Liang Ruyu, Xu Haojie, Yao Ranran, Pei Wenwen, Wang Ziye, Liang Renge, Han Xiao, Zhou Yunshan, An Yuan, Su Yin
Department of Rheumatology and Immunology, Peking University People's Hospital, 11 Xizhimen South Street, Beijing, 100044, China.
Peking University People's Hospital, Qingdao, China.
Clin Rheumatol. 2024 May;43(5):1541-1550. doi: 10.1007/s10067-024-06934-3. Epub 2024 Apr 2.
Systemic lupus erythematosus (SLE) is associated with a significant risk of atherosclerotic cardiovascular disease, especially in the development of premature atherosclerosis. Specific prediction models for premature atherosclerosis in SLE patients are still limited. The objective of this study was to establish a predictive model for premature atherosclerosis in SLE.
The study collected clinical and laboratory data from 148 SLE patients under the age of 55, between January 2021 and June 2023. The least absolute shrinkage and selection operator logistic regression model was utilized to identify potentially relevant features. Subsequently, a nomogram was developed using multivariable logistic analysis. The performance of the nomogram was evaluated through a receiver-operating characteristic curve, calibration curve, and decision curve analysis (DCA).
A total of 148 SLE patients who fulfilled the inclusion criteria were enrolled in the study, of whom 53 patients (35.81%) met the definition of premature atherosclerosis. Hypertension, antiphospholipid syndrome, azathioprine use, duration of glucocorticoid, and age of patients were included in the multivariable regression. The nomogram, based on the non-overfitting multivariable model, was internally validated and demonstrated sufficient clinical utility for assessing the risk of premature atherosclerosis (area under curve: 0.867).
The comprehensive nomogram constructed in this study serves as a useful and convenient tool for evaluating the risk of premature atherosclerosis in SLE patients. It is helpful for clinicians to early identify SLE patients with premature atherosclerosis and facilitates the implementation of more effective preventive measures. Key Points • SLE patients are at a significantly higher risk of developing premature atherosclerosis compared to the general population, and this risk persists even in cases with low disease activity. Traditional models used to evaluate and predict premature atherosclerosis in SLE patients often underestimate the risk. • This study establishes a comprehensive and visually orientated predictive model of premature atherosclerosis in SLE patients, based on clinical characteristics. • The scoring system allows for convenient and effective prediction of individual incidence of premature atherosclerosis, and could provide valuable information for identification and making further intervention decision.
系统性红斑狼疮(SLE)与动脉粥样硬化性心血管疾病的显著风险相关,尤其是在过早发生动脉粥样硬化方面。针对SLE患者过早发生动脉粥样硬化的特定预测模型仍然有限。本研究的目的是建立一个SLE患者过早发生动脉粥样硬化的预测模型。
本研究收集了2021年1月至2023年6月期间148例年龄在55岁以下的SLE患者的临床和实验室数据。采用最小绝对收缩和选择算子逻辑回归模型来识别潜在的相关特征。随后,使用多变量逻辑分析开发了一个列线图。通过受试者操作特征曲线、校准曲线和决策曲线分析(DCA)对列线图的性能进行评估。
共有148例符合纳入标准的SLE患者纳入本研究,其中53例(35.81%)符合过早发生动脉粥样硬化的定义。多变量回归纳入了高血压、抗磷脂综合征、硫唑嘌呤使用情况、糖皮质激素使用时长和患者年龄。基于非过拟合多变量模型的列线图经过内部验证,显示出在评估过早发生动脉粥样硬化风险方面具有足够的临床实用性(曲线下面积:0.867)。
本研究构建的综合列线图是评估SLE患者过早发生动脉粥样硬化风险的有用且便捷的工具。有助于临床医生早期识别有过早发生动脉粥样硬化的SLE患者,并促进实施更有效的预防措施。要点 • 与一般人群相比,SLE患者发生过早动脉粥样硬化的风险显著更高,且即使在疾病活动度低的情况下,这种风险依然存在。用于评估和预测SLE患者过早动脉粥样硬化的传统模型往往低估了风险。 • 本研究基于临床特征建立了一个全面且直观的SLE患者过早动脉粥样硬化预测模型。 • 评分系统能够方便有效地预测个体过早发生动脉粥样硬化的发生率,并可为识别和做出进一步干预决策提供有价值的信息。