非洲血统是多发性硬化症临床过程中继发性进展的预测因素。

ISRN Neurology Pub Date : 2012-01-01 DOI:10.5402/2012/410629
Claudia Cristina Ferreira Vasconcelos, Gutemberg Augusto Cruz Dos Santos, Luiz Claudio Thuler, Solange Maria Camargo, Regina Maria Papais Alvarenga
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引用次数: 20

摘要

背景。对多发性硬化症临床病程的研究表明,某些初始临床因素可预测疾病进展。疾病低流行地区的环境和遗传因素与高流行地区不同,缺乏对疾病进展过程和致残特征的研究。目标。分析混合人群复发缓解型多发性硬化症向进展期的长期演变及其预后因素。方法。我们进行了一项生存研究和逻辑回归,以检验人口统计学和初始临床因素对疾病进展的影响。在巴西多发性硬化症参考中心接受治疗的553名复发缓解型患者中,我们回顾了150名患病10年或以上的患者的医疗记录。结果。非洲血统是继发性进展风险较高的一个因素,其次是发病年龄和诊断后一年内复发次数。更好地了解祖先对预后的影响有助于促进遗传学和药物基因组学研究,并可能阐明尚不清楚的多发性硬化症神经退行性进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

African ancestry is a predictor factor to secondary progression in clinical course of multiple sclerosis.

African ancestry is a predictor factor to secondary progression in clinical course of multiple sclerosis.

Background. Studies on the clinical course of multiple sclerosis have indicated that certain initial clinical factors are predictive of disease progression. Regions with a low prevalence for disease, which have environmental and genetic factors that differ from areas of high prevalence, lack studies on the progressive course and disabling characteristics of the disease. Objective. To analyse the long-term evolution to the progressive phase of the relapsing-remitting multiple sclerosis and its prognosis factors in mixed population. Methods. We performed a survival study and logistic regression to examine the influence of demographic and initial clinical factors on disease progression. Among 553 relapsing-remitting patients assisted at a Brazilian reference centre for multiple sclerosis, we reviewed the medical records of 150 patients who had a disease for ten or more years. Results. African ancestry was a factor that conferred more risk for secondary progression followed by age at the onset of the disease and the number of relapses in the year after diagnosis. A greater understanding of the influence of ancestry on prognosis serves to stimulate genetics and pharmacogenomics research and may clarify the poorly understood neurodegenerative progression of MS.

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