Your browser doesn't support javascript.
loading
Organ Transplantation in Hereditary Fibrinogen A α-Chain Amyloidosis: A Case Series of French Patients.
Meyer, Lara; Ulrich, Marc; Ducloux, Didier; Garrigue, Valérie; Vigneau, Cécile; Nochy, Dominique; Bobrie, Guillaume; Ferlicot, Sophie; Colombat, Magalie; Boffa, Jean-Jacques; Clabault, Karine; Mansour, Jeannette; Mousson, Christiane; Azar, Raymond; Bacri, Jean-Louis; Dürrbach, Antoine; Duvic, Christian; El Karoui, Khalil; Hoffmann, Maxime; Lionet, Arnaud; Panescu, Victor; Plaisier, Emmanuelle; Ratsimbazafy, Anderson; Guerrot, Dominique; Vrigneaud, Laurence; Valleix, Sophie; François, Hélène.
Afiliación
  • Meyer L; Department of Nephrology, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris (AP-HP), Department of Nephrology, Université Paris Descartes, Paris.
  • Ulrich M; Department of Nephrology, Hôpital Jean Bernard, Valenciennes, France.
  • Ducloux D; Department of Nephrology, Centre Hospitalier Universitaire de Besançon, France.
  • Garrigue V; Department of Nephrology, Hôpital Lapeyronie, Montpellier, France.
  • Vigneau C; Department of Nephrology, Centre Hospitalier Universitaire de Rennes, France.
  • Nochy D; Departments of Pathology, Hôpital Européen Georges Pompidou, AP-HP, Université Paris Descartes, Paris, France.
  • Bobrie G; Departments of Hypertension, Hôpital Européen Georges Pompidou, AP-HP, Université Paris Descartes, France.
  • Ferlicot S; Hôpital Européen Georges Pompidou, AP-HP, Université Paris Descartes, Paris, Department of Pathology, Hôpital Bicêtre, AP-HP, Université Paris-Sud, Le Kremlin-Bicêtre, France.
  • Colombat M; Department of Pathology, Centre Hospitalier Universitaire de Toulouse, France.
  • Boffa JJ; Department of Nephrology and Dialysis, Hôpital Tenon, AP-HP, Sorbonne Université, Paris, France.
  • Clabault K; Department of Nephrology, Le Havre Hospital, France.
  • Mansour J; Department of Nephrology, Soisson Hospital, France.
  • Mousson C; Department of Nephrology, Centre Hospitalier Unversitaire de Dijon, France.
  • Azar R; Department of Nephrology, Centre Hospitalier de Dunkerque, France.
  • Bacri JL; Department of Nephrology, Hôpital Jean Bernard, Valenciennes, France.
  • Dürrbach A; Department of Nephrology, Dialysis and Transplantation, Hôpital Bicêtre, AP-HP, Université Paris-Sud, Le Kremlin-Bicêtre.
  • Duvic C; Department of Hemodialysis Clinique de Choisy, Le Gosier, Guadeloupe.
  • El Karoui K; Department of Nephrology, Hôpital Henri Mondor, Créteil.
  • Hoffmann M; Department of Nephrology and Dialysis, Hôpital Privé La Louvière, Groupe Ramsay Générale de Santé, Lille.
  • Lionet A; Department of Nephrology, and Transplantation, Centre Hospitalier Régional et Universitaire de Lille, France.
  • Panescu V; Department of Nephrology and Hemodialysis, Polyclinique de Gentilly, Gentilly, France.
  • Plaisier E; Department of Nephrology and Dialysis, Hôpital Tenon, AP-HP, Sorbonne Université, Paris, France.
  • Ratsimbazafy A; Department of Nephrology, Centre Hospitalier de Béthune, Beuvry.
  • Guerrot D; Department of Nephrology and Dialysis, Centre Hospitalier Bois Guillaume, Rouen.
  • Vrigneaud L; Department of Nephrology and Dialysis, Hôpital Privé La Louvière, Groupe Ramsay Générale de Santé, Lille.
  • Valleix S; Department of Genetic Necker Hospital, AP-HP, Université Paris Descartes, Paris AP-HP, France. Electronic address: sophie.valleix@aphp.fr.
  • François H; Department of Nephrology and Transplantation, Hôpital Tenon, Sorbonne Université, Paris, France. Electronic address: helene.francois@aphp.fr.
Am J Kidney Dis ; 76(3): 384-391, 2020 09.
Article en En | MEDLINE | ID: mdl-32660897
RATIONALE & OBJECTIVE: Fibrinogen A α-chain amyloidosis (AFib amyloidosis) is a form of amyloidosis resulting from mutations in the fibrinogen A α-chain gene (FGA), causing progressive kidney disease leading to kidney failure. Treatment may include kidney transplantation (KT) or liver-kidney transplantation (LKT), but it is not clear what factors should guide this decision. The aim of this study was to characterize the natural history and long-term outcomes of this disease, with and without organ transplantation, among patients with AFib amyloidosis and various FGA variants. STUDY DESIGN: Case series. SETTING & PARTICIPANTS: 32 patients with AFib amyloidosis diagnosed by genetic testing in France between 1983 and 2014, with a median follow-up of 93 (range, 4-192) months, were included. RESULTS: Median age at diagnosis was 51.5 (range, 12-77) years. Clinical presentation consisted of proteinuria (93%), hypertension (83%), and kidney failure (68%). Manifestations of kidney disease appeared on average at age 57 (range, 36-77) years in patients with the E526V variant, at age 45 (range, 12-59) years in those with the R554L variant (P<0.001), and at age 24.5 (range, 12-31) years in those with frameshift variants (P<0.001). KT was performed in 15 patients and LKT was performed in 4. In KT patients with the E526V variant, recurrence of AFib amyloidosis in the kidney graft was less common than with a non-E526V (R554L or frameshift) variant (22% vs 83%; P=0.03) and led to graft loss less frequently (33% vs 100%). Amyloid recurrence was not observed in patients after LKT. LIMITATIONS: Analyses were based on clinically available historical data. Small number of patients with non-E526V and frameshift variants. CONCLUSIONS: Our study suggests phenotypic variability in the natural history of AFib amyloidosis, depending on the FGA mutation type. KT appears to be a viable option for patients with the most common E526V variant, whereas LKT may be a preferred option for patients with frameshift variants.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Trasplante de Riñón / Trasplante de Hígado / Amiloidosis Familiar Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Am J Kidney Dis Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Trasplante de Riñón / Trasplante de Hígado / Amiloidosis Familiar Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Am J Kidney Dis Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos