A thorough clinical study pipeline to discover and validate biomarkers in kidney transplantation: The European BIOMARGIN program
The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is...
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Published in | Journal of pharmaceutical and biomedical analysis Vol. 263; p. 116911 |
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Language | English |
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15.09.2025
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Abstract | The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is subject to large inter-operator variability. Non-invasive biomarkers able to detect graft lesions early would help reduce or eliminate the use of biopsies and propose medical intervention earlier. BIOMARGIN entails a thorough clinical research pipeline for the untargeted discovery, selection and repeated validation of urine, blood and biopsy biomarkers (mRNAs, miRNAs, metabolites, peptides or proteins) of kidney graft rejection or interstitial fibrosis/tubular atrophy. It combines: (i) two case-control studies to identify, confirm and select the best biomarker signatures; (ii) a cross-sectional study to assess their diagnostic performance in a representative population; (iii) a longitudinal cohort study to evaluate their diagnostic and predictive performance in adult and pediatric patients; (iv) very thoroughly standardized and monitored sample collection, preparation, storage and shipment; (v) gold-standard outcomes through centralized, consensus histological assessment of graft biopsies; (vi) untargeted -omics techniques for the discovery, and targeted techniques for the quantitation, of candidate biomarkers; and (vii) a sophisticated statistical pipeline to select biomarker candidates (avoiding confounders), combine them with clinical data and evaluate their diagnostic and prognostic performances. More than 2500 biopsies, 4200 plasma and 9700 urine samples have been collected from > 1300 patients. To the best of our knowledge, there has never been such a comprehensive research program for clinical biomarkers.
•BIOMARGIN (Biomarkers of Renal Graft Injuries) is a European research program.•It aims to identify and validate non-invasive biomarkers of kidney graft lesions.•It combines two case-control, a cross-sectional and a longitudinal cohort study.•Sample collection, preparation, storage and shipment conditions are standardized.•It entails a sophisticated statistical /machine learning analysis pipeline.•The outcome is set through centralized characterization of graft biopsies. |
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AbstractList | The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is subject to large inter-operator variability. Non-invasive biomarkers able to detect graft lesions early would help reduce or eliminate the use of biopsies and propose medical intervention earlier. BIOMARGIN entails a thorough clinical research pipeline for the untargeted discovery, selection and repeated validation of urine, blood and biopsy biomarkers (mRNAs, miRNAs, metabolites, peptides or proteins) of kidney graft rejection or interstitial fibrosis/tubular atrophy. It combines: (i) two case-control studies to identify, confirm and select the best biomarker signatures; (ii) a cross-sectional study to assess their diagnostic performance in a representative population; (iii) a longitudinal cohort study to evaluate their diagnostic and predictive performance in adult and pediatric patients; (iv) very thoroughly standardized and monitored sample collection, preparation, storage and shipment; (v) gold-standard outcomes through centralized, consensus histological assessment of graft biopsies; (vi) untargeted -omics techniques for the discovery, and targeted techniques for the quantitation, of candidate biomarkers; and (vii) a sophisticated statistical pipeline to select biomarker candidates (avoiding confounders), combine them with clinical data and evaluate their diagnostic and prognostic performances. More than 2500 biopsies, 4200 plasma and 9700 urine samples have been collected from > 1300 patients. To the best of our knowledge, there has never been such a comprehensive research program for clinical biomarkers. The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is subject to large inter-operator variability. Non-invasive biomarkers able to detect graft lesions early would help reduce or eliminate the use of biopsies and propose medical intervention earlier. BIOMARGIN entails a thorough clinical research pipeline for the untargeted discovery, selection and repeated validation of urine, blood and biopsy biomarkers (mRNAs, miRNAs, metabolites, peptides or proteins) of kidney graft rejection or interstitial fibrosis/tubular atrophy. It combines: (i) two case-control studies to identify, confirm and select the best biomarker signatures; (ii) a cross-sectional study to assess their diagnostic performance in a representative population; (iii) a longitudinal cohort study to evaluate their diagnostic and predictive performance in adult and pediatric patients; (iv) very thoroughly standardized and monitored sample collection, preparation, storage and shipment; (v) gold-standard outcomes through centralized, consensus histological assessment of graft biopsies; (vi) untargeted -omics techniques for the discovery, and targeted techniques for the quantitation, of candidate biomarkers; and (vii) a sophisticated statistical pipeline to select biomarker candidates (avoiding confounders), combine them with clinical data and evaluate their diagnostic and prognostic performances. More than 2500 biopsies, 4200 plasma and 9700 urine samples have been collected from > 1300 patients. To the best of our knowledge, there has never been such a comprehensive research program for clinical biomarkers. •BIOMARGIN (Biomarkers of Renal Graft Injuries) is a European research program.•It aims to identify and validate non-invasive biomarkers of kidney graft lesions.•It combines two case-control, a cross-sectional and a longitudinal cohort study.•Sample collection, preparation, storage and shipment conditions are standardized.