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A combined biomarker and clinical panel for chronic graft versus host disease diagnosis

Whilst many chronic graft versus host disease (cGVHD) biomarkers have been previously reported, few have been verified in an independent cGVHD cohort. We aimed to verify the diagnostic accuracy of previously reported markers of cGVHD in a multi‐centre Chronic GVHD Consortium. A total of 42 RNA and 1...

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Autores principales: Pidala, Joseph, Sigdel, Tara K, Wang, Anyou, Hsieh, Sue, Inamoto, Yoshi, Martin, Paul J, Flowers, Mary ED, Hansen, John A, Lee, Stephanie J, Sarwal, Minnie M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259564/
https://www.ncbi.nlm.nih.gov/pubmed/28138397
http://dx.doi.org/10.1002/cjp2.58
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author Pidala, Joseph
Sigdel, Tara K
Wang, Anyou
Hsieh, Sue
Inamoto, Yoshi
Martin, Paul J
Flowers, Mary ED
Hansen, John A
Lee, Stephanie J
Sarwal, Minnie M
author_facet Pidala, Joseph
Sigdel, Tara K
Wang, Anyou
Hsieh, Sue
Inamoto, Yoshi
Martin, Paul J
Flowers, Mary ED
Hansen, John A
Lee, Stephanie J
Sarwal, Minnie M
author_sort Pidala, Joseph
collection PubMed
description Whilst many chronic graft versus host disease (cGVHD) biomarkers have been previously reported, few have been verified in an independent cGVHD cohort. We aimed to verify the diagnostic accuracy of previously reported markers of cGVHD in a multi‐centre Chronic GVHD Consortium. A total of 42 RNA and 18 protein candidate biomarkers were assessed amongst 59 cGVHD cases and 33 matched non‐GVHD controls. Total RNA was isolated from PBMC, and RNA markers were quantified using PCR. Serum protein markers were quantified using ELISA. A combined 3 RNA biomarker (IRS2, PLEKHF1 and IL1R2) and 2 clinical variables (recipient CMV serostatus and conditioning regimen intensity) panel accurately (AUC 0.81) segregated cGVHD cases from controls. Other studied RNA and protein markers were not confirmed as accurate cGVHD diagnostic biomarkers. The studied markers failed to segregate higher risk cGVHD (per overall NIH 0‐3 score, and overlap versus classic cGVHD status). These data support the need for multiple independent verification studies for the ultimate clinical application of cGVHD diagnostic biomarkers.
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spelling pubmed-52595642017-01-30 A combined biomarker and clinical panel for chronic graft versus host disease diagnosis Pidala, Joseph Sigdel, Tara K Wang, Anyou Hsieh, Sue Inamoto, Yoshi Martin, Paul J Flowers, Mary ED Hansen, John A Lee, Stephanie J Sarwal, Minnie M J Pathol Clin Res Original Articles Whilst many chronic graft versus host disease (cGVHD) biomarkers have been previously reported, few have been verified in an independent cGVHD cohort. We aimed to verify the diagnostic accuracy of previously reported markers of cGVHD in a multi‐centre Chronic GVHD Consortium. A total of 42 RNA and 18 protein candidate biomarkers were assessed amongst 59 cGVHD cases and 33 matched non‐GVHD controls. Total RNA was isolated from PBMC, and RNA markers were quantified using PCR. Serum protein markers were quantified using ELISA. A combined 3 RNA biomarker (IRS2, PLEKHF1 and IL1R2) and 2 clinical variables (recipient CMV serostatus and conditioning regimen intensity) panel accurately (AUC 0.81) segregated cGVHD cases from controls. Other studied RNA and protein markers were not confirmed as accurate cGVHD diagnostic biomarkers. The studied markers failed to segregate higher risk cGVHD (per overall NIH 0‐3 score, and overlap versus classic cGVHD status). These data support the need for multiple independent verification studies for the ultimate clinical application of cGVHD diagnostic biomarkers. John Wiley and Sons Inc. 2016-11-29 /pmc/articles/PMC5259564/ /pubmed/28138397 http://dx.doi.org/10.1002/cjp2.58 Text en © 2016 The Authors The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Pidala, Joseph
Sigdel, Tara K
Wang, Anyou
Hsieh, Sue
Inamoto, Yoshi
Martin, Paul J
Flowers, Mary ED
Hansen, John A
Lee, Stephanie J
Sarwal, Minnie M
A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title_full A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title_fullStr A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title_full_unstemmed A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title_short A combined biomarker and clinical panel for chronic graft versus host disease diagnosis
title_sort combined biomarker and clinical panel for chronic graft versus host disease diagnosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259564/
https://www.ncbi.nlm.nih.gov/pubmed/28138397
http://dx.doi.org/10.1002/cjp2.58
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