Evidence map›Paper›PMID 40526686›Full record

ArticlePLOS digital health2025

Sociodemographically differential patterns of chronic pain progression revealed by analyzing the all of us research program data.

Edwin Baldwin, Jin Zhou, Wenting Luo, W Michael Hooten, Jungwei W Fan, Haiquan Li

Abstract read
In one paragraph

Article in PLOS digital health, 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

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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Edwin BaldwinDepartment of Biosystems Engineering, University of Arizona, Tucson, Arizona, United States of America.ORCID https://orcid.org/0009-0003-2280-0615
Jin ZhouDepartment of Biostatistics, University of California at Los Angeles, Los Angeles, California, United States of America.
Wenting LuoStatistics and Data Science Graduate Interdisciplinary Program, University of Arizona, Tucson, Arizona United States of America.
W Michael HootenDivision of Pain Medicine, Department of Anesthesiology, Mayo Clinic, Rochester, Minnesota, United States of America.
Jungwei W FanDepartment of Artificial Intelligence & Informatics, Mayo Clinic, Rochester, Minnesota, United States of America.
Haiquan LiDepartment of Biosystems Engineering, University of Arizona, Tucson, Arizona, United States of America.ORCID https://orcid.org/0000-0002-8049-0278

Funding

Identify the heterogeneity and commonality of chronic overlapping pain conditions (COPCs) through phenotypic and genomic perspectivesR21DE031424 · NIDCR · MAYO CLINIC ROCHESTER · PI FAN, JUNGWEI WILFRED, HOOTEN, W. MICHAEL · 2022 to 2023
$446k
NIDCR NIH HHS R21 DE031424
6 · The paper itself

Abstract

The differential progression of ten chronic overlapping pain conditions (COPC) and four comorbid mental disorders across demographic groups have rarely been reported in the literature. To fill in this gap, we conducted retrospective cohort analyses using All of Us Research Program data from 1970 to 2023. Separate cohorts were created to assess the differential patterns across sex, race, and ethnicity. Logistic regression models, controlling for demographic variables and household income level, were employed to identify significant sociodemographic factors associated with the differential progression from one COPC or mental condition to another. Among the 139 frequent disease pairs, we identified group-specific patterns in 15 progression pathways. Black or African Americans with a COPC condition had a significantly increased association in progression to other COPCs (CLBP- > IBS, CLBP- > MHA, or IBS- > MHA, OR≥1.25, adj.p ≤ 4.0x10-3) or mental disorders (CLBP- > anxiety, CLBP- > depression, MHA- > anxiety, MHA- > depression, OR≥1.25, adj.p ≤ 1.9x10-2) after developing a COPC. Females had an increased likelihood of chronic low back pain after anxiety and depression (OR≥1.12, adj.p ≤ 1.5x10-2). Additionally, the lowest income bracket was associated with an increased risk of developing another COPC from a COPC (CLBP- > MHA, IBS- > MHA, MHA- > CLBP, or MHA- > IBS, OR≥1.44, adj.p ≤ 2.6x10-2) or from a mental disorder (depression- > MHA, depression- > CLBP, anxiety- > CLBP, or anxiety- > IBS, OR≥1.50, adj.p ≤ 2.0x10-2), as well as developing a mental disorder after a COPC (CLBP- > depression, CBLP- > anxiety, MHA- > anxiety, OR≥1.37,adj.p ≤ 1.6x10-2). To our knowledge, this is the first study that unveils the sociodemographic influence on COPC progression. These findings suggest the importance of considering sociodemographic factors to achieve optimal prognostication and preemptive management of COPCs.

Identifiers

PMID40526686
PMCPMC12173358

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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.