Evidence map›Paper›PMID 42226125›Full record

ArticleBMC cardiovascular disorders2026

Associations of chronic pain and genetic risks with incident atrial fibrillation: a prospective cohort study.

Zexin Lou, Yu Wang, Mengtong Sun, Guoxian Li, Jianing Li, Yujie Shi, Ziqing Sun, Boyan Liu, Hanqing Zhao, Ze Ma and 4 more

Abstract read
In one paragraph

Article in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Zexin LouDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Yu WangDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Mengtong SunDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Guoxian LiDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Jianing LiDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Yujie ShiDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Ziqing SunDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Boyan LiuThe Fourth Affiliated Hospital of Soochow University, Suzhou, 215000, Jiangsu, China.
Hanqing ZhaoDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Ze MaDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Qiang HanDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Qida HeDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China.
Shigang QiaoDepartment of Anesthesiology, Kunshan Hospital of Chinese Medicine, Affiliated Hospital of Yangzhou University, Kunshan, 215300, Jiangsu, China. sgqiao@yzu.edu.cn.
Yueping ShenDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou City, 215123, Jiangsu Province, P. R. China. shenyueping@suda.edu.cn.

Funding

National Natural Science Foundation of China 81973143Natural Science Foundation of Gansu Province 23JRRA1466Project of Jiangsu Society of Traditional Chinese Medicine PDJH2024042Science and Technology Program of Suzhou SYWD2025307
6 · The paper itself

Abstract

backgroundCurrent knowledge on whether chronic pain contributes to atrial fibrillation (AF) risk, especially under varying genetic susceptibilities, is limited. This study aimed to explore the association between chronic pain and AF risk and assess the combined impact of chronic pain and genetic susceptibility to AF, as defined by polygenic risk scores (PRS), in the UK Biobank cohort.

methodsWe analyzed data from 290,345 UK Biobank participants who were initially AF-free. Based on pain duration and location, participants were categorized into four groups: no pain, short-term pain, chronic localized pain, and chronic widespread pain (CWP). Genetic susceptibility to AF was quantified using PRS, categorizing individuals into low, intermediate, and high genetic risk groups. Cox proportional hazard regression analyses were conducted to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for assessing the risk of AF about chronic pain and genetic susceptibility.

resultsOver a median follow-up of 14.2 years, 19,998 participants (6.9%) developed AF. All pain categories were associated with a statistically significant increased risk of AF compared with the no pain category. Both chronic pain and higher PRS were independently associated with incident AF. Joint analyses revealed that, in the high genetic risk group, individuals with chronic localized pain and CWP had HRs of 3.52 (95% CI: 3.25-3.81) and 3.32 (95% CI: 2.71-4.08), respectively, compared to the low genetic risk and no pain group.

conclusionsChronic pain and PRS were independently associated with an increased risk of AF, and individuals with combined exposures had the highest risk.

Indexed as

Atrial FibrillationChronic PainAgedFemaleGenetic Predisposition to DiseaseGenetic Risk ScoreHumansIncidenceMaleMiddle AgedPhenotypeProspective StudiesRisk AssessmentRisk FactorsTime FactorsUK BiobankAtrial fibrillationChronic painGenetic riskUK Biobank

Identifiers

PMID42226125
PMCPMC13439901

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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.