Evidence map›Paper›PMID 40685637›Full record

ArticleAge and ageing2025

Development of a midlife-specific CogDrisk algorithm (CogDrisk-ML) to enable validated implementation of dementia risk assessment from midlife to late life.

Md Hamidul Huque, Heidi Jane Welberry, Ranmalee Eramudugolla, Nicola T Lautenschlager, Kaarin J Anstey

Abstract readValidation Study
In one paragraph

Article in Age and ageing, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
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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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

5 authors.

Md Hamidul HuqueSchool of Psychology, University of New South Wales, Sydney, NSW, Australia.ORCID 0000-0002-5605-3801
Heidi Jane WelberryCentre for Big Data Research in Health, University of New South Wales, Sydney, NSW, Australia.ORCID 0000-0002-2220-3664
Ranmalee EramudugollaSchool of Psychology, University of New South Wales, Sydney, NSW, Australia.
Nicola T LautenschlagerAcademic Unit for Psychiatry of Old Age, Department of Psychiatry, University of Melbourne, Melbourne, VIC, Australia.
Kaarin J AnsteySchool of Psychology, University of New South Wales, Sydney, NSW, Australia.ORCID 0000-0002-9706-9316

Funding

ARC Laureate Fellowship FL190100011UNSW Ageing Futures Institute Grant. M.H.H. is supported by NHMRC FL190100011UNSW Ageing Futures Institute Grant. M.H.H. is supported by NHMRC GNT1171279
6 · The paper itself

Abstract

backgroundExisting dementia risk assessment tools, such as The Australian National University Alzheimer's Disease Risk Index (ANU-ADRI), LIfestyle for BRAin health (LIBRA) and Cognitive health and Dementia Risk Assessment (CogDrisk), show limited validation for middle-aged adults (age 40-64 years). The Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE) tool, developed almost two decades ago, demonstrated moderate predictive accuracy. As key modifiable dementia risk factors emerge in midlife, there is a need for a new, more accurate midlife dementia risk assessment tool.

objectivesTo develop CogDrisk-ML, a midlife dementia risk assessment tool that can complement the existing CogDrisk tool for late-life dementia risk assessment. DESIGN AND SETTINGS: Data from the UK Biobank and the Atherosclerosis Risk in Communities (ARIC) study were used to develop and validate CogDrisk-ML, which was also externally validated using the Whitehall II cohort. PARTICIPANTS AND COVARIATES: Participants without dementia at baseline were included, with CogDrisk predictors along with additional midlife risk factors based on recent evidence.

main outcome measuresCox regression models estimated the relationship between risk factors and dementia for each sex. A random-effects meta-analysis model aggregated cohort- and sex-specific regression coefficients to develop CogDrisk-ML. Harrell's C statistics measured predictability, with multiple imputation used for missing data.

resultsCogDrisk-ML outperformed CAIDE in the UK Biobank and Whitehall II cohorts; however, it provided similar C statistics in the ARIC dataset. C statistics (95% confidence interval) for CogDrisk-ML were 0.71 (0.69, 0.74) for the ARIC, 0.75 (0.73, 0.77) for the UK Biobank and 0.70 (0.62, 0.79) for the Whitehall II study.

conclusionThe novel CogDrisk-ML for assessing dementia risk in midlife offers improved predictive accuracy. Combined with the CogDrisk tool for late life, it provides a comprehensive framework for dementia prevention throughout the life course.

Indexed as

AlgorithmsDecision Support TechniquesDementiaAdultAgedAge FactorsFemaleHumansMaleMiddle AgedPredictive Value of TestsReproducibility of ResultsRisk AssessmentRisk FactorsUnited Kingdomdementia predictiondementia preventionmidlife risk factorsolder peoplerisk assessmentrisk tool

Identifiers

PMID40685637
PMCPMC12277239

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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.