Journal Article

Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population

Vicente, Antonio, Vergara, Inés, Chocron, Sara, Oliet, Aniana, Rodríguez-Rubio, Enrique, Santos, Fernando, Ferrando, Susana, Gil, Marta, González-Rodríguez, Juan David, Espinosa, Laura, de la Cerda-Ojeda, Francisco, Madariaga, Leire, Gil-Peña, Helena, Fernández-Escribano, Angustias, Fernández-Fernández, Marta, de Lucas-Collantes, Carmen, Carrasco Hidalgo-Barquero, Marta, Fernández-Maseda, Mº Ángeles, Antón-Gamero, Montserrat, Luis-Yanes, María Isabel, Ariceta, Gema

2021

Overview

Background X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in PHEX gene leading tohypophosphatemia and high renal loss of phosphate. Rickets and growth retardation are the major manifestations of XLH in children, but there is a broad phenotypic variability. Few publications have reported large series of patients. Current data on the clinical spectrum of the disease, the correlation with the underlying gene mutations, and the long-term outcome of patients on conventional treatment are needed, particularly because of the recent availability of new specific medications to treat XLH. Results The RenalTube database was used to retrospectively analyze 48 Spanish patients (15 men) from 39 different families, ranging from 3 months to 8 years and 2 months of age at the time of diagnosis (median age of 2.0 years), and with XLH confirmed by genetic analysis. Bone deformities, radiological signs of active rickets and growth retardation were the most common findings at diagnosis. Mean (± SEM) height was − 1.89 ± 0.19 SDS and 55% (22/40) of patients had height SDS below—2. All cases had hypophosphatemia, serum phosphate being − 2.81 ± 0.11 SDS. Clinical manifestations and severity of the disease were similar in both genders. No genotype—phenotype correlation was found. Conventional treatment did not attenuate growth retardation after a median follow up of 7.42 years (IQR = 11.26; n = 26 patients) and failed to normalize serum concentrations of phosphate. Eleven patients had mild hyperparathyroidism and 8 patients nephrocalcinosis. Conclusions This study shows that growth retardation and rickets were the most prevalent clinical manifestations at diagnosis in a large series of Spanish pediatric patients with XLH confirmed by mutations in the PHEX gene. Traditional treatment with phosphate and vitamin D supplements did not improve height or corrected hypophosphatemia and was associated with a risk of hyperparathyroidism and nephrocalcinosis. The severity of the disease was similar in males and females.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Age / Body mass index / Bone deformities / Calcinosis / Causes of / Complications and side effects / Diagnosis / Gene mutations / Genetic analysis / Genetic aspects / Genetic variability / Genotype & phenotype / Genotypes / Growth rate / Growth retardation / Human Genetics / Hyperparathyroidism / Hypophosphatemia / Inherited hypophosphatemia / Kidney diseases / Medical research / Medicine / Medicine & Public Health / Mutation / Patients / Pediatric research / Pediatrics / Pharmacology/Toxicology / Phenotype / Phenotypes / Rare bone diseases and skeletal dysplasias / Rare diseases / Rickets / Vitamin D / XLH