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Exploring C-peptide loss in type 1 diabetes using growth curve analysis

OBJECTIVES: C-peptide (CP) loss in type 1 diabetes (T1D) is highly variable, and factors influencing it are poorly understood. We modelled CP values in T1D patients from diagnosis for up to 6 years, treating the serial data as growth curves plotted against time since diagnosis. The aims were to summ...

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Autores principales: Besser, Rachel E. J., Ludvigsson, Johnny, Hindmarsh, Peter C., Cole, Tim J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029769/
https://www.ncbi.nlm.nih.gov/pubmed/29969494
http://dx.doi.org/10.1371/journal.pone.0199635
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author Besser, Rachel E. J.
Ludvigsson, Johnny
Hindmarsh, Peter C.
Cole, Tim J.
author_facet Besser, Rachel E. J.
Ludvigsson, Johnny
Hindmarsh, Peter C.
Cole, Tim J.
author_sort Besser, Rachel E. J.
collection PubMed
description OBJECTIVES: C-peptide (CP) loss in type 1 diabetes (T1D) is highly variable, and factors influencing it are poorly understood. We modelled CP values in T1D patients from diagnosis for up to 6 years, treating the serial data as growth curves plotted against time since diagnosis. The aims were to summarise the pattern of CP loss (i.e. growth curve shape) in individual patients in simple terms, and to identify baseline characteristics that predict this pattern in individuals. MATERIALS AND METHODS: Between 1976 and 2011, 442 T1D patients initially aged <18y underwent 120-minute mixed meal tolerance tests (MMTT) to calculate area under the curve (AUC) CP, at 3, 9, 18, 30, 48 and 72 months after diagnosis (n = 1537). The data were analysed using the novel SITAR mixed effects growth curve model (SuperImposition by Translation And Rotation). It fits a mean AUC growth curve, but also allows the curve’s mean level and rate of fall to vary between individuals so as to best fit the individual patient curves. These curve adjustments define individual curve shape. RESULTS: The square root (√) AUC scale provided the best fit. The mean levels and rates of fall for individuals were normally distributed and uncorrelated with each other. Age at diagnosis and √AUC at 3 months strongly predicted the patient-specific mean levels, while younger age at diagnosis (p<0.0001) and the 120-minute CP value of the 3-month MMTT (p = 0.002) predicted the patient-specific rates of fall. CONCLUSIONS: SITAR growth curve analysis is a useful tool to assess CP loss in type 1 diabetes, explaining patient differences in terms of their mean level and rate of fall. A definition of rapid CP loss could be based on a quantile of the rate of fall distribution, allowing better understanding of factors determining CP loss and stratification of patients into targeted therapies.
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spelling pubmed-60297692018-07-19 Exploring C-peptide loss in type 1 diabetes using growth curve analysis Besser, Rachel E. J. Ludvigsson, Johnny Hindmarsh, Peter C. Cole, Tim J. PLoS One Research Article OBJECTIVES: C-peptide (CP) loss in type 1 diabetes (T1D) is highly variable, and factors influencing it are poorly understood. We modelled CP values in T1D patients from diagnosis for up to 6 years, treating the serial data as growth curves plotted against time since diagnosis. The aims were to summarise the pattern of CP loss (i.e. growth curve shape) in individual patients in simple terms, and to identify baseline characteristics that predict this pattern in individuals. MATERIALS AND METHODS: Between 1976 and 2011, 442 T1D patients initially aged <18y underwent 120-minute mixed meal tolerance tests (MMTT) to calculate area under the curve (AUC) CP, at 3, 9, 18, 30, 48 and 72 months after diagnosis (n = 1537). The data were analysed using the novel SITAR mixed effects growth curve model (SuperImposition by Translation And Rotation). It fits a mean AUC growth curve, but also allows the curve’s mean level and rate of fall to vary between individuals so as to best fit the individual patient curves. These curve adjustments define individual curve shape. RESULTS: The square root (√) AUC scale provided the best fit. The mean levels and rates of fall for individuals were normally distributed and uncorrelated with each other. Age at diagnosis and √AUC at 3 months strongly predicted the patient-specific mean levels, while younger age at diagnosis (p<0.0001) and the 120-minute CP value of the 3-month MMTT (p = 0.002) predicted the patient-specific rates of fall. CONCLUSIONS: SITAR growth curve analysis is a useful tool to assess CP loss in type 1 diabetes, explaining patient differences in terms of their mean level and rate of fall. A definition of rapid CP loss could be based on a quantile of the rate of fall distribution, allowing better understanding of factors determining CP loss and stratification of patients into targeted therapies. Public Library of Science 2018-07-03 /pmc/articles/PMC6029769/ /pubmed/29969494 http://dx.doi.org/10.1371/journal.pone.0199635 Text en © 2018 Besser et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Besser, Rachel E. J.
Ludvigsson, Johnny
Hindmarsh, Peter C.
Cole, Tim J.
Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title_full Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title_fullStr Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title_full_unstemmed Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title_short Exploring C-peptide loss in type 1 diabetes using growth curve analysis
title_sort exploring c-peptide loss in type 1 diabetes using growth curve analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029769/
https://www.ncbi.nlm.nih.gov/pubmed/29969494
http://dx.doi.org/10.1371/journal.pone.0199635
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