Associations of clinical biomarker-based biological aging with suicide attempts and suicidal ideation: evidence from 124,529 UK Biobank participants.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Wei Hu, Zhenzhen Shen, Ge Tian, Baopeng Liu, Cunxian Jia
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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.

基于临床生物标志物的生物衰老与自杀企图和自杀意念的关联:来自124,529名英国生物银行参与者的证据
生物衰老与多种心理障碍有关,但其与自杀的外推仍不存在。我们的目的是研究生物衰老与自杀意念(SI)和自杀企图(SA)的关系,并探讨可能的调节因素。来自英国生物银行的124529名中老年参与者被纳入研究。表型年龄(PhenoAge)是根据实足年龄和9个临床生物标志物计算的。利用对实足年龄进行回归的表型年龄残差来量化生物衰老,称为表型年龄加速(PAA)。大约三分之一的基线参与者完成了包括自杀相关信息的心理健康随访问卷。采用多变量logistic回归模型来估计相关性。记录了2718例SA(2.2%)和5207例SI(4.4%)。与PAA最低四分位数的参与者相比,PAA最高四分位数的参与者的风险为21.8%[比值比(OR) = 1.218;95%可信区间(CI): 1.087-1.198)和12.5% (OR = 1.125, 95% CI: 1.035-1.224) SA和SI的几率分别高。生物学上年龄较大的参与者(PAA bb 0)更有可能报告SA (OR = 1.104, 95% CI: 1.018-1.198)和SI (OR = 1.064, 95% CI: 1.003-1.129)。性别、年龄、社会经济地位(SES)、身体活动、躯体和精神疾病可以改变这种关联(P为相互作用)
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
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.
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