Gender and Ethnicity Based Differences in Clinical and Laboratory Features of Myasthenia Gravis.

IF 1.7 Q4 IMMUNOLOGY Autoimmune Diseases Pub Date : 2015-01-01 Epub Date: 2015-06-14 DOI:10.1155/2015/197893
Fawzi Abukhalil, Bijal Mehta, Erin Saito, Sejal Mehta, Aaron McMurtray
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引用次数: 10

Abstract

Background. Previous reports describe ethnicity based differences in clinical and laboratory features between Caucasians and African Americans with myasthenia gravis. However, it is not known whether these findings apply to other ethnicities. Methods. Retrospective analysis of all patients treated for myasthenia gravis during a three-year period at a community based medical center. Results. A total of 44 patients were included, including 19 of Hispanic, 16 of African American, 6 of Caucasian, and 3 of Asian ethnicities. Female gender was more common among those with Hispanic, Asian, and African American ethnicities compared to Caucasian ethnicity (p = 0.029). Anti-acetylcholine receptor antibody subtypes demonstrated no significant ethnicity based differences in either generalized or ocular myasthenia gravis. A trend was noted towards greater frequency of blocking antibodies among Hispanics (52.6%) compared to African American (37.5%) and Caucasian (33.3%) patients (p = 0.059). Generalized but not ocular myasthenia patients showed greater frequency of anti-muscle specific kinase antibodies in Asians and Hispanics compared to African Americans and Caucasians (p = 0.041). Conclusions. The results of this study support the existence of ethnicity based differences in clinical and laboratory features of myasthenia gravis. Further study of genetic factors influencing clinical features of myasthenia gravis is indicated.

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重症肌无力临床和实验室特征的性别和种族差异。
背景。以前的报告描述了白人和非裔美国人重症肌无力的临床和实验室特征的种族差异。然而,尚不清楚这些发现是否适用于其他种族。方法。回顾性分析在社区医疗中心治疗重症肌无力三年期间的所有患者。结果。共纳入44例患者,其中西班牙裔19例,非洲裔16例,高加索6例,亚洲3例。与白种人相比,女性在西班牙裔、亚裔和非裔美国人中更为常见(p = 0.029)。抗乙酰胆碱受体抗体亚型在全身性或眼型重症肌无力中均无明显的种族差异。与非裔美国人(37.5%)和高加索人(33.3%)相比,西班牙裔患者(52.6%)出现阻断抗体的频率更高(p = 0.059)。与非裔美国人和白种人相比,亚洲人和西班牙裔患者出现抗肌肉特异性激酶抗体的频率更高(p = 0.041)。结论。本研究结果支持重症肌无力的临床和实验室特征存在基于种族的差异。建议进一步研究影响重症肌无力临床特征的遗传因素。
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来源期刊
Autoimmune Diseases
Autoimmune Diseases IMMUNOLOGY-
CiteScore
6.10
自引率
0.00%
发文量
9
审稿时长
17 weeks
期刊最新文献
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