Cargando…

Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus

AIMS: This study aims to evaluate the stability of C‐peptide over time and to compare fasting C‐peptide and C‐peptide response after mixed‐meal tolerance test (MMTT) at T90 or T120 with C‐peptide area under the curve (AUC) in long‐standing type 1 diabetes. METHODS: We included 607 type 1 diabetes in...

Descripción completa

Detalles Bibliográficos
Autores principales: Vollenbrock, Charlotte E., Mul, Dick, Dekker, Pim, Birnie, Erwin, de Vries‐Velraeds, Martine M. C., Boesten, Lianne, Groen, Joost, Geelhoed‐Duijvestijn, Petronella H. L. M., Aanstoot, Henk‐Jan, Wolffenbuttel, Bruce H. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107202/
https://www.ncbi.nlm.nih.gov/pubmed/36398450
http://dx.doi.org/10.1111/dme.15012
_version_ 1785026555504754688
author Vollenbrock, Charlotte E.
Mul, Dick
Dekker, Pim
Birnie, Erwin
de Vries‐Velraeds, Martine M. C.
Boesten, Lianne
Groen, Joost
Geelhoed‐Duijvestijn, Petronella H. L. M.
Aanstoot, Henk‐Jan
Wolffenbuttel, Bruce H. R.
author_facet Vollenbrock, Charlotte E.
Mul, Dick
Dekker, Pim
Birnie, Erwin
de Vries‐Velraeds, Martine M. C.
Boesten, Lianne
Groen, Joost
Geelhoed‐Duijvestijn, Petronella H. L. M.
Aanstoot, Henk‐Jan
Wolffenbuttel, Bruce H. R.
author_sort Vollenbrock, Charlotte E.
collection PubMed
description AIMS: This study aims to evaluate the stability of C‐peptide over time and to compare fasting C‐peptide and C‐peptide response after mixed‐meal tolerance test (MMTT) at T90 or T120 with C‐peptide area under the curve (AUC) in long‐standing type 1 diabetes. METHODS: We included 607 type 1 diabetes individuals with diabetes duration >5 years. C‐peptide concentrations (ultrasensitive assay) were collected in the fasting state, and in a subpopulation after MMTT (T0, just prior to, T30‐T60‐T90‐T120, 30–120 min after ingestion of mixed‐meal) (n = 168). Fasting C‐peptide concentrations (in n = 535) at Year 0 and Year 1 were compared. The clinical determinants associated with residual C‐peptide secretion and the correspondence of C‐peptide at MMTT T90 / T120 and total AUC were assessed. RESULTS: A total of 153 participants (25%) had detectable fasting serum C‐peptide (i.e ≥ 3.8 pmol/L). Fasting C‐peptide was significantly lower at Year 1 (p < 0.001, effect size = −0.16). Participants with higher fasting C‐peptide had a higher age at diagnosis and shorter disease duration and were less frequently insulin pump users. Overall, 109 of 168 (65%) participants had both non‐detectable fasting and post‐meal serum C‐peptide concentrations. The T90 and T120 C‐peptide values at MMTT were concordant with total AUC. In 17 (10%) individuals, C‐peptide was only detectable at MMTT and not in the fasting state. CONCLUSIONS: Stimulated C‐peptide was detectable in an additional 10% of individuals compared with fasting in individuals with >5 years of diabetes duration. T90 and T120 MMTT measurements showed good concordance with the MMTT total AUC. Overall, there was a decrease of C‐peptide at 1‐year follow‐up.
format Online
Article
Text
id pubmed-10107202
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-101072022023-04-18 Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus Vollenbrock, Charlotte E. Mul, Dick Dekker, Pim Birnie, Erwin de Vries‐Velraeds, Martine M. C. Boesten, Lianne Groen, Joost Geelhoed‐Duijvestijn, Petronella H. L. M. Aanstoot, Henk‐Jan Wolffenbuttel, Bruce H. R. Diabet Med Research: Pathophysiology AIMS: This study aims to evaluate the stability of C‐peptide over time and to compare fasting C‐peptide and C‐peptide response after mixed‐meal tolerance test (MMTT) at T90 or T120 with C‐peptide area under the curve (AUC) in long‐standing type 1 diabetes. METHODS: We included 607 type 1 diabetes individuals with diabetes duration >5 years. C‐peptide concentrations (ultrasensitive assay) were collected in the fasting state, and in a subpopulation after MMTT (T0, just prior to, T30‐T60‐T90‐T120, 30–120 min after ingestion of mixed‐meal) (n = 168). Fasting C‐peptide concentrations (in n = 535) at Year 0 and Year 1 were compared. The clinical determinants associated with residual C‐peptide secretion and the correspondence of C‐peptide at MMTT T90 / T120 and total AUC were assessed. RESULTS: A total of 153 participants (25%) had detectable fasting serum C‐peptide (i.e ≥ 3.8 pmol/L). Fasting C‐peptide was significantly lower at Year 1 (p < 0.001, effect size = −0.16). Participants with higher fasting C‐peptide had a higher age at diagnosis and shorter disease duration and were less frequently insulin pump users. Overall, 109 of 168 (65%) participants had both non‐detectable fasting and post‐meal serum C‐peptide concentrations. The T90 and T120 C‐peptide values at MMTT were concordant with total AUC. In 17 (10%) individuals, C‐peptide was only detectable at MMTT and not in the fasting state. CONCLUSIONS: Stimulated C‐peptide was detectable in an additional 10% of individuals compared with fasting in individuals with >5 years of diabetes duration. T90 and T120 MMTT measurements showed good concordance with the MMTT total AUC. Overall, there was a decrease of C‐peptide at 1‐year follow‐up. John Wiley and Sons Inc. 2022-12-04 2023-02 /pmc/articles/PMC10107202/ /pubmed/36398450 http://dx.doi.org/10.1111/dme.15012 Text en © 2022 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research: Pathophysiology
Vollenbrock, Charlotte E.
Mul, Dick
Dekker, Pim
Birnie, Erwin
de Vries‐Velraeds, Martine M. C.
Boesten, Lianne
Groen, Joost
Geelhoed‐Duijvestijn, Petronella H. L. M.
Aanstoot, Henk‐Jan
Wolffenbuttel, Bruce H. R.
Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title_full Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title_fullStr Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title_full_unstemmed Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title_short Fasting and meal‐stimulated serum C‐peptide in long‐standing type 1 diabetes mellitus
title_sort fasting and meal‐stimulated serum c‐peptide in long‐standing type 1 diabetes mellitus
topic Research: Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107202/
https://www.ncbi.nlm.nih.gov/pubmed/36398450
http://dx.doi.org/10.1111/dme.15012
work_keys_str_mv AT vollenbrockcharlottee fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT muldick fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT dekkerpim fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT birnieerwin fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT devriesvelraedsmartinemc fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT boestenlianne fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT groenjoost fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT geelhoedduijvestijnpetronellahlm fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT aanstoothenkjan fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus
AT wolffenbuttelbrucehr fastingandmealstimulatedserumcpeptideinlongstandingtype1diabetesmellitus