Evidence map›Paper›PMID 40009844›Full record

ArticleJMIR aging2025

Estimation of Machine Learning-Based Models to Predict Dementia Risk in Patients With Atherosclerotic Cardiovascular Diseases: UK Biobank Study.

Zhengsheng Gu, Shuang Liu, Huijuan Ma, Yifan Long, Xuehao Jiao, Xin Gao, Bingying Du, Xiaoying Bi, Xingjie Shi

Abstract read
In one paragraph

Article in JMIR aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

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

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 synthesis or guideline pooled it.

  1. Pooled it
  2. 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.

Zhengsheng Gu *Department of Neurology, First Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID 0009-0000-5568-4911
Shuang Liu *KLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University, Shanghai, China.ORCID 0009-0001-0199-2959
Huijuan Ma *KLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University, Shanghai, China.ORCID 0000-0003-2790-7035
Yifan LongKLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University, Shanghai, China.ORCID 0009-0009-7955-2759
Xuehao JiaoDepartment of Neurology, First Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID 0009-0009-9124-7888
Xin GaoDepartment of Neurology, First Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID 0009-0001-5965-9817
Bingying Du *Department of Neurology, First Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID 0000-0003-3124-780X
Xiaoying Bi *Department of Neurology, First Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID 0000-0001-5784-7294
Xingjie Shi *KLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University, Shanghai, China.ORCID 0000-0002-9866-8599

Funding

UK Biobank 97366
6 · The paper itself

Abstract

backgroundThe atherosclerotic cardiovascular disease (ASCVD) is associated with dementia. However, the risk factors of dementia in patients with ASCVD remain unclear, necessitating the development of accurate prediction models.

objectiveThe aim of the study is to develop a machine learning model for use in patients with ASCVD to predict dementia risk using available clinical and sociodemographic data.

methodsThis prognostic study included patients with ASCVD between 2006 and 2010, with registration of follow-up data ending on April 2023 based on the UK Biobank. We implemented a data-driven strategy, identifying predictors from 316 variables and developing a machine learning model to predict the risk of incident dementia, Alzheimer disease, and vascular dementia within 5, 10, and longer-term follow-up in patients with ASCVD.

resultsA total of 29,561 patients with ASCVD were included, and 1334 (4.51%) developed dementia during a median follow-up time of 10.3 (IQR 7.6-12.4) years. The best prediction model (UK Biobank ASCVD risk prediction model) was light gradient boosting machine, comprising 10 predictors including age, time to complete pairs matching tasks, mean time to correctly identify matches, mean sphered cell volume, glucose levels, forced expiratory volume in 1 second z score, C-reactive protein, forced vital capacity, time engaging in activities, and age first had sexual intercourse. This model achieved the following performance metrics for all incident dementia: area under the receiver operating characteristic curve: mean 0.866 (SD 0.027), accuracy: mean 0.883 (SD 0.010), sensitivity: mean 0.637 (SD 0.084), specificity: mean 0.914 (SD 0.012), precision: mean 0.479 (SD 0.031), and F

conclusionsThe findings of this study suggest that predictive modeling could inform patients and clinicians about ASCVD at risk for dementia.

Indexed as

AtherosclerosisDementiaMachine LearningAgedBiological Specimen BanksFemaleHumansMaleMiddle AgedPrognosisRisk AssessmentRisk FactorsUK BiobankUnited KingdomAlzheimer diseaseatherosclerotic cardiovascular diseasedementiamachine learningUK Biobankvascular dementia

Identifiers

PMID40009844
PMCPMC11904384

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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.