Wei Hu, Zhenzhen Shen, Ge Tian, Baopeng Liu, Cunxian Jia
{"title":"Associations of clinical biomarker-based biological aging with suicide attempts and suicidal ideation: evidence from 124,529 UK Biobank participants.","authors":"Wei Hu, Zhenzhen Shen, Ge Tian, Baopeng Liu, Cunxian Jia","doi":"10.1038/s41398-025-03412-5","DOIUrl":null,"url":null,"abstract":"<p><p>Biological aging has been linked to multiple psychological disorders, yet its extrapolation to suicide remains absent. We aimed to examine the associations of biological aging with suicidal ideation (SI) and suicide attempt (SA) and to explore possible moderators of the associations. A total of 124,529 middle and older participants from the UK Biobank were included. Phenotypic age (PhenoAge) indicating biological aging was calculated based on chronological age and nine clinical biomarkers. The residuals of PhenoAge regressed on chronological age were utilized to quantify biological aging, termed PhenoAge acceleration (PAA). Approximately one-third of baseline participants completed mental health follow-up questionnaires including suicide-related information. Multivariate logistic regression models were performed to estimate the associations. 2718 (2.2%) SA and 5207 (4.4%) SI cases were documented. Compared with participants in the lowest quartile of PAA, those in the highest quartile had a 21.8% [odds ratio (OR) = 1.218; 95% confidence interval (CI): 1.087-1.198) and 12.5% (OR = 1.125, 95% CI: 1.035-1.224) higher odds of SA and SI, respectively. Biologically older participants (PAA > 0) were more likely to report SA (OR = 1.104, 95% CI: 1.018-1.198) and SI (OR = 1.064, 95% CI: 1.003-1.129). Gender, age, socioeconomic status (SES), physical activity, and somatic and psychiatric disorders could modify the associations (P for interaction <0.05). Our findings indicated that PAA-measured aging might be positively associated with SA/SI. Interventions aimed at slowing aging might contribute to suicide prevention, especially among males, young adults, low SES, the physically inactive, and vulnerable populations.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"204"},"PeriodicalIF":5.8000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03412-5","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
Biological aging has been linked to multiple psychological disorders, yet its extrapolation to suicide remains absent. We aimed to examine the associations of biological aging with suicidal ideation (SI) and suicide attempt (SA) and to explore possible moderators of the associations. A total of 124,529 middle and older participants from the UK Biobank were included. Phenotypic age (PhenoAge) indicating biological aging was calculated based on chronological age and nine clinical biomarkers. The residuals of PhenoAge regressed on chronological age were utilized to quantify biological aging, termed PhenoAge acceleration (PAA). Approximately one-third of baseline participants completed mental health follow-up questionnaires including suicide-related information. Multivariate logistic regression models were performed to estimate the associations. 2718 (2.2%) SA and 5207 (4.4%) SI cases were documented. Compared with participants in the lowest quartile of PAA, those in the highest quartile had a 21.8% [odds ratio (OR) = 1.218; 95% confidence interval (CI): 1.087-1.198) and 12.5% (OR = 1.125, 95% CI: 1.035-1.224) higher odds of SA and SI, respectively. Biologically older participants (PAA > 0) were more likely to report SA (OR = 1.104, 95% CI: 1.018-1.198) and SI (OR = 1.064, 95% CI: 1.003-1.129). Gender, age, socioeconomic status (SES), physical activity, and somatic and psychiatric disorders could modify the associations (P for interaction <0.05). Our findings indicated that PAA-measured aging might be positively associated with SA/SI. Interventions aimed at slowing aging might contribute to suicide prevention, especially among males, young adults, low SES, the physically inactive, and vulnerable populations.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.