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  • The Journal of Rheumatology  (6)
  • Medizin  (6)
Materialart
Verlag/Herausgeber
  • The Journal of Rheumatology  (6)
Sprache
Erscheinungszeitraum
Fachgebiete(RVK)
  • Medizin  (6)
RVK
  • 1
    Online-Ressource
    Online-Ressource
    The Journal of Rheumatology ; 2009
    In:  The Journal of Rheumatology Vol. 36, No. 8 ( 2009-08), p. 1691-1698
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 36, No. 8 ( 2009-08), p. 1691-1698
    Kurzfassung: The relationship among serum uric acid (SUA), metabolic syndrome, and chronic kidney disease (CKD) is unclear. We examined whether SUA level is an independent risk factor for chronic kidney disease and whether the association between SUA and metabolic syndrome is affected by kidney function. Methods. We analyzed 28,745 subjects (17,478 men, 11,267 women, age 20–49 yrs) who underwent health examinations at this hospital between 2000 and 2007. Hyperuricemia was defined as SUA level 〉 7.7 mg/dl in men or 〉 6.6 mg/dl in women. Kidney function was assessed by estimated glomerular filtration rate (eGFR) using the Modification of Diet in Renal Disease Study equation modified for Chinese subjects. Impaired renal function with low GFR was defined as eGFR 〈 90 ml/min/1.73 m 2 . The UA-low GFR groups were defined according to the observed combination of hyperuricemia and low GFR: Group A (absence of both hyperuricemia and low GFR); Group B (presence of low GFR but no hyperuricemia); Group C (presence of hyperuricemia but not low GFR); and Group D (presence of both hyperuricemia and low GFR). Results. The prevalence of hyperuricemia, metabolic syndrome, and impaired kidney function with low GFR was 20.3% (27.6% in men, 8.9% in women), 7.6% (10.6% in men, 3.0% in women), and 9.9% (11.6% in men, 7.1% in women), respectively. The Pearson correlation between SUA and eGFR was only −0.26 (−0.21 in men, −0.22 in women; p 〈 0.001). In men, the age-adjusted odds ratio (OR) of metabolic syndrome was 1.41 (Group B), 2.45 (Group C), and 2.58 (Group D) in comparison with Group A. In women, the age-adjusted OR of metabolic syndrome was 0.83 (Group B), 5.47 (Group C), and 3.31 (Group D) in comparison with Group A. Conclusion. Hyperuricemia is prevalent in the Taiwan population. Hyperuricemia is only weakly associated with renal function, but is strongly associated with metabolic syndrome with or without a low eGFR.
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2009
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 41, No. 8 ( 2014-08), p. 1662-1669
    Kurzfassung: Pulmonary involvement is common in patients with systemic sclerosis (SSc), and this condition causes substantial morbidity and mortality. Disrupted immunity from the disease or associated medication may render such patients subject to tuberculosis (TB) infection. However, the relationship between SSc and TB has not yet been investigated. Methods. Using the Taiwan National Health Insurance Research Database, 838 patients with SSc diagnosed in Taiwan during 2000–2006 were identified and followed for emergence of TB infection. Incidence rate ratios (IRR) of TB compared to 8380 randomly selected age-, sex-, and comorbidity-matched controls without SSc were calculated. The Cox proportional hazards model was used for multivariate adjustment to identify independent risk factors for TB infection. Results. The risk of TB infection was higher in the SSc cohort than in controls (IRR 2.81, 95% CI 1.36–5.37; p = 0.004), particularly for pulmonary TB (IRR 2.53, 95% CI 1.08–5.30; p = 0.022). Other independent risk factors for TB infection in patients with SSc were age ≥ 60 years [hazard ratio (HR) 3.52, 95% CI 1.10–11.33; p = 0.035] and pulmonary hypertension (PH; HR 6.06, 95% CI 1.59–23.17; p = 0.008). Mortality did not differ for SSc patients with or without TB. Conclusion. In this nationwide study, the incidence of TB infection was significantly higher among patients with SSc than in controls without SSc. Special care should be taken in managing patients with SSc who are at high risk for TB, especially those aged ≥ 60 years or who also have PH.
