Saragoça M A, Cassiolatto J L, Vanetta A M, Canziani M E, Abreu P, Ventura R T, Ramos O L
Hypertension-Nephrology Division, Paulista School of Medicine, São Paulo, Brazil.
Am J Hypertens. 1993 Mar;6(3 Pt 2):89S-91S. doi: 10.1093/ajh/6.3.89s.
The left ventricular hypertrophy (LVH) of hypertension is often associated with ventricular arrhythmias, which may increase the risk of cardiovascular mortality. Our study was therefore designed to assess whether pharmacological reversal of LVH was associated with the diminution of LV ectopic beats. The antihypertensive agent selected for the study was the dihydropyridine calcium antagonist isradipine (2.5 to 5.0 mg/day orally), which induces rapid regression of LVH. A marked temporal association was observed between regression of LV mass and reductions in the total number of ventricular extrasystoles and in paired beats. Furthermore, there was a diminution of the complexity of the form of ventricular ectopic beats during antihypertensive treatment. No changes in serum electrolytes were documented to account for this control of cardiac arrhythmias. We conclude that the reversal of LVH obtained with isradipine is accompanied by control of the ventricular arrhythmias in hypertensive patients. It is possible that this cardioprotective action may be associated non-specifically with the reduction in LV mass, although a drug- or class-specific action cannot be ruled out.
高血压引起的左心室肥厚(LVH)常与室性心律失常相关,这可能会增加心血管疾病死亡风险。因此,我们开展本研究旨在评估LVH的药物逆转是否与左心室异位搏动减少有关。本研究选用的降压药物是二氢吡啶类钙拮抗剂伊拉地平(口服剂量为每日2.5至5.0毫克),该药可使LVH迅速消退。LV质量的消退与室性期前收缩总数及成对搏动的减少之间存在明显的时间关联。此外,在降压治疗期间,室性异位搏动的形态复杂性有所降低。未发现血清电解质变化可解释心律失常的这种控制情况。我们得出结论,伊拉地平使LVH逆转的同时,高血压患者的室性心律失常也得到了控制。尽管不能排除药物或药物类别特异性作用,但这种心脏保护作用可能与LV质量的降低非特异性相关。