Liver and/or kidney transplantation in amino and organic acid‐related inborn errors of metabolism: An overview on European data. Issue 3 (29th October 2020)
- Record Type:
- Journal Article
- Title:
- Liver and/or kidney transplantation in amino and organic acid‐related inborn errors of metabolism: An overview on European data. Issue 3 (29th October 2020)
- Main Title:
- Liver and/or kidney transplantation in amino and organic acid‐related inborn errors of metabolism: An overview on European data
- Authors:
- Molema, Femke
Martinelli, Diego
Hörster, Friederike
Kölker, Stefan
Tangeraas, Trine
de Koning, Barbara
Dionisi‐Vici, Carlo
Williams, Monique - Abstract:
- Abstract: Background: This study provides a general overview on liver and/or kidney transplantation in patients with an amino and organic acid‐related disorder (AOA) with the aim to investigate patient characteristics and global outcome in Europe. This study was an initiative of the E‐IMD and the AOA subnetwork of MetabERN. Methods: A questionnaire was sent to all clinically active European Society for the Study of Inborn Errors of Metabolism (SSIEM) members. The questionnaire focused on transplanted individuals with methylmalonic acidemia (MMA), propionic acidemia (PA), maple syrup urine disease (MSUD), and urea‐cycle disorders (UCDs). Results: We identified 280 transplanted AOA patients (liver transplantation in 20 MMA, 37 PA, 47 MSUD, and 111 UCD patients, kidney or combined liver and kidney transplantation in 57 MMA patients and undefined transplantation type in 8 MMA patients), followed by 51 metabolic centers. At a median follow‐up of 3.5 years, posttransplant survival ranged between 78% and 100%, being the lowest in PA patients. Overall, the risk of mortality was highest within 14 days posttransplantation. Neurological complications were mainly reported in Mut 0 type MMA ( n = 8). Nonneurological complications occurred in MMA ( n = 28), PA ( n = 7), and UCD ( n = 14) patients, while it was virtually absent in MSUD patients. Only 116/280 patients were psychologically tested. In all, except MSUD patients, the intelligence quotient (IQ) remained unchanged in theAbstract: Background: This study provides a general overview on liver and/or kidney transplantation in patients with an amino and organic acid‐related disorder (AOA) with the aim to investigate patient characteristics and global outcome in Europe. This study was an initiative of the E‐IMD and the AOA subnetwork of MetabERN. Methods: A questionnaire was sent to all clinically active European Society for the Study of Inborn Errors of Metabolism (SSIEM) members. The questionnaire focused on transplanted individuals with methylmalonic acidemia (MMA), propionic acidemia (PA), maple syrup urine disease (MSUD), and urea‐cycle disorders (UCDs). Results: We identified 280 transplanted AOA patients (liver transplantation in 20 MMA, 37 PA, 47 MSUD, and 111 UCD patients, kidney or combined liver and kidney transplantation in 57 MMA patients and undefined transplantation type in 8 MMA patients), followed by 51 metabolic centers. At a median follow‐up of 3.5 years, posttransplant survival ranged between 78% and 100%, being the lowest in PA patients. Overall, the risk of mortality was highest within 14 days posttransplantation. Neurological complications were mainly reported in Mut 0 type MMA ( n = 8). Nonneurological complications occurred in MMA ( n = 28), PA ( n = 7), and UCD ( n = 14) patients, while it was virtually absent in MSUD patients. Only 116/280 patients were psychologically tested. In all, except MSUD patients, the intelligence quotient (IQ) remained unchanged in the majority (76/94, 81%). Forty‐one percentage (9/22) of MSUD patient showed improved IQ. Conclusion: The survival in AOA individuals receiving liver and/or kidney transplantation seems satisfactory. Evidence‐based guidelines, systematic data collection, and improved cooperation between transplantation centers and European Reference Networks are indispensable to improve patient care and outcomes. … (more)
- Is Part Of:
- Journal of inherited metabolic disease. Volume 44:Issue 3(2021)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 44:Issue 3(2021)
- Issue Display:
- Volume 44, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 44
- Issue:
- 3
- Issue Sort Value:
- 2021-0044-0003-0000
- Page Start:
- 593
- Page End:
- 605
- Publication Date:
- 2020-10-29
- Subjects:
- amino acid and organic acid diseases -- development -- inborn errors of metabolism -- MetabERN -- morbidity -- mortality -- quality of life -- solid organ transplantation
Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1002/jimd.12318 ↗
- 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:
- 16900.xml