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免疫抑制治疗在 3 或 4 期慢性肾脏病 IgA 肾病中的预后作用。

The prognostic effect of immunosuppressive therapy in IgA nephropathy with stage 3 or 4 chronic kidney disease.

机构信息

Department of Nephrology, Xijing Hospital, the Fourth Military Medical University, Xi'an, China.

出版信息

Ren Fail. 2021 Aug 10;43(1):1180-1187. doi: 10.1080/0886022X.2021.1956536.

Abstract

BACKGROUND

It is debated whether patients with IgAN with heavy proteinuria and decreased eGFR benefit from aggressive treatment consisting of corticosteroids alone or combined with immunosuppressive agents.

METHODS

A retrospective study was performed between January 2008 and December 2016 on patients with IgAN who had urinary protein excretion > 1.0 g/d and an eGFR between 15 and 59 mL/min/1.73 m. These patients were assigned to receive supportive care alone or supportive care plus immunosuppressive therapy. The primary outcome was defined as the first occurrence of a 50% decrease in eGFR or the development of ESKD.

RESULTS

All 208 included patients were followed for a median of 43 months, and 92 (44%) patients experienced the primary outcome. Cumulative kidney survival was better in the immunosuppression group than in the supportive care group ( < .001). The median annual rate of eGFR decline in the immunosuppression group was -2.0 (-7.3 to 4.2), compared with -8.4 (-18.9 to -4.1) mL/min/1.73 m in the supportive care group ( < .001). In multivariate Cox regression analyses, immunosuppressive therapy was associated with a lower risk of progression to ESKD, independent of age, sex, eGFR, proteinuria, MAP, kidney histologic findings and the use of RASi agents (HR = 0.335; 95% CI 0.209-0.601). Among the adverse events, infection requiring hospitalization occurred at similar rates in both groups ( = .471).

CONCLUSION

Immunosuppressive therapy attenuated the rate of eGFR decline and was associated with a favorable kidney outcome in IgAN patients with heavy proteinuria and decreased eGFR, and the side effects were tolerable.

摘要

背景

目前对于存在大量蛋白尿和 eGFR 降低的 IgAN 患者,单独使用皮质激素或联合免疫抑制剂进行强化治疗是否获益仍存在争议。

方法

本研究为回顾性队列研究,纳入了 2008 年 1 月至 2016 年 12 月期间患有 IgAN 且尿蛋白排泄量>1.0 g/d 和 eGFR 为 15-59 mL/min/1.73 m2 的患者。这些患者被分为接受单纯支持治疗或支持治疗联合免疫抑制治疗。主要结局定义为 eGFR 下降 50%或进展至终末期肾病(ESKD)的首次发生。

结果

共纳入 208 例患者,中位随访时间为 43 个月,92 例(44%)患者发生了主要结局。与支持治疗组相比,免疫抑制组的肾脏存活率更高( < .001)。免疫抑制组的 eGFR 年下降率中位数为-2.0(-7.3 至 4.2),而支持治疗组为-8.4(-18.9 至-4.1)mL/min/1.73 m2( < .001)。多因素 Cox 回归分析显示,免疫抑制治疗与 ESKD 进展风险降低相关,与年龄、性别、eGFR、蛋白尿、平均动脉压、肾脏组织学发现和 RASi 药物的使用无关(HR = 0.335;95%CI 0.209-0.601)。在不良反应方面,两组因感染需要住院治疗的发生率相似( = .471)。

结论

免疫抑制治疗可减缓 eGFR 下降速度,并改善大量蛋白尿和 eGFR 降低的 IgAN 患者的肾脏预后,且副作用可耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7edd/8366668/9344f981bb94/IRNF_A_1956536_F0001_C.jpg

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