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Browsing by Author "Zivanovic, Sandra (35732872100)"

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    Publication
    Evaluation of the effects of different supplementation on oxidative status in patients with rheumatoid arthritis
    (2016)
    Vasiljevic, Dragan (56820314500)
    ;
    Veselinovic, Mirjana (54418120000)
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    Jovanovic, Maja (56727572000)
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    Jeremic, Nevena (56609154900)
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    Arsic, Aleksandra (14031166400)
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    Vucic, Vesna (14049380100)
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    Lucic-Tomic, Aleksandra (36005544100)
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    Zivanovic, Sandra (35732872100)
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    Djuric, Dragan (36016317400)
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    Jakovljevic, Vladimir (56425747600)
    Rheumatoid arthritis is a chronic inflammatory disease. Reactive oxygen species have been considered as aggravating factors for autoimmune diseases. Fatty acids had been linked in reduction of various diseases by augment of their antioxidant potential and antiinflammatory mechanisms. The aim of this study was to assess the oxidative status in patients with rheumatoid arthritis who used concentrated fish oil only or concentrated fish oil in combination with evening primrose oil in a period of 3 months. Subjects were divided into three groups. The group I consists of patients who had been taking only their regular rheumatologic therapy; group II, patients who had been taking concentrated fish oil; and group III, patients who had been taking concentrated fish oil and evening primrose oil. Peripheral blood samples were used for all the assays. We assessed the following oxidative stress markers: index of lipid peroxidation (thiobarbituric acid-reactive substances (TBARS)), hydrogen peroxide (H2O2), superoxide anion radical (O2 −), nitric oxide (NO), superoxide dismutase activity (SOD), catalase activity (CAT), and glutathione levels (GSH) in erythrocytes. There were no statistically significant changes for any of the oxidative stress parameters in group I. In group II, levels of TBARS, NO2 −, and GSH were increased, while levels of H2O2 decreased. Increased values of TBARS, NO2 −, and SOD were found in group III. Our findings indicate that intakes of fish oil and evening primrose oil may be of importance in mitigation of inflammation, disease activity, and oxidative stress biomarkers, through increased activities of antioxidant enzymes. © 2016, International League of Associations for Rheumatology (ILAR).
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    Publication
    Late-onset systemic lupus erythematosus: Clinical features, course, and prognosis
    (2013)
    Tomic-Lucic, Aleksandra (36005544100)
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    Petrovic, Radmila (35475760900)
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    Radak-Perovic, Marija (6507787195)
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    Milovanovic, Dragan (57204473227)
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    Milovanovic, Jasmina (23502044000)
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    Zivanovic, Sandra (35732872100)
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    Pantovic, Suzana (8339783800)
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    Veselinovic, Mirjana (54418120000)
    There are contradictory opinions if late-onset systemic lupus erythematosus (SLE) is associated with a different, more benign disease course and better prognosis than early-onset SLE. The objective of this study was to evaluate the clinical manifestations, course, treatment, and prognosis of late-onset SLE. Patients who developed SLE after/or at the age of 50 years were considered late-onset SLE and compared to a group of randomly selected patients aged younger than 50 years at the diagnosis, matched for disease duration. Lower frequency of cutaneous manifestations (p = 0.01) and higher frequency of cytopenias (p = 0.02) were registrated at the SLE onset in the late-onset group. Atypical clinical presentation of SLE contributed to a longer delay of diagnosis in late-onset SLE patients (p = 0.005), who fullfiled less American College of Rheumatology criteria at the diagnosis (p = 0.022). Cumulative incidence of clinical manifestations showed lower frequency of cutaneous (p = 0.017), neuropsychiatric manifestations (p = 0.021), lupus nephritis (p = 0.006), and higher frequency of Sjogren′s syndrome (p = 0.025) in the late-onset group. Late-onset SLE patients received lower doses of corticosteroid (p = 0.006) and cyclophosphamide (p = 0.001) and had more cyclophosphamide- induced complications (p = 0.005). Higher prevalence of comorbid conditions in the late-onset group (p = 0.025), and higher Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index was noticed (p = 0.018). Despite the less major organ involvement and more benign course of disease, late-onset SLE has poorer prognosis, because of the higher frequency of comorbid conditions and higher organ damage, due to the aging and longer exposition to a classical vascular risk factors. © 2013 Clinical Rheumatology.

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