Blumenthal James A, Feger Bryan J, Smith Patrick J, Watkins Lana L, Jiang Wei, Davidson Jonathan, Hoffman Benson M, Ashworth Megan, Mabe Stephanie K, Babyak Michael A, Kraus William E, Hinderliter Alan, Sherwood Andrew
Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC.
Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC.
Am Heart J. 2016 Jun;176:53-62. doi: 10.1016/j.ahj.2016.03.003. Epub 2016 Mar 12.
Anxiety is highly prevalent among patients with coronary heart disease (CHD), and there is growing evidence that high levels of anxiety are associated with worse prognosis. However, few studies have evaluated the efficacy of treating anxiety in CHD patients for reducing symptoms and improving clinical outcomes. Exercise and selective serotonin reuptake inhibitors have been shown to be effective in treating patients with depression, but have not been studied in cardiac patients with high anxiety.
The UNWIND trial is a randomized clinical trial of patients with CHD who are at increased risk for adverse events because of comorbid anxiety. One hundred fifty participants with CHD and elevated anxiety symptoms and/or with a diagnosed anxiety disorder will be randomly assigned to 12 weeks of aerobic exercise (3×/wk, 35 min, 70%-85% VO2peak), escitalopram (5-20 mg qd), or placebo. Before and after 12 weeks of treatment, participants will undergo assessments of anxiety symptoms and CHD biomarkers of risk, including measures of inflammation, lipids, hemoglobin A1c, heart rate variability, and vascular endothelial function. Primary outcomes include post-intervention effects on symptoms of anxiety and CHD biomarkers. Secondary outcomes include clinical outcomes (cardiovascular hospitalizations and all-cause death) and measures of quality of life.
The UNWIND trial (ClinicalTrials.gov NCT02516332) will evaluate the efficacy of aerobic exercise and escitalopram for improving anxiety symptoms and reducing risk for adverse clinical events in anxious CHD patients.
焦虑在冠心病(CHD)患者中极为普遍,且越来越多的证据表明,高度焦虑与更差的预后相关。然而,很少有研究评估治疗冠心病患者焦虑症对减轻症状和改善临床结局的疗效。运动和选择性5-羟色胺再摄取抑制剂已被证明对治疗抑郁症患者有效,但尚未在焦虑程度高的心脏病患者中进行研究。
“放松”试验是一项针对因合并焦虑症而发生不良事件风险增加的冠心病患者的随机临床试验。150名有冠心病且焦虑症状加重和/或被诊断患有焦虑症的参与者将被随机分配至进行12周的有氧运动(每周3次,每次35分钟,70%-85%最大摄氧量)、艾司西酞普兰(每日5-20毫克)或安慰剂治疗组。在治疗12周前后,参与者将接受焦虑症状评估以及冠心病风险生物标志物评估,包括炎症、血脂、糖化血红蛋白、心率变异性和血管内皮功能测量。主要结局包括干预后对焦虑症状和冠心病生物标志物的影响。次要结局包括临床结局(心血管住院和全因死亡)以及生活质量测量。
“放松”试验(ClinicalTrials.gov NCT02516332)将评估有氧运动和艾司西酞普兰对改善焦虑症冠心病患者焦虑症状和降低不良临床事件风险的疗效。