Evidence map›Paper›PMID 42844259›Full record

ArticleTranslational psychiatry2026

Associations between lifestyle, genetic liability for severe mental illness and risk of incident somatic illnesses.

Ulker Isayeva, Sinan Guloksuz, Bochao Danae Lin, Nini de Boer, Bart P F Rutten, David E J Linden, Mirko Manchia, Jurjen J Luykx

Abstract read
In one paragraph

Article in Translational psychiatry, 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
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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

8 authors.

Ulker IsayevaUnit of Psychiatry, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy. ulker.isayeva@unica.it.ORCID http://orcid.org/0000-0003-3927-4810
Sinan GuloksuzDepartment of Psychiatry, University of British Columbia, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0002-6626-1874
Bochao Danae LinDepartment of Psychiatry and Neuropsychology, Mental Health and Neuroscience Research Institute, Maastricht University Medical Centre, Maastricht, The Netherlands.
Nini de BoerDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.
Bart P F RuttenDepartment of Psychiatry and Neuropsychology, Mental Health and Neuroscience Research Institute, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-9834-6346
David E J LindenDepartment of Psychiatry and Neuropsychology, Mental Health and Neuroscience Research Institute, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0002-5638-9292
Mirko ManchiaUnit of Psychiatry, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.ORCID http://orcid.org/0000-0003-4175-6413
Jurjen J LuykxDepartment of Psychiatry and Neuropsychology, Mental Health and Neuroscience Research Institute, Maastricht University Medical Centre, Maastricht, The Netherlands. j.j.luykx@amsterdamumc.nl.ORCID http://orcid.org/0000-0002-6439-2774

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

People with severe mental illness (SMI), including schizophrenia (SCZ) and bipolar disorder (BD), show elevated risk for somatic conditions and premature mortality. Both genetic liability and modifiable lifestyle factors have been implicated in this comorbidity, yet large-scale studies examining their independent and combined effects across multiple somatic conditions are lacking. We therefore examined whether modifiable lifestyle factors (i.e. smoking, alcohol intake, diet, and exercise) and polygenic risk scores (PRS) for SCZ and BD are associated with the risk of developing somatic illnesses. Data were drawn from 315,313 unrelated individuals in the UK Biobank cohort, with a median follow up of 14 years. Cox proportional hazards models were used to estimate the independent, joint, and interaction effects of PRS-SCZ and PRS-BD and lifestyle factors on the incidence of nine chronic somatic illnesses. Healthy lifestyle was associated with lower risks of type 2 diabetes (T2D), cardiovascular disease (CVD), dementia, rheumatoid arthritis, asthma, chronic liver disease (CLD), and cancer (HRs ranging from 0.43 to 0.80). In addition, higher PRS for SCZ was associated with increased risks of asthma and dementia and lower risk of T2D, while higher PRS for BD was associated with increased risk of T2D. Moreover, likelihood ratio tests confirmed that PRS-SCZ and PRS-BD each contribute independent information to the joint Cox model for T2D, indicating that the opposing directions of their associations with T2D risk are not driven by shared genetic variance between the two scores. Finally, individuals with a healthy lifestyle consistently showed lower risks of CLD, T2D, CVD, and dementia across genetic risk strata; however, no significant additive interaction was observed between genetic risk and lifestyle factors. In conclusion, these findings indicate that genetic liabilities for SCZ and BD show outcome-specific associations with somatic illnesses, while a healthy lifestyle is associated with lower somatic illness risk regardless of genetic risk level.

Indexed as

Bipolar DisorderGenetic Predisposition to DiseaseLife StyleMental DisordersSchizophreniaAdultAlcohol DrinkingCardiovascular DiseasesChronic DiseaseComorbidityDiabetes Mellitus, Type 2FemaleGenetic Risk ScoreHumansIncidenceMale

Identifiers

PMID42844259
PMCPMC13646258

What Socratic holds

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Registered trials

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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 Socratic graph.