Savoia Carmine, Touyz Rhian M, Endemann Dierk H, Pu Qian, Ko Eun A, De Ciuceis Carolina, Schiffrin Ernesto L
Multidisciplinary Research Group on Hypertension, Clinical Research Institute of Montreal, University of Montreal, Montreal, Quebec, Canada.
Hypertension. 2006 Aug;48(2):271-7. doi: 10.1161/01.HYP.0000230234.84356.36. Epub 2006 Jun 19.
Lowering elevated blood pressure (BP) in diabetic hypertensive individuals decreases cardiovascular events. We questioned whether remodeling of resistance arteries from hypertensive diabetic patients would improve after 1 year of tight BP control with addition of either the angiotensin receptor blocker (ARB) valsartan or the beta-blocker (BB) atenolol to previous therapy, which included angiotensin-converting enzyme inhibitors (ACEIs) and/or calcium channel blockers. Twenty-eight hypertensive type 2 diabetic patients treated with oral hypoglycemic and antihypertensive agents (not receiving ARBs or BBs) were randomly assigned to double-blind treatment for 1 year with valsartan (80 to 160 mg) or atenolol (50 to 100 mg) daily, added to previous therapy. Resistance arteries dissected from gluteal subcutaneous tissues were assessed on a pressurized myograph. After 1 year of treatment, systolic and diastolic BP and glycemia were equally well controlled in the valsartan and atenolol groups. Endothelium-dependent and independent relaxation did not change in the treated groups. After 1 year of treatment, resistance artery media:lumen ratio decreased in the valsartan group (7.9+/-0.5% after versus 9.8+/-0.6% before; P < 0.05) but not in the atenolol-treated group (9.9+/-0.9% versus 10.6+/-1%; P value not significant). Artery walls from atenolol-treated patients became stiffer, with no change in the valsartan-treated patients. In conclusion, similar intensive BP control for 1 year with valsartan was associated with improved structure of resistance arteries in diabetic hypertensive patients, whereas vessels from atenolol-treated patients exhibited unchanged remodeling and a stiffer wall. The addition of ARBs but not BBs to antihypertensive medications that may include angiotensin-converting enzyme inhibitors and/or calcium channel blockers results in an improvement in resistance artery remodeling in diabetic hypertensive patients.
降低糖尿病高血压患者的血压可减少心血管事件。我们探讨了在先前使用血管紧张素转换酶抑制剂(ACEIs)和/或钙通道阻滞剂的治疗基础上,添加血管紧张素受体阻滞剂(ARB)缬沙坦或β受体阻滞剂(BB)阿替洛尔进行1年严格血压控制后,高血压糖尿病患者的阻力动脉重塑是否会得到改善。28例接受口服降糖药和抗高血压药物治疗(未接受ARB或BB)的2型高血压糖尿病患者被随机分配接受为期1年的双盲治疗,每天添加缬沙坦(80至160毫克)或阿替洛尔(50至100毫克)到先前的治疗中。从臀皮下组织分离的阻力动脉在压力肌动描记器上进行评估。治疗1年后,缬沙坦组和阿替洛尔组的收缩压、舒张压和血糖得到同等程度的良好控制。治疗组的内皮依赖性和非依赖性舒张功能没有改变。治疗1年后,缬沙坦组的阻力动脉中膜与管腔比值下降(治疗后为7.9±0.5%,治疗前为9.8±0.6%;P<0.05),而阿替洛尔治疗组未下降(9.9±0.9%对10.6±1%;P值无统计学意义)。阿替洛尔治疗患者的动脉壁变得更硬,而缬沙坦治疗患者的动脉壁没有变化。总之,缬沙坦进行1年类似的强化血压控制与糖尿病高血压患者阻力动脉结构改善相关,而阿替洛尔治疗患者的血管重塑未改变且动脉壁更硬。在可能包括血管紧张素转换酶抑制剂和/或钙通道阻滞剂的抗高血压药物中添加ARB而非BB可改善糖尿病高血压患者的阻力动脉重塑。