1. East Asians Variant Mitochondrial Aldehyde Dehydrogenase 2 Genotype Exacerbates Nitrate Tolerance in Patients With Coronary Spastic Angina.
- Author
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Mizuno Y, Harada E, Kugimiya F, Shono M, Kusumegi I, Yoshimura M, Kinoshita K, and Yasue H
- Subjects
- Aged, Angina Pectoris ethnology, Angina Pectoris physiopathology, Coronary Vasospasm ethnology, Coronary Vasospasm physiopathology, Female, Humans, Japan epidemiology, Male, Middle Aged, Nitroglycerin adverse effects, Vasoconstriction genetics, Vasodilator Agents adverse effects, Aldehyde Dehydrogenase, Mitochondrial genetics, Angina Pectoris drug therapy, Angina Pectoris genetics, Asian People genetics, Coronary Vasospasm drug therapy, Coronary Vasospasm genetics, Drug Resistance genetics, Nitroglycerin administration & dosage, Polymorphism, Genetic, Vasoconstriction drug effects, Vasodilator Agents administration & dosage
- Abstract
Background: Aldehyde dehydrogenase 2 (ALDH2) plays a central role in the biotransformation of glyceryl trinitrate (GTN) or nitroglycerin, which is widely used for the treatment of coronary artery disease (CAD). The deficient variant ALDH2 genotype (ALDH2*2) is prevalent among East Asians. This study examined whether there are differences in nitroglycerine-mediated dilation (NMD) and flow-mediated dilation (FMD) response between wildALDH2*1/*1and variantALDH2*2patients with CAD., Methods and results: The study subjects comprised 55 coronary spastic angina (CSA) patients, confirmed by coronary angiography and intracoronary injection of acetylcholine (42 men and 13 women, mean age 68.0±9.0 years). They underwent NMD and FMD tests in the morning before and after continuous transdermal GTN administration for 48 h. NMD was lower at baseline inALDH2*2than in theALDH2*1/*1group (P=0.0499) and decreased significantly in both groups (P<0.0001 and P<0.0001, respectively) after GTN, with significantly lower levels in theALDH2*2group (P=0.0002). FMD decreased significantly in bothALDH2*1/*1andALDH2*2groups (P<0.0001and P=0.0002, respectively) after continuous GTN administration, with no significant differences between the 2 groups both before and after GTN., Conclusions: Continuous administration of GTN produced endothelial dysfunction as well as nitrate tolerance in bothALDH2*1/1andALDH2*2patients with CSA.ALDH2*2attenuated GTN response and exacerbated GTN tolerance, but not endothelial dysfunction, as compared toALDH2*1/*1in patients with CSA.
- Published
- 2020
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