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Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently

Objective: To evaluate the value of combined interferon β (IFN-β) and platelet (PLT) detection for Kawasaki disease (KD) identification. Methods: Forty-four children who were newly diagnosed with KD were selected as the KD group. They were divided into acute phase of KD and subacute phase of KD. The...

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Autores principales: Huijuan, Kan, Yaping, Dong, Bo, Wang, Miao, Hou, Guanghui, Qian, Wenhua, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100027/
https://www.ncbi.nlm.nih.gov/pubmed/33968843
http://dx.doi.org/10.3389/fped.2021.624818
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author Huijuan, Kan
Yaping, Dong
Bo, Wang
Miao, Hou
Guanghui, Qian
Wenhua, Yan
author_facet Huijuan, Kan
Yaping, Dong
Bo, Wang
Miao, Hou
Guanghui, Qian
Wenhua, Yan
author_sort Huijuan, Kan
collection PubMed
description Objective: To evaluate the value of combined interferon β (IFN-β) and platelet (PLT) detection for Kawasaki disease (KD) identification. Methods: Forty-four children who were newly diagnosed with KD were selected as the KD group. They were divided into acute phase of KD and subacute phase of KD. They were also separated into groups with and without coronary artery disease (CAD) (CAD+ and CAD–, respectively). Meanwhile, 44 children hospitalized with febrile disease and 44 healthy children were selected as a febrile control group and normal control group, whom were attended to at Children's Hospital of Soochow University at the same time. We detected the concentration of IFN-β and PLT of peripheral blood serum for all three groups and analyzed the difference. Results: At acute and subacute phases of KD, both IFN-β and PLT are higher than both the febrile control group and healthy control group, especially at subacute phase; the difference between groups was statistically significant, P < 0.05. Receiver operating characteristic (ROC) curve showed that the areas under the ROC curve (AUCs) of IFN-β and PLT at acute phase of KD were 0.81 and 0.72, respectively; the sensitivity and specificity were 97.22 and 63.64%, and 57.89 and 73.86%, respectively. The AUCs of combined IFN-β and PLT were 0.81 at acute phase and 0.96 at subacute phase of KD, with sensitivity and specificity of 97.22 and 55.26%, and 86.36 and 100%, respectively. The cutoff value of combined IFN-β and PLT detection was IFN-β = 3.51 pg/ml and PLT = 303 × 10(9)/L at acute phase of KD, IFN-β = 4.21 pg/ml and PLT = 368 × 10(9)/L at subacute phase from plot vs. criterion values. However, there are no significant differences between the CAD– group and the CAD+ group for combined IFN-β and PLT, both P > 0.5, neither at acute nor at subacute phase of KD. Conclusion: Combined IFN-β and PLT detection is an efficient biomarker for KD identification. The cutoff values are IFN-β = 3.51 pg/ml and PLT = 303 × 10(9)/L at acute phase of KD and IFN-β = 4.21 pg/ml and PLT = 368 × 10(9)/L at subacute phase.
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spelling pubmed-81000272021-05-07 Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently Huijuan, Kan Yaping, Dong Bo, Wang Miao, Hou Guanghui, Qian Wenhua, Yan Front Pediatr Pediatrics Objective: To evaluate the value of combined interferon β (IFN-β) and platelet (PLT) detection for Kawasaki disease (KD) identification. Methods: Forty-four children who were newly diagnosed with KD were selected as the KD group. They were divided into acute phase of KD and subacute phase of KD. They were also separated into groups with and without coronary artery disease (CAD) (CAD+ and CAD–, respectively). Meanwhile, 44 children hospitalized with febrile disease and 44 healthy children were selected as a febrile control group and normal control group, whom were attended to at Children's Hospital of Soochow University at the same time. We detected the concentration of IFN-β and PLT of peripheral blood serum for all three groups and analyzed the difference. Results: At acute and subacute phases of KD, both IFN-β and PLT are higher than both the febrile control group and healthy control group, especially at subacute phase; the difference between groups was statistically significant, P < 0.05. Receiver operating characteristic (ROC) curve showed that the areas under the ROC curve (AUCs) of IFN-β and PLT at acute phase of KD were 0.81 and 0.72, respectively; the sensitivity and specificity were 97.22 and 63.64%, and 57.89 and 73.86%, respectively. The AUCs of combined IFN-β and PLT were 0.81 at acute phase and 0.96 at subacute phase of KD, with sensitivity and specificity of 97.22 and 55.26%, and 86.36 and 100%, respectively. The cutoff value of combined IFN-β and PLT detection was IFN-β = 3.51 pg/ml and PLT = 303 × 10(9)/L at acute phase of KD, IFN-β = 4.21 pg/ml and PLT = 368 × 10(9)/L at subacute phase from plot vs. criterion values. However, there are no significant differences between the CAD– group and the CAD+ group for combined IFN-β and PLT, both P > 0.5, neither at acute nor at subacute phase of KD. Conclusion: Combined IFN-β and PLT detection is an efficient biomarker for KD identification. The cutoff values are IFN-β = 3.51 pg/ml and PLT = 303 × 10(9)/L at acute phase of KD and IFN-β = 4.21 pg/ml and PLT = 368 × 10(9)/L at subacute phase. Frontiers Media S.A. 2021-04-22 /pmc/articles/PMC8100027/ /pubmed/33968843 http://dx.doi.org/10.3389/fped.2021.624818 Text en Copyright © 2021 Huijuan, Yaping, Bo, Miao, Guanghui and Wenhua. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Huijuan, Kan
Yaping, Dong
Bo, Wang
Miao, Hou
Guanghui, Qian
Wenhua, Yan
Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title_full Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title_fullStr Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title_full_unstemmed Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title_short Combined IFN-β and PLT Detection Can Identify Kawasaki Disease Efficiently
title_sort combined ifn-β and plt detection can identify kawasaki disease efficiently
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100027/
https://www.ncbi.nlm.nih.gov/pubmed/33968843
http://dx.doi.org/10.3389/fped.2021.624818
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