Xiang Jiao-Jiao, Hong Su, Ran Liu-Yi, Zeng Qi, Kong Yi-Ting, Zhang Chen-Yu, Liao Jing, Kuang Li
Department of Psychiatry, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Mental Health Center, University-Town Hospital of Chongqing Medical University, Chongqing 401331, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2023 Mar;54(2):310-315. doi: 10.12182/20230360204.
To investigate the changes in serum inflammatory cytokines and the predictive factors for the efficacy of sertraline following medication therapy in adolescents with first-episode major depressive disorder (MDD).
A total of 61 adolescent patients with first-episode drug-naïve MDD were enrolled for the MDD group and 55 healthy adolescents were enrolled for the healthy control (HC) group. Sertraline tablets were administered to the MDD group for 8 weeks after enrollment, while no medication was given to the HC group. In the MDD group, blood samples were collected to measure the cytokine levels and clinical data, including scores for the 17-item Hamilton Depression Scale (HAMD-17) and the Connor-Davidson Resilience Scale (CD-RISC), were assessed at baseline and at the end of the 8-week medication, whereas in the HC group, blood samples and clinical data were collected only at baseline. The correlation between the levels of serum inflammatory cytokines and depression severity in the MDD group was analyzed and stepwise linear regression of HAMD-17 in the MDD group was performed to find serologic indicators that could be used to predict the efficacy of sertraline.
At baseline, the levels of interleukin (IL)-1β and IL-6 in the MDD group were significantly higher than those in the HC group (all <0.0001), while the tumor necrosis factor (TNF)-α level in the MDD group was significantly lower than that in the HC group ( =0.006). After 8 weeks of medication treatment, the MDD group showed decreased levels of IL-1β and IL-6 and increased level of TNF-α compared to the pre-treatment levels. In addition, the HAMD-17 score, CD-RISC total score, and scores for perceived competence, trust and tolerance, and control, three factors of CD-RISC, all improved after treatment. There was no significant difference in serum cytokine levels at baseline between the subgroup showing response to the treatment and the non-responding subgroup. There was a weak correlation between IL-6 levels before and after treatment and CD-RISC scores and the scores for the trust and tolerance factor of CD-RISC before and after treatment. The baseline IL-1β and TNF-α levels did not show significant effect on posttreatment HAMD-17 scores.
Serum cytokine levels of adolescents with first-episode MDD differ significantly from those of healthy adolescents. Although IL-6 was found to be correlated with depression severity, there was not enough support for it to be used as a predictor of the antidepression efficacy of sertraline.
探讨首发重度抑郁症(MDD)青少年药物治疗后血清炎症细胞因子的变化及舍曲林疗效的预测因素。
共纳入61例首发未用药的MDD青少年患者作为MDD组,55例健康青少年作为健康对照组(HC组)。MDD组入组后给予舍曲林片治疗8周,HC组未给予药物治疗。MDD组在基线和8周药物治疗结束时采集血样检测细胞因子水平,并评估临床数据,包括17项汉密尔顿抑郁量表(HAMD - 17)评分和康纳 - 戴维森心理弹性量表(CD - RISC)评分,而HC组仅在基线时采集血样和临床数据。分析MDD组血清炎症细胞因子水平与抑郁严重程度之间的相关性,并对MDD组的HAMD - 17进行逐步线性回归,以寻找可用于预测舍曲林疗效的血清学指标。
基线时,MDD组白细胞介素(IL)-1β和IL - 6水平显著高于HC组(均<0.0001),而MDD组肿瘤坏死因子(TNF)-α水平显著低于HC组(=0.006)。药物治疗8周后,与治疗前水平相比,MDD组IL - 1β和IL - 6水平降低,TNF - α水平升高。此外,治疗后MDD组的HAMD - 17评分、CD - RISC总分以及CD - RISC的三个因子即感知能力、信任和容忍度以及掌控力评分均有所改善。治疗反应亚组和无反应亚组在基线时血清细胞因子水平无显著差异。治疗前后IL - 6水平与CD - RISC评分以及治疗前后CD - RISC的信任和容忍度因子评分之间存在弱相关性。基线IL - 1β和TNF - α水平对治疗后HAMD - 17评分无显著影响。
首发MDD青少年的血清细胞因子水平与健康青少年有显著差异。尽管发现IL - 6与抑郁严重程度相关,但尚无足够证据支持其作为舍曲林抗抑郁疗效的预测指标。