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Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications

OBJECTIVE: To evaluate the levels of periostin in patients with systemic sclerosis (SSc) and their association with features of systemic sclerosis. METHODS: The levels of periostin were assessed in the serum of 106 SSc patients and 22 healthy controls and by immunofluorescence staining in cardiac ti...

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Autores principales: El-Adili, Fatima, Lui, Justin K., Najem, Mortada, Farina, Giuseppina, Trojanowska, Maria, Sam, Flora, Bujor, Andreea M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650849/
https://www.ncbi.nlm.nih.gov/pubmed/36369212
http://dx.doi.org/10.1186/s13075-022-02943-2
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author El-Adili, Fatima
Lui, Justin K.
Najem, Mortada
Farina, Giuseppina
Trojanowska, Maria
Sam, Flora
Bujor, Andreea M.
author_facet El-Adili, Fatima
Lui, Justin K.
Najem, Mortada
Farina, Giuseppina
Trojanowska, Maria
Sam, Flora
Bujor, Andreea M.
author_sort El-Adili, Fatima
collection PubMed
description OBJECTIVE: To evaluate the levels of periostin in patients with systemic sclerosis (SSc) and their association with features of systemic sclerosis. METHODS: The levels of periostin were assessed in the serum of 106 SSc patients and 22 healthy controls and by immunofluorescence staining in cardiac tissue from 4 SSc patients and 4 controls. Serum periostin was measured via enzyme-linked immunosorbent assay. The results were analyzed using Mann-Whitney test or Kruskal-Wallis test followed by Dunn’s multiple comparisons tests and Spearman’s test for correlations. Cardiac tissue from SSc patients and controls was stained for periostin and co-stained for periostin and collagen type I using immunofluorescence. RESULTS: Periostin levels were higher in patients with SSc compared to controls and directly correlated to modified Rodnan skin score and echocardiography parameters of left ventricular measurements. Immunofluorescence staining in SSc cardiac tissue showed patchy periostin expression in all SSc patients, but not in controls. Furthermore, there was extensive periostin expression even in areas without collagen deposition, while all established fibrotic areas showed colocalization of collagen and periostin. There was no association between periostin levels and interstitial lung disease, pulmonary hypertension or other vascular complications. CONCLUSION: Periostin is elevated in SSc cardiac tissue in vivo and circulating levels of periostin are increased in SSc, correlating with the extent of disease duration, degree of skin fibrosis, and left ventricular structural assessments. Periostin may be a potential biomarker that can provide further pathogenic insight into cardiac fibrosis in SSc.
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spelling pubmed-96508492022-11-15 Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications El-Adili, Fatima Lui, Justin K. Najem, Mortada Farina, Giuseppina Trojanowska, Maria Sam, Flora Bujor, Andreea M. Arthritis Res Ther Research OBJECTIVE: To evaluate the levels of periostin in patients with systemic sclerosis (SSc) and their association with features of systemic sclerosis. METHODS: The levels of periostin were assessed in the serum of 106 SSc patients and 22 healthy controls and by immunofluorescence staining in cardiac tissue from 4 SSc patients and 4 controls. Serum periostin was measured via enzyme-linked immunosorbent assay. The results were analyzed using Mann-Whitney test or Kruskal-Wallis test followed by Dunn’s multiple comparisons tests and Spearman’s test for correlations. Cardiac tissue from SSc patients and controls was stained for periostin and co-stained for periostin and collagen type I using immunofluorescence. RESULTS: Periostin levels were higher in patients with SSc compared to controls and directly correlated to modified Rodnan skin score and echocardiography parameters of left ventricular measurements. Immunofluorescence staining in SSc cardiac tissue showed patchy periostin expression in all SSc patients, but not in controls. Furthermore, there was extensive periostin expression even in areas without collagen deposition, while all established fibrotic areas showed colocalization of collagen and periostin. There was no association between periostin levels and interstitial lung disease, pulmonary hypertension or other vascular complications. CONCLUSION: Periostin is elevated in SSc cardiac tissue in vivo and circulating levels of periostin are increased in SSc, correlating with the extent of disease duration, degree of skin fibrosis, and left ventricular structural assessments. Periostin may be a potential biomarker that can provide further pathogenic insight into cardiac fibrosis in SSc. BioMed Central 2022-11-11 2022 /pmc/articles/PMC9650849/ /pubmed/36369212 http://dx.doi.org/10.1186/s13075-022-02943-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
El-Adili, Fatima
Lui, Justin K.
Najem, Mortada
Farina, Giuseppina
Trojanowska, Maria
Sam, Flora
Bujor, Andreea M.
Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title_full Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title_fullStr Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title_full_unstemmed Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title_short Periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
title_sort periostin overexpression in scleroderma cardiac tissue and its utility as a marker for disease complications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650849/
https://www.ncbi.nlm.nih.gov/pubmed/36369212
http://dx.doi.org/10.1186/s13075-022-02943-2
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