Oxidative stress in systemic lupus erythematosus and allied conditions with vascular involvement

被引:86
作者
Ames, PRJ
Alves, J
Inanc, M
Isenberg, DA
Nourooz-Zadeh, J
机构
[1] St Thomas Hosp, Dept Haematol, London SE1 7EH, England
[2] Curry Cabral Hosp, Autoimmune Dis Unit, Lisbon, Portugal
[3] UCL, Bloomsbury Ctr Rheumatol, London, England
[4] UCL, Inst Nephrol, Dept Med, London, England
关键词
systemic lupus erythematosus; vasculitis; atherosclerosis; prednisolone; oxidative stress;
D O I
10.1093/rheumatology/38.6.529
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To evaluate the occurrence and clinical significance of lipid peroxidation (oxidative stress) in rheumatic diseases characterized by vascular involvement. Patients and methods. Plasma 8-epi-PGF(2 alpha) (oxidative stress marker) was measured by gas chromatography-mass spectrometry in 36 patients with systemic lupus erythematosus (SLE), 13 with systemic sclerosis (SSc), 13 with systemic vasculitis [Wegener's granulomatosis (WG), n = 4; Churg-Strauss syndrome (CSS), n = 3; Behcet syndrome, rr = 6], 12 with rheumatoid arthritis (RA) and in 23 healthy controls (n = 23). Results. 8-epi-PGF(2 alpha) levels were higher in patients with SLE (P = 0.007), SSc (P < 0.001) and vasculitis (P = 0.001) than in controls. In SLE, a positive Coombs' test and arterial hypertension independently predicted 8-epi-PGF(2 alpha) concentrations (P = 0.004 and P = 0.001, respectively). SLE patients not taking prednisolone showed higher 8-epi-PGF(2 alpha) concentrations than SLE patients on prednisolone (P = 0.02). In the latter group, a dose-response relationship was noted between 8-epi-PGF(2 alpha) and steroid dosage (I = 0.6, P = 0.0003). In WG and CSS, 8-epi-PGF(2 alpha) concentrations correlated with disease activity (r = 0.8, P = 0.01) and were higher than in patients with Behcet disease (P = 0.003). Conclusions. Oxidative stress may be pathogenetically relevant in some autoimmune rheumatic diseases with vascular involvement. Amelioration of some clinical manifestations of these diseases may be envisaged by targeting lipid peroxidation with dietary or pharmacological antioxidants.
引用
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页码:529 / 534
页数:6
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