Yetman Anji T, Bornemeier Renee A, McCrindle Brian W
Division of Cardiology, Department of Pediatrics, The Children's Hospital, University of Colorado Health Sciences Center, Denver, Colorado 80220, USA.
Am J Cardiol. 2005 May 1;95(9):1125-7. doi: 10.1016/j.amjcard.2005.01.032.
Despite variable clinical results, beta blockers have become the primary therapy for prevention of aortic dilation in patients with the Marfan syndrome. This study examines the use of the angiotensin-converting enzyme inhibitor enalapril for treatment of these patients. We sought to examine the effects of enalapril versus beta-blocker therapy in patients with the Marfan syndrome and noted improved aortic distensibility (3.0 +/- 0.3 vs 1.9 +/- 0.4 cm2 dynes(-1); p <0.02) and a reduced aortic stiffness index (8.0 +/- 2.9 vs 18.4 +/- 3.8; p <0.05) in patients receiving enalapril compared with those receiving beta blockers. These favorable hemodynamic changes were associated with a smaller increase in aortic root diameter (0.1 +/- 1.0 vs 5.8 +/- 5.2 mm) and fewer clinical end points during follow-up.
尽管临床结果存在差异,但β受体阻滞剂已成为马方综合征患者预防主动脉扩张的主要治疗方法。本研究探讨了血管紧张素转换酶抑制剂依那普利在这些患者治疗中的应用。我们试图研究依那普利与β受体阻滞剂治疗对马方综合征患者的影响,结果发现,与接受β受体阻滞剂治疗的患者相比,接受依那普利治疗的患者主动脉扩张性有所改善(3.0±0.3对1.9±0.4 cm2达因-1;p<0.02),主动脉僵硬度指数降低(8.0±2.9对18.4±3.8;p<0.05)。这些有利的血流动力学变化与主动脉根部直径较小的增加幅度(0.1±1.0对5.8±5.2 mm)以及随访期间较少的临床终点相关。