Sharma Abhinav, de Souza Brito Flávio, Sun Jie-Lena, Thomas Laine, Haffner Steven, Holman Rury R, Lopes Renato D
Duke Clinical Research Institute, Duke University, Durham, NC; Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada.
Duke Clinical Research Institute, Duke University, Durham, NC.
Am Heart J. 2017 Apr;186:73-82. doi: 10.1016/j.ahj.2016.12.011. Epub 2016 Dec 29.
Patients with impaired glucose tolerance have an elevated risk of cardiovascular (CV) death; however, the causes and risk factors associated with non-CV deaths are poorly understood.
The NAVIGATOR trial enrolled 9,306 participants with impaired glucose tolerance and CV disease or at high CV risk, with a median follow-up of 6.4years. Using this population, we identified (1) the proportion of deaths attributed to CV, non-CV, and unknown causes, and (2) the risk factors associated with non-CV death.
During the NAVIGATOR trial follow-up, 622 patients died. Investigators reported 244 (39.2%) CV deaths, 313 (50.3%) non-CV deaths, and 65 (10.5%) deaths of unknown cause. Myocardial infarction was the leading cause of investigator-reported death (57/622 [9.2%]). Among non-CV deaths, the most commonly identified cause related to malignancy (177/313 [56.5%]). Using adjudicated causes of death, Cox proportional hazard models identified 3 independent prognostic markers that increased the risk of non-CV death: history of non-melanoma skin cancer (hazard ratio 2.67 [95% CI 1.65-4.33]; P<.0001), white blood cell count (1 unit >5000/mm; 1.10 [1.02-1.18]; P=.011), and serum potassium levels (per 1mmol/L above any value; 1.67 [1.302.15]; P<.0001).
Despite the high baseline CV risk among patients in the NAVIGATOR trial, the most common cause of death was non-CV. The high burden of non-CV death in this population has potential implications for future CV event-driven trials.
糖耐量受损患者心血管(CV)死亡风险升高;然而,与非CV死亡相关的原因和风险因素却知之甚少。
NAVIGATOR试验纳入了9306例糖耐量受损且患有CV疾病或CV风险较高的参与者,中位随访时间为6.4年。利用这一人群,我们确定了(1)归因于CV、非CV和不明原因的死亡比例,以及(2)与非CV死亡相关的风险因素。
在NAVIGATOR试验随访期间,622例患者死亡。研究者报告244例(39.2%)CV死亡、313例(50.3%)非CV死亡和65例(10.5%)不明原因死亡。心肌梗死是研究者报告死亡的主要原因(57/622 [9.2%])。在非CV死亡中,最常见的确定原因与恶性肿瘤有关(177/313 [56.5%])。使用经判定的死亡原因,Cox比例风险模型确定了3个增加非CV死亡风险的独立预后标志物:非黑色素瘤皮肤癌病史(风险比2.67 [95% CI 1.65 - 4.33];P <.0001)、白细胞计数(每升高1个单位>5000/mm;1.10 [1.02 - 1.18];P = 0.011)和血清钾水平(每高于任何值1mmol/L;1.67 [1.30 - 2.15];P <.0001)。
尽管NAVIGATOR试验中的患者基线CV风险较高,但最常见的死亡原因是非CV原因。该人群中非CV死亡的高负担对未来以CV事件为驱动的试验具有潜在影响。