抗高血压治疗和预防中风和痴呆

Ji-Guang Wang , Jan A. Staessen , Willem H. Birkenhäger
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引用次数: 17

摘要

高血压是中风最一致和最有力的预测因子,与近70%的中风有关。安慰剂对照试验证明,降压治疗可使以舒张期高血压为主的中年或老年高血压患者卒中发生率降低40%,使孤立性收缩期高血压的老年患者卒中发生率降低30%。最近的试验比较了新药物(钙通道阻滞剂、α-阻滞剂、血管紧张素转换酶抑制剂或血管紧张素1型受体阻滞剂)与旧药物(利尿剂或β-阻滞剂)。钙通道阻滞剂,包括维拉帕米(- 8%,P =0.07)或不包括维拉帕米(- 10%,P =0.02),以及血管紧张素1型受体阻滞剂(- 24%,P =0.0002)比旧药物预防中风的效果更好,而血管紧张素转换酶抑制剂的趋势相反(+10%,P =0.03)。对有脑血管病史的患者进行的6项试验的综述表明,抗高血压药物治疗可使卒中复发率降低25% (P =0.004)。荟萃回归分析显示,在大多数试验中,收缩压的试验内差异是预防中风的原因。在5项试验中,痴呆是次要结果。总体而言,降压治疗并没有降低血管性痴呆或退行性痴呆的发生率(- 11%,P =0.15)。然而,当分析仅限于以二氢吡啶或利尿剂为主要治疗手段的3项试验时,这种获益增加到25% (P =0.01)。随机临床试验应该尽快解决降血压治疗在多大程度上可以预防退行性痴呆的问题。
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Antihypertensive treatment and prevention of stroke and dementia

Hypertension is the most consistent and powerful predictor of stroke and is involved in nearly 70% of strokes. Placebo-controlled trials have proven that blood-pressure-lowering treatment reduces the incidence of stroke by 40% in middle-aged or older hypertensive patients with predominantly diastolic hypertension and by 30% in older patients with isolated systolic hypertension. Recent trials have compared new agents (calcium-channel blockers, α-blockers, angiotensin converting enzyme inhibitors or angiotensin type-1 receptor blockers) with old durg classes (diuretics or β-blockers). Calcium-channel blockers, including (−8%, P=0.07) or excluding verapamil (−10%, P=0.02), as well as angiotensin type-1 receptor blockers (−24%, P=0.0002) resulted in better stroke prevention than did the old drugs, whereas the opposite trend was observed for angiotension converting enzyme inhibitors (+10%, P=0.03). An overview of 6 trials conducted in patients with a history of cerebrovascular disease demonstrated that antihypertensive drug treatment reduced stroke recurrence by 25% (P=0.004). A meta-regression analysis showed that within-trial differences in systolic blood pressure accounted for the prevention of stroke in most trials. In 5 trials, dementia was a secondary outcome. Overall, antihypertensive treatment did not reduce the incidence of vascular or degenerative dementia (−11%, P=0.15). However, when the analysis was limited to 3 trials involving a dihydropyridine or a diuretic as the mainstay of therapy, this benefit increased to 25% (P=0.01). Randomized clinical trials should urgently address the question to what extent blood-pressure-lowering therapy may prevent degenerative dementia.

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