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Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity

Spondyloarthritis (SpA) is a family of inflammatory diseases sharing clinical, genetic, and radiological features. While crucial for tailoring early interventions, validated prognostic biomarkers are scarce in SpA. We analyze the correlation between serum levels of vasoactive intestinal peptide (VIP...

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Autores principales: Seoane, Iria V., Tomero, Eva, Martínez, Carmen, Garcia-Vicuña, Rosario, Juarranz, Yasmina, Lamana, Amalia, Ocón, Elena, Ortiz, Ana M., Gómez-León, Nieves, González-Álvaro, Isidoro, Gomariz, Rosa P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477066/
https://www.ncbi.nlm.nih.gov/pubmed/25711477
http://dx.doi.org/10.1007/s12031-015-0517-6
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author Seoane, Iria V.
Tomero, Eva
Martínez, Carmen
Garcia-Vicuña, Rosario
Juarranz, Yasmina
Lamana, Amalia
Ocón, Elena
Ortiz, Ana M.
Gómez-León, Nieves
González-Álvaro, Isidoro
Gomariz, Rosa P.
author_facet Seoane, Iria V.
Tomero, Eva
Martínez, Carmen
Garcia-Vicuña, Rosario
Juarranz, Yasmina
Lamana, Amalia
Ocón, Elena
Ortiz, Ana M.
Gómez-León, Nieves
González-Álvaro, Isidoro
Gomariz, Rosa P.
author_sort Seoane, Iria V.
collection PubMed
description Spondyloarthritis (SpA) is a family of inflammatory diseases sharing clinical, genetic, and radiological features. While crucial for tailoring early interventions, validated prognostic biomarkers are scarce in SpA. We analyze the correlation between serum levels of vasoactive intestinal peptide (VIP) and disease activity/severity in patients with early chronic inflammatory back pain. The study population comprised 54 patients enrolled in our early chronic inflammatory back pain register. We collected demographic information, clinical data, laboratory data, and imaging findings. VIP levels were measured by enzyme immunoassay in serum samples from 162 visits. The association between independent variables and VIP levels was analyzed using longitudinal multivariate analysis nested by patient and visit. No significant differences were observed in VIP levels between these two groups. Lower levels of VIP were significantly associated with a higher Bath Ankylosing Spondylitis Disease Activity Index (BASFI) score, presence of bone edema in magnetic resonance imaging (MRI) scan, and lower hemoglobin levels. Coexistence of cutaneous psoriasis was independently associated with lower VIP levels, and similar trend was observed for enthesitis. We conclude that SpA patients with low serum VIP levels had worse 2-year disease outcome, suggesting that serum VIP levels could be a valid prognostic biomarker.
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spelling pubmed-44770662015-06-24 Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity Seoane, Iria V. Tomero, Eva Martínez, Carmen Garcia-Vicuña, Rosario Juarranz, Yasmina Lamana, Amalia Ocón, Elena Ortiz, Ana M. Gómez-León, Nieves González-Álvaro, Isidoro Gomariz, Rosa P. J Mol Neurosci Article Spondyloarthritis (SpA) is a family of inflammatory diseases sharing clinical, genetic, and radiological features. While crucial for tailoring early interventions, validated prognostic biomarkers are scarce in SpA. We analyze the correlation between serum levels of vasoactive intestinal peptide (VIP) and disease activity/severity in patients with early chronic inflammatory back pain. The study population comprised 54 patients enrolled in our early chronic inflammatory back pain register. We collected demographic information, clinical data, laboratory data, and imaging findings. VIP levels were measured by enzyme immunoassay in serum samples from 162 visits. The association between independent variables and VIP levels was analyzed using longitudinal multivariate analysis nested by patient and visit. No significant differences were observed in VIP levels between these two groups. Lower levels of VIP were significantly associated with a higher Bath Ankylosing Spondylitis Disease Activity Index (BASFI) score, presence of bone edema in magnetic resonance imaging (MRI) scan, and lower hemoglobin levels. Coexistence of cutaneous psoriasis was independently associated with lower VIP levels, and similar trend was observed for enthesitis. We conclude that SpA patients with low serum VIP levels had worse 2-year disease outcome, suggesting that serum VIP levels could be a valid prognostic biomarker. Springer US 2015-02-25 2015 /pmc/articles/PMC4477066/ /pubmed/25711477 http://dx.doi.org/10.1007/s12031-015-0517-6 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Seoane, Iria V.
Tomero, Eva
Martínez, Carmen
Garcia-Vicuña, Rosario
Juarranz, Yasmina
Lamana, Amalia
Ocón, Elena
Ortiz, Ana M.
Gómez-León, Nieves
González-Álvaro, Isidoro
Gomariz, Rosa P.
Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title_full Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title_fullStr Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title_full_unstemmed Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title_short Vasoactive Intestinal Peptide in Early Spondyloarthritis: Low Serum Levels as a Potential Biomarker for Disease Severity
title_sort vasoactive intestinal peptide in early spondyloarthritis: low serum levels as a potential biomarker for disease severity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477066/
https://www.ncbi.nlm.nih.gov/pubmed/25711477
http://dx.doi.org/10.1007/s12031-015-0517-6
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