Long‐term outcome of methylmalonic aciduria after kidney, liver, or combined liver‐kidney transplantation: The French experience. Issue 2 (11th February 2020)
- Record Type:
- Journal Article
- Title:
- Long‐term outcome of methylmalonic aciduria after kidney, liver, or combined liver‐kidney transplantation: The French experience. Issue 2 (11th February 2020)
- Main Title:
- Long‐term outcome of methylmalonic aciduria after kidney, liver, or combined liver‐kidney transplantation: The French experience
- Authors:
- Brassier, Anaïs
Krug, Pauline
Lacaille, Florence
Pontoizeau, Clément
Krid, Saoussen
Sissaoui, Samira
Servais, Aude
Arnoux, Jean‐Baptiste
Legendre, Christophe
Charbit, Marina
Scemla, Anne
Francoz, Claire
Benoist, Jean‐François
Schiff, Manuel
Mochel, Fanny
Touati, Guy
Broué, Pierre
Cano, Aline
Tardieu, Marine
Querciagrossa, Stefania
Grévent, David
Boyer, Olivia
Dupic, Laurent
Oualha, Mehdi
Girard, Muriel
Aigrain, Yves
Debray, Dominique
Capito, Carmen
Ottolenghi, Chris
Salomon, Rémi
Chardot, Christophe
de Lonlay, Pascale
… (more) - Abstract:
- 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.
- Is Part Of:
- Journal of inherited metabolic disease. Volume 43:Issue 2(2020)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 43:Issue 2(2020)
- Issue Display:
- Volume 43, Issue 2 (2020)
- Year:
- 2020
- Volume:
- 43
- Issue:
- 2
- Issue Sort Value:
- 2020-0043-0002-0000
- Page Start:
- 234
- Page End:
- 243
- Publication Date:
- 2020-02-11
- Subjects:
- combined liver‐kidney transplantation -- kidney transplantation -- liver transplantation -- metabolic outcome -- methylmalonic aciduria -- renal failure
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1002/jimd.12174 ↗
- Languages:
- English
- ISSNs:
- 0141-8955
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5006.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19211.xml