dc.contributor.author | Oram, RA | |
dc.contributor.author | Rawlingson, A | |
dc.contributor.author | Shields, BM | |
dc.contributor.author | Bingham, C | |
dc.contributor.author | Besser, REJ | |
dc.contributor.author | McDonald, TJ | |
dc.contributor.author | Knight, BA | |
dc.contributor.author | Hattersley, AT | |
dc.date.accessioned | 2018-05-04T15:14:18Z | |
dc.date.issued | 2013-12-18 | |
dc.description.abstract | OBJECTIVES: The current assessment of insulin resistance (IR) in epidemiology studies relies on the blood measurement of C-peptide or insulin. A urine C-peptide creatinine ratio (UCPCR) can be posted from home unaided. It is validated against serum measures of the insulin in people with diabetes. We tested whether UCPCR could be a surrogate measure of IR by examining the correlation of UCPCR with serum insulin, C-peptide and HOMA2 (Homeostasis Model Assessment 2)-IR in participants without diabetes and with chronic kidney disease (CKD). DESIGN: Observational study. SETTING: Single-centre clinical research facility. PARTICIPANTS: 37 healthy volunteers and 30 patients with CKD (glomerular filtration rate 15-60) were recruited. PRIMARY AND SECONDARY ENDPOINTS: Serum insulin, C-peptide and glucose at fasting (0), 30, 60, 90 and 120 min were measured during an oral glucose tolerance test (OGTT). Second-void fasting UCPCR and 120 min post-OGTT UCPCR were collected. HOMA2-IR was calculated using fasting insulin and glucose. The associations between UCPCR and serum measures were assessed using Spearman's correlations. RESULTS: In healthy volunteers, fasting second-void UCPCR strongly correlated with serum insulin (rs=0.69, p<0.0001), C-peptide (rs=0.73, p<0.0001) and HOMA2-IR (rs=-0.69, p<0.0001). 120 min post-OGTT UCPCR correlated strongly with C-peptide and insulin area under the curve. In patients with CKD, UCPCR did not correlate with serum C-peptide, insulin or HOMA2-IR. CONCLUSIONS: In participants with normal renal function, UCPCR may be a simple, practical method for the assessment of IR in epidemiology studies. | en_GB |
dc.description.sponsorship | The material costs for the project were provided by a Royal Devon and Exeter NHS Foundation Trust Small Projects Grant. This study was supported by PenCLAHRC and the NIHR Exeter Clinical Research Facility. ATH, BAK and BMS are core members of the NIHR Exeter Clinical Research Facility. ATH is supported by a Wellcome Trust Senior Investigator award(grant number 067463/Z/2/Z). RAO is a Clinical Training Fellow funded by Diabetes UK (grant number 11/0004171). TJM is an NIHR CSO Clinical Scientist Fellow. AGJ is an NIHR Doctoral Research Fellow (grant number DRF-2010-03-72). REJB was a DUK Clinical Training Fellow (grant number BDA09/0003825) when she contributed to this work. | en_GB |
dc.identifier.citation | Vol. 3, article e003193 | en_GB |
dc.identifier.doi | 10.1136/bmjopen-2013-003193 | |
dc.identifier.uri | http://hdl.handle.net/10871/32734 | |
dc.language.iso | en | en_GB |
dc.publisher | BMJ Publishing Group | en_GB |
dc.relation.source | Additional data are available from Richard Oram (including individual anonymous results on UCPCR, serum blood measurements, HOMA2IR calculations and baseline characteristics of cohort. For extrainformation please write to:-r.oram@exeter.ac.uk | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/24353253 | en_GB |
dc.rights | This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/3.0/ | en_GB |
dc.title | Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2018-05-04T15:14:18Z | |
dc.identifier.issn | 2044-6055 | |
exeter.place-of-publication | England | en_GB |
dc.description | This is the final version of the article. Available from BMJ Publishing Group via the DOI in this record. | en_GB |
dc.identifier.journal | BMJ Open | en_GB |