New biomarkers for early diagnosis of Lesch-Nyhan disease revealed by metabolic analysis on a large cohort of patients.

Autor: Ceballos-Picot I; Laboratoire de Biochimie métabolomique et protéomique, Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. irene.ceballos@nck.aphp.fr.; Université Paris Descartes Sorbonne Paris Cité, 15 rue de l'Ecole de Médecine, Paris, 75006, France. irene.ceballos@nck.aphp.fr.; Centre de référence 'Maladies Métaboliques Héréditaires de l'enfant à l'adulte' Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. irene.ceballos@nck.aphp.fr., Le Dantec A; Université de Bordeaux, IBGC UMR 5095, 1 rue Camille Saint-Saëns, Bordeaux, F-33077, France. aureliald@gmail.com.; Institut de Biochimie et Génétique Cellulaires, CNRS UMR 5095 1 rue C. Saint-Saëns CS 61390 F-33077, Bordeaux, France. aureliald@gmail.com., Brassier A; Centre de référence 'Maladies Métaboliques Héréditaires de l'enfant à l'adulte' Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. anais.brassier@nck.aphp.fr., Jaïs JP; Service de Biostatistique, Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. jean-philippe.jais@nck.aphp.fr., Ledroit M; Laboratoire de Biochimie métabolomique et protéomique, Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. ledroit.morgan@gmail.com., Cahu J; Laboratoire de Biochimie métabolomique et protéomique, Hôpital Necker-Enfants Malades, AP-HP, 149 rue de Sèvres, Paris, 75015, France. julie.cahu@gmail.com., Ea HK; Université Paris 7 Denis Diderot, Hôpital Lariboisière, Centre Viggo Petersen, Inserm UMR 1132 (Ex-606), 2 rue Ambroise Paré, Paris, 75010, France. korngea@yahoo.fr., Daignan-Fornier B; Université de Bordeaux, IBGC UMR 5095, 1 rue Camille Saint-Saëns, Bordeaux, F-33077, France. b.daignan-fornier@ibgc.cnrs.fr.; Institut de Biochimie et Génétique Cellulaires, CNRS UMR 5095 1 rue C. Saint-Saëns CS 61390 F-33077, Bordeaux, France. b.daignan-fornier@ibgc.cnrs.fr., Pinson B; Université de Bordeaux, IBGC UMR 5095, 1 rue Camille Saint-Saëns, Bordeaux, F-33077, France. benoit.pinson@ibgc.cnrs.fr.; Institut de Biochimie et Génétique Cellulaires, CNRS UMR 5095 1 rue C. Saint-Saëns CS 61390 F-33077, Bordeaux, France. benoit.pinson@ibgc.cnrs.fr.
Jazyk: angličtina
Zdroj: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2015 Jan 23; Vol. 10, pp. 7. Date of Electronic Publication: 2015 Jan 23.
DOI: 10.1186/s13023-014-0219-0
Abstrakt: Background: Lesch-Nyhan disease is a rare X-linked neurodevelopemental metabolic disorder caused by a wide variety of mutations in the HPRT1 gene leading to a deficiency of the purine recycling enzyme hypoxanthine-guanine phosphoribosyltransferase (HGprt). The residual HGprt activity correlates with the various phenotypes of Lesch-Nyhan (LN) patients and in particular with the different degree of neurobehavioral disturbances. The prevalence of this disease is considered to be underestimated due to large heterogeneity of its clinical symptoms and the difficulty of diagnosing of the less severe forms of the disease. We therefore searched for metabolic changes that would facilitate an early diagnosis and give potential clues on the disease pathogenesis and potential therapeutic approaches.
Methods: Lesch-Nyhan patients were diagnosed using HGprt enzymatic assay in red blood cells and identification of the causal HPRT1 gene mutations. These patients were subsequently classified into the three main phenotypic subgroups ranging from patients with only hyperuricemia to individuals presenting motor dysfunction, cognitive disability and self-injurious behavior. Metabolites from the three classes of patients were analyzed and quantified by High Performance Ionic Chromatography and biomarkers of HGprt deficiency were then validated by statistical analyses.
Results: A cohort of 139 patients, from 112 families, diagnosed using HGprt enzymatic assay in red blood cells, was studied. 98 displayed LN full phenotype (86 families) and 41 (26 families) had attenuated clinical phenotypes. Genotype/phenotype correlations show that LN full phenotype was correlated to genetic alterations resulting in null enzyme function, while variant phenotypes are often associated with missense mutations allowing some residual HGprt activity. Analysis of metabolites extracted from red blood cells from 56 LN patients revealed strong variations specific to HGprt deficiency for six metabolites (AICAR mono- and tri-phosphate, nicotinamide, nicotinic acid, ATP and Succinyl-AMP) as compared to controls including hyperuricemic patients without HGprt deficiency.
Conclusions: A highly significant correlation between six metabolites and the HGprt deficiency was established, each of them providing an easily measurable marker of the disease. Their combination strongly increases the probability of an early and reliable diagnosis for HGprt deficiency.
Databáze: MEDLINE
Externí odkaz: