Evidence map›Paper›PMID 40603145›Full record

Trial reportThe journal of prevention of Alzheimer's disease2025

The Alzheimer's Disease Cooperative Study - Activities of Daily Living dependence score: revision and validation of an algorithm evaluating patient dependence across the spectrum of AD severity.

Julie M Chandler, Claire J Lansdall, Wenyu Ye, Fiona McDougall, Mark Belger, Balazs Toth, Xiaojuan Mi, Kaycee M Sink, Alexandra S Atkins

12 registry-linked trialsAbstract readValidation StudyRandomized Controlled Trial
In one paragraph

Trial report in The journal of prevention of Alzheimer's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 12 registered trials, which are not on this map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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.

NCT00904683 phase3completednot on this map

Effect of Passive Immunization on the Progression of Alzheimer's Disease: LY2062430 Versus Placebo

TypeinterventionalSponsorEli Lilly and CompanyRan2009 to 2012Enrolled1,040ConditionsAlzheimer's DiseaseArmsLY2062430, Placebo
NCT00905372 phase3completednot on this map

Effect of LY2062430, an Anti-Amyloid Beta Monoclonal Antibody, on the Progression of Alzheimer's Disease as Compared With Placebo

TypeinterventionalSponsorEli Lilly and CompanyRan2009 to 2012Enrolled1,000ConditionsAlzheimer's DiseaseArmsLY2062430, Placebo
NCT01900665 phase3terminatednot on this map

Effect of Passive Immunization on the Progression of Mild Alzheimer's Disease: Solanezumab (LY2062430) Versus Placebo

TypeinterventionalSponsorEli Lilly and CompanyRan2013 to 2017Enrolled2,129ConditionsAlzheimer's DiseaseArmsSolanezumab, Placebo
NCT02245737 phase2 / phase3terminatednot on this map

A 24-month, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Efficacy, Safety, Tolerability, Biomarker, and Pharmacokinetic Study of AZD3293 in Early Alzheimer's Disease (The AMARANTH Study)

TypeinterventionalSponsorAstraZenecaRan2014 to 2018Enrolled2,218ConditionsAlzheimer´s DiseaseArmsLanabecestat, Placebo
NCT02670083 phase3terminatednot on this map

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy And Safety Study of Crenezumab in Patients With Prodromal to Mild Alzheimer's Disease.

TypeinterventionalSponsorHoffmann-La RocheRan2016 to 2019Enrolled813ConditionsAlzheimer's DiseaseArmsCrenezumab, Placebo
NCT03114657 phase3terminatednot on this map

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy and Safety Study of Crenezumab in Patients With Prodromal to Mild Alzheimer's Disease

TypeinterventionalSponsorHoffmann-La RocheRan2017 to 2019Enrolled806ConditionsAlzheimer's DiseaseArmsCrenezumab, Placebo
NCT03289143 phase2terminatednot on this map

A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy, and Safety Study of MTAU9937A in Patients With Prodromal to Mild Alzheimer's Disease

TypeinterventionalSponsorGenentech, Inc.Ran2017 to 2021Enrolled457ConditionsAlzheimer's DiseaseArmsSemorinemab, Placebo, [18F]GTP1
NCT03367403 phase2completednot on this map

Assessment of Safety, Tolerability and Efficacy of LY3002813 in Early Symptomatic Alzheimer's Disease

TypeinterventionalSponsorEli Lilly and CompanyRan2017 to 2021Enrolled272ConditionsAlzheimer DiseaseArmsDonanemab, Placebo, LY3202626
NCT03443973 phase3terminatednot on this map

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy, and Safety Study of Gantenerumab in Patients With Early (Prodromal to Mild) Alzheimer's Disease

TypeinterventionalSponsorHoffmann-La RocheRan2018 to 2022Enrolled975ConditionsAlzheimer DiseaseArmsGantenerumab, Placebo
NCT03444870 phase3terminatednot on this map

A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy, and Safety Study of Gantenerumab in Patients With Early (Prodromal to Mild) Alzheimer's Disease

TypeinterventionalSponsorHoffmann-La RocheRan2018 to 2023Enrolled1,053ConditionsAlzheimer DiseaseArmsGantenerumab, Placebo
NCT03828747 phase2completednot on this map

