Is there a Role for Genetics in Cardiac Calcification?

U. Hellman, S. Mörner, M. Henein
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Abstract

Calcific coronary artery disease (CCAD) may cause abnormal myocardial perfusion and hence generalized ischaemia, despite potential discrepancy in its expression pattern compared to the well-known atherosclerotic disease which raises questions about the exact pathophysiology of coronary calcification and whether there is a genetic aetiology for it.  In a pilot study we studied three candidate genes, ENPP1, ABCC6 and NTE5 which may predispose to coronary arterial or valvular calcification. We studied 65 patients with CCAD and 5 patients with calcific aortic valve disease (CAVD).  Five DNA variants potentially affecting protein function were found in six patients. Our findings support genetic variants might influence the development of CCAD and CAVD, however, segregation in the families must first be performed to ascertain any damaging effect of these variants. The search for direct causative genetic variants in coronary artery and aortic valve calcification must be broadened with other genes.
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基因在心脏钙化中起作用吗?
钙化性冠状动脉疾病(CCAD)可能导致心肌灌注异常,从而导致全身性缺血,尽管与众所周知的动脉粥样硬化性疾病相比,其表达模式可能存在差异,这使得人们对冠状动脉钙化的确切病理生理以及是否存在遗传病因提出了疑问。在一项初步研究中,我们研究了三个候选基因,ENPP1, ABCC6和NTE5,它们可能易导致冠状动脉或瓣膜钙化。我们研究了65例CCAD患者和5例钙化主动脉瓣疾病(CAVD)患者。在6名患者中发现了5种可能影响蛋白质功能的DNA变异。我们的研究结果支持遗传变异可能影响CCAD和CAVD的发展,然而,必须首先在家族中进行分离以确定这些变异的任何破坏性影响。对冠状动脉和主动脉瓣钙化的直接致病基因变异的研究必须扩大到其他基因。
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