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Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study

Background: High mobility group box 1 (HMGB1) is an important mediator of systemic inflammatory response syndrome (SIRS) in humans with severe acute pancreatitis (AP), but there is little information regarding its role in dogs. Aim: To compare the serum concentrations of C-reactive protein (CRP) and...

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Autores principales: Kim, Hakhyun, Kim, Hyung-Jin, Kang, Ji-Houn, Kang, Byeong-Teck, Yang, Mhan-Pyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830977/
https://www.ncbi.nlm.nih.gov/pubmed/31401946
http://dx.doi.org/10.1080/01652176.2019.1655178
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author Kim, Hakhyun
Kim, Hyung-Jin
Kang, Ji-Houn
Kang, Byeong-Teck
Yang, Mhan-Pyo
author_facet Kim, Hakhyun
Kim, Hyung-Jin
Kang, Ji-Houn
Kang, Byeong-Teck
Yang, Mhan-Pyo
author_sort Kim, Hakhyun
collection PubMed
description Background: High mobility group box 1 (HMGB1) is an important mediator of systemic inflammatory response syndrome (SIRS) in humans with severe acute pancreatitis (AP), but there is little information regarding its role in dogs. Aim: To compare the serum concentrations of C-reactive protein (CRP) and HMGB1 in healthy dogs and those with AP with or without SIRS. Methods: The study included 22 dogs with AP and 20 healthy dogs. CRP and HMGB1 were assessed by ELISA. Statistical analyses were conducted by non-parametric tests. Results: Median (interquartile range) serum CRP and HMGB1 concentrations were significantly (P < 0.05) higher in dogs with AP [60.56 (14.50–140.10) µg/mL and 0.35 (0.03–1.12) ng/mL, respectively] than in healthy dogs [2.23 (1.75–5.14) µg/mL and 0.02 (0.01–0.05) ng/mL, respectively]. After the recommended treatments for AP, serum CRP concentration in AP dogs significantly decreased, but that of HMGB1 in AP dogs significantly increased. There was also a significant difference in median serum HMGB1 concentration between AP dogs with and without SIRS. The use of serum HMGB1 concentration of 0.35 ng/mL to distinguish AP dogs with and without SIRS was associated with a sensitivity of 87.5% and a specificity of 71.5%. A positive correlation was identified between HMGB1 and clinical severity of AP. All AP dogs had a positive outcome during hospitalization [6.0 (1.5–6.0) days]. Conclusion: Results indicate that HMGB1 might be a useful biomarker for the progression of AP and may play a role in progression of AP into SIRS in dogs.
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spelling pubmed-68309772019-11-19 Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study Kim, Hakhyun Kim, Hyung-Jin Kang, Ji-Houn Kang, Byeong-Teck Yang, Mhan-Pyo Vet Q Article Background: High mobility group box 1 (HMGB1) is an important mediator of systemic inflammatory response syndrome (SIRS) in humans with severe acute pancreatitis (AP), but there is little information regarding its role in dogs. Aim: To compare the serum concentrations of C-reactive protein (CRP) and HMGB1 in healthy dogs and those with AP with or without SIRS. Methods: The study included 22 dogs with AP and 20 healthy dogs. CRP and HMGB1 were assessed by ELISA. Statistical analyses were conducted by non-parametric tests. Results: Median (interquartile range) serum CRP and HMGB1 concentrations were significantly (P < 0.05) higher in dogs with AP [60.56 (14.50–140.10) µg/mL and 0.35 (0.03–1.12) ng/mL, respectively] than in healthy dogs [2.23 (1.75–5.14) µg/mL and 0.02 (0.01–0.05) ng/mL, respectively]. After the recommended treatments for AP, serum CRP concentration in AP dogs significantly decreased, but that of HMGB1 in AP dogs significantly increased. There was also a significant difference in median serum HMGB1 concentration between AP dogs with and without SIRS. The use of serum HMGB1 concentration of 0.35 ng/mL to distinguish AP dogs with and without SIRS was associated with a sensitivity of 87.5% and a specificity of 71.5%. A positive correlation was identified between HMGB1 and clinical severity of AP. All AP dogs had a positive outcome during hospitalization [6.0 (1.5–6.0) days]. Conclusion: Results indicate that HMGB1 might be a useful biomarker for the progression of AP and may play a role in progression of AP into SIRS in dogs. Taylor & Francis 2019-08-10 /pmc/articles/PMC6830977/ /pubmed/31401946 http://dx.doi.org/10.1080/01652176.2019.1655178 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Kim, Hakhyun
Kim, Hyung-Jin
Kang, Ji-Houn
Kang, Byeong-Teck
Yang, Mhan-Pyo
Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title_full Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title_fullStr Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title_full_unstemmed Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title_short Evaluation of serum C-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
title_sort evaluation of serum c-reactive protein and high mobility group box 1 concentrations in 22 dogs with acute pancreatitis: a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830977/
https://www.ncbi.nlm.nih.gov/pubmed/31401946
http://dx.doi.org/10.1080/01652176.2019.1655178
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