银屑病关节炎风险预测模型:NHANES 数据和多算法方法。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-01-01 Epub Date: 2024-11-25 DOI:10.1007/s10067-024-07244-4
Jinshan Zhan, Fangqi Chen, Yanqiu Li, Changzheng Huang
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引用次数: 0

摘要

目的:开发一种用于识别银屑病患者银屑病关节炎(PsA)的简化预测模型:建立一个简化的预测模型,用于识别银屑病患者的银屑病关节炎(PsA):方法:分析美国国家健康与营养调查(NHANES)数据库中的数据,包括无关节炎银屑病(PsC)或PsA患者。采用最小绝对收缩和选择算子、Boruta 算法、随机森林和逐步回归等方法从 38 个潜在预测因子中选择关键变量。针对所选变量的每种组合构建了逻辑回归模型,并使用接收器操作特征曲线(ROC)、精确度-召回曲线(PR)、校准图、布赖尔评分和决策曲线分析(DCA)进行了评估:研究纳入了 587 名银屑病患者,其中 238 人患有 PsA。博鲁塔算法提出的变量组合表现出最佳的整体性能。博鲁塔模型的主要预测因素包括年龄、空腹血糖、教育水平、甲状腺疾病、高血压和慢性支气管炎。在 ROC 曲线分析中,该模型的训练集曲线下面积(AUC)为 0.781(95% CI,0.737-0.826),测试集曲线下面积(AUC)为 0.780(95% CI,0.712-0.848)。PR 曲线的 AUC 值分别为 0.687(95% CI,0.611-0.757)和 0.653(95% CI,0.535-0.770)。测试集和训练集的 Brier 评分分别为 0.186 和 0.191,表明拟合度良好,校准曲线也进一步证实了这一点。在两个数据集中,当决策阈值为 0.2 至 0.8 时,DCA 显示出净临床效益:结论:Borutamodel是一种很有前途的PsA早期风险评估工具。要点 - 国家数据库的利用:本研究利用 NHANES 数据库预测银屑病关节炎风险,解决了以往因地区或种族限制而造成的局限性。- 综合变量分析:研究采用四种不同的筛查方法和对模型性能的全面评估,检查了 38 个变量,包括人口统计学、健康状况、实验室结果和生活方式因素。- 创新的风险模型:该研究引入了一个新颖的风险评估模型,该模型综合了年龄、空腹血糖、教育程度以及包括高血压、甲状腺疾病和慢性支气管炎在内的合并症,从而超越了传统的只关注皮肤病变和关节症状的做法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk prediction model for psoriatic arthritis: NHANES data and multi-algorithm approach.

Objective: To develop a simplified predictive model for identifying psoriatic arthritis (PsA) in psoriasis patients.

Methods: Data from the National Health and Nutrition Examination Survey (NHANES) database were analyzed, including patients with psoriasis without arthritis (PsC) or PsA. The least absolute shrinkage and selection operator, Boruta algorithm, random forest, and stepwise regression were employed to select key variables from 38 potential predictors. Logistic regression models were constructed for each combination of selected variables and evaluated using receiver operating characteristic (ROC) curves, precision-recall (PR) curves, calibration plots, Brier scores, and decision curve analysis (DCA).

Results: The study included 587 patients with psoriasis, 238 of whom had PsA. The variable combinations proposed by the Boruta algorithm exhibited the best overall performance. Key predictors in the Borutamodel included age, fasting glucose, education level, thyroid disease, hypertension, and chronic bronchitis. This model achieved area under the curve (AUC) of 0.781 (95% CI, 0.737-0.826) for the training set and 0.780 (95% CI, 0.712-0.848) for the testing set in the ROC curve analyses. The AUC values in the PR curves were 0.687 (95% CI, 0.611-0.757) and 0.653 (95% CI, 0.535-0.770), respectively. The Brier scores of 0.186 and 0.191 for the testing and training sets indicated a good fit, further supported by the calibration curves. DCA showed a net clinical benefit for decision thresholds ranging from 0.2 to 0.8 in both datasets.

Conclusion: The Borutamodel represents a promising tool for early risk assessment of PsA. Key Points • National Database Utilization: This study leverages the NHANES database to predict psoriatic arthritis risk, addressing previous limitations tied to regional or ethnic constraints. • Comprehensive Variable Analyses: The research examines 38 variables, including demographics, health conditions, laboratory results, and lifestyle factors, using four distinct screening methods and thorough evaluations of model performance. • Innovative Risk Model: The study introduces a novel risk assessment model that integrates age, fasting glucose, education, and comorbidities including hypertension, thyroid disease, and chronic bronchitis, thus moving beyond traditional focus on skin lesions and joint symptoms.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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