Risk assessment tool for anemia of chronic disease in systemic lupus erythematosus: a prediction model

Objective This study aims to develop a predictive model for estimating the likelihood of anemia of chronic disease (ACD) in patients with systemic lupus erythematosus (SLE) and to elucidate the relationship between various factors and ACD Methods Individuals diagnosed with SLE for at least one year...

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Veröffentlicht in:Clinical rheumatology 2024-09, Vol.43 (9), p.2857-2866
Hauptverfasser: Jinshan, Zhan, Fangqi, Chen, Juanmei, Cao, Yifan, Jin, Yuqing, Wang, Ting, Wu, Jing, Zhang, Changzheng, Huang
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container_end_page 2866
container_issue 9
container_start_page 2857
container_title Clinical rheumatology
container_volume 43
creator Jinshan, Zhan
Fangqi, Chen
Juanmei, Cao
Yifan, Jin
Yuqing, Wang
Ting, Wu
Jing, Zhang
Changzheng, Huang
description Objective This study aims to develop a predictive model for estimating the likelihood of anemia of chronic disease (ACD) in patients with systemic lupus erythematosus (SLE) and to elucidate the relationship between various factors and ACD Methods Individuals diagnosed with SLE for at least one year were enrolled and categorized into two groups: those with ACD and those without anemia symptoms. Patients were randomly assigned to training and test sets at an 8:2 ratio. The least absolute shrinkage and selection operator (LASSO) method was used to select predictors, followed by logistic regression for modeling. Model performance was assessed using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA) for both training and test sets. Results The study included a total of 216 patients, with 172 in the training set and 44 in the test set. LASSO identified 6 variables for constructing the predictive model, resulting in an area under the curve (AUC) of 0.833 (95% CI, 0.773-0.892) in the training set and 0.861 (95% CI, 0.750-0.972) in the test set. Calibration curves indicated consistency between expected and observed probabilities. DCA indicated that the model yielded a net benefit with threshold probabilities ranging from 20% to 90% in the training set and from 10% to 80% in the test set. Conclusion This study presents a predictive model for assessing the risk of ACD in SLE patients. The model effectively captures the underlying mechanism of ACD in SLE and empowers clinicians to make well-informed treatment adjustments. Key Points • Development of a New Predictive Model: This study introduces a new predictive model to evaluate the likelihood of anemia of chronic disease (ACD) in patients with systemic lupus erythematosus (SLE). The model utilizes routine laboratory parameters to identify high-risk individuals, addressing a significant gap in current clinical practice. • Reflection of Potential Mechanisms for ACD Development: By incorporating the factors needed to construct the predictive model, this study also sheds light on the potential mechanisms of ACD development in SLE patients.
doi_str_mv 10.1007/s10067-024-07067-3
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Patients were randomly assigned to training and test sets at an 8:2 ratio. The least absolute shrinkage and selection operator (LASSO) method was used to select predictors, followed by logistic regression for modeling. Model performance was assessed using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA) for both training and test sets. Results The study included a total of 216 patients, with 172 in the training set and 44 in the test set. LASSO identified 6 variables for constructing the predictive model, resulting in an area under the curve (AUC) of 0.833 (95% CI, 0.773-0.892) in the training set and 0.861 (95% CI, 0.750-0.972) in the test set. Calibration curves indicated consistency between expected and observed probabilities. DCA indicated that the model yielded a net benefit with threshold probabilities ranging from 20% to 90% in the training set and from 10% to 80% in the test set. Conclusion This study presents a predictive model for assessing the risk of ACD in SLE patients. The model effectively captures the underlying mechanism of ACD in SLE and empowers clinicians to make well-informed treatment adjustments. Key Points • Development of a New Predictive Model: This study introduces a new predictive model to evaluate the likelihood of anemia of chronic disease (ACD) in patients with systemic lupus erythematosus (SLE). The model utilizes routine laboratory parameters to identify high-risk individuals, addressing a significant gap in current clinical practice. • Reflection of Potential Mechanisms for ACD Development: By incorporating the factors needed to construct the predictive model, this study also sheds light on the potential mechanisms of ACD development in SLE patients.</description><identifier>ISSN: 0770-3198</identifier><identifier>ISSN: 1434-9949</identifier><identifier>EISSN: 1434-9949</identifier><identifier>DOI: 10.1007/s10067-024-07067-3</identifier><identifier>PMID: 39023656</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult ; Anemia ; Anemia - complications ; Anemia - diagnosis ; Chronic Disease ; chronic diseases ; Chronic illnesses ; Female ; Humans ; Logistic Models ; Lupus ; lupus erythematosus ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - diagnosis ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; model validation ; Original Article ; Patients ; Prediction models ; regression analysis ; Rheumatology ; risk ; Risk Assessment ; Risk Factors ; ROC Curve ; Systemic lupus erythematosus</subject><ispartof>Clinical rheumatology, 2024-09, Vol.43 (9), p.2857-2866</ispartof><rights>The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR) 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. 