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非典型性抑郁症与非非典型性抑郁症:HPA 轴功能是否为生物标志物?系统综述。

Atypical depression and non-atypical depression: Is HPA axis function a biomarker? A systematic review.

机构信息

Centre for Affective Disorders, Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Biomedical Research Centre (BRC) at South London and Maudsley NHS Foundation Trust (SLaM) and King's College London, UK; Department of Neuroscience and Behavior, School of Medicine of Ribeirao Preto, University of Sao Paulo, Sao Paulo, Brazil.

Centre for Affective Disorders, Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Biomedical Research Centre (BRC) at South London and Maudsley NHS Foundation Trust (SLaM) and King's College London, UK.

出版信息

J Affect Disord. 2018 Jun;233:45-67. doi: 10.1016/j.jad.2017.09.052. Epub 2017 Oct 6.

DOI:10.1016/j.jad.2017.09.052
PMID:29150144
Abstract

BACKGROUND

The link between the abnormalities of the Hypothalamic-pituitary-adrenal (HPA) axis and depression has been one of the most consistently reported findings in psychiatry. At the same time, multiple studies have demonstrated a stronger association between the increased activation of HPA-axis and melancholic, or endogenous depression subtype. This association has not been confirmed for the atypical subtype, and some researchers have suggested that as an antinomic depressive subtype, it may be associated with the opposite type, i.e. hypo-function, of the HPA-axis, similarly to PTSD. The purpose of this systematic review is to summarise existing studies addressing the abnormalities of the HPA-axis in melancholic and/or atypical depression.

METHOD

We conducted a systematic review in the literature by searching MEDLINE, PsycINFO, OvidSP and Embase databases until June 2017. The following search items were used: "hypothalamic-pituitary-adrenal" OR "HPA" OR "cortisol" OR "corticotropin releasing hormone" OR "corticotropin releasing factor" OR "glucocorticoid*" OR "adrenocorticotropic hormone" OR "ACTH" AND "atypical depression" OR "non-atypical depression" OR "melancholic depression" OR "non-melancholic depression" OR "endogenous depression" OR "endogenomorphic depression" OR "non-endogenous depression". Search limits were set to include papers in English or German language published in peer-reviewed journals at any period. All studies were scrutinized to determine the main methodological characteristics, and particularly possible sources of bias influencing the results reported.

RESULTS

We selected 48 relevant studies. Detailed analysis of the methodologies used in the studies revealed significant variability especially regarding the samples' definition comparing the HPA axis activity of melancholic patients to atypical depression, including healthy controls. The results were subdivided into 4 sections: (1) 27 studies which compared melancholic OR endogenous depression vs. non-melancholic or non-endogenous depression or controls; (2) 9 studies which compared atypical depression or atypical traits vs. non-atypical depression or controls; (3) 7 studies which compared melancholic or endogenous and atypical depression subtypes and (4) 5 studies which used a longitudinal design, comparing the measures of HPA-axis across two or more time points. While the majority of studies did confirm the association between melancholic depression and increased post-challenge cortisol levels, the association with increases in basal cortisol and basal ACTH were less consistent. Some studies, particularly those focusing on reversed vegetative symptoms, demonstrated a decrease in the activity of the HPA axis in atypical depression compared to controls, but the majority did not distinguish it from healthy controls.

CONCLUSIONS

In conclusion, our findings indicate that there is a difference in the activity of the HPA-axis between melancholic and atypical depressive subtypes. However, these are more likely explained by hypercortisolism in melancholia; and most often normal than decreased function in atypical depression. Further research should seek to distinguish a particular subtype of depression linked to HPA-axis abnormalities, based on symptom profile, with a focus on vegetative symptoms, neuroendocrine probes, and the history of adverse childhood events. New insights into the dichotomy addressed in this review might be obtained from genetic and epigenetic studies of HPA-axis related genes in both subtypes, with an emphasis on the presence of vegetative symptoms.

摘要

背景

下丘脑-垂体-肾上腺(HPA)轴的异常与抑郁症之间的联系一直是精神病学中最一致的发现之一。同时,多项研究表明,HPA 轴的过度激活与忧郁型或内源性抑郁亚型之间存在更强的关联。这种关联尚未得到非典型亚型的证实,一些研究人员认为,作为一种矛盾的抑郁亚型,它可能与 HPA 轴的相反类型相关,即功能减退,类似于创伤后应激障碍。本系统评价的目的是总结现有的研究,探讨 HPA 轴在忧郁型和/或非典型抑郁中的异常。

方法

我们在文献中进行了系统的文献检索,检索了 MEDLINE、PsycINFO、OvidSP 和 Embase 数据库,检索时间截至 2017 年 6 月。使用了以下搜索项:“下丘脑-垂体-肾上腺”或“HPA”或“皮质醇”或“促肾上腺皮质激素释放激素”或“促肾上腺皮质激素释放因子”或“糖皮质激素*”或“促肾上腺皮质激素”或“ACTH”和“非典型抑郁”或“非典型抑郁”或“忧郁型抑郁”或“非忧郁型抑郁”或“内源性抑郁”或“内源性抑郁”或“非内源性抑郁”。搜索限制设置为包括在任何时期以英文或德文发表的同行评议期刊上的论文。仔细分析了研究中使用的方法学特征,特别是可能影响报告结果的偏倚来源。

结果

我们选择了 48 项相关研究。对研究中使用的方法的详细分析显示出显著的变异性,特别是在将忧郁型患者的 HPA 轴活性与非忧郁型或非内源性抑郁症进行比较时,包括健康对照组。结果分为 4 个部分:(1)27 项研究比较了忧郁型或内源性抑郁与非忧郁型或非内源性抑郁或对照组;(2)9 项研究比较了非典型抑郁或非典型特征与非非典型抑郁或对照组;(3)7 项研究比较了忧郁型或内源性和非典型抑郁亚型;(4)5 项研究采用了纵向设计,比较了 HPA 轴在两个或更多时间点的测量值。虽然大多数研究确实证实了忧郁型抑郁症与应激后皮质醇水平升高之间的关联,但与基础皮质醇和基础 ACTH 升高之间的关联则不太一致。一些研究,特别是那些关注逆转植物性症状的研究,表明与对照组相比,非典型抑郁症中 HPA 轴的活性下降,但大多数研究并没有将其与健康对照组区分开来。

结论

总之,我们的研究结果表明,在忧郁型和非典型抑郁亚型之间 HPA 轴的活性存在差异。然而,这些更可能是由于忧郁症中的皮质醇过度活跃所致,而不是非典型抑郁症中常见的功能减退。进一步的研究应根据症状特征,重点关注植物性症状、神经内分泌探针和儿童期不良事件史,寻求区分与 HPA 轴异常相关的特定抑郁亚型。通过对 HPA 轴相关基因的遗传和表观遗传学研究,可能会对本综述中所讨论的二分法有新的认识,重点是存在植物性症状。

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