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Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model
SUMMARY: To establish a model for osteoporosis risk in patients with rheumatoid arthritis and validate the model. A newly generated predictive model has been suggested to have good differentiation, calibration, and clinical validity and may be a useful clinical model for predicting osteoporosis in p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer London
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782444/ https://www.ncbi.nlm.nih.gov/pubmed/33394305 http://dx.doi.org/10.1007/s11657-020-00867-5 |
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author | Yan, Xiaobin Xu, Zhenhong Li, Shilin Yan, Lisheng Lyu, Guorong Wang, Zecheng |
author_facet | Yan, Xiaobin Xu, Zhenhong Li, Shilin Yan, Lisheng Lyu, Guorong Wang, Zecheng |
author_sort | Yan, Xiaobin |
collection | PubMed |
description | SUMMARY: To establish a model for osteoporosis risk in patients with rheumatoid arthritis and validate the model. A newly generated predictive model has been suggested to have good differentiation, calibration, and clinical validity and may be a useful clinical model for predicting osteoporosis in patients with rheumatoid arthritis. PURPOSE: To establish a prediction model for osteoporosis risk in patients with rheumatoid arthritis and validate the model internally and externally. METHODS: A total of 270 patients with rheumatoid arthritis who underwent bone mineral density measurement at our hospital from June 2019 to June 2020 were enrolled in the study. The patients were divided into two groups according to their entry time: a training set containing the first 2/3 of the patients (n = 180) and a validation set containing the remaining 1/3 of the patients (n = 90). Binary logistic regression analysis was used to establish the regression models, and the concordance index (C-index), calibration plot, and decision curve analysis were used to evaluate the prediction model. RESULTS: Five variables, including age (X1), course of disease (X2), the disease activity score using 28 joint counts (DAS28) (X4), anti-cyclic citrullinated peptide antibody (CCP) (X7), and 7-joint ultrasonic bone erosion (X14), were selected to enter the model. The prediction model is Logit Y = − 12.647 + 0.133X1 + 0.011X2 + 0.754X4 + 0.001X7 + 0.605X14. The model had good differentiation; the C-index in the internal verification was 0.947 (95% CI is 0.932–0.977) and the C-index in the external verification was 0.946 (95% CI is 0.940–0.994). The calibration plot of the model showed excellent consistency between the prediction probability and actual probability. When > 0.483 was taken as the cutoff value for the diagnosis of osteoporosis, the sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and Jordan index of the model were 90.24%, 87.76%, 7.37, 0.11, and 78.00%, respectively. CONCLUSION: A newly generated predictive model has been suggested to have good differentiation, calibration, and clinical validity and may be a useful clinical model for predicting osteoporosis in patients with rheumatoid arthritis. |
format | Online Article Text |
id | pubmed-7782444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer London |
record_format | MEDLINE/PubMed |
spelling | pubmed-77824442021-01-11 Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model Yan, Xiaobin Xu, Zhenhong Li, Shilin Yan, Lisheng Lyu, Guorong Wang, Zecheng Arch Osteoporos Original Article SUMMARY: To establish a model for osteoporosis risk in patients with rheumatoid arthritis and validate the model. A newly generated predictive model has been suggested to have good differentiation, calibration, and clinical validity and may be a useful clinical model for predicting osteoporosis in patients with rheumatoid arthritis. PURPOSE: To establish a prediction model for osteoporosis risk in patients with rheumatoid arthritis and validate the model internally and externally. METHODS: A total of 270 patients with rheumatoid arthritis who underwent bone mineral density measurement at our hospital from June 2019 to June 2020 were enrolled in the study. The patients were divided into two groups according to their entry time: a training set containing the first 2/3 of the patients (n = 180) and a validation set containing the remaining 1/3 of the patients (n = 90). Binary logistic regression analysis was used to establish the regression models, and the concordance index (C-index), calibration plot, and decision curve analysis were used to evaluate the prediction model. RESULTS: Five variables, including age (X1), course of disease (X2), the disease activity score using 28 joint counts (DAS28) (X4), anti-cyclic citrullinated peptide antibody (CCP) (X7), and 7-joint ultrasonic bone erosion (X14), were selected to enter the model. The prediction model is Logit Y = − 12.647 + 0.133X1 + 0.011X2 + 0.754X4 + 0.001X7 + 0.605X14. The model had good differentiation; the C-index in the internal verification was 0.947 (95% CI is 0.932–0.977) and the C-index in the external verification was 0.946 (95% CI is 0.940–0.994). The calibration plot of the model showed excellent consistency between the prediction probability and actual probability. When > 0.483 was taken as the cutoff value for the diagnosis of osteoporosis, the sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, and Jordan index of the model were 90.24%, 87.76%, 7.37, 0.11, and 78.00%, respectively. CONCLUSION: A newly generated predictive model has been suggested to have good differentiation, calibration, and clinical validity and may be a useful clinical model for predicting osteoporosis in patients with rheumatoid arthritis. Springer London 2021-01-04 2021 /pmc/articles/PMC7782444/ /pubmed/33394305 http://dx.doi.org/10.1007/s11657-020-00867-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Original Article Yan, Xiaobin Xu, Zhenhong Li, Shilin Yan, Lisheng Lyu, Guorong Wang, Zecheng Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title | Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title_full | Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title_fullStr | Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title_full_unstemmed | Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title_short | Establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
title_sort | establishment and verification of an osteoporosis risk model in patients with rheumatoid arthritis: a valuable new model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782444/ https://www.ncbi.nlm.nih.gov/pubmed/33394305 http://dx.doi.org/10.1007/s11657-020-00867-5 |
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