Back to Search Start Over

Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls

Authors :
Van Ginkel, Willem W.G.
Goyens, Philippe
McKiernan, Patrick
Van Spronsen, Francjan
Jahja, Rianne
Huijbregts, Stephan C J
Daly, Anne
MacDonald, Anita
De Laet, Corinne
Cassiman, David
Eyskens, François
Körver-Keularts, Irene M L W I.M.L.W.
Van Ginkel, Willem W.G.
Goyens, Philippe
McKiernan, Patrick
Van Spronsen, Francjan
Jahja, Rianne
Huijbregts, Stephan C J
Daly, Anne
MacDonald, Anita
De Laet, Corinne
Cassiman, David
Eyskens, François
Körver-Keularts, Irene M L W I.M.L.W.
Source :
Orphanet journal of rare diseases, 11 (1
Publication Year :
2016

Abstract

Background: Hereditary Tyrosinemia type 1 (HT1) is a rare metabolic disorder caused by a defect in the enzyme Fumarylacetoacetate Hydrolase. Due to this defect, toxic products accumulate which, in turn, cause liver and kidney dysfunction. Treatment with 2-(2-nitro-4-trifluoromethylbenoyl)-1,3-cyclohexanedione (NTBC) and diet has diminished these problems, but recent data indicate that HT1 patients have neurocognitive problems. However, the neuropsychological profile of these patients is unknown. Therefore, this study aimed to investigate this neuropsychological profile by comparing HT1 patients with healthy controls. Methods: Neurocognitive testing was performed in a heterogeneous group of 19 NTBC and dietary treated HT1 patients (five female, fourteen male; mean age 12.9 ± 4.8 years; range 7.9-23.6 years) and 19 age and gender matched controls (five female, fourteen male; mean age 13.2 ± 4.6 years; range 8.1-24.8 years). IQ scores were estimated and all participants performed the Amsterdam Neuropsychological Tasks, measuring executive functions (inhibition, cognitive flexibility and working memory) and social cognition (face recognition and identification of facial emotions). Results: HT1 patients showed poorer estimated IQ, executive functioning (working memory and cognitive flexibility), and social cognition compared to healthy controls. Lower IQ scores in HT1 patients were mostly unrelated to scores on executive function- and social cognition tasks and therefore did not account for group differences in these domains. Further analyses within the HT1 patient group (comparing different groups of patients based on the age at diagnosis and the clinical symptoms at diagnosis) did not reveal any significant results. The duration of NTBC treatment was negatively correlated with IQ. Conclusions: Despite the heterogeneity of the patient group, these data clearly show that IQ, executive functioning and social cognition are affected in HT1 patients, and that IQ screening is<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
Orphanet journal of rare diseases, 11 (1
Notes :
1 full-text file(s): application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn961112098
Document Type :
Electronic Resource