Serum biomarkers of collagen remodeling are associated with intestinal fibrosis and differentiate stenotic from luminal Crohn's disease patients: a pre- and post-resection longitudinal study.

IF 8.7
Anja Poulsen, Marta Sorokina Alexdóttir, Lene Buhl Riis, Pernille Dige Ovesen, Julie Rasmussen, Mads Damsgaard Wewer, Viviane Lin, Ronja M B Lagström, Marwah Al-Sheikh, Emilie Dahl, Annedorte Ries, Martin Pehrsson, Thomai Tsapanou-Katranara, Peter-Martin Krarup, Ismail Gögenur, Florian Rieder, Johan Burisch, Joachim Høg Mortensen, Jakob Benedict Seidelin
{"title":"Serum biomarkers of collagen remodeling are associated with intestinal fibrosis and differentiate stenotic from luminal Crohn's disease patients: a pre- and post-resection longitudinal study.","authors":"Anja Poulsen, Marta Sorokina Alexdóttir, Lene Buhl Riis, Pernille Dige Ovesen, Julie Rasmussen, Mads Damsgaard Wewer, Viviane Lin, Ronja M B Lagström, Marwah Al-Sheikh, Emilie Dahl, Annedorte Ries, Martin Pehrsson, Thomai Tsapanou-Katranara, Peter-Martin Krarup, Ismail Gögenur, Florian Rieder, Johan Burisch, Joachim Høg Mortensen, Jakob Benedict Seidelin","doi":"10.1093/ecco-jcc/jjaf085","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and aims: </strong>Crohn's disease (CD) is characterized by progressive intestinal transmural damage, including fibrosis and strictures, which impair quality of life and require surgical intervention. No anti-stricture therapies are available, and no accurate biomarkers have been validated allowing prediction of strictures. Collagen fragments synthesis and remodeling show potential as markers of transmural disease activity. This study aimed to evaluate serum collagen markers for their accuracy in differentiating between stenosing and luminal CD and assessing their correlation with histopathology.</p><p><strong>Methods: </strong>Sixty-two patients undergoing resection for stricturing CD and 49 with luminal CD were prospectively included. Extracellular matrix (ECM) markers were quantified using ELISA, and histological assessments of fibrosis and inflammation were performed on full-thickness tissue samples. Clinical outcomes, biomarkers, and histology were analyzed over a 12-month follow-up.</p><p><strong>Results: </strong>Extracellular matrix markers, including PRO-C6, PRO-C3, PRO-C5, C4M, and PRO-C4, distinguished stenosing from luminal CD with and the combination of PRO-C6, PRO-C3, and PRO-C5 achieved the highest discriminative power of (AUC 0.91). Significant changes in levels of the collagen biomarker were observed post-resection. Histological analysis revealed extensive intestinal fibrosis in the submucosa of the stenotic segments, which correlated with PRO-C6 levels. C4M and PRO-C4 positively correlated with neutrophils in the lamina propria. CTX-III correlated negatively with the D'Haens score and neutrophils and mononuclear cells in the lamina propria and in the epithelium.</p><p><strong>Conclusions: </strong>Collagen markers distinguished stenosing from luminal CD, and they correlated with histological fibrosis and chronic inflammation, promising for understanding ECM remodeling. This study highlights the need for extended follow-up to assess long-term stenosis-related outcomes.</p>","PeriodicalId":94074,"journal":{"name":"Journal of Crohn's & colitis","volume":" ","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12148806/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Crohn's & colitis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ecco-jcc/jjaf085","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background and aims: Crohn's disease (CD) is characterized by progressive intestinal transmural damage, including fibrosis and strictures, which impair quality of life and require surgical intervention. No anti-stricture therapies are available, and no accurate biomarkers have been validated allowing prediction of strictures. Collagen fragments synthesis and remodeling show potential as markers of transmural disease activity. This study aimed to evaluate serum collagen markers for their accuracy in differentiating between stenosing and luminal CD and assessing their correlation with histopathology.

Methods: Sixty-two patients undergoing resection for stricturing CD and 49 with luminal CD were prospectively included. Extracellular matrix (ECM) markers were quantified using ELISA, and histological assessments of fibrosis and inflammation were performed on full-thickness tissue samples. Clinical outcomes, biomarkers, and histology were analyzed over a 12-month follow-up.

Results: Extracellular matrix markers, including PRO-C6, PRO-C3, PRO-C5, C4M, and PRO-C4, distinguished stenosing from luminal CD with and the combination of PRO-C6, PRO-C3, and PRO-C5 achieved the highest discriminative power of (AUC 0.91). Significant changes in levels of the collagen biomarker were observed post-resection. Histological analysis revealed extensive intestinal fibrosis in the submucosa of the stenotic segments, which correlated with PRO-C6 levels. C4M and PRO-C4 positively correlated with neutrophils in the lamina propria. CTX-III correlated negatively with the D'Haens score and neutrophils and mononuclear cells in the lamina propria and in the epithelium.

Conclusions: Collagen markers distinguished stenosing from luminal CD, and they correlated with histological fibrosis and chronic inflammation, promising for understanding ECM remodeling. This study highlights the need for extended follow-up to assess long-term stenosis-related outcomes.

Abstract Image

Abstract Image

Abstract Image

胶原重塑的血清生物标志物与肠纤维化相关,并可区分狭窄性和管腔性克罗恩病患者:一项切除前后的纵向研究
背景和目的:克罗恩病(CD)的特点是进行性肠跨壁损伤,包括纤维化和狭窄,影响生活质量,需要手术干预。目前还没有抗狭窄的治疗方法,也没有准确的生物标志物被证实可以预测狭窄。胶原碎片的合成和重塑显示出作为跨壁疾病活动性标志物的潜力。本研究旨在评估血清胶原标记物在区分狭窄和腔内CD方面的准确性,并评估其与组织病理学的相关性。方法:回顾性分析62例狭窄性CD患者和49例管腔性CD患者。使用ELISA定量ECM标记物,并对全层组织样本进行纤维化和炎症的组织学评估。在12个月的随访中分析了临床结果、生物标志物和组织学。结果:包括PRO-C6、PRO-C3、PRO-C5、C4M和PRO-C4在内的ECM标记物,使用PRO-C6、PRO-C3和PRO-C5以及联合使用PRO-C5区分狭窄与腔内CD的能力最高(AUC为0.91)。术后观察到胶原生物标志物水平的显著变化。组织学分析显示狭窄段粘膜下层广泛的肠纤维化,这与PRO-C6水平相关。C4M、PRO-C4与固有层中性粒细胞呈正相关。CTX-III与D'Haens评分、固有层和上皮内的中性粒细胞和单核细胞呈负相关。结论:胶原蛋白标志物可区分管腔CD和狭窄,并与组织学纤维化和慢性炎症相关,有望理解ECM重塑。本研究强调需要延长随访时间以评估长期狭窄相关结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信