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Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study

IMPORTANCE: Racial and ethnic groups with higher rates of clinical Alzheimer disease (AD) are underrepresented in studies of AD biomarkers, including amyloid positron emission tomography (PET). OBJECTIVE: To compare amyloid PET positivity among a diverse cohort of individuals with mild cognitive imp...

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Autores principales: Wilkins, Consuelo H., Windon, Charles C., Dilworth-Anderson, Peggye, Romanoff, Justin, Gatsonis, Constantine, Hanna, Lucy, Apgar, Charles, Gareen, Ilana F., Hill, Carl V., Hillner, Bruce E., March, Andrew, Siegel, Barry A., Whitmer, Rachel A., Carrillo, Maria C., Rabinovici, Gil D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531087/
https://www.ncbi.nlm.nih.gov/pubmed/36190710
http://dx.doi.org/10.1001/jamaneurol.2022.3157
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author Wilkins, Consuelo H.
Windon, Charles C.
Dilworth-Anderson, Peggye
Romanoff, Justin
Gatsonis, Constantine
Hanna, Lucy
Apgar, Charles
Gareen, Ilana F.
Hill, Carl V.
Hillner, Bruce E.
March, Andrew
Siegel, Barry A.
Whitmer, Rachel A.
Carrillo, Maria C.
Rabinovici, Gil D.
author_facet Wilkins, Consuelo H.
Windon, Charles C.
Dilworth-Anderson, Peggye
Romanoff, Justin
Gatsonis, Constantine
Hanna, Lucy
Apgar, Charles
Gareen, Ilana F.
Hill, Carl V.
Hillner, Bruce E.
March, Andrew
Siegel, Barry A.
Whitmer, Rachel A.
Carrillo, Maria C.
Rabinovici, Gil D.
author_sort Wilkins, Consuelo H.
collection PubMed
description IMPORTANCE: Racial and ethnic groups with higher rates of clinical Alzheimer disease (AD) are underrepresented in studies of AD biomarkers, including amyloid positron emission tomography (PET). OBJECTIVE: To compare amyloid PET positivity among a diverse cohort of individuals with mild cognitive impairment (MCI) or dementia. DESIGN, SETTING, AND PARTICIPANTS: Secondary analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS), a single-arm multisite cohort study of Medicare beneficiaries who met appropriate-use criteria for amyloid PET imaging between February 2016 and September 2017 with follow-up through January 2018. Data were analyzed between April 2020 and January 2022. This study used 2 approaches: the McNemar test to compare amyloid PET positivity proportions between matched racial and ethnic groups and multivariable logistic regression to assess the odds of having a positive amyloid PET scan. IDEAS enrolled participants at 595 US dementia specialist practices. A total of 21 949 were enrolled and 4842 (22%) were excluded from the present analysis due to protocol violations, not receiving an amyloid PET scan, not having a positive or negative scan, or because of small numbers in some subgroups. EXPOSURES: In the IDEAS study, participants underwent a single amyloid PET scan. MAIN OUTCOMES AND MEASURES: The main outcomes were amyloid PET positivity proportions and odds. RESULTS: Data from 17 107 individuals (321 Asian, 635 Black, 829 Hispanic, and 15 322 White) with MCI or dementia and amyloid PET were analyzed between April 2020 and January 2022. The median (range) age of participants was 75 (65-105) years; 8769 participants (51.3%) were female and 8338 (48.7%) were male. In the optimal 1:1 matching analysis (n = 3154), White participants had a greater proportion of positive amyloid PET scans compared with Asian participants (181 of 313; 57.8%; 95% CI, 52.3-63.2 vs 142 of 313; 45.4%; 95% CI, 39.9-50.9, respectively; P = .001) and Hispanic participants (482 of 780; 61.8%; 95% CI, 58.3-65.1 vs 425 of 780; 54.5%; 95% CI, 51.0-58.0, respectively; P = .003) but not Black participants (359 of 615; 58.4%; 95% CI, 54.4-62.2 vs 333 of 615; 54.1%; 95% CI, 50.2-58.0, respectively; P = .13). In the adjusted model, the odds of having a positive amyloid PET scan were lower for Asian participants (odds ratio [OR], 0.47; 95% CI, 0.37-0.59; P < .001), Black participants (OR, 0.71; 95% CI, 0.60-0.84; P < .001), and Hispanic participants (OR, 0.68; 95% CI, 0.59-0.79; P < .001) compared with White participants. CONCLUSIONS AND RELEVANCE: Racial and ethnic differences found in amyloid PET positivity among individuals with MCI and dementia in this study may indicate differences in underlying etiology of cognitive impairment and guide future treatment and prevention approaches.
