Daniel Guldager Kring Rasmussen

ORCID: 0000-0003-1642-7482
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About
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Research Areas
  • Cell Adhesion Molecules Research
  • Chronic Kidney Disease and Diabetes
  • Connective Tissue Growth Factor Research
  • Protease and Inhibitor Mechanisms
  • Diabetes Treatment and Management
  • Liver Disease Diagnosis and Treatment
  • Neuropeptides and Animal Physiology
  • Liver Diseases and Immunity
  • Peptidase Inhibition and Analysis
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Systemic Sclerosis and Related Diseases
  • Advanced Glycation End Products research
  • Renal Diseases and Glomerulopathies
  • Liver physiology and pathology
  • Cardiovascular Function and Risk Factors
  • S100 Proteins and Annexins
  • Adenosine and Purinergic Signaling
  • Neurological and metabolic disorders
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Diabetes and associated disorders
  • Peripheral Artery Disease Management
  • Diabetes Management and Research
  • Parathyroid Disorders and Treatments
  • Biomedical Research and Pathophysiology
  • Platelet Disorders and Treatments

Nordic Bioscience (Denmark)
2016-2024

Gentofte Hospital
2020

University of Southern Denmark
2016-2018

Institute of Molecular Medicine
2018

Copenhagen University Hospital
2015-2017

Rigshospitalet
2015-2017

Type 2 diabetes is a common risk factor for the development of chronic kidney disease (CKD). Enhanced de novo collagen type VI (COL VI) formation has been associated with renal fibrosis and CKD. We investigated hypothesis that PRO-C6, product specifically generated during COL formation, prognostic adverse outcomes in patients microalbuminuria.In prospective, observational study, we measured PRO-C6 serum (S-PRO-C6) urine (U-PRO-C6) 198 microalbuminuria without symptoms coronary artery...

10.2337/dc17-2392 article EN Diabetes Care 2018-04-11

The development of accurate non-invasive tests to detect and measure the extent fibrosis disease activity in patients with non-alcoholic steatohepatitis (NASH) - progressive phenotype fatty liver (NAFLD) is great clinical importance. Herein, we aimed validate performance PRO-C3 ADAPT for detection moderate/severe within CENTAUR screening population.PRO-C3 was assessed plasma from population phase IIb study (NCT02217475) adults NASH fibrosis. relation between histologic features evaluated, as...

10.1016/j.jhep.2021.08.016 article EN cc-by-nc-nd Journal of Hepatology 2021-08-27

Abstract Renal fibrosis is the central pathogenic process in progression of chronic kidney disease (CKD). Collagen type VI (COL VI) upregulated renal fibrosis. Endotrophin released from COL and promotes pleiotropic pro-fibrotic effects. Kidney severity varies considerably accurate information regarding CKD may improve clinical decisions. We tested hypothesis that urinary endotrophin derived during deposition fibrotic human kidneys a marker for Impairment Secondary Care (RIISC) cohort,...

10.1038/s41598-017-17470-3 article EN cc-by Scientific Reports 2017-12-05

There is a need for noninvasive biomarkers that can identify patients with progressive liver fibrosis and monitor response to antifibrotic therapy. An equally important identification of spontaneous regression, since they may not treatment nor be included in clinical studies as end point. Circulating biomarkers, originating from defined fragments the scar tissue itself, serve valuable tools this aspect precision medicine. We investigated panel serological collagen formation degradation...

