Serum concentrations of alpha tocopherol, beta carotene, and retinol preceding the diagnosis of rheumatoid arthritis and systemic lupus erythematosus

被引:92
作者
Comstock, GW
Burke, AE
Hoffman, SC
Helzlsouer, KJ
Bendich, A
Masi, AT
Norkus, EP
Malamet, RL
Gershwin, ME
机构
[1] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,DEPT EPIDEMIOL,BALTIMORE,MD
[2] HOFFMANN LAROCHE,HUMAN NUTR RES,PARAMUS,NJ
[3] UNIV ILLINOIS,COLL MED,DEPT MED,PEORIA,IL 61656
[4] OUR LADY MERCY MED CTR,BRONX,NY
[5] UNIV CALIF DAVIS,SCH MED,DIV RHEUMATOL ALLERGY & CLIN IMMUNOL,DAVIS,CA 95616
关键词
D O I
10.1136/ard.56.5.323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives-Because oxidative damage has been implicated in the pathogenesis of rheumatoid arthritis and systemic lupus erythematosus, this study was designed to see if serum concentrations of alpha tocopherol, beta carotene, and retinol, substances believed to be involved in the prevention or repair of oxidative damage, might be lower among persons who develop rheumatoid arthritis or systemic lupus erythematosus than among those who do not. Methods-For this prospective case-control study, persons with rheumatoid arthritis and systemic lupus erythematosus that developed two to 15 years after donating blood for a serum bank in 1974 were designated as cases. For each case, four controls were selected from the serum bank donors, matched for race, sex, and age. Stored serum samples from cases and controls were assayed for alpha tocopherol, beta carotene, and retinol. Results-Cases of both diseases had lower serum concentrations of alpha tocopherol, beta carotene, and retinol in 1974 than their matched controls. For rheumatoid arthritis, the difference for beta carotene (-29%) was statistically significant. Conclusions-These findings support those of a previous study that low antioxidant status is a risk factor for rheumatoid arthritis. They suggest a similar association for systemic lupus erythematosus.
引用
收藏
页码:323 / 325
页数:3
相关论文
共 15 条
[1]  
Bendich Adrianne, 1996, Journal of Nutritional Immunology, V4, P47
[2]   REACTIVE OXYGEN SPECIES DAMAGE TO DNA AND ITS ROLE IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
BLOUNT, S ;
GRIFFITHS, HR ;
LUNEC, J .
MOLECULAR ASPECTS OF MEDICINE, 1991, 12 (02) :93-105
[3]   SERUM ANTIOXIDANTS AND RISK OF RHEUMATOID-ARTHRITIS [J].
HELIOVAARA, M ;
KNEKT, P ;
AHO, K ;
AARAN, RK ;
ALFTHAN, G ;
AROMAA, A .
ANNALS OF THE RHEUMATIC DISEASES, 1994, 53 (01) :51-53
[4]   ADULT AND JUVENILE RHEUMATOID-ARTHRITIS - CURRENT EPIDEMIOLOGIC CONCEPTS [J].
HOCHBERG, MC .
EPIDEMIOLOGIC REVIEWS, 1981, 3 :27-44
[5]  
HONKANEN V, 1989, CLIN EXP RHEUMATOL, V7, P465
[6]  
LUNEC J, 1981, J RHEUMATOL, V8, P233
[7]   FLUORESCENT LIPID-PEROXIDATION PRODUCTS IN SYNOVIAL-FLUID [J].
LUNEC, J ;
DORMANDY, TL .
CLINICAL SCIENCE AND MOLECULAR MEDICINE, 1979, 56 (01) :53-59
[8]   FREE-RADICALS AND INFLAMMATION - PROTECTION OF SYNOVIAL-FLUID BY SUPEROXIDE-DISMUTASE [J].
MCCORD, JM .
SCIENCE, 1974, 185 (4150) :529-531
[9]   OXYGEN FREE-RADICALS, INFLAMMATION, AND SYNOVITIS - THE CURRENT STATUS [J].
MERRY, P ;
WINYARD, PG ;
MORRIS, CJ ;
GROOTVELD, M ;
BLAKE, DR .
ANNALS OF THE RHEUMATIC DISEASES, 1989, 48 (10) :864-870
[10]  
ROPES M W, 1958, Bull Rheum Dis, V9, P175