Mutations in Mitochondrial DNA and Hypertension
Abstract: Hypertension is one of the most common cardiovascular disease. It is one of the main risk factors associated with cardiovascular death. Mutations in mitochondrial DNA lead to failures in metabolism, affecting mitochondrial protein synthesis and oxidative phosphorylation function. These mutations result in a deficit in ATP synthesis and an increase of generation of reactive oxygen species. As a result, mitochondrial DNA mutation has been the highlight in this filed. These findings will be helpful for understanding the molecular mechanism of maternally inherited hypertension. It may provide new insights into management and treatment of maternally inherited hypertension. This review summarized the association between mtDNA mutations and hypertension.
文章引用: 秦文蓓 , 张富春 , 郑秀芬 (2012) 线粒体DNA突变与高血压。 临床医学进展， 2， 1-5. doi: 10.12677/acm.2012.21001
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