Evidence map›Paper›PMID 40225240›Full record

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

Measuring time saved in Alzheimer's disease: What is a meaningful slowing of progression?

Krista Lanctot, Linus Jönsson, Alireza Atri, Russ Paulsen, Soeren Mattke, Julie Hviid Hahn-Pedersen, Pepa Polavieja, Thomas Maltesen, Teresa León, Anders Gustavsson and 1 more

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Brain patterns and risk factors in the FINGER RCT multimodal lifestyle intervention.The journal of prevention of Alzheimer's disease · 2025
    Trial
  2. Review
  3. Article
  4. 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

11 authors.

Krista LanctotDepartment of Psychiatry, Temerty Faculty of Medicine, Hurvitz Brain Sciences Research Program University of Toronto Toronto Ontario Canada.ORCID https://orcid.org/0000-0001-7024-6637
Linus JönssonDivision of Neurogeriatrics, Department of Neurobiology, CareSciences and Society Karolinska Institutet Solna Sweden.
Alireza AtriBanner Sun Health Research Institute and Banner Alzheimer's Institute Banner Health, Sun City and Phoenix Arizona USA.
Russ PaulsenUsAgainstAlzheimer's and UsAgainstAlzheimer's Action Washington District of Columbia USA.
Soeren MattkeUniversity of Southern California Los Angeles California USA.
Julie Hviid Hahn-PedersenNovo Nordisk A/S Søborg Søborg Denmark.
Pepa PolaviejaNovo Nordisk A/S Søborg Søborg Denmark.
Thomas MaltesenNovo Nordisk A/S Søborg Søborg Denmark.
Teresa LeónNovo Nordisk A/S Søborg Søborg Denmark.
Anders GustavssonDivision of Neurogeriatrics, Department of Neurobiology, CareSciences and Society Karolinska Institutet Solna Sweden.
Alzheimer's Disease Neuroimaging Initiative

Funding

Project 1U19AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI MONICA G. RIVERA-MINDT · 2016 to 2026
$226.7M
Research Education ComponentP30AG072980 · NIA · BANNER HEALTH · PI ALIREZA ATRI · 2021 to 2026
$24.9M
NIA NIH HHS P30 AG072980NIA NIH HHS U19 AG024904
6 · The paper itself

Abstract

introductionMinimal clinically important differences (MCIDs) for Alzheimer's disease (AD) have previously been estimated using clinician-based anchors. However, MCIDs have been criticized for not reflecting the preferences of people living with AD (PLWAD). Furthermore, interpretations of clinical trial results have been criticized for conflating within-person meaningfulness thresholds and between-group differences. Here, we simulate scenarios of disease slowing and compare those to published MCIDs.

methodsScenarios of 5%-95% disease slowing were simulated using Alzheimer's Disease Neuroimaging Initiative (ADNI) data. Time saved and point differences on the Clinical Dementia Rating scale-Sum of Boxes (CDR-SB) were estimated for these scenarios and compared to published MCIDs.

resultsScenario analyses resulted in estimates of time saved at ∼3 weeks-17 months and mean changes at 0.08-1.5 CDR-SB points over 18 months. The often referenced MCID for mild cognitive impairment (0.98) thereby corresponded to 11 months slowing, whereas the MCID for mild dementia (1.63) corresponded to >17 months slowing. DISCUSSION: Translating trial endpoints to estimates of time saved supports that often-referenced MCIDs may not be aligned with realistic and meaningful slowing of clinical progression. Highlights: AD slowing of clinical progression by 5%-95% resulted in 0.74-17 months saved and 0.08-1.5 CDR-SB points change at 18 months.Slowing of at least 60% or 11 months of time saved over 18 months met an often-cited MCID threshold of 0.98 points for mild cognitive impairment.For mild AD dementia, an MCID of 1.63 meant that even an 18-month delay over 18 months would be considered only borderline meaningful-a face invalid and unrealistic proposition.

Indexed as

ADNI dataAlzheimer's diseaseClinical Dementia Rating scale—Sum of the Boxesmeaningful within‐person changeminimal clinically important differencepatient perspectivePLWAD

Identifiers

PMID40225240
PMCPMC11992356

What OpenQuestion holds

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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.