{"title":"布鲁斯特关于文章“CKM Glu83Gly与钝化肌酸激酶变异有关,但与肌痛无关”的信函。","authors":"Lizzy M Brewster","doi":"10.1161/CIRCGENETICS.117.001938","DOIUrl":null,"url":null,"abstract":"In a recent article, Siddiqui et al1 aimed to gain insight in the known negative association between constitutive plasma creatine kinase (CK) and a rare single-nucleotide polymorphism in the CK gene coding for the cytoplasmic M isoenzyme monomer, CKM Glu83Gly (rs11559024). The authors report that the polymorphism is associated with lower plasma CK variability and inducibility, but not with myalgia. It is concluded that the findings represent a novel mechanistic rationale for a subpopulation of individuals presenting with statin intolerance or myalgia without raised CK levels.1 Although the data are promising, the authors should have included cytoplasmic CK in the discussion.\n\nThere is no …","PeriodicalId":10277,"journal":{"name":"Circulation: Cardiovascular Genetics","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1161/CIRCGENETICS.117.001938","citationCount":"0","resultStr":"{\"title\":\"Letter by Brewster Regarding Article, \\\"<i>CKM</i> Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia\\\".\",\"authors\":\"Lizzy M Brewster\",\"doi\":\"10.1161/CIRCGENETICS.117.001938\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In a recent article, Siddiqui et al1 aimed to gain insight in the known negative association between constitutive plasma creatine kinase (CK) and a rare single-nucleotide polymorphism in the CK gene coding for the cytoplasmic M isoenzyme monomer, CKM Glu83Gly (rs11559024). The authors report that the polymorphism is associated with lower plasma CK variability and inducibility, but not with myalgia. It is concluded that the findings represent a novel mechanistic rationale for a subpopulation of individuals presenting with statin intolerance or myalgia without raised CK levels.1 Although the data are promising, the authors should have included cytoplasmic CK in the discussion.\\n\\nThere is no …\",\"PeriodicalId\":10277,\"journal\":{\"name\":\"Circulation: Cardiovascular Genetics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1161/CIRCGENETICS.117.001938\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Circulation: Cardiovascular Genetics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1161/CIRCGENETICS.117.001938\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Circulation: Cardiovascular Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1161/CIRCGENETICS.117.001938","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Letter by Brewster Regarding Article, "CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia".
In a recent article, Siddiqui et al1 aimed to gain insight in the known negative association between constitutive plasma creatine kinase (CK) and a rare single-nucleotide polymorphism in the CK gene coding for the cytoplasmic M isoenzyme monomer, CKM Glu83Gly (rs11559024). The authors report that the polymorphism is associated with lower plasma CK variability and inducibility, but not with myalgia. It is concluded that the findings represent a novel mechanistic rationale for a subpopulation of individuals presenting with statin intolerance or myalgia without raised CK levels.1 Although the data are promising, the authors should have included cytoplasmic CK in the discussion.
There is no …
期刊介绍:
Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.