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Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort

AIMS: To assess urinary C peptide creatinine ratio (UCPCR) used in a modified Matsuda equation to measure insulin sensitivity (IS) in pregnancy. RESEARCH AND DESIGN METHODS: In this cross-sectional study, two IS measurements were calculated in 73 pregnant women at ~28 weeks of gestation by two separ...

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Autores principales: Markoska, Ankica, Mendoza, Lilian C, Valaiyapathi, Rajalakshmi, Thorn, Chloe, Dornhorst, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5942436/
https://www.ncbi.nlm.nih.gov/pubmed/29724737
http://dx.doi.org/10.1136/bmjopen-2017-020029
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author Markoska, Ankica
Mendoza, Lilian C
Valaiyapathi, Rajalakshmi
Thorn, Chloe
Dornhorst, Anne
author_facet Markoska, Ankica
Mendoza, Lilian C
Valaiyapathi, Rajalakshmi
Thorn, Chloe
Dornhorst, Anne
author_sort Markoska, Ankica
collection PubMed
description AIMS: To assess urinary C peptide creatinine ratio (UCPCR) used in a modified Matsuda equation to measure insulin sensitivity (IS) in pregnancy. RESEARCH AND DESIGN METHODS: In this cross-sectional study, two IS measurements were calculated in 73 pregnant women at ~28 weeks of gestation by two separate methods using modified Matsuda equations. The first using the 0 and 120 min serum C peptide concentration during a 75 g oral glucose tolerance test (OGTT) and the second using the 0 and 120 min UCPCR values. The calculated IS measurements from the two methodologies were evaluated using Person’s test and linear regression analysis. The relationship between IS(OGTT) UCPCR and the fasting second void UCPCR and 120 min UCPCR was assessed using Pearson correlation and linear regression analysis after logarithmic transformation of the variables. Statistical analysis was performed using SPSS V.22. RESULTS: The IS measured using serum C peptide (IS(OGTTc-pep)) in the modified Matsuda equation correlated with the IS measurement using serum UCPCR (IS(OGTT-UCPCR)) (r 0.704, p<0.0001). A strong correlation was found between the IS(OGTT-UCPCR) and the fasting UCPCR (r −0.916, p<0.0001), displaying a hyperbolic relationship. CONCLUSION: The UCPCR provides a practical methodology to assess IS and β-cell function in pregnancy.
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spelling pubmed-59424362018-05-11 Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort Markoska, Ankica Mendoza, Lilian C Valaiyapathi, Rajalakshmi Thorn, Chloe Dornhorst, Anne BMJ Open Diabetes and Endocrinology AIMS: To assess urinary C peptide creatinine ratio (UCPCR) used in a modified Matsuda equation to measure insulin sensitivity (IS) in pregnancy. RESEARCH AND DESIGN METHODS: In this cross-sectional study, two IS measurements were calculated in 73 pregnant women at ~28 weeks of gestation by two separate methods using modified Matsuda equations. The first using the 0 and 120 min serum C peptide concentration during a 75 g oral glucose tolerance test (OGTT) and the second using the 0 and 120 min UCPCR values. The calculated IS measurements from the two methodologies were evaluated using Person’s test and linear regression analysis. The relationship between IS(OGTT) UCPCR and the fasting second void UCPCR and 120 min UCPCR was assessed using Pearson correlation and linear regression analysis after logarithmic transformation of the variables. Statistical analysis was performed using SPSS V.22. RESULTS: The IS measured using serum C peptide (IS(OGTTc-pep)) in the modified Matsuda equation correlated with the IS measurement using serum UCPCR (IS(OGTT-UCPCR)) (r 0.704, p<0.0001). A strong correlation was found between the IS(OGTT-UCPCR) and the fasting UCPCR (r −0.916, p<0.0001), displaying a hyperbolic relationship. CONCLUSION: The UCPCR provides a practical methodology to assess IS and β-cell function in pregnancy. BMJ Publishing Group 2018-05-03 /pmc/articles/PMC5942436/ /pubmed/29724737 http://dx.doi.org/10.1136/bmjopen-2017-020029 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Diabetes and Endocrinology
Markoska, Ankica
Mendoza, Lilian C
Valaiyapathi, Rajalakshmi
Thorn, Chloe
Dornhorst, Anne
Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title_full Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title_fullStr Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title_full_unstemmed Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title_short Insulin sensitivity assessed using urine C peptide creatinine ratio (UCPCR) in pregnancy: cross-sectional analysis of an English multiethnic cohort
title_sort insulin sensitivity assessed using urine c peptide creatinine ratio (ucpcr) in pregnancy: cross-sectional analysis of an english multiethnic cohort
topic Diabetes and Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5942436/
https://www.ncbi.nlm.nih.gov/pubmed/29724737
http://dx.doi.org/10.1136/bmjopen-2017-020029
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