabetes, smoking, and physical activity. On the other hand, low physical activity was associated with a significantly reduced risk of developing clinical AD compared to physical inactivity.
CONCLUSIONS
Our results support that AD pathology may be detectable and associated with reduced weight even in middle adulthood, many years before clinical diagnosis of AD. Physical activity might reduce the risk of onset of AD symptoms.

Identifiants

pubmed: 34461995
doi: 10.1186/s13195-021-00889-2
pii: 10.1186/s13195-021-00889-2
pmc: PMC8406782
doi:

Substances chimiques

Amyloid beta-Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

145

Informations de copyright

© 2021. The Author(s).

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Auteurs

Tobias Möllers (T)

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Im Neuenheimer Feld 581, Heidelberg, Germany. t.moellers@dkfz-heidelberg.de.
Network Aging Research, Heidelberg University, Bergheimer Straße 20, Heidelberg, Germany. t.moellers@dkfz-heidelberg.de.

Hannah Stocker (H)

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Im Neuenheimer Feld 581, Heidelberg, Germany.
Network Aging Research, Heidelberg University, Bergheimer Straße 20, Heidelberg, Germany.
Medical Faculty, Heidelberg University, Im Neuenheimer Feld 572, Heidelberg, Germany.

Laura Perna (L)

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Im Neuenheimer Feld 581, Heidelberg, Germany.
Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Kraepelinstraße 2-10, München, Germany.

Andreas Nabers (A)

Department of Biophysics, Ruhr-University Bochum, Universitätsstraße 150, Bochum, Germany.
Department of Biophysics, Center for Protein Diagnostics (ProDi), Biospectroscopy, Ruhr-University Bochum, Universitätsstraße 150, Bochum, Germany.

Dan Rujescu (D)

University Clinic and Outpatient Clinic for Psychiatry, Psychotherapy and Psychosomatics, Martin-Luther-University Halle-Wittenberg, Julius-Kühn-Straße 7, Halle (Saale), Germany.

Annette M Hartmann (AM)

University Clinic and Outpatient Clinic for Psychiatry, Psychotherapy and Psychosomatics, Martin-Luther-University Halle-Wittenberg, Julius-Kühn-Straße 7, Halle (Saale), Germany.

Bernd Holleczek (B)

Saarland Cancer Registry, Präsident-Baltz-Straße 5, Saarbrücken, Germany.

Ben Schöttker (B)

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Im Neuenheimer Feld 581, Heidelberg, Germany.
Network Aging Research, Heidelberg University, Bergheimer Straße 20, Heidelberg, Germany.

Klaus Gerwert (K)

Department of Biophysics, Ruhr-University Bochum, Universitätsstraße 150, Bochum, Germany.
Department of Biophysics, Center for Protein Diagnostics (ProDi), Biospectroscopy, Ruhr-University Bochum, Universitätsstraße 150, Bochum, Germany.

Hermann Brenner (H)

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Im Neuenheimer Feld 581, Heidelberg, Germany.
Network Aging Research, Heidelberg University, Bergheimer Straße 20, Heidelberg, Germany.

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