Evidence map›Paper›PMID 41161813›Full record

ArticleBMJ mental health2025

Identifying modifiable factors and their joint associations on late-onset schizophrenia risk in the UK Biobank: a prospective exposure-wide association study.

Fan Jiang, Qiuyue Dong, Emilio Fernandez-Egea, Rudolf N Cardinal, Xinyu Li, Huizhi Liang, Wenbo Song, Alimu Dayimu, Haibo Wang, Lei Xu and 1 more

Abstract read
In one paragraph

Article in BMJ mental 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

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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Fan JiangShandong ENT Hospital, School of Public Health, Shandong University, Jinan, Shandong, China.
Qiuyue DongShandong ENT Hospital, School of Public Health, Shandong University, Jinan, Shandong, China.
Emilio Fernandez-EgeaDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
Rudolf N CardinalDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
Xinyu LiShandong ENT Hospital, School of Public Health, Shandong University, Jinan, Shandong, China.
Huizhi LiangSchool of Computing, Newcastle University, Newcastle upon Tyne, England, UK.
Wenbo SongDepartment of Non-communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, England, UK.ORCID 0000-0002-1588-8597
Alimu DayimuCambridge Clinical Trials Unit Cancer Theme, University of Cambridge, Cambridge, England, UK.
Haibo WangShandong ENT Hospital, School of Public Health, Shandong University, Jinan, Shandong, China.
Lei XuShandong ENT Hospital, School of Public Health, Shandong University, Jinan, Shandong, China shanquan.chen@hku.hk sdphxl@email.sdu.edu.cn.
Shanquan ChenSchool of Public Health, LKS Faculty of Medicine, University of Hong Kong, Hong Kong, China shanquan.chen@hku.hk sdphxl@email.sdu.edu.cn.ORCID 0000-0002-4724-4892

Funding

Medical Research Council MRC MR/W014386/1MRC Medical Research Council MR/W029987/1MRC Medical Research Council MR/Z504816/1
6 · The paper itself

Abstract

backgroundOne in four cases of schizophrenia begins in late life, resulting in high unemployment and reduced life expectancy. However, knowledge of the modifiable risk factors for late-onset schizophrenia and their combined effects is limited.

aimsTo identify modifiable risk factors for late-onset schizophrenia and estimate their joint disease risk effects.

methodsThis prospective cohort study using UK Biobank data included 482 708 participants without late-onset schizophrenia at baseline, followed up for a mean of 14.36 years. We conducted an exposure-wide association study of 232 potentially modifiable factors linked to late-onset schizophrenia risk. Late-onset schizophrenia is diagnosed using ICD-10 (International Classification of Diseases, 10th Revision) criteria. Cox proportional hazard models identified significant factors across six domains: lifestyle, environment, medical history, physical measures, mental health and socioeconomic status (SES). Domain-specific weighted scores were calculated from Cox model coefficients and stratified into tertiles (favourable, intermediate, unfavourable) for risk assessment. Population attributable fractions (PAFs) quantified prevention potential.

resultsDuring follow-up, 1276 participants developed late-onset schizophrenia. We identified 109 significant potentially modifiable factors, with intellectual disability (HR 35.15, 95% CI 11.23 to 110.09), manic episode (HR 33.14, 95% CI 21.16 to 51.90) and bipolar affective disorder (HR 32.91, 95% CI 27.07 to 40.01) showing the strongest risks, while higher household income (>£100 000: HR 0.14, 95% CI 0.09 to 0.22), regular friends/family visits (HR 0.23, 95% CI 0.18 to 0.28) and higher hand grip strength (HR 0.35, 95% CI 0.29 to 0.44) showed the strongest protection. PAF estimations indicated that shifting individuals from unfavourable to intermediate/favourable risk profiles could prevent 71.3% (95% CI 71.2% to 71.4%) of late-onset schizophrenia cases, mainly from mental health (25.1%, 95% CI 25.0% to 25.2%), medical history (13.6%, 95% CI 13.5% to 13.7%) and SES domain (11.2%, 95% CI 11.1% to 11.3%); shifting individuals from intermediate/unfavourable risk profiles to favourable could prevent 89.2% of cases.

conclusionsA substantial proportion of late-onset schizophrenia risk appears modifiable, with mental health and medical history as key contributors. Physical health and natural environment exposure provided protective benefits. Findings supported integrating clinical interventions and structural changes addressing socioeconomic and environmental factors to reduce late-onset schizophrenia burden.

Indexed as

SchizophreniaAdultAgedAge of OnsetBiological Specimen BanksFemaleHumansMaleMiddle AgedProportional Hazards ModelsProspective StudiesRisk FactorsUK BiobankUnited KingdomSchizophrenia

Identifiers

PMID41161813
PMCPMC12574375

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.