A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy, and Safety Study of MTAU9937A in Patients With Moderate Alzheimer's Disease

TypeinterventionalSponsorGenentech, Inc.Ran2019 to 2023Enrolled272ConditionsAlzheimer's DiseaseArmsSemorinemab, Placebo, [18F]GTP1
NCT04437511 phase3active not recruitingnot on this map

Assessment of Safety, Tolerability, and Efficacy of Donanemab in Early Symptomatic Alzheimer's Disease

TypeinterventionalSponsorEli Lilly and CompanyRan2020 to 2028Enrolled1,736ConditionsAlzheimer DiseaseArmsDonanemab, Placebo
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Julie M ChandlerEli Lilly and Company, Indianapolis, Indiana, USA. Electronic address: juliechandler24@gmail.com.
Claire J LansdallF. Hoffman-LaRoche AG, Basel, Switzerland. Electronic address: claire.lansdall@roche.com.
Wenyu YeEli Lilly and Company, Indianapolis, Indiana, USA. Electronic address: ye_wendy_wenyu@lilly.com.
Fiona McDougallGenentech, Inc., South San Francisco, California, USA. Electronic address: mcdougall.fiona@gene.com.
Mark BelgerEli Lilly and Company, Indianapolis, Indiana, USA. Electronic address: belger_mark@lilly.com.
Balazs TothGenentech, Inc., South San Francisco, California, USA. Electronic address: toth.balazs@gene.com.
Xiaojuan MiTechData Services Company, King of Prussia, Pennsylvania, USA. Electronic address: mi_xiaojuan@network.lilly.com.
Kaycee M SinkGenentech, Inc., South San Francisco, California, USA. Electronic address: ksink@cogstate.com.
Alexandra S AtkinsEli Lilly and Company, Indianapolis, Indiana, USA. Electronic address: atkins_alexandra@lilly.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing dependence on informal and formal caregivers in Alzheimer's disease (AD) contributes to high societal cost. Treatments that delay time to increased dependence/care needs would be clinically meaningful, but these outcomes are rarely collected in early AD clinical trials. The 2015 ADCS-ADL dependence algorithm was created to estimate level of dependence in AD.

objectivesTo revise the original dependence algorithm to improve accuracy of dependence scores (DS) across AD severity, including early symptomatic AD.

designSecondary data analysis

settingCommunity cohort; randomized clinical trial

participants14,000 participants enrolled across GERAS-EU observational study and 12 AD clinical trials. MEASUREMENTS: Three-phase algorithm revision: 1) reassess ADCS-ADL items to identify those appropriate for assessing dependence; 2) (a) assign individual item responses to degrees of assistance and (b) to operationalize assignment of DS based on extent of total assistance needed; and 3) validate revised algorithm in multiple datasets across AD severity from mild cognitive impairment due to AD to moderate-severe AD.

resultsThe revised DS (0-6) algorithm classified most participants with early symptomatic AD as independent or moderately independent (DS<3) at baseline. With disease progression over time, the proportion of participants who were mildly to fully dependent (DS≥3) increased across AD severity. Increased DS was associated with incremental worsening of clinical outcomes.

conclusionsThe revised ADCS-ADL DS algorithm provides a supplementary approach to evaluate the impact of emerging treatments on independence/care needs in AD and may be useful in clinical trials where the ADCS-ADL has been collected. CLINICAL TRIAL REGISTRATION INFORMATION: EXPEDITION 1 NCT00905372; EXPEDITION 2 NCT00904683; EXPEDITION 3 NCT01900665; AMARANTH NCT02245737; TRAILBLAZER-ALZ NCT03367403; TRAILBLAZER-ALZ 2 NCT04437511; GRADUATE I NCT03444870; GRADUATE II NCT03443973; CREAD NCT02670083; CREAD 2, NCT03114657; TAURIEL NCT03289143; LAURIET NCT03828747.

Indexed as

Activities of Daily LivingAlgorithmsAlzheimer DiseaseAgedAged, 80 and overCaregiversCognitive DysfunctionFemaleHumansMaleSeverity of Illness IndexAlzheimer’s diseaseAlzheimer’s Disease Cooperative Study-Activities of Daily Living scaleCare partnerDependence

Identifiers

PMID40603145
PMCPMC12413719

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

and 6 more above

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.