Evidence map›Paper›PMID 39949872›Full record

ArticleAlzheimer's & dementia (New York, N. Y.)

Assessing the clinical meaningfulness of slowing CDR-SB progression with disease-modifying therapies for Alzheimer's disease.

Sarah M Hartz, Suzanne E Schindler, Marissa L Streitz, Krista L Moulder, Jessica Mozersky, Guoqiao Wang, Chengjie Xiong, John C Morris

Abstract read
In one paragraph

Article in Alzheimer's & dementia (New York, N. Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Cognitive Outcomes After Hip Fracture Surgery: The Association of Postoperative Delirium on Previously Cognitively Normal Older Adults.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2026
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  16. Anti-amyloid treatments: Why we think they are worth it.Alzheimer's & dementia (New York, N. Y.)
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Sarah M HartzDepartment of Psychiatry Washington University School of Medicine in St. Louis St. Louis Missouri USA.ORCID https://orcid.org/0000-0002-5429-3799
Suzanne E SchindlerDepartment of Neurology Washington University School of Medicine in St. Louis St. Louis Missouri USA.
Marissa L StreitzDepartment of Neurology Washington University School of Medicine in St. Louis St. Louis Missouri USA.
Krista L MoulderDepartment of Neurology Washington University School of Medicine in St. Louis St. Louis Missouri USA.
Jessica MozerskyDepartment of Medicine Washington University School of Medicine in St. Louis St. Louis Missouri USA.
Guoqiao WangDepartment of Neurology Washington University School of Medicine in St. Louis St. Louis Missouri USA.
Chengjie XiongDivision of Biostatistics Washington University School of Medicine in St. Louis St. Louis Missouri USA.
John C MorrisDepartment of Neurology Washington University School of Medicine in St. Louis St. Louis Missouri USA.

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI Jacquelyn Leigh Meyers · 1989 to 2026
$162.7M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Smartphone-Based "Burst" Cognitive AssessmentsP01AG003991 · NIA · WASHINGTON UNIVERSITY · PI JOHN MORRIS · 1985 to 2026
$69.5M
The natural history of AB accumulation in preclinical ADP01AG026276 · NIA · WASHINGTON UNIVERSITY · PI MORRIS, JOHN · 2005 to 2025
$49.5M
Neuropathology CoreP30AG013854 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ROGALSKI, EMILY J · 1996 to 2020
$28.9M
Research Education ComponentP30AG066444 · NIA · WASHINGTON UNIVERSITY · PI DAVID M. HOLTZMAN · 2020 to 2026
$28.7M
Research Education Core FP30AG072977 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SANDRA WEINTRAUB · 2021 to 2026
$26.3M
Cross Sectional and Longitudinal Racial Disparity in Molecular Biomarkers of Alzheimer DiseaseR01AG067505 · NIA · WASHINGTON UNIVERSITY · PI XIONG, CHENGJIE · 2020 to 2024
$14.7M
Staging Alzheimer disease with blood-based biomarkersR01AG070941 · NIA · WASHINGTON UNIVERSITY · PI SCHINDLER, SUZANNE ELIZABETH · 2021 to 2025
$4.3M
Returning Research Results that Indicate Risk of Alzheimer Disease to Healthy Participants in Longitudinal StudiesR01AG065234 · NIA · WASHINGTON UNIVERSITY · PI HARTZ, SARAH, MOZERSKY, JESSICA · 2020 to 2024
$3.8M
Returning AD biomarker Results to Community Dwelling Older Adults: Testing Modalities and ImpactR01AG084723 · NIA · WASHINGTON UNIVERSITY · PI Sarah Hartz, Jessica Mozersky · 2024 to 2026
$2.0M
Investigating the longitudinal relationship between alcohol use, neurophysiological functioning, and Alzheimer disease biomarkers in the Collaborative Study on the Genetics of AlcoholismR01AA029308 · NIAAA · WASHINGTON UNIVERSITY · PI HARTZ, SARAH · 2020 to 2024
$2.0M
NCATS NIH HHS UL1 TR002345NIAAA NIH HHS R01 AA029308NIAAA NIH HHS U10 AA008401NIA NIH HHS P01 AG003991NIA NIH HHS P01 AG026276NIA NIH HHS P30 AG013854NIA NIH HHS P30 AG066444NIA NIH HHS P30 AG072977NIA NIH HHS R01 AG065234NIA NIH HHS R01 AG067505NIA NIH HHS R01 AG070941NIA NIH HHS R01 AG084723
6 · The paper itself

Abstract

introductionFor many patients and caregivers, a major goal of disease-modifying treatments (DMTs) for Alzheimer's disease (AD) dementia is to extend independence in instrumental and basic activities of daily living (IADLs and BADLs). The goal of this study was to estimate the effect of treatments on the time remaining independent in IADLs and BADLs.

methodsParticipants at the Knight Alzheimer Disease Research Center (Knight ADRC) who met eligibility criteria for recent DMT trials were studied: age ≥60 years at baseline, clinical diagnosis of very mild or mild AD dementia (global Clinical Dementia Rating [CDR] score 0.5 or 1), biomarker confirmation of amyloid pathology, and at least one follow-up CDR assessment within 5 years. For IADLs, a subset of the Functional Assessment Questionnaire (FAQ) was examined that rated the degree of independence in the following: paying bills, driving, remembering medications and appointments, and preparing meals. For BADLs, the Personal Care domain of the CDR was used. Mixed-effects logistic and ordinal regression models were used to examine the relationship between CDR Sum of Boxes (CDR-SB) and the individual functional outcomes and their components. The change in CDR-SB over time was estimated with linear mixed-effects models.

resultsA total of 282 participants were followed for an average of 2.9 years (standard deviation [SD] 1.3 years). For 50% of individuals, loss of independence in IADLs occurred at CDR-SB >4.5 and in BADLs at CDR-SB >11.5. For individuals with a baseline CDR-SB = 2, treatment with lecanemab would extend independence in IADLs for 10 months (95% confidence interval [CI] 4-18 months) and treatment with donanemab in the low/medium tau group would extend independence in IADLs by 13 months (95% CI 6-24 months). DISCUSSION: Independence in ADLs can be related to CDR-SB and used to demonstrate the effect of AD treatments in extending the time of independent function, a meaningful outcome for patients and their families. Highlights: We estimated time to loss of independence for people with AD dementiaEstimating time to loss of independence can help with clinical decision-makingDisease-modifying treatments for AD dementia can extend independence.

Indexed as

AD dementiaclinical meaningfulnessfunctional independence

Identifiers

PMID39949872
PMCPMC11822626

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.