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Long-Term Predictive Value of High-Sensitivity C-Reactive Protein for Cancer Mortality in Patients Undergoing Percutaneous Coronary Intervention

机译:高敏感性C反应蛋白对接受经皮冠状动脉介入治疗的患者的癌症死亡率的长期预测价值

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Background: High-sensitivity C-reactive protein (hs-CRP) is a well known risk factor for the development of cardiovascular disease and cancer. We investigated the long-term impact of hs-CRP on cancer mortality in patients with stable coronary artery disease (CAD). Methods?and?Results: This study was a retrospective analysis of 2,867 consecutive patients who underwent percutaneous coronary intervention for stable CAD from 2000 to 2016. The patients were divided into 2 groups according to median hs-CRP. We then evaluated the association between baseline hs-CRP and both all-cause and cancer deaths. Median hs-CRP was 0.10 mg/dL (IQR, 0.04–0.27 mg/dL). The median follow-up period was 5.8 years (IQR, 2.3–10.0 years). There were 416 deaths (14.5%), including 149 cardiovascular deaths (5.2%) and 115 (4.0%) cancer deaths. On Kaplan-Meier analysis the higher hs-CRP group had a significantly higher incidence of both all-cause and cancer death (log-rank, P0.001 and P=0.001, respectively). On multivariable analysis higher hs-CRP was significantly associated with higher risk of cancer death (HR, 1.74; 95% CI: 1.18–2.61, P=0.005). Conclusions: Elevated baseline hs-CRP was significantly associated with cancer mortality in patients with stable CAD. Hs-CRP measurement may be useful for the identification of subjects with an increased risk of cancer death.
机译:背景:高敏C反应蛋白(hs-CRP)是心血管疾病和癌症发展的众所周知的危险因素。我们研究了hs-CRP对稳定冠状动脉疾病(CAD)患者癌症死亡率的长期影响。方法和结果:本研究是回顾性分析2000年至2016年间2867例行经皮冠状动脉介入治疗以稳定CAD的患者。根据hs-CRP中位数将患者分为两组。然后,我们评估了基线hs-CRP与全因和癌症死亡之间的关联。 hs-CRP中位数为0.10 mg / dL(IQR,0.04-0.27 mg / dL)。中位随访期为5.8年(IQR,2.3-10.0年)。有416例死亡(14.5%),包括149例心血管死亡(5.2%)和115例(4.0%)癌症死亡。在Kaplan-Meier分析中,较高hs-CRP组的全因和癌症死亡发生率均显着较高(分别为log-rank,P <0.001和P = 0.001)。在多变量分析中,较高的hs-CRP与较高的癌症死亡风险显着相关(HR,1.74; 95%CI:1.12-2.61,P = 0.005)。结论:基线hs-CRP升高与稳定CAD患者的癌症死亡率显着相关。 Hs-CRP测量可能有助于识别罹患癌症死亡风险增加的受试者。

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