Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
Sep 2019
Historique:
entrez: 3 10 2019
pubmed: 3 10 2019
medline: 11 10 2019
Statut: ppublish

Résumé

Treatment with nitisinone (NTBC) has brought about a drastic improvement in the treatment and prognosis of hereditary tyrosinemia type I (HT1). We conducted a retrospective observational multicentric study in Spanish HT1 patients treated with NTBC to assess clinical and biochemical long-term evolution.We evaluated 52 patients, 7 adults and 45 children, treated with NTBC considering: age at diagnosis, diagnosis by clinical symptoms, or by newborn screening (NBS); phenotype (acute/subacute/chronic), mutational analysis; symptoms at diagnosis and clinical course; biochemical markers; doses of NTBC; treatment adherence; anthropometric evolution; and neurocognitive outcome.The average follow-up period was 6.1 ± 4.9 and 10.6 ± 5.4 years in patients with early and late diagnosis respectively. All patients received NTBC from diagnosis with an average dose of 0.82 mg/kg/d. All NBS-patients (n = 8) were asymptomatic at diagnosis except 1 case with acute liver failure, and all remain free of liver and renal disease in follow-up. Liver and renal affectation was markedly more frequent at diagnosis in patients with late diagnosis (P < .001 and .03, respectively), with ulterior positive hepatic and renal course in 86.4% and 93.2% of no-NBS patients, although 1 patient with good metabolic control developed hepatocarcinoma.Despite a satisfactory global nutritional evolution, 46.1% of patients showed overweight/obesity. Interestingly lower body mass index was observed in patients with good dietary adherence (20.40 ± 4.43 vs 24.30 ± 6.10; P = .08) and those with good pharmacological adherence (21.19 ± 4.68 vs 28.58 ± 213.79).intellectual quotient was ≥85 in all NBS- and 68.75% of late diagnosis cases evaluated, 15% of which need pedagogical support, and 6.8% (3/44) showed school failure.Among the 12 variants identified in fumarylacetoacetate hydrolase gene, 1 of them novel (H63D), the most prevalent in Spanish population is c.554-1 G>T.After NTBC treatment a reduction in tyrosine and alpha-fetoprotein levels was observed in all the study groups, significant for alpha-fetoprotein in no NBS-group (P = .03), especially in subacute/chronic forms (P = .018).This series confirms that NTBC treatment had clearly improved the prognosis and quality of life of HT1 patients, but it also shows frequent cognitive dysfunctions and learning difficulties in medium-term follow-up, and, in a novel way, a high percentage of overweight/obesity.

Identifiants

pubmed: 31574857
doi: 10.1097/MD.0000000000017303
pii: 00005792-201909270-00066
pmc: PMC6775438
doi:

Substances chimiques

Cyclohexanones 0
Enzyme Inhibitors 0
Nitrobenzoates 0
nitisinone K5BN214699

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e17303

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Auteurs

María Luz Couce (ML)

Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Clínico Universitario de Santiago de Compostela, CIBERER, Health Research Institute of Santiago de Compostela (IDIS).

Paula Sánchez-Pintos (P)

Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Clínico Universitario de Santiago de Compostela, CIBERER, Health Research Institute of Santiago de Compostela (IDIS).

Luís Aldámiz-Echevarría (L)

Unit of Metabolism, Department of Pediatrics, Hospital de Cruces, Group of Metabolism, Biocruces Health Research Institute, CIBERER.

Isidro Vitoria (I)

Unit of Metabolopathies Hospital Universitario La Fe.

Victor Navas (V)

Pediatric Gastroenterology and Nutrition Unit Hospital Carlos Haya, Málaga.

Elena Martín-Hernández (E)

Unit of Mitochondrial and Congenital Metabolic Diseases, Hospital 12 de Octubre.

Camila García-Volpe (C)

Pediatric Gastroenterology, Hepatology and Nutrition Unit, H. San Joan de Deu, Barcelona.

Guillem Pintos (G)

Minority disease Unit, Hospital Vall d'Hebron.

Luis Peña-Quintana (L)

Gastroenterology and Nutrition Unit Complejo Hospitalario Universitario Insular-Materno Infantil, CIBEROBN, Las Palmas de Gran Canaria University, Las Palmas.

Tomás Hernández (T)

Pediatric Service, Hospital General de Albacete.

David Gil (D)

Pediatric Gastroenterology, Hepatology and Nutrition Unit Hospital Virgen da Arrixaca, Murcia.

Félix Sánchez-Valverde (F)

Gastroenterology and Nutrition Unit, Hospital Virgen del Camino, Pamplona.

María Bueno (M)

Metabolic Congenital Diseases Unit, Hospital Virgen del Rocío, Sevilla.

Iria Roca (I)

Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Clínico Universitario de Santiago de Compostela, CIBERER, Health Research Institute of Santiago de Compostela (IDIS).

Encarna López-Ruzafa (E)

Gastroenterology Unit, H. de Torrecárdenas, Almería.

Carmen Díaz-Fernández (C)

Unit of Hepatology and Infantile Hepatic Transplantation, Hospital Universitario La Paz, Madrid, Spain.

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Classifications MeSH