Oligoclonal bands in multiple sclerosis patients: worse prognosis?

被引:20
|
作者
Rojas, J. I. [1 ]
Tizio, S. [2 ]
Patrucco, L. [1 ]
Cristiano, E. [1 ]
机构
[1] Hosp Italiano Buenos Aires, Dept Neurol, Buenos Aires, DF, Argentina
[2] Hosp Interzonal Gen Agudos Gen San Martin La Plat, Buenos Aires, DF, Argentina
关键词
Multiple sclerosis; Oligoclonal bands; Prognosis; INTRATHECAL IGM SYNTHESIS; DIAGNOSTIC-CRITERIA; DISEASE COURSE; CEREBROSPINAL-FLUID; MRI; GUIDELINES; DISABILITY; PREDICTS; ONSET; EVENT;
D O I
10.1179/1743132812Y.0000000088
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Cerebrospinal fluid (CSF) oligoclonal bands (OB) imply intrathecal immunoglobulin synthesis and B-cell immune process. There is scarce evidence of OB having a role in disease prognosis. The objective of the present study was to determine OB's prognostic value regarding disease progression. Methods: Between January 1994 and January 2007, relapsing-remitting MS (RRMS) patients in which OB were determined were included. Demographic, clinical aspects and presence of OB were analyzed. We compared OB+ versus OB- patients regarding progression to expanded disability status scale (EDSS) of 6.0 and to secondary progressive MS (SPMS). Cox proportional hazard models were used to compare the outcome between groups. P values <0.05 were considered significant. Results: One hundred and ninety-six patients were included. In 176 patients (90%), the CSF showed type II OB, 20 (10%) patients were OB negative. There were no differences between age, clinical presentation and EDSS at onset or in the immunomodulatory treatment received between OB+ and OB- patients. Sixty-two (31.6%) patients converted to SPMS during the follow-up, 59 (33.5%) were OB+ and 3 (15%) were OB-. EDSS of 6 was recorded in 56 (28.5%) patients during the follow-up; 54 (31%) were OB+ while only 2 (10%) OB- patients reached this outcome (reach SP phase, P=0.032; HR: 2.2; 95% CI: 1.3-7.5 and EDSS of 6, P=0.037; HR: 1.9; 95% CI: 1.3-8.5). Conclusion: We observed during the follow-up that OB- patients had a better prognosis and milder disability compared to OB+ patients.
引用
收藏
页码:889 / 892
页数:4
相关论文
共 50 条
  • [1] CSF Oligoclonal Bands in Multiple Sclerosis Patients: Worse Prognosis?
    Patrucco, Liliana
    Patrucco, Liliana
    Ignacio Rojas, Juan
    Cristiano, Edgardo
    NEUROLOGY, 2010, 74 (09) : A157 - A157
  • [2] CSF IgG oligoclonal bands and prognosis in multiple sclerosis
    Valado, A.
    Sousa, L.
    Baldeiras, I.
    EUROPEAN JOURNAL OF PUBLIC HEALTH, 2019, 29 : 6 - 6
  • [3] The Effect of Oligoclonal Bands in Patients with Multiple Sclerosis
    Tutar, Nurhan Kaya
    Soylemez, Elif
    Omerhoca, Sami
    Icen, Nilufer Kale
    TURKISH JOURNAL OF NEUROLOGY, 2022, 28 (04) : 217 - 222
  • [4] The identity of oligoclonal bands in patients with multiple sclerosis
    Pointon, Tiffany
    Sundet, Alec
    Ibrahim, Nadeen
    Vollmer, Timothy
    Yu, Xiaoli
    JOURNAL OF NEUROIMMUNOLOGY, 2014, 275 (1-2) : 16 - 16
  • [5] Cerebrospinal fluid oligoclonal bands in multiple sclerosis: prevelance and prognosis
    Acar, N. P.
    Kurne, A. Tuncer
    Sayat, G.
    Pinar, A.
    Karabudak, R.
    MULTIPLE SCLEROSIS JOURNAL, 2013, 19 (11) : 542 - 542
  • [6] Oligoclonal IgG bands in Japanese multiple sclerosis patients
    Nakashima, I
    Fujihara, K
    Itoyama, Y
    JOURNAL OF NEUROIMMUNOLOGY, 1999, 101 (02) : 205 - 206
  • [7] Turkish multiple sclerosis patients with and without oligoclonal bands
    Bilgili, F.
    Akman-Demir, G.
    Saruhan-Direskeneli, G.
    Gurvit, H.
    Coban, O.
    Tumac, A.
    Cetin, S.
    Tanor, O. O.
    Eraksoy, M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2004, 11 : 261 - 262
  • [8] Oligoclonal IgG bands in Japanese multiple sclerosis patients
    Nakashima, I
    Fujihara, K
    Okita, N
    Takase, S
    Itoyama, Y
    NEUROLOGY, 1999, 52 (06) : A437 - A438
  • [9] OLIGOCLONAL BANDS IN SERUM OF PATIENTS WITH MULTIPLE-SCLEROSIS
    MADIEDO, G
    CHERAYIL, GD
    CLINICAL CHEMISTRY, 1988, 34 (10) : 2183 - 2184
  • [10] Multiple sclerosis and oligoclonal bands in tears
    Forzy, G
    Gallois, P
    Hautecoeur, P
    ANNALES DE BIOLOGIE CLINIQUE, 1999, 57 (02) : 240 - 241