Mycophenolate Mofetil in C3 Glomerulopathy and Pathogenic Drivers of the Disease

Fernando Caravaca‐Fontán(Universidad Complutense de Madrid), Montserrat M. Díaz Encarnación(Puigvert Foundation), Laura Lucientes(Universidad Complutense de Madrid), Teresa Cavero(Hospital Universitario 12 De Octubre), Virginia Cabello(Hospital Universitario Virgen del Rocío), Gema Ariceta(Universitat Autònoma de Barcelona), Luís F. Quintana(Hospital Clínic de Barcelona), Helena Marco(Hospital Universitari Germans Trias i Pujol), Xoana Barros(Hospital Universitari de Girona Doctor Josep Trueta), Natàlia Ramos(Vall d'Hebron Hospital Universitari), Nuria Rodríguez-Mendiola(Hospital Universitario Ramón y Cajal), Sonia Cruz(Hospital Juan Ramón Jiménez), Gema Fernández‐Juárez(Hospital Universitario Fundación Alcorcón), A. Bernardos Rodríguez(Hospital Universitario Virgen del Rocío), Ana Pérez de José(Hospital General Universitario Gregorio Marañón), Cristina Rabasco(Hospital Universitario Reina Sofía), Raquél Rodado(Hospital Universitario Virgen de la Arrixaca), Loreto Fernández(Complejo Hospitalario de Navarra), María Vanessa Pérez-Gómez(Hospital Universitario Fundación Jiménez Díaz), Ana I Ávila(Hospital Universitario Doctor Peset), Luis Eduardo Bravo(Complexo Hospitalario Universitario A Coruña), Javier Lumbreras(Health Research Institute of the Balearic Islands), Natalia Allende(Hospital Universitario Son Espases), María Dolores Sánchez de la Nieta(Hospital General Universitario de Ciudad Real), Eva Rodríguez(Hospital Del Mar), Teresa Olea(Hospital Universitario La Paz), Marta Melgosa(Hospital Universitario La Paz), Ana Huerta(Hospital Universitario Puerta de Hierro Majadahonda), Rosa Miquel(Hospital Universitario de Canarias), Carmen Mon(Hospital Universitario Severo Ochoa), Gloria Fraga(Universitat Autònoma de Barcelona), Alberto de Lorenzo(Hospital Universitario de Getafe), Juliana Draibe(Bellvitge University Hospital), Marta Cano-Megías(Hospital Universitario Príncipe de Asturias), Fayna González(Hospital Universitario de Gran Canaria Doctor Negrín), Amir Shabaka(Hospital Clínico San Carlos), Maria Esperanza López-Rubio(Complejo Hospitalario Universitario de Albacete), María Ángeles Fenollosa(Hospital General Universitari de Castelló), Luis Martín‐Penagos(Marqués de Valdecilla University Hospital), Iara Da Silva(Puigvert Foundation), Juana Alonso Titos(Hospital Regional Universitario de Málaga), Santiago Rodrı́guez de Córdoba(Consejo Superior de Investigaciones Científicas), Elena Goicoechea de Jorge(Consejo Superior de Investigaciones Científicas), Manuel Praga(Universidad Complutense de Madrid), on behalf of the Spanish Group for the Study of Glomerular Diseases GLOSEN
Clinical Journal of the American Society of Nephrology
August 19, 2020
Cited by 78Open Access
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Abstract

BACKGROUND AND OBJECTIVES: C3 glomerulopathy is a complement-mediated disease arising from abnormalities in complement genes and/or antibodies against complement components. Previous studies showed that treatment with corticosteroids plus mycophenolate mofetil (MMF) was associated with improved outcomes, although the genetic profile of these patients was not systematically analyzed. This study aims to analyze the main determinants of disease progression and response to this therapeutic regimen. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: =16) between January 1995 and March 2018 were enrolled. Multivariable and propensity score matching analyses were used to evaluate the association of clinical and genetic factors with response to treatment with corticosteroids and MMF as measured by proportion of patients with disease remission and kidney survival (status free of kidney failure). RESULTS: The study group comprised 97 patients (84% C3 glomerulopathy, 16% dense deposit disease). Forty-two patients were treated with corticosteroids plus MMF, and this treatment was associated with a higher rate of remission and lower probability of kidney failure (79% and 14%, respectively) compared with patients treated with other immunosuppressives (24% and 59%, respectively), or ecluzimab (33% and 67%, respectively), or conservative management (18% and 65%, respectively). The therapeutic superiority of corticosteroids plus MMF was observed both in patients with complement abnormalities and with autoantibodies. However, patients with pathogenic variants in complement genes only achieved partial remission, whereas complete remissions were common among patients with autoantibody-mediated forms. The main determinant of no remission was baseline proteinuria. Relapses occurred after treatment discontinuation in 33% of the patients who had achieved remission with corticosteroids plus MMF, and a longer treatment length of MMF was associated with a lower risk of relapse. CONCLUSIONS: The beneficial response to corticosteroids plus MMF treatment in C3 glomerulopathy appears independent of the pathogenic drivers analyzed in this study.


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