Camacho Álvaro, Larsen Britta, McClelland Robyn L, Morgan Cindy, Criqui Michael H, Cushman Mary, Allison Matthew A
Department of Family & Preventive Medicine, University of California, San Diego, USA.
Department of Family & Preventive Medicine, University of California, San Diego, USA.
J Affect Disord. 2014 Aug;164:165-70. doi: 10.1016/j.jad.2014.04.018. Epub 2014 Apr 19.
Depressive symptoms are associated with inflammation yet the association between inflammation and different levels of depression remains unclear. Therefore, we studied the association of subsyndromal and depressive symptoms with inflammatory markers in a large multi-ethnic cohort.
C-reactive protein (CRP) (n=6269), interleukin-6 (IL-6) (n=6135) and tumor necrosis factor-alpha (TNF-α) (n=1830) were measured in selected participants from the multi-ethnic study of atherosclerosis (MESA). Subsyndromal depressive symptoms were defined as a CES-D value from 8 to 15, depressive symptoms as a CES-D≥16 and normal as a CES-D≤7. Depressive states (subsyndromal and depressed) were entered into multivariable linear regression models incrementally adjusting for demographic, behavioral, biologic and comorbidities.
Among 6289 participants not taking antidepressants and free from CVD, the mean age was 62.2, while 52% were women, 36.4% were Caucasian, 28.9% African-American, 22.3% Hispanics and 12.4% Chinese-American. Of the total, 24.2% had subsyndromal depression and 11.8% had depressive symptoms. Compared to the non-depressed group and after controlling for demographics, there was no association between both subsyndromal and depressive symptoms with logCRP (β=-0.01, p=0.80 and β=-0.05, p=0.25 respectively), logIL-6 (β=0.01, p=0.71 and β=-0.04, p=0.07 respectively) and logTNF-α (β=-0.03, p=0.29 and β=0.06, p=0.18 respectively). Moreover, fully adjusted models showed no significant associations for logIL-6 and logTNF-α and the different depressive categories. However, with full adjustment, we found a significant inverse association between depressive symptoms and lnCRP (β=-0.10, p=0.01) that was not present for subsyndromal depression (β=-0.05, p=0.11).
Among participants not taking anti-depressants, subsyndromal depression is not associated with inflammation. However, depressive symptoms measured by CES-D≥16 are associated with a lower inflammation (CRP).
抑郁症状与炎症相关,但炎症与不同程度抑郁之间的关联尚不清楚。因此,我们在一个大型多民族队列中研究了亚综合征性抑郁症状和抑郁症状与炎症标志物之间的关联。
在动脉粥样硬化多民族研究(MESA)的部分参与者中测量了C反应蛋白(CRP)(n = 6269)、白细胞介素-6(IL-6)(n = 6135)和肿瘤坏死因子-α(TNF-α)(n = 1830)。亚综合征性抑郁症状定义为CES-D值为8至15,抑郁症状定义为CES-D≥16,正常定义为CES-D≤7。将抑郁状态(亚综合征性和抑郁)逐步纳入多变量线性回归模型,对人口统计学、行为、生物学和合并症进行调整。
在6289名未服用抗抑郁药且无心血管疾病的参与者中,平均年龄为62.2岁,其中52%为女性,36.4%为白人,28.9%为非裔美国人,22.3%为西班牙裔,12.4%为华裔美国人。总体中,24.2%有亚综合征性抑郁,11.8%有抑郁症状。与非抑郁组相比,在控制人口统计学因素后,亚综合征性抑郁症状和抑郁症状与logCRP(β = -0.01,p = 0.80和β = -0.05,p = 0.25)、logIL-6(β = 0.01,p = 0.71和β = -0.04,p = 0.07)以及logTNF-α(β = -0.03,p = 0.29和β = 0.06,p = 0.18)之间均无关联。此外,完全调整后的模型显示logIL-6和logTNF-α与不同抑郁类别之间无显著关联。然而,在完全调整后,我们发现抑郁症状与lnCRP之间存在显著的负相关(β = -0.10,p = 0.01),而亚综合征性抑郁则不存在这种关联(β = -0.05,p = 0.11)。
在未服用抗抑郁药的参与者中,亚综合征性抑郁与炎症无关。然而,通过CES-D≥16测量的抑郁症状与较低水平的炎症(CRP)相关。