Evidence map›Paper›PMID 38031083›Full record

ArticleAlzheimer's research & therapy2023

Identification of high likelihood of dementia in population-based surveys using unsupervised clustering: a longitudinal analysis.

Amin Gharbi-Meliani, François Husson, Henri Vandendriessche, Eleonore Bayen, Kristine Yaffe, Anne-Catherine Bachoud-Lévi, Laurent Cleret de Langavant

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Amin Gharbi-MelianiNeuropsychologie Interventionnelle, U955 E01, Institut Mondor de Recherche Biomédicale & Département d'études Cognitives, INSERM, Ecole Normale Supérieure, Université PSL, Université Paris-Est Créteil, Creteil, 94000, France.ORCID 0000-0001-7788-3321
François HussonInstitut Agro, Univ Rennes1, CNRS, IRMAR, Rennes, 35000, France.ORCID 0000-0002-7271-8877
Henri VandendriesscheLaboratoire de Neurosciences Cognitives et Computationnelles, Département d'études Cognitives, Ecole Normale Supérieure, Université PSL, INSERM, Paris, 75005, France.ORCID 0000-0001-9319-0031
Eleonore BayenDépartement de Rééducation Neurologique, Sorbonne Université, Hôpital Pitié-Salpêtrière-Assistance Publique Hôpitaux de Paris, Paris, 75013, France.ORCID 0000-0002-0286-5521
Kristine YaffeGlobal Brain Health Institute, University of California, San Francisco, CA, 94143, USA.ORCID 0000-0003-0919-3825
Anne-Catherine Bachoud-LéviNeuropsychologie Interventionnelle, U955 E01, Institut Mondor de Recherche Biomédicale & Département d'études Cognitives, INSERM, Ecole Normale Supérieure, Université PSL, Université Paris-Est Créteil, Creteil, 94000, France.ORCID 0000-0003-3000-2210
Laurent Cleret de LangavantNeuropsychologie Interventionnelle, U955 E01, Institut Mondor de Recherche Biomédicale & Département d'études Cognitives, INSERM, Ecole Normale Supérieure, Université PSL, Université Paris-Est Créteil, Creteil, 94000, France. laurent.cleret@gbhi.org.ORCID 0000-0001-6551-4641
Inserm · FRUniversity of California, San Francisco · USCentre National de la Recherche Scientifique · FR

Funding

Project-001R01AG017644 · NIA · UNIVERSITY OF LONDON INST OF NEUROLOGY · PI Andrew Steptoe · 2000 to 2026
$56.2M
Integrting Information About Aging SurveysR01AG030153 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sara Adar, Alden L. Gross · 2007 to 2026
$41.7M
Stress, diet quality, and biological aging across the lifespanR24AG048024 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI EPEL, ELISSA S., MENDES, WENDY BERRY · 2014 to 2025
$6.2M
Enhancing the Comparability of SHARE with HRS and ELSAR01AG052527 · NIA · MAX PLANCK INST/SOCIAL LAW/SOCIAL POLICY · PI BOERSCH-SUPAN, AXEL H · 2016 to 2020
$2.1M
Mega Meta Data Set of the Health and Retirement Surveys Around the WorldRC2AG036619 · NIA · RAND CORPORATION · PI KAPTEYN, ARIE · 2009 to 2010
$2.0M
Archiving & Creating User Friendly Data: the Longitudinal Aging Survey in IndiaR03AG043052 · NIA · RAND CORPORATION · PI LEE, JINKOOK · 2012 to 2012
$95k
NIA NIH HHS HHSN271201300071CNIA NIH HHS R01 AG017644NIA NIH HHS R01 AG030153NIA NIH HHS R01 AG052527NIA NIH HHS R03 AG043052NIA NIH HHS R24 AG048024NIA NIH HHS RC2 AG036619
6 · The paper itself

Abstract

backgroundDementia is defined as a cognitive decline that affects functional status. Longitudinal ageing surveys often lack a clinical diagnosis of dementia though measure cognition and daily function over time. We used unsupervised machine learning and longitudinal data to identify transition to probable dementia.

methodsMultiple Factor Analysis was applied to longitudinal function and cognitive data of 15,278 baseline participants (aged 50 years and more) from the Survey of Health, Ageing, and Retirement in Europe (SHARE) (waves 1, 2 and 4-7, between 2004 and 2017). Hierarchical Clustering on Principal Components discriminated three clusters at each wave. We estimated probable or "Likely Dementia" prevalence by sex and age, and assessed whether dementia risk factors increased the risk of being assigned probable dementia status using multistate models. Next, we compared the "Likely Dementia" cluster with self-reported dementia status and replicated our findings in the English Longitudinal Study of Ageing (ELSA) cohort (waves 1-9, between 2002 and 2019, 7840 participants at baseline).

resultsOur algorithm identified a higher number of probable dementia cases compared with self-reported cases and showed good discriminative power across all waves (AUC ranged from 0.754 [0.722-0.787] to 0.830 [0.800-0.861]). "Likely Dementia" status was more prevalent in older people, displayed a 2:1 female/male ratio, and was associated with nine factors that increased risk of transition to dementia: low education, hearing loss, hypertension, drinking, smoking, depression, social isolation, physical inactivity, diabetes, and obesity. Results were replicated in ELSA cohort with good accuracy.

conclusionsMachine learning clustering can be used to study dementia determinants and outcomes in longitudinal population ageing surveys in which dementia clinical diagnosis is lacking.

Indexed as

Cognitive DysfunctionDementiaAgedAgingCognitionFemaleHumansLongitudinal StudiesMaleMiddle AgedDementiaIdentificationLongitudinal analysisMachine LearningMultistate modelsPopulation-based surveysUnsupervised clustering

Identifiers

PMID38031083
PMCPMC10688099
OpenAlexW4389138091

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Registered trials

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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.