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在肌萎缩侧索硬化症和脑循环障碍患者血清中检测针对潜在淀粉样蛋白生成蛋白γ-突触核蛋白的自身抗体。

Detection of autoantibodies to potentially amyloidogenic protein, gamma-synuclein, in the serum of patients with amyotrophic lateral sclerosis and cerebral circulatory disorders.

作者信息

Roman A Yu, Kovrazhkina E A, Razinskaya O D, Kukharsky M S, Maltsev A V, Ovchinnikov R K, Lytkina O A, Smirnov A P, Moskovtsev A A, Borodina Yu V, Surguchov A P, Ustyugov A A, Ninkina N N, Skvortsova V I

机构信息

Institute of Physiologically Active Compounds, Russian Academy of Sciences, Chernogolovka, Moscow oblast, 142432, Russia.

Aix-Marseille Université, Inserm, France.

出版信息

Dokl Biochem Biophys. 2017 Jan;472(1):64-67. doi: 10.1134/S1607672917010197. Epub 2017 Apr 19.

Abstract

In this study, we analyzed serum for the presence of antibodies to gamma-synuclein in patients with amyotrophic lateral sclerosis (ALS) compared to the control group of patients with other neurological diseases and healthy control donors. As a result, antibodies against gamma-synuclein are not an ALS-specific feature and have been identified in patients with ALS as well as in the control group patients. Patients with the impaired cerebral circulation showed increased incidence of autoantibodies to gamma-synuclein, yet the difference lacks statistical representativeness due to limited sample size.

摘要

在本研究中,我们分析了肌萎缩侧索硬化症(ALS)患者血清中γ-突触核蛋白抗体的存在情况,并与患有其他神经系统疾病的患者对照组以及健康对照供体进行了比较。结果显示,抗γ-突触核蛋白抗体并非ALS的特异性特征,在ALS患者以及对照组患者中均已检测到。脑循环受损的患者中,γ-突触核蛋白自身抗体的发生率有所增加,但由于样本量有限,这种差异缺乏统计学代表性。

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