Clinical Trial Service Unit & Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, Big Data Institute Building, University of Oxford, Old Road Campus, Roosevelt Drive, Oxford, OX3 7LF, UK.
Medical Research Council Population Health Research Unit (MRC PHRU) at the University of Oxford, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
J Cardiovasc Transl Res. 2022 Dec;15(6):1474-1476. doi: 10.1007/s12265-022-10261-w. Epub 2022 May 5.
Tissue remodelling and fibrosis which occur in response to injury play a central role in the development of many diseases. Chymase is a key enzyme believed to mediate these pathological processes. As such, chymase inhibitors have been under active development for the treatment of a number of conditions. To investigate the impact of reduced chymase function, we constructed a genetic score from two pLoF mutations in the gene encoding chymase and tested its association with diseases and biomarkers. Our study found no association between the genetically-predicted reduced chymase function score and heart failure, chronic kidney disease or other predefined conditions. We additionally found no association of the score with any physical measurements or biomarkers. Our results provide no evidence in support of chymase inhibition as a novel therapeutic strategy for the treatment or prevention of heart failure, chronic kidney disease or major cardiovascular events, as previously proposed.
组织重塑和纤维化是对损伤的反应,它们在许多疾病的发展中起着核心作用。糜酶是一种被认为介导这些病理过程的关键酶。因此,糜酶抑制剂一直是治疗多种疾病的研究热点。为了研究糜酶功能降低的影响,我们构建了一个基因评分,该评分来自编码糜酶的基因中的两个 pLoF 突变,并测试了其与疾病和生物标志物的相关性。我们的研究发现,基因预测的糜酶功能降低评分与心力衰竭、慢性肾脏病或其他预先定义的疾病之间没有相关性。我们还没有发现评分与任何身体测量或生物标志物之间的关联。我们的研究结果没有提供支持糜酶抑制作为治疗或预防心力衰竭、慢性肾脏病或主要心血管事件的新治疗策略的证据,这与之前的提议相反。