Washington University School of Medicine, St. Louis, Missouri, USA.
J Cardiovasc Electrophysiol. 2011 Feb;22(2):122-7. doi: 10.1111/j.1540-8167.2010.01967.x. Epub 2010 Dec 6.
We examined whether heart rate turbulence (HRT) and C-reactive protein (CRP) add to traditional risk factors for cardiac mortality in older adults at low, intermediate, and high risk.
One thousand two hundred and seventy-two individuals, age ≥ 65 years, with 24-hour Holter recordings were studied. HRT, which quantifies heart rate response to ventricular premature contractions, was categorized as: both turbulence onset (TO) and turbulence slope (TS) normal; TO abnormal; TS abnormal; or both abnormal. Independent risks for cardiac mortality associated with HRT or, for comparison, elevated CRP (>3.0 mg/L), were calculated using Cox regression analysis adjusted for traditional cardiovascular disease risk factors and stratified by the presence of no, isolated subclinical (i.e., intermediate risk) or clinical cardiovascular disease. Having TS + TO abnormal compared to both normal was associated with cardiac mortality in the low-risk group [HR 7.9, 95% confidence interval (CI) 2.8-22.5, (P < 0.001)]. In the high and intermediate risk groups, abnormal TS and TS + TO ([HR 2.2, 95% CI 1.5-4.0, P = 0.016] and [HR 2.7, 95% CI 1.2-5.9, P = 0.012]), respectively, were also significantly associated with cardiac mortality. In contrast, elevated CRP was associated with increased cardiac mortality risk only in low-risk individuals [HR 2.5, 95% CI 1.3-5.1, P = 0.009]. Among low risk, the c-statistic was 0.706 for the base model, 0.725 for the base model with CRP, and 0.767 for the base model with HRT.
Abnormal HRT independently adds to risk stratification of low, intermediate and high-risk individuals, but HRT and CRP appear to both add to stratification of those considered low risk.
我们研究了心率震荡(HRT)和 C 反应蛋白(CRP)是否会增加低、中、高危老年人的传统心脏死亡风险因素。
对 1272 名年龄≥65 岁、进行 24 小时 Holter 记录的个体进行了研究。HRT 量化了室性早搏后心率的反应,可以分为:均正常(TO 和 TS);TO 异常;TS 异常;或两者均异常。使用 Cox 回归分析,根据传统心血管疾病风险因素和无、孤立亚临床(即中危)或临床心血管疾病的存在进行分层,计算与 HRT 相关的心脏死亡的独立风险,或与 CRP(>3.0mg/L)升高相比。与低危组相比,TO 和 TS 均异常与心脏死亡率相关[HR 7.9,95%置信区间(CI)2.8-22.5,(P<0.001)]。在高危和中危组中,异常 TS 和 TS + TO([HR 2.2,95%CI 1.5-4.0,P=0.016]和[HR 2.7,95%CI 1.2-5.9,P=0.012])也与心脏死亡率显著相关。相比之下,CRP 升高仅与低危个体的心脏死亡风险增加相关[HR 2.5,95%CI 1.3-5.1,P=0.009]。在低危人群中,基础模型的 C 统计量为 0.706,基础模型加 CRP 的 C 统计量为 0.725,基础模型加 HRT 的 C 统计量为 0.767。
异常 HRT 独立增加了低、中、高危人群的风险分层,但 HRT 和 CRP 似乎都增加了低危人群的分层。