Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.
Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.
Brain Behav Immun. 2014 Oct;41:109-15. doi: 10.1016/j.bbi.2014.05.004. Epub 2014 May 13.
Growing evidence suggests immune and metabolic dysregulation among depressed persons, possibly restricted to specific subgroups. This study explores the association between depressive disorders and characteristics with immunometabolic functioning among older persons. Data are from the baseline assessment of the Netherlands Study of Depression in Older Persons, including 131 non-depressed and 358 depressed (6-month DSM-IV major depressive disorder) persons (60-93 years). Immune (C-reactive protein, interleukin [IL]-6) and metabolic (waist circumference, triglycerides, high-density lipoprotein cholesterol, blood pressure, fasting glucose) factors were measured. Depression characteristics included severity, age of onset, symptom profile (atypical/melancholic) and antidepressant use. Depressed persons showed lower IL-6 levels compared with non-depressed persons. Depressed persons, except those with atypical depression, had lower waist circumference, lower glucose levels and scored lower on an overall index including all immunometabolic factors. Low waist circumference was more pronounced among those with less severe depression and those with a later age of onset, whom also had lower blood pressure levels. Atypical depression was associated with higher triglyceride levels. Antidepressant use was not clearly associated with immunometabolic functioning. To conclude, contrary to our expectations, we found overall immunometabolic downregulation in older depressed persons, in particular among those with less severe symptoms and those with late-life onset. However, persons with atypical depression presented with metabolic upregulation compared with other depressed persons. Taking depression symptom profiles into account is important when examining biological dysregulation in late-life depression.
越来越多的证据表明抑郁患者存在免疫和代谢紊乱,这种紊乱可能局限于特定的亚组。本研究旨在探讨老年人群中抑郁障碍与免疫代谢功能特征之间的关系。研究数据来自荷兰老年人抑郁研究的基线评估,共纳入 131 名非抑郁者和 358 名抑郁者(6 个月 DSM-IV 重度抑郁障碍)(60-93 岁)。检测了免疫(C 反应蛋白、白细胞介素 [IL]-6)和代谢(腰围、甘油三酯、高密度脂蛋白胆固醇、血压、空腹血糖)因素。抑郁特征包括严重程度、发病年龄、症状谱(非典型/忧郁型)和抗抑郁药物的使用情况。与非抑郁者相比,抑郁者的 IL-6 水平较低。除了非典型抑郁者之外,抑郁者的腰围较小,血糖水平较低,所有免疫代谢因素综合指数得分也较低。在轻度抑郁和发病年龄较晚的患者中,腰围较小的情况更为明显,他们的血压水平也较低。非典型抑郁与甘油三酯水平升高有关。抗抑郁药物的使用与免疫代谢功能之间没有明显的关联。总之,与我们的预期相反,我们发现老年抑郁患者的整体免疫代谢功能下降,尤其是在症状较轻和发病较晚的患者中。然而,与其他抑郁患者相比,非典型抑郁患者表现出代谢功能的上调。在检查老年抑郁患者的生物学紊乱时,考虑抑郁症状谱非常重要。