10.1152/ajpgi.00158.2018 article EN AJP Gastrointestinal and Liver Physiology 2018-08-30
Katherine Johnson Peter Leary Olivier Govaere Matthew J. Barter Sarah Charlton and 95 more Simon Cockell Dina Tiniakos Michalina Zatorska Pierre Bédossa M. Julia Brosnan Jeremy Cobbold Mattias Ekstedt Guruprasad P. Aithal Karine Clément Jörn M. Schattenberg Jérôme Boursier Vlad Ratziu Elisabetta Bugianesi Quentin M. Anstee Ann K. Daly James Clark Heather J. Cordell Rebecca Darlay Christopher P. Day Timothy Hardy Yang‐Lin Liu Fiona Oakley Jeremy M. Palmer Rachel Queen Kristy Wonders Patrick M. Bossuyt Adriaan G. Holleboom Hadi Zafarmand Yasaman Vali Jenny Lee Karine Clément Raluca Pais Detlef Schuppan Michael Allison Sergio Rodriguez Cuenca Vanessa Pellegrinelli Michèle Vacca Antonio Vidal‐Puig Tuulia Hyötyläinen Aidan McGlinchey Matej Orešič Partho Sen José M. Mato Óscar Millet Jean‐François Dufour Stephen A. Harrison Stefan Neubauer Michael Pavlides Ferenc Mózes Salma Akhtar Rajarshi Banerjee Matt Kelly Elizabeth Shumbayawonda Andrea Dennis Charlotte Erpicum Manuel Romero‐Gómez Rocío Gallego‐Durán Isabel Fernández-Lizaranzu M.A. Karsdal Jenny Lee Mette Juul Fisker Elisabeth Erhardtsen Daniel Guldager Kring Rasmussen Per Qvist Antonia Sinisi Estelle Sandt Maria Manuela Tonini Maurizio Parola Chiara Rosso Fabio Marra Amalia Gastaldelli Sven Francque Stergios Kechagias Hannele Yki‐Järvinen Kimmo Porthan Saskia W. C. van Mil George Papatheodoridis Helena Cortez‐Pinto Luca Valenti Salvatore Petta Luca Miele Andreas Geier Christian Trautwein Paul Hockings Philip N. Newsome David Wenn Cecília M. P. Rodrigues Rémy Hanf Pierre Chaumat Christian Rosenquist Aldo Trylesinski Pablo A. Ortiz Kevin L. Duffin Carla Yunis Melissa Miller

Serum microRNA (miRNA) levels are known to change in non-alcoholic fatty liver disease (NAFLD) and may serve as useful biomarkers. This study aimed profile miRNAs comprehensively at all NAFLD stages.

10.1016/j.jhepr.2021.100409 article EN cc-by-nc-nd JHEP Reports 2021-11-25

OBJECTIVE Patients with type 1 diabetes (T1D) have a higher risk of developing chronic kidney disease, cardiovascular events (CVEs), and mortality than the general population. We hypothesized that two previously published biomarkers, namely PRO-C6, biomarker collagen VI formation, C3M, III degradation, may be associated impaired renal function prognostic value for adverse renal, CVE, in patients T1D. RESEARCH DESIGN AND METHODS PRO-C6 C3M serum (sPRO-C6, sC3M) urine (uPRO-C6, uC3M) were...

10.2337/dc18-2599 article EN Diabetes Care 2019-07-01

Renal fibrosis is a hallmark of chronic kidney disease (CKD) caused by an imbalance between formation and degradation extracellular matrix proteins. We investigated the collagen turnover profile 81 non-dialysis CKD stage 2-5 patients measuring peptides reflecting type (COL) I, III, IV, VI. Based on profile, we identified four clusters patients. Cluster 1 contained one patient with prostate cancer, who had distinct turnover. The other generally severe (Cluster 2), moderate 4), or mild 3). 4...

10.1038/s41598-019-51905-3 article EN cc-by Scientific Reports 2019-11-05

Renal fibrosis is the hallmark of chronic kidney disease (CKD) and characterized by an imbalanced extracellular matrix remodelling. Endotrophin (ETP) a signalling molecule released from collagen type VI (COL VI). ETP can be measured PRO-C6 assay, which quantifies levels COL formation. were previously associated with mortality progression in patients CKD. We hypothesized that serum urinary correlate degree interstitial biopsies immunoglobulin A nephropathy (IgAN) anti-neutrophil cytoplasmic...

10.1093/ndt/gfab163 article EN cc-by-nc Nephrology Dialysis Transplantation 2021-04-28

•A normal reference range in healthy adult volunteers was established for PRO-C3.•PRO-C3 levels were not affected by age, sex, BMI, or ethnicity.•PRO-C3 increased with liver fibrosis stage.•PRO-C3 identified patients significant and advanced fibrosis. Background & AimsProgressive has been as the major predictor of mortality non-alcoholic fatty disease (NAFLD). Several biomarkers are currently being evaluated their ability to substitute biopsy standard. Recent clinical studies NAFLD/NASH...

