Development of a nomogram model for predicting coronary heart disease in patients with metabolic-associated fatty liver disease.

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Frontiers in Cardiovascular Medicine Pub Date : 2025-09-23 eCollection Date: 2025-01-01 DOI:10.3389/fcvm.2025.1652321
Zhengliang Li, Xiaokai Chen, Juan Wang, Weirui Chen, Run Zhang, Lihua Cao, Shaoting Shi, Linlin Ren, Wenzhong Zhang
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引用次数: 0

Abstract

Objective: To investigate the risk factors associated with coronary heart disease (CHD) in patients with metabolic-associated fatty liver disease (MAFLD) and develop a nomogram prediction model.

Methods: This study included 394 patients with MAFLD who underwent coronary angiography at The Affiliated Hospital of Qingdao University between December 2019 and December 2024. The study cohort was divided in a 7:3 ratio into training and validation sets comprising 277 and 117 cases, respectively. The training group was further divided into the MAFLD-only (n = 57) and MAFLD-plus-CHD (n = 220) groups. LASSO and multivariable logistic regression analyses were performed to identify the risk factors of concomitant coronary heart disease in patients with MAFLD. A nomogram was constructed and validated internally to predict CHD risk in the patients. We evaluated the nomogram's predictive performance using receiver operating characteristic (ROC) curves, calibration plots, and decision curve analysis (DCA) in the training and validation groups.

Results: Of the 394 MAFLD cases, 313 had CHD-related complications. Of the 277 patients in the training set, 220 had CHD, and of the 117 patients in the validation set, 93 had CHD. LASSO regression analysis revealed that the following variables were associated with the risk of CHD: sex, lipoprotein(a) (Lp[a]), low-density lipoprotein cholesterol, white blood cell count (WBC), glycated triglyceride-glucose index (TyG), and atherosclerosis index (AIP). Multivariate logistic regression analysis revealed that sex, Lp(a), WBC, TyG, and AIP were independent risk factors for CHD in MAFLD cases. A nomogram was constructed and an ROC curve was plotted, based on which the optimal cutoff value was determined as 0.698. The area under the curve of the nomogram in the training and validation cohorts was 0.860 (95% CI = 0.807-0.913) and 0.843 (95% CI = 0.757-0.929), respectively. Calibration curves for CHD risk probability showed good agreement between the nomogram's predicted probabilities and the observed event rates. DCA demonstrated the net clinical benefit of the constructed nomogram.

Conclusion: Sex, Lp(a), WBC, TyG, and AIP emerged as independent risk factors for CHD in patients with MAFLD and the nomogram prediction model constructed using these factors could effectively predict CHD occurrence.

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代谢相关脂肪肝患者冠心病的nomogram预测模型的建立
目的:探讨代谢性脂肪性肝病(MAFLD)患者冠心病(CHD)的相关危险因素,并建立nomogram预测模型。方法:本研究纳入了2019年12月至2024年12月在青岛大学附属医院行冠状动脉造影的394例MAFLD患者。研究队列按7:3的比例分为训练组和验证组,分别包括277例和117例。训练组进一步分为仅mafld组(n = 57)和mafld加冠心病组(n = 220)。采用LASSO和多变量logistic回归分析来确定MAFLD患者并发冠心病的危险因素。构建并内部验证了一个nomogram来预测患者的冠心病风险。在训练组和验证组中,我们使用受试者工作特征(ROC)曲线、校准图和决策曲线分析(DCA)来评估nomogram的预测性能。结果:在394例MAFLD病例中,313例有冠心病相关并发症。在训练组的277例患者中,有220例患有冠心病,而在验证组的117例患者中,有93例患有冠心病。LASSO回归分析显示,与冠心病发生风险相关的变量有:性别、脂蛋白(a) (Lp[a])、低密度脂蛋白胆固醇、白细胞计数(WBC)、糖化甘油三酯-葡萄糖指数(TyG)、动脉粥样硬化指数(AIP)。多因素logistic回归分析显示,性别、Lp(a)、WBC、TyG和AIP是MAFLD患者冠心病的独立危险因素。构建模态图,绘制ROC曲线,确定最佳截止值为0.698。训练组和验证组的曲线下面积分别为0.860 (95% CI = 0.807-0.913)和0.843 (95% CI = 0.757-0.929)。冠心病风险概率的校准曲线显示,nomogram预测概率与观测到的事件发生率之间具有良好的一致性。DCA显示了构建的nomogram临床益处。结论:性别、Lp(a)、WBC、TyG、AIP是MAFLD患者冠心病的独立危险因素,利用这些因素构建的nomogram预测模型可以有效预测冠心病的发生。
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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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