The fibroblast hormone endotrophin is a biomarker of mortality in chronic diseases

Federica Genovese, Cecilie Bager, Peder Frederiksen, Dario Vazquez, Jannie Marie Bülow Sand, R Gisli Jenkins, Toby M Maher, Iain D Stewart, Philip L Molyneaux, William A Fahy, Louise V Wain, Jørgen Vestbo, Carmel Nanthakumar, Saher Burhan Shaker, Nils Hoyer, Diana Julie Leeming, Jacob George, Jonel Trebicka, Daniel Guldager Kring Rasmussen, Michael K HansenPaul Cockwell, Daan Kremer, Stephan Jl Bakker, Nicholas M Selby, Alexander Lynge Reese-Petersen, Arantxa González, Julio Núñez, Peter Rossing, Neel I Nissen, Mogens Karsbøl Boisen, Inna M Chen, Lei Zhao, Morten A Karsdal, Detlef Schuppan

6 Citationer (Scopus)

Abstract

Fibrosis, driven by fibroblast activities, is an important contributor to morbidity and mortality in most chronic diseases. Endotrophin, a signaling molecule derived from processing of type VI collagen by highly activated fibroblasts, is involved in fibrotic tissue remodeling. Circulating levels of endotrophin have been associated with an increased risk of mortality in multiple chronic diseases. We conducted a systematic literature review collecting evidence from original papers published between 2012 and January 2023 that reported associations between circulating endotrophin (PRO-C6) and mortality. Cohorts with data available to the study authors were included in an Individual Patient Data (IPD) meta-analysis that evaluated the association of PRO-C6 with mortality (PROSPERO registration number: CRD42023340215) after adjustment for age, sex and BMI, where available. In the IPD meta-analysis including sixteen cohorts of patients with different non-communicable chronic diseases (NCCDs) (N=15,205) the estimated summary hazard ratio for 3-years all-cause mortality was 2.10 (95% CI 1.75-2.52) for a 2-fold increase in PRO-C6, with some heterogeneity observed between the studies (I2=70%). This meta-analysis is the first study documenting that fibroblast activities, as quantified by circulating endotrophin, are independently associated with mortality across a broad range of NCCDs. This indicates that, irrespective of disease, interstitial tissue remodeling, and consequently fibroblast activities, has a central role in adverse clinical outcomes, and should be considered with urgency from drug developers as a target to treat.

OriginalsprogEngelsk
TidsskriftMatrix biology : journal of the International Society for Matrix Biology
Vol/bind132
Sider (fra-til)1-9
Antal sider9
ISSN0945-053X
DOI
StatusUdgivet - sep. 2024

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