Evidence map›Paper›PMID 39481175›Full record

ArticleInternational journal of medical informatics2025

Modeling the impact of socioeconomic disparity, biological markers and environmental exposures on phenotypic age using mediation analysis and structural equation models.

Daniele Pala, Yuezhi Xie, Jia Xu, Li Shen

Abstract read
In one paragraph

Article in International journal of medical informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Daniele PalaDepartment of Computer, Electrical and Biomedical Engineering, University of Pavia, Pavia, Italy; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: daniele.pala@unipv.it.
Yuezhi XieDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Jia XuDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Li ShenDepartment of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

Technology Identification and Training CoreP30AG073105 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DEMIRIS, GEORGE, KARLAWISH, JASON H · 2021 to 2025
$21.2M
Ultrascale Machine Learning to Empower Discovery in Alzheimers Disease BiobanksU01AG068057 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Christos Davatzikos, Heng Huang · 2020 to 2026
$20.7M
Translational big data analytic approaches to advance drug repurposing for Alzheimer's diseaseR01AG071470 · NIA · UNIVERSITY OF PENNSYLVANIA · PI KIM, DOKYOON, NING, XIA · 2021 to 2025
$3.8M
NIA NIH HHS P30 AG073105NIA NIH HHS R01 AG071470NIA NIH HHS U01 AG068057
6 · The paper itself

Abstract

introductionAverage age is increasing worldwide, raising the public health burden of age-related diseases, as more resources will be required to manage treatments. Phenotypic Age is a score that can be useful to provide an estimate of the probability of developing aging-related conditions, and prevention of such conditions could be performed efficiently studying the mechanisms leading to an increased phenotypic age. The objective of this study is to characterize the mechanisms that lead to aging acceleration from the interactions among socio-demographic factors, health predispositions and biological phenotypes.

methodsWe present an approach based on the combination of mediation analysis and structural equation models (SEM) to better characterize these mechanisms, quantifying the interactions between biological and external factors and the effects of preexisting health conditions and socioeconomic disparities. We use two independent cohorts of the NHANES dataset: we use the largest (n = 13,186) to select the variables that enlarge the gap between phenotypic and chronological ages, we then create a SEM based on nested linear regressions to quantify the influence of all sociodemographic variables expressed in three latent variables indicating ethnicity, socioeconomic status and preexisting health status. We then replicate the model and apply it to the second cohort (n = 4,425) to compare the results.

resultsResults show that phenotypic age increases with poor glucose control or obesity-related biomarkers, especially if combined with a low socioeconomic status or the presence of chronic or vascular diseases, and provide a framework to quantify these relationships. Black ethnicity, low income/education and a history of chronic diseases are also associated with a higher phenotypic age. Although these findings are already known in literature, the proposed SEM-based framework provides an useful tool to assess the combinations of these heterogeneous factors from a quantitative point of view.

conclusionIn an aging society, phenotypic age is an important metric that can be used to estimate the individual health risk, however its value is influenced by a myriad of external factors, both biological and sociodemographic. The framework proposed in this paper can help quantifying the combined effects of these factors and be a starting point to the creation of personalized prevention and intervention strategies.

Indexed as

AgingBiomarkersEnvironmental ExposurePhenotypeAdultAgedFemaleHumansLatent Class AnalysisMaleMediation AnalysisMiddle AgedNutrition SurveysSocioeconomic Disparities in HealthSocioeconomic FactorsBiomarkersAgingLatent VariablesPhenotypic AgeSocial Determinats of HealthStructural Equation Model

Identifiers

PMID39481175
PMCPMC11973974

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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.