Chaikijurajai Thanat, Wu Yuping, Grodin Justin L, Harb Serge, Jaber Wael, Tang W H Wilson
Department of Cardiovascular Medicine, Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, OH, United States of America.
Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, United States of America.
Am Heart J Plus. 2022 Jun;18. doi: 10.1016/j.ahjo.2022.100174. Epub 2022 Jul 14.
Recently, the hemodynamic gain index (HGI) has shown to be a strong independent predictor of all-cause mortality and associated with metabolic equivalents (METs) in a cohort of male patients. However, the prognostic implications of the HGI have never been externally validated with subgroup analyses based on gender, body mass index (BMI) of 35 kg/m, history of heart failure (HF), coronary artery disease (CAD) and beta-blocker use.
We identified 126,356 consecutive patients undergoing treadmill exercise testing between January 1st, 1991 and February 27th, 2015. HGI was calculated using the formula: [(SBP × HR) - (SBP × HR)] / (SBP × HR). Cox regression models were used to determine the associations between HGI quartiles and all-cause mortality with adjustment for cardiovascular risk factors and exercise testing parameters.
Mean age was 53.5 ± 12.6 years. There were 74,724 (59.1 %) male, 5940 (4.7 %) HF, 21,123 (16.7 %) CAD, and 30,568 (24.2 %) beta-blocker-using patients. During the median follow up of 7.1 years, 9929 (7.9 %) died. Median HGI was 1.93 (interquartile range [IQR] 1.40-2.54) bpm/mmHg. After adjustment for the covariates, lower HGI was independently associated with all-cause mortality in the entire cohort (quartile 1 vs 4, adjusted hazard ratio [95 % confidence interval] 1.33 [IQR 1.21-1.45], 0.001), and subgroups of men, women, patients with body mass index <35 kg/m, with and without HF, CAD, and beta-blocker use. The HGI also correlates well with METs in every subgroup.
The HGI is a strong predictor of long-term mortality independently of traditional cardiovascular risk factors, and exercise performance across patient subgroups.
最近,血流动力学增益指数(HGI)已被证明是全因死亡率的一个强有力的独立预测因子,并且在一组男性患者中与代谢当量(METs)相关。然而,HGI的预后意义从未通过基于性别、体重指数(BMI)35kg/m、心力衰竭(HF)病史、冠状动脉疾病(CAD)和β受体阻滞剂使用情况的亚组分析进行外部验证。
我们确定了1991年1月1日至2015年2月27日期间连续接受跑步机运动试验的126356例患者。HGI使用公式计算:[(收缩压×心率)-(收缩压×心率)]/(收缩压×心率)。使用Cox回归模型来确定HGI四分位数与全因死亡率之间的关联,并对心血管危险因素和运动试验参数进行调整。
平均年龄为53.5±12.6岁。有74724例(59.1%)男性、5940例(4.7%)HF患者、21123例(16.7%)CAD患者和30568例(24.2%)使用β受体阻滞剂的患者。在中位随访7.1年期间,9929例(7.9%)死亡。HGI中位数为1.93(四分位间距[IQR]1.40 - 2.54)bpm/mmHg。在对协变量进行调整后,较低的HGI与整个队列的全因死亡率独立相关(四分位数1与4相比,调整后的危险比[95%置信区间]为1.33[IQR 1.21 - 1.45],P<0.001),以及男性、女性、体重指数<35kg/m的患者、有和无HF病史、CAD病史以及使用β受体阻滞剂的亚组。HGI在每个亚组中也与METs密切相关。
HGI是长期死亡率的一个强有力的预测因子,独立于传统心血管危险因素以及各患者亚组的运动表现。