原发性高血压儿童血清转化生长因子β1与颈股动脉脉搏波传导速度的关系

Relationship between serum transforming growth factor β1 and carotid-femoral pulse wave velocity in children with primary hypertension

  • 摘要: 目的 探讨原发性高血压儿童血清转化生长因子β1(TGF-β1)与颈股动脉脉搏波传导速度(cfPWV)的关系。方法 此研究为横断面研究设计,选取2021年1月至2022年8月住院诊断为原发性高血压且未经治疗的82例患儿为研究对象,男68例(82.9%),女14例(17.1%),选取42名正常血压儿童为对照组。分析临床特征,应用SphygmoCor心血管功能检测仪检测,以cfPWV作为早期动脉僵硬度增加的评估指标。应用酶联免疫吸附试验(ELISA)法检测血清TGF-β1水平。采用Spearman相关系数分析血清TGF-β1水平与cfPWV的相关性;采用多因素逐步logistic回归分析早期动脉僵硬度增加的独立危险因素,应用受试者工作特征(ROC)曲线分析各变量诊断早期动脉僵硬度增加的价值。结果 高血压组患儿血清TGF-β1水平明显高于正常血压组46.1(38.8~49.0)比41.3(30.3~47.1)ng/L,Z=-2.322,P=0.020。82例原发性高血压患儿中,高血压2级组血清TGF-β1水平较1级组高46.1(38.8~49.7)比38.8(35.6~46.1)ng/L,Z=-2.424,P=0.015;16例动脉僵硬度增加组患儿体重指数、血清TGF-β1水平较66例动脉弹性正常组高(31.4±5.1)比(26.3±4.0)kg/m2,t=-4.382,P<0.001;48.8(46.1~55.1)比46.0(38.8~48.1)ng/L,Z=-3.189,P=0.001。Spearman相关性分析显示,体重指数、心率、舒张压、24 h平均舒张压(24hDBP)、24 h平均动脉压(24hMAP)、TGF-β1与cfPWV呈正相关(rs=0.318,P=0.004;rs=0.239,P=0.031;rs=0.244,P=0.027;rs=0.294,P=0.007;rs=0.267,P=0.015;rs=0.482,P<0.001)。多因素逐步logistic回归分析结果显示,体重指数(OR=1.260,95%CI 1.041~1.525)和TGF-β1(OR=1.149,95%CI 1.013~1.305)是早期动脉僵硬度增加的危险因素。ROC曲线分析显示,联合体重指数、TGF-β1诊断早期动脉僵硬度增加的曲线下面积为0.887(95%CI 0.805~0.970,P<0.001),灵敏度和特异度分别为81.3%和80.3%。结论 血清TGF-β1与cfPWV呈正相关,体重指数、TGF-β1是早期动脉僵硬度增加的独立危险因素,联合体重指数、TGF-β1对原发性高血压儿童早期动脉僵硬度增加具有一定的诊断价值。

     

    Abstract: Objective To investigate the correlation between serum transforming growth factor β1(TGF-β1) and carotid-femoral pulse wave velocity(cfPWV) in children with primary hypertension. Methods This was a cross-sectional study in which 82 children, 68 males(82.9%) and 14 females(17.1%), hospitalized with a diagnosis of essential hypertension and untreated from January 2021 to August 2022 were selected, and 42 normotensive children were selected as the control group. The clinical data were analyzed. cfPWV measured by SphygmoCor cardiovascular function detector was assessed as the parameter of early arterial stiffness. Concentration of serum TGF-β1 was detected by enzyme linked immunosorbent assay test(ELISA). Spearman correlation coefficient was used to analyze the correlation between serum TGF-β1 and cfPWV. Multivariable logistic regression was used to analyze the independent risk factors of early arterial stiffness. The receiver operating characteristic(ROC) curve was used to explore the value of variables in the diagnosis of early arterial stiffness. Results The case group had a TGF-β1 level of 46.1(38.8, 49.0) ng/L, significantly higher than the 41.3(30.3, 47.1)ng/L from the control group(Z=-2.322, P=0.020). Among 82 children with primary hypertension, the concentration of serum TGF-β1 in stage 2 hypertension was higher than that in stage 1 46.1(38.8, 49.7) vs 38.8(35.6, 46.1)ng/L, Z=-2.424, P=0.015. The body mass index(BMI) and serum TGF-β1 level in 16 patients with early arterial stiffness group were higher than those in 66 patients with normal arterial elasticity group (31.4±5.1) vs(26.3±4.0)kg/m~2, 48.8(46.1, 55.1) vs 46.0(38.8, 48.1)ng/L. The difference was statistically significant(t=-4.382, P<0.001; Z=-3.189, P=0.001). Spearman correlation analysis showed that BMI, heart rate, diastolic blood pressure(DBP), 24 h mean diastolic blood pressure(24hDBP), 24 h mean pulsatile pressure(24hMAP) and TGF-β1 were positively correlated with cfPWV(rs=0.318, P=0.004; rs=0.239, P=0.031; rs=0.244, P=0.027; rs=0.294, P=0.007; rs=0.267, P=0.015; rs=0.482, P<0.001). The multivariate logistic regression analysis showed that BMI(OR, 1.260; 95%CI 1.041-1.525) and TGF-β1(OR, 1.149; 95%CI 1.013-1.305) were the risk factors for early arterial stiffness. ROC curve analysis showed that the area under the curve of combined BMI and TGF-β1 for the diagnosis of increased early arterial stiffness was 0.887(95%CI 0.805 to 0.970, P<0.001), with a sensitivity and specificity of 81.3% and 80.3%, respectively. Conclusion Serum TGF-β1 is positively correlated with cfPWV, and BMI and TGF-β1 are independent risk factors for early increased arterial stiffness, and combined BMI and TGF-β1 have diagnostic value for early increased arterial stiffness in children with essential hypertension.

     

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