A nomogram for predicting the adverse pregnancy outcomes of systemic lupus erythematosus: a single-center study.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Wei Kong, Xin Zhang, Linyu Geng, Chen Chen, Yue Sun, Xue Xu, Shengnan Zhao, Ziyi Jin, Yang Huang, Dandan Wang, Jun Liang, Yun Zhu, Lingyun Sun
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引用次数: 0

Abstract

Objectives: As systemic lupus erythematosus (SLE) primarily impacts women of childbearing age, a considerable number of patients have fertility needs. However, the risk of experiencing adverse pregnancy outcomes (APOs) was higher in these patients. Our study aimed to construct a predictive model to assess the risks for APOs of SLE.

Method: We retrospectively analyzed the data of pregnant SLE patients hospitalized at Nanjing Drum Tower Hospital from August 2010 to April 2023. The Least Absolute Shrinkage and Selection Operator (LASSO) regression analysis was used to explore the risk factors for APOs, and a nomogram was established. Afterward, the efficacy of the nomogram was evaluated by analyzing the areas under the curves (AUCs) of Receiver Operating Characteristic (ROC), calibration curves, and Decision Curve Analysis (DCA).

Results: Our study involved 259 pregnant patients with a median age of 29.00 years, and identified 129 cases of APOs, including preterm birth, low birth weight, congenital anomalies, stillbirth/miscarriage, and fetal distress. Through LASSO regression analysis, nine optimal features were selected as risk factors, including age, lupus nephritis, antepartum body mass index, antinuclear antibody, anti-U1RNP/Sm antibody, anti-ribosomal P protein antibody, platelet, albumin levels, SLEDAI scores, diabetes mellitus, rash, and the use of aspirin therapy. These factors were integrated into a predictive nomogram model, which showed good predictive accuracy, with AUC values of 0.870 and 0.830 in training and validation groups, respectively. The calibration curves and DCA also confirmed the good performance of the model.

Conclusions: We developed a tool to predict APOs in SLE patients, offering personalized risk assessments and clinical decision support. As the data used to build the predictive model was obtained from a single center, the tool is currently best suited for application within our center. Further validation in diverse populations is needed to expand its generalizability. Key Points • Our study revealed the independent predictors for APOs of SLE through LASSO regression analysis. • We developed a nomogram to predict APOs in SLE based on the results of LASSO regression analysis. • The predictive model may aid clinical decision-making, enabling timely interventions to reduce the incidence of APOs.

预测系统性红斑狼疮不良妊娠结局的提名图:一项单中心研究。
目的:由于系统性红斑狼疮(SLE)主要影响育龄妇女,相当数量的患者有生育需求。然而,这些患者出现不良妊娠结局(APOs)的风险较高。我们的研究旨在建立一个预测模型来评估SLE患者apo的风险。方法:回顾性分析2010年8月至2023年4月南京鼓楼医院SLE孕妇住院资料。采用最小绝对收缩和选择算子(LASSO)回归分析探讨APOs的危险因素,并建立nomogram。随后,通过分析受试者工作特征(ROC)、校准曲线和决策曲线分析(DCA)的曲线下面积(auc)来评价nomogram疗效。结果:我们的研究纳入了259例中位年龄为29.00岁的孕妇,确定了129例apo,包括早产、低出生体重、先天性异常、死产/流产和胎儿窘迫。通过LASSO回归分析,筛选出年龄、狼疮肾炎、产前体重指数、抗核抗体、抗u1rnp /Sm抗体、抗核糖体P蛋白抗体、血小板、白蛋白水平、SLEDAI评分、糖尿病、皮疹、阿司匹林使用情况等9个最优特征作为危险因素。将这些因素整合到预测模态图模型中,该模型具有较好的预测准确性,训练组和验证组的AUC分别为0.870和0.830。标定曲线和DCA验证了该模型的良好性能。结论:我们开发了一种预测SLE患者apo的工具,提供个性化的风险评估和临床决策支持。由于用于构建预测模型的数据是从单个中心获得的,因此该工具目前最适合在我们中心内应用。需要在不同人群中进一步验证以扩大其普遍性。•本研究通过LASSO回归分析揭示了SLE APOs的独立预测因子。•基于LASSO回归分析的结果,我们开发了一个nomogram来预测SLE患者的apo。•预测模型可以帮助临床决策,及时干预,减少apo的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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