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Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias

INTRODUCTION: The Kaiser Healthy Aging and Diverse Life Experiences (KHANDLE) study enrolled Asian, Black, Latino, and White adults ages 65+ without prior dementia diagnosis (N = 1709). We evaluated the prevalence of cognitive impairment (mild cognitive impairment or dementia) accounting for potenti...

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Autores principales: Mungas, Dan, Shaw, Crystal, Hayes‐Larson, Eleanor, DeCarli, Charles, Farias, Sarah Tomaszewski, Olichney, John, Saucedo, Hector Hernandez, Gilsanz, Paola, Glymour, M Maria, Whitmer, Rachel A, Mayeda, Elizabeth Rose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719430/
https://www.ncbi.nlm.nih.gov/pubmed/35005198
http://dx.doi.org/10.1002/dad2.12265
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author Mungas, Dan
Shaw, Crystal
Hayes‐Larson, Eleanor
DeCarli, Charles
Farias, Sarah Tomaszewski
Olichney, John
Saucedo, Hector Hernandez
Gilsanz, Paola
Glymour, M Maria
Whitmer, Rachel A
Mayeda, Elizabeth Rose
author_facet Mungas, Dan
Shaw, Crystal
Hayes‐Larson, Eleanor
DeCarli, Charles
Farias, Sarah Tomaszewski
Olichney, John
Saucedo, Hector Hernandez
Gilsanz, Paola
Glymour, M Maria
Whitmer, Rachel A
Mayeda, Elizabeth Rose
author_sort Mungas, Dan
collection PubMed
description INTRODUCTION: The Kaiser Healthy Aging and Diverse Life Experiences (KHANDLE) study enrolled Asian, Black, Latino, and White adults ages 65+ without prior dementia diagnosis (N = 1709). We evaluated the prevalence of cognitive impairment (mild cognitive impairment or dementia) accounting for potential biases. METHODS: A random subgroup (N = 541) received clinical evaluation and others were evaluated if they failed a cognitive screen. Diagnoses were made under two conditions: (1) demographics‐blind, based on clinical exam and demographically adjusted neuropsychological test scores; and (2) all available information (clinical exam, demographics, and adjusted and unadjusted test scores). RESULTS: Cognitive impairment prevalence was 28% for blinded‐adjusted diagnosis and 25% using all available information. Black participants had higher impairment rates than White (both conditions) and Latino (blinded‐adjusted diagnosis) participants. Incomplete assessments negatively biased prevalence estimates for White participants. DISCUSSION: Racial/ethnic disparities in cognitive impairment were amplified by attrition bias in White participants but were unaffected by type of test norms and diagnosticians’ knowledge of demographics.
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spelling pubmed-87194302022-01-07 Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias Mungas, Dan Shaw, Crystal Hayes‐Larson, Eleanor DeCarli, Charles Farias, Sarah Tomaszewski Olichney, John Saucedo, Hector Hernandez Gilsanz, Paola Glymour, M Maria Whitmer, Rachel A Mayeda, Elizabeth Rose Alzheimers Dement (Amst) Cognitive & Behavioral Assessment INTRODUCTION: The Kaiser Healthy Aging and Diverse Life Experiences (KHANDLE) study enrolled Asian, Black, Latino, and White adults ages 65+ without prior dementia diagnosis (N = 1709). We evaluated the prevalence of cognitive impairment (mild cognitive impairment or dementia) accounting for potential biases. METHODS: A random subgroup (N = 541) received clinical evaluation and others were evaluated if they failed a cognitive screen. Diagnoses were made under two conditions: (1) demographics‐blind, based on clinical exam and demographically adjusted neuropsychological test scores; and (2) all available information (clinical exam, demographics, and adjusted and unadjusted test scores). RESULTS: Cognitive impairment prevalence was 28% for blinded‐adjusted diagnosis and 25% using all available information. Black participants had higher impairment rates than White (both conditions) and Latino (blinded‐adjusted diagnosis) participants. Incomplete assessments negatively biased prevalence estimates for White participants. DISCUSSION: Racial/ethnic disparities in cognitive impairment were amplified by attrition bias in White participants but were unaffected by type of test norms and diagnosticians’ knowledge of demographics. John Wiley and Sons Inc. 2021-12-31 /pmc/articles/PMC8719430/ /pubmed/35005198 http://dx.doi.org/10.1002/dad2.12265 Text en © 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cognitive & Behavioral Assessment
Mungas, Dan
Shaw, Crystal
Hayes‐Larson, Eleanor
DeCarli, Charles
Farias, Sarah Tomaszewski
Olichney, John
Saucedo, Hector Hernandez
Gilsanz, Paola
Glymour, M Maria
Whitmer, Rachel A
Mayeda, Elizabeth Rose
Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title_full Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title_fullStr Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title_full_unstemmed Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title_short Cognitive impairment in racially/ethnically diverse older adults: Accounting for sources of diagnostic bias
title_sort cognitive impairment in racially/ethnically diverse older adults: accounting for sources of diagnostic bias
topic Cognitive & Behavioral Assessment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719430/
https://www.ncbi.nlm.nih.gov/pubmed/35005198
http://dx.doi.org/10.1002/dad2.12265
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