Tousoulis Dimitris, Antoniades Charalambos, Drolias Apostolos, Stefanadi Elli, Marinou Kyriakoyla, Vasiliadou Carmen, Tsioufis Costas, Toutouzas Kostas, Latsios George, Stefanadis Christodoulos
1st Cardiology Department, Athens University Medical School, Athens, Greece.
J Card Fail. 2008 Aug;14(6):456-64. doi: 10.1016/j.cardfail.2008.02.015. Epub 2008 May 27.
Major depression (MD) is a key feature in heart failure (HF), and it is unclear whether common antidepressive medications interact with cardiovascular drugs used for the treatment of patients with MD and HF, affecting their efficacy. We examined the impact of MD on long-term survival of patients with end-stage severe HF. We also evaluated the interaction between antidepressive medication and beta-blockers on the clinical outcome of these patients.
The study population consisted of 250 patients with end-stage severe HF. Sixty-one percent of these patients suffered MD and were receiving selective serotonin reuptake inhibitors (SSRIs), serotonin norepinephrine reuptake inhibitors (SNRIs), or tricyclic antidepressants (TCA). All patients were followed prospectively for 18 months. The primary end point was cardiovascular death. At baseline, patients with severe MD had higher serum interleukin 6 (P < .05) and soluble vascular cell adhesion molecule (P < .01). During the follow-up, 167 cardiovascular deaths were reported, and MD was 1 of the major predictors of cardiovascular death (P = .031), whereas treatment with angiotensin receptor inhibitors and statins were also important negative predictors of mortality (P = .036 and P = .039, respectively). Although beta-blockers had a borderline nonsignificant effect on cardiovascular mortality in the overall population, they had a striking beneficial effect among those patients with major depression receiving SSRIs (P = .006), whereas they had a negative effect on mortality in those patients receiving SNRIs/TCAs (P = .025).
MD is an independent predictor of cardiovascular death in patients with end-stage HF. beta-blockers are associated with lower cardiovascular mortality in patients with end-stage HF and depression only when they are combined with SSRIs.
重度抑郁症(MD)是心力衰竭(HF)的一个关键特征,目前尚不清楚常用的抗抑郁药物是否会与用于治疗MD合并HF患者的心血管药物相互作用,从而影响其疗效。我们研究了MD对终末期重度HF患者长期生存的影响。我们还评估了抗抑郁药物与β受体阻滞剂对这些患者临床结局的相互作用。
研究人群包括250例终末期重度HF患者。其中61%的患者患有MD,正在接受选择性5-羟色胺再摄取抑制剂(SSRI)、5-羟色胺去甲肾上腺素再摄取抑制剂(SNRI)或三环类抗抑郁药(TCA)治疗。所有患者均接受了为期18个月的前瞻性随访。主要终点是心血管死亡。基线时,重度MD患者的血清白细胞介素6水平较高(P < .05),可溶性血管细胞黏附分子水平较高(P < .01)。随访期间,共报告了167例心血管死亡病例,MD是心血管死亡的主要预测因素之一(P = .031),而使用血管紧张素受体抑制剂和他汀类药物治疗也是死亡率的重要负性预测因素(分别为P = .036和P = .039)。虽然β受体阻滞剂对总体人群的心血管死亡率影响不显著,但在接受SSRI治疗的重度抑郁症患者中具有显著的有益作用(P = .006),而在接受SNRI/TCA治疗的患者中对死亡率有负面影响(P = .025)。
MD是终末期HF患者心血管死亡的独立预测因素。β受体阻滞剂仅在与SSRI联合使用时,才与终末期HF合并抑郁症患者较低的心血管死亡率相关。