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Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis
BACKGROUND: To investigate the association of D-dimer with gut inflammation in spondyloarthritis (SpA). METHODS: Sixty-five patients with SpA and 70 healthy controls were included. Demographic, clinical, and laboratory parameters were collected. The differences of clinical and laboratory parameters...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815704/ https://www.ncbi.nlm.nih.gov/pubmed/35127771 http://dx.doi.org/10.3389/fmed.2021.816422 |
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author | Feng, Jiaqi Li, Jia Li, Yixuan Jin, Yuyang Du, Fang Chen, Xiaoxiang |
author_facet | Feng, Jiaqi Li, Jia Li, Yixuan Jin, Yuyang Du, Fang Chen, Xiaoxiang |
author_sort | Feng, Jiaqi |
collection | PubMed |
description | BACKGROUND: To investigate the association of D-dimer with gut inflammation in spondyloarthritis (SpA). METHODS: Sixty-five patients with SpA and 70 healthy controls were included. Demographic, clinical, and laboratory parameters were collected. The differences of clinical and laboratory parameters were compared between patients with SpA and healthy controls, and between patients with SpA, with and without gut inflammation. The associations of D-dimer with laboratory data were analyzed. The predictive value of D-dimer was obtained by a receiver operator characteristic (ROC) curve analysis. The independent risk factors for gut inflammation in SpA were investigated by binary logistic regression analysis. RESULTS: Patients with SpA had higher D-dimer than healthy controls (P = 0.016). D-dimer was positively correlated with platelet (PLT), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP), and negatively correlated with hemoglobin (Hb). Besides, significant differences were observed in D-dimer between SpA patients with and without gut inflammation (P < 0.001). Furthermore, SpA patients with gut inflammation were more likely to have peripheral joint involvement than those without gut inflammation (P < 0.001). The AUC of D-dimer was 0.865 at cut-off value of 0.29 mg/L, with a sensitivity of 82.6%, and a specificity of 81%. Elevated D-dimer (OR = 15.451, 95% CI: 3.030–78.780, P = 0.001) was independently associated with gut inflammation in SpA. CONCLUSION: D-dimer may be a potential biomarker for identifying SpA patients with gut inflammation. |
format | Online Article Text |
id | pubmed-8815704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88157042022-02-05 Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis Feng, Jiaqi Li, Jia Li, Yixuan Jin, Yuyang Du, Fang Chen, Xiaoxiang Front Med (Lausanne) Medicine BACKGROUND: To investigate the association of D-dimer with gut inflammation in spondyloarthritis (SpA). METHODS: Sixty-five patients with SpA and 70 healthy controls were included. Demographic, clinical, and laboratory parameters were collected. The differences of clinical and laboratory parameters were compared between patients with SpA and healthy controls, and between patients with SpA, with and without gut inflammation. The associations of D-dimer with laboratory data were analyzed. The predictive value of D-dimer was obtained by a receiver operator characteristic (ROC) curve analysis. The independent risk factors for gut inflammation in SpA were investigated by binary logistic regression analysis. RESULTS: Patients with SpA had higher D-dimer than healthy controls (P = 0.016). D-dimer was positively correlated with platelet (PLT), erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP), and negatively correlated with hemoglobin (Hb). Besides, significant differences were observed in D-dimer between SpA patients with and without gut inflammation (P < 0.001). Furthermore, SpA patients with gut inflammation were more likely to have peripheral joint involvement than those without gut inflammation (P < 0.001). The AUC of D-dimer was 0.865 at cut-off value of 0.29 mg/L, with a sensitivity of 82.6%, and a specificity of 81%. Elevated D-dimer (OR = 15.451, 95% CI: 3.030–78.780, P = 0.001) was independently associated with gut inflammation in SpA. CONCLUSION: D-dimer may be a potential biomarker for identifying SpA patients with gut inflammation. Frontiers Media S.A. 2022-01-21 /pmc/articles/PMC8815704/ /pubmed/35127771 http://dx.doi.org/10.3389/fmed.2021.816422 Text en Copyright © 2022 Feng, Li, Li, Jin, Du and Chen. 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 | Medicine Feng, Jiaqi Li, Jia Li, Yixuan Jin, Yuyang Du, Fang Chen, Xiaoxiang Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title | Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title_full | Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title_fullStr | Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title_full_unstemmed | Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title_short | Elevated Serum D-Dimer May Reflect the Presence of Gut Inflammation in Spondyloarthritis |
title_sort | elevated serum d-dimer may reflect the presence of gut inflammation in spondyloarthritis |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8815704/ https://www.ncbi.nlm.nih.gov/pubmed/35127771 http://dx.doi.org/10.3389/fmed.2021.816422 |
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