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Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients
BACKGROUND: Allostatic load (AL) is defined as the cumulative dysregulation of neuroendocrine, immunological, metabolic, and cardiovascular systems that increases the susceptibility to stress-related health problems. Several dementia and Alzheimer's disease (AD) risk factors have been identifie...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937889/ https://www.ncbi.nlm.nih.gov/pubmed/36820052 http://dx.doi.org/10.1016/j.bbih.2023.100592 |
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author | Adedeji, Dickson O. Holleman, Jasper Juster, Robert-Paul Udeh-Momoh, Chinedu T. Kåreholt, Ingemar Hagman, Göran Aspö, Malin Adagunodo, Sofia Håkansson, Krister Kivipelto, Miia Solomon, Alina Sindi, Shireen |
author_facet | Adedeji, Dickson O. Holleman, Jasper Juster, Robert-Paul Udeh-Momoh, Chinedu T. Kåreholt, Ingemar Hagman, Göran Aspö, Malin Adagunodo, Sofia Håkansson, Krister Kivipelto, Miia Solomon, Alina Sindi, Shireen |
author_sort | Adedeji, Dickson O. |
collection | PubMed |
description | BACKGROUND: Allostatic load (AL) is defined as the cumulative dysregulation of neuroendocrine, immunological, metabolic, and cardiovascular systems that increases the susceptibility to stress-related health problems. Several dementia and Alzheimer's disease (AD) risk factors have been identified, yet little is known about the role of AL and its associations with AD biomarkers (e.g., beta-amyloid (Aβ) or tau) and cognitive function among memory clinic patients. Hence, this study aims to assess the association between AL and AD biomarkers, cognitive performance, and cognitive decline after 3-years of follow-up. METHODS: Data from 188 memory clinic patients were derived from the Cortisol and Stress in AD (Co-STAR) study in Sweden. Participants underwent baseline assessments including blood tests for AL measures (including cortisol, thyroid stimulating hormone, cobalamin, homocysteine, leukocytes, glycated hemoglobin, albumin, high-density and low-density lipoprotein cholesterol, triglycerides, and creatinine), cerebrospinal fluid (CSF) sampling for AD biomarkers and neuropsychological tests including five cognitive domains. Linear regressions were conducted, adjusting for age, sex, and education. RESULTS: Higher AL was associated with lower CSF Aβ1-42 levels (β = −0.175, p = 0.025), reflecting higher brain levels of Aβ1-42. Stratified analyses suggested a significant association among women but not men, although the AL-sex interaction was not statistically significant. AL was not significantly associated with T-tau level (β = −0.030, p = 0.682) and P-tau level (β = 0.091, p = 0.980). There were no significant associations between AL and cognition or cognitive decline after 3 years. CONCLUSION: This study showed that higher AL was associated with increased brain amyloid accumulation. This suggests that AL may play a role in AD/dementia pathophysiology. Potential sex-related differences should be assessed in further larger studies. |
format | Online Article Text |
id | pubmed-9937889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99378892023-02-19 Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients Adedeji, Dickson O. Holleman, Jasper Juster, Robert-Paul Udeh-Momoh, Chinedu T. Kåreholt, Ingemar Hagman, Göran Aspö, Malin Adagunodo, Sofia Håkansson, Krister Kivipelto, Miia Solomon, Alina Sindi, Shireen Brain Behav Immun Health Full Length Article BACKGROUND: Allostatic load (AL) is defined as the cumulative dysregulation of neuroendocrine, immunological, metabolic, and cardiovascular systems that increases the susceptibility to stress-related health problems. Several dementia and Alzheimer's disease (AD) risk factors have been identified, yet little is known about the role of AL and its associations with AD biomarkers (e.g., beta-amyloid (Aβ) or tau) and cognitive function among memory clinic patients. Hence, this study aims to assess the association between AL and AD biomarkers, cognitive performance, and cognitive decline after 3-years of follow-up. METHODS: Data from 188 memory clinic patients were derived from the Cortisol and Stress in AD (Co-STAR) study in Sweden. Participants underwent baseline assessments including blood tests for AL measures (including cortisol, thyroid stimulating hormone, cobalamin, homocysteine, leukocytes, glycated hemoglobin, albumin, high-density and low-density lipoprotein cholesterol, triglycerides, and creatinine), cerebrospinal fluid (CSF) sampling for AD biomarkers and neuropsychological tests including five cognitive domains. Linear regressions were conducted, adjusting for age, sex, and education. RESULTS: Higher AL was associated with lower CSF Aβ1-42 levels (β = −0.175, p = 0.025), reflecting higher brain levels of Aβ1-42. Stratified analyses suggested a significant association among women but not men, although the AL-sex interaction was not statistically significant. AL was not significantly associated with T-tau level (β = −0.030, p = 0.682) and P-tau level (β = 0.091, p = 0.980). There were no significant associations between AL and cognition or cognitive decline after 3 years. CONCLUSION: This study showed that higher AL was associated with increased brain amyloid accumulation. This suggests that AL may play a role in AD/dementia pathophysiology. Potential sex-related differences should be assessed in further larger studies. Elsevier 2023-02-01 /pmc/articles/PMC9937889/ /pubmed/36820052 http://dx.doi.org/10.1016/j.bbih.2023.100592 Text en © 2023 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Adedeji, Dickson O. Holleman, Jasper Juster, Robert-Paul Udeh-Momoh, Chinedu T. Kåreholt, Ingemar Hagman, Göran Aspö, Malin Adagunodo, Sofia Håkansson, Krister Kivipelto, Miia Solomon, Alina Sindi, Shireen Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title | Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title_full | Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title_fullStr | Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title_full_unstemmed | Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title_short | Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
title_sort | longitudinal study of alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937889/ https://www.ncbi.nlm.nih.gov/pubmed/36820052 http://dx.doi.org/10.1016/j.bbih.2023.100592 |
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