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Angiotensin-converting enzyme 2 polymorphisms and cardiovascular risk

机译:血管紧张素转换酶2基因多态性与心血管风险

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摘要

We read with interest the meta-analysis performed by Y. Li, analysing the angiotensin-converting enzyme (ACE) gene insertion/deletion polymorphism and its association with essential hypertension in the Chinese population. The association between genes of the 'classic', ACE-mediated renin-angiotensin system (RAS) with hypertension has been extensively studied and has yielded important insights. However, an area of more recent interest concerns the ACE structural homologue, ACE2. The discovery of this enzyme in 2000 has opened up research into an 'alternate arm' of the RAS, which in many cases opposes the deleterious effects of the 'classic' arm. In this regard, ACE2 has emerged as a critical regulator of heart function, at least partly because it hydrolyses angiotensin II to the truncated peptide angi-otensin 1-7, which is reported to have vasodilatory and anti-fibrotic effects.
机译:我们感兴趣地阅读了Y. Li进行的荟萃分析,分析了中国人群中血管紧张素转换酶(ACE)基因的插入/缺失多态性及其与原发性高血压的关系。 “经典的” ACE介导的肾素-血管紧张素系统(RAS)的基因与高血压之间的关联已得到广泛研究,并产生了重要的见解。然而,最近关注的领域涉及ACE结构同系物ACE2。这种酶在2000年的发现为RAS的“另类臂”开辟了研究领域,在许多情况下,它都抵制了“经典”臂的有害作用。在这方面,ACE2已成为心脏功能的关键调节剂,至少部分是因为它能将血管紧张素II水解为截短的肽血管紧张素1-7,据报道它具有血管舒张和抗纤维化作用。

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