Efficacy of low dose nitisinone in the management of alkaptonuria.
Mol Genet Metab
; 127(3): 184-190, 2019 07.
Article
en En
| MEDLINE
| ID: mdl-31235217
ABSTRACT
AIM:
To study the efficacy of low dosage of nitisinone in alkaptonuria.BACKGROUND:
Alkaptonuria (AKU) is a rare genetic disease which induces deposition of homogentisic acid (HGA) in connective inducing premature arthritis, lithiasis, cardiac valve disease, fractures, muscle and tendon ruptures and osteopenia. Recent studies showed that nitisinone decreases HGA and is a beneficial therapy in AKU. This treatment induces an increase in tyrosine levels which can induces adverse effects as keratopathy.METHODS:
We described the evolution HGA excretion and tyrosine evolution in 3 AKU patients treated by very low dosage of nitisinone with regards to their daily protein intakes. We also described the first pregnancy in an AKU patient treated by nitisinone.RESULTS:
We found mild clinical signs of alkaptonuria on vertebra MRI in two young adults and homogentisate deposition in teeth of a 5â¯years old girl. Very low dose of nitisinone (10% of present recommended dose 0.2â¯mg/day) allowed to decrease homogentisic acid by >90% without increasing tyrosine levels above 500⯵mol/ in these three patients. INTERPRETATIONS The analysis of the follow-up data shows that, in our three patients, a low-dosage of nitisinone is sufficient to decrease urinary HGA without increasing plasma tyrosine levels above the threshold of 500⯵mol/L.Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Ciclohexanonas
/
Alcaptonuria
/
Nitrobenzoatos
Límite:
Adult
/
Child, preschool
/
Female
/
Humans
/
Male
Idioma:
En
Revista:
Mol Genet Metab
Asunto de la revista:
BIOLOGIA MOLECULAR
/
BIOQUIMICA
/
METABOLISMO
Año:
2019
Tipo del documento:
Article
País de afiliación:
Francia