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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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 |
format | Article |
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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.</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 & 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. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c359t-2db5c6ba7538a473a55a0a13424172d9b81773a45b5ec126247e60eda3bec8b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10067-024-07067-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10067-024-07067-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39023656$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jinshan, Zhan</creatorcontrib><creatorcontrib>Fangqi, Chen</creatorcontrib><creatorcontrib>Juanmei, Cao</creatorcontrib><creatorcontrib>Yifan, Jin</creatorcontrib><creatorcontrib>Yuqing, Wang</creatorcontrib><creatorcontrib>Ting, Wu</creatorcontrib><creatorcontrib>Jing, Zhang</creatorcontrib><creatorcontrib>Changzheng, Huang</creatorcontrib><title>Risk assessment tool for anemia of chronic disease in systemic lupus erythematosus: a prediction model</title><title>Clinical rheumatology</title><addtitle>Clin Rheumatol</addtitle><addtitle>Clin Rheumatol</addtitle><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.</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 & 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 ; Fangqi, Chen ; Juanmei, Cao ; Yifan, Jin ; Yuqing, Wang ; Ting, Wu ; Jing, Zhang ; Changzheng, Huang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-2db5c6ba7538a473a55a0a13424172d9b81773a45b5ec126247e60eda3bec8b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Anemia</topic><topic>Anemia - complications</topic><topic>Anemia - diagnosis</topic><topic>Chronic Disease</topic><topic>chronic diseases</topic><topic>Chronic illnesses</topic><topic>Female</topic><topic>Humans</topic><topic>Logistic Models</topic><topic>Lupus</topic><topic>lupus erythematosus</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - diagnosis</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>model validation</topic><topic>Original Article</topic><topic>Patients</topic><topic>Prediction models</topic><topic>regression analysis</topic><topic>Rheumatology</topic><topic>risk</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>ROC Curve</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jinshan, Zhan</creatorcontrib><creatorcontrib>Fangqi, Chen</creatorcontrib><creatorcontrib>Juanmei, Cao</creatorcontrib><creatorcontrib>Yifan, Jin</creatorcontrib><creatorcontrib>Yuqing, Wang</creatorcontrib><creatorcontrib>Ting, Wu</creatorcontrib><creatorcontrib>Jing, Zhang</creatorcontrib><creatorcontrib>Changzheng, Huang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Clinical rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jinshan, Zhan</au><au>Fangqi, Chen</au><au>Juanmei, Cao</au><au>Yifan, Jin</au><au>Yuqing, Wang</au><au>Ting, Wu</au><au>Jing, Zhang</au><au>Changzheng, Huang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk assessment tool for anemia of chronic disease in systemic lupus erythematosus: a prediction model</atitle><jtitle>Clinical rheumatology</jtitle><stitle>Clin Rheumatol</stitle><addtitle>Clin Rheumatol</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>43</volume><issue>9</issue><spage>2857</spage><epage>2866</epage><pages>2857-2866</pages><issn>0770-3198</issn><issn>1434-9949</issn><eissn>1434-9949</eissn><abstract>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.</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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