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Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children

PURPOSE: To determine clinically useful biochemical markers reflecting disease activity and/or gastrointestinal (GI) tract involvement in Henoch-Schönlein purpura (HSP). METHODS: A total of 185 children with HSP and 130 controls were included. Laboratory data indicating inflammation, standard coagul...

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Autores principales: Hong, Jeana, Yang, Hye Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391999/
https://www.ncbi.nlm.nih.gov/pubmed/25866732
http://dx.doi.org/10.5223/pghn.2015.18.1.39
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author Hong, Jeana
Yang, Hye Ran
author_facet Hong, Jeana
Yang, Hye Ran
author_sort Hong, Jeana
collection PubMed
description PURPOSE: To determine clinically useful biochemical markers reflecting disease activity and/or gastrointestinal (GI) tract involvement in Henoch-Schönlein purpura (HSP). METHODS: A total of 185 children with HSP and 130 controls were included. Laboratory data indicating inflammation, standard coagulation, and activated coagulation were analyzed for the HSP patients, including measurements of the hemoglobin level, white blood cell (WBC) count, absolute neutrophil count (ANC), platelet count, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) level, prothrombin time, activated partial thromboplastin time, and fibrinogen, D-dimer, and fibrin degradation product (FDP) levels. The clinical scores of the skin, joints, abdomen, and kidneys were assessed during the acute and convalescence phases of HSP. RESULTS: The WBC count, ANC, ESR, and CRP, fibrinogen, D-dimer, and FDP levels were significantly higher in the acute phase compared with the convalescent phase of HSP (p<0.05). The total clinical scores were more strongly correlated with the D-dimer (r=0.371, p<0.001) and FDP (r=0.369, p<0.001) levels than with inflammatory markers, such as the WBC count (r=0.241, p=0.001), ANC (r=0.261, p<0.001), and CRP (r=0.260, p<0.001) levels. The patients with GI symptoms had significantly higher ANC (median [interquartile range], 7,138.0 [4,446.4-9,470.0] vs. 5,534.1 [3,263.0-8,153.5], p<0.05) and CRP (0.49 [0.15-1.38] vs. 0.23 [0.01-0.67], p<0.05), D-dimer (2.63 [1.20-4.09] vs. 1.75 [0.62-3.39]), and FDP (7.10 [0.01-13.65] vs. 0.10 [0.01-7.90], p<0.05) levels than those without GI symptoms. CONCLUSION: D-dimer and FDPs are more strongly associated with disease activity and more consistently reflect GI involvement than inflammatory markers during the acute phase of HSP.
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spelling pubmed-43919992015-04-10 Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children Hong, Jeana Yang, Hye Ran Pediatr Gastroenterol Hepatol Nutr Original Article PURPOSE: To determine clinically useful biochemical markers reflecting disease activity and/or gastrointestinal (GI) tract involvement in Henoch-Schönlein purpura (HSP). METHODS: A total of 185 children with HSP and 130 controls were included. Laboratory data indicating inflammation, standard coagulation, and activated coagulation were analyzed for the HSP patients, including measurements of the hemoglobin level, white blood cell (WBC) count, absolute neutrophil count (ANC), platelet count, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) level, prothrombin time, activated partial thromboplastin time, and fibrinogen, D-dimer, and fibrin degradation product (FDP) levels. The clinical scores of the skin, joints, abdomen, and kidneys were assessed during the acute and convalescence phases of HSP. RESULTS: The WBC count, ANC, ESR, and CRP, fibrinogen, D-dimer, and FDP levels were significantly higher in the acute phase compared with the convalescent phase of HSP (p<0.05). The total clinical scores were more strongly correlated with the D-dimer (r=0.371, p<0.001) and FDP (r=0.369, p<0.001) levels than with inflammatory markers, such as the WBC count (r=0.241, p=0.001), ANC (r=0.261, p<0.001), and CRP (r=0.260, p<0.001) levels. The patients with GI symptoms had significantly higher ANC (median [interquartile range], 7,138.0 [4,446.4-9,470.0] vs. 5,534.1 [3,263.0-8,153.5], p<0.05) and CRP (0.49 [0.15-1.38] vs. 0.23 [0.01-0.67], p<0.05), D-dimer (2.63 [1.20-4.09] vs. 1.75 [0.62-3.39]), and FDP (7.10 [0.01-13.65] vs. 0.10 [0.01-7.90], p<0.05) levels than those without GI symptoms. CONCLUSION: D-dimer and FDPs are more strongly associated with disease activity and more consistently reflect GI involvement than inflammatory markers during the acute phase of HSP. The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2015-03 2015-03-30 /pmc/articles/PMC4391999/ /pubmed/25866732 http://dx.doi.org/10.5223/pghn.2015.18.1.39 Text en Copyright © 2015 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hong, Jeana
Yang, Hye Ran
Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title_full Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title_fullStr Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title_full_unstemmed Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title_short Laboratory Markers Indicating Gastrointestinal Involvement of Henoch-Schönlein Purpura in Children
title_sort laboratory markers indicating gastrointestinal involvement of henoch-schönlein purpura in children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391999/
https://www.ncbi.nlm.nih.gov/pubmed/25866732
http://dx.doi.org/10.5223/pghn.2015.18.1.39
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