Bortolasci C C, Voigt C, Turner A, Mohebbi M, Gray L, Dodd S, Walder K, Berk M, Cotton S M, Malhi G S, Ng C H, Dowling N, Sarris J, Dean O M
The Institute for Mental and Physical Health and Clinical Translation, Deakin University, Barwon Health, Geelong, Australia.
University of Bremen, Bremen, Germany.
Acta Neuropsychiatr. 2020 Dec;32(6):313-320. doi: 10.1017/neu.2020.25. Epub 2020 Jun 30.
The aims of this study were to evaluate changes in inflammatory and oxidative stress levels following treatment with N-acetylcysteine (NAC) or mitochondrial-enhancing agents (CT), and to assess the how these changes may predict and/or moderate clinical outcomes primarily the Montgomery-Åsberg Depression Rating Scale (MADRS).
This study involved secondary analysis of a placebo-controlled randomised trial (n = 163). Serum samples were collected at baseline and week 16 of the clinical trial to determine changes in Interleukin-6 (IL-6) and total antioxidant capacity (TAC) following adjunctive CT and/or NAC treatment, and to explore the predictability of the outcome or moderator effects of these markers.
In the NAC-treated group, no difference was observed in serum IL-6 and TAC levels after 16 weeks of treatment with NAC or CT. However, results from a moderator analysis showed that in the CT group, lower IL-6 levels at baseline was a significant moderator of MADRS χ2 (df) = 4.90, p = 0.027) and Clinical Global Impression-Improvement (CGI-I, χ2 (df) = 6.28 p = 0.012). In addition, IL-6 was a non-specific but significant predictor of functioning (based on the Social and Occupational Functioning Assessment Scale (SOFAS)), indicating that individuals with higher IL-6 levels at baseline had a greater improvement on SOFAS regardless of their treatment (p = 0.023).
Participants with lower IL-6 levels at baseline had a better response to the adjunctive treatment with the mitochondrial-enhancing agents in terms of improvements in MADRS and CGI-I outcomes.
本研究旨在评估用N-乙酰半胱氨酸(NAC)或线粒体增强剂(CT)治疗后炎症和氧化应激水平的变化,并评估这些变化如何预测和/或调节主要基于蒙哥马利-Åsberg抑郁评定量表(MADRS)的临床结局。
本研究涉及对一项安慰剂对照随机试验(n = 163)的二次分析。在临床试验的基线和第16周采集血清样本,以确定辅助CT和/或NAC治疗后白细胞介素-6(IL-6)和总抗氧化能力(TAC)的变化,并探讨这些标志物对结局或调节效应的可预测性。
在NAC治疗组中,用NAC或CT治疗16周后,血清IL-6和TAC水平未观察到差异。然而,调节分析结果显示,在CT组中,基线时较低的IL-6水平是MADRS(χ2(自由度)= 4.90,p = 0.027)和临床总体印象改善(CGI-I,χ2(自由度)= 6.28,p = 0.012)的显著调节因素。此外,IL-6是功能的非特异性但显著的预测指标(基于社会和职业功能评估量表(SOFAS)),表明基线时IL-6水平较高的个体无论接受何种治疗,在SOFAS上的改善都更大(p = 0.023)。
就MADRS和CGI-I结局的改善而言,基线时IL-6水平较低的参与者对线粒体增强剂辅助治疗的反应更好。