A study on risk factor analysis and prediction model construction for dilated cardiomyopathy complicated with pulmonary hypertension
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摘要:
目的 探讨扩张型心肌病(DCM)合并肺动脉高压(PH)的风险因素,构建并验证其预测模型,为早期识别高危人群及优化临床管理提供依据。 方法 选取2022年10月—2024年10月杭州师范大学附属医院收治的122例DCM患者,按是否合并PH分为PH组与非PH组(各61例)。采用二元logistic回归分析研究DCM合并PH的风险因素并构建预测模型,通过ROC曲线评估预测模型的效能,并在训练集和验证集上验证模型性能。 结果 2组心电图QRS波、心电图中V1导联的R波+V5导联的S波振幅(RV1+SV5)、N末端脑钠肽前体(NT-proBNP)、左前降支冠状动脉(LAD)、肺动脉收缩压(PASP)差异有统计学意义(P < 0.05)。二元logistic回归分析结果显示,心电图QRS波、RV1+SV5、NT-proBNP、PASP均是DCM合并PH的影响因素(P < 0.05)。ROC分析显示心电图QRS波、RV1+SV5、NT-proBNP、PASP预测DCM出现PH的AUC为0.862、0.362、0.840、0.848,灵敏度分别为70.50%、88.50%、68.90%、86.90%,特异度分别为95.10%、9.80%、90.20%、73.80%;采用校准曲线评估模型的校准度,结果提示该列线图分度良好。依据预测模型计算公式得到预测模型数据,将预测模型数据作为检验变量,并以组别作为状态变量。建立ROC曲线分析各项模型的区分度,结果显示预测模型的AUC为0.985,灵敏度为91.80%,特异度为98.40%;绘制列线图校准曲线,训练集与验证集中校准曲线与理想曲线有较高的一致性,预测模型与实际验证差距较小。 结论 心电图QRS波、NT-proBNP、PASP是DCM合并PH的关键预测因子,综合模型预测效能优异,可为早期筛查及个体化治疗提供重要参考。 Abstract:Objective To investigate risk factors for pulmonary hypertension (PH) in patients diagnosed with dilated cardiomyopathy (DCM) and develop a predictive model to facilitate early identification of patients who are at high risk, thus enabling optimized clinical management. Methods A total of 122 patients diagnosed with DCM patients were admitted to the Affiliated Hospital of Hangzhou Normal University between October 2022 and October 2024, were divided into PH and non-PH groups (61 each). Binary logistic regression was used to identify risk factors for PH in DCM and construct a predictive model. The predictive model ' s performance was evaluated using ROC curves, with calibration assessment being conducted in both the training and validation sets. Results Statistically significant differences were identified (P < 0.05) between the two groups with regard to QRS wave duration on electrocardiogram (ECG), the sum of R-wave amplitude in lead V1 and S-wave amplitude in lead V5 (RV1+SV5) on ECG, N-terminal pro-brain natriuretic peptide (NT-proBNP), left anterior descending coronary artery (LAD), and pulmonary artery systolic pressure (PASP). Binary logistic regression analysis revealed that QRS wave duration, RV1+SV5, NT-proBNP, and PASP were all influential factors for DCM complicated by PH (P < 0.05). ROC analysis demonstrated that the AUCs for predicting PH in DCM using QRS wave duration, RV1+SV5, NT-proBNP, and PASP were 0.862, 0.362, 0.840, and 0.848, respectively, the sensitivity were 70.50%, 88.50%, 68.90% and 86.90%, and the specificity were 95.10%, 9.80%, 90.20% and 73.80%, respectively. The calibration curve was utilized to evaluate the calibration of the model, and the results indicated effective discrimination of the nomogram. The prediction model ' s calculation formula was utilized to obtain prediction model data, which was then employed as test variables, with group assignment designated as the state variable. An ROC curve was undertaken for the purpose of