Lifestyle and BrainAGE in adult depression.

IF 7.5 1区 医学 Q1 PSYCHIATRY
Nicole Sanford, Yuetong Yu, Ruiyang Ge, Shalaila S Haas, Liisa A M Galea, Sophia Frangou
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Abstract

This study investigates how heterogeneity in lifestyle and physical fitness shapes patterns of brain ageing in depression. The study sample included medically healthy adults from the UK Biobank (44-82 years) with a history of depression (n = 896) and non-psychiatric controls (n = 36,206). Heterogeneity through Discriminative Analysis (HYDRA) was used to derive data-driven subgroups within the depression sample based on 224 behavioural and physical health features. Global and voxel-based brain-age-gap-estimates (brainAGE) computed from structural neuroimaging data were used for personalized assessment of brain ageing. Four depression clusters were identified: the "balanced-active" cluster (n = 253) characterized by an active lifestyle and balanced diet; the "low metabolic risk-active" cluster (n = 178) characterized by a health-conscious dietary and exercise lifestyle; the "high metabolic risk-sedentary" cluster (n = 315) who had higher body mass, poor diet, and sedentary behaviour; and the "frailty-moderately active" cluster (n = 150) who had a varied diet but coupled with physical frailty. Mood symptoms were lowest in the "balanced-active" cluster and highest in the "high metabolic risk-sedentary" cluster. While depression overall was associated with minimally accelerated global and local brain ageing in fronto-limbic regions, the "high metabolic risk-sedentary" cluster showed additional, regionally specific acceleration in prefrontal, parahippocampal, and thalamic areas. This work underscores the importance of lifestyle and fitness heterogeneity when examining associations between depression and neurobiological ageing and supports lifestyle-informed stratification as a pathway toward more targeted intervention strategies.

成人抑郁症的生活方式与脑龄。
这项研究探讨了生活方式和身体健康的异质性如何影响抑郁症患者大脑衰老的模式。研究样本包括来自英国生物银行(UK Biobank)的医学上健康的成年人(44-82岁),有抑郁症史(n = 896)和非精神病对照组(n = 36,206)。通过判别分析(HYDRA)的异质性,基于224个行为和身体健康特征,在抑郁症样本中得出数据驱动的亚组。从结构神经成像数据计算的全局和基于体素的脑年龄差距估计(brainAGE)用于个性化脑老化评估。确定了四种抑郁症类型:“平衡-活跃”类型(n = 253),其特征是积极的生活方式和均衡的饮食;“低代谢风险活跃”组(n = 178),以注重健康的饮食和锻炼生活方式为特征;“高代谢风险-久坐”组(n = 315),他们有较高的体重、不良饮食和久坐行为;“虚弱-适度运动”组(n = 150)饮食多样,但伴有身体虚弱。情绪症状在“平衡-活跃”组中最低,在“高代谢-久坐”组中最高。虽然抑郁症总体上与额边缘区域的整体和局部大脑衰老的最小加速有关,但“高代谢风险-久坐”集群在前额叶、海马体旁和丘脑区域显示出额外的、区域特异性的加速。这项工作强调了生活方式和健康异质性在研究抑郁症和神经生物学老化之间的关系时的重要性,并支持生活方式分层作为更有针对性的干预策略的途径。
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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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