Yifeng Li, Dandan Zhang, Wei Jin, Chunhong Shao, Pengrong Yan, Congjian Xu, Haihui Sheng, Yan Liu, Jinde Yu, Yuying Xie, Yingnan Zhao, Daru Lu, Daniel W. Nebert, Donald C. Harrison, Wei Huang, Li Jin
J Clin Invest.
2006;
116(2):506–511
doi:10.1172/JCI26564
This article Copyright © 2006, The American Society for Clinical Investigation
Abstract
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G
lyceryl trinitrate (GTN), also known as nitroglycerin, has been used to treat angina and heart failure for more than 130 years. Recently, it was shown that mitochondrial aldehyde dehydrogenase-2 (ALDH2) is responsible for formation of NO, the metabolite needed for GTN efficacy. In the present study, we show that the common G-to-A polymorphism in exon 12 of ALDH2 — resulting in a Glu504Lys replacement that virtually eliminates ALDH2 activity in both heterozygotes and homozygotes — is associated with a lack of efficacy of sublingual GTN in Chinese subjects. We also show that the catalytic efficiency (Vmax/Km) of GTN metabolism of the Glu504 protein is approximately 10-fold higher than that of the Lys504 enzyme. We conclude that the presence of the Lys504 allele contributes in large part to the lack of an efficacious clinical response to nitroglycerin; we recommend that this genetic factor be considered when administering nitroglycerin to patients, especially Asians, 30–50% of whom possess the inactive ALDH2*2 mutant allele.
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