| Literature DB >> 31525265 |
Anaïs Brassier1, Pauline Krug2, Florence Lacaille3, Clément Pontoizeau1,4, Saoussen Krid2, Samira Sissaoui3, Aude Servais1,5, Jean-Baptiste Arnoux1, Christophe Legendre5, Marina Charbit2, Anne Scemla1,5, Claire Francoz6, Jean-François Benoist7, Manuel Schiff8, Fanny Mochel9, Guy Touati1,10, Pierre Broué10, Aline Cano11, Marine Tardieu12, Stefania Querciagrossa13, David Grévent14, Olivia Boyer2, Laurent Dupic15, Mehdi Oualha15, Muriel Girard3, Yves Aigrain16, Dominique Debray3, Carmen Capito16, Chris Ottolenghi1,4, Rémi Salomon2, Christophe Chardot16, Pascale de Lonlay1.
Abstract
Organ transplantation is discussed in methylmalonic aciduria (MMA) for renal failure, and poor quality of life and neurological outcome. We retrospectively evaluated 23 French MMA patients after kidney (KT), liver-kidney (LKT), and liver transplantation (LT). Two patients died, one after LKT, one of hepatoblastoma after KT. One graft was lost early after KT. Of 18 evaluable patients, 12 previously on dialysis, 8 underwent KT (mean 12.5 years), 8 LKT (mean 7 years), and 2 LT (7 and 2.5 years). At a median follow-up of 7.3 (KT), 2.3 (LKT), and 1.0 years (LT), no metabolic decompensation occurred except in 1 KT. Plasma and urine MMA levels dramatically decreased, more after LKT. Protein intake was increased more significantly after LKT than KT. Enteral nutrition was stopped in 7/8 LKT, 1/8 KT. Early complications were frequent after LKT. Neurological disorders occurred in four LKT, reversible in one. Five years after KT, four patients had renal failure. The metabolic outcomes were much better after LKT than KT. LKT in MMA is difficult but improves the quality of life. KT will be rarely indicated. We need more long-term data to indicate early LT, in the hope to delay renal failure and prevent neurodevelopmental complications.Entities:
Keywords: combined liver-kidney transplantation; kidney transplantation; liver transplantation; metabolic outcome; methylmalonic aciduria; renal failure
Mesh:
Year: 2020 PMID: 31525265 DOI: 10.1002/jimd.12174
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982