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IgA/C3 比值在 IgA 肾病预后中的作用?一项基于欧洲人群的结局分析。

Is There a Role for IgA/C3 Ratio in IgA Nephropathy Prognosis? An Outcome Analysis on An European Population.

机构信息

Dr. Carol Davila Teaching Hospital of Nephrology, University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

出版信息

Iran J Kidney Dis. 2020 Dec;14(6):470-477.

Abstract

INTRODUCTION

Serum immunoglobulin A (IgA)/C3 ratio has been reported as a predictor of histological lesions and prognosis in asian patients with IgA nephropathy (IgAN). Since its validity in other populations is unclear, we aimed to evaluate the relationship between IgA/C3 ratio and renal outcome in Caucasian European patients with biopsy-proven IgAN.

METHODS

We conducted a retrospective, observational study on 95 patients with primary IgAN patients diagnosed between 2010 to 2017 (70% male, age 41 (34 to 49) years, eGFR 39.4 (25.2 to 56.5) mL/ min, proteinuria 1.7 (0.8 to 3.0) g/g). The primary study composite end-point was doubling of serum creatinine, ESRD (dialysis or renal transplant) or death, whichever came first.

RESULTS

Median follow-up was 30 (95% CI: 27.5 to 32.4) months; 11% developed ESRD, 10% experienced serum creatinine doubling, and 1% died. The endpoint was reached by 21% of the patients. They had lower eGFR, higher proteinuria and hematuria, and lower serum albumin. The distribution in Oxford classes was alike. The AUROC for IgA/C3 ratio was 0.60 (95% CI: 0.45 to 0.74) and generated an optimal cut-off of 2.91 (sensitivity 68%, specificity 55%). The mean event-free survival of the whole cohort was 5.2 (95% CI: 4.7 to 5.8) years. Patients with IgA/C3 ratio < 2.9 had a tendency to better renal survival (P > .05). In Cox proportional hazard ratio model, the independent predictors of a poorer eventfree survival were higher serum creatinine, higher proteinuria and increased IgA/C3 ratio, while renin angiotensin system inhibitors predicted better outcome.

CONCLUSION

Our study reports evidence that supports IgA/C3 ratio as a reasonable predictor of IgAN prognosis in European patients.

摘要

简介

血清免疫球蛋白 A(IgA)/C3 比值已被报道为亚洲 IgA 肾病(IgAN)患者组织学病变和预后的预测指标。由于其在其他人群中的有效性尚不清楚,我们旨在评估 IgA/C3 比值与经活检证实的 IgAN 欧洲白人患者肾结局之间的关系。

方法

我们对 2010 年至 2017 年间诊断为原发性 IgAN 的 95 例患者进行了回顾性、观察性研究(70%为男性,年龄 41(34 至 49)岁,eGFR 39.4(25.2 至 56.5)mL/min,蛋白尿 1.7(0.8 至 3.0)g/g)。主要研究复合终点是血清肌酐加倍、终末期肾病(透析或肾移植)或死亡,以先发生者为准。

结果

中位随访时间为 30 个月(95%CI:27.5 至 32.4);11%的患者发展为终末期肾病,10%的患者发生血清肌酐加倍,1%的患者死亡。21%的患者达到了终点。他们的 eGFR 较低,蛋白尿和血尿较多,血清白蛋白较低。牛津分类的分布相似。IgA/C3 比值的 AUROC 为 0.60(95%CI:0.45 至 0.74),并产生了 2.91 的最佳截断值(敏感性 68%,特异性 55%)。整个队列的平均无事件生存时间为 5.2 年(95%CI:4.7 至 5.8)。IgA/C3 比值<2.91 的患者有更好的肾脏生存趋势(P>0.05)。在 Cox 比例风险比例模型中,较差的无事件生存的独立预测因素是较高的血清肌酐、较高的蛋白尿和增加的 IgA/C3 比值,而肾素-血管紧张素系统抑制剂预测更好的结果。

结论

我们的研究报告了支持 IgA/C3 比值作为欧洲患者 IgAN 预后合理预测指标的证据。

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