Effect of gender on late-onset multiple sclerosis

被引:88
作者
Bove, Riley M. [1 ]
Healy, Brian [1 ,2 ]
Augustine, Ann [1 ]
Musallam, Alexander [1 ]
Gholipour, Taha [1 ]
Chitnis, Tanuja [1 ]
机构
[1] Brigham & Womens Hosp, Partners Multiple Sclerosis Ctr, Brookline, MA 02445 USA
[2] Massachusetts Gen Hosp, Biostat Ctr, Boston, MA 02114 USA
关键词
multiple sclerosis; geriatrics; progression; disability; female; menopause; CLINICAL CHARACTERISTICS; SEX-RATIO; AGE; DISABILITY; BRAIN; RISK; ENHANCEMENT; POPULATION; IMPAIRMENT; PREDICTORS;
D O I
10.1177/1352458512438236
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: We aimed to examine the incidence and disease course of late-onset multiple sclerosis (LOMS) compared with adult-onset MS (AOMS) in our clinic cohort, stratified based on gender and race, since both have been reported as important modifiers of disease outcomes in MS. Methods: Patients with LOMS and AOMS were compared in terms of demographic characteristics and disease course characteristics. Combined effects were investigated with a logistic regression model. Time from disease onset to sustained Expanded Disability Status Scale (EDSS) score of 6 was investigated using an extension of log-rank test appropriate for interval-censored data. Results: Some 7.96% of 4273 patients studied had an onset of MS after the age of 50 years (LOMS), and 1.33% experienced an onset after age 60. Progressive onset was more common in LOMS relative to AOMS. The proportion of women with progressive-onset disease was similar in AOMS and LOMS. Time to EDSS 6 was delayed in AOMS females compared with males; however, it was similar between males and females in the LOMS group. Conclusions: Women with LOMS have a different trajectory in terms of disease progression than women with AOMS. The effect of menopause combined with race/ethnicity on the MS disease course requires further investigation.
引用
收藏
页码:1472 / 1479
页数:8
相关论文
共 51 条
[1]   MULTIPLE-SCLEROSIS WITH VERY LATE-ONSET - REPORT OF 6 CASES AND REVIEW OF THE LITERATURE [J].
AZZIMONDI, G ;
STRACCIARI, A ;
RINALDI, R ;
DALESSANDRO, R ;
PAZZAGLIA, P .
EUROPEAN NEUROLOGY, 1994, 34 (06) :332-336
[2]   Risk factors for and management of cognitive dysfunction in multiple sclerosis [J].
Benedict, Ralph H. B. ;
Zivadinov, Robert .
NATURE REVIEWS NEUROLOGY, 2011, 7 (06) :332-342
[3]   Demographics of pediatric-onset multiple sclerosis in an MS center population from the Northeastern United States [J].
Chitnis, T. ;
Glanz, B. ;
Jaffin, S. ;
Healy, B. .
MULTIPLE SCLEROSIS, 2009, 15 (05) :627-631
[4]   Pediatric multiple sclerosis [J].
Chitnis, Tanuja .
NEUROLOGIST, 2006, 12 (06) :299-310
[5]   Modification of Multiple Sclerosis Phenotypes by African Ancestry at HLA [J].
Cree, Bruce A. C. ;
Reich, David E. ;
Khan, Omar ;
De Jager, Philip L. ;
Nakashima, Ichiro ;
Takahashi, Toshiyuki ;
Bar-Or, Amit ;
Tong, Christine ;
Hauser, Stephen L. ;
Oksenberg, Jorge R. .
ARCHIVES OF NEUROLOGY, 2009, 66 (02) :226-233
[6]  
de Seze J, 2005, EUR J NEUROL, V12, P241
[7]  
Dean G, 1970, Trans Am Neurol Assoc, V95, P232
[8]  
Delalande S, 2002, REV NEUROL-FRANCE, V158, P1082
[9]   Enhancement frequency decreases with increasing age in relapsing-remitting multiple sclerosis [J].
Filippi, M ;
Wolinsky, JS ;
Sormani, MP ;
Comi, G .
NEUROLOGY, 2001, 56 (03) :422-423
[10]   A PROPORTIONAL HAZARDS MODEL FOR INTERVAL-CENSORED FAILURE TIME DATA [J].
FINKELSTEIN, DM .
BIOMETRICS, 1986, 42 (04) :845-854