FGF23-Related Hypophosphataemic Bone Disease

4Citations
Citations of this article
12Readers
Mendeley users who have this article in their library.

Abstract

Metabolic skeletal dysplasias comprise an extensive group of diseases capable of causing changes, usually progressive, in the bone and are due to hereditary disorders in many cases. The diagnosis and treatment of these diseases are not without difficulty, both because of their rarity and their possible confusion with more common diseases. A paradigmatic case of these metabolic skeletal dysplasias is X-linked hypophosphataemic rickets, which causes phosphaturia, a condition that alters the phosphate–calcium metabolism balance consequently causing, among other conditions, skeletal deformities and short stature. The genetic advances in recent years allow a much more accurate diagnosis of this disease when suspected, making differential diagnosis easier with similar entities but whose real causes are different. A better understanding of the phosphate–calcium metabolism allows us to replace the symptomatic treatment currently available with one that involves rebalancing the excess of fibroblast growth factor 23 (FGF23) by using monoclonal antibodies. In November 2018, a symposium sponsored by Kyowa Kirin Pharmaceuticals took place in Madrid, in which national and international experts addressed several aspects of these rare kidney diseases. Some topics addressed were the present and future genetic diagnosis, the use of multi-gene panels in renal or skeletal diseases, the role of animal models to better understand underlying skeletal changes, and the role of conventional radiology and surgery in the diagnosis and final treatment of bone deformities; all these without forgetting the important role of FGF23 and Klotho imbalances that result in the genetic change causing this disease. The optimization and limitations of conventional treatments currently available was also a topic addressed extensively, as well as the implications that new treatments against FGF23 could have in the future. This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by the author.

References Powered by Scopus

Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia

368Citations
N/AReaders
Get full text

Review of clinical next-generation sequencing

281Citations
N/AReaders
Get full text

Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial

265Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Burden of disease of X-linked hypophosphatemia in Japanese and Korean patients: a cross-sectional survey

15Citations
N/AReaders
Get full text

Safety and Efficacy of Burosumab in Pediatric Patients With X-Linked Hypophosphatemia: A Phase 3/4 Open-Label Trial

13Citations
N/AReaders
Get full text

Cellular and Molecular Alterations Underlying Abnormal Bone Growth in X-Linked Hypophosphatemia

7Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

González-Meneses López, A. (2020, May 1). FGF23-Related Hypophosphataemic Bone Disease. Advances in Therapy. Adis. https://doi.org/10.1007/s12325-019-01177-0

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 5

63%

Researcher 3

38%

Readers' Discipline

Tooltip

Biochemistry, Genetics and Molecular Bi... 4

44%

Medicine and Dentistry 3

33%

Pharmacology, Toxicology and Pharmaceut... 2

22%

Save time finding and organizing research with Mendeley

Sign up for free