Literature DB >> 20524110

Phenotype presentation of hypophosphatemic rickets in adults.

Signe S Beck-Nielsen1, Klaus Brusgaard, Lars M Rasmussen, Kim Brixen, Bendt Brock-Jacobsen, Mette R Poulsen, Peter Vestergaard, Stuart H Ralston, Omar M E Albagha, Sven Poulsen, Dorte Haubek, Hans Gjørup, Hanne Hintze, Mette G Andersen, Lene Heickendorff, Jacob Hjelmborg, Jeppe Gram.   

Abstract

Hypophosphatemic rickets (HR) is a group of rare disorders caused by excessive renal phosphate wasting. The purpose of this cross-sectional study of 38 HR patients was to characterize the phenotype of adult HR patients. Moreover, skeletal and endodontic severity scores were defined to assess possible gender differences in disease severity in patients with genetically verified X-linked HR. Compared to normal reference data, i.e., z = 0, HR patients had significantly lower final height, with a mean difference in z-score of -1.9 (95% CI -2.4 to -1.4, P < 0.001). Compared to paired z-scores of final height, z-scores of leg length were significantly lower and those of sitting height were significantly higher (P < 0.001), resulting in disproportion as indicated by the significantly elevated sitting height ratio, mean difference in z-score of 2.6 (95% CI 2.1-3.1, P < 0.001). Z-scores of head circumference (median 1.4, range -0.4 to 5.5, P < 0.001) and z-scores of bone mineral density (BMD) of the lumbar spine (median 1.9, range -1.5 to 8.6, P < 0.001) were significantly elevated compared to normal reference data. The relative risk (RR) of fracture was reduced (RR = 0.34, 95% CI 0.20-0.57, P < 0.001). The skeletal severity score tended to be higher in males compared to females (P = 0.07), and no gender difference in endodontic severity was found. In conclusion, adult HR patients were characterized by short stature and were disproportioned. They had elevated BMD of the lumbar spine and a reduced risk of fractures. We found a tendency for males to be more severely affected than females.

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Year:  2010        PMID: 20524110     DOI: 10.1007/s00223-010-9373-0

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  28 in total

1.  Evaluation of bone mineral density and microarchitectural parameters by DXA and HR-pQCT in 37 children and adults with X-linked hypophosphatemic rickets.

Authors:  G P Colares Neto; R M R Pereira; J C Alvarenga; L Takayama; M F A Funari; R M Martin
Journal:  Osteoporos Int       Date:  2017-02-13       Impact factor: 4.507

2.  Skeletal mineralization defects in adult hypophosphatasia--a clinical and histological analysis.

Authors:  F Barvencik; F Timo Beil; M Gebauer; B Busse; T Koehne; S Seitz; J Zustin; P Pogoda; T Schinke; M Amling
Journal:  Osteoporos Int       Date:  2011-01-26       Impact factor: 4.507

3.  Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron.

Authors:  Camille Ansermet; Matthias B Moor; Gabriel Centeno; Muriel Auberson; Dorothy Zhang Hu; Roland Baron; Svetlana Nikolaeva; Barbara Haenzi; Natalya Katanaeva; Ivan Gautschi; Vladimir Katanaev; Samuel Rotman; Robert Koesters; Laurent Schild; Sylvain Pradervand; Olivier Bonny; Dmitri Firsov
Journal:  J Am Soc Nephrol       Date:  2016-10-31       Impact factor: 10.121

Review 4.  X-linked hypophosphatemia and growth.

Authors:  R Fuente; H Gil-Peña; D Claramunt-Taberner; O Hernández; A Fernández-Iglesias; L Alonso-Durán; E Rodríguez-Rubio; F Santos
Journal:  Rev Endocr Metab Disord       Date:  2017-03       Impact factor: 6.514

Review 5.  Congenital Conditions of Hypophosphatemia Expressed in Adults.

Authors:  Gemma Marcucci; Maria Luisa Brandi
Journal:  Calcif Tissue Int       Date:  2020-05-14       Impact factor: 4.333

6.  X-Linked Hypophosphatemic Rickets Manifesting as Sclerotic Bone Disease and Enthesopathy.

Authors:  Hiya Boro; Shailendra Singh Naik; Charandeep Singh; Saurav Khatiwada; Rajesh Khadgawat
Journal:  Cureus       Date:  2020-10-10

Review 7.  FGF23 and Associated Disorders of Phosphate Wasting.

Authors:  Anisha Gohil; Erik A Imel
Journal:  Pediatr Endocrinol Rev       Date:  2019-09

8.  Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemia.

Authors:  Hans Gjørup; Signe Sparre Beck-Nielsen; Dorte Haubek
Journal:  Clin Oral Investig       Date:  2017-06-12       Impact factor: 3.573

9.  High bone mineral apparent density in children with X-linked hypophosphatemia.

Authors:  S S Beck-Nielsen; K Brixen; J Gram; C Mølgaard
Journal:  Osteoporos Int       Date:  2013-02-07       Impact factor: 4.507

Review 10.  Pharmacological management of X-linked hypophosphataemia.

Authors:  Erik A Imel; Kenneth E White
Journal:  Br J Clin Pharmacol       Date:  2018-10-29       Impact factor: 4.335

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