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Development and validation of a new nomogram to screen for MAFLD
BACKGROUND AND AIM: Metabolic dysfunction-associated fatty liver disease (MAFLD) poses significant health and economic burdens on all nations. Thus, identifying patients at risk early and managing them appropriately is essential. This study’s goal was to develop a new predictive model for MAFLD. Add...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730620/ https://www.ncbi.nlm.nih.gov/pubmed/36482400 http://dx.doi.org/10.1186/s12944-022-01748-1 |
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author | Zou, Haoxuan Zhao, Fanrong Lv, Xiuhe Ma, Xiaopu Xie, Yan |
author_facet | Zou, Haoxuan Zhao, Fanrong Lv, Xiuhe Ma, Xiaopu Xie, Yan |
author_sort | Zou, Haoxuan |
collection | PubMed |
description | BACKGROUND AND AIM: Metabolic dysfunction-associated fatty liver disease (MAFLD) poses significant health and economic burdens on all nations. Thus, identifying patients at risk early and managing them appropriately is essential. This study’s goal was to develop a new predictive model for MAFLD. Additionally, to improve the new model’s clinical utility, researchers limited the variables to readily available simple clinical and laboratory measures. METHODS: Based on the National Health and Nutrition Examination Survey (NHANES) cycle 2017–2020.3, the study was a retrospective cross-sectional study involving 7300 participants. By least absolute shrinkage and selection operator (LASSO) regression, significant indicators independently associated with MAFLD were identified, and a predictive model called the MAFLD prediction nomogram (MPN) was developed. The study then compared the MPN with six existing predictive models for MAFLD. The model was evaluated by measuring the area under receiver operating characteristic curve (AUC), net reclassification index (NRI), integrated discrimination improvement (IDI), calibration curve, and decision curve analysis (DCA) curve. RESULTS: In this study, researchers identified nine predictors from 33 variables, including age, race, arm circumference (AC), waist circumference (WC), body mass index (BMI), alanine aminotransferase (ALT)-to-aspartate aminotransferase (AST) ratio, triglyceride-glucose index (TyG), hypertension, and diabetes. The diagnostic accuracy of the MPN for MAFLD was significantly better than that of the other six existing models in both the training and validation cohorts (AUC 0.868, 95% confidence interval (CI) 0.858–0.877, and AUC 0.863, 95% CI 0.848–0.878, respectively). The MPN showed a higher net benefit than the other existing models. CONCLUSIONS: This nonimaging-assisted nomogram based on demographics, laboratory factors, anthropometrics, and comorbidities better predicted MAFLD than the other six existing predictive models. Using this model, the general population with MAFLD can be assessed rapidly. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01748-1. |
format | Online Article Text |
id | pubmed-9730620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97306202022-12-09 Development and validation of a new nomogram to screen for MAFLD Zou, Haoxuan Zhao, Fanrong Lv, Xiuhe Ma, Xiaopu Xie, Yan Lipids Health Dis Research BACKGROUND AND AIM: Metabolic dysfunction-associated fatty liver disease (MAFLD) poses significant health and economic burdens on all nations. Thus, identifying patients at risk early and managing them appropriately is essential. This study’s goal was to develop a new predictive model for MAFLD. Additionally, to improve the new model’s clinical utility, researchers limited the variables to readily available simple clinical and laboratory measures. METHODS: Based on the National Health and Nutrition Examination Survey (NHANES) cycle 2017–2020.3, the study was a retrospective cross-sectional study involving 7300 participants. By least absolute shrinkage and selection operator (LASSO) regression, significant indicators independently associated with MAFLD were identified, and a predictive model called the MAFLD prediction nomogram (MPN) was developed. The study then compared the MPN with six existing predictive models for MAFLD. The model was evaluated by measuring the area under receiver operating characteristic curve (AUC), net reclassification index (NRI), integrated discrimination improvement (IDI), calibration curve, and decision curve analysis (DCA) curve. RESULTS: In this study, researchers identified nine predictors from 33 variables, including age, race, arm circumference (AC), waist circumference (WC), body mass index (BMI), alanine aminotransferase (ALT)-to-aspartate aminotransferase (AST) ratio, triglyceride-glucose index (TyG), hypertension, and diabetes. The diagnostic accuracy of the MPN for MAFLD was significantly better than that of the other six existing models in both the training and validation cohorts (AUC 0.868, 95% confidence interval (CI) 0.858–0.877, and AUC 0.863, 95% CI 0.848–0.878, respectively). The MPN showed a higher net benefit than the other existing models. CONCLUSIONS: This nonimaging-assisted nomogram based on demographics, laboratory factors, anthropometrics, and comorbidities better predicted MAFLD than the other six existing predictive models. Using this model, the general population with MAFLD can be assessed rapidly. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01748-1. BioMed Central 2022-12-08 /pmc/articles/PMC9730620/ /pubmed/36482400 http://dx.doi.org/10.1186/s12944-022-01748-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zou, Haoxuan Zhao, Fanrong Lv, Xiuhe Ma, Xiaopu Xie, Yan Development and validation of a new nomogram to screen for MAFLD |
title | Development and validation of a new nomogram to screen for MAFLD |
title_full | Development and validation of a new nomogram to screen for MAFLD |
title_fullStr | Development and validation of a new nomogram to screen for MAFLD |
title_full_unstemmed | Development and validation of a new nomogram to screen for MAFLD |
title_short | Development and validation of a new nomogram to screen for MAFLD |
title_sort | development and validation of a new nomogram to screen for mafld |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730620/ https://www.ncbi.nlm.nih.gov/pubmed/36482400 http://dx.doi.org/10.1186/s12944-022-01748-1 |
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