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 in | Alzheimer's & dementia Vol. 21; no. 2; pp. e14623 - n/a |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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. |
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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 – name: 10 Eli Lilly and Company Indianapolis Indiana USA – name: 11 Center for Alzheimer Research and Treatment, Brigham and Women's Hospital, Harvard Medical School Boston Massachusetts USA – name: 3 Department of Neurobiology and Behavior University of California Irvine Irvine Irvine California USA – name: 4 Alzheimer's Therapeutic Research Institute University of Southern California San Diego California USA – name: 2 Department of Psychiatry and Human Behavior University of California Irvine Irvine Irvine California USA – name: 6 Department of Psychiatry and Behavioral Medicine University of South Florida Tampa Florida USA – name: 5 Department of Neurology Oregon Health and Science University Portland Oregon USA – name: 8 Department of Neurology University of Kansas Alzheimer's Disease Research Center Kansas City Kansas USA – name: 7 Department of Psychiatry and Behavioral Sciences Johns Hopkins School of Medicine Baltimore Maryland USA – name: 9 Department of Medicine University of Pennsylvania Philadelphia Pennsylvania USA |
Author_xml | – sequence: 1 givenname: Joshua D. surname: Grill fullname: Grill, Joshua D. email: jgrill@uci.edu organization: Irvine – sequence: 2 givenname: Rema surname: Raman fullname: Raman, Rema organization: University of Southern California – sequence: 3 givenname: Charlene surname: Flournoy fullname: Flournoy, Charlene organization: University of Southern California – sequence: 4 givenname: Karin surname: Ernstrom fullname: Ernstrom, Karin organization: University of Southern California – sequence: 5 givenname: Aimee surname: Pierce fullname: Pierce, Aimee organization: Oregon Health and Science University – sequence: 6 givenname: Amanda surname: Smith fullname: Smith, Amanda organization: University of South Florida – sequence: 7 givenname: Paul surname: Rosenberg fullname: Rosenberg, Paul organization: Johns Hopkins School of Medicine – sequence: 8 givenname: Jeffrey surname: Burns fullname: Burns, Jeffrey organization: University of Kansas Alzheimer's Disease Research Center – sequence: 9 givenname: Jason surname: Karlawish fullname: Karlawish, Jason organization: University of Pennsylvania – sequence: 10 givenname: Paul surname: Aisen fullname: Aisen, Paul organization: Irvine – sequence: 11 givenname: Karen Chilcott surname: Holdridge fullname: Holdridge, Karen Chilcott organization: Eli Lilly and Company – sequence: 12 givenname: Michele surname: Mancini fullname: Mancini, Michele organization: Eli Lilly and Company – sequence: 13 givenname: Reisa surname: Sperling fullname: Sperling, Reisa organization: Center for Alzheimer Research and Treatment, Brigham and Women's Hospital, Harvard Medical School – sequence: 14 givenname: David surname: Sultzer fullname: Sultzer, David organization: Irvine |
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Cites_doi | 10.1002/alz.13726 10.1176/appi.ajp.2011.10111704 10.1001/jamapsychiatry.2021.0150 10.1001/jamaneurol.2022.3094 10.1212/WNL.0000000000001451 10.1016/S1474-4422(23)00508-2 10.1016/j.trci.2015.12.001 10.1016/j.jalz.2011.03.003 10.1056/NEJMoa2305032 10.1001/jamaneurol.2020.2734 10.1001/jamaneurol.2019.0797 10.1016/j.mayocp.2014.05.016 10.1097/WAD.0000000000000097 |
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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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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 |
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