Evidence map›Paper›PMID 37212095›Full record

ArticleJournal of Alzheimer's disease : JAD2023

Signatures of Neuropsychological Test Results in the Long Life Family Study: A Cluster Analysis.

Qingyan Xiang, Stacy L Andersen, Benjamin Sweigart, Sophia Gunn, Marianne Nygaard, Thomas T Perls, Paola Sebastiani

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

7 authors.

Qingyan XiangDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Stacy L AndersenSection of Geriatrics, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Benjamin SweigartDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Sophia GunnDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
Marianne NygaardThe Danish Aging Research Center and The Danish Twin Registry, Epidemiology, Biostatistics and Biodemography, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Thomas T PerlsSection of Geriatrics, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Paola SebastianiInstitute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.

Funding

The Long Life Family StudyU19AG063893 · NIA · WASHINGTON UNIVERSITY · PI Michael A. Province · 2019 to 2026
$125.4M
Protein Signatures of APOE2 and Cognitive AgingR01AG061844 · NIA · TUFTS MEDICAL CENTER · PI PERLS, THOMAS T, SEBASTIANI, PAOLA · 2018 to 2022
$3.1M
Digital Markers of Cognition Across the Spectrum of Preclinical Cognitive Impairment to DementiaK01AG057798 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ANDERSEN, STACY · 2018 to 2022
$596k
NIA NIH HHS K01 AG057798NIA NIH HHS R01 AG061844NIA NIH HHS U19 AG063893
6 · The paper itself

Abstract

backgroundDiscovering patterns of cognitive domains and characterizing how these patterns associate with other risk factors and biomarkers can improve our understanding of the determinants of cognitive aging.

objectiveTo discover patterns of cognitive domains using neuropsychological test results in Long Life Family Study (LLFS) and characterize how these patterns associate with aging markers.

methods5,086 LLFS participants were administered neuropsychological tests at enrollment. We performed a cluster analysis of six baseline neuropsychological test scores and tested the association between the identified clusters and various clinical variables, biomarkers, and polygenic risk scores using generalized estimating equations and the Chi-square test. We used Cox regression to correlate the clusters with the hazard of various medical events. We investigated whether the cluster information could enhance the prediction of cognitive decline using Bayesian beta regression.

resultsWe identified 12 clusters with different cognitive signatures that represent profiles of performance across multiple neuropsychological tests. These signatures significantly correlated with 26 variables including polygenic risk scores, physical and pulmonary functions, and blood biomarkers and were associated with the hazard of mortality (p < 0.01), cardiovascular disease (p = 0.03), dementia (p = 0.01), and skin cancer (p = 0.03).

conclusionThe identified cognitive signatures capture multiple domains simultaneously and provide a holistic vision of cognitive function, showing that different patterns of cognitive function can coexist in aging individuals. Such patterns can be used for clinical intervention and primary care.

Indexed as

Cluster AnalysisCognitive AgingFamily HealthLongevityNeuropsychological TestsAgedAged, 80 and overBayes TheoremBiomarkersCardiovascular DiseasesCognitionCognitive DysfunctionDementiaFemaleHolistic HealthHumansBiomarkersAgingAlzheimer’s diseasecluster analysiscognitionlongevityneuropsychologysurvival

Identifiers

PMID37212095
PMCPMC10635779

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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.