AAT: A Comparative Study in HCM and DCM

作者:Veronica M; Ali Altaf; Venkateshwari A; Narsimhan C; Nallari Pratibha*
来源:International Journal of Human Genetics, 2010, 10(4): 235-238.

摘要

Cardiomyopathies are the sub-acute, chronic disorders of the myocardium that result in cardiac muscle injury thus disrupting the normal contractile function of the heart. HCM and DCM are inflammatory disorders where the role of AAT as a disease marker and cardiac remodeler has been identified. AAT acts as a major serine protease inhibitor and immunomodulator with high degree of polymorphism. Its main role is inhibition of the matrix metalloproteinases, collagen and the enzyme elastase apart from ECM and microfibrillar components degradation. The present study aims to evaluate the role of AAT, in 83 HCM, 97 DCM patients and 100 Control individuals to identify its association with cardiomyopathy. Our results implicate the role of the Z and S alleles in the etiopathogenesis of HCM and DCM, and also their role in cardiomyocyte remodelling through ECM changes. Thus decreased production of AAT may lead to further damage of the myocardiocytes.

  • 出版日期2010-12