TY - JOUR
T1 - Amyloid PET and clinical management in a diverse, cognitively impaired population
T2 - The New IDEAS Study
AU - Windon, Charles C.
AU - Gatsonis, Constantine
AU - Carrillo, Maria C.
AU - Romanoff, Justin
AU - Hanna, Lucy
AU - Glavin, Emily
AU - Gareen, Ilana
AU - Gutman, Roee
AU - Hillner, Bruce E.
AU - March, Andrew
AU - O'Bryant, Sid
AU - Rissman, Robert A.
AU - Siegel, Barry A.
AU - Smith, Karen
AU - Whitmer, Rachel A.
AU - Weber, Christopher J.
AU - Wilkins, Consuelo H.
AU - Dilworth-Anderson, Peggye
AU - Rabinovici, Gil D.
N1 - Publisher Copyright:
© 2025 The Author(s). Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/7
Y1 - 2025/7
N2 - INTRODUCTION: The New Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) study (NCT04426539) evaluated the association between amyloid positron emission tomography (PET) and changes in clinical management among ethnoracially diverse, clinically heterogeneous patients. METHODS: We assessed diagnosis and management plan before and 90 ± 30 days after amyloid PET among Medicare beneficiaries who met 2018 National Institute on Aging–Alzheimer's Association criteria for mild cognitive impairment (MCI) or dementia. We aimed to identify ≥ 30% change in a composite patient management endpoint (CPME; i.e., changes in Alzheimer's disease [AD]/non-AD medications, changes in counseling). RESULTS: Among 5757 participants (median age 75 years; 21.7% Black, 20.3% Latinx, 58.1% all other races/ethnicities [AORE]), a change in CPME occurred in 59.0% (95% confidence interval 57.6%–60.5%) of individuals post PET. Change varied by ethnoracial identity and type of clinical presentation: Black (MCI: 55.3%, dementia: 55.8%), Latinx (MCI: 53.7%, dementia: 61.9%), AORE (MCI: 62.0%, dementia: 58.3%), typical (MCI: 64.8%, dementia: 60.9%), atypical (MCI 45.5%, dementia: 53.6%). DISCUSSION: Amyloid PET is associated with clinical management among diverse, clinically heterogeneous populations. Highlights: Changes in management plan occurred in 59% of patients 90 days after amyloid positron emission tomography. Rates of change in management exceeded the pre-specified goal of > 30% across ethnoracial groups. Rates of change in management also exceeded > 30% among amnestic and non-amnestic Alzheimer's disease presentations.
AB - INTRODUCTION: The New Imaging Dementia–Evidence for Amyloid Scanning (IDEAS) study (NCT04426539) evaluated the association between amyloid positron emission tomography (PET) and changes in clinical management among ethnoracially diverse, clinically heterogeneous patients. METHODS: We assessed diagnosis and management plan before and 90 ± 30 days after amyloid PET among Medicare beneficiaries who met 2018 National Institute on Aging–Alzheimer's Association criteria for mild cognitive impairment (MCI) or dementia. We aimed to identify ≥ 30% change in a composite patient management endpoint (CPME; i.e., changes in Alzheimer's disease [AD]/non-AD medications, changes in counseling). RESULTS: Among 5757 participants (median age 75 years; 21.7% Black, 20.3% Latinx, 58.1% all other races/ethnicities [AORE]), a change in CPME occurred in 59.0% (95% confidence interval 57.6%–60.5%) of individuals post PET. Change varied by ethnoracial identity and type of clinical presentation: Black (MCI: 55.3%, dementia: 55.8%), Latinx (MCI: 53.7%, dementia: 61.9%), AORE (MCI: 62.0%, dementia: 58.3%), typical (MCI: 64.8%, dementia: 60.9%), atypical (MCI 45.5%, dementia: 53.6%). DISCUSSION: Amyloid PET is associated with clinical management among diverse, clinically heterogeneous populations. Highlights: Changes in management plan occurred in 59% of patients 90 days after amyloid positron emission tomography. Rates of change in management exceeded the pre-specified goal of > 30% across ethnoracial groups. Rates of change in management also exceeded > 30% among amnestic and non-amnestic Alzheimer's disease presentations.
KW - Alzheimer's disease
KW - Medicare
KW - amyloid positron emission tomography
KW - dementia
KW - ethnicity
KW - mild cognitive impairment
UR - https://www.scopus.com/pages/publications/105011988620
U2 - 10.1002/alz.70504
DO - 10.1002/alz.70504
M3 - Article
C2 - 40728069
AN - SCOPUS:105011988620
SN - 1552-5260
VL - 21
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
IS - 7
M1 - e70504
ER -