Evidence map›Paper›PMID 41926844›Full record

ArticleThe journal of prevention of Alzheimer's disease2026

Increase in healthcare utilization and Medicare payment with progression of preclinical Alzheimer's disease.

Julie Beyrer, Zachary Sheff, Nalin Payakachat, Julie M Chandler, Yun-Fei Chen, Joanna Kubisiak, Angelina Lee, Karen C Holdridge, Roy Yaari, Paul Aisen and 3 more

2 registry-linked trialsAbstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

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

NCT02008357 phase3completednot on this map

Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4 Study)

TypeinterventionalSponsorEli Lilly and CompanyRan2014 to 2023Enrolled1,169ConditionsCognition DisordersArmsPlacebo, Solanezumab
NCT02488720 completednot on this map

Longitudinal Evaluation of Amyloid Risk and Neurodegeneration - the LEARN Study. A Companion Observational Study to Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4) Trial

TypeobservationalSponsorUniversity of Southern CaliforniaRan2015 to 2023Enrolled538ConditionsCognition Disorders
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Julie BeyrerEli Lilly and Company, Indianapolis, IN, United States. Electronic address: beyrer_julie_kay@lilly.com.
Zachary SheffEli Lilly and Company, Indianapolis, IN, United States. Electronic address: zachary.sheff@lilly.com.
Nalin PayakachatEli Lilly and Company, Indianapolis, IN, United States. Electronic address: npayakachat@lilly.com.
Julie M ChandlerEli Lilly and Company, Indianapolis, IN, United States.
Yun-Fei ChenEli Lilly and Company, Indianapolis, IN, United States. Electronic address: chen_yun-fei@lilly.com.
Joanna KubisiakWestat, Rockville, MD, United States. Electronic address: joannakubisiak@westat.com.
Angelina LeeWestat, Rockville, MD, United States. Electronic address: angelinalee@westat.com.
Karen C HoldridgeEli Lilly and Company, Indianapolis, IN, United States. Electronic address: kholdridge@lilly.com.
Roy YaariEli Lilly and Company, Indianapolis, IN, United States. Electronic address: yaari_roy@lilly.com.
Paul AisenUniversity of Southern California, San Diego, CA, United States. Electronic address: paisen@usc.edu.
Michael S RafiiUniversity of Southern California, San Diego, CA, United States. Electronic address: mrafii@usc.edu.
Reisa A SperlingBrigham and Women's Hospital, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States. Electronic address: reisa@bwh.harvard.edu.
A4 and LEARN Study TeamsA4 and LEARN Study Teams - Alzheimer Clinical Trials Consortium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) begins with the preclinical stage (Stages 1 and 2) where individuals are cognitively unimpaired but have AD pathology. Healthcare utilization and medical cost of cognitively unimpaired (preclinical) AD have not been previously evaluated.

objectivesTo describe healthcare resource utilization (HRU) and Medicare payments among cognitively unimpaired individuals with and without elevated amyloid and to evaluate the association of AD progression with HRU and Medicare payments.

designRetrospective cohort analysis of the randomized controlled trial (Anti-Amyloid Treatment in Asymptomatic AD [A4]) and companion observational study (Longitudinal Evaluation of Amyloid Risk and Neurodegeneration [LEARN]) linked with Medicare.

settingClinical trials sites in the United States

participants246 cparticipants with cognitively unimpaired AD in A4 and 121 amyloid-negative participants in LEARN Medicare cohorts. MEASUREMENTS: Measures from Medicare claims included medical conditions (diagnosis codes), HRU (inpatient, emergency room, outpatient, professional, skilled nursing facility, home health), and Medicare payments. AD progression (or cognitive or functional decline) was measured using Clinical Dementia Rating Scale-Global Score (CDR-GS) in A4/LEARN and diagnosis codes for cognitive impairment, AD, and JEN Frailty Index (JFI) of ≥6 (high frailty) in Medicare data.

resultsHRU and payments were overall similar between A4 and LEARN Medicare. Claims indicators suggesting AD progression in A4 Medicare were associated with higher inpatient, outpatient, emergency room, and home health utilization (any utilization) and increased number of inpatient stays. Payments were significantly greater in A4 Medicare with AD progression vs without progression: 45% payment increase for cognitive impairment (p=0.035) with a mean incremental cost of $140 per person per month (PPPM) (95% confidence interval [CI] $125-$155), 66% payment increase for AD (p=0.011) with a mean incremental cost of $207 PPPM (95% CI $188-$226), and 103% payment increase for high frailty (p<0.001) with a mean incremental cost of $303 PPPM (95% CI $283-$323).

conclusionsOverall, individuals with cognitively unimpaired AD in A4 Medicare did not have increased utilization and payments vs LEARN. HRU and payments were significantly greater in A4 Medicare participants with AD progression indicators in claims vs those without progression. These results highlight the need for additional research on both health and economic impacts of progression in a real-world (routine care) cohort of individuals with cognitively unimpaired AD and the potential cost savings associated with effective therapy that delays AD progression in cognitively unimpaired AD. CLINICAL TRIAL REGISTRATION INFORMATION: NCT02008357, NCT02488720.

Indexed as

Alzheimer DiseaseMedicarePatient Acceptance of Health CareAgedAged, 80 and overDisease ProgressionFemaleHealth Care CostsHumansMaleMulticenter Studies as TopicObservational Studies as TopicRandomized Controlled Trials as TopicRetrospective StudiesUnited StatesA4AD disease progressionAlzheimer’s diseaseCognitively unimpaired (preclinical) ADHealth resource utilizationLEARNMedicare

Identifiers

PMID41926844
PMCPMC13084671

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.