8-epi-prostaglandin-f2alpha and Lupus-Erythematosus--Systemic

8-epi-prostaglandin-f2alpha has been researched along with Lupus-Erythematosus--Systemic* in 3 studies

Trials

1 trial(s) available for 8-epi-prostaglandin-f2alpha and Lupus-Erythematosus--Systemic

ArticleYear
A randomised interventional trial of omega-3-polyunsaturated fatty acids on endothelial function and disease activity in systemic lupus erythematosus.
    Annals of the rheumatic diseases, 2008, Volume: 67, Issue:6

    To determine the clinical effect of dietary supplementation with low-dose omega-3-polyunsaturated fatty acids on disease activity and endothelial function in patients with systemic lupus erythematosus.. A 24-week randomised double-blind placebo-controlled parallel trial of the effect of 3 g of omega-3-polyunsaturated fatty acids on 60 patients with systemic lupus erythematosus was performed. Serial measurements of disease activity using the revised Systemic Lupus Activity Measure (SLAM-R) and British Isles Lupus Assessment Group index of disease activity for systemic lupus erythematosus (BILAG), endothelial function using flow-mediated dilation (FMD) of the brachial artery, oxidative stress using platelet 8-isoprostanes and analysis of platelet membrane fatty acids were taken at baseline, 12 and 24 weeks.. In the fish oil group there was a significant improvement at 24 weeks in SLAM-R (from 9.4 (SD 3.0) to 6.3 (2.5), p<0.001); in BILAG (from 13.6 (6.0) to 6.7 (3.8), p<0.001); in FMD (from 3.0% (-0.5 to 8.2) to 8.9% (1.3 to 16.9), p<0.001) and in platelet 8-isoprostanes (from 177 pg/mg protein (23-387) to 90 pg/mg protein (32-182), p = 0.007).. Low-dose dietary supplementation with omega-3 fish oils in systemic lupus erythematosus not only has a therapeutic effect on disease activity but also improves endothelial function and reduces oxidative stress and may therefore confer cardiovascular benefits.

    Topics: Adult; Biomarkers; Brachial Artery; Cell Membrane; Dietary Supplements; Dinoprost; Docosahexaenoic Acids; Double-Blind Method; Eicosapentaenoic Acid; Endothelium, Vascular; Fatty Acids, Omega-3; Fatty Acids, Unsaturated; Female; Humans; Lupus Erythematosus, Systemic; Male; Middle Aged; Nitroglycerin; Regional Blood Flow; Statistics, Nonparametric; Treatment Outcome; Ultrasonography, Doppler, Pulsed; Vasodilation; Vasodilator Agents

2008

Other Studies

2 other study(ies) available for 8-epi-prostaglandin-f2alpha and Lupus-Erythematosus--Systemic

ArticleYear
Relationship between iron metabolism, oxidative stress, and insulin resistance in patients with systemic lupus erythematosus.
    Scandinavian journal of rheumatology, 2013, Volume: 42, Issue:4

    The aim of the present study was to assess oxidative stress and iron metabolism in systemic lupus erythematosus (SLE) patients with and without insulin resistance (IR).. This study included 236 subjects (125 controls and 111 SLE patients). Patients with SLE were divided in two groups: with (n = 72) or without (n = 39) IR.. SLE patients with IR showed higher advanced oxidation protein product (AOPP) levels (p = 0.030) and gamma-glutamyltransferase (GGT) levels (p = 0.001) and lower sulfhydryl groups of proteins (p = 0.0002) and total radical-trapping antioxidant parameter (TRAP) corrected by uric acid (UA) levels (p = 0.04) when compared to SLE patients without IR. However, SLE patients with IR presented lower serum 8-isoprostane (p = 0.05) and carbonyl protein levels (p = 0.04) when compared to SLE patients without IR. Serum ferritin levels were significantly higher in SLE patients (p = 0.0006) than in controls, and SLE patients with IR presented higher serum ferritin levels (p = 0.01) than SLE patients without IR. Patients with SLE showed that IR was inversely correlated to TRAP/UA (r = -0.2724, p = 0.0008) and serum ferritin was positively correlated to AOPP (r = 0.2870, p = 0.004).. This study found that oxidative stress was higher in the group of SLE patients with IR, and increased ferritin, whether caused by the inflammatory process per se or hyperinsulinaemia, can favour the redox process. In addition, the preset data reinforce the need to measure oxidative stress with several methodologies with different assumptions.

    Topics: Adult; Age Factors; Anthropometry; Biomarkers; Case-Control Studies; Dinoprost; Disease Progression; Female; Ferritins; Follow-Up Studies; gamma-Glutamyltransferase; Humans; Insulin Resistance; Lupus Erythematosus, Systemic; Male; Middle Aged; Oxidative Stress; Sex Factors; Statistics, Nonparametric

2013
Oxidative stress in systemic lupus erythematosus and allied conditions with vascular involvement.
    Rheumatology (Oxford, England), 1999, Volume: 38, Issue:6

    To evaluate the occurrence and clinical significance of lipid peroxidation (oxidative stress) in rheumatic diseases characterized by vascular involvement.. Plasma 8-epi-PGF2alpha (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, n = 6], 12 with rheumatoid arthritis (RA) and in 23 healthy controls (n = 23).. 8-epi-PGF2alpha 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-PGF2alpha concentrations (P = 0.004 and P = 0.001, respectively). SLE patients not taking prednisolone showed higher 8-epi-PGF2alpha concentrations than SLE patients on prednisolone (P = 0.02). In the latter group, a dose response relationship was noted between 8-epi-PGF2alpha and steroid dosage (r = 0.6, P = 0.0003). In WG and CSS, 8-epi-PGF2alpha concentrations correlated with disease activity (r = 0.8, P = 0.01) and were higher than in patients with Behcet disease (P = 0.003).. 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.

    Topics: Adult; Aged; Autoimmune Diseases; Dinoprost; Female; Humans; Lipid Peroxidation; Lupus Erythematosus, Systemic; Male; Middle Aged; Oxidative Stress; Vascular Diseases; Vasoconstrictor Agents

1999