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Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes
OBJECTIVE: To propose a new definition of partial remission (PR) for patients with type 1 diabetes (T1D) of all-ages using insulin dose and glycated albumin (GA), and find the optimal cut-off values for stimulated C-peptide to diagnose PR in different age-groups. RESEARCH DESIGN AND METHODS: Patient...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344919/ https://www.ncbi.nlm.nih.gov/pubmed/35928900 http://dx.doi.org/10.3389/fendo.2022.938059 |
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author | Shi, Mei Ji, Xiaolin Xie, Yuting Zhong, Ting Tang, Rong Fan, Li Li, Xia |
author_facet | Shi, Mei Ji, Xiaolin Xie, Yuting Zhong, Ting Tang, Rong Fan, Li Li, Xia |
author_sort | Shi, Mei |
collection | PubMed |
description | OBJECTIVE: To propose a new definition of partial remission (PR) for patients with type 1 diabetes (T1D) of all-ages using insulin dose and glycated albumin (GA), and find the optimal cut-off values for stimulated C-peptide to diagnose PR in different age-groups. RESEARCH DESIGN AND METHODS: Patients with newly diagnosed T1D (n=301) were included. GA/insulin dose was used to diagnose PR, and insulin dose-adjusted glycated albumin (IDAGA) was proposed to facilitate clinical application. The optimal diagnostic levels of IDAGA and stimulated C-peptide were determined in different age-groups (≤ 12y, 12-18y and ≥ 18y). Furthermore, the diagnostic consistency between different PR definitions was studied. RESULTS: GA≤ 23%/insulin dose ≤ 0.5u/kg/day was used to define PR, and IDAGA (GA (%) + 40 * insulin dose(u/kg/day)) ≤ 40 was feasible in all age-groups. Whereas, the optimal diagnostic level showed difference for stimulated C-peptide (265.5, 449.3 and 241.1 pmol/L for the ≤ 12y, 12-18y and ≥ 18y age-group, respectively). About 40% of patients met the PR definition by stimulated C-peptide but not GA/insulin dose or IDAGA, who showed dyslipidemia and higher insulin resistance. CONCLUSIONS: A new definition of the PR phase is proposed using GA/insulin dose, and the calculated IDAGA≤ 40 applies to all age-groups. The stimulated C-peptide to diagnose PR is the highest in the 12-18y age-group, which reflects the effect of puberty on metabolism. For patients with insulin resistance, it is not recommended to use stimulated C-peptide alone to diagnose PR. |
format | Online Article Text |
id | pubmed-9344919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93449192022-08-03 Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes Shi, Mei Ji, Xiaolin Xie, Yuting Zhong, Ting Tang, Rong Fan, Li Li, Xia Front Endocrinol (Lausanne) Endocrinology OBJECTIVE: To propose a new definition of partial remission (PR) for patients with type 1 diabetes (T1D) of all-ages using insulin dose and glycated albumin (GA), and find the optimal cut-off values for stimulated C-peptide to diagnose PR in different age-groups. RESEARCH DESIGN AND METHODS: Patients with newly diagnosed T1D (n=301) were included. GA/insulin dose was used to diagnose PR, and insulin dose-adjusted glycated albumin (IDAGA) was proposed to facilitate clinical application. The optimal diagnostic levels of IDAGA and stimulated C-peptide were determined in different age-groups (≤ 12y, 12-18y and ≥ 18y). Furthermore, the diagnostic consistency between different PR definitions was studied. RESULTS: GA≤ 23%/insulin dose ≤ 0.5u/kg/day was used to define PR, and IDAGA (GA (%) + 40 * insulin dose(u/kg/day)) ≤ 40 was feasible in all age-groups. Whereas, the optimal diagnostic level showed difference for stimulated C-peptide (265.5, 449.3 and 241.1 pmol/L for the ≤ 12y, 12-18y and ≥ 18y age-group, respectively). About 40% of patients met the PR definition by stimulated C-peptide but not GA/insulin dose or IDAGA, who showed dyslipidemia and higher insulin resistance. CONCLUSIONS: A new definition of the PR phase is proposed using GA/insulin dose, and the calculated IDAGA≤ 40 applies to all age-groups. The stimulated C-peptide to diagnose PR is the highest in the 12-18y age-group, which reflects the effect of puberty on metabolism. For patients with insulin resistance, it is not recommended to use stimulated C-peptide alone to diagnose PR. Frontiers Media S.A. 2022-07-19 /pmc/articles/PMC9344919/ /pubmed/35928900 http://dx.doi.org/10.3389/fendo.2022.938059 Text en Copyright © 2022 Shi, Ji, Xie, Zhong, Tang, Fan and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Shi, Mei Ji, Xiaolin Xie, Yuting Zhong, Ting Tang, Rong Fan, Li Li, Xia Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title | Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title_full | Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title_fullStr | Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title_full_unstemmed | Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title_short | Using Glycated Albumin and Stimulated C-Peptide to Define Partial Remission in Type 1 Diabetes |
title_sort | using glycated albumin and stimulated c-peptide to define partial remission in type 1 diabetes |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344919/ https://www.ncbi.nlm.nih.gov/pubmed/35928900 http://dx.doi.org/10.3389/fendo.2022.938059 |
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