Neurocognitive profiles in MSUD school‐age patients. Issue 3 (21st March 2017)
- Record Type:
- Journal Article
- Title:
- Neurocognitive profiles in MSUD school‐age patients. Issue 3 (21st March 2017)
- Main Title:
- Neurocognitive profiles in MSUD school‐age patients
- Authors:
- Bouchereau, Juliette
Leduc‐Leballeur, Julie
Pichard, Samia
Imbard, Apolline
Benoist, Jean‐François
Abi Warde, Marie‐Thérèse
Arnoux, Jean‐Baptiste
Barbier, Valérie
Brassier, Anaïs
Broué, Pierre
Cano, Aline
Chabrol, Brigitte
Damon, Gilles
Gay, Claire
Guillain, Isabelle
Habarou, Florence
Lamireau, Delphine
Ottolenghi, Chris
Paermentier, Laetitia
Sabourdy, Frédérique
Touati, Guy
Ogier de Baulny, Hélène
de Lonlay, Pascale
Schiff, Manuel - Abstract:
- Abstract: Maple syrup urine disease (MSUD), an inborn error of amino acids catabolism is characterized by accumulation of branched chain amino acids (BCAAs) leucine, isoleucine, valine and their corresponding alpha‐ketoacids. Impact on the cognitive development has been reported historically, with developmental delays of varying degree. Currently, earlier diagnosis and improved management allow a better neurodevelopment, without requirement of special education. However, specific impairments can be observed, and so far, results of detailed neurocognitive assessments are not available. The aim of this study was to analyse neurocognitive profiles of French MSUD patients. This was a multicentre retrospective study on MSUD patients who underwent neurocognitive evaluation at primary school age. Twenty‐one patients with classical neonatal onset MSUD were included. The patients' mean age at the time of evaluation was 8.7 years. The mean intellectual quotient (IQ) score was in the normal range (95.1 ± 12.6). In a subset of eight patients, a consistent developmental pattern of higher verbal than performance IQ was observed (mean of the difference 25.7 ± 8.7, p < 0.0001). No correlation could be established between this pattern and long‐term metabolic balance (BCAA blood levels), or severity of acute metabolic imbalances, or leucine blood levels at diagnosis and time to toxin removal procedure. These data show that some MSUD patients may exhibit an abnormal neurocognitive profileAbstract: Maple syrup urine disease (MSUD), an inborn error of amino acids catabolism is characterized by accumulation of branched chain amino acids (BCAAs) leucine, isoleucine, valine and their corresponding alpha‐ketoacids. Impact on the cognitive development has been reported historically, with developmental delays of varying degree. Currently, earlier diagnosis and improved management allow a better neurodevelopment, without requirement of special education. However, specific impairments can be observed, and so far, results of detailed neurocognitive assessments are not available. The aim of this study was to analyse neurocognitive profiles of French MSUD patients. This was a multicentre retrospective study on MSUD patients who underwent neurocognitive evaluation at primary school age. Twenty‐one patients with classical neonatal onset MSUD were included. The patients' mean age at the time of evaluation was 8.7 years. The mean intellectual quotient (IQ) score was in the normal range (95.1 ± 12.6). In a subset of eight patients, a consistent developmental pattern of higher verbal than performance IQ was observed (mean of the difference 25.7 ± 8.7, p < 0.0001). No correlation could be established between this pattern and long‐term metabolic balance (BCAA blood levels), or severity of acute metabolic imbalances, or leucine blood levels at diagnosis and time to toxin removal procedure. These data show that some MSUD patients may exhibit an abnormal neurocognitive profile with higher verbal than performance abilities. This might suggest an executive dysfunction disorder that would need to be further investigated by specialized testing. This pattern is important to detect in MSUD, as appropriate neuropsychological treatment strategies should be proposed. … (more)
- Is Part Of:
- Journal of inherited metabolic disease. Volume 40:Issue 3(2017)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 40:Issue 3(2017)
- Issue Display:
- Volume 40, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 40
- Issue:
- 3
- Issue Sort Value:
- 2017-0040-0003-0000
- Page Start:
- 377
- Page End:
- 383
- Publication Date:
- 2017-03-21
- Subjects:
- Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1007/s10545-017-0033-7 ↗
- 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:
- 9778.xml