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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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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.
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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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