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Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline

BACKGROUND: Mild behavioral impairment (MBI) and subjective cognitive decline (SCD) are dementia risk states, and potentially represent neurobehavioral and neurocognitive manifestations, respectively, of early stage neurodegeneration. Both MBI and SCD predict incident cognitive decline and dementia,...

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Autores principales: Ismail, Zahinoor, McGirr, Alexander, Gill, Sascha, Hu, Sophie, Forkert, Nils D., Smith, Eric E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075401/
https://www.ncbi.nlm.nih.gov/pubmed/33554909
http://dx.doi.org/10.3233/JAD-201184
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author Ismail, Zahinoor
McGirr, Alexander
Gill, Sascha
Hu, Sophie
Forkert, Nils D.
Smith, Eric E.
author_facet Ismail, Zahinoor
McGirr, Alexander
Gill, Sascha
Hu, Sophie
Forkert, Nils D.
Smith, Eric E.
author_sort Ismail, Zahinoor
collection PubMed
description BACKGROUND: Mild behavioral impairment (MBI) and subjective cognitive decline (SCD) are dementia risk states, and potentially represent neurobehavioral and neurocognitive manifestations, respectively, of early stage neurodegeneration. Both MBI and SCD predict incident cognitive decline and dementia, are associated with known dementia biomarkers, and are both represented in the NIA-AA research framework for AD in Stage 2 (preclinical disease). OBJECTIVE: To assess the associations of MBI and SCD, alone and in combination, with incident cognitive and functional decline in a population of older adults. We tested the hypothesis that MBI and SCD confer additive risk for decline. METHODS: Cognitively normal participants were followed up annually at Alzheimer’s Disease Centers. Logistic regression assessed the relationship between baseline classification (MBI-SCD-, MBI-SCD+, MBI+SCD-, or MBI+SCD+) and 3-year outcome. RESULTS: Of 2,769 participants (mean age=76), 1,536 were MBI-SCD-, 254 MBI-SCD+, 743 MBI+SCD-, and 236 MBI+SCD+. At 3 years, 349 (12.6%) declined to CDR >0, including 23.1% of the MBI+group, 23.5% of the SCD+group, and 30.9% of the intersection group of both MBI+and SCD+participants. Compared to SCD-MBI-, we observed an ordinal progression in risk (ORs [95% CI]): 3.61 [2.42–5.38] for MBI-SCD+ (16.5% progression), 4.76 [3.57–6.34] for MBI+SCD- (20.7%), and 8.15 [5.71–11.64] for MBI+SCD+(30.9%). CONCLUSION: MBI and SCD together were associated with the greatest risk of decline. These complementary dementia risk syndromes can be used as simple and scalable methods to identify high-risk patients for workup or for clinical trial enrichment.
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spelling pubmed-80754012021-05-11 Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline Ismail, Zahinoor McGirr, Alexander Gill, Sascha Hu, Sophie Forkert, Nils D. Smith, Eric E. J Alzheimers Dis Research Article BACKGROUND: Mild behavioral impairment (MBI) and subjective cognitive decline (SCD) are dementia risk states, and potentially represent neurobehavioral and neurocognitive manifestations, respectively, of early stage neurodegeneration. Both MBI and SCD predict incident cognitive decline and dementia, are associated with known dementia biomarkers, and are both represented in the NIA-AA research framework for AD in Stage 2 (preclinical disease). OBJECTIVE: To assess the associations of MBI and SCD, alone and in combination, with incident cognitive and functional decline in a population of older adults. We tested the hypothesis that MBI and SCD confer additive risk for decline. METHODS: Cognitively normal participants were followed up annually at Alzheimer’s Disease Centers. Logistic regression assessed the relationship between baseline classification (MBI-SCD-, MBI-SCD+, MBI+SCD-, or MBI+SCD+) and 3-year outcome. RESULTS: Of 2,769 participants (mean age=76), 1,536 were MBI-SCD-, 254 MBI-SCD+, 743 MBI+SCD-, and 236 MBI+SCD+. At 3 years, 349 (12.6%) declined to CDR >0, including 23.1% of the MBI+group, 23.5% of the SCD+group, and 30.9% of the intersection group of both MBI+and SCD+participants. Compared to SCD-MBI-, we observed an ordinal progression in risk (ORs [95% CI]): 3.61 [2.42–5.38] for MBI-SCD+ (16.5% progression), 4.76 [3.57–6.34] for MBI+SCD- (20.7%), and 8.15 [5.71–11.64] for MBI+SCD+(30.9%). CONCLUSION: MBI and SCD together were associated with the greatest risk of decline. These complementary dementia risk syndromes can be used as simple and scalable methods to identify high-risk patients for workup or for clinical trial enrichment. IOS Press 2021-03-09 /pmc/articles/PMC8075401/ /pubmed/33554909 http://dx.doi.org/10.3233/JAD-201184 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ismail, Zahinoor
McGirr, Alexander
Gill, Sascha
Hu, Sophie
Forkert, Nils D.
Smith, Eric E.
Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title_full Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title_fullStr Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title_full_unstemmed Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title_short Mild Behavioral Impairment and Subjective Cognitive Decline Predict Cognitive and Functional Decline
title_sort mild behavioral impairment and subjective cognitive decline predict cognitive and functional decline
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075401/
https://www.ncbi.nlm.nih.gov/pubmed/33554909
http://dx.doi.org/10.3233/JAD-201184
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