Emilio Rodrigo, Luis F Quintana, Teresa Vázquez-Sánchez, Ana Sánchez-Fructuoso, Anna Buxeda, Eva Gavela, Juan M Cazorla, Sheila Cabello, Isabel Beneyto, María O López-Oliva, Fritz Diekmann, José M Gómez-Ortega, Natividad Calvo Romero, María J Pérez-Sáez, Asunción Sancho, Auxiliadora Mazuecos, Jordi Espí-Reig, Carlos Jiménez, Domingo Hernández
{"title":"Tubulo-interstitial inflammation increases the risk of graft loss after the recurrence of IgA nephropathy","authors":"Emilio Rodrigo, Luis F Quintana, Teresa Vázquez-Sánchez, Ana Sánchez-Fructuoso, Anna Buxeda, Eva Gavela, Juan M Cazorla, Sheila Cabello, Isabel Beneyto, María O López-Oliva, Fritz Diekmann, José M Gómez-Ortega, Natividad Calvo Romero, María J Pérez-Sáez, Asunción Sancho, Auxiliadora Mazuecos, Jordi Espí-Reig, Carlos Jiménez, Domingo Hernández","doi":"10.1093/ckj/sfad259","DOIUrl":null,"url":null,"abstract":"ABSTRACT Background Immunoglobulin A nephropathy (IgAN) is the most frequent recurrent disease in kidney transplant recipients and its recurrence contributes to reducing graft survival. Several variables at the time of recurrence have been associated with a higher risk of graft loss. The presence of clinical or subclinical inflammation has been associated with a higher risk of kidney graft loss, but it is not precisely known how it influences the outcome of patients with recurrent IgAN. Methods We performed a multicentre retrospective study including kidney transplant recipients with biopsy-proven recurrence of IgAN in which Banff and Oxford classification scores were available. ‘Tubulo-interstitial inflammation’ (TII) was defined when ‘t’ or ‘i’ were ≥2. The main endpoint was progression to chronic kidney disease (CKD) stage 5 or to death censored-graft loss (CKD5/DCGL). Results A total of 119 kidney transplant recipients with IgAN recurrence were included and 23 of them showed TII. Median follow-up was 102.9 months and 39 (32.8%) patients reached CKD5/DCGL. TII related to a higher risk of CKD5/DCGL (3 years 18.0% vs 45.3%, log-rank 7.588, P = .006). After multivariate analysis, TII remained related to the risk of CKD5/DCGL (HR 2.344, 95% CI 1.119–4.910, P = .024) independently of other histologic and clinical variables. Conclusions In kidney transplant recipients with IgAN recurrence, TII contributes to increasing the risk of CKD5/DCGL independently of previously well-known variables. We suggest adding TII along with the Oxford classification to the clinical variables to identify recurrent IgAN patients at increased risk of graft loss who might benefit from intensified immunosuppression or specific IgAN therapies.","PeriodicalId":18987,"journal":{"name":"NDT Plus","volume":"939 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NDT Plus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ckj/sfad259","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
ABSTRACT Background Immunoglobulin A nephropathy (IgAN) is the most frequent recurrent disease in kidney transplant recipients and its recurrence contributes to reducing graft survival. Several variables at the time of recurrence have been associated with a higher risk of graft loss. The presence of clinical or subclinical inflammation has been associated with a higher risk of kidney graft loss, but it is not precisely known how it influences the outcome of patients with recurrent IgAN. Methods We performed a multicentre retrospective study including kidney transplant recipients with biopsy-proven recurrence of IgAN in which Banff and Oxford classification scores were available. ‘Tubulo-interstitial inflammation’ (TII) was defined when ‘t’ or ‘i’ were ≥2. The main endpoint was progression to chronic kidney disease (CKD) stage 5 or to death censored-graft loss (CKD5/DCGL). Results A total of 119 kidney transplant recipients with IgAN recurrence were included and 23 of them showed TII. Median follow-up was 102.9 months and 39 (32.8%) patients reached CKD5/DCGL. TII related to a higher risk of CKD5/DCGL (3 years 18.0% vs 45.3%, log-rank 7.588, P = .006). After multivariate analysis, TII remained related to the risk of CKD5/DCGL (HR 2.344, 95% CI 1.119–4.910, P = .024) independently of other histologic and clinical variables. Conclusions In kidney transplant recipients with IgAN recurrence, TII contributes to increasing the risk of CKD5/DCGL independently of previously well-known variables. We suggest adding TII along with the Oxford classification to the clinical variables to identify recurrent IgAN patients at increased risk of graft loss who might benefit from intensified immunosuppression or specific IgAN therapies.
免疫球蛋白A肾病(IgAN)是肾移植受者中最常见的复发疾病,其复发会降低移植物的存活率。复发时的几个变量与移植物丢失的高风险相关。临床或亚临床炎症的存在与肾移植丢失的高风险相关,但尚不清楚它如何影响复发性IgAN患者的预后。方法我们进行了一项多中心回顾性研究,包括活检证实IgAN复发的肾移植受者,其中有Banff和Oxford分类评分。当t或i≥2时定义为“小管间质炎症”(TII)。主要终点是进展为慢性肾脏疾病(CKD)第5期或死亡检查-移植物丢失(CKD5/DCGL)。结果共纳入119例IgAN复发肾移植受者,其中23例出现TII。中位随访时间为102.9个月,39例(32.8%)患者达到CKD5/DCGL。TII与CKD5/DCGL的高风险相关(3年18.0% vs 45.3%, log-rank为7.588,P = 0.006)。多因素分析后,TII与CKD5/DCGL的风险相关(HR 2.344, 95% CI 1.119-4.910, P = 0.024),独立于其他组织学和临床变量。结论:在IgAN复发的肾移植受者中,TII有助于增加CKD5/DCGL的风险,独立于先前已知的变量。我们建议在临床变量中加入TII和牛津分类,以确定移植物丢失风险增加的复发性IgAN患者,这些患者可能受益于强化免疫抑制或特异性IgAN治疗。