Nick Hales Young Investigator Award

Nick Hales Young Investigator Award A71 (P115) Association of tryptic peptides with progression of kidney disease in Type 1 diabetesM COLOMBO1, S McGurnaghan2, L Blackbourn2, RN Dalton3, PM McKeigue1 and HM Colhoun21Usher Institute of Population Health Sciences and Informatics, The University of Edinburgh, Edinburgh, UK, 2Institute of Genetics and Molecular Medicine, The University of Edinburgh, Edinburgh, UK, 3WellChild Laboratory, King's College London, London, UKAims: To identify biomarkers associated with and predictors of renal function decline in patients with contemporary Type 1 diabetes.Methods: From the Scottish Diabetes Research Network Type 1 Bioresource (SDRNT1BIO) cohort of 6,127 people representative of the adult population with Type 1 diabetes in Scotland, we selected 789 patients with estimated glomerular filtration rate (eGFR) <70ml/min/1.73 m2 at recruitment. Prospective trajectories of eGFR were summarised with a linear slope for each patient, and patients with a loss >3ml/min/1.73 m2/year were defined as rapid progressors. In non‐fasting serum samples, following tryptic digestion, we measured 147 peptides by tandem mass spectrometry and tested them through linear/logistic regression models where biomarkers were evaluated independently. Significance was declared at p < 3.4 × 10−4.Results: Median age was 55.7 years and diabetes duration 26.6 years. Over four‐year follow‐up, median annual change in eGFR was −1.17ml/min/1.73 m2/year (interquartile range −3.12, 0.66), categorising 26.5% of the patients as http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Diabetic Medicine Wiley

Nick Hales Young Investigator Award

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Publisher
Wiley
Copyright
Diabetic Medicine © 2018 Diabetes UK
ISSN
0742-3071
eISSN
1464-5491
D.O.I.
10.1111/dme.13_13570
Publisher site
See Article on Publisher Site

Abstract

A71 (P115) Association of tryptic peptides with progression of kidney disease in Type 1 diabetesM COLOMBO1, S McGurnaghan2, L Blackbourn2, RN Dalton3, PM McKeigue1 and HM Colhoun21Usher Institute of Population Health Sciences and Informatics, The University of Edinburgh, Edinburgh, UK, 2Institute of Genetics and Molecular Medicine, The University of Edinburgh, Edinburgh, UK, 3WellChild Laboratory, King's College London, London, UKAims: To identify biomarkers associated with and predictors of renal function decline in patients with contemporary Type 1 diabetes.Methods: From the Scottish Diabetes Research Network Type 1 Bioresource (SDRNT1BIO) cohort of 6,127 people representative of the adult population with Type 1 diabetes in Scotland, we selected 789 patients with estimated glomerular filtration rate (eGFR) <70ml/min/1.73 m2 at recruitment. Prospective trajectories of eGFR were summarised with a linear slope for each patient, and patients with a loss >3ml/min/1.73 m2/year were defined as rapid progressors. In non‐fasting serum samples, following tryptic digestion, we measured 147 peptides by tandem mass spectrometry and tested them through linear/logistic regression models where biomarkers were evaluated independently. Significance was declared at p < 3.4 × 10−4.Results: Median age was 55.7 years and diabetes duration 26.6 years. Over four‐year follow‐up, median annual change in eGFR was −1.17ml/min/1.73 m2/year (interquartile range −3.12, 0.66), categorising 26.5% of the patients as

Journal

Diabetic MedicineWiley

Published: Jan 1, 2018

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