Evidence map›Paper›PMID 41180962›Full record

ArticleJournal of Alzheimer's disease reports

Red-flagging multimorbidity clusters for Alzheimer's disease risk using explainable machine learning: Evidence from a national emergency department sample.

Tursun Alkam, Ebrahim Tarshizi, Andrew H Van Benschoten

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

3 authors.

Tursun AlkamMaster's Program of Applied Artificial Intelligence, University of San Diego, San Diego, CA, USA.ORCID https://orcid.org/0009-0001-4150-8383
Ebrahim TarshiziMaster's Program of Applied Artificial Intelligence, University of San Diego, San Diego, CA, USA.
Andrew H Van BenschotenMaster's Program of Applied Artificial Intelligence, University of San Diego, San Diego, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Emergency-department (ED) visits capture diagnostic data that could flag patients at heightened risk for Alzheimer's disease (AD) long before cognitive symptoms are formally recognized. Objective: To examine how age and multimorbidity interact to predict AD and to test whether explainable machine learning enhances risk stratification using national ED data. Methods: We analyzed 554,985 ED visits (2010-2014 National Emergency Department Sample) from adults ≥ 60 y. ICD-9-CM codes identified AD and 17 chronic conditions. Logistic regression estimated odds ratios (ORs) for single and combined comorbidities across five age bands. Predictive performance of logistic regression, decision tree, random forest and XGBoost was compared; Shapley Additive exPlanations (SHAP) interpreted model output. Results: Urinary-tract infection (UTI; OR = 2.74), depression (1.93), hypothyroidism (1.68) and anemia (1.57) independently increased AD odds. Possessing all four "red-flag" conditions tripled risk (OR = 3.31), and each additional red-flag raised risk by 74%. Age showed a steep gradient: relative to 60-65 y, ORs climbed from 2.58 (66-70 y) to 25.8 (86-90 y; all p < 0.001). XGBoost performed best (AUC = 0.782; recall = 0.821), and SHAP confirmed age and red-flag multimorbidity as dominant predictors. Conclusions: Routine ED codes reveal an age-dependent, dose-response relationship between specific multimorbidity clusters and AD. An interpretable XGBoost model accurately identifies high-risk patients, outlining a practical pathway for real-time cognitive-risk alerts in acute-care settings.

Indexed as

age groupsAlzheimer's diseasecognitive healthrisk predictionSHAPXGBoost

Identifiers

PMID41180962
PMCPMC12576166

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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.