Disclosure of elevated amyloid status is not associated with long‐term suicidality in a preclinical AD trial

INTRODUCTION The long‐term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. METHODS We compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not ele...

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Published inAlzheimer's & dementia Vol. 21; no. 2; pp. e14623 - n/a
Main Authors Grill, Joshua D., Raman, Rema, Flournoy, Charlene, Ernstrom, Karin, Pierce, Aimee, Smith, Amanda, Rosenberg, Paul, Burns, Jeffrey, Karlawish, Jason, Aisen, Paul, Holdridge, Karen Chilcott, Mancini, Michele, Sperling, Reisa, Sultzer, David
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Published United States John Wiley and Sons Inc 01.02.2025
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Abstract INTRODUCTION The long‐term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. METHODS We compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not elevated result and enrolled in an observational cohort that underwent parallel assessments. Our primary outcome was a score > 0 on the Columbia Suicidality Severity Rating Scale (CSSRS) at any visit; we also considered suicidal behaviors (CSSRS > 5). RESULTS Among 1707 total participants (68% elevated amyloid, mean [standard deviation] age 71.5 [4.7], 60% female, 90% non‐Hispanic White), followed for a mean 218 (74.1) weeks, there were no suicides and few indications of suicidal thoughts (n = 124 [7%]) or behaviors (n = 13 [<1%]). In a generalized estimating equation model controlling for covariates, we observed no effect of amyloid status on the primary outcome of CSSRS > 0 (odds ratio = 1.6, 95% confidence interval = 0.76, 3.37). DISCUSSION With a structured approach, brain amyloid results can be returned safely. Highlights The Anti‐Amyloid Treatment in Asymptomatic Alzheimer's study was among the first and largest studies to include biomarker disclosure in a population without cognitive impairment. Routine psychological assessment provided a novel assessment of the impact of disclosure in this sample. Learning an elevated brain amyloid result through a protocolized approach was not associated with suicidal thoughts or behaviors compared to a matched cohort who learned they did not have elevated brain amyloid. Future research will be needed to ensure similar safety in more real‐world settings.
AbstractList The long-term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown.INTRODUCTIONThe long-term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown.We compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not elevated result and enrolled in an observational cohort that underwent parallel assessments. Our primary outcome was a score > 0 on the Columbia Suicidality Severity Rating Scale (CSSRS) at any visit; we also considered suicidal behaviors (CSSRS > 5).METHODSWe compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not elevated result and enrolled in an observational cohort that underwent parallel assessments. Our primary outcome was a score > 0 on the Columbia Suicidality Severity Rating Scale (CSSRS) at any visit; we also considered suicidal behaviors (CSSRS > 5).Among 1707 total participants (68% elevated amyloid, mean [standard deviation] age 71.5 [4.7], 60% female, 90% non-Hispanic White), followed for a mean 218 (74.1) weeks, there were no suicides and few indications of suicidal thoughts (n = 124 [7%]) or behaviors (n = 13 [<1%]). In a generalized estimating equation model controlling for covariates, we observed no effect of amyloid status on the primary outcome of CSSRS > 0 (odds ratio = 1.6, 95% confidence interval = 0.76, 3.37).RESULTSAmong 1707 total participants (68% elevated amyloid, mean [standard deviation] age 71.5 [4.7], 60% female, 90% non-Hispanic White), followed for a mean 218 (74.1) weeks, there were no suicides and few indications of suicidal thoughts (n = 124 [7%]) or behaviors (n = 13 [<1%]). In a generalized estimating equation model controlling for covariates, we observed no effect of amyloid status on the primary outcome of CSSRS > 0 (odds ratio = 1.6, 95% confidence interval = 0.76, 3.37).With a structured approach, brain amyloid results can be returned safely.DISCUSSIONWith a structured approach, brain amyloid results can be returned safely.The Anti-Amyloid Treatment in Asymptomatic Alzheimer's study was among the first and largest studies to include biomarker disclosure in a population without cognitive impairment. Routine psychological assessment provided a novel assessment of the impact of disclosure in this sample. Learning an elevated brain amyloid result through a protocolized approach was not associated with suicidal thoughts or behaviors compared to a matched cohort who learned they did not have elevated brain amyloid. Future research will be needed to ensure similar safety in more real-world settings.HIGHLIGHTSThe Anti-Amyloid Treatment in Asymptomatic Alzheimer's study was among the first and largest studies to include biomarker disclosure in a population without cognitive impairment. Routine psychological assessment provided a novel assessment of the impact of disclosure in this sample. Learning an elevated brain amyloid result through a protocolized approach was not associated with suicidal thoughts or behaviors compared to a matched cohort who learned they did not have elevated brain amyloid. Future research will be needed to ensure similar safety in more real-world settings.