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2014
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 41, No. 6 ( 2014-06), p. 1104-1111
    Kurzfassung: Bone loss is a recognized feature of ankylosing spondylitis (AS). The binding of microRNA-21 (miR-21) to programmed cell death 4 (PDCD4) could inhibit the expression of PDCD4 and further induce the activation of osteoclasts. In the present study, we compared the difference in miR-21 expression between patients with AS and healthy controls, and evaluated the relationships of miR-21, PDCD4 mRNA, and bone erosion in patients with AS. The influences of nonsteroidal antiinflammatory drugs (NSAID) and disease-modifying antirheumatic drugs (DMARD) on the expressions of miR-21 and PDCD4 mRNA in patients with AS were also assessed. Methods. Whole blood miR-21 and PDCD4 mRNA expression were evaluated by quantitative real-time PCR among 122 patients with AS and 122 healthy controls. The serum level of collagen cross-linked C-telopeptide (CTX) was measured using ELISA. Results. When compared to controls, patients with AS had significantly higher levels of miR-21, PDCD4 mRNA, and CTX. MiR-21 expression was negatively correlated with PDCD4 mRNA expression in patients with AS who were taking neither NSAID nor DMARD. Interestingly, significantly positive correlations between miR-21 expression with PDCD4 mRNA expression (r = 0.33, p = 0.01) and CTX level (r = 0.44, p 〈 0.01) were observed in patients with AS who were taking sulfasalazine. Positive correlations of miR-21 and CTX level were also observed in AS patients with disease duration 〈 7.0 years (r = 0.36, p = 0.004) and active disease (r = 0.42, p = 0.001). Conclusion. The expression of miR-21 might have a role in the development of AS.
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2014
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 37, No. 1 ( 2010-01), p. 45-52
    Kurzfassung: Systemic lupus erythematosus (SLE) is a prototype of systemic autoimmune disease in which cytokines such as B lymphocyte chemoattractant (BLC, or CXC motif ligand 13, CXCL13) may play important roles in pathogenesis. We investigated the implications of CXCL13 in SLE and lupus nephritis. Methods. Serum samples from 425 patients with SLE and 106 healthy control individuals were analyzed for the concentration of CXCL13 by ELISA. Tissue expression of CXCL13 and its corresponding receptor CXCR5 were observed in lupus kidney. The CXCR5-bearing B cells in SLE patients were analyzed by flow cytometry. Results. Serum levels of CXCL13 were higher in SLE patients compared to controls. SLE patients with lupus nephritis or positive anti-dsDNA antibodies had significantly higher serum CXCL13 levels. The peripheral venous blood B cells that bear CXCR5 were more abundant in SLE patients as detected by flow cytometry. CXCR5 and CXCL13 were highly expressed in the renal cortex from patients with lupus nephritis. Conclusions. Our results suggest that BLC/CXCL13 as well as its corresponding receptor, CXCR5, may play important roles in the pathogenesis of SLE and in lupus nephritis.
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2010
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Online-Ressource
    Online-Ressource
    The Journal of Rheumatology ; 2014
    In:  The Journal of Rheumatology Vol. 41, No. 5 ( 2014-05), p. 909-915
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 41, No. 5 ( 2014-05), p. 909-915
    Kurzfassung: Studies of the risks of deep vein thrombosis (DVT) and pulmonary embolism (PE) in patients with Sjögren syndrome (SS) in Asia are scant. We evaluated the effect of SS on the incidences of DVT and PE in a nationwide, population-based cohort in Taiwan. Methods. We identified patients in Taiwan diagnosed with SS between 1998 and 2008 in the Catastrophic Illness Patient Database and the National Health Insurance Research Database. Each patient with SS was matched to 4 control patients based on age, sex, and index year, and all patients were followed up from the index date to December 31, 2010. We calculated the hazard ratios (HR) and 95% CI of DVT and PE in the SS and comparison cohorts by using Cox proportional hazards regression models. Results. We followed 8920 patients with SS and a comparison cohort of 35,680 for about 50,000 and 200,000 person-years, respectively. The mean age of the SS and comparison cohorts was 53.5 and 53.1 years, respectively, and 88.9% of the patients were women. The risks of DVT and PE among the patients with SS were a 1.83-fold and 3.29-fold greater, respectively, than those for the general population after adjusting for age, sex, comorbidities, and frequency of hospitalization. The patients with a secondary SS had a greater risk of PE (adjusted HR: 5.06; 95% CI: 1.22–21.1) than those with a primary SS (adjusted HR: 3.21; 95% CI: 1.96–5.23). Conclusion. Patients with SS have a significantly greater risk of developing DVT or PE than the general population.
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2014
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Online-Ressource
    Online-Ressource
    The Journal of Rheumatology ; 2011
    In:  The Journal of Rheumatology Vol. 38, No. 11 ( 2011-11), p. 2488-2489
    In: The Journal of Rheumatology, The Journal of Rheumatology, Vol. 38, No. 11 ( 2011-11), p. 2488-2489
    Materialart: Online-Ressource
    ISSN: 0315-162X , 1499-2752
    RVK:
    Sprache: Englisch
    Verlag: The Journal of Rheumatology
    Publikationsdatum: 2011
    Standort Signatur Einschränkungen Verfügbarkeit
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