TY - JOUR
T1 - Recurrence of membranous nephropathy after kidney transplantation
T2 - A multicenter retrospective cohort study
AU - Hullekes, Frank
AU - Uffing, Audrey
AU - Verhoeff, Rucháma
AU - Seeger, Harald
AU - von Moos, Seraina
AU - Mansur, Juliana
AU - Mastroianni-Kirsztajn, Gianna
AU - Silva, Helio Tedesco
AU - Buxeda, Anna
AU - Pérez-Sáez, María José
AU - Arias-Cabrales, Carlos
AU - Collins, A. Bernard
AU - Swett, Christie
AU - Morená, Leela
AU - Loucaidou, Marina
AU - Kousios, Andreas
AU - Malvezzi, Paolo
AU - Bugnazet, Mathilde
AU - Russo, Luis Sanchez
AU - Muhsin, Saif A.
AU - Agrawal, Nikhil
AU - Nissaisorakarn, Pitchaphon
AU - Patel, Het
AU - Al Jurdi, Ayman
AU - Akalin, Enver
AU - Neto, Elias David
AU - Agena, Fabiana
AU - Ventura, Carlucci
AU - Manfro, Roberto C.
AU - Bauer, Andrea Carla
AU - Mazzali, Marilda
AU - Vinicius de Sousa, Marcos
AU - La Manna, Gaetano
AU - Bini, Claudia
AU - Comai, Giorgia
AU - Reindl-Schwaighofer, Roman
AU - Berger, Stefan
AU - Cravedi, Paolo
AU - Riella, Leonardo V.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/6
Y1 - 2024/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85186082256&partnerID=8YFLogxK
U2 - 10.1016/j.ajt.2024.01.036
DO - 10.1016/j.ajt.2024.01.036
M3 - Article
C2 - 38341027
AN - SCOPUS:85186082256
SN - 1600-6135
VL - 24
SP - 1016
EP - 1026
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 6
ER -