Cargando…

Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia

Methylmalonic and propionic acidemia (MMA/PA) are inborn errors of metabolism characterized by accumulation of propionic acid and/or methylmalonic acid due to deficiency of methylmalonyl-CoA mutase (MUT) or propionyl-CoA carboxylase (PCC). MMA has an estimated incidence of ~ 1: 50,000 and PA of ~ 1:...

Descripción completa

Detalles Bibliográficos
Autores principales: Baumgartner, Matthias R, Hörster, Friederike, Dionisi-Vici, Carlo, Haliloglu, Goknur, Karall, Daniela, Chapman, Kimberly A, Huemer, Martina, Hochuli, Michel, Assoun, Murielle, Ballhausen, Diana, Burlina, Alberto, Fowler, Brian, Grünert, Sarah C, Grünewald, Stephanie, Honzik, Tomas, Merinero, Begoña, Pérez-Cerdá, Celia, Scholl-Bürgi, Sabine, Skovby, Flemming, Wijburg, Frits, MacDonald, Anita, Martinelli, Diego, Sass, Jörn Oliver, Valayannopoulos, Vassili, Chakrapani, Anupam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180313/
https://www.ncbi.nlm.nih.gov/pubmed/25205257
http://dx.doi.org/10.1186/s13023-014-0130-8
_version_ 1782337204600700928
author Baumgartner, Matthias R
Hörster, Friederike
Dionisi-Vici, Carlo
Haliloglu, Goknur
Karall, Daniela
Chapman, Kimberly A
Huemer, Martina
Hochuli, Michel
Assoun, Murielle
Ballhausen, Diana
Burlina, Alberto
Fowler, Brian
Grünert, Sarah C
Grünewald, Stephanie
Honzik, Tomas
Merinero, Begoña
Pérez-Cerdá, Celia
Scholl-Bürgi, Sabine
Skovby, Flemming
Wijburg, Frits
MacDonald, Anita
Martinelli, Diego
Sass, Jörn Oliver
Valayannopoulos, Vassili
Chakrapani, Anupam
author_facet Baumgartner, Matthias R
Hörster, Friederike
Dionisi-Vici, Carlo
Haliloglu, Goknur
Karall, Daniela
Chapman, Kimberly A
Huemer, Martina
Hochuli, Michel
Assoun, Murielle
Ballhausen, Diana
Burlina, Alberto
Fowler, Brian
Grünert, Sarah C
Grünewald, Stephanie
Honzik, Tomas
Merinero, Begoña
Pérez-Cerdá, Celia
Scholl-Bürgi, Sabine
Skovby, Flemming
Wijburg, Frits
MacDonald, Anita
Martinelli, Diego
Sass, Jörn Oliver
Valayannopoulos, Vassili
Chakrapani, Anupam
author_sort Baumgartner, Matthias R
collection PubMed
description Methylmalonic and propionic acidemia (MMA/PA) are inborn errors of metabolism characterized by accumulation of propionic acid and/or methylmalonic acid due to deficiency of methylmalonyl-CoA mutase (MUT) or propionyl-CoA carboxylase (PCC). MMA has an estimated incidence of ~ 1: 50,000 and PA of ~ 1:100’000 -150,000. Patients present either shortly after birth with acute deterioration, metabolic acidosis and hyperammonemia or later at any age with a more heterogeneous clinical picture, leading to early death or to severe neurological handicap in many survivors. Mental outcome tends to be worse in PA and late complications include chronic kidney disease almost exclusively in MMA and cardiomyopathy mainly in PA. Except for vitamin B(12) responsive forms of MMA the outcome remains poor despite the existence of apparently effective therapy with a low protein diet and carnitine. This may be related to under recognition and delayed diagnosis due to nonspecific clinical presentation and insufficient awareness of health care professionals because of disease rarity. These guidelines aim to provide a trans-European consensus to guide practitioners, set standards of care and to help to raise awareness. To achieve these goals, the guidelines were developed using the SIGN methodology by having professionals on MMA/PA across twelve European countries and the U.S. gather all the existing evidence, score it according to the SIGN evidence level system and make a series of conclusive statements supported by an associated level of evidence. Although the degree of evidence rarely exceeds level C (evidence from non-analytical studies like case reports and series), the guideline should provide a firm and critical basis to guide practice on both acute and chronic presentations, and to address diagnosis, management, monitoring, outcomes, and psychosocial and ethical issues. Furthermore, these guidelines highlight gaps in knowledge that must be filled by future research. We consider that these guidelines will help to harmonize practice, set common standards and spread good practices, with a positive impact on the outcomes of MMA/PA patients.
format Online
Article
Text
id pubmed-4180313
