Sandor George G S, Alghamdi Mohammed H, Raffin Leslie A, Potts Mary T, Williams Lindsey D, Potts James E, Kiess Marla, van Breemen Casey
Children's Heart Centre, British Columbia Children's Hospital, The University of British Columbia, Vancouver, Canada.
Children's Heart Centre, British Columbia Children's Hospital, The University of British Columbia, Vancouver, Canada.
Int J Cardiol. 2015 Jan 20;179:470-5. doi: 10.1016/j.ijcard.2014.11.082. Epub 2014 Nov 8.
Patients with Marfan (MFS) and Loeys-Dietz (LDS) syndromes have been shown to have abnormal aortic biophysical properties. The purpose of this study was to compare the effects of 12-months of therapy with atenolol or losartan on vascular function in young patients with MFS and LDS.
Seventeen patients with MFS or LDS were recruited and randomized to treatment with atenolol, 25-50mg, or losartan, 25mg daily. Prior to treatment and following therapy, echocardiography for left ventricular size, function and aortic root size was performed. Pulse wave velocity (PWV), input (Zi, ZiF) and characteristic (Zc, ZcF) impedances, arterial stiffness (Ep and β-index), total arterial compliance (TAC), mean (Wm) and total (Wt) hydraulic power, efficiency, power cost per unit of forward flow (Wt/CI) and brachial artery flow-mediated dilation (FMD) were measured.
The atenolol group consisted of 9 females (17.6years) and the losartan group 7 males and 1 female (17.0years). Their height, weight, BSA, BMI, systolic and diastolic blood pressures were similar. Baseline to 12-month changes for atenolol and losartan were PWV (20% vs -14%), Zi (-2% vs -27%), Zc (-20% vs -27%), Ep (1%, vs -13%), β-index (10% vs 14%), FMD (11% vs 20%), TAC (3% vs 42%), Wm (-24% vs 15%), Wt (-24% vs 17%), and Wt/CI (3% vs 21%). There was a trend for losartan to decrease PWV and stiffness indexes while atenolol decreased power and power/unit flow.
This pilot study suggests that atenolol and losartan may have different mechanisms of action on vascular function. A larger clinical trial is needed to confirm these effects.Clinical trials registration NCT00593710 (ClinicalTrials.gov).
已证实患有马凡综合征(MFS)和洛伊迪茨综合征(LDS)的患者具有异常的主动脉生物物理特性。本研究的目的是比较阿替洛尔或氯沙坦治疗12个月对年轻MFS和LDS患者血管功能的影响。
招募了17例MFS或LDS患者,并随机分为阿替洛尔(25 - 50mg)或氯沙坦(25mg)每日治疗组。在治疗前和治疗后,进行超声心动图检查以评估左心室大小、功能和主动脉根部大小。测量脉搏波速度(PWV)、输入(Zi、ZiF)和特征(Zc、ZcF)阻抗、动脉僵硬度(Ep和β指数)、总动脉顺应性(TAC)、平均(Wm)和总(Wt)水力功率、效率、单位向前血流的功率成本(Wt/CI)以及肱动脉血流介导的扩张(FMD)。
阿替洛尔组包括9名女性(17.6岁),氯沙坦组包括7名男性和1名女性(17.0岁)。他们的身高、体重、体表面积、体重指数、收缩压和舒张压相似。阿替洛尔和氯沙坦从基线到12个月的变化分别为:PWV(20%对 - 14%)、Zi(-2%对 - 27%)、Zc(-20%对 - 27%)、Ep(1%对 - 13%)、β指数(10%对14%)、FMD(11%对20%)、TAC(3%对42%)、Wm(-24%对15%)、Wt(-24%对17%)以及Wt/CI(3%对21%)。氯沙坦有降低PWV和僵硬度指数的趋势,而阿替洛尔降低功率和单位血流功率。
这项初步研究表明,阿替洛尔和氯沙坦对血管功能可能有不同的作用机制。需要进行更大规模的临床试验来证实这些效果。临床试验注册号:NCT00593710(ClinicalTrials.gov)。