首页|期刊导航|广东医学|以"络病学说"构建的2型糖尿病周围神经病变电导法经络测量预警模型及其外部验证

以"络病学说"构建的2型糖尿病周围神经病变电导法经络测量预警模型及其外部验证OA

Development and independent validation of a meridian electrical conductance-based screening model for diabetic peripheral neuropathy guided by the collateral disease theory

中文摘要英文摘要

目的 基于中医"络病学说",利用电导法经络测量技术构建2型糖尿病周围神经病变(DPN)的预警模型,并通过外部验证评估其预测效能和临床应用价值.方法 收集广东省中医院189例2型糖尿病患者资料,其中DPN组53例,非DPN组136例.采集患者基本信息及穴位电导值.由于经络测量与实验室检查并非在同一天完成,提取了受试者经络检测日期前1个月内的血糖相关数据,包括空腹血糖(FPG)、餐后2 h血糖(2hPG)及糖化血红蛋白(HbA1C).对于在该时间窗内存在多次FPG或2hPG检测结果的受试者,采用其平均值作为主要分析指标;HbA1C采用距离经络检测日期最近的一次检测值作为代表值.采用LASSO回归筛选关键穴位电导特征变量,并构建多层前馈神经网络模型.针对训练集类别不平衡问题,在训练阶段使用SMOTE过采样进行优化.采用敏感度、特异度、F1值等指标综合评价模型性能,并在30例独立样本中进行外部验证.结果 基线资料显示两组患者在年龄、性别、BMI及血糖指标方面差异无统计学意义.LASSO回归筛选出11个关键电导变量(如厉兑左、中冲右、冲阳左等).最优神经网络模型(隐藏层节点数为4,截断值0.4)在训练集上表现出较好的拟合表现(准确率97.35%,敏感度90.57%,特异度100.00%,F1值95.05%).在30例外部验证样本中,模型准确率为90.00%,敏感度为87.50%,特异度为90.91%,F1值为82.35%.结论 基于"络病学说"指导,利用电导法经络测量构建的神经网络预警模型,能够较好地区分糖尿病患者是否伴有DPN,展现出一定的预测准确性和稳定性.该方法具有无创、便捷、经济的特点,为DPN的早期风险评估和筛查提供了一种有潜力的中医特色新途径.

Objective To develop a screening model for diabetic peripheral neuropathy(DPN)in patients with type 2 diabetes mellitus(T2DM)based on meridian electrical conductance measurement guided by the traditional Chinese medicine(TCM)Collateral Disease Theory and to evaluate its screening performance and clinical applicability through in-dependent validation.Methods Clinical data from 189 patients with T2DM treated at Guangdong Provincial Hospital of Chinese Medicine were collected,including 53 patients with DPN and 136 without DPN.Demographic and clinical charac-teristics and electrical conductance values at selected acupoints were collected.Because meridian electrical conductance measurements and laboratory tests were not performed on the same day,glucose-related laboratory data obtained within 1 month before the meridian measurement were extracted,including fasting plasma glucose(FPG),2-h postprandial plas-ma glucose(2hPG),and glycated hemoglobin A1c(HbA1c).For patients with multiple FPG or 2hPG measurements during this period,the mean value was used for the primary analysis,whereas the HbA1c measurement closest to the date of meridian measurement was selected.Least absolute shrinkage and selection operator(LASSO)regression was used to i-dentify key electrical conductance features of the acupoints,followed by construction of a multilayer feedforward neural net-work model.Synthetic Minority Over-sampling Technique(SMOTE)was applied during model training to address class imbalance in the training set.Model performance was evaluated using accuracy,sensitivity,specificity,and F1 score and was subsequently validated in a separate cohort of 30 patients.Results No statistically significant differences were ob-served between the DPN and non-DPN groups in age,sex,body mass index,or glucose-related indicators at baseline.LASSO regression identified 11 key electrical conductance variables,including left Lidui(ST45),right Zhongchong(PC9),and left Chongyang(ST42).The optimal neural network model,with four hidden-layer nodes and a cutoff value of 0.4,showed good performance in the training set,with an accuracy of 97.35%,sensitivity of 90.57%,specificity of 100.00%,and F1 score of 95.05%.In the separate validation cohort of 30 patients,the model achieved an accuracy of 90.00%,sensitivity of 87.50%,specificity of 90.91%,and F1 score of 82.35%.Conclusion Guided by the TCM Collateral Disease Theory,the neural network screening model based on meridian electrical conductance measurement dem-onstrated good discriminatory performance and relatively stable results in identifying DPN among patients with T2DM.This noninvasive,convenient,and economical approach may provide a promising TCM-based strategy for early screening and risk assessment of DPN.

原嘉民;李秀铭;孙晨;何春香;徐福平;黄鹂;杨志敏

广东省中医院治未病中心(广东 广州 510120)广东省中医院内分泌科(广东 广州 510120)广东省中医院治未病中心(广东 广州 510120)广东省中医院治未病中心(广东 广州 510120)广东省中医院治未病中心(广东 广州 510120)广东省中医院治未病中心(广东 广州 510120)广东省中医院治未病中心(广东 广州 510120)

医药卫生

糖尿病周围神经病变电导法经络测量预警模型

diabetic peripheral neuropathymeridian electrical conductance measurementscreening model

《广东医学》 2026 (8)

1144-1149,6

国家重点研发计划项目(2024YFC3506303)广州市科技局市校联合专项(2023A03J0754)

10.13820/j.cnki.gdyx.20254445

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