Department of Public Health, Juntendo University Graduate School of Medicine.
Department of Epidemiology and Public Health, Faculty of Population Health Sciences, University College London.
J Atheroscler Thromb. 2021 Aug 1;28(8):852-864. doi: 10.5551/jat.53926. Epub 2020 Oct 10.
Stress is known to be a potential contributor to the development of diabetes and hypertension. However, the biological mechanisms underlying the association between cardiometabolic risk markers and the biological stress response have not yet been determined. Therefore, we examined salivary alpha-amylase and heart rate variability in relation to cardiometabolic status in a sample of healthy Japanese men and women.
Participants (473 men and 1,029 women aged 30-84) underwent a 75 g oral glucose tolerance test after a 10-hr fast. The homeostasis model assessment index for insulin resistance was based on fasting and 2-hr postload glucose and insulin concentrations. Sitting blood pressure was measured twice after rest. A saliva sample was collected in the morning and salivary alpha-amylase was assayed. A 5-min heart rate variability recording was evaluated using time-domain indices of standard deviations of normal-to-normal intervals and root mean square of successive differences. Multivariate linear regression models were used to estimate associations between salivary alpha-amylase and each outcome measure.
Salivary alpha-amylase was associated with fasting glucose (β=0.008; 95% CI=0.002, 0.014), 2-hr postload glucose (β=0.023; 95% CI=0.004, 0.041), homeostasis model assessment index for insulin resistance (β=0.032; 95%CI=0.000, 0.064), systolic (β=1.603; 95% CI=0.479, 2.726) and diastolic (β=0.906; 95% CI=0.212, 1.600) blood pressures among women. These associations remained significant after further adjustment for heart rate variability measures.
The elevation of salivary alpha-amylase may reflect a dysfunction of the sympathetic nervous system associated with cardiometabolic abnormalities in women.
压力已知是糖尿病和高血压发展的一个潜在因素。然而,心血管代谢风险标志物与生物应激反应之间关联的生物学机制尚未确定。因此,我们在日本健康男性和女性样本中检查了唾液α-淀粉酶和心率变异性与心血管代谢状态的关系。
参与者(30-84 岁,男性 473 人,女性 1029 人)禁食 10 小时后进行 75 g 口服葡萄糖耐量试验。胰岛素抵抗的稳态模型评估指数基于空腹和 2 小时餐后血糖和胰岛素浓度。休息后两次测量坐姿血压。早上采集唾液样本并测定唾液α-淀粉酶。使用正常-正常间隔标准差和连续差异均方根的时域指数评估 5 分钟心率变异性记录。使用多元线性回归模型估计唾液α-淀粉酶与每个结果测量之间的关联。
唾液α-淀粉酶与空腹血糖(β=0.008;95%CI=0.002,0.014)、2 小时餐后血糖(β=0.023;95%CI=0.004,0.041)、胰岛素抵抗的稳态模型评估指数(β=0.032;95%CI=0.000,0.064)、女性的收缩压(β=1.603;95%CI=0.479,2.726)和舒张压(β=0.906;95%CI=0.212,1.600)相关。这些关联在进一步调整心率变异性测量后仍然显著。
唾液α-淀粉酶的升高可能反映了与女性心血管代谢异常相关的交感神经系统功能障碍。