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Osteoporosis Assessment among Adults with Liver Cirrhosis

Osteopenic bone disease occurs frequently in patients with chronic liver cirrhosis, which most frequently presents with hepatic osteodystrophy. Thus, the relationship between nutritional status and bone mineral density has been poorly measured in liver cirrhosis. This single-center study consisted o...

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Autores principales: Ionele, Claudiu Marinel, Turcu-Stiolica, Adina, Subtirelu, Mihaela Simona, Ungureanu, Bogdan Silviu, Sas, Teodor Nicusor, Rogoveanu, Ion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820827/
https://www.ncbi.nlm.nih.gov/pubmed/36614954
http://dx.doi.org/10.3390/jcm12010153
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author Ionele, Claudiu Marinel
Turcu-Stiolica, Adina
Subtirelu, Mihaela Simona
Ungureanu, Bogdan Silviu
Sas, Teodor Nicusor
Rogoveanu, Ion
author_facet Ionele, Claudiu Marinel
Turcu-Stiolica, Adina
Subtirelu, Mihaela Simona
Ungureanu, Bogdan Silviu
Sas, Teodor Nicusor
Rogoveanu, Ion
author_sort Ionele, Claudiu Marinel
collection PubMed
description Osteopenic bone disease occurs frequently in patients with chronic liver cirrhosis, which most frequently presents with hepatic osteodystrophy. Thus, the relationship between nutritional status and bone mineral density has been poorly measured in liver cirrhosis. This single-center study consisted of a group of 70 patients diagnosed with liver cirrhosis. The nutritional status was evaluated with the Controlling Nutritional Status index, and volumetric vertebral bone mineral density was measured with quantitative computed tomography. Among the 70 patients included, osteopenia and osteoporosis were found in 71% and 24.3%, respectively. Malnutrition assessed with the Controlling Nutritional Status index was observed in 56 (80%) patients and was more frequent in alcoholic cirrhosis patients than viral cirrhosis patients (87.24% vs. 65.22%). Significant positive correlation with Controlling Nutritional Status score was found with Model for End-Stage Liver Disease (rho = 0.576, p-value < 0.0001), Child–Pugh score (rho = 0.670, p-value < 0.0001), International Normalized Ratio (rho = 0.517, p-value = 0.001), aspartate aminotransferase (rho = 0.293, p-value = 0.045), and bilirubin (rho =0.395, p-value = 0.02). Among the liver cirrhosis patients, 15 had osteoporosis and 49 had osteopenia at the lumbar spine (L1-L4 vertebrae), as determined by bone mass density via quantitative computed tomography. A non-significant relationship between Controlling Nutritional Status index-assessed nutritional status and bone mass density was documented. Regarding osteoporosis, no differences were found between the viral and alcohol types of liver cirrhosis patients (p-value = 0.870). Age, obesity, grade of varices, Child–Pugh score, and Model for End-Stage Liver Disease score were associated with osteoporosis in patients with liver cirrhosis.
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spelling pubmed-98208272023-01-07 Osteoporosis Assessment among Adults with Liver Cirrhosis Ionele, Claudiu Marinel Turcu-Stiolica, Adina Subtirelu, Mihaela Simona Ungureanu, Bogdan Silviu Sas, Teodor Nicusor Rogoveanu, Ion J Clin Med Article Osteopenic bone disease occurs frequently in patients with chronic liver cirrhosis, which most frequently presents with hepatic osteodystrophy. Thus, the relationship between nutritional status and bone mineral density has been poorly measured in liver cirrhosis. This single-center study consisted of a group of 70 patients diagnosed with liver cirrhosis. The nutritional status was evaluated with the Controlling Nutritional Status index, and volumetric vertebral bone mineral density was measured with quantitative computed tomography. Among the 70 patients included, osteopenia and osteoporosis were found in 71% and 24.3%, respectively. Malnutrition assessed with the Controlling Nutritional Status index was observed in 56 (80%) patients and was more frequent in alcoholic cirrhosis patients than viral cirrhosis patients (87.24% vs. 65.22%). Significant positive correlation with Controlling Nutritional Status score was found with Model for End-Stage Liver Disease (rho = 0.576, p-value < 0.0001), Child–Pugh score (rho = 0.670, p-value < 0.0001), International Normalized Ratio (rho = 0.517, p-value = 0.001), aspartate aminotransferase (rho = 0.293, p-value = 0.045), and bilirubin (rho =0.395, p-value = 0.02). Among the liver cirrhosis patients, 15 had osteoporosis and 49 had osteopenia at the lumbar spine (L1-L4 vertebrae), as determined by bone mass density via quantitative computed tomography. A non-significant relationship between Controlling Nutritional Status index-assessed nutritional status and bone mass density was documented. Regarding osteoporosis, no differences were found between the viral and alcohol types of liver cirrhosis patients (p-value = 0.870). Age, obesity, grade of varices, Child–Pugh score, and Model for End-Stage Liver Disease score were associated with osteoporosis in patients with liver cirrhosis. MDPI 2022-12-25 /pmc/articles/PMC9820827/ /pubmed/36614954 http://dx.doi.org/10.3390/jcm12010153 Text en © 2022 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
Ionele, Claudiu Marinel
Turcu-Stiolica, Adina
Subtirelu, Mihaela Simona
Ungureanu, Bogdan Silviu
Sas, Teodor Nicusor
Rogoveanu, Ion
Osteoporosis Assessment among Adults with Liver Cirrhosis
title Osteoporosis Assessment among Adults with Liver Cirrhosis
title_full Osteoporosis Assessment among Adults with Liver Cirrhosis
title_fullStr Osteoporosis Assessment among Adults with Liver Cirrhosis
title_full_unstemmed Osteoporosis Assessment among Adults with Liver Cirrhosis
title_short Osteoporosis Assessment among Adults with Liver Cirrhosis
title_sort osteoporosis assessment among adults with liver cirrhosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820827/
https://www.ncbi.nlm.nih.gov/pubmed/36614954
http://dx.doi.org/10.3390/jcm12010153
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