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41803132014-10-03 Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia Baumgartner, Matthias R Hörster, Friederike Dionisi-Vici, Carlo Haliloglu, Goknur Karall, Daniela Chapman, Kimberly A Huemer, Martina Hochuli, Michel Assoun, Murielle Ballhausen, Diana Burlina, Alberto Fowler, Brian Grünert, Sarah C Grünewald, Stephanie Honzik, Tomas Merinero, Begoña Pérez-Cerdá, Celia Scholl-Bürgi, Sabine Skovby, Flemming Wijburg, Frits MacDonald, Anita Martinelli, Diego Sass, Jörn Oliver Valayannopoulos, Vassili Chakrapani, Anupam Orphanet J Rare Dis Review Methylmalonic and propionic acidemia (MMA/PA) are inborn errors of metabolism characterized by accumulation of propionic acid and/or methylmalonic acid due to deficiency of methylmalonyl-CoA mutase (MUT) or propionyl-CoA carboxylase (PCC). MMA has an estimated incidence of ~ 1: 50,000 and PA of ~ 1:100’000 -150,000. Patients present either shortly after birth with acute deterioration, metabolic acidosis and hyperammonemia or later at any age with a more heterogeneous clinical picture, leading to early death or to severe neurological handicap in many survivors. Mental outcome tends to be worse in PA and late complications include chronic kidney disease almost exclusively in MMA and cardiomyopathy mainly in PA. Except for vitamin B(12) responsive forms of MMA the outcome remains poor despite the existence of apparently effective therapy with a low protein diet and carnitine. This may be related to under recognition and delayed diagnosis due to nonspecific clinical presentation and insufficient awareness of health care professionals because of disease rarity. These guidelines aim to provide a trans-European consensus to guide practitioners, set standards of care and to help to raise awareness. To achieve these goals, the guidelines were developed using the SIGN methodology by having professionals on MMA/PA across twelve European countries and the U.S. gather all the existing evidence, score it according to the SIGN evidence level system and make a series of conclusive statements supported by an associated level of evidence. Although the degree of evidence rarely exceeds level C (evidence from non-analytical studies like case reports and series), the guideline should provide a firm and critical basis to guide practice on both acute and chronic presentations, and to address diagnosis, management, monitoring, outcomes, and psychosocial and ethical issues. Furthermore, these guidelines highlight gaps in knowledge that must be filled by future research. We consider that these guidelines will help to harmonize practice, set common standards and spread good practices, with a positive impact on the outcomes of MMA/PA patients. BioMed Central 2014-09-02 /pmc/articles/PMC4180313/ /pubmed/25205257 http://dx.doi.org/10.1186/s13023-014-0130-8 Text en © Baumgartner et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Baumgartner, Matthias R
Hörster, Friederike
Dionisi-Vici, Carlo
Haliloglu, Goknur
Karall, Daniela
Chapman, Kimberly A
Huemer, Martina
Hochuli, Michel
Assoun, Murielle
Ballhausen, Diana
Burlina, Alberto
Fowler, Brian
Grünert, Sarah C
Grünewald, Stephanie
Honzik, Tomas
Merinero, Begoña
Pérez-Cerdá, Celia
Scholl-Bürgi, Sabine
Skovby, Flemming
Wijburg, Frits
MacDonald, Anita
Martinelli, Diego
Sass, Jörn Oliver
Valayannopoulos, Vassili
Chakrapani, Anupam
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title_full Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title_fullStr Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title_full_unstemmed Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title_short Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
title_sort proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180313/
https://www.ncbi.nlm.nih.gov/pubmed/25205257
http://dx.doi.org/10.1186/s13023-014-0130-8
work_keys_str_mv AT baumgartnermatthiasr proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT horsterfriederike proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT dionisivicicarlo proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT haliloglugoknur proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT karalldaniela proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT chapmankimberlya proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT huemermartina proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT hochulimichel proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT assounmurielle proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT ballhausendiana proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT burlinaalberto proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT fowlerbrian proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT grunertsarahc proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT grunewaldstephanie proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT honziktomas proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT merinerobegona proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT perezcerdacelia proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT schollburgisabine proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT skovbyflemming proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT wijburgfrits proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT macdonaldanita proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT martinellidiego proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT sassjornoliver proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT valayannopoulosvassili proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia
AT chakrapanianupam proposedguidelinesforthediagnosisandmanagementofmethylmalonicandpropionicacidemia