Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis

被引:0
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作者
S. V. Ramagopalan
G. C. DeLuca
K. M. Morrison
B. M. Herrera
D. A. Dyment
M. R. Lincoln
S.-M. Orton
M. J. Chao
A. Degenhardt
M. Pugliatti
A. D. Sadovnick
S. Sotgiu
G. C. Ebers
机构
[1] Level 3,Dept. of Clinical Neurology, University of Oxford
[2] West Wing,Wellcome Trust Centre for Human Genetics
[3] John Radcliffe Hospital,Dept. of Medical Genetics and Faculty of Medicine
[4] University of Oxford,Institute of Clinical Neurology
[5] Division of Neurology,undefined
[6] University of British Columbia,undefined
[7] University of Sassari,undefined
来源
Journal of Neurology | 2008年 / 255卷
关键词
multiple sclerosis; genetics; outcome;
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摘要
Multiple sclerosis (MS) is a common inflammatory disease of the central nervous system unsurpassed for its variability in disease outcome. As little is conclusively known about MS disease mechanisms, we have selected a variety of candidate genes that may influence the prognosis of the disease based on their function. A cohort of sporadic MS cases, taken from opposite extremes of the putative distribution of long-term outcome using the most stringent clinical criteria to date, was used to determine the role of on MS disease severity. The MS cases selected represent the prognostic best 5 % (benign MS) and worst 5 % (malignant MS) of cases in terms of clinical outcome assessed by the EDSS. Genotyping the two sets of MS patients (112 benign and 51 malignant) and a replication cohort from Sardinia provided no evidence to suggest that the genes selected have any outcome modifying activity, although small effects of these genes cannot be ruled out.
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