Development of Spinal Enthesopathies in Adults With X-linked Hypophosphatemia

Author:

Herrou Julia12ORCID,Fechtenbaum Jacques2,Rothenbuhler Anya345,Kamenický Peter36,Roux Christian123,Linglart Agnès345ORCID,Briot Karine123ORCID

Affiliation:

1. Department of Rheumatology, INSERM UMR 1153, Université de Paris-Cité, APHP Centre, Cochin Hospital , 75014 Paris , France

2. Department of Rheumatology, APHP Centre, Cochin Hospital , 75014 Paris , France

3. Reference Center for Rare Diseases of the Calcium and Phosphate Metabolism, OSCAR Network for Rare Bone and Calcium Phosphate Disorders , Paris , France

4. Department of Endocrinology and Diabetes for Children, APHP, Bicêtre Paris Saclay Hospital , 94270 Le Kremlin Bicêtre , France

5. APHP, Plateforme d’expertise Paris Saclay maladies rares, Bicêtre Paris Saclay Hospital , 94270 Le Kremlin Bicêtre , France

6. Université Paris-Saclay, INSERM UMR-S 1185, Physiologie et Physiopathologie Endocriniennes , 94270 Le Kremlin-Bicêtre , France

Abstract

Abstract Context Musculoskeletal complications are the main manifestations in adults with X-linked hypophosphatemia (XLH). Enthesopathy significantly impairs quality of life. Objective To identify the risk factors associated with the development and progression of spinal enthesopathies in adults with XLH. Design and setting We conducted a retrospective study in the French Reference Center for Rare Diseases of the Calcium and Phosphate Metabolism. Patients Adults XLH patients with 2 EOS® imaging performed at least 2 years apart at the same center between June 2011 and March 2022. The progression of enthesopathies was defined as a new enthesopathy at least 1 intervertebral level in patients with or without presence of enthesopathy at baseline. Main outcome measures Demographic, treatment, PHEX mutation with the progression of enthesopathies. Results Fifty-one patients (66.7% of women, mean age 42.1 ± 13.4 years) underwent 2 EOS imaging with an average interval of 5.7 (± 2.31) years. Progression of spinal enthesopathies was observed in 27 (52.9%) patients. In univariate analysis, patients with a progression of spinal enthesopathies were significantly older (P < .0005), were significantly older at treatment initiation (P = .02), presented with dental complications (P = .03), received less frequently treatment during childhood with phosphate and/or vitamin D analogs (P = .06), and presented more frequently with hip osteoarthritis (P = .002) at baseline. In multivariate analysis, none of these factors was associated with a progression of spinal enthesopathies. Conclusion This study confirms the high proportion of patients with a progression of spinal enthesopathies. Age seems to be the main factor associated with progression.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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