The natural history of secondary progressive multiple sclerosis

被引:170
作者
Koch, Marcus [1 ,2 ]
Kingwell, Elaine [2 ]
Rieckmann, Peter [2 ]
Tremlett, Helen [2 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Neurol, NL-9713 GZ Groningen, Netherlands
[2] Univ British Columbia, Fac Med, Div Neurol, Vancouver, BC V5Z 1M9, Canada
基金
加拿大健康研究院;
关键词
PROGNOSTIC-FACTORS; DISABILITY; AGE; ONSET; PHASE;
D O I
10.1136/jnnp.2010.208173
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background The onset of secondary progression is a pivotal event in the course of relapsing-remitting (RR) multiple sclerosis (MS). Patients with secondary progressive MS (SPMS) experience continuous worsening of symptoms independent of the occurrence of relapses. Possible risk factors associated with the onset of SPMS remain under investigated in natural history studies of MS disease course. Methods We used Kaplan-Meier survival analyses and Cox regression models to investigate the influence of gender, onset age and onset symptoms on time to and age at SPMS in British Columbia (BC) MS patients with a RR disease onset who were not exposed to immunomodulatory drugs. Results Of 5778 patients in the BCMS database with definite MS, 5207 (90%) had an RR onset. Median time to SPMS was 21.4 years (95% CI 20.6 to 22.2), reached at a median age of 53.7 years (95% CI 53.1 to 54.3). Male gender and motor onset symptoms were associated with a shorter time to and a younger age at SPMS. A younger age at disease onset was associated with a longer time to SPMS but also with a younger age at secondary progression. Other onset symptoms were not associated with time to, or age at, SPMS. Conclusions We identified three factors influencing the onset of SPMS in untreated patients with RRMS: motor onset symptoms and male gender were associated with both a shorter time to and a younger age at SPMS. A younger age at disease onset should not be viewed as indicating a better prognosis.
引用
收藏
页码:1039 / 1043
页数:5
相关论文
共 29 条
[1]   A prospective study on the natural history of multiple sclerosis: clues to the conduct and interpretation of clinical trials [J].
Amato, MP ;
Ponziani, G ;
Bartolozzi, ML ;
Siracusa, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 168 (02) :96-106
[2]   Predicting secondary progression in relapsing-remitting multiple sclerosis: a Bayesian analysis [J].
Bergamaschi, R ;
Berzuini, C ;
Romani, A ;
Cosi, V .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2001, 189 (1-2) :13-21
[3]   Multiple sclerosis [J].
Compston, A ;
Coles, A .
LANCET, 2002, 359 (9313) :1221-1231
[4]  
Compston A., 1998, MCALPINES MULTIPLE S
[5]   Age at disability milestones in multiple sclerosis [J].
Confavreux, C ;
Vukusic, S .
BRAIN, 2006, 129 :595-605
[6]   Rate of pregnancy-related relapse in multiple sclerosis [J].
Confavreux, C ;
Hutchinson, M ;
Hours, MM ;
Cortinovis-Tourniaire, P ;
Moreau, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (05) :285-291
[7]   Multiple sclerosis with a progressive course from onset in Lorraine-Eastern France [J].
Debouverie, Marc ;
Louis, Sarah ;
Pittion-Vouyovitch, Sophie ;
Roederer, Thomas ;
Vespignani, Herve .
JOURNAL OF NEUROLOGY, 2007, 254 (10) :1370-1375
[8]   SPINAL-CORD MRI USING MULTIARRAY COILS AND FAST SPIN-ECHO .2. FINDINGS IN MULTIPLE-SCLEROSIS [J].
KIDD, D ;
THORPE, JW ;
THOMPSON, AJ ;
KENDALL, BE ;
MOSELEY, IF ;
MACMANUS, DG ;
MCDONALD, WI ;
MILLER, DH .
NEUROLOGY, 1993, 43 (12) :2632-2637
[9]   Factors associated with the risk of secondary progression in multiple sclerosis [J].
Koch, M. ;
Uyttenboogaart, M. ;
van Harten, A. ;
De Keyser, J. .
MULTIPLE SCLEROSIS JOURNAL, 2008, 14 (06) :799-803
[10]   Progression in multiple sclerosis: Further evidence of an age dependent process [J].
Koch, Marcus ;
Mostert, Jop ;
Heersema, Dorothea ;
De Keyser, Jacques .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2007, 255 (1-2) :35-41