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Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis

BACKGROUND: This study investigated whether serum progranulin could act as a predictive marker for high disease activity of antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV). METHODS: Fifty‐eight AAV patients were included in this study. Clinical and laboratory data were obtaine...

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Autores principales: Yoon, Taejun, Lee, Lucy Eunju, Ahn, Sung Soo, Pyo, Jung Yoon, Song, Jason Jungsik, Park, Yong‐Beom, Lee, Sang‐Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605163/
https://www.ncbi.nlm.nih.gov/pubmed/34626000
http://dx.doi.org/10.1002/jcla.24048
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author Yoon, Taejun
Lee, Lucy Eunju
Ahn, Sung Soo
Pyo, Jung Yoon
Song, Jason Jungsik
Park, Yong‐Beom
Lee, Sang‐Won
author_facet Yoon, Taejun
Lee, Lucy Eunju
Ahn, Sung Soo
Pyo, Jung Yoon
Song, Jason Jungsik
Park, Yong‐Beom
Lee, Sang‐Won
author_sort Yoon, Taejun
collection PubMed
description BACKGROUND: This study investigated whether serum progranulin could act as a predictive marker for high disease activity of antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV). METHODS: Fifty‐eight AAV patients were included in this study. Clinical and laboratory data were obtained at blood collection. The Short‐Form 36‐Item Health Survey Physical and Mental Component Summaries (SF‐36 PCS and SF‐36 MCS), Birmingham Vasculitis activity score (BVAS), Five‐Factor Score (FFS), and Vasculitis Damage Index (VDI) were assessed as AAV‐specific indices. Whole blood was collected and serum samples were isolated and stored at −80°C. Serum progranulin concentration was quantified by ELISA kits. RESULTS: The median age of patients was 63.0 years (19 men). The median BVAS was 11.0, and the median serum progranulin level was 49.0 ng/ml. Serum progranulin was significantly correlated with BVAS, FFS, erythrocyte sedimentation rate, C‐reactive protein level, SF‐36 PCS, haemoglobin, and serum albumin. Severe AAV was arbitrarily defined as the highest tertile of BVAS (BVAS ≥16). When the cut‐offs of serum progranulin were set as 55.16 ng/ml and 43.01 ng/ml for severe AAV, AAV patients with serum progranulin ≥55.16 and 43.01 ng/ml had significantly higher risks of severe AAV than those without (relative risk (RR) 4.167 and 4.524, respectively). CONCLUSIONS: Progranulin might play an anti‐inflammatory role in AAV pathogenesis and serum progranulin could be used as a predictive marker for high activity of AAV.
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spelling pubmed-86051632021-11-24 Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis Yoon, Taejun Lee, Lucy Eunju Ahn, Sung Soo Pyo, Jung Yoon Song, Jason Jungsik Park, Yong‐Beom Lee, Sang‐Won J Clin Lab Anal Research Articles BACKGROUND: This study investigated whether serum progranulin could act as a predictive marker for high disease activity of antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV). METHODS: Fifty‐eight AAV patients were included in this study. Clinical and laboratory data were obtained at blood collection. The Short‐Form 36‐Item Health Survey Physical and Mental Component Summaries (SF‐36 PCS and SF‐36 MCS), Birmingham Vasculitis activity score (BVAS), Five‐Factor Score (FFS), and Vasculitis Damage Index (VDI) were assessed as AAV‐specific indices. Whole blood was collected and serum samples were isolated and stored at −80°C. Serum progranulin concentration was quantified by ELISA kits. RESULTS: The median age of patients was 63.0 years (19 men). The median BVAS was 11.0, and the median serum progranulin level was 49.0 ng/ml. Serum progranulin was significantly correlated with BVAS, FFS, erythrocyte sedimentation rate, C‐reactive protein level, SF‐36 PCS, haemoglobin, and serum albumin. Severe AAV was arbitrarily defined as the highest tertile of BVAS (BVAS ≥16). When the cut‐offs of serum progranulin were set as 55.16 ng/ml and 43.01 ng/ml for severe AAV, AAV patients with serum progranulin ≥55.16 and 43.01 ng/ml had significantly higher risks of severe AAV than those without (relative risk (RR) 4.167 and 4.524, respectively). CONCLUSIONS: Progranulin might play an anti‐inflammatory role in AAV pathogenesis and serum progranulin could be used as a predictive marker for high activity of AAV. John Wiley and Sons Inc. 2021-10-09 /pmc/articles/PMC8605163/ /pubmed/34626000 http://dx.doi.org/10.1002/jcla.24048 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yoon, Taejun
Lee, Lucy Eunju
Ahn, Sung Soo
Pyo, Jung Yoon
Song, Jason Jungsik
Park, Yong‐Beom
Lee, Sang‐Won
Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title_full Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title_fullStr Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title_full_unstemmed Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title_short Serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
title_sort serum progranulin as a predictive marker for high activity of antineutrophil cytoplasmic antibody‐associated vasculitis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605163/
https://www.ncbi.nlm.nih.gov/pubmed/34626000
http://dx.doi.org/10.1002/jcla.24048
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