Hasumi M, Hiroe M, Fujita N, Hasumi S, Toyosaki T, Nagao H, Hosoda S, Kasajima T, Sekiguchi M
Heart Institute of Japan, Tokyo Women's Medical College, Japan.
Heart Vessels Suppl. 1990;5:31-6.
To study the pathogenesis of idiopathic ventricular tachycardia with left bundle branch block morphology (LBBB-VT), histopathological findings in 34 patients and adrenergic receptor (AR) density obtained by micro-autoradiography in 11 patients were analyzed, using endomyocardial biopsy samples. According to the ventricular volume, we divided the patients into 3 groups. Group A patients (n = 8) were diagnosed as having arrhythmogenic right ventricular dysplasia (ARVD) showing right ventricular enlargement, group B patients (n = 7) showed decreased left ventricular function and/or enlarged left ventricle, and group C (n = 19) included patients with idiopathic ventricular tachycardia (VT) without enlargement or dysfunction of either ventricle. Histologically, there was a high incidence of significant pathology showing myocardial hypertrophy, degeneration, abnormal branching, and interstitial fibrosis in all groups (group A, 100%; group B, 86%; group C, 56%). There was a higher incidence of fatty tissue infiltration in groups A (100%), B (71%), C (48%) than in the control groups. As for AR, specific grains of alpha 1- and beta-AR were 23.0, and 18.3 (grains/25 x 25 mm square) respectively, in patients with LBBB-VT. The number of alpha 1 grains in patients with LBBB-VT was apparently higher than in the control group, sick sinus syndrome (SSS; 11.2), and the beta-AR density in the LBBB-VT group was the same as in the control group (SSS; 15.4). We concluded that the significant pathology in cases with VT might affect the arrhythmogenic condition. Moreover, these results suggested that the increase in the number of alpha 1-AR might have a great influence in idiopathic VT.
为研究具有左束支传导阻滞形态的特发性室性心动过速(LBBB-VT)的发病机制,我们使用心内膜活检样本分析了34例患者的组织病理学发现,并对11例患者通过微放射自显影获得的肾上腺素能受体(AR)密度进行了分析。根据心室容积,我们将患者分为3组。A组患者(n = 8)被诊断为致心律失常性右心室发育不良(ARVD),表现为右心室扩大;B组患者(n = 7)表现为左心室功能减退和/或左心室扩大;C组(n = 19)包括无任何心室扩大或功能障碍的特发性室性心动过速(VT)患者。组织学上,所有组均有较高比例的显著病理改变,表现为心肌肥大、变性、分支异常和间质纤维化(A组,100%;B组,86%;C组,56%)。A组(100%)、B组(71%)、C组(48%)脂肪组织浸润的发生率高于对照组。至于AR,LBBB-VT患者的α1-AR和β-AR特异性颗粒分别为23.0和18.3(颗粒/25×25平方毫米)。LBBB-VT患者的α1颗粒数量明显高于对照组、病态窦房结综合征(SSS;11.2),LBBB-VT组的β-AR密度与对照组(SSS;15.4)相同。我们得出结论,VT病例中的显著病理改变可能影响致心律失常状态。此外,这些结果表明α1-AR数量的增加可能对特发性VT有很大影响。