Factors influencing early response of IgA nephropathy following targeted-release budesonide (TRB) treatment: preliminary results from a multicenter study.

IF 4.6 2区 医学 Q1 UROLOGY & NEPHROLOGY Clinical Kidney Journal Pub Date : 2024-11-19 eCollection Date: 2025-01-01 DOI:10.1093/ckj/sfae364
Christodoulos Keskinis, Eleni Moysidou, Eleni Kapsia, Vasilios Vaios, Christos Bintas, Maria Trivyza, Michalis Christodoulou, Georgios Lioulios, Stamatia Stai, Christina Nikolaidou, Panagiotis Pateinakis, Marios Papasotiriou, Vassilios Liakopoulos, Smaragdi Marinaki, Maria Stangou
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Abstract

Background: Formation of galactose-deficient IgA1 (Gd-IgA1) immunoglobulin is the initial step in the immunological cascade leading to IgA nephropathy (IgAN). Targeted-release budesonide (TRB), an evidence-based regimen without major side-effects, has recently been approved for IgAN treatment; herein we present our preliminary real-world data regarding prompt response to TRB.

Methods: Patients with primary IgAN who remained with Uprot >1 g/24 h despite conventional treatment for 6 months were started on TRB, and re-evaluated at 3 (T3) and 6 (T6) months. Reduction of proteinuria by ≥30%, at T3 and T6 was regarded as very early (VER) and early response (ER), respectively. Kidney biopsies were evaluated according to Oxford classification (MEST-C) score.

Results: Thirty-seven IgAN patients, male/female 26/11, mean ± standard deviation age 50.38 ± 14.32 years and mean time since diagnosis 45.65 ± 56.67 months, were included. Seventeen (45.94%) patients demonstrated VER, increasing to 29 (78.3%) as ER (P = .004). Patients who demonstrated VER had a shorter time interval since diagnosis compared with non-VER, 29.41 ± 6.96 vs 65.37 ± 17.64 months (P = .05), and preserved estimated glomerular filtration rate at diagnosis and T0, while time since diagnosis was the main factor associated with ER, 38.36 ± 19.6 vs 78.67 ± 18.64 months, in ER and non-ER respectively (P = .05). Patients with M0, E0, S0 and T0 had no significant changes during T0-T6, while patients with M1, E1, S1 and even T1 had significantly reduced proteinuria (P = .006, P = .0011, P < .0001 and P < .0001, respectively).

Conclusions: Almost half of the patients showed proteinuria reduction after TRB treatment at 3 months, and the proportion increased significantly at 6 months. Patients likely to have a prompt proteinuria reduction were relatively close to diagnosis, retained kidney function and had active lesions in kidney biopsy.

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影响靶向释放布地奈德(TRB)治疗后IgA肾病早期反应的因素:来自多中心研究的初步结果
背景:半乳糖缺乏IgA1 (Gd-IgA1)免疫球蛋白的形成是导致IgA肾病(IgAN)的免疫级联反应的第一步。靶向释放布地奈德(TRB)是一种无重大副作用的循证方案,最近已被批准用于IgAN治疗;在此,我们给出了关于TRB快速响应的初步真实数据。方法:原发性IgAN患者在常规治疗6个月后仍继续使用Uprot bb0 1 g/24 h,并在3 (T3)和6 (T6)个月时重新评估TRB。在T3和T6时,蛋白尿减少≥30%分别被视为非常早期(VER)和早期反应(ER)。肾活检按照牛津分级(MEST-C)评分进行评估。结果:纳入IgAN患者37例,男/女26/11,平均±标准差年龄50.38±14.32岁,平均诊断时间45.65±56.67个月。VER 17例(45.94%),ER 29例(78.3%)(P = 0.004)。与非ER患者相比,VER患者自诊断后的时间间隔较短,分别为29.41±6.96和65.37±17.64个月(P = 0.05),并且在诊断和T0时保留了估计的肾小球滤过率,而诊断后的时间是与ER相关的主要因素,ER和非ER患者分别为38.36±19.6和78.67±18.64个月(P = 0.05)。M0、E0、S0、T0患者在T0- t6期间无明显变化,而M1、E1、S1甚至T1患者的蛋白尿明显减少(P = 0.006, P = 0.0011, P)。结论:TRB治疗3个月时,几乎有一半的患者出现蛋白尿减少,6个月时比例明显增加。可能出现蛋白尿迅速减少的患者相对接近诊断,保留肾功能,肾活检有活动性病变。
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来源期刊
Clinical Kidney Journal
Clinical Kidney Journal Medicine-Transplantation
CiteScore
6.70
自引率
10.90%
发文量
242
审稿时长
8 weeks
期刊介绍: About the Journal Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.
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