Cargando…

Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes

BACKGROUND: To develop and validate a multivariable risk prediction model for ketosis‐prone type 2 diabetes mellitus (T2DM) based on clinical characteristics. METHODS: A total of 964 participants newly diagnosed with T2DM were enrolled in the modeling and validation cohort. Baseline clinical data we...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Jia, Shen, Shiyi, Xu, Hanwen, Zhao, Yu, Hu, Ye, Xing, Yubo, Song, Yingxiang, Wu, Xiaohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509513/
https://www.ncbi.nlm.nih.gov/pubmed/37165751
http://dx.doi.org/10.1111/1753-0407.13407
_version_ 1785107750724829184
author Zheng, Jia
Shen, Shiyi
Xu, Hanwen
Zhao, Yu
Hu, Ye
Xing, Yubo
Song, Yingxiang
Wu, Xiaohong
author_facet Zheng, Jia
Shen, Shiyi
Xu, Hanwen
Zhao, Yu
Hu, Ye
Xing, Yubo
Song, Yingxiang
Wu, Xiaohong
author_sort Zheng, Jia
collection PubMed
description BACKGROUND: To develop and validate a multivariable risk prediction model for ketosis‐prone type 2 diabetes mellitus (T2DM) based on clinical characteristics. METHODS: A total of 964 participants newly diagnosed with T2DM were enrolled in the modeling and validation cohort. Baseline clinical data were collected and analyzed. Multivariable logistic regression analysis was performed to select independent risk factors, develop the prediction model, and construct the nomogram. The model's reliability and validity were checked using the receiver operating characteristic curve and the calibration curve. RESULTS: A high morbidity of ketosis‐prone T2DM was observed (20.2%), who presented as lower age and fasting C‐peptide, and higher free fatty acids, glycated hemoglobin A(1c) and urinary protein. Based on these five independent influence factors, we developed a risk prediction model for ketosis‐prone T2DM and constructed the nomogram. Areas under the curve of the modeling and validation cohorts were 0.806 (95% confidence interval [CI]: 0.760–0.851) and 0.856 (95% CI: 0.803–0.908). The calibration curves that were both internally and externally checked indicated that the projected results were reasonably close to the actual values. CONCLUSIONS: Our study provided an effective clinical risk prediction model for ketosis‐prone T2DM, which could help for precise classification and management.
format Online
Article
Text
id pubmed-10509513
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Wiley Publishing Asia Pty Ltd
record_format MEDLINE/PubMed
spelling pubmed-105095132023-09-21 Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes Zheng, Jia Shen, Shiyi Xu, Hanwen Zhao, Yu Hu, Ye Xing, Yubo Song, Yingxiang Wu, Xiaohong J Diabetes Original Articles BACKGROUND: To develop and validate a multivariable risk prediction model for ketosis‐prone type 2 diabetes mellitus (T2DM) based on clinical characteristics. METHODS: A total of 964 participants newly diagnosed with T2DM were enrolled in the modeling and validation cohort. Baseline clinical data were collected and analyzed. Multivariable logistic regression analysis was performed to select independent risk factors, develop the prediction model, and construct the nomogram. The model's reliability and validity were checked using the receiver operating characteristic curve and the calibration curve. RESULTS: A high morbidity of ketosis‐prone T2DM was observed (20.2%), who presented as lower age and fasting C‐peptide, and higher free fatty acids, glycated hemoglobin A(1c) and urinary protein. Based on these five independent influence factors, we developed a risk prediction model for ketosis‐prone T2DM and constructed the nomogram. Areas under the curve of the modeling and validation cohorts were 0.806 (95% confidence interval [CI]: 0.760–0.851) and 0.856 (95% CI: 0.803–0.908). The calibration curves that were both internally and externally checked indicated that the projected results were reasonably close to the actual values. CONCLUSIONS: Our study provided an effective clinical risk prediction model for ketosis‐prone T2DM, which could help for precise classification and management. Wiley Publishing Asia Pty Ltd 2023-05-10 /pmc/articles/PMC10509513/ /pubmed/37165751 http://dx.doi.org/10.1111/1753-0407.13407 Text en © 2023 The Authors. Journal of Diabetes published by Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zheng, Jia
Shen, Shiyi
Xu, Hanwen
Zhao, Yu
Hu, Ye
Xing, Yubo
Song, Yingxiang
Wu, Xiaohong
Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title_full Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title_fullStr Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title_full_unstemmed Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title_short Development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
title_sort development and validation of a multivariable risk prediction model for identifying ketosis‐prone type 2 diabetes
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509513/
https://www.ncbi.nlm.nih.gov/pubmed/37165751
http://dx.doi.org/10.1111/1753-0407.13407
work_keys_str_mv AT zhengjia developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT shenshiyi developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT xuhanwen developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT zhaoyu developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT huye developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT xingyubo developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT songyingxiang developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes
AT wuxiaohong developmentandvalidationofamultivariableriskpredictionmodelforidentifyingketosispronetype2diabetes