Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA; Groningen Transplant Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA; Department of Surgery, Erasmus Medical Center Transplant Institute, Erasmus University, Rotterdam, The Netherlands.
Am J Transplant. 2024 Jun;24(6):1016-1026. doi: 10.1016/j.ajt.2024.01.036. Epub 2024 Feb 8.
Membranous nephropathy (MN) is a leading cause of kidney failure worldwide and frequently recurs after transplant. Available data originated from small retrospective cohort studies or registry analyses; therefore, uncertainties remain on risk factors for MN recurrence and response to therapy. Within the Post-Transplant Glomerular Disease Consortium, we conducted a retrospective multicenter cohort study examining the MN recurrence rate, risk factors, and response to treatment. This study screened 22,921 patients across 3 continents and included 194 patients who underwent a kidney transplant due to biopsy-proven MN. The cumulative incidence of MN recurrence was 31% at 10 years posttransplant. Patients with a faster progression toward end-stage kidney disease were at higher risk of developing recurrent MN (hazard ratio [HR], 0.55 per decade; 95% confidence interval [CI], 0.35-0.88). Moreover, elevated pretransplant levels of anti-phospholipase A2 receptor (PLA2R) antibodies were strongly associated with recurrence (HR, 18.58; 95% CI, 5.37-64.27). Patients receiving rituximab for MN recurrence had a higher likelihood of achieving remission than patients receiving renin-angiotensin-aldosterone system inhibition alone. In sum, MN recurs in one-third of patients posttransplant, and measurement of serum anti-PLA2R antibody levels shortly before transplant could aid in risk-stratifying patients for MN recurrence. Moreover, patients receiving rituximab had a higher rate of treatment response.
膜性肾病 (MN) 是全球范围内导致肾衰竭的主要原因,并且在移植后经常复发。现有数据源自小型回顾性队列研究或登记分析;因此,MN 复发的风险因素和对治疗的反应仍存在不确定性。在移植后肾小球疾病联盟内,我们进行了一项回顾性多中心队列研究,调查 MN 复发率、风险因素和治疗反应。该研究在三大洲筛查了 22921 名患者,包括 194 名因活检证实的 MN 而接受肾移植的患者。移植后 10 年 MN 复发的累积发生率为 31%。向终末期肾病进展更快的患者发生复发性 MN 的风险更高(风险比 [HR],每十年 0.55;95%置信区间 [CI],0.35-0.88)。此外,移植前抗磷脂酶 A2 受体 (PLA2R) 抗体水平升高与复发密切相关(HR,18.58;95%CI,5.37-64.27)。接受利妥昔单抗治疗 MN 复发的患者比单独接受肾素-血管紧张素-醛固酮系统抑制治疗的患者更有可能获得缓解。总之,三分之一的移植后患者会发生 MN 复发,并且在移植前短时间测量血清抗 PLA2R 抗体水平可以帮助对 MN 复发的患者进行风险分层。此外,接受利妥昔单抗治疗的患者治疗反应率更高。