Department of Biology, City University of New York-College of Staten Island, Staten Island, NY 10314, USA.
Oxid Med Cell Longev. 2022 Sep 16;2022:1061274. doi: 10.1155/2022/1061274. eCollection 2022.
Major depressive disorder (MDD) and treatment-resistant depression (TRD) represent a global source of societal and health burden. To advise proper management of inflammation-related depression among TRD patients, it is important to identify therapeutic clinical treatments. A key factor is related to proinflammatory cytokines such as interleukin- (IL-) 1, IL-6, and tumor necrosis factor- (TNF-) which have been implicated in the pathogenesis of depressive symptoms in MDD patients. Ketamine may provide an anti-inflammatory therapeutic strategy by targeting proinflammatory pathways associated with depressive disorders, which may be exacerbated in the ageing population with TRD.
Despite a burgeoning body of literature demonstrating that inflammation is linked to TRD, there is still a lack of comprehensive research on the relationship between proinflammatory biomarkers and ketamine's antidepressant effect on TRD patients.
The Cochrane Library and PubMed/MEDLINE databases were systematically searched from inception up to February 1, 2022, adopting broad inclusion criteria to assess clinical topics related to the impact of ketamine on inflammatory cytokines in TRD patients. The present work is in compliance with the World Health Organization Rapid Review Guide.
Five out of the seven studies examined in this review show that ketamine infusion may reduce depressive symptoms with a quick start of effect on TRD patients. Based on the Montgomery-Åsberg Depression Rating Scale (MADRS) and Hamilton Depression Rating Scale (HAM-D) scores, the overall response rate for ketamine was 56%; that is, 56% of those treated with ketamine had MADRS/HAM-D scores decreased by at least 50%.
While the anti-inflammatory effects of ketamine modulate specific proinflammatory cytokines, its rapid antidepressant effect on TRD patients remains inconsistent. However, our study findings can provide a reliable basis for future research on how to improve systemic inflammatory immune disorders and mental health. We suggest that ketamine infusion may be part of a comprehensive treatment approach in TRD patients with elevated levels of depression-specific inflammatory biomarkers.
重度抑郁症(MDD)和治疗抵抗性抑郁症(TRD)是全球社会和健康负担的主要来源。为了建议适当管理 TRD 患者的炎症相关抑郁症,确定治疗性临床治疗方法很重要。一个关键因素与促炎细胞因子有关,如白细胞介素(IL)-1、IL-6 和肿瘤坏死因子(TNF),它们与 MDD 患者的抑郁症状发病机制有关。氯胺酮通过靶向与抑郁障碍相关的促炎途径可能提供一种抗炎治疗策略,这在 TRD 伴年龄增长的人群中可能会加剧。
尽管越来越多的文献表明炎症与 TRD 有关,但关于促炎生物标志物与氯胺酮对 TRD 患者抗抑郁作用之间的关系,仍缺乏全面的研究。
系统检索了 Cochrane 图书馆和 PubMed/MEDLINE 数据库,从成立到 2022 年 2 月 1 日,采用广泛的纳入标准评估与氯胺酮对 TRD 患者炎症细胞因子影响相关的临床主题。本工作符合世界卫生组织快速审查指南。
在本综述中检查的七项研究中有五项表明,氯胺酮输注可能会减轻 TRD 患者的抑郁症状,并且对 TRD 患者的起效迅速。根据蒙哥马利-阿斯伯格抑郁评定量表(MADRS)和汉密尔顿抑郁评定量表(HAM-D)评分,氯胺酮的总体反应率为 56%;即 56%的接受氯胺酮治疗的患者的 MADRS/HAM-D 评分降低至少 50%。
虽然氯胺酮的抗炎作用调节特定的促炎细胞因子,但它对 TRD 患者的快速抗抑郁作用仍不一致。然而,我们的研究结果可为如何改善系统性炎症免疫障碍和心理健康提供可靠的依据。我们建议氯胺酮输注可能是治疗具有升高的抑郁特异性炎症生物标志物的 TRD 患者的综合治疗方法的一部分。