analyzing the discrimination of each model, and the results showed an AUC of 0.985 for the prediction model, with a sensitivity of 91.80% and a specificity of 98.40%. A calibration curve for the nomogram was plotted, and there was a high degree of consistency between the calibration curves for the training and validation sets and the ideal curve, indicating a minor discrepancy between the prediction model and the actual validation. Conclusion QRS duration, NT-proBNP, and PASP are key predictors of PH in DCM. The model offers excellent predictive performance, supporting early screening and personalized treatment strategies for improved precision medicine. -
Key words:
- Dilated cardiomyopathy /
- Pulmonary hypertension /
- Risk factors /
- Prediction model
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表 1 2组DCM患者临床资料比较
Table 1. Comparison of clinical data between two groups of DCM patients
项目 类别 PH组(n=61) 非PH组(n=61) 统计量 P值 年龄(x ±s,岁) 48.93±12.66 47.31±12.03 0.726a 0.469 性别[例(%)] 男性 43(70.49) 36(59.02) 1.760b 0.185 女性 18(29.51) 25(40.98) BMI(x ±s) 24.03±3.68 23.51±3.07 0.847a 0.398 吸烟[例(%)] 是 30(49.18) 27(44.26) 0.296b 0.586 否 31(50.82) 34(55.74) 糖尿病[例(%)] 是 13(21.31) 14(22.95) 0.048b 0.827 否 48(78.69) 47(77.05) NYHA心功能分级[例(%)] Ⅱ级 23(37.70) 31(50.82) 2.126b 0.145 Ⅲ~Ⅳ级 38(62.30) 30(49.18) HR(x ±s,次/min) 99.03±12.07 94.07±17.98 1.791a 0.076 SBP(x ±s,mmHg) 114.00±13.99 114.05±13.05 0.020a 0.984 DBP(x ±s,mmHg) 71.00±12.96 71.03±12.04 0.013a 0.989 HGB(x ±s,g/L) 137.00±15.00 135.98±12.97 0.402a 0.689 心电图QRS波(x ±s,ms) 129.85±13.02 114.17±9.66 7.554a < 0.001 RV1+SV5(x ±s,mV) 0.71±0.13 0.83±0.21 3.798a < 0.001 NT-proBNP(x ±s,ng/L) 2 445.23±378.46 2 033.19±257.70 7.029a < 0.001 ALB(x ±s,mg/L) 41.58±3.31 42.07±3.14 0.839a 0.403 LAD(x ±s,mm) 47.59±4.38 43.89±3.89 4.933a < 0.001 PASP(x ±s,mmHg) 33.16±2.32 29.58±2.68 7.888a < 0.001 LVEDD(x ±s,mm) 65.28±4.52 64.17±5.71 1.190a 0.236 LVEF(x ±s,%) 34.13±3.39 35.32±3.75 1.839a 0.068 MPAD(x ±s,mm) 26.74±2.81 25.74±3.63 1.702a 0.091 RVTD(x ±s,mm) 37.59±4.26 36.43±3.80 1.587a 0.115 注:a为t值,b为χ2值;1 mmHg=0.133 kPa。 表 2 DCM合并PH风险因素的二元logistic回归分析
Table 2. Binary logistic regression analysis of risk factors for DCM combined with PH
变量 B SE Waldχ2 P值 OR值 95% CI 心电图QRS波 -0.133 0.061 4.672 0.031 0.876 0.777~0.988 RV1+SV5 -23.265 8.877 6.867 0.002 0.000 0.000~0.003 NT-proBNP -0.007 0.003 6.135 0.013 0.993 0.988~0.999 LAD -0.223 0.181 1.529 0.216 0.800 0.562~1.140 PASP -0.733 0.268 7.481 0.006 0.481 0.284~0.812 表 3 心电图QRS波、RV1+SV5、NT-proBNP、PASP预测DCM出现PH的价值
Table 3. The value of ECG QRS wave, RV1+SV5, NT-proBNP, and PASP for PH prediction in DCM
指标 AUC 95% CI SE P值 cut-off值 约登指数 灵敏度(%) 特异度(%) 心电图QRS波 0.862 0.793~0.930 0.035 < 0.001 125.305 0.656 70.50 95.10 RV1+SV5 0.362 0.259~0.464 0.052 0.008 0.565 -0.017 88.50 9.80 NT-proBNP 0.840 0.768~0.912 0.037 < 0.001 2 257.675 0.591 68.90 90.20 PASP 0.848 0.777~0.918 0.036 < 0.001 31.145 0.607 86.90 73.80 -
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