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Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study

INTRODUCTION: To assess the association between growth differentiation factor-15 (GDF15) and radiographic features including bone marrow edema and bone erosion in Spondyloarthritis (SpA). METHODS: Patients with SpA (n = 120) receiving treatment in the Guangdong General Hospital, China, between Augus...

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Autores principales: Song, Yingyu, Cui, Yang, Zhang, Xiao, Lin, Haobo, Zhang, Guangfeng, Zeng, Hui, Zeng, Yonghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320148/
https://www.ncbi.nlm.nih.gov/pubmed/30572513
http://dx.doi.org/10.1097/MD.0000000000013733
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author Song, Yingyu
Cui, Yang
Zhang, Xiao
Lin, Haobo
Zhang, Guangfeng
Zeng, Hui
Zeng, Yonghan
author_facet Song, Yingyu
Cui, Yang
Zhang, Xiao
Lin, Haobo
Zhang, Guangfeng
Zeng, Hui
Zeng, Yonghan
author_sort Song, Yingyu
collection PubMed
description INTRODUCTION: To assess the association between growth differentiation factor-15 (GDF15) and radiographic features including bone marrow edema and bone erosion in Spondyloarthritis (SpA). METHODS: Patients with SpA (n = 120) receiving treatment in the Guangdong General Hospital, China, between August 2012 and December 2016 were retrospectively included. Serum of patients and healthy controls (n = 30) were collected and GDF15 levels were measured using ELISA. Inflammation was assessed by C-reactive protein (CRP), and magnetic resonance imaging (MRI) of the sacroiliac joint using Spondyloarthritis Research Consortium of Canada score and a method of dichotomy to assess fat metaplasia, bone erosion, and ankylosis. Radiographs of the pelvis were scored using the modified New York (mNY) score. RESULTS: Serum GDF15 levels were higher in SpA patients compared to controls (503.52 ± 222.92 vs. 190.86 ± 104.18 pg/mL, P < .0001). Patients who suffered from bone erosion on MRI had higher levels of GDF15 (525.72 [186.33, 801.62]vs. 428.06 [255.15, 670.98] pg/mL, P = .0375). There was a positive correlation between serum GDF15 and CRP (r = 0.5442, P < .0001). Moreover, GDF15 levels were related to CRP levels (r = 0.5658, P < .0001) in those X-ray scores were III, according to 1984mNY criteria. Receiver operating characteristic (ROC) analysis showed that GDF15 levels above 501.98pg/mL could predict presence of bone erosion on MRI. CONCLUSION: The present study suggested that serum GDF15 levels are higher in SpA patients than in healthy controls. The GDF15 level was correlated with CRP and may be a surrogate biomarker in bone erosion.
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spelling pubmed-63201482019-01-14 Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study Song, Yingyu Cui, Yang Zhang, Xiao Lin, Haobo Zhang, Guangfeng Zeng, Hui Zeng, Yonghan Medicine (Baltimore) Research Article INTRODUCTION: To assess the association between growth differentiation factor-15 (GDF15) and radiographic features including bone marrow edema and bone erosion in Spondyloarthritis (SpA). METHODS: Patients with SpA (n = 120) receiving treatment in the Guangdong General Hospital, China, between August 2012 and December 2016 were retrospectively included. Serum of patients and healthy controls (n = 30) were collected and GDF15 levels were measured using ELISA. Inflammation was assessed by C-reactive protein (CRP), and magnetic resonance imaging (MRI) of the sacroiliac joint using Spondyloarthritis Research Consortium of Canada score and a method of dichotomy to assess fat metaplasia, bone erosion, and ankylosis. Radiographs of the pelvis were scored using the modified New York (mNY) score. RESULTS: Serum GDF15 levels were higher in SpA patients compared to controls (503.52 ± 222.92 vs. 190.86 ± 104.18 pg/mL, P < .0001). Patients who suffered from bone erosion on MRI had higher levels of GDF15 (525.72 [186.33, 801.62]vs. 428.06 [255.15, 670.98] pg/mL, P = .0375). There was a positive correlation between serum GDF15 and CRP (r = 0.5442, P < .0001). Moreover, GDF15 levels were related to CRP levels (r = 0.5658, P < .0001) in those X-ray scores were III, according to 1984mNY criteria. Receiver operating characteristic (ROC) analysis showed that GDF15 levels above 501.98pg/mL could predict presence of bone erosion on MRI. CONCLUSION: The present study suggested that serum GDF15 levels are higher in SpA patients than in healthy controls. The GDF15 level was correlated with CRP and may be a surrogate biomarker in bone erosion. Wolters Kluwer Health 2018-12-21 /pmc/articles/PMC6320148/ /pubmed/30572513 http://dx.doi.org/10.1097/MD.0000000000013733 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Song, Yingyu
Cui, Yang
Zhang, Xiao
Lin, Haobo
Zhang, Guangfeng
Zeng, Hui
Zeng, Yonghan
Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title_full Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title_fullStr Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title_full_unstemmed Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title_short Increased serum levels of MIC1/GDF15 correlated with bone erosion in spondyloarthritis: A pilot study
title_sort increased serum levels of mic1/gdf15 correlated with bone erosion in spondyloarthritis: a pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320148/
https://www.ncbi.nlm.nih.gov/pubmed/30572513
http://dx.doi.org/10.1097/MD.0000000000013733
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