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肾脏病与透析肾移植杂志 ›› 2026, Vol. 35 ›› Issue (2): 134-140.DOI: 10.3969/j.issn.1006-298X.2026.02.006

• 论著 • 上一篇    下一篇

骨骼肌密度联合传统因素判别透析患者二尖瓣钙化风险:一项多中心回顾性横断面研究

  

  • 出版日期:2026-04-28 发布日期:2026-04-23

Skeletal muscle density combined with traditional factors to identify the risk of mitral valve calcification in dialysis patients:a multicenter retrospective cross-sectional study

  • Online:2026-04-28 Published:2026-04-23

摘要: 目的:探讨维持性透析患者二尖瓣钙化 (MVC) 的相关因素,构建多维度风险判别模型。方法:纳入 2020 年 1 月至 2023 年 6 月江苏省四家透析中心的 1642 例维持性透析患者。通过多元螺旋 CT 扫描获取骨骼肌密度 (SMD)。通过最小绝对收缩和选择算子 (Lasso) 筛选 MVC 的独立相关因素,并结合多因素 Logistic 回归构建风险判别模型及可视化列线图,评估 SMD 的增量价值。采用受试者工作特征曲线、校正曲线、Hosmer-Lemeshow 检验、临床决策曲线、净重分类改善 (NRI) 和综合判别改善指数 (IDI) 来评价模型性能,并进行亚组分析验证稳健性。结果:MVC 组 289 例 (17.60%), 非 MVC 组 1353 例 (82.40%)。Lasso 回归和多因素 Logistic 回归分析显示,年龄、透析龄、碱性磷酸酶和甲状旁腺激素与 MVC 呈正相关,而 SMD、淋巴细胞与单核细胞比值及载脂蛋白 A1 (ApoA1) 与 MVC 呈负相关。引入 SMD 后,模型 AUC 略有提升 (训练集:0.780vs0.772,P=0.267; 验证集 0.739vs0.731,P=0.513),IDI 与 NRI 显著改善 (IDI=0.024,NRI=0.316)。亚组分析未见明显交互效应。结论:基于 SMD、年龄、透析龄、碱性磷酸酶、甲状旁腺激素、淋巴细胞与单核细胞比值和 ApoA1 构建的 MVC 发生风险的列线图模型具有较好的判别价值,有助于识别发生 MVC 的高危患者并进行早期干预。

关键词: 维持性透析, 二尖瓣钙化, 骨骼肌密度, 相关因素, 判别模型

Abstract: Objective:To investigate factors associated with mitral valve calcification (MVC) in maintenance dialysis patients and to construct a multidimensional risk discrimination model. Methods:A total of 1642 maintenance dialysis patients from four dialysis centers in Jiangsu Province,China,between January 2020 and June 2023 were included. Skeletal muscle density (SMD) was measured using multidetector spiral computed tomography.The least absolute shrinkage and selection operator (Lasso) regression was applied to identify independent factors associated with MVC,which were then incorporated into a multivariable logistic regression to develop a risk discrimination model and a visualized nomogram. The incremental value of SMD was assessed.Model performance was evaluated using receiver operating characteristic (ROC) curves,calibration plots,Hosmer-Lemeshow goodness-of-fit test,decision curve analysis (DCA),net reclassification improvement (NRI),and integrated discrimination improvement (IDI).Stratified analyses were performed to verify model robustness. Results:MVC was present in 289 patients (17.60%) and absent in 1353 patients (82.40%).Lasso and multivariable logistic regression analyses showed that age,dialysis vintage,alkaline phosphatase (ALP),and parathyroid hormone (PTH) were positively associated with MVC,whereas SMD,lymphocyte-to-monocyte ratio (LMR),and apolipoprotein A1 (ApoA1) were negatively associated.Incorporation of SMD into the model slightly increased the area under the ROC curve (training set:0.780vs0.772,P=0.267; validation set:0.739vs0.731,P=0.513) and significantly improved both IDI (0.024) and NRI (0.316).No significant interaction effects were identified in stratified analyses. Conclusion:The nomogram-based risk discrimination model incorporating SMD,age,dialysis vintage,ALP,PTH,LMR,and ApoA1 demonstrated good discriminative ability for MVC occurrence in maintenance dialysis patients.This model may facilitate early identification of high-risk patients and guide timely intervention.