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Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases
The association between bone mineral density (BMD) and hepatic glycogen storage diseases (GSDs) is still unclear. To evaluate the BMD of patients with GSD I, IIIa and IXα, a cross-sectional study was performed, including 23 patients (GSD Ia = 13, Ib = 5, IIIa = 2 and IXα = 3; median age = 11.9 years...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469033/ https://www.ncbi.nlm.nih.gov/pubmed/34578865 http://dx.doi.org/10.3390/nu13092987 |
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author | Jacoby, Jésica Tamara Bento dos Santos, Bruna Nalin, Tatiele Colonetti, Karina Farret Refosco, Lília F. M. de Souza, Carolina Spritzer, Poli Mara Poloni, Soraia Hack-Mendes, Roberta Schwartz, Ida Vanessa Doederlein |
author_facet | Jacoby, Jésica Tamara Bento dos Santos, Bruna Nalin, Tatiele Colonetti, Karina Farret Refosco, Lília F. M. de Souza, Carolina Spritzer, Poli Mara Poloni, Soraia Hack-Mendes, Roberta Schwartz, Ida Vanessa Doederlein |
author_sort | Jacoby, Jésica Tamara |
collection | PubMed |
description | The association between bone mineral density (BMD) and hepatic glycogen storage diseases (GSDs) is still unclear. To evaluate the BMD of patients with GSD I, IIIa and IXα, a cross-sectional study was performed, including 23 patients (GSD Ia = 13, Ib = 5, IIIa = 2 and IXα = 3; median age = 11.9 years; IQ = 10.9–20.1) who underwent a dual-energy X-ray absorptiometry (DXA). Osteocalcin (OC, n = 18), procollagen type 1 N-terminal propeptide (P1NP, n = 19), collagen type 1 C-terminal telopeptide (CTX, n = 18) and 25-OH Vitamin D (n = 23) were also measured. The participants completed a 3-day food diary (n = 20). Low BMD was defined as a Z-score ≤ −2.0. All participants were receiving uncooked cornstarch (median dosage = 6.3 g/kg/day) at inclusion, and 11 (47.8%) presented good metabolic control. Three (13%) patients (GSD Ia = 1, with poor metabolic control; IIIa = 2, both with high CPK levels) had a BMD ≤ −2.0. CTX, OC and P1NP correlated negatively with body weight and age. 25-OH Vitamin D concentration was decreased in seven (30.4%) patients. Our data suggest that patients with hepatic GSDs may have low BMD, especially in the presence of muscular involvement and poor metabolic control. Systematic nutritional monitoring of these patients is essential. |
format | Online Article Text |
id | pubmed-8469033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84690332021-09-27 Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases Jacoby, Jésica Tamara Bento dos Santos, Bruna Nalin, Tatiele Colonetti, Karina Farret Refosco, Lília F. M. de Souza, Carolina Spritzer, Poli Mara Poloni, Soraia Hack-Mendes, Roberta Schwartz, Ida Vanessa Doederlein Nutrients Article The association between bone mineral density (BMD) and hepatic glycogen storage diseases (GSDs) is still unclear. To evaluate the BMD of patients with GSD I, IIIa and IXα, a cross-sectional study was performed, including 23 patients (GSD Ia = 13, Ib = 5, IIIa = 2 and IXα = 3; median age = 11.9 years; IQ = 10.9–20.1) who underwent a dual-energy X-ray absorptiometry (DXA). Osteocalcin (OC, n = 18), procollagen type 1 N-terminal propeptide (P1NP, n = 19), collagen type 1 C-terminal telopeptide (CTX, n = 18) and 25-OH Vitamin D (n = 23) were also measured. The participants completed a 3-day food diary (n = 20). Low BMD was defined as a Z-score ≤ −2.0. All participants were receiving uncooked cornstarch (median dosage = 6.3 g/kg/day) at inclusion, and 11 (47.8%) presented good metabolic control. Three (13%) patients (GSD Ia = 1, with poor metabolic control; IIIa = 2, both with high CPK levels) had a BMD ≤ −2.0. CTX, OC and P1NP correlated negatively with body weight and age. 25-OH Vitamin D concentration was decreased in seven (30.4%) patients. Our data suggest that patients with hepatic GSDs may have low BMD, especially in the presence of muscular involvement and poor metabolic control. Systematic nutritional monitoring of these patients is essential. MDPI 2021-08-27 /pmc/articles/PMC8469033/ /pubmed/34578865 http://dx.doi.org/10.3390/nu13092987 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jacoby, Jésica Tamara Bento dos Santos, Bruna Nalin, Tatiele Colonetti, Karina Farret Refosco, Lília F. M. de Souza, Carolina Spritzer, Poli Mara Poloni, Soraia Hack-Mendes, Roberta Schwartz, Ida Vanessa Doederlein Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title | Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title_full | Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title_fullStr | Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title_full_unstemmed | Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title_short | Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases |
title_sort | bone mineral density in patients with hepatic glycogen storage diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469033/ https://www.ncbi.nlm.nih.gov/pubmed/34578865 http://dx.doi.org/10.3390/nu13092987 |
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