Increased Prevalence of Nephrolithiasis and Hyperoxaluria in Paget Disease of Bone

Author:

Rendina Domenico1,De Filippo Gianpaolo2ORCID,Merlotti Daniela3,Di Stefano Marco4,Mingiano Christian3,Giaquinto Alfonso1,Evangelista Marco1,Bo Mario4ORCID,Arpino Sergio5,Faraonio Raffaella5,Strazzullo Pasquale1,Gennari Luigi3ORCID

Affiliation:

1. Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy

2. Assistance Publique-Hôpitaux de Paris, Hôpital Robert-Debré, Service d’Endocrinologie et Diabétologie Pédiatrique, Paris, France

3. Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy

4. Department of Medical Science, Gerontology and Bone Metabolic Diseases, University of Torino, Torino, Italy

5. Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy

Abstract

Abstract Context Nephrolithiasis (NL) and primary hyperparathyroidism (HPTH) are metabolic complications of Paget disease of bone (PDB), but recent data regarding their prevalence in PDB patients are lacking. Objectives Study 1: To compare the prevalence of primary HPTH and NL in 708 patients with PDB and in 1803 controls. Study 2: To evaluate the prevalence of NL-metabolic risk factors in 97 patients with PDB and NL, 219 PDB patients without NL, 364 NL patients without PDB, and 219 controls, all of them without HPTH. Design Cross-sectional multicentric study. Setting Italian referral centers for metabolic bone disorders. Participants Patients with PDB from the Associazione Italiana malati di osteodistrofia di Paget registry. Participants in the Olivetti Heart and the Siena Osteoporosis studies. Main Outcome Measures HPTH; NL; NL-metabolic risk factors. Results Patients with PDB showed higher prevalence of primary HPTH and NL compared with controls (P < 0.01). The NL recurrence occurs more frequently in patients with polyostotic PDB. About one-half of patients with PDB but without NL showed 1 or more NL-related metabolic risk factors. The hyperoxaluria (HyperOx) prevalence was higher in patients with PDB and NL compared with patients with NL but without PDB and in patients with PDB without NL compared with controls (P = 0.01). Patients with PDB and HyperOx showed a longer lapse of time from the last aminobisphosphonate treatment. Conclusions NL and HPTH are frequent metabolic complication of PDB. The NL occurrence should be evaluated in patients with PDB, particularly in those with polyostotic disease and/or after aminobisphosphonate treatment to apply an adequate prevention strategy.

Publisher

The Endocrine Society

Subject

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

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