基于残差卷积网络的心脏年龄预测偏差校正方法研究OA
Study on bias correction methods for cardiac age prediction based on residual convolutional networks
目的:提出一种基于残差卷积网络的心脏年龄预测偏差校正方法并验证其有效性,同时探究校正后年龄差值(age gap,AG)在疾病分类与死亡风险中的应用价值.方法:首先,整合CODE-15%心电图(electrocardiogram,ECG)数据集、MIMIC-Ⅳ数据库、PTB_XL ECG数据集和英国生物样本库4个公开数据库的12导联ECG数据,筛选185 005例健康样本并按照8∶1∶1的比例划分为健康训练集(n=148 022)、健康验证集(n=18 479)和健康测试集(n=18 504),另外筛选23 917例疾病样本构建疾病测试集.其次,基于残差卷积网络构建心脏年龄预测模型,使用健康样本训练预测模型,将基于验证集预测结果计算的各年龄段的预测残差均值作为年龄偏差系数,并将测试集每个样本的预测心脏年龄减去相应偏差系数实现对测试集预测结果的校正.最后,在校正前后的健康测试集上评估AG分布变化,并通过平均绝对误差(mean absolute error,MAE)和偏差标准差(standard deviation,SD)指标与大脑年龄研究中常用的线性校正方法进行对比.此外,采用独立样本t检验比较健康测试集与疾病测试集的AG差异,并采用生存分析及Cox回归探究校正后AG与全因死亡风险的关联.结果:偏差校正结果表明,校正前模型在健康测试集中表现出显著的年龄偏差(在生理年龄约为20岁的受试者中,AG的平均值接近10岁;在约80岁的高龄受试者中,AG的平均值约为-10岁),校正后各年龄段AG分布均接近0.方法对比分析结果表明,与线性校正后在高龄区间(71~85岁)的结果(MAE=5.12,SD=4.44)相比,本研究提出的残差校正方法在该区间的MAE更低(5.00)、SD更小(4.30),偏差校正更彻底、AG分布更集中.疾病判别分析结果表明,在疾病测试集中校正后的AG显著高于健康测试集,尤其在高龄患者中校正后AG由负值转为正值,更符合临床病理特征.生存分析结果表明,基于校正后AG划分的高风险人群生存率显著低于低风险人群.将AG按五分位分组后作为有序变量纳入Cox回归模型后,显示AG与全因死亡风险呈显著相关,死亡风险比为 1.40,分组级别每升高一级,死亡风险平均上升约40%.结论:提出的残差校正方法显著降低了心脏年龄预测中的系统性年龄偏差,提高了预测准确性.校正后的AG是反映病理性心脏衰老、区分健康和疾病状态并预测死亡风险的可靠生物标志物,为心血管疾病早期筛查与风险分层管理提供了新思路.
Objective To propose a bias-correction method for cardiac age prediction based on residual convolutional networks and verify its effectiveness,and to investigate the application value of the corrected age gap(AG)for disease classification and mortality risk assessment.Methods First,from four public databases of the CODE-15%ECG dataset,the MIMIC-Ⅳ database,the PTB_XL ECG dataset and the UK Biobank,the 12-lead ECG data of 185 005 healthy samples were selected and divided into a healthy training set(n=148 022),a healthy validation set(n=18 479)and a healthy test set(n=18 504).Additionally,23 917 disease samples were enrolled into a disease test set.Second,a cardiac age prediction model was constructed using a residual convolutional network and then trained with the healthy samples;the mean prediction residuals across all age groups calculated with the validation set was used as the age bias coefficient,and the prediction results for the test set were corrected by subtracting the corresponding bias coefficient from the predicted cardiac age of each sample in the test set.Finally,changes in the AG distribution were evaluated on the healthy test set before and after correction,and the method proposed was compared with the linear correction method commonly used in brain age studies using the mean absolute error(MAE)and standard deviation(SD)metrics.An independent sample t-test was used to compare AG differences between the healthy and diseased test sets,and survival analysis and Cox regression were employed to explore the association between adjusted AG and the risk of all-cause mortality.Results The results of the bias correction indicated that,prior to correction,the model exhibited significant age bias in the healthy test set(among the participants with a physiological age of approximately 20 years,the mean AG was close to 10 years;among elderly participants aged approximately 80 years,the mean AG was approximately-10 years);after correction,the AG distribution for all age groups approached 0.A comparative analysis of methods showed that,compared with the linear correction method with the results in the older age range(71-85 years)(MAE=5.12,SD=4.44),the residual correction method proposed yielded a lower MAE(5.00)and smaller SD(4.30)in this range,indicating more thorough bias correction and a more concentrated AG distribution.Disease discrimination analysis showed that the corrected AG in the disease test set was significantly higher than that in the healthy test set;notably,the corrected AG shifted from negative to positive in elderly patients,which was consistent with clinical and pathological characteristics.Survival analysis results proved that the survival rate of the high-risk population,defined based on the corrected AG,was significantly lower than that of the low-risk population;after grouping AG into quintiles and incorporating it as an ordinal variable into the Cox regression model,AG was found to be significantly positively correlated with all-cause mortality risk,with the hazard ratio being 1.40 and the risk of death increasing by approximately 40%on average with each higher quintile.Conclusion The proposed residual correction method significantly reduces systematic age bias in cardiac age prediction and improves predictive accuracy.The corrected AG serves as a reliable biomarker for reflecting pathological cardiac aging,distinguishing between healthy and diseased states and predicting mortality risk,thereby offering a new approach for early screening and risk stratification of cardiovascular diseases.[Chinese Medical Equipment Journal,2026,47(4):1-12]
王晓娟;余睿;周著黄;高小峰;朱红玲;宾光宇
北京工业大学化学与生命科学学院,北京 100124北京工业大学化学与生命科学学院,北京 100124北京工业大学化学与生命科学学院,北京 100124北京麦迪克斯科技有限公司,北京 100095华中科技大学同济医学院附属同济医院心血管内科,武汉 430030北京工业大学化学与生命科学学院,北京 100124
医药卫生
残差卷积网络心脏年龄偏差校正深度学习心血管疾病生物标志物
residual convolutional networkcardiac agebias correctiondeep learningcardiovascular diseasebiomarker
《医疗卫生装备》 2026 (4)
1-12,12
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