Evidence map›Paper›PMID 39211881›Full record

ArticlemedRxiv : the preprint server for health sciences2024

De Novo Exposomic Geospatial Assembly of Chronic Disease Regions with Machine Learning & Network Analysis.

Andrew Deonarine, Ayushi Batwara, Roy Wada, Shoba Nair, Puneet Sharma, Joseph Loscalzo, Bisola Ojikutu, Kathryn Hall

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Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Andrew Deonarine
Ayushi Batwara
Roy Wada
Shoba Nair
Puneet Sharma
Joseph Loscalzo
Bisola Ojikutu
Kathryn Hall

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDetermining spatial relationships between disease and the exposome is limited by available methodologies. aPEER (algorithm for Projection of Exposome and Epidemiological Relationships) uses machine learning (ML) and network analysis to find spatial relationships between diseases and the exposome in the United States.

methodsUsing aPEER we examined the relationship between 12 chronic diseases and 186 pollutants. PCA, K-means clustering, and map projection produced clusters of counties derived from pollutants, and the Jaccard correlation of these clusters with counties with high rates of disease was calculated. Pollution correlation matrices were used together with network analysis to identify the strongest disease-pollution relationships. Results were compared to LISA, Moran's I, univariate, elastic net, and random forest regression.

findingsaPEER produced 68,820 maps with human interpretable, distinct pollution-derived regions. Diseases with the strongest pollution associations were hypertension (J=0.5316, p=3.89x10-208), COPD (J=0.4545, p=8.27x10-131), stroke (J=0.4517, p=1.15x10-127), stroke mortality (J=0.4445, p=4.28x10-125), and diabetes mellitus (J=0.4425, p=2.34x10-127). Methanol, acetaldehyde, and formaldehyde were identified as strongly associated with stroke, COPD, stroke mortality, hypertension, and diabetes mellitus in the southeast United States (which correlated with both the Stroke and Diabetes Belt). Pollutants were strongly predictive of chronic disease geography and outperformed conventional prediction models based on preventive services and social determinants of health (using elastic net and random forest regression).

interpretationaPEER used machine learning to identify disease and air pollutant relationships with similar or superior AUCs compared to social determinants of health (SDOH) and healthcare preventive service models. These findings highlight the utility of aPEER in epidemiological and geospatial analysis as well as the emerging role of exposomics in understanding chronic disease pathology.

fundingBoston Public Health Commission, NHLBI (R03 HL157890) and the CDC.

Identifiers

PMID39211881
PMCPMC11361230

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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.