期刊论文详细信息
Kidney and Blood Pressure Research
The Clinical Significance of Uric Acid and Complement Activation in the Progression of IgA Nephropathy
Caliskan Y.1  Oztop N.3  Aksoy A.3  Kilicaslan I.2  Sever M.S.1  Celik D.1  Ucar A.S.1  Ozluk Y.2  Yazici H.1 
[1] Division of Nephrology, Department of Internal Medicine, $$;Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey$$
关键词: Biomarkers;    Complement;    End stage renal disease;    IgA Nephropathy;    Uric acid;   
DOI  :  10.1159/000443415
来源: S Karger AG
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【 摘 要 】

Background/Aims: The aim of this study is to investigate the utility of clinical [age, gender, mean arterial pressure (MAP)] and laboratory parameters [eGFR, hemoglobin (Hgb), serum levels of creatinine, uric acid, albumin, proteinuria, hematuria] and also histopathological lesions (Oxford classification parameters, crescents, intensity and pattern of staining for C3, C1Q, IgA, IgG, IgM) as progression markers in patients with IgA Nephropathy (IgAN). Methods: A total of 111 IgAN patients with a follow-up period >1 year or who reached kidney failure [GFR category G5 chronic kidney disease (CKD)] <1 year were investigated. Primary endpoint was the development of kidney failure or eGFR decline ≥50% from the baseline. Kaplan-Meier and Cox proportional hazards analyses were performed. Results: Mean follow-up period was 33±29 months. Thirty-seven (33.3%) patients progressed to kidney failure and 4 (3.6%) patients developed eGFR decline ≥50% from the baseline after a median of 23 and 65 months, respectively. In multivariate Cox regression analysis, baseline levels of Hgb (HR:0.782, 95% CI 0.559-0.973, p=0.037), serum uric acid (HR:1.293, 95% CI 1.023-1.621, p=0.046), eGFR (HR:0.966, 95% CI 0.947-0.984, p=0.004) and intensity of C3 staining (HR:1.550, 95% CI 1.198-1.976, p=0.049) predicted primary endpoint. Serum uric acid level was associated independently with T score (β=0.303, p=0.005) in patients with eGFR>30 ml/min/m2. Conclusions: Hyperuricemia and the deposition of C3 are independent risk factors for IgAN progression.

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