INTRODUCTION The long‐term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. METHODS We compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not elevated result and enrolled in an observational cohort that underwent parallel assessments. Our primary outcome was a score > 0 on the Columbia Suicidality Severity Rating Scale (CSSRS) at any visit; we also considered suicidal behaviors (CSSRS > 5). RESULTS Among 1707 total participants (68% elevated amyloid, mean [standard deviation] age 71.5 [4.7], 60% female, 90% non‐Hispanic White), followed for a mean 218 (74.1) weeks, there were no suicides and few indications of suicidal thoughts (n = 124 [7%]) or behaviors (n = 13 [<1%]). In a generalized estimating equation model controlling for covariates, we observed no effect of amyloid status on the primary outcome of CSSRS > 0 (odds ratio = 1.6, 95% confidence interval = 0.76, 3.37). DISCUSSION With a structured approach, brain amyloid results can be returned safely. Highlights The Anti‐Amyloid Treatment in Asymptomatic Alzheimer's study was among the first and largest studies to include biomarker disclosure in a population without cognitive impairment. Routine psychological assessment provided a novel assessment of the impact of disclosure in this sample. Learning an elevated brain amyloid result through a protocolized approach was not associated with suicidal thoughts or behaviors compared to a matched cohort who learned they did not have elevated brain amyloid. Future research will be needed to ensure similar safety in more real‐world settings.
The long-term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. We compared participants who disclosed their elevated amyloid imaging result in a preclinical AD trial to those who disclosed a not elevated result and enrolled in an observational cohort that underwent parallel assessments. Our primary outcome was a score > 0 on the Columbia Suicidality Severity Rating Scale (CSSRS) at any visit; we also considered suicidal behaviors (CSSRS > 5). Among 1707 total participants (68% elevated amyloid, mean [standard deviation] age 71.5 [4.7], 60% female, 90% non-Hispanic White), followed for a mean 218 (74.1) weeks, there were no suicides and few indications of suicidal thoughts (n = 124 [7%]) or behaviors (n = 13 [<1%]). In a generalized estimating equation model controlling for covariates, we observed no effect of amyloid status on the primary outcome of CSSRS > 0 (odds ratio = 1.6, 95% confidence interval = 0.76, 3.37). With a structured approach, brain amyloid results can be returned safely. The Anti-Amyloid Treatment in Asymptomatic Alzheimer's study was among the first and largest studies to include biomarker disclosure in a population without cognitive impairment. Routine psychological assessment provided a novel assessment of the impact of disclosure in this sample. Learning an elevated brain amyloid result through a protocolized approach was not associated with suicidal thoughts or behaviors compared to a matched cohort who learned they did not have elevated brain amyloid. Future research will be needed to ensure similar safety in more real-world settings.
Author Ernstrom, Karin
Aisen, Paul
Karlawish, Jason
Sperling, Reisa
Holdridge, Karen Chilcott
Flournoy, Charlene
Raman, Rema
Grill, Joshua D.
Pierce, Aimee
Smith, Amanda
Burns, Jeffrey
Mancini, Michele
Rosenberg, Paul
Sultzer, David
AuthorAffiliation 7 Department of Psychiatry and Behavioral Sciences Johns Hopkins School of Medicine Baltimore Maryland USA
3 Department of Neurobiology and Behavior University of California Irvine Irvine Irvine California USA
4 Alzheimer's Therapeutic Research Institute University of Southern California San Diego California USA
5 Department of Neurology Oregon Health and Science University Portland Oregon USA
10 Eli Lilly and Company Indianapolis Indiana USA
1 Institute for Memory Impairments and Neurological Disorder University of California Irvine Irvine Irvine California USA
2 Department of Psychiatry and Human Behavior University of California Irvine Irvine Irvine California USA
6 Department of Psychiatry and Behavioral Medicine University of South Florida Tampa Florida USA
9 Department of Medicine University of Pennsylvania Philadelphia Pennsylvania USA
11 Center for Alzheimer Research and Treatment, Brigham and Women's Hospital, Harvard Medical School Boston Massachusetts USA
8 Department of Neurology Uni
AuthorAffiliation_xml – name: 1 Institute for Memory Impairments and Neurological Disorder University of California Irvine Irvine Irvine California USA
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– name: 3 Department of Neurobiology and Behavior University of California Irvine Irvine Irvine California USA
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– name: 6 Department of Psychiatry and Behavioral Medicine University of South Florida Tampa Florida USA
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– name: 8 Department of Neurology University of Kansas Alzheimer's Disease Research Center Kansas City Kansas USA
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Snippet INTRODUCTION The long‐term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. METHODS...
The long-term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown. We compared...
The long-term implications of disclosing Alzheimer's disease (AD) biomarker information to cognitively unimpaired individuals are unknown.INTRODUCTIONThe...
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SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage e14623
SubjectTerms Aged
Aged, 80 and over
Alzheimer Disease - diagnostic imaging
Alzheimer Disease - metabolism
Alzheimer Disease - psychology
Amyloid - metabolism
Amyloid beta-Peptides - metabolism
biomarker
Biomarkers - metabolism
Brain - diagnostic imaging
Brain - metabolism
Cohort Studies
Disclosure
Female
Humans
Male
Middle Aged
Positron-Emission Tomography
preclinical
Short Report
Suicidal Ideation
suicide
Suicide - psychology
Title Disclosure of elevated amyloid status is not associated with long‐term suicidality in a preclinical AD trial
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Falz.14623
https://www.ncbi.nlm.nih.gov/pubmed/39988989
https://www.proquest.com/docview/3170267263
https://pubmed.ncbi.nlm.nih.gov/PMC11847990
Volume 21
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