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Febuxostat is superior to allopurinol in delaying the progression of renal impairment in patients with chronic kidney disease and hyperuricemia

机译:Febuxostat优于Allopurinol,延迟慢性肾病患者肾损伤进展和高尿酸血症

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Purpose This study aimed to compare efficacy of renal-protective function between febuxostat and allopurinol in patients with chronic kidney disease (CKD) and hyperuricemia (HUA). Methods Totally 152 CKD stage 2-3 patients complicated with HUA were recruited. According to their uric acid-lowering therapy, there were 67 patients included in febuxostat group and 85 in allopurinol group, respectively. Estimated glomerular filtration rate (eGFR), serum creatinine (Scr), 24-h proteinuria, serum uric acid (SUA) were measured at M0, M1, M3 and M6 after the treatment. Primary outcome was proportion of patients showing >= 10% decline in eGFR from baseline at M6. Results The eGFR at M6 was numerically higher at M6 and eGFR change (M6-M0) was increased in febuxostat group compared with allopurinol group. Most importantly, the proportion of patients showing a >= 10% decline in eGFR from baseline at M6 was reduced in febuxostat group compared with allopurinol group. Multivariate logistic regression analyses further validated that febuxostat vs. allopurinol was an independent predictor for reduced risk of eGFR decline >= 10% from baseline. Besides, SUA change (M6-M0) was decreased, but Scr change (M6-M0) and 24-h proteinuria change (M6-M0) were similar in febuxostat group compared with allopurinol group. Conclusions Febuxostat presents a superior effect in delaying renal impairment progression compared with allopurinol in CKD patients complicated with HUA.
机译:目的本研究旨在比较慢性肾疾病(CKD)和高尿血症(HUA)患者肾脏保护功能与血尿病患者的疗效。方法完全152阶段2-3款复杂的华盛患者被招募。根据尿酸酸性酸性治疗,分别存在67名患者,分别包括85例Allopurinol组。在治疗后,测量估计肾小球过滤速率(EGFR),血清肌酐(SCR),24-H蛋白浆液,血清尿酸(SUA)。主要结果是患者的比例显示> =从M6的基线egfr下降10%。结果M6的EGFR在M6的数量上较高,与Allopurinol基团相比,Febuxostat组的EGFR变化(M6-M0)增加。最重要的是,与Allopurinol基团相比,Febuxostat组的患者从M6的基线下降的患者的比例从M6的基线降低。多变量逻辑回归分析进一步验证了Febuxostat与Allopurinol是一个独立的预测因子,用于降低EGFR下降的风险> = =基线10%。此外,SUA变化(M6-M0)降低,但与Allopurinol基团相比,SCS变化(M6-M0)和24-H蛋白豇豆(M6-M0)相似。结论Febuxostat对延迟肾脏损伤进展的效果促进了肾脏损伤,与CKD患者的Allopurinol复杂化。

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