Hiles Sarah A, Baker Amanda L, de Malmanche Theo, McEvoy Mark, Boyle Michael, Attia John
Priority Research Centre for Translational Neuroscience and Mental Health, Faculty of Health, University of Newcastle, New South Wales, Australia.
Priority Research Centre for Translational Neuroscience and Mental Health, Faculty of Health, University of Newcastle, New South Wales, Australia.
J Psychiatr Res. 2015 Apr;63:65-74. doi: 10.1016/j.jpsychires.2015.02.010. Epub 2015 Feb 25.
Depression and inflammatory markers have a reliable cross-sectional association although less is known about the prospective relationship. The current study investigated whether pro-inflammatory markers are prospectively associated with depression, and whether indicators of unhealthy lifestyle, physical health and psychosocial functioning may drive this association. Participants were drawn from the Hunter Community Study, a community-dwelling cohort of individuals aged 55-85 years (N = 1410). Participants completed baseline physiological assessment, health-related questionnaires, and blood sampling for the analysis of inflammatory markers, C-reactive protein (CRP) and interleukin (IL)-6. Participants completed the same depressive symptom questionnaire again after 3.5-5.5 years. Depression outcomes at follow-up were analysed dichotomously using established scale cut-off scores and continuously as a "residual score", representing the variation in follow-up depressive symptoms not explained by baseline symptoms and age. Analyses were conducted on males and females separately. At baseline, indicators of unhealthy lifestyle, physical health and psychosocial functioning were associated with depressive symptoms and inflammatory markers. For males, there were no relationships between inflammatory markers and follow-up depression outcomes. In females, IL-6 was significantly associated with depression outcomes in univariate, but not multivariate analyses. However, IL-6 significantly mediated the association between the predictors of waist-to-hip ratio, smoking and psychological coping at baseline, and follow-up depression outcomes. The results support the inflammatory hypothesis of depression, although females may be more vulnerable to effects. The findings raise the possibility that unhealthy lifestyle and psychosocial stress may drive inflammation and subsequent depressive symptoms.
抑郁症与炎症标志物之间存在可靠的横断面关联,尽管对于前瞻性关系的了解较少。本研究调查了促炎标志物是否与抑郁症存在前瞻性关联,以及不健康生活方式、身体健康和心理社会功能指标是否可能驱动这种关联。参与者来自亨特社区研究,这是一个由55 - 85岁个体组成的社区居住队列(N = 1410)。参与者完成了基线生理评估、健康相关问卷,并进行了血液采样以分析炎症标志物、C反应蛋白(CRP)和白细胞介素(IL)-6。3.5 - 5.5年后,参与者再次完成相同的抑郁症状问卷。随访时的抑郁结果采用既定量表的截断分数进行二分法分析,并作为“残余分数”进行连续分析,该分数代表随访时抑郁症状中无法由基线症状和年龄解释的变异。分别对男性和女性进行了分析。在基线时,不健康生活方式、身体健康和心理社会功能指标与抑郁症状和炎症标志物相关。对于男性,炎症标志物与随访时的抑郁结果之间没有关系。在女性中,IL - 6在单变量分析中与抑郁结果显著相关,但在多变量分析中并非如此。然而,IL - 6显著介导了基线时腰臀比、吸烟和心理应对等预测因素与随访时抑郁结果之间的关联。结果支持抑郁症的炎症假说,尽管女性可能更容易受到影响。研究结果提出了一种可能性,即不健康的生活方式和心理社会压力可能会引发炎症及随后的抑郁症状。