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

AI Article Synopsis

  • The study aimed to assess how disease-modifying treatments (DMT) for Alzheimer’s disease (AD) affect the duration of independence in daily living activities among individuals with very mild to mild AD dementia.
  • It followed 282 participants over about 2.9 years, finding that loss of independence in instrumental activities (IADLs) typically occurred when CDR-SB scores reached above 4.5, and for basic activities (BADLs) above 11.5.
  • Notably, treatments like lecanemab and donanemab were associated with extended periods of independence in IADLs, with lecanemab offering an average of 10 months and donanemab providing an average of 13

Article Abstract

Introduction: For many patients and caregivers, a major goal of disease-modifying treatments (DMT) for Alzheimer 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.

Methods: Participants at the Knight Alzheimer Disease Research Center were selected who were potentially eligible for recent DMT trials: 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 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.

Results: 282 participants were followed for an average of 2.9 years (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% 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11302622PMC
http://dx.doi.org/10.1101/2024.07.16.24310511DOI Listing

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