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日本胸腺瘤组织学与肌特异性受体酪氨酸激酶抗体阳性重症肌无力伴发自身免疫性疾病的相关性。

Thymus histology and concomitant autoimmune diseases in Japanese patients with muscle-specific receptor tyrosine kinase-antibody-positive myasthenia gravis.

机构信息

Department of Clinical Neuroscience and Neurology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

出版信息

Eur J Neurol. 2013 Sep;20(9):1272-6. doi: 10.1111/ene.12169. Epub 2013 May 17.

DOI:10.1111/ene.12169
PMID:23679930
Abstract

BACKGROUND AND PURPOSE

The differences in the characteristics of thymus histology, coexisting autoimmune diseases and related autoantibodies between anti-muscle-specific receptor tyrosine kinase (MuSK)-antibody (Ab)-positive myasthenia gravis (MG) patients, and anti-acetylcholine receptor (AChR)-Ab-positive MG patients are not clearly defined.

METHODS

The types of thymus histology, coexisting autoimmune diseases and associated Abs in 83 MuSK-Ab-positive patients nationwide were investigated and were compared with those in AChR-Ab-positive patients followed at our institute (n = 83). As for the autoantibodies associated with thymoma, titin Abs were measured.

RESULTS

Thymoma was not present in any of the MuSK-Ab-positive patients but presented in 21 patients (25.3%) amongst the AChR-Ab-positive patients. Titin Abs were absent in MuSK-Ab-positive patients but positive in 25 (30.1%) of the AChR-Ab-positive patients. Concomitant autoimmune diseases were present in eight MuSK-Ab-positive patients (9.6%) amongst whom Hashimoto's thyroiditis and rheumatoid arthritis predominated, whereas 22 AChR-Ab-positive patients (26.5%) had one or more concomitant autoimmune diseases of which Graves' disease predominated.

CONCLUSIONS

Differences in frequency of thymoma and thymic hyperplasia, coexisting autoimmune diseases and autoantibody positivity between MuSK-Ab-positive and AChR-Ab-positive MG were indicated, suggesting that, in contrast with AChR-Ab-positive MG, thymus does not seem to be involved in the pathogenic mechanisms of MuSK-Ab-positive MG.

摘要

背景与目的

抗肌肉特异性受体酪氨酸激酶(MuSK)抗体阳性重症肌无力(MG)患者与抗乙酰胆碱受体(AChR)抗体阳性 MG 患者的胸腺组织学特征、共存自身免疫性疾病及相关自身抗体存在差异,但尚未明确。

方法

对全国 83 例 MuSK-Ab 阳性患者的胸腺组织学类型、共存自身免疫性疾病及相关抗体进行调查,并与我院收治的 83 例 AChR-Ab 阳性患者进行比较。针对与胸腺瘤相关的自身抗体,检测了titin 抗体。

结果

MuSK-Ab 阳性患者中无一例存在胸腺瘤,而 AChR-Ab 阳性患者中则有 21 例(25.3%)存在胸腺瘤。MuSK-Ab 阳性患者 titin 抗体均为阴性,而 AChR-Ab 阳性患者中有 25 例(30.1%)为阳性。8 例 MuSK-Ab 阳性患者(9.6%)存在伴发自身免疫性疾病,其中以桥本甲状腺炎和类风湿关节炎为主,而 22 例 AChR-Ab 阳性患者(26.5%)存在一种或多种伴发自身免疫性疾病,其中以格雷夫斯病为主。

结论

MuSK-Ab 阳性与 AChR-Ab 阳性 MG 患者在胸腺瘤和胸腺增生的发生率、共存自身免疫性疾病及自身抗体阳性率方面存在差异,表明与 AChR-Ab 阳性 MG 不同,胸腺似乎并不参与 MuSK-Ab 阳性 MG 的发病机制。

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