Klein W
Kardiologische Abteilung, Medizinische Universitätsklinik Graz.
Z Kardiol. 1992 Jun;81(6):295-302.
Meta-analysis of several large interventional trials in patients with mild to moderate hypertension has shown that coronary events are reduced to a much lesser extent than expected. One of the possible explanations for this are the metabolic side-effects of diuretics and betablockers used in these trials that may counteract their beneficial blood-pressure-lowering effect. Diuretics, especially thiazide, increase total cholesterol (+5%) and LDL-cholesterol (+10%), while betablockers decrease HDL-cholesterol (-5%) and increase triglycerides (+20%). Calcium antagonists and ACE-inhibitors do not affect lipids, and alpha-blockers have some beneficial effects. Regarding the carbohydrate metabolism, diuretics and betablockers decrease insulin sensitivity, increase plasma insulin, LDL-cholesterol, and triglycerides, and reduce HDL-cholesterol. Calcium channel blockers are neutral, while alpha-blockers and ACE-inhibitors improve glucose tolerance and reduce insulin resistance. To date, the clinical relevance of this side-effects is not known. Controlled, long-term trials in hypertensive patients with calcium channel blockers, ACE-inhibitors, and alpha-blockers are needed.
对多项针对轻至中度高血压患者的大型干预试验进行的荟萃分析表明,冠状动脉事件的减少幅度远低于预期。对此的一种可能解释是,这些试验中使用的利尿剂和β受体阻滞剂的代谢副作用可能会抵消其有益的降压效果。利尿剂,尤其是噻嗪类利尿剂,会使总胆固醇升高(5%),低密度脂蛋白胆固醇升高(10%),而β受体阻滞剂会使高密度脂蛋白胆固醇降低(5%),甘油三酯升高(20%)。钙拮抗剂和血管紧张素转换酶抑制剂对血脂没有影响,而α受体阻滞剂有一些有益作用。关于碳水化合物代谢,利尿剂和β受体阻滞剂会降低胰岛素敏感性,增加血浆胰岛素、低密度脂蛋白胆固醇和甘油三酯,并降低高密度脂蛋白胆固醇。钙通道阻滞剂无影响,而α受体阻滞剂和血管紧张素转换酶抑制剂可改善糖耐量并降低胰岛素抵抗。迄今为止,这种副作用的临床相关性尚不清楚。需要对高血压患者使用钙通道阻滞剂、血管紧张素转换酶抑制剂和α受体阻滞剂进行对照的长期试验。