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首页> 外文期刊>Autoimmunity reviews >Anti-HMGCR antibodies as a biomarker for immune-mediated necrotizing myopathies: A history of statins and experience from a large international multi-center study
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Anti-HMGCR antibodies as a biomarker for immune-mediated necrotizing myopathies: A history of statins and experience from a large international multi-center study

机译:抗HMGCR抗体可作为免疫介导的坏死性肌病的生物标志物:他汀类药物的历史和大型国际多中心研究的经验

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摘要

In an effort to find naturally occurring substances that reduce cholesterol by inhibiting 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR), statins were first discovered by Endo in 1972. With the widespread prescription and use of statins to decrease morbidity from myocardial infarction and stroke, it was noted that approximately 5% of all statin users experienced muscle pain and weakness during treatment In a smaller proportion of patients, the myopathy progressed to severe morbidity marked by proximal weakness and severe muscle wasting. Remarkably, Mammen and colleagues were the first to discover that the molecular target of statins, 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR), is an autoantibody target in patients that develop an immune-mediated necrotizing myopathy (IMNM). These observations have been confirmed in a number of studies but, until today, a multi-center, international study of IMNM, related idiopathic inflammatory myopathies (IIM), other auto-inflammatory conditions and controls has not been published. Accordingly, an international, multi-center study investigated the utility of anti-HMGCR antibodies in the diagnosis of statin-associated IMNM in comparison to different forms of IIM and controls. This study included samples from patients with different forms of IIM (n = 1250) and patients with other diseases (n = 656) that were collected from twelve sites and tested for anti-HMGCR antibodies by ELISA. This study confirmed that anti-HMGCR autoantibodies, when found in conjunction with statin use, characterize a subset of IIM who are older and have necrosis on muscle biopsy. Taken together, the data to date indicates that testing for anti-HMGCR antibodies is important in the differential diagnosis of IIM and might be considered for future classification criteria. (C) 2016 Published by Elsevier B.V.
机译:为了寻找可通过抑制3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)降低胆固醇的天然物质,他汀类药物于1972年由Endo首次发现。他汀类药物的广泛处方和使用可降低心肌病的发病率在脑梗塞和中风中,应注意的是,在使用他汀类药物的患者中,约有5%的患者在治疗期间经历了肌肉疼痛和无力。在较小比例的患者中,肌病进展为以近端无力和严重的肌肉消瘦为特征的严重发病。值得注意的是,Mammen及其同事是第一个发现他汀类药物的分子靶标3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)是发展为免疫介导的坏死性肌病(IMNM)的患者的自身抗体靶标。这些观察已在许多研究中得到证实,但是直到今天,关于IMNM,相关特发性炎症性肌病(IIM),其他自发性炎症和控制的多中心国际研究尚未发表。因此,一项国际,多中心研究与不同形式的IIM和对照相比,研究了抗HMGCR抗体在他汀类药物相关IMNM诊断中的效用。这项研究包括从十二种部位采集的不同形式IIM患者(n = 1250)和其他疾病患者(n = 656)的样品,并通过ELISA检测抗HMGCR抗体。这项研究证实,当与他汀类药物联合使用时,抗HMGCR自身抗体具有IIM的一个亚群的特征,该亚群年龄较大且肌肉活检坏死。综上所述,迄今为止的数据表明抗HMGCR抗体的测试在IIM的鉴别诊断中很重要,并且可能被认为是将来的分类标准。 (C)2016由Elsevier B.V.发布

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