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[血管紧张素转换酶和血管紧张素原基因多态性对西班牙肥厚型心肌病患者表型表达的影响]

[The effect of polymorphisms of the angiotensin-converting enzyme and angiotensinogen genes on the phenotypic expression of Spanish patients with hypertrophic cardiomyopathy].

作者信息

López-Haldón J, García-Lozano J R, Martínez Martínez A, Núñez-Roldán A, Burgos Cornejo J

机构信息

Servicio de Cardiología, Hospital Universitario Virgen del Rocío, Sevilla.

出版信息

Med Clin (Barc). 1999 Jul 10;113(5):161-3.

PMID:10480137
Abstract

BACKGROUND

Hypertrophic cardiomyopathy (HCM) has a great variability in its morphofunctional expression. This study analyzes whether angiotensin-converting enzyme (ACE) and angiotensinogen (AGT) gene polymorphisms modulate the phenotypic expression in Spanish patients with HCM.

PATIENTS AND METHODS

Forty Spanish HCM patients were studied. Twenty-six out of these 40 patients belonged to 7 families with familial HCM, and the remaining 14 patients had either a sporadic HCM or a HCM with unknown family incidence. A group of 269 healthy subjects was included as control for the genotype study. Maximal wall thickness, ventricular mass and several diastolic function indexes were measured in each patient by Doppler-echocardiography. The insertion/deletion (I/D) polymorphism of ACE gene and the M235T polymorphism of AGT gene were studied in both patients and healthy subjects.

RESULTS

A higher frequency in patients than in controls was found for D allele (0.79 vs 0.64; p = 0.02) and for DD genotype (62.5 vs 41.2%; p = 0.02). Conversely, no difference was observed in M235T polymorphism between both groups. Neither DD genotype of ACE, nor TT genotype of AGT determined a greater degree of ventricular hypertrophy or a worse diastolic function in patients with HCM.

CONCLUSIONS

D allele and DD genotype are predisposing factors to express HCM. In this series of Spanish patients, I/D polymorphism of ACE and M235T polymorphism of AGT do not modify phenotypic expression of HCM.

摘要

背景

肥厚型心肌病(HCM)在形态功能表达上具有很大的变异性。本研究分析血管紧张素转换酶(ACE)和血管紧张素原(AGT)基因多态性是否调节西班牙HCM患者的表型表达。

患者和方法

对40例西班牙HCM患者进行了研究。这40例患者中有26例属于7个家族性HCM家族,其余14例患者患有散发性HCM或家族发病率未知的HCM。纳入269名健康受试者作为基因型研究的对照。通过多普勒超声心动图测量每位患者的最大壁厚、心室质量和几个舒张功能指标。对患者和健康受试者均研究了ACE基因的插入/缺失(I/D)多态性和AGT基因的M235T多态性。

结果

患者中D等位基因(0.79对0.64;p = 0.02)和DD基因型(62.5对41.2%;p = 0.02)的频率高于对照组。相反,两组之间在M235T多态性上未观察到差异。ACE的DD基因型和AGT的TT基因型均未在HCM患者中确定更大程度的心室肥厚或更差的舒张功能。

结论

D等位基因和DD基因型是表达HCM的易感因素。在这一系列西班牙患者中,ACE的I/D多态性和AGT的M235T多态性不会改变HCM的表型表达。

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