Predictors of the location of multiple sclerosis relapse

被引:18
|
作者
Deen, S. [1 ]
Bacchetti, P. [2 ]
High, A. [3 ]
Waubant, E. [1 ]
机构
[1] Univ San Francisco, MS Ctr, San Francisco, CA 94117 USA
[2] Univ San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94117 USA
[3] Univ San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94117 USA
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D O I
10.1136/jnnp.2007.136440
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: While clinical relapses are the defining feature of relapsing-remitting multiple sclerosis (RRMS), their characteristics vary widely from patient to patient. This study sought to identify predictors of MS relapse location. Based on the current literature, two potential predictors were identified: treatment with interferon beta (IFNB) and location of previous relapse. Methods: Patients with RRMS were identified from the UCSF MS Center database who underwent at least 3 months of treatment with IFNB or glatiramer acetate (GA). The relapse immediately preceding the initiation of treatment (pretreatment relapse) and the first relapse occurring after the initiation of treatment (on-treatment relapse) were coded as affecting the spinal cord (SC), optic nerve (ON), brainstem/cerebellum (BC) or cerebrum. Logistic regression was performed to identify independent predictors of on-treatment relapse location. Results: The 134 IFNB and 56 GA patients did not differ in gender, race, age at symptom onset (30.3 years) or disease duration at the start of treatment (5.7 years). Patients with pretreatment SC relapses had increased odds of having on-treatment SC compared with non-SC relapses (OR 2.31, p=0.013); the same tendency for localisation occurred with BC (OR 3.05, p=0.013) and ON (OR 3.63, p=0.011) relapses. Additionally, patients who relapsed on treatment had a higher SC (but not ON or BC) relapse risk when they were receiving IFNB compared with GA (OR 2.05, p=0.041), independent of pretreatment relapse location. Conclusion: These results show a tendency for patients to have localised exacerbations, which could be mediated by genetic or immunological factors. In addition, and to be confirmed in subsequent studies, IFNB treatment may influence SC relapse risk.
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页码:1190 / 1193
页数:4
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