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Patients were randomly assigned to training and test sets at an 8:2 ratio. The least absolute shrinkage and selection operator (LASSO) method was used to select predictors, followed by logistic regression for modeling. Model performance was assessed using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA) for both training and test sets. Results The study included a total of 216 patients, with 172 in the training set and 44 in the test set. LASSO identified 6 variables for constructing the predictive model, resulting in an area under the curve (AUC) of 0.833 (95% CI, 0.773-0.892) in the training set and 0.861 (95% CI, 0.750-0.972) in the test set. Calibration curves indicated consistency between expected and observed probabilities. DCA indicated that the model yielded a net benefit with threshold probabilities ranging from 20% to 90% in the training set and from 10% to 80% in the test set. 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The model utilizes routine laboratory parameters to identify high-risk individuals, addressing a significant gap in current clinical practice. • Reflection of Potential Mechanisms for ACD Development: By incorporating the factors needed to construct the predictive model, this study also sheds light on the potential mechanisms of ACD development in SLE patients.</description><subject>Adult</subject><subject>Anemia</subject><subject>Anemia - complications</subject><subject>Anemia - diagnosis</subject><subject>Chronic Disease</subject><subject>chronic diseases</subject><subject>Chronic illnesses</subject><subject>Female</subject><subject>Humans</subject><subject>Logistic Models</subject><subject>Lupus</subject><subject>lupus erythematosus</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - diagnosis</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>model validation</subject><subject>Original Article</subject><subject>Patients</subject><subject>Prediction models</subject><subject>regression analysis</subject><subject>Rheumatology</subject><subject>risk</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>ROC Curve</subject><subject>Systemic lupus erythematosus</subject><issn>0770-3198</issn><issn>1434-9949</issn><issn>1434-9949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUGL1TAQx4Mo7nP1C3iQgBcv1SSTNI03WVZ3YUEQPYc0nbpZ2-aZaQ_v25vnWxU86CUJmd_8h-HH2HMpXksh7BuqZ2sboXQj7PEFD9hOatCNc9o9ZDthrWhAuu6MPSG6E0KozsnH7AycUNCadsfGT4m-8UCERDMuK19znviYCw8LzinwPPJ4W_KSIh8SYSDkaeF0oLWWI5-2_UYcy2G9xTmsmTZ6ywPfFxxSXFNe-JwHnJ6yR2OYCJ_d3-fsy_vLzxdXzc3HD9cX726aCMatjRp6E9s-WANd0BaCMUEECVppadXg-k7a-qtNbzBK1SptsRU4BOgxdr2Dc_bqlLsv-fuGtPo5UcRpqtvkjTxIA1ZLAfL_qOgUSOFMV9GXf6F3eStLXaRSDpw2bXecrU5ULJmo4Oj3Jc2hHLwU_ijMn4T5Ksz_FOahNr24j976GYffLb8MVQBOANXS8hXLn9n_iP0Bof2gbA</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Jinshan, Zhan</creator><creator>Fangqi, Chen</creator><creator>Juanmei, Cao</creator><creator>Yifan, Jin</creator><creator>Yuqing, Wang</creator><creator>Ting, Wu</creator><creator>Jing, Zhang</creator><creator>Changzheng, Huang</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240901</creationdate><title>Risk assessment tool for anemia of chronic disease in systemic lupus erythematosus: a prediction model</title><author>Jinshan, Zhan ; 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Patients were randomly assigned to training and test sets at an 8:2 ratio. The least absolute shrinkage and selection operator (LASSO) method was used to select predictors, followed by logistic regression for modeling. Model performance was assessed using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA) for both training and test sets. Results The study included a total of 216 patients, with 172 in the training set and 44 in the test set. LASSO identified 6 variables for constructing the predictive model, resulting in an area under the curve (AUC) of 0.833 (95% CI, 0.773-0.892) in the training set and 0.861 (95% CI, 0.750-0.972) in the test set. Calibration curves indicated consistency between expected and observed probabilities. DCA indicated that the model yielded a net benefit with threshold probabilities ranging from 20% to 90% in the training set and from 10% to 80% in the test set. Conclusion This study presents a predictive model for assessing the risk of ACD in SLE patients. The model effectively captures the underlying mechanism of ACD in SLE and empowers clinicians to make well-informed treatment adjustments. Key Points • Development of a New Predictive Model: This study introduces a new predictive model to evaluate the likelihood of anemia of chronic disease (ACD) in patients with systemic lupus erythematosus (SLE). The model utilizes routine laboratory parameters to identify high-risk individuals, addressing a significant gap in current clinical practice. • Reflection of Potential Mechanisms for ACD Development: By incorporating the factors needed to construct the predictive model, this study also sheds light on the potential mechanisms of ACD development in SLE patients.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>39023656</pmid><doi>10.1007/s10067-024-07067-3</doi><tpages>10</tpages></addata></record>
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subjects Adult
Anemia
Anemia - complications
Anemia - diagnosis
Chronic Disease
chronic diseases
Chronic illnesses
Female
Humans
Logistic Models
Lupus
lupus erythematosus
Lupus Erythematosus, Systemic - complications
Lupus Erythematosus, Systemic - diagnosis
Male
Medicine
Medicine & Public Health
Middle Aged
model validation
Original Article
Patients
Prediction models
regression analysis
Rheumatology
risk
Risk Assessment
Risk Factors
ROC Curve
Systemic lupus erythematosus
title Risk assessment tool for anemia of chronic disease in systemic lupus erythematosus: a prediction model
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