Mental Health Centre Copenhagen, Faculty of Health Sciences, University of Copenhagen, Denmark.
Brain Behav Immun. 2014 Jan;35:70-6. doi: 10.1016/j.bbi.2013.08.014. Epub 2013 Sep 7.
The purpose of this study was to assess the association between IL-6 and CRP with depressive items and cognitive function. We included 112 outpatients with major depression from an exercise trial and 57 healthy controls. IL-6, high sensitive CRP (hsCRP), and cognitive function were assessed in all subjects. After baseline assessment, patients were randomised to either a 3months exercise intervention or an exercise control group. Post-intervention IL-6, hsCRP, depressive symptoms, and cognitive function were reassessed in the patient group. IL-6 and hsCRP were significantly increased in depressed patients compared to healthy controls (p=0.02 and 0.04). These differences were no longer significant after adjustment for lifestyle associated variables. We found no association between immune markers and specific depressive symptoms at baseline or as change over time. Regarding the cognitive tests, IL-6 was positively associated with Serial sevens (p=0.008) and hsCRP was inversely associated with Trail making A (p=0.02) and design fluency (p=0.001) at baseline. At 3months follow-up IL-6 and hsCRP levels did not significantly change from baseline and did not differ between the two patient groups. Depression scores was lower compared to baseline but did not differ between groups. Combining the two groups, a decrease in IL-6 was associated to decreased verbal fluency (p=0.02), and a decrease in hsCRP was associated with improvement in Trail making A (p=0.005). In conclusion, the level of IL-6 and hsCRP was increased in depressed outpatients but was not associated to specific depressive symptoms. In terms of cognitive function, we found that higher hsCRP levels were associated to lower psychomotor speed both at baseline and at follow-up.
本研究旨在评估白细胞介素 6(IL-6)和 C 反应蛋白(CRP)与抑郁症状和认知功能的相关性。我们纳入了 112 名来自运动试验的重度抑郁症门诊患者和 57 名健康对照者。所有受试者均接受了 IL-6、高敏 CRP(hsCRP)和认知功能评估。基线评估后,患者被随机分为 3 个月运动干预组或运动对照组。干预后,患者组再次评估了 IL-6、hsCRP、抑郁症状和认知功能。与健康对照组相比,抑郁患者的 IL-6 和 hsCRP 显著升高(p=0.02 和 0.04)。这些差异在调整与生活方式相关的变量后不再显著。我们没有发现基线时免疫标志物与特定抑郁症状之间或随时间变化的相关性。关于认知测试,IL-6 与连续七项测试呈正相关(p=0.008),hsCRP 与连线测试 A(p=0.02)和设计流畅性(p=0.001)呈负相关。在 3 个月随访时,IL-6 和 hsCRP 水平与基线相比没有显著变化,两组患者之间也没有差异。与基线相比,抑郁评分降低,但两组之间没有差异。将两组患者合并后,IL-6 降低与言语流畅性降低相关(p=0.02),hsCRP 降低与连线测试 A 改善相关(p=0.005)。总之,抑郁门诊患者的 IL-6 和 hsCRP 水平升高,但与特定抑郁症状无关。在认知功能方面,我们发现 hsCRP 水平较高与基线和随访时的心理运动速度降低有关。