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Epidemiology of Tumor-Induced Osteomalacia in Denmark

Tumor-induced osteomalacia (TIO) is a rare, acquired condition of phosphate wasting due to phosphaturic mesenchymal tumors. Because the incidence and prevalence of TIO is unknown, we conducted an observational cohort study using national Danish health registers for the period 2008 to 2018 to obtain...

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Autores principales: Abrahamsen, Bo, Smith, Christopher D., Minisola, Salvatore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273058/
https://www.ncbi.nlm.nih.gov/pubmed/33818653
http://dx.doi.org/10.1007/s00223-021-00843-2
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author Abrahamsen, Bo
Smith, Christopher D.
Minisola, Salvatore
author_facet Abrahamsen, Bo
Smith, Christopher D.
Minisola, Salvatore
author_sort Abrahamsen, Bo
collection PubMed
description Tumor-induced osteomalacia (TIO) is a rare, acquired condition of phosphate wasting due to phosphaturic mesenchymal tumors. Because the incidence and prevalence of TIO is unknown, we conducted an observational cohort study using national Danish health registers for the period 2008 to 2018 to obtain such information. The study also aimed to describe the demographics of the TIO population and the prognosis. The operational definition was based on hypophosphatemia or adult osteomalacia diagnoses, combined with prescriptions used in the initial management and procedures consistent with advanced imaging used for locating tumors. The incidence of TIO in Denmark was found to be below 0.13 per 100,000 person years for the total population of the country and 0.10 per 100,000 in adult-onset disease. The prevalence of TIO was estimated to be no more than 0.70 per 100,000 persons for the total population and 0.43 per 100,000 in adults. In 2018, there were a maximum of nine new cases of TIO in Danish adults. Mortality was low but few patients fulfilled the protocol cure criterion during the observation period. TIO has no ICD-10 code and limitations to the study include lack of information on serum biochemistry and on the use of phosphate supplements. Strengths include the use of long-term longitudinal, national hospital and prescription data from a country with universal healthcare. Given the very small patient population with TIO and the known delay to diagnosis and cure, management of patients with suspected TIO should be centralized. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00223-021-00843-2.
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spelling pubmed-82730582021-07-20 Epidemiology of Tumor-Induced Osteomalacia in Denmark Abrahamsen, Bo Smith, Christopher D. Minisola, Salvatore Calcif Tissue Int Original Research Tumor-induced osteomalacia (TIO) is a rare, acquired condition of phosphate wasting due to phosphaturic mesenchymal tumors. Because the incidence and prevalence of TIO is unknown, we conducted an observational cohort study using national Danish health registers for the period 2008 to 2018 to obtain such information. The study also aimed to describe the demographics of the TIO population and the prognosis. The operational definition was based on hypophosphatemia or adult osteomalacia diagnoses, combined with prescriptions used in the initial management and procedures consistent with advanced imaging used for locating tumors. The incidence of TIO in Denmark was found to be below 0.13 per 100,000 person years for the total population of the country and 0.10 per 100,000 in adult-onset disease. The prevalence of TIO was estimated to be no more than 0.70 per 100,000 persons for the total population and 0.43 per 100,000 in adults. In 2018, there were a maximum of nine new cases of TIO in Danish adults. Mortality was low but few patients fulfilled the protocol cure criterion during the observation period. TIO has no ICD-10 code and limitations to the study include lack of information on serum biochemistry and on the use of phosphate supplements. Strengths include the use of long-term longitudinal, national hospital and prescription data from a country with universal healthcare. Given the very small patient population with TIO and the known delay to diagnosis and cure, management of patients with suspected TIO should be centralized. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00223-021-00843-2. Springer US 2021-04-05 2021 /pmc/articles/PMC8273058/ /pubmed/33818653 http://dx.doi.org/10.1007/s00223-021-00843-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Research
Abrahamsen, Bo
Smith, Christopher D.
Minisola, Salvatore
Epidemiology of Tumor-Induced Osteomalacia in Denmark
title Epidemiology of Tumor-Induced Osteomalacia in Denmark
title_full Epidemiology of Tumor-Induced Osteomalacia in Denmark
title_fullStr Epidemiology of Tumor-Induced Osteomalacia in Denmark
title_full_unstemmed Epidemiology of Tumor-Induced Osteomalacia in Denmark
title_short Epidemiology of Tumor-Induced Osteomalacia in Denmark
title_sort epidemiology of tumor-induced osteomalacia in denmark
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273058/
https://www.ncbi.nlm.nih.gov/pubmed/33818653
http://dx.doi.org/10.1007/s00223-021-00843-2
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