Department of Cardiology, Institute of Cardiovascular Diseases, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning.
School of Public Health, Dalian Medical University, Dalian, Liaoning, China.
J Hypertens. 2019 Jan;37(1):84-91. doi: 10.1097/HJH.0000000000001857.
Resting heart rate (RHR) and SBP are important risk markers for all-cause mortality. However, the link between increased RHR and SBP for all causes of death remained unclear. We investigated the link between an increased visit-to-visit variation of RHR and SBP for risk of all-cause mortality in the general population.
We examined long-term visit-to-visit variation of RHR and blood pressure among 46 751 residents of Tangshan city, China (mean age: 52.58 ± 11.64 years; 78% men). Cox proportional hazard model was used to estimate the hazard ratios and 95% confidence interval (CI) adjusting for clinical characteristics assessed at the last examination (2010-2011).
A total of 1667 deaths were recorded over 4.97 ± 0.69 years follow-up. A rise in 1 SD of heart rate (4 bpm) was associated with an increased risk of death among the participants in third and fourth quartile of SBP-SD in the subgroups of general population [hazard ratio (95% CI) = 1.10 (1.03-1.67) and 1.16 (1.03-1.30), respectively], men [hazard ratio (95% CI) = 1.10 (1.02-1.17) and 1.16 (1.03-1.30), respectively], and participants under 65 years of age [hazard ratio (95% CI) = 1.16 (1.02-1.33) and 1.20 (1.03-1.39), respectively]. Similarly, 1-SD increase of SBP (7 mmHg) was associated with an increased risk of death among the participants in the highest quartiles of RHR-SD in the subgroups of the general population, men, and under 65 years of age.
An elevated long-term SBP variability combined with an increased RHR variability or vice versa may amplify the risk of all-cause mortality in general population, as well as in men and middle-age group.
静息心率(RHR)和 SBP 是全因死亡率的重要风险标志物。然而,RHR 升高与 SBP 升高对所有死因的关系仍不清楚。我们研究了 RHR 和 SBP 就诊间变异性增加与一般人群全因死亡率风险之间的关系。
我们在中国唐山市的 46751 名居民中检查了 RHR 和血压的长期就诊间变异性(平均年龄:52.58±11.64 岁;78%为男性)。使用 Cox 比例风险模型,根据最后一次检查(2010-2011 年)评估的临床特征,估计风险比和 95%置信区间(CI)。
在 4.97±0.69 年的随访中,共记录了 1667 例死亡。在 SBP-SD 第三和第四四分位数的参与者中,RHR 升高 1 SD(4 bpm)与死亡率增加相关,在一般人群亚组中[风险比(95%CI)=1.10(1.03-1.67)和 1.16(1.03-1.30)],男性[风险比(95%CI)=1.10(1.02-1.17)和 1.16(1.03-1.30)],以及 65 岁以下的参与者[风险比(95%CI)=1.16(1.02-1.33)和 1.20(1.03-1.39)]。同样,SBP 升高 1-SD(7mmHg)与一般人群、男性和 65 岁以下参与者中 RHR-SD 最高四分位数的参与者的死亡风险增加相关。
长期 SBP 变异性升高与 RHR 变异性升高相结合,或反之,可能会放大一般人群、男性和中年人群全因死亡率的风险。