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spelling pubmed-95310872022-10-20 Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study Wilkins, Consuelo H. Windon, Charles C. Dilworth-Anderson, Peggye Romanoff, Justin Gatsonis, Constantine Hanna, Lucy Apgar, Charles Gareen, Ilana F. Hill, Carl V. Hillner, Bruce E. March, Andrew Siegel, Barry A. Whitmer, Rachel A. Carrillo, Maria C. Rabinovici, Gil D. JAMA Neurol Original Investigation IMPORTANCE: Racial and ethnic groups with higher rates of clinical Alzheimer disease (AD) are underrepresented in studies of AD biomarkers, including amyloid positron emission tomography (PET). OBJECTIVE: To compare amyloid PET positivity among a diverse cohort of individuals with mild cognitive impairment (MCI) or dementia. DESIGN, SETTING, AND PARTICIPANTS: Secondary analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS), a single-arm multisite cohort study of Medicare beneficiaries who met appropriate-use criteria for amyloid PET imaging between February 2016 and September 2017 with follow-up through January 2018. Data were analyzed between April 2020 and January 2022. This study used 2 approaches: the McNemar test to compare amyloid PET positivity proportions between matched racial and ethnic groups and multivariable logistic regression to assess the odds of having a positive amyloid PET scan. IDEAS enrolled participants at 595 US dementia specialist practices. A total of 21 949 were enrolled and 4842 (22%) were excluded from the present analysis due to protocol violations, not receiving an amyloid PET scan, not having a positive or negative scan, or because of small numbers in some subgroups. EXPOSURES: In the IDEAS study, participants underwent a single amyloid PET scan. MAIN OUTCOMES AND MEASURES: The main outcomes were amyloid PET positivity proportions and odds. RESULTS: Data from 17 107 individuals (321 Asian, 635 Black, 829 Hispanic, and 15 322 White) with MCI or dementia and amyloid PET were analyzed between April 2020 and January 2022. The median (range) age of participants was 75 (65-105) years; 8769 participants (51.3%) were female and 8338 (48.7%) were male. In the optimal 1:1 matching analysis (n = 3154), White participants had a greater proportion of positive amyloid PET scans compared with Asian participants (181 of 313; 57.8%; 95% CI, 52.3-63.2 vs 142 of 313; 45.4%; 95% CI, 39.9-50.9, respectively; P = .001) and Hispanic participants (482 of 780; 61.8%; 95% CI, 58.3-65.1 vs 425 of 780; 54.5%; 95% CI, 51.0-58.0, respectively; P = .003) but not Black participants (359 of 615; 58.4%; 95% CI, 54.4-62.2 vs 333 of 615; 54.1%; 95% CI, 50.2-58.0, respectively; P = .13). In the adjusted model, the odds of having a positive amyloid PET scan were lower for Asian participants (odds ratio [OR], 0.47; 95% CI, 0.37-0.59; P < .001), Black participants (OR, 0.71; 95% CI, 0.60-0.84; P < .001), and Hispanic participants (OR, 0.68; 95% CI, 0.59-0.79; P < .001) compared with White participants. CONCLUSIONS AND RELEVANCE: Racial and ethnic differences found in amyloid PET positivity among individuals with MCI and dementia in this study may indicate differences in underlying etiology of cognitive impairment and guide future treatment and prevention approaches. American Medical Association 2022-10-03 2022-11 /pmc/articles/PMC9531087/ /pubmed/36190710 http://dx.doi.org/10.1001/jamaneurol.2022.3157 Text en Copyright 2022 Wilkins CH et al. JAMA Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Wilkins, Consuelo H.
Windon, Charles C.
Dilworth-Anderson, Peggye
Romanoff, Justin
Gatsonis, Constantine
Hanna, Lucy
Apgar, Charles
Gareen, Ilana F.
Hill, Carl V.
Hillner, Bruce E.
March, Andrew
Siegel, Barry A.
Whitmer, Rachel A.
Carrillo, Maria C.
Rabinovici, Gil D.
Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title_full Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title_fullStr Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title_full_unstemmed Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title_short Racial and Ethnic Differences in Amyloid PET Positivity in Individuals With Mild Cognitive Impairment or Dementia: A Secondary Analysis of the Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) Cohort Study
title_sort racial and ethnic differences in amyloid pet positivity in individuals with mild cognitive impairment or dementia: a secondary analysis of the imaging dementia–evidence for amyloid scanning (ideas) cohort study
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531087/
https://www.ncbi.nlm.nih.gov/pubmed/36190710
http://dx.doi.org/10.1001/jamaneurol.2022.3157
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