Cargando…

Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP

Background. Prolonged immobilization, nutritional and vitamin D deficiency, and specific drug administration may lead to significant bone resorption. Methods and Patients. We prospectively evaluated critically ill patients admitted to the ICU for at least 10 days. Demographics, APACHE II, SOFA score...

Descripción completa

Detalles Bibliográficos
Autores principales: Gavala, Alexandra, Makris, Konstantinos, Korompeli, Anna, Myrianthefs, Pavlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153473/
https://www.ncbi.nlm.nih.gov/pubmed/28025639
http://dx.doi.org/10.1155/2016/1951707
_version_ 1782474698824613888
author Gavala, Alexandra
Makris, Konstantinos
Korompeli, Anna
Myrianthefs, Pavlos
author_facet Gavala, Alexandra
Makris, Konstantinos
Korompeli, Anna
Myrianthefs, Pavlos
author_sort Gavala, Alexandra
collection PubMed
description Background. Prolonged immobilization, nutritional and vitamin D deficiency, and specific drug administration may lead to significant bone resorption. Methods and Patients. We prospectively evaluated critically ill patients admitted to the ICU for at least 10 days. Demographics, APACHE II, SOFA scores, length of stay (LOS), and drug administration were recorded. Blood collections were performed at baseline and on a weekly basis for five consecutive weeks. Serum levels of PINP, β-CTx, iPTH, and 25(OH)vitamin D were measured at each time-point. Results. We enrolled 28 patients of mean age 67.4 ± 2.3 years, mean APACHE II 22.2 ± 0.9, SOFA 10.1 ± 0.6, and LOS 31.6 ± 5.7 days. Nineteen patients were receiving low molecular weight heparin, 17 nor-epinephrine and low dose hydrocortisone, 18 transfusions, and 3 phenytoin. 25(OH)vitamin D serum levels were very low in all patients at all time-points; iPTH serum levels were increased at baseline tending to normalize on 5th week; β-CTx serum levels were significantly increased compared to baseline on 2nd week (peak values), whereas PINP levels were increased significantly after the 4th week. Conclusions. Our data show that critically ill patients had a pattern of hypovitaminosis D, increased iPTH, hypocalcaemia, and BTMs compatible with altered bone metabolism.
format Online
Article
Text
id pubmed-5153473
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-51534732016-12-26 Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP Gavala, Alexandra Makris, Konstantinos Korompeli, Anna Myrianthefs, Pavlos Biomed Res Int Research Article Background. Prolonged immobilization, nutritional and vitamin D deficiency, and specific drug administration may lead to significant bone resorption. Methods and Patients. We prospectively evaluated critically ill patients admitted to the ICU for at least 10 days. Demographics, APACHE II, SOFA scores, length of stay (LOS), and drug administration were recorded. Blood collections were performed at baseline and on a weekly basis for five consecutive weeks. Serum levels of PINP, β-CTx, iPTH, and 25(OH)vitamin D were measured at each time-point. Results. We enrolled 28 patients of mean age 67.4 ± 2.3 years, mean APACHE II 22.2 ± 0.9, SOFA 10.1 ± 0.6, and LOS 31.6 ± 5.7 days. Nineteen patients were receiving low molecular weight heparin, 17 nor-epinephrine and low dose hydrocortisone, 18 transfusions, and 3 phenytoin. 25(OH)vitamin D serum levels were very low in all patients at all time-points; iPTH serum levels were increased at baseline tending to normalize on 5th week; β-CTx serum levels were significantly increased compared to baseline on 2nd week (peak values), whereas PINP levels were increased significantly after the 4th week. Conclusions. Our data show that critically ill patients had a pattern of hypovitaminosis D, increased iPTH, hypocalcaemia, and BTMs compatible with altered bone metabolism. Hindawi Publishing Corporation 2016 2016-11-29 /pmc/articles/PMC5153473/ /pubmed/28025639 http://dx.doi.org/10.1155/2016/1951707 Text en Copyright © 2016 Alexandra Gavala et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gavala, Alexandra
Makris, Konstantinos
Korompeli, Anna
Myrianthefs, Pavlos
Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title_full Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title_fullStr Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title_full_unstemmed Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title_short Evaluation of Bone Metabolism in Critically Ill Patients Using CTx and PINP
title_sort evaluation of bone metabolism in critically ill patients using ctx and pinp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153473/
https://www.ncbi.nlm.nih.gov/pubmed/28025639
http://dx.doi.org/10.1155/2016/1951707
work_keys_str_mv AT gavalaalexandra evaluationofbonemetabolismincriticallyillpatientsusingctxandpinp
AT makriskonstantinos evaluationofbonemetabolismincriticallyillpatientsusingctxandpinp
AT korompelianna evaluationofbonemetabolismincriticallyillpatientsusingctxandpinp
AT myrianthefspavlos evaluationofbonemetabolismincriticallyillpatientsusingctxandpinp