10.1016/j.jhepr.2021.100317 article EN cc-by JHEP Reports 2021-07-10

Renal fibrogenesis is associated with increased ECM remodeling and release of collagen fragments in urine progressive renal disease. We investigated the diagnostic value urinary degradation products a proteinuria-driven fibrosis rat model without anti-fibrotic S1P-receptor modulator FTY720 treatment. Proteinuria was induced male Wistar rats by Adriamycin (ADR) injection (n = 16). Healthy served as controls 12). Six weeks post-injection, all underwent biopsy, FTY720-treatment started ADR-rats...

10.1186/s12967-017-1163-2 article EN cc-by Journal of Translational Medicine 2017-03-20

Natural cytokine-specific autoantibodies (c-aAb) have been measured in healthy and diseased individuals, considered as both endogenous immune-regulators pathogenic factors. Overall, the etiology potential pathology of c-aAb are still undefined. To further characterize sero-prevalence, predictors consequences high levels, we performed largest population-based study to date, using participants epidemiological data from Danish Blood Donor Study. Using a validated bead-based multiplex assay...

10.1371/journal.pone.0179981 article EN cc-by PLoS ONE 2017-06-30

Background Diabetic kidney disease is a major cause of morbidity and mortality. Dysregulated turnover collagen type III associated with development fibrosis. We investigated whether degradation product (C3M) was risk marker for progression chronic (CKD), occurrence cardiovascular (CVD), mortality during follow up in people 2 diabetes (T2D) microalbuminuria. Moreover, we C3M correlated markers inflammation endothelial dysfunction at baseline. Methods measured serum (sC3M) urine (uC3M) 200...

10.1371/journal.pone.0283296 article EN cc-by PLoS ONE 2023-03-17

Tubulointerstitial fibrosis is a major pathological feature in chronic kidney disease (CKD) and collagen type III (COL3) component of the renal fibrotic scar. We hypothesized that dysregulated turnover COL3 an important determinant CKD progression. assessed relationship between fragments reflecting active formation (PRO-C3) degradation (C3M) progression mortality prospective cohort patients.We measured PRO-C3 C3M urine (uPRO-C3 uC3M) serum (sPRO-C3 sC3M) 500 patients from Renal Impairment...

10.1093/ckj/sfz174 article EN cc-by-nc Clinical Kidney Journal 2019-11-18

Delayed graft function after kidney transplantation is common and increases morbidity health care costs. There evidence that endotrophin, a specific fragment of pro-collagen type VI, promotes the inflammatory response in diseases. We tested hypothesis pretransplant endotrophin transplant recipients may be associated with risk delayed function. Pretransplant plasma was assessed using an enzyme-linked immunosorbent assay three independent cohorts 806 recipients. The primary outcome function,...

10.1038/s41598-022-07645-y article EN cc-by Scientific Reports 2022-03-08

Abstract Extracellular matrix (ECM) remodeling is a hallmark of the pathology gastrointestinal disorders. Collagen type VI (COL6) produced by fibroblasts, and COL6 α3-chain has shown to be elevated in patients with ulcerative colitis (UC), Crohn’s disease (CD) colorectal cancer (CRC). Measuring COL6α3 serum may therefore have potential as biomarker for The aims this study were develop validate competitive ELISA targeting specific neo-epitope evaluate its associations disorders UC, CD CRC,...

10.1038/s41598-020-62474-1 article EN cc-by Scientific Reports 2020-04-03

OBJECTIVE We investigated endotrophin, a profibrotic signaling molecule reflecting collagen VI formation, in serum and urine as risk marker for complications to type 2 diabetes. RESEARCH DESIGN AND METHODS Endotrophin was measured 774 individuals with Outcomes included composite kidney end point, first major adverse cardiovascular event (MACE), mortality, progression of albuminuria, incident heart failure, sight-threatening eye disease. Adjusted Cox proportional hazards models were applied....

10.2337/dc22-0852 article EN Diabetes Care 2022-09-12

Abstract Background Enhanced de-novo collagen type VI (COL VI) formation has been associated with kidney and cardiovascular fibrosis. We hypothesized that endotrophin (ETP), a product specifically generated during formation, may be prognostic for heart failure (HF), death (CVD), endpoints, all-cause mortality in patients 2 diabetes. Methods measured ETP plasma (P-ETP) urine (U-ETP) samples collected at baseline follow-up (year 3) from the randomized controlled trial, CANagliflozin...

10.1186/s12933-022-01666-7 article EN cc-by Cardiovascular Diabetology 2022-11-28
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