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本文引用的文献

1
Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma.与童年创伤相关的应激反应基因中的表观遗传修饰
Front Psychiatry. 2019 Nov 8;10:808. doi: 10.3389/fpsyt.2019.00808. eCollection 2019.
2
Peripheral cytokine levels and response to antidepressant treatment in depression: a systematic review and meta-analysis.外周细胞因子水平与抗抑郁治疗反应在抑郁症中的系统评价和荟萃分析。
Mol Psychiatry. 2020 Feb;25(2):339-350. doi: 10.1038/s41380-019-0474-5. Epub 2019 Aug 19.
3
Low-Grade Inflammation as a Predictor of Antidepressant and Anti-Inflammatory Therapy Response in MDD Patients: A Systematic Review of the Literature in Combination With an Analysis of Experimental Data Collected in the EU-MOODINFLAME Consortium.低度炎症作为重度抑郁症患者抗抑郁和抗炎治疗反应的预测指标:结合欧盟情绪炎症联盟收集的实验数据分析的文献系统综述
Front Psychiatry. 2019 Jul 9;10:458. doi: 10.3389/fpsyt.2019.00458. eCollection 2019.
4
Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-κB-driven inflammation and cardiovascular risk.衰老和应激导致 FKBP5 的表观遗传上调,从而导致 NF-κB 驱动的炎症和心血管风险。
Proc Natl Acad Sci U S A. 2019 Jun 4;116(23):11370-11379. doi: 10.1073/pnas.1816847116. Epub 2019 May 21.
5
Childhood Adversity and Current Stress are related to Pro- and Anti-inflammatory Cytokines in Major Depression.儿童期逆境和当前压力与重度抑郁症中的促炎和抗炎细胞因子有关。
J Affect Disord. 2019 Jun 15;253:270-276. doi: 10.1016/j.jad.2019.04.088. Epub 2019 Apr 22.
6
Childhood trauma history is linked to abnormal brain connectivity in major depression.童年创伤史与重度抑郁症患者大脑连接异常有关。
Proc Natl Acad Sci U S A. 2019 Apr 23;116(17):8582-8590. doi: 10.1073/pnas.1900801116. Epub 2019 Apr 8.
7
Association between childhood trauma exposure and pro-inflammatory cytokines in schizophrenia and bipolar-I disorder.精神分裂症和双相情感障碍患者童年创伤与促炎细胞因子的关联。
Psychol Med. 2019 Dec;49(16):2736-2744. doi: 10.1017/S0033291718003690. Epub 2018 Dec 18.
8
Inflammatory Measures in Depressed Patients With and Without a History of Adverse Childhood Experiences.有和没有童年不良经历史的抑郁症患者的炎症指标
Front Psychiatry. 2018 Nov 27;9:610. doi: 10.3389/fpsyt.2018.00610. eCollection 2018.
9
Adverse Childhood Experiences and the Consequences on Neurobiological, Psychosocial, and Somatic Conditions Across the Lifespan.童年不良经历及其对一生的神经生物学、心理社会和躯体状况的影响。
Front Psychiatry. 2018 Sep 4;9:420. doi: 10.3389/fpsyt.2018.00420. eCollection 2018.
10
Replication and reproducibility issues in the relationship between C-reactive protein and depression: A systematic review and focused meta-analysis.C 反应蛋白与抑郁关系中复制和可重复性问题的系统评价和重点荟萃分析。
Brain Behav Immun. 2018 Oct;73:85-114. doi: 10.1016/j.bbi.2018.06.016. Epub 2018 Jun 19.

评估儿童期创伤、C 反应蛋白与情感障碍患者抗抑郁治疗反应之间的关系。

Assessing the links between childhood trauma, C-reactive protein and response to antidepressant treatment in patients with affective disorders.

机构信息

Department of Psychiatry and Psychotherapy, University Hospital, LMU Munich, Nußbaumstraße 7, 80336, München, Germany.

Institute of Mental Health at UBC, University of British Columbia, Vancouver, Canada.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2021 Oct;271(7):1331-1341. doi: 10.1007/s00406-021-01245-z. Epub 2021 Mar 17.

DOI:10.1007/s00406-021-01245-z
PMID:33733300
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8429368/
Abstract

Adverse Childhood Experiences (ACE) are a well-known risk-factor for depression. Additionally, (high-sensitive) C-reactive Protein (hsCRP) is elevated in subgroups of depressed patients and high following ACE. In this context the literature considers hsCRP and ACE to be associated with treatment resistant depression. With the data being heterogenous, this study aimed to explore the associations of ACE, hsCRP levels and response to antidepressant treatment in uni- and bipolar depression. N = 76 patients diagnosed with uni- or bipolar depression and N = 53 healthy controls were included. Treatment was over 6 weeks in an inpatient psychiatric setting within an observatory study design. Depressive symptoms were assessed by the Montgomery-Asberg Depression Rating Scale (MADRS), ACE were assessed by the Childhood Trauma Questionnaire (CTQ); the body-mass-index (BMI) and hsCRP were measured. HsCRP levels did not differ between the study population and the healthy controls. While the depressive symptoms decreased, the hsCRP levels increased. Sexual abuse was associated with significant higher and emotional abuse with lower levels of hsCRP after 6 weeks. The baseline hsCRP levels and the ACE subgroups did not show significant associations with the treatment response in unipolar depressed patients. The long-lasting effects of specific forms of ACE may have relevant impact on inflammation, supporting hsCRP to be a suitable biomarker. With ACE and hsCRP not showing any significant associations with treatment response in the unipolar depressed subgroup, a more differentiate research concerning biomarkers and treatment regimens is needed when talking about treatment response.

摘要

童年期逆境经历(ACE)是抑郁的一个众所周知的风险因素。此外,(高敏)C 反应蛋白(hsCRP)在抑郁患者亚组中升高,且在 ACE 后升高。在这种情况下,文献认为 hsCRP 和 ACE 与治疗抵抗性抑郁有关。由于数据存在异质性,本研究旨在探讨 ACE、hsCRP 水平与单相和双相抑郁患者抗抑郁治疗反应的关系。共纳入 76 例单相或双相抑郁患者和 53 名健康对照者。在观察性研究设计的住院精神病学环境中,进行为期 6 周的治疗。采用蒙哥马利-阿斯伯格抑郁评定量表(MADRS)评估抑郁症状,采用儿童创伤问卷(CTQ)评估 ACE;测量体重指数(BMI)和 hsCRP。研究人群与健康对照组的 hsCRP 水平无差异。随着抑郁症状的减轻,hsCRP 水平升高。6 周后,性虐待与 hsCRP 水平显著升高相关,情感虐待与 hsCRP 水平降低相关。hsCRP 基线水平和 ACE 亚组与单相抑郁患者的治疗反应无显著相关性。特定形式的 ACE 的长期影响可能对炎症有重要影响,支持 hsCRP 成为一种合适的生物标志物。由于 ACE 和 hsCRP 与单相抑郁亚组的治疗反应无显著相关性,因此在讨论治疗反应时,需要对生物标志物和治疗方案进行更具针对性的研究。