Autonomic Nervous System Dysfunction and Inflammation Contribute to the Increased Cardiovascular Mortality Risk Associated With Depression

被引:145
作者
Kop, Willem J. [1 ]
Stein, Phyllis K. [2 ]
Tracy, Russell P. [3 ]
Barzilay, Joshua I. [4 ]
Schulz, Richard [5 ]
Gottdiener, John S.
机构
[1] Univ Maryland, Med Ctr, Div Cardiol, Dept Med, Baltimore, MD 21201 USA
[2] Washington Univ, Sch Med, Div Cardiovasc, St Louis, MO 63110 USA
[3] Univ Vermont Coll, Dept Pathol & Biochem, Burlington, VT USA
[4] Emory Univ, Sch Med, Dept Endocrinol, Atlanta, GA USA
[5] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
来源
PSYCHOSOMATIC MEDICINE | 2010年 / 72卷 / 07期
关键词
depression; autonomic nervous system; inflammation; risk factors; cardiovascular disease; mortality; HEART-RATE-VARIABILITY; C-REACTIVE PROTEIN; MYOCARDIAL-INFARCTION; RATE TURBULENCE; OLDER-ADULTS; ANTIDEPRESSANT TREATMENT; MAJOR DEPRESSION; DISEASE; SYMPTOMS; MARKERS;
D O I
10.1097/PSY.0b013e3181eadd2b
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To investigate prospectively whether autonomic nervous system (ANS) dysfunction and inflammation play a role in the increased cardiovascular disease (CVD)-related mortality risk associated with depression. Methods: Participants in the Cardiovascular Health Study (n = 907; mean age, 71.3 +/- 4.6 years; 59.1% women) were evaluated for ANS indices derived from heart rate variability (HRV) analysis (frequency and time domain HRV, and nonlinear indices, including detrended fluctuation analysis (DFA(1)) and heart rate turbulence). Inflammation markers included C-reactive protein, interleukin-6, fibrinogen, and white blood cell count). Depressive symptoms were assessed, using the 10-item Centers for Epidemiological Studies Depression scale. Cox proportional hazards models were used to investigate the mortality risk associated with depression, ANS, and inflammation markers, adjusting for demographic and clinical covariates. Results: Depression was associated with ANS dysfunction (DFA(1), p = .018), and increased inflammation markers (white blood cell count, p = .012, fibrinogen p = .043) adjusting for covariates. CVD-related mortality occurred in 121 participants during a median follow-up of 13.3 years. Depression was associated with an increased CVD mortality risk (hazard ratio, 1.88; 95% confidence interval, 1.23-2.86). Multivariable analyses showed that depression was an independent predictor of CVD mortality (hazard ratio, 1.72; 95% confidence interval, 1.05-2.83) when adjusting for independent HRV and inflammation predictors (DFA(1), heart rate turbulence, interleukin-6), attenuating the depression-CVD mortality association by 12.7% (p < .001). Conclusion: Autonomic dysfunction and inflammation contribute to the increased cardiovascular mortality risk associated with depression, but a large portion of the predictive value of depression remains unexplained by these neuroimmunological measures.
引用
收藏
页码:626 / 635
页数:10
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