Forette Françoise, Seux Marie-Laure, Staessen Jan A, Thijs Lutgarde, Babarskiene Marija-Ruta, Babeanu Speranta, Bossini Alfredo, Fagard Robert, Gil-Extremera Blas, Laks Tovio, Kobalava Zhanna, Sarti Cinzia, Tuomilehto Jaakko, Vanhanen Hannu, Webster John, Yodfat Yair, Birkenhäger Willem H
Department of Geriatrics, Hôpital Broca, CHU Cochin, University of Paris V, 54-56 rue Pascal, 75013 Paris, France.
Arch Intern Med. 2002 Oct 14;162(18):2046-52. doi: 10.1001/archinte.162.18.2046.
After the double-blind, placebo-controlled Systolic Hypertension in Europe (Syst-Eur) trial ended in February 1997, randomized patients were offered active study medication for a further period of observation.
To refine the estimates of the long-term effects of antihypertensive therapy on the incidence of dementia.
Eligible patients had no dementia and were at least 60 years old. Their systolic blood pressure at entry was 160 to 219 mm Hg, with diastolic blood pressure below 95 mm Hg. Antihypertensive therapy was started immediately after randomization in the active treatment group, but only after termination of the double-blind trial in the control patients. Treatment consisted of nitrendipine (10-40 mg/d), with the possible addition of enalapril maleate (5-20 mg/d), hydrochlorothiazide (12.5-25 mg/d), or both add-on drugs.
Median follow-up increased from 2.0 years in the double-blind trial to 3.9 years overall. The incidence of dementia doubled from 32 to 64 cases, 41 of whom had Alzheimer disease. Throughout follow-up, systolic/diastolic blood pressure was 7.0/3.2 mm Hg higher in the 1417 control patients than in the 1485 subjects randomized to active treatment. At the last examination, the blood pressure difference was still 4.2/2.9 mm Hg; 48.1%, 26.4%, and 11.4% of the control patients were taking nitrendipine, enalapril, and/or hydrochlorothiazide, whereas in the active treatment group these proportions were 70.2%, 35.4%, and 18.4%, respectively. Compared with the controls, long-term antihypertensive therapy reduced the risk of dementia by 55%, from 7.4 to 3.3 cases per 1000 patient-years (43 vs 21 cases, P<.001). After adjustment for sex, age, education, and entry blood pressure, the relative hazard rate associated with the use of nitrendipine was 0.38 (95% confidence interval, 0.23-0.64; P<.001). Treatment of 1000 patients for 5 years can prevent 20 cases of dementia (95% confidence interval, 7-33).
The extended follow-up of Syst-Eur patients reinforces the evidence that blood pressure-lowering therapy initiated with a long-acting dihydropyridine protects against dementia in older patients with systolic hypertension.
1997年2月欧洲收缩期高血压(Syst-Eur)双盲、安慰剂对照试验结束后,为随机分组的患者提供了活性研究药物,以进行进一步观察。
完善抗高血压治疗对痴呆发病率长期影响的评估。
符合条件的患者无痴呆且年龄至少60岁。入组时收缩压为160至219毫米汞柱,舒张压低于95毫米汞柱。活性治疗组在随机分组后立即开始抗高血压治疗,而对照组患者仅在双盲试验结束后开始治疗。治疗药物为尼群地平(10 - 40毫克/天),可能加用马来酸依那普利(5 - 20毫克/天)、氢氯噻嗪(12.5 - 25毫克/天)或两种加用药物。
中位随访时间从双盲试验中的2.0年增加到总体的3.9年。痴呆发病率从32例翻倍至64例,其中41例为阿尔茨海默病。在整个随访期间,1417名对照患者的收缩压/舒张压比随机接受活性治疗的1485名受试者高7.0/3.2毫米汞柱。在最后一次检查时,血压差值仍为4.2/2.9毫米汞柱;48.1%、26.4%和11.4%的对照患者正在服用尼群地平、依那普利和/或氢氯噻嗪, 而在活性治疗组中这些比例分别为70.2%、35.4%和18.4%。与对照组相比,长期抗高血压治疗使痴呆风险降低了55%,从每1000患者年7.4例降至3.3例(43例对21例,P<0.001)。对性别、年龄、教育程度和入组时血压进行调整后,使用尼群地平的相对风险率为0.38(95%置信区间,0.23 - 0.64;P<0.001)。对1,000名患者进行5年治疗可预防20例痴呆(95%置信区间,7 - 33)。
Syst-Eur患者的延长随访强化了以下证据:长效二氢吡啶类药物起始的降压治疗可预防老年收缩期高血压患者发生痴呆。