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肌萎缩侧索硬化症和神经病变中抗GM1抗体的临床相关性

Clinical correlations of anti-GM1 antibodies in amyotrophic lateral sclerosis and neuropathies.

作者信息

Lamb N L, Patten B M

机构信息

Department of Neurology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Muscle Nerve. 1991 Oct;14(10):1021-7. doi: 10.1002/mus.880141014.

Abstract

Clinical correlations of antiganglioside GM1 antibodies are important because high titers of these antibodies may have therapeutic significance. To further evaluate this significance, we reviewed our experience with 78 patients who had the following diagnoses: amyotrophic lateral sclerosis (ALS), ALS syndromes in patients with gammopathy or thyroid abnormalities, cervical spondylosis simulating ALS, motor neuropathies, and chronic inflammatory demyelinating polyneuropathies (CIDP). Antiganglioside antibody titers were measured "blind" by ELISA assay at the neuromuscular clinical laboratory, Johns Hopkins School of Medicine. We conclude that anti-GM1 antibodies are found in a wide variety of neuromuscular conditions. Patients with classical ALS had a mean anti-GM1 antibody titer significantly lower than patients with CIDP or motor neuropathy. Patients with ALS associated with gammopathy or thyroid disorders had higher anti-GM1 titers than seen in classical ALS. The highest mean titer occurred in patients with CIDP, a treatable neuropathy.

摘要

抗神经节苷脂GM1抗体的临床相关性很重要,因为这些抗体的高滴度可能具有治疗意义。为了进一步评估这种意义,我们回顾了78例患者的情况,这些患者有以下诊断:肌萎缩侧索硬化症(ALS)、患有丙种球蛋白病或甲状腺异常患者的ALS综合征、模拟ALS的颈椎病、运动神经病以及慢性炎症性脱髓鞘性多发性神经病(CIDP)。抗神经节苷脂抗体滴度由约翰霍普金斯医学院神经肌肉临床实验室通过ELISA检测法“盲法”测定。我们得出结论,抗GM1抗体在多种神经肌肉疾病中均可发现。典型ALS患者的抗GM1抗体平均滴度显著低于CIDP或运动神经病患者。患有丙种球蛋白病或甲状腺疾病相关ALS的患者,其抗GM1滴度高于典型ALS患者。平均滴度最高的是CIDP患者,这是一种可治疗的神经病。

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