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香港华人重症肌无力亚分类中的人类白细胞抗原及乙酰胆碱受体抗体

HLA antigens and acetylcholine receptor antibody in the subclassification of myasthenia gravis in Hong Kong Chinese.

作者信息

Hawkins B R, Ip M S, Lam K S, Ma J T, Wy C L, Yeung R T, Dawkins R L

出版信息

J Neurol Neurosurg Psychiatry. 1986 Mar;49(3):316-9. doi: 10.1136/jnnp.49.3.316.

Abstract

Thirty seven Chinese adults and 23 children in Hong Kong with myasthenia gravis were tested for HLA-A and -B antigens and acetylcholine receptor (AChR) antibody. HLA BW46 had a significantly increased prevalence in patients with juvenile onset ocular myasthenia gravis. Only one third of the juvenile ocular patients had AChR antibodies and the titres were generally low. In the adult patients taken as a whole there was a non-significant increase in the prevalence of HLA B5 and HLA B15. HLA BW46 was more prevalent in adult patients without AChR antibody and less prevalent in patients with AChR antibody but the findings were not statistically significant. It is suggested that ocular myasthenia gravis is determined by a pathological mechanism for which susceptibility is determined by HLA BW46. There was a strong correlation between ocular myasthenia gravis and Graves' disease in the adult patients. The possibility that ocular myasthenia gravis is accentuated by a BW46-associated predisposition to ocular Graves' disease is considered.

摘要

对37名患有重症肌无力的中国香港成年人及23名儿童进行了HLA - A和 - B抗原以及乙酰胆碱受体(AChR)抗体检测。HLA BW46在青少年起病的眼肌型重症肌无力患者中的患病率显著升高。仅三分之一的青少年眼肌型患者有AChR抗体,且滴度通常较低。在整体成年患者中,HLA B5和HLA B15的患病率有不显著的升高。HLA BW46在无AChR抗体的成年患者中更为常见,而在有AChR抗体的患者中则较少见,但这些结果无统计学意义。提示眼肌型重症肌无力由一种病理机制决定,对该机制的易感性由HLA BW46决定。成年患者中眼肌型重症肌无力与格雷夫斯病之间存在强相关性。考虑到眼肌型重症肌无力可能因与BW46相关的眼型格雷夫斯病易感性而加重。

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本文引用的文献

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Association of HLA-DR4 with myasthenia gravis in the Chinese.
Tissue Antigens. 1984 Feb;23(2):127-9. doi: 10.1111/j.1399-0039.1984.tb00021.x.
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HLA antigens and myasthenia gravis in Japan.日本的人类白细胞抗原(HLA)抗原与重症肌无力
J Neurol Sci. 1977 Jun;32(2):195-201. doi: 10.1016/0022-510x(77)90234-9.
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Myasthenia gravis (first of two parts).重症肌无力(两部分中的第一部分)
N Engl J Med. 1978 Jan 19;298(3):136-42. doi: 10.1056/NEJM197801192980305.

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