首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >A reassessment of the risk of multiple sclerosis developing in patients with optic neuritis after extended follow-up.
【2h】

A reassessment of the risk of multiple sclerosis developing in patients with optic neuritis after extended follow-up.

机译:长期随访后对视神经炎患者发生多发性硬化症的风险进行了重新评估。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

One hundred and one of 146 patients presenting with isolated idiopathic optic neuritis, previously reviewed in 1978, were reassessed clinically, and retyped for HLA antigens and Factor B alleles, after a mean follow-up of 11.6 years. Fifty eight patients (57%) had developed multiple sclerosis at the time of reassessment in the present study, of whom 51 (88%) had clinically definite disease. This compared with 40% of the original group, in 1978, of whom 62% then had clinically definite multiple sclerosis. When the life-table method of analysis was used, the probability of developing multiple sclerosis was 75%, 15 years after the initial episode of optic neuritis. The frequencies of HLA-DR2 and the recently defined D-region antigen, DQw1, were significantly increased in patients with isolated optic neuritis and those who subsequently developed multiple sclerosis compared with normal controls, but neither allele appears to influence progression from optic neuritis to multiple sclerosis. Patients with optic neuritis who were HLA-DR3 positive had an increased risk for the development of multiple sclerosis (RR = 2.8) and this risk was further enhanced when DR3 occurred in combination with DR2 (RR = 6.7). The overall increased risk of developing multiple sclerosis for patients with this combination was 26 times that for the normal population. When the patients' original tissue-typing was considered BT 101 no longer influenced conversion of optic neuritis to multiple sclerosis. This may partly be explained by improved methods of tissue-typing, since not all BT 101 patients were subsequently found to be positive for HLA-DR2 or HLA-DQw1 and vice versa and by extended follow-up as multiple sclerosis conversion in HLA-DR2 negative individuals increased with time. All 101 patients were typed for Factor B alleles. No significant differences in frequencies were found between individuals with isolated optic neuritis or those who progressed to multiple sclerosis compared with the control population. Recurrent episodes of optic neuritis were associated with an increased risk for the development of multiple sclerosis in this study.
机译:在平均随访11.6年后,对先前在1978年进行回顾的146例患有孤立性特发性视神经炎的患者中的101例进行了临床评估,并对HLA抗原和因子B等位基因进行了重新分型。在本研究中,有58名患者(57%)在重新评估时出现了多发性硬化症,其中51名患者(88%)有临床明确的疾病。相比之下,1978年,原始组中有40%的人中有62%具有临床明确的多发性硬化症。当使用生命表分析方法时,视神经炎初发15年后,发生多发性硬化的可能性为75%。与正常对照相比,孤立性视神经炎和随后发展为多发性硬化症的患者,HLA-DR2和最近定义的D区抗原DQw1的频率显着增加,但没有等位基因似乎影响视神经炎向多发性硬化的进展硬化。 HLA-DR3阳性的视神经炎患者发生多发性硬化症的风险增加(RR = 2.8),当DR3与DR2合并发生时,这种风险进一步增加(RR = 6.7)。具有这种组合的患者发生多发性硬化症的总风险增加是正常人群的26倍。当考虑患者的原始组织类型时,BT 101不再影响视神经炎向多发性硬化的转化。部分原因可以通过改进的组织分型方法来解释,因为并非随后所有的BT 101患者都被发现对HLA-DR2或HLA-DQw1呈阳性,反之亦然,并且由于对HLA-DR2中的多发性硬化症进行了转换而进行了后续随访消极个体随时间增加。所有101例患者均输入了B因子等位基因。与对照组相比,单纯性视神经炎患者或进展为多发性硬化症患者之间的频率无明显差异。在这项研究中,视神经炎的复发发作与多发性硬化症发展的风险增加有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号