Rodrigo Emilio, Quintana Luis F, Vázquez-Sánchez Teresa, Sánchez-Fructuoso Ana, Buxeda Anna, Gavela Eva, Cazorla Juan M, Cabello Sheila, Beneyto Isabel, López-Oliva María O, Diekmann Fritz, Gómez-Ortega José M, Calvo Romero Natividad, Pérez-Sáez María J, Sancho Asunción, Mazuecos Auxiliadora, Espí-Reig Jordi, Jiménez Carlos, Hernández Domingo
Nephrology Department, Hospital Universitario Marqués de Valdecilla/IDIVAL, Santander, SpainRD21/0005/0010 (ISCIII RICORS2040).
Nephrology and Renal Transplantation Department, Hospital Clinic, Barcelona, Spain.
Clin Kidney J. 2023 Oct 16;17(1):sfad259. doi: 10.1093/ckj/sfad259. eCollection 2024 Jan.
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.
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).
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, = .006). After multivariate analysis, TII remained related to the risk of CKD5/DCGL (HR 2.344, 95% CI 1.119-4.910, = .024) independently of other histologic and clinical variables.
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性疾病,其复发会导致移植肾存活率降低。复发时的几个变量与移植肾丢失风险较高有关。临床或亚临床炎症的存在与肾移植丢失风险较高有关,但尚不清楚其如何影响复发性IgAN患者的预后。
我们进行了一项多中心回顾性研究,纳入经活检证实为IgAN复发的肾移植受者,且可获得Banff和牛津分类评分。当“t”或“i”≥2时定义为“肾小管间质炎症”(TII)。主要终点是进展至慢性肾脏病(CKD)5期或死亡删失的移植肾丢失(CKD5/DCGL)。
共纳入119例复发IgAN的肾移植受者,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风险较高相关(3年时分别为18.0%和45.3%,对数秩检验7.588,P = 0.006)。多变量分析后,TII仍然与CKD5/DCGL风险相关(风险比2.344,95%置信区间1.119 - 4.910,P = 0.024),独立于其他组织学和临床变量。
在复发IgAN的肾移植受者中,TII独立于先前已知变量,会增加CKD5/DCGL风险。我们建议将TII与牛津分类一起纳入临床变量,以识别移植肾丢失风险增加的复发性IgAN患者,这些患者可能从强化免疫抑制或特定的IgAN治疗中获益。