Arbelaez Jose J, Ariyo Abraham A, Crum Rosa M, Fried Linda P, Ford Daniel E
Department of Epidemiology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland, USA.
J Am Geriatr Soc. 2007 Nov;55(11):1825-30. doi: 10.1111/j.1532-5415.2007.01393.x. Epub 2007 Oct 3.
To investigate the mediator role of inflammation in any relationship between depressive symptoms and ischemic stroke.
Longitudinal prospective study.
Review of medical records, death certificates, and the Medicare healthcare utilization database for hospitalizations.
Total of 5,525 elderly men and women aged 65 and older who were prospectively followed from 1989 to 2000 as participants in the Cardiovascular Health Study.
Depression symptom scores, inflammatory markers.
Greater depressive symptoms were associated with risk of ischemic stroke (unadjusted hazard ratio (HR)=1.32, 95% confidence interval (CI)=1.09-1.59; HR=1.26, 95% CI=1.03-1.54, adjusted for traditional risk factors). When a term for inflammation (C-reactive protein (CRP)) was introduced in the model, the HRs were not appreciably altered (unadjusted HR=1.31, 95% CI=1.08-1.58; adjusted HR=1.25, 95% CI=1.02-1.53), indicating that CRP at baseline was not a mediator in this relationship. In analyses stratified according to CRP levels, a J-shaped relationship between depressive symptoms and stroke was evident in the unadjusted analyses; in the fully adjusted model, only CRP in the highest tertile was associated with a higher risk for stroke in the presence of higher depressive symptoms scores.
The analyses from this prospective study provide evidence of a positive association between depressive symptoms and risk of incident stroke. Inflammation, as measured according to CRP at baseline, did not appear to mediate the relationship between depressive symptoms and stroke.
探讨炎症在抑郁症状与缺血性卒中之间的关系中所起的中介作用。
纵向前瞻性研究。
回顾医疗记录、死亡证明以及医疗保险住院医疗利用数据库。
共有5525名65岁及以上的老年男性和女性,他们作为心血管健康研究的参与者,于1989年至2000年接受前瞻性随访。
抑郁症状评分、炎症标志物。
抑郁症状越严重,缺血性卒中风险越高(未调整的风险比(HR)=1.32,95%置信区间(CI)=1.09 - 1.59;调整传统危险因素后,HR = 1.26,95% CI = 1.03 - 1.54)。当在模型中引入炎症指标(C反应蛋白(CRP))时,HR没有明显变化(未调整的HR = 1.31,95% CI = 1.08 - 1.58;调整后的HR = 1.25,95% CI = 1.02 - 1.53),这表明基线时的CRP并非这种关系中的中介因素。在根据CRP水平分层的分析中,未调整的分析显示抑郁症状与卒中之间呈J形关系;在完全调整模型中,仅最高三分位数的CRP与存在较高抑郁症状评分时的卒中风险升高相关。
这项前瞻性研究的分析提供了抑郁症状与新发卒中风险之间存在正相关的证据。根据基线CRP测量的炎症似乎并未介导抑郁症状与卒中之间的关系。