•It entails a sophisticated statistical /machine learning analysis pipeline.•The outcome is set through centralized characterization of graft biopsies. The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is subject to large inter-operator variability. Non-invasive biomarkers able to detect graft lesions early would help reduce or eliminate the use of biopsies and propose medical intervention earlier. BIOMARGIN entails a thorough clinical research pipeline for the untargeted discovery, selection and repeated validation of urine, blood and biopsy biomarkers (mRNAs, miRNAs, metabolites, peptides or proteins) of kidney graft rejection or interstitial fibrosis/tubular atrophy. It combines: (i) two case-control studies to identify, confirm and select the best biomarker signatures; (ii) a cross-sectional study to assess their diagnostic performance in a representative population; (iii) a longitudinal cohort study to evaluate their diagnostic and predictive performance in adult and pediatric patients; (iv) very thoroughly standardized and monitored sample collection, preparation, storage and shipment; (v) gold-standard outcomes through centralized, consensus histological assessment of graft biopsies; (vi) untargeted -omics techniques for the discovery, and targeted techniques for the quantitation, of candidate biomarkers; and (vii) a sophisticated statistical pipeline to select biomarker candidates (avoiding confounders), combine them with clinical data and evaluate their diagnostic and prognostic performances. More than 2500 biopsies, 4200 plasma and 9700 urine samples have been collected from > 1300 patients. To the best of our knowledge, there has never been such a comprehensive research program for clinical biomarkers.The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney transplant patients. Graft biopsies represent the gold standard to identify graft lesions, but they are invasive, and their interpretation is subject to large inter-operator variability. Non-invasive biomarkers able to detect graft lesions early would help reduce or eliminate the use of biopsies and propose medical intervention earlier. BIOMARGIN entails a thorough clinical research pipeline for the untargeted discovery, selection and repeated validation of urine, blood and biopsy biomarkers (mRNAs, miRNAs, metabolites, peptides or proteins) of kidney graft rejection or interstitial fibrosis/tubular atrophy. It combines: (i) two case-control studies to identify, confirm and select the best biomarker signatures; (ii) a cross-sectional study to assess their diagnostic performance in a representative population; (iii) a longitudinal cohort study to evaluate their diagnostic and predictive performance in adult and pediatric patients; (iv) very thoroughly standardized and monitored sample collection, preparation, storage and shipment; (v) gold-standard outcomes through centralized, consensus histological assessment of graft biopsies; (vi) untargeted -omics techniques for the discovery, and targeted techniques for the quantitation, of candidate biomarkers; and (vii) a sophisticated statistical pipeline to select biomarker candidates (avoiding confounders), combine them with clinical data and evaluate their diagnostic and prognostic performances. More than 2500 biopsies, 4200 plasma and 9700 urine samples have been collected from > 1300 patients. To the best of our knowledge, there has never been such a comprehensive research program for clinical biomarkers. |
ArticleNumber | 116911 |
Author | Anglicheau, Dany Thevenot, Etienne A. Labriffe, Marc Marquet, Pierre Gwinner, Wilfried Essig, Marie Naesens, Maarten Humeau, Antoine |
Author_xml | – sequence: 1 givenname: Pierre surname: Marquet fullname: Marquet, Pierre email: pierre.marquet@unilim.fr organization: Pharmacology & Transplantation, Universite de Limoges, UMR1248 INSERM, Limoges, France – sequence: 2 givenname: Antoine orcidid: 0000-0002-2971-7254 surname: Humeau fullname: Humeau, Antoine organization: Pharmacology & Transplantation, Universite de Limoges, UMR1248 INSERM, Limoges, France – sequence: 3 givenname: Dany surname: Anglicheau fullname: Anglicheau, Dany organization: Department of Nephrology and Kidney Transplantation, Necker Hospital, Assistance Publique-Hopitaux de Paris, Paris, France – sequence: 4 givenname: Maarten surname: Naesens fullname: Naesens, Maarten organization: Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium – sequence: 5 givenname: Wilfried surname: Gwinner fullname: Gwinner, Wilfried organization: Department of Nephrology, Hannover Medical School, Hannover, Germany – sequence: 6 givenname: Etienne A. surname: Thevenot fullname: Thevenot, Etienne A. organization: CEA, LIST, Laboratory for Data Analysis and Systems' Intelligence, MetaboHUB Gif-sur-Yvette, France – sequence: 7 givenname: Marc orcidid: 0000-0001-5840-8904 surname: Labriffe fullname: Labriffe, Marc organization: Pharmacology & Transplantation, Universite de Limoges, UMR1248 INSERM, Limoges, France – sequence: 8 givenname: Marie surname: Essig fullname: Essig, Marie organization: Department of Nephrology, Dialysis, Hopital Ambroise Pare, Assistance Publique-Hopitaux de Paris, Paris, France |
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Keywords | Biomarkers Omics Kidney transplantation Graft rejection Clinical study |
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Snippet | The European research program BIOMARGIN (Biomarkers of Renal Graft Injuries) seeks to identify and validate non-invasive biomarkers of graft lesions in kidney... |
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SubjectTerms | Biomarkers Biomarkers - analysis Biomarkers - blood Biomarkers - metabolism Biopsy - methods Case-Control Studies Clinical study Cross-Sectional Studies Europe Graft rejection Graft Rejection - diagnosis Graft Rejection - metabolism Humans Kidney transplantation Kidney Transplantation - adverse effects Kidney Transplantation - methods Longitudinal Studies Omics |
Title | A thorough clinical study pipeline to discover and validate biomarkers in kidney transplantation: The European BIOMARGIN program |
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