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Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters

AIM: To determine if there are correlations between joint and fascial chronic graft-vs-host disease (cGVHD) with clinical findings, laboratory parameters, and measures of functional capacity. METHODS: 29 patients were diagnosed with cGVHD based on National Institutes of Health (NIH) Consensus Criter...

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Autores principales: Vukić, Tamara, Smith, Sean Robinson, Ljubas Kelečić, Dina, Desnica, Lana, Prenc, Ema, Pulanić, Dražen, Vrhovac, Radovan, Nemet, Damir, Pavletic, Steven Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937232/
https://www.ncbi.nlm.nih.gov/pubmed/27374828
http://dx.doi.org/10.3325/cmj.2016.57.266
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author Vukić, Tamara
Smith, Sean Robinson
Ljubas Kelečić, Dina
Desnica, Lana
Prenc, Ema
Pulanić, Dražen
Vrhovac, Radovan
Nemet, Damir
Pavletic, Steven Z.
author_facet Vukić, Tamara
Smith, Sean Robinson
Ljubas Kelečić, Dina
Desnica, Lana
Prenc, Ema
Pulanić, Dražen
Vrhovac, Radovan
Nemet, Damir
Pavletic, Steven Z.
author_sort Vukić, Tamara
collection PubMed
description AIM: To determine if there are correlations between joint and fascial chronic graft-vs-host disease (cGVHD) with clinical findings, laboratory parameters, and measures of functional capacity. METHODS: 29 patients were diagnosed with cGVHD based on National Institutes of Health (NIH) Consensus Criteria at the University Hospital Centre Zagreb from October 2013 to October 2015. Physical examination, including functional measures such as 2-minute walk test and hand grip strength, as well as laboratory tests were performed. The relationship between these evaluations and the severity of joint and fascial cGVHD was tested by logistical regression analysis. RESULTS: 12 of 29 patients (41.3%) had joint and fascial cGVHD diagnosed according to NIH Consensus Criteria. There was a significant positive correlation of joint and fascial cGVHD and skin cGVHD (P < 0.001), serum C3 complement level (P = 0.045), and leukocytes (P = 0.032). There was a significant negative correlation between 2-minute walk test (P = 0.016), percentage of cytotoxic T cells CD3+/CD8+ (P = 0.022), serum albumin (P = 0.047), and Karnofsky score (P < 0.001). Binary logistic regression model found that a significant predictor for joint and fascial cGVHD was cGVHD skin involvement (odds ratio, 7.79; 95 confidence interval 1.87-32.56; P = 0.005). CONCLUSION: Joint and fascial cGVHD manifestations correlated with multiple laboratory measurements, clinical features, and cGVHD skin involvement, which was a significant predictor for joint and fascial cGVHD.
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spelling pubmed-49372322016-07-18 Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters Vukić, Tamara Smith, Sean Robinson Ljubas Kelečić, Dina Desnica, Lana Prenc, Ema Pulanić, Dražen Vrhovac, Radovan Nemet, Damir Pavletic, Steven Z. Croat Med J Graft-VS-Host Disease AIM: To determine if there are correlations between joint and fascial chronic graft-vs-host disease (cGVHD) with clinical findings, laboratory parameters, and measures of functional capacity. METHODS: 29 patients were diagnosed with cGVHD based on National Institutes of Health (NIH) Consensus Criteria at the University Hospital Centre Zagreb from October 2013 to October 2015. Physical examination, including functional measures such as 2-minute walk test and hand grip strength, as well as laboratory tests were performed. The relationship between these evaluations and the severity of joint and fascial cGVHD was tested by logistical regression analysis. RESULTS: 12 of 29 patients (41.3%) had joint and fascial cGVHD diagnosed according to NIH Consensus Criteria. There was a significant positive correlation of joint and fascial cGVHD and skin cGVHD (P < 0.001), serum C3 complement level (P = 0.045), and leukocytes (P = 0.032). There was a significant negative correlation between 2-minute walk test (P = 0.016), percentage of cytotoxic T cells CD3+/CD8+ (P = 0.022), serum albumin (P = 0.047), and Karnofsky score (P < 0.001). Binary logistic regression model found that a significant predictor for joint and fascial cGVHD was cGVHD skin involvement (odds ratio, 7.79; 95 confidence interval 1.87-32.56; P = 0.005). CONCLUSION: Joint and fascial cGVHD manifestations correlated with multiple laboratory measurements, clinical features, and cGVHD skin involvement, which was a significant predictor for joint and fascial cGVHD. Croatian Medical Schools 2016-06 /pmc/articles/PMC4937232/ /pubmed/27374828 http://dx.doi.org/10.3325/cmj.2016.57.266 Text en Copyright © 2016 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Graft-VS-Host Disease
Vukić, Tamara
Smith, Sean Robinson
Ljubas Kelečić, Dina
Desnica, Lana
Prenc, Ema
Pulanić, Dražen
Vrhovac, Radovan
Nemet, Damir
Pavletic, Steven Z.
Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title_full Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title_fullStr Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title_full_unstemmed Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title_short Joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
title_sort joint and fascial chronic graft-vs-host disease: correlations with clinical and laboratory parameters
topic Graft-VS-Host Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937232/
https://www.ncbi.nlm.nih.gov/pubmed/27374828
http://dx.doi.org/10.3325/cmj.2016.57.266
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