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基于进化精神病学的抑郁分类:近似机制和终极功能。

Depression subtyping based on evolutionary psychiatry: Proximate mechanisms and ultimate functions.

机构信息

Department of Biology, University of Turku, FIN-20014 Turku, Finland; Turku Brain and Mind Center, University of Turku, FIN-20014 Turku, Finland.

English, Drama and Writing Studies, University of Auckland, 1010 Auckland, New Zealand; School of Psychology, University of Auckland, 1010 Auckland, New Zealand.

出版信息

Brain Behav Immun. 2018 Mar;69:603-617. doi: 10.1016/j.bbi.2017.10.012. Epub 2017 Oct 16.

Abstract

Major depressive disorder constitutes one of the leading causes of disability worldwide. However, it is not a unitary disease-it is a heterogeneous syndrome, with patients differing remarkably in symptom profile, pathophysiology and treatment responsiveness. Previous attempts to subtype major depressive disorder have showed limited clinical applicability. We present a classification of major depressive disorder episodes based on the proximate mechanisms that led to the original mood change that caused the depressive episode. We identify discrete depression subtypes that are induced by: 1) infection, 2) long-term stress, 3) loneliness, 4) traumatic experience, 5) hierarchy conflict, 6) grief, 7) romantic rejection, 8) postpartum events, 9) the season, 10) chemicals, 11) somatic diseases and 12) starvation. We further examine the ultimate functions of these subtypes and show that not all types of mood changes that trigger depression are adaptive. Instead, some are clearly maladaptive and some are byproducts of other adaptations. In modern societies, low mood after adverse life events may turn into a pathological depressive state. Modern lifestyle increases susceptibility to inflammatory dysregulation and chronic stress, both of which increase the amount of proinflammatory cytokines in peripheral blood, leading to low mood and sickness behaviour. Proinflammatory cytokines may aggravate the previously adaptive short-term mood changes to a chronic maladaptive depressive state by preventing the normalization of mood after adverse life events. Subtyping depression enables an effective and intelligent long-term treatment of patients in each subtype by treating the underlying causes of depression.

摘要

重度抑郁症是全球导致残疾的主要原因之一。然而,它并不是一种单一的疾病——而是一种异质性综合征,患者在症状特征、病理生理学和治疗反应方面差异显著。以前对重度抑郁症进行亚型分类的尝试显示出其临床应用的局限性。我们提出了一种基于导致抑郁发作的原始情绪变化的近端机制对重度抑郁症发作进行分类的方法。我们确定了由以下原因引起的离散抑郁亚型:1)感染,2)长期压力,3)孤独,4)创伤性经历,5)等级冲突,6)悲伤,7)浪漫拒绝,8)产后事件,9)季节,10)化学物质,11)躯体疾病和 12)饥饿。我们进一步研究了这些亚型的最终功能,并表明并非所有引发抑郁的情绪变化都是适应不良的。相反,有些显然是适应不良的,有些则是其他适应的副产品。在现代社会中,不良生活事件后的情绪低落可能会变成病理性抑郁状态。现代生活方式增加了对炎症失调和慢性应激的易感性,这两者都会增加外周血中促炎细胞因子的数量,导致情绪低落和疾病行为。促炎细胞因子可能会通过阻止不良生活事件后情绪的正常化,将以前适应的短期情绪变化加剧为慢性适应不良的抑郁状态。对抑郁症进行亚型分类,可以通过治疗抑郁症的根本原因,对每种亚型的患者进行有效的、智能的长期治疗。

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