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Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling

BACKGROUND: The fatty liver index (FLI) is frequently used as a non-invasive clinical marker for research, prognostic and diagnostic purposes. It is also used to stratify individuals with hepatic steatosis such as non-alcoholic fatty liver disease (NAFLD), and to detect the presence of type 2 diabet...

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Autores principales: Asaturyan, Hykoush A., Basty, Nicolas, Thanaj, Marjola, Whitcher, Brandon, Thomas, E. Louise, Bell, Jimmy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469950/
https://www.ncbi.nlm.nih.gov/pubmed/36099244
http://dx.doi.org/10.1371/journal.pone.0273171
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author Asaturyan, Hykoush A.
Basty, Nicolas
Thanaj, Marjola
Whitcher, Brandon
Thomas, E. Louise
Bell, Jimmy D.
author_facet Asaturyan, Hykoush A.
Basty, Nicolas
Thanaj, Marjola
Whitcher, Brandon
Thomas, E. Louise
Bell, Jimmy D.
author_sort Asaturyan, Hykoush A.
collection PubMed
description BACKGROUND: The fatty liver index (FLI) is frequently used as a non-invasive clinical marker for research, prognostic and diagnostic purposes. It is also used to stratify individuals with hepatic steatosis such as non-alcoholic fatty liver disease (NAFLD), and to detect the presence of type 2 diabetes or cardiovascular disease. The FLI is calculated using a combination of anthropometric and blood biochemical variables; however, it reportedly excludes 8.5-16.7% of individuals with NAFLD. Moreover, the FLI cannot quantitatively predict liver fat, which might otherwise render an improved diagnosis and assessment of fatty liver, particularly in longitudinal studies. We propose FLI+ using predictive regression modelling, an improved index reflecting liver fat content that integrates 12 routinely-measured variables, including the original FLI. METHODS AND FINDINGS: We evaluated FLI+ on a dataset from the UK Biobank containing 28,796 individual estimates of proton density fat fraction derived from magnetic resonance imaging across normal to severe levels and interpolated to align with the original FLI range. The results obtained for FLI+ outperform the original FLI by delivering a lower mean absolute error by approximately 47%, a lower standard deviation by approximately 20%, and an increased adjusted R(2) statistic by approximately 49%, reflecting a more accurate representation of liver fat content. CONCLUSIONS: Our proposed model predicting FLI+ has the potential to improve diagnosis and provide a more accurate stratification than FLI between absent, mild, moderate and severe levels of hepatic steatosis.
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spelling pubmed-94699502022-09-14 Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling Asaturyan, Hykoush A. Basty, Nicolas Thanaj, Marjola Whitcher, Brandon Thomas, E. Louise Bell, Jimmy D. PLoS One Research Article BACKGROUND: The fatty liver index (FLI) is frequently used as a non-invasive clinical marker for research, prognostic and diagnostic purposes. It is also used to stratify individuals with hepatic steatosis such as non-alcoholic fatty liver disease (NAFLD), and to detect the presence of type 2 diabetes or cardiovascular disease. The FLI is calculated using a combination of anthropometric and blood biochemical variables; however, it reportedly excludes 8.5-16.7% of individuals with NAFLD. Moreover, the FLI cannot quantitatively predict liver fat, which might otherwise render an improved diagnosis and assessment of fatty liver, particularly in longitudinal studies. We propose FLI+ using predictive regression modelling, an improved index reflecting liver fat content that integrates 12 routinely-measured variables, including the original FLI. METHODS AND FINDINGS: We evaluated FLI+ on a dataset from the UK Biobank containing 28,796 individual estimates of proton density fat fraction derived from magnetic resonance imaging across normal to severe levels and interpolated to align with the original FLI range. The results obtained for FLI+ outperform the original FLI by delivering a lower mean absolute error by approximately 47%, a lower standard deviation by approximately 20%, and an increased adjusted R(2) statistic by approximately 49%, reflecting a more accurate representation of liver fat content. CONCLUSIONS: Our proposed model predicting FLI+ has the potential to improve diagnosis and provide a more accurate stratification than FLI between absent, mild, moderate and severe levels of hepatic steatosis. Public Library of Science 2022-09-13 /pmc/articles/PMC9469950/ /pubmed/36099244 http://dx.doi.org/10.1371/journal.pone.0273171 Text en © 2022 Asaturyan et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Asaturyan, Hykoush A.
Basty, Nicolas
Thanaj, Marjola
Whitcher, Brandon
Thomas, E. Louise
Bell, Jimmy D.
Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title_full Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title_fullStr Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title_full_unstemmed Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title_short Improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
title_sort improving the accuracy of fatty liver index to reflect liver fat content with predictive regression modelling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469950/
https://www.ncbi.nlm.nih.gov/pubmed/36099244
http://dx.doi.org/10.1371/journal.pone.0273171
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