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A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis
OBJECTIVE: The objective of this study was to identify biochemical and clinical predictors of poor response (including incomplete response and non-response) to standard treatment in autoimmune hepatitis (AIH) patients. METHODS: This study retrospectively collected clinical data from 297 patients who...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams And Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695339/ https://www.ncbi.nlm.nih.gov/pubmed/37942733 http://dx.doi.org/10.1097/MEG.0000000000002661 |
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author | Wang, Xin Liu, Hui Wang, Peng Wang, Yuqi Yi, Yunyun Li, Xin |
author_facet | Wang, Xin Liu, Hui Wang, Peng Wang, Yuqi Yi, Yunyun Li, Xin |
author_sort | Wang, Xin |
collection | PubMed |
description | OBJECTIVE: The objective of this study was to identify biochemical and clinical predictors of poor response (including incomplete response and non-response) to standard treatment in autoimmune hepatitis (AIH) patients. METHODS: This study retrospectively collected clinical data from 297 patients who were first diagnosed with AIH in Beijing Ditan Hospital from 2010 to 2019. Finally, 149 patients were screened out. Risk factors were screened by univariate and multifactorial logistic regression. Then they were used to establish the nomogram. The ROC curve, calibration curve, decision curves analysis (DCA) and clinical impact curves (CIC) were used to evaluate the nomogram. RESULTS: 149 patients were divided into two groups: the response group (n = 120, 80%) and the poor response group (n = 29, 20%). Multivariate logistic regression analysis found that IgG > 26.5 g/L (OR: 22.016; 95% CI: 4.677–103.640) in AIH patients increased the risk. In contrast, treatment response status was better in women (OR: 0.085; 95% CI: 0.015–0.497) aged >60 years (OR: 0.159; 95% CI: 0.045–0.564) with AST > 4.49 × ULN (OR: 0.066; 95% CI: 0.009–0.494). The C index (0.853) and the calibration curve show that the nomogram is well differentiated and calibrated; the DCA and CIC indicate that the model has good clinical benefits and implications. CONCLUSION: The study found that male patients aged ≤ 60 years with IgG > 26.5 g/L and elevated AST ≤ 4.49 × ULN were more likely to have a non-response/incomplete response to standard treatment. |
format | Online Article Text |
id | pubmed-10695339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams And Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-106953392023-12-05 A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis Wang, Xin Liu, Hui Wang, Peng Wang, Yuqi Yi, Yunyun Li, Xin Eur J Gastroenterol Hepatol Original Articles: Hepatology OBJECTIVE: The objective of this study was to identify biochemical and clinical predictors of poor response (including incomplete response and non-response) to standard treatment in autoimmune hepatitis (AIH) patients. METHODS: This study retrospectively collected clinical data from 297 patients who were first diagnosed with AIH in Beijing Ditan Hospital from 2010 to 2019. Finally, 149 patients were screened out. Risk factors were screened by univariate and multifactorial logistic regression. Then they were used to establish the nomogram. The ROC curve, calibration curve, decision curves analysis (DCA) and clinical impact curves (CIC) were used to evaluate the nomogram. RESULTS: 149 patients were divided into two groups: the response group (n = 120, 80%) and the poor response group (n = 29, 20%). Multivariate logistic regression analysis found that IgG > 26.5 g/L (OR: 22.016; 95% CI: 4.677–103.640) in AIH patients increased the risk. In contrast, treatment response status was better in women (OR: 0.085; 95% CI: 0.015–0.497) aged >60 years (OR: 0.159; 95% CI: 0.045–0.564) with AST > 4.49 × ULN (OR: 0.066; 95% CI: 0.009–0.494). The C index (0.853) and the calibration curve show that the nomogram is well differentiated and calibrated; the DCA and CIC indicate that the model has good clinical benefits and implications. CONCLUSION: The study found that male patients aged ≤ 60 years with IgG > 26.5 g/L and elevated AST ≤ 4.49 × ULN were more likely to have a non-response/incomplete response to standard treatment. Lippincott Williams And Wilkins 2023-11-23 2024-01 /pmc/articles/PMC10695339/ /pubmed/37942733 http://dx.doi.org/10.1097/MEG.0000000000002661 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Articles: Hepatology Wang, Xin Liu, Hui Wang, Peng Wang, Yuqi Yi, Yunyun Li, Xin A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title | A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title_full | A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title_fullStr | A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title_full_unstemmed | A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title_short | A nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
title_sort | nomogram for analyzing risk factors of poor treatment response in patients with autoimmune hepatitis |
topic | Original Articles: Hepatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695339/ https://www.ncbi.nlm.nih.gov/pubmed/37942733 http://dx.doi.org/10.1097/MEG.0000000000002661 |
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