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Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients

OBJECTIVE: This study aims to investigate the relationship between diurnal cortisol patterns, cognition and Alzheimer’s disease (AD) biomarkers in memory clinic patients. METHOD: Memory clinic patients were recruited from Karolinska University Hospital in Sweden (n=155). Diurnal cortisol patterns we...

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Autores principales: Holleman, Jasper, Adagunodo, Sofia, Kåreholt, Ingemar, Hagman, Göran, Aspö, Malin, Udeh-Momoh, Chinedu T, Solomon, Alina, Kivipelto, Miia, Sindi, Shireen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582323/
https://www.ncbi.nlm.nih.gov/pubmed/36277478
http://dx.doi.org/10.1136/bmjno-2022-000344
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author Holleman, Jasper
Adagunodo, Sofia
Kåreholt, Ingemar
Hagman, Göran
Aspö, Malin
Udeh-Momoh, Chinedu T
Solomon, Alina
Kivipelto, Miia
Sindi, Shireen
author_facet Holleman, Jasper
Adagunodo, Sofia
Kåreholt, Ingemar
Hagman, Göran
Aspö, Malin
Udeh-Momoh, Chinedu T
Solomon, Alina
Kivipelto, Miia
Sindi, Shireen
author_sort Holleman, Jasper
collection PubMed
description OBJECTIVE: This study aims to investigate the relationship between diurnal cortisol patterns, cognition and Alzheimer’s disease (AD) biomarkers in memory clinic patients. METHOD: Memory clinic patients were recruited from Karolinska University Hospital in Sweden (n=155). Diurnal cortisol patterns were assessed using five measures: awakening levels, cortisol awakening response, bedtime levels, the ratio of awakening to bedtime levels (AM/PM ratio) and total daily output. Cognition was measured in five domains: memory, working memory, processing speed, perceptual reasoning and overall cognition. AD biomarkers Aβ(42), total tau and phosphorylated tau were assessed from cerebrospinal fluid (CSF). Cognition was measured at follow-up (average 32 months) in a subsample of participants (n=57). RESULTS: In assessing the associations between cortisol and cognition, higher awakening cortisol levels were associated with greater processing speed at baseline. No relationship was found between diurnal cortisol patterns and change in cognition over time or CSF AD biomarkers in the total sample. After stratification by CSF Aβ(42) levels, higher awakening cortisol levels were associated with worse memory performance in amyloid-positive participants. In amyloid-negative participants, higher bedtime cortisol levels and a lower AM/PM ratio were associated with lower overall cognition, greater awakening cortisol levels were associated with better processing speed, and a higher AM/PM ratio was associated with better perceptual reasoning. Additionally, higher awakening cortisol levels were associated with lower CSF Aβ(42) levels in amyloid-positive participants, while higher bedtime cortisol levels and a lower AM/PM ratio were associated with higher CSF total tau in amyloid-negative participants. CONCLUSIONS: Our findings suggest that diurnal cortisol patterns are associated with cognitive function and provide new insights into the association between diurnal cortisol patterns and AD-related CSF biomarkers. Further research is needed to examine the complex relationship between cortisol, cognition and brain pathology.
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spelling pubmed-95823232022-10-21 Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients Holleman, Jasper Adagunodo, Sofia Kåreholt, Ingemar Hagman, Göran Aspö, Malin Udeh-Momoh, Chinedu T Solomon, Alina Kivipelto, Miia Sindi, Shireen BMJ Neurol Open Original Research OBJECTIVE: This study aims to investigate the relationship between diurnal cortisol patterns, cognition and Alzheimer’s disease (AD) biomarkers in memory clinic patients. METHOD: Memory clinic patients were recruited from Karolinska University Hospital in Sweden (n=155). Diurnal cortisol patterns were assessed using five measures: awakening levels, cortisol awakening response, bedtime levels, the ratio of awakening to bedtime levels (AM/PM ratio) and total daily output. Cognition was measured in five domains: memory, working memory, processing speed, perceptual reasoning and overall cognition. AD biomarkers Aβ(42), total tau and phosphorylated tau were assessed from cerebrospinal fluid (CSF). Cognition was measured at follow-up (average 32 months) in a subsample of participants (n=57). RESULTS: In assessing the associations between cortisol and cognition, higher awakening cortisol levels were associated with greater processing speed at baseline. No relationship was found between diurnal cortisol patterns and change in cognition over time or CSF AD biomarkers in the total sample. After stratification by CSF Aβ(42) levels, higher awakening cortisol levels were associated with worse memory performance in amyloid-positive participants. In amyloid-negative participants, higher bedtime cortisol levels and a lower AM/PM ratio were associated with lower overall cognition, greater awakening cortisol levels were associated with better processing speed, and a higher AM/PM ratio was associated with better perceptual reasoning. Additionally, higher awakening cortisol levels were associated with lower CSF Aβ(42) levels in amyloid-positive participants, while higher bedtime cortisol levels and a lower AM/PM ratio were associated with higher CSF total tau in amyloid-negative participants. CONCLUSIONS: Our findings suggest that diurnal cortisol patterns are associated with cognitive function and provide new insights into the association between diurnal cortisol patterns and AD-related CSF biomarkers. Further research is needed to examine the complex relationship between cortisol, cognition and brain pathology. BMJ Publishing Group 2022-10-19 /pmc/articles/PMC9582323/ /pubmed/36277478 http://dx.doi.org/10.1136/bmjno-2022-000344 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Holleman, Jasper
Adagunodo, Sofia
Kåreholt, Ingemar
Hagman, Göran
Aspö, Malin
Udeh-Momoh, Chinedu T
Solomon, Alina
Kivipelto, Miia
Sindi, Shireen
Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title_full Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title_fullStr Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title_full_unstemmed Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title_short Cortisol, cognition and Alzheimer’s disease biomarkers among memory clinic patients
title_sort cortisol, cognition and alzheimer’s disease biomarkers among memory clinic patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582323/
https://www.ncbi.nlm.nih.gov/pubmed/36277478
http://dx.doi.org/10.1136/bmjno-2022-000344
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