Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

作者：Palacin Maria; Alvarez Victoria; Martin Maria; Diaz Marta; Corao Ana I; Alonso Beien; Diaz Molina Beatriz; Lozano Inigo; Avanzas Pablo; Moris Cesar; Reguero Julian R; Rodriguez Isabel; Lopez Larrea Carlos; Cannata Andia Jorge; Batalla Alberto; Ruiz Ortega Marta; Martinez Camblor Pablo; Coto Eliecer^*

来源：Mitochondrion, 2011, 11(1): 176-181.

DOI：10.1016/j.mito.2010.09.004

• Atherosclerosis
• Myocardial infarction
• Mitochondria
• Haplogroups
• Mitochondrial transcription factor

The main objective of this research was to define the association between common mitochondrial DNA (mtDNA) polymorphisms and mitochondrial transcription A gene (TFAM) variants and myocardial infarction (MI) in patients with atherosclerotic diseased vessels. Ten mitochondrial polymorphisms that defined the nine common European haplogroups were genotyped in 500 male patients with early onset MI (<55 years) and at least one atherosclerotic coronary vessel (angiographically confirmed), and 500 healthy controls. In addition, we searched for DNA variants in the coding region of the TFAM gene and compared patients and controls for the allele and genotype frequencies.
Early onset MI was strongly associated with male gender and tobacco smoking in our population. MtDNA haplogroup H (defined by allele 7028 degrees C) was significantly more frequent in a first group of patients (n=250) compared to controls (n=300), and the association was confirmed in a second group of only smokers (250 patients and 200 controls). For total patients and controls, we obtained a p = 0.002 (OR = 1.50; 95% CI = 1.17-1.92) for H vs. the other haplogroups. We found four common TFAM polymorphisms, with allele/genotype frequencies that did not differ between patients and controls.
In conclusion, mitochondrial haplogroup H was associated with early onset MI in male smokers. Our work supported a role for the mtDNA variation in the risk for atherosclerosis and ischemic associated events, likely due to differences in mitochondrial function and reactive oxygen production between the different haplogroups.

• 出版日期2011-1