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Article: All-cause and cause-specific mortality in people with mental disorders: a population-based study on risk evaluation, effect modifiers and excess life-years lost in Hong Kong

TitleAll-cause and cause-specific mortality in people with mental disorders: a population-based study on risk evaluation, effect modifiers and excess life-years lost in Hong Kong
Authors
Issue Date1-Mar-2026
PublisherElsevier
Citation
European Neuropsychopharmacology, 2026, v. 104 How to Cite?
Abstract

Mental-disorders (MDs) are associated with premature mortality. Previous studies had limitations including confounding by physical-morbidities and lack of cause-specific mortality evaluation. We aimed to quantify mortality risk and life-expectancy gap across MDs in an Asian population. This retrospective population-based study investigated people with MDs (ascertained by ICD10-codes) in 2006–2021, utilizing comprehensive health-record-database of public-healthcare services in Hong-Kong. Individuals without MDs attending primary-care-clinics during study period served as comparisons. We estimated relative all-cause and cause-specific mortality risk using Cox-proportional hazards-regression models, and calculated excess life-years-lost (LYLs). Effect modification (sex, age, Charlson-comorbidity-index, socioeconomic-status (SES)) on relative risks was evaluated with subgroup-analyses. This analysis included 332,298 people with and 902,927 people without MDs. Any MD was associated with increased all-cause mortality (hazard-ratio (HR): 2.04 [95%Confidence-interval (CI)=2.02–2.07]) and excess LYLs (13.81 years [95%CI=13.60–13.98]). Eating-disorders exhibited the highest all-cause mortality (HR=9.43 [95%CI=6.83–13.02]), followed by developmental-disorders (HR=5.55 [95%CI=4.45–6.92]), personality-disorders (HR=4.50 [95%CI=4.06–4.98]) and substance-use disorders (HR=3.83 [95%CI=3.70–3.96]), with pronounced excess LYLs (14.18–17.41 years). Psychiatric-multimorbidity further increased excess mortality. Suicide was associated with the highest mortality risk (HR=8.69 [95%CI=7.97–9.45]). Natural causes accounted for most deaths (85%; HR range=1.50–2.76), while external causes explained 5% of all deaths (suicide: HR=8.69 [95%CI=7.97–9.45]). Men, younger age and lower SES were associated with increased all-cause and natural-cause mortality, while women and higher SES were linked to elevated external-cause mortality. This study highlighted transdiagnostic nature of premature mortality associated with MDs. Implementation of comprehensive multilevel interventions is warranted to narrow this mortality gap.


Persistent Identifierhttp://hdl.handle.net/10722/368340
ISSN
2023 Impact Factor: 6.1
2023 SCImago Journal Rankings: 1.756

 

DC FieldValueLanguage
dc.contributor.authorChan, Joe Kwun-Nam-
dc.contributor.authorLi, Ryan Cheuk-Yin-
dc.contributor.authorPlana-Ripoll, Oleguer-
dc.contributor.authorMomen, Natalie C.-
dc.contributor.authorCorrell, Christoph U.-
dc.contributor.authorSolmi, Marco-
dc.contributor.authorWong, Corine Sau-Man-
dc.contributor.authorKu, Kam-Ming-
dc.contributor.authorMahboobani, Vanessa Ramesh-
dc.contributor.authorChung, Albert Kar-Kin-
dc.contributor.authorLui, Simon Sai-Yu-
dc.contributor.authorSham, Pak-Chung-
dc.contributor.authorChang, Wing-Chung-
dc.date.accessioned2025-12-24T00:37:45Z-
dc.date.available2025-12-24T00:37:45Z-
dc.date.issued2026-03-01-
dc.identifier.citationEuropean Neuropsychopharmacology, 2026, v. 104-
dc.identifier.issn0924-977X-
dc.identifier.urihttp://hdl.handle.net/10722/368340-
dc.description.abstract<p>Mental-disorders (MDs) are associated with premature mortality. Previous studies had limitations including confounding by physical-morbidities and lack of cause-specific mortality evaluation. We aimed to quantify mortality risk and life-expectancy gap across MDs in an Asian population. This retrospective population-based study investigated people with MDs (ascertained by ICD10-codes) in 2006–2021, utilizing comprehensive health-record-database of public-healthcare services in Hong-Kong. Individuals without MDs attending primary-care-clinics during study period served as comparisons. We estimated relative all-cause and cause-specific mortality risk using Cox-proportional hazards-regression models, and calculated excess life-years-lost (LYLs). Effect modification (sex, age, Charlson-comorbidity-index, socioeconomic-status (SES)) on relative risks was evaluated with subgroup-analyses. This analysis included 332,298 people with and 902,927 people without MDs. Any MD was associated with increased all-cause mortality (hazard-ratio (HR): 2.04 [95%Confidence-interval (CI)=2.02–2.07]) and excess LYLs (13.81 years [95%CI=13.60–13.98]). Eating-disorders exhibited the highest all-cause mortality (HR=9.43 [95%CI=6.83–13.02]), followed by developmental-disorders (HR=5.55 [95%CI=4.45–6.92]), personality-disorders (HR=4.50 [95%CI=4.06–4.98]) and substance-use disorders (HR=3.83 [95%CI=3.70–3.96]), with pronounced excess LYLs (14.18–17.41 years). Psychiatric-multimorbidity further increased excess mortality. Suicide was associated with the highest mortality risk (HR=8.69 [95%CI=7.97–9.45]). Natural causes accounted for most deaths (85%; HR range=1.50–2.76), while external causes explained 5% of all deaths (suicide: HR=8.69 [95%CI=7.97–9.45]). Men, younger age and lower SES were associated with increased all-cause and natural-cause mortality, while women and higher SES were linked to elevated external-cause mortality. This study highlighted transdiagnostic nature of premature mortality associated with MDs. Implementation of comprehensive multilevel interventions is warranted to narrow this mortality gap.<br></p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofEuropean Neuropsychopharmacology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleAll-cause and cause-specific mortality in people with mental disorders: a population-based study on risk evaluation, effect modifiers and excess life-years lost in Hong Kong-
dc.typeArticle-
dc.identifier.doi10.1016/j.euroneuro.2025.112742-
dc.identifier.volume104-
dc.identifier.eissn1873-7862-
dc.identifier.issnl0924-977X-

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