Curb J D, Pressel S L, Cutler J A, Savage P J, Applegate W B, Black H, Camel G, Davis B R, Frost P H, Gonzalez N, Guthrie G, Oberman A, Rutan G H, Stamler J
John A. Burns School of Medicine, Honolulu, Hawaii, USA.
JAMA. 1996 Dec 18;276(23):1886-92.
To assess the effect of low-dose, diuretic-based antihypertensive treatment on major cardiovascular disease (CVD) event rates in older, non-insulin-treated diabetic patients with isolated systolic hypertension (ISH), compared with nondiabetic patients.
Double-blind, randomized, placebo-controlled trial: the Systolic Hypertension in the Elderly Program (SHEP).
Multiple clinical and support centers in the United States.
A total of 4736 men and women aged 60 years and older at baseline with ISH (systolic blood pressure [BP], > or = 160 mm Hg; diastolic BP, <90 mm Hg) at baseline, 583 non-insulin-dependent diabetic patients and 4149 nondiabetic patients (4 additional patients not so classifiable were randomized but not included in these analyses). Diabetes mellitus defined as physician diagnosis, taking oral hypoglycemic drugs, fasting glucose level of 7.8 mmol/L or more (> or = 140 mg/dL), or any combination of these characteristics.
The active treatment group received a low dose of chlorthalidone (12.5-25.0 mg/d) with a step-up to atenolol (25.0-50.0 mg/d) or reserpine (0.05-0.10 mg/d) if needed. The placebo group received placebo and any active antihypertensive drugs prescribed by patient's private physician for persistently high BP.
The 5-year rates of major CVD events, nonfatal plus fatal stroke, nonfatal myocardial infarction (MI) and fatal coronary heart disease (CHD), major CHD events, and all-cause mortality.
The SHEP antihypertensive drug regimen lowered BP of both diabetic and nondiabetic patients, with few adverse effects. For both diabetic and nondiabetic patients, all outcome rates were lower for participants randomized to the active treatment group than for those randomized to the placebo group. Thus, 5-year major CVD rate was lower by 34% for active treatment compared with placebo, both for diabetic patients (95% confidence interval [CI], 6%-54%) and nondiabetic patients (95% CI, 21%-45%). Absolute risk reduction with active treatment compared with placebo was twice as great for diabetic vs nondiabetic patients (101/1000 vs 51/1000 randomized participants at the 5-year follow-up), reflecting the higher risk of diabetic patients.
Low-dose diuretic-based (chlorthalidone) treatment is effective in preventing major CVD events, cerebral and cardiac, in both non-insulin-treated diabetic and nondiabetic older patients with ISH.
评估低剂量、基于利尿剂的降压治疗对老年非胰岛素治疗的单纯收缩期高血压(ISH)糖尿病患者主要心血管疾病(CVD)事件发生率的影响,并与非糖尿病患者进行比较。
双盲、随机、安慰剂对照试验:老年收缩期高血压计划(SHEP)。
美国多个临床和支持中心。
共有4736名60岁及以上的男性和女性,基线时患有ISH(收缩压[BP]≥160mmHg;舒张压BP<90mmHg),其中583名非胰岛素依赖型糖尿病患者和4149名非糖尿病患者(另外4名无法分类的患者被随机分组但未纳入这些分析)。糖尿病定义为医生诊断、服用口服降糖药、空腹血糖水平≥7.8mmol/L(≥140mg/dL)或这些特征的任意组合。
活性治疗组接受低剂量氢氯噻酮(12.5 - 25.0mg/d),必要时加用阿替洛尔(25.0 - 50.0mg/d)或利血平(0.05 - 0.10mg/d)。安慰剂组接受安慰剂以及患者私人医生为持续性高血压开具的任何活性降压药物。
主要CVD事件、非致命性加致命性卒中、非致命性心肌梗死(MI)和致命性冠心病(CHD)的5年发生率、主要CHD事件以及全因死亡率。
SHEP降压药物方案降低了糖尿病和非糖尿病患者的血压,且不良反应较少。对于糖尿病和非糖尿病患者,随机分配到活性治疗组的参与者的所有结局发生率均低于随机分配到安慰剂组的参与者。因此,活性治疗组的5年主要CVD发生率比安慰剂组低34%,糖尿病患者(95%置信区间[CI],6% - 54%)和非糖尿病患者(95%CI,21% - 45%)均如此。与安慰剂相比,活性治疗的绝对风险降低在糖尿病患者中是非糖尿病患者的两倍(5年随访时,随机参与者分别为101/1000和51/1000),这反映了糖尿病患者的较高风险。
基于低剂量利尿剂(氢氯噻酮)的治疗对预防非胰岛素治疗的糖尿病和非糖尿病老年ISH患者的主要CVD事件(包括脑和心脏事件)有效。