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[未确诊慢性肌病中与坏死性肌病相关自身抗体的筛查]

[Screening of autoantibodies associated with necrotizing myopathy among undiagnosed chronic myopathy].

作者信息

Kuru Satoshi, Suzuki Shigeaki, Ogata Katsuhisa, Kobayashi Michio, Ishida Chiho, Watanabe Chigusa, Matsumura Tsuyoshi

机构信息

Department of Neurology, National Hospital Organization Suzuka Hospital.

Department of Neurology, Keio University School of Medicine.

出版信息

Rinsho Shinkeigaku. 2017 Oct 27;57(10):562-566. doi: 10.5692/clinicalneurol.cn-001075. Epub 2017 Sep 28.

Abstract

We screened anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies among 42 patients who had undiagnosed chronic myopathy from six national hospitals. Anti-SRP and anti-HMGCR antibodies were determined by RNA immuneprecipitation and enzyme-linked immune-sorbent assay (ELISA), respectively. We identified two patients with anti-SRP antibodies (4.7%) and, two with anti-HMGCR antibodies (4.7%). Both of anti-SRP-positive patients showed dysphagia with a high level of creatine kinase. Anti-HMGCR antibodies were associated with mild muscle weakness with a relatively late disease onset. Our study suggests the importance of autoantibody testing among undiagnosed chronic myopathy.

摘要

我们在来自六家国立医院的42例未确诊慢性肌病患者中筛查了抗信号识别颗粒(SRP)抗体和抗3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)抗体。抗SRP抗体和抗HMGCR抗体分别通过RNA免疫沉淀和酶联免疫吸附测定(ELISA)来检测。我们鉴定出两名抗SRP抗体阳性患者(4.7%)和两名抗HMGCR抗体阳性患者(4.7%)。两名抗SRP抗体阳性患者均表现出吞咽困难且肌酸激酶水平较高。抗HMGCR抗体与轻度肌无力及相对较晚的疾病发病相关。我们的研究表明了在未确诊慢性肌病中进行自身抗体检测的重要性。

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