Adolescent onset of lupus results in moire aggressive disease and worse outcomes:: results of a nested matched case-control study within LUMINA, a multiethnic US cohort (LUMINA LVII)

被引:271
作者
Tucker, L. B. [2 ]
Uribe, A. G. [2 ]
Fenandez, M. [1 ,3 ]
Vila, L. M.
McGwin, G. [1 ]
Apte, M. [1 ]
Fessler, B. J. [1 ]
Bastian, H. M. [1 ]
Reveille, J. D. [4 ]
Alarcon, G. S. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Rheumatol, Birmingham, AL 35294 USA
[2] BC Childrens Hosp, Dept Pediat, Div Pediat, Vancouver, BC, Canada
[3] Univ Puerto Rico, Dept Med, San Juan, PR 00936 USA
[4] Univ Texas Houston, Dept Med, Hlth Sci Ctr, Houston, TX USA
关键词
juvenile-onset SLE; outcome;
D O I
10.1177/0961203307087875
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of this study is to examine the clinical features and outcomes of patients with systemic lupus erythematosus (SLE) whose disease began in adolescence buvenile-onset SLE OSLE)] compared with adult-onset patients [adult-onset SLE (aSLE)] from a large multiethnic cohort. Systemic lupus erythematosus patients of African-American, Caucasian, or Hispanic ethnicity and >= 1 year follow-up were studied in two groups: jSLE (diagnosed at : 18 years); aSLE (diagnosed at 1950 years; matched for gender and disease duration at enrolment). Sociodemographic data, SLE manifestations, disease activity, damage accrual, SLE-related hospitalizations or emergency room visits, drug utilization, mortality and psychosocial characteristics and quality of life were compared. Data were analysed by univariable and multivariable analyses. Seventy-nine patients were studied (31 jSLE, 48 aSLE); 90% were women. Mean (SD) total disease duration was 6.8 (2.7) years in jSLE and 5.6 (3.3) years in aSLE (p = 0.077). Mean age at cohort entry was 18.4 (1.8) and 33.9 (9.2) years in jSLE and aSLE respectively. By univariable analysis, jSLE patients were more commonly of African-American descent, were more likely to have renal and neurological involvements, and to accrue renal damage; jSLE patients had lower levels of helplessness and scored higher in the physical component measure of the SF-36 than aSLE patients. Renal involvement [OR = 1.549, 95% CI (1.397-15.856)] and neurological involvement [OR = 1.642, 95% CI (1.689-15.786)] were independently associated with jSLE by multivariable analysis. There was a larger proportion of African-Americans within the jSLE group. After adjusting for ethnicity and follow-up time, jSLE patients experienced more renal and neurological manifestations, with more renal damage. There was a two-fold higher mortality rate in the jSLE group.
引用
收藏
页码:314 / 322
页数:9
相关论文
共 31 条
[1]   Systemic lupus erythematosus in three ethnic groups.: XIV.: Poverty, wealth, and their influence on disease activity [J].
Alarcón, GS ;
McGwin, G ;
Sanchez, ML ;
Bastian, HM ;
Fessler, BJ ;
Friedman, AW ;
Baethge, BA ;
Roseman, J ;
Reveille, JD .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2004, 51 (01) :73-77
[2]  
Alarcón GS, 1998, ARTHRITIS RHEUM-US, V41, P1173, DOI 10.1002/1529-0131(199807)41:7<1173::AID-ART5>3.0.CO
[3]  
2-A
[4]   Systemic lupus erythematosus in three ethnic groups:: III A comparison of characteristics early in the natural history of the LUMINA cohort [J].
Alarcón, GS ;
Friedman, AW ;
Straaton, KV ;
Moulds, JM ;
Lisse, J ;
Bastian, HM ;
McGwin, G ;
Bartolucci, AA ;
Roseman, JM ;
Reveille, JD .
LUPUS, 1999, 8 (03) :197-209
[5]   Systemic lupus erythematosus in a multiethnic US cohort -: Clinical features, course, and outcome in patients with late-onset disease [J].
Bertoli, Ana M. ;
Alarcon, Graciela S. ;
Calvo-Alen, Jaime ;
Fernandez, Monica ;
Vila, Luis M. ;
Reveille, John D. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (05) :1580-1587
[6]   Risk factors for damage in childhood-onset systemic lupus erythematosus - Cumulative disease activity and medication use predict disease damage [J].
Brunner, HI ;
Silverman, ED ;
To, T ;
Bombardier, C ;
Feldman, BM .
ARTHRITIS AND RHEUMATISM, 2002, 46 (02) :436-444
[7]  
CHALOM EC, 2004, PEDIAT RHEUMATOL ONL, V2, P207
[8]  
Cohen S., 1985, SOCIAL SUPPORT THEOR, P73, DOI DOI 10.1007/978-94-009-5115-0_5
[9]   LEARNED HELPLESSNESS IN SYSTEMIC LUPUS-ERYTHEMATOSUS - ANALYSIS USING THE RHEUMATOLOGY ATTITUDES INDEX [J].
ENGLE, EW ;
CALLAHAN, LF ;
PINCUS, T ;
HOCHBERG, MC .
ARTHRITIS AND RHEUMATISM, 1990, 33 (02) :281-286
[10]   Systemic lupus erythematosus (SLE) in childhood:: analysis of clinical and immunological findings in 34 patients and comparison with SLE characteristics in adults [J].
Font, J ;
Cervera, R ;
Espinosa, G ;
Pallarés, L ;
Ramos-Casals, M ;
Jiménez, S ;
García-Carrasco, M ;
Seisdedos, L ;
Ingelmo, M .
ANNALS OF THE RHEUMATIC DISEASES, 1998, 57 (08) :456-459