Mazidi Mohsen, Katsiki Niki, Mikhailidis Dimitri P, Radenkovic Dina, Pella Daniel, Banach Maciej
Department of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital, Strand, London SE1 7EH, UK.
First Department of Internal Medicine, Center for Diabetes, Metabolism and Endocrinology, AHEPA University Hospital, 546 36 Thessaloniki, Greece.
J Clin Med. 2020 Jan 8;9(1):170. doi: 10.3390/jcm9010170.
There is a lack of evidence regarding the link between apolipoproteins and cancer mortality. By using two nationally representative samples of US adults, we prospectively evaluated the associations between apolipoprotein B (apoB) levels and apoB/apoA-I ratio with cancer mortality. We also examined the role of C-reactive protein (CRP) in these associations.
Adults aged ≥20 years, enrolled in the 3rd National Health and Nutrition Examination Survey (NHANES III, 1988-1994) and continuous NHANES (2005-2010), and followed up to 31 December 2011, were included in the analysis. Multiple Cox regressions were applied to evaluate the associations between the variables of interest and cancer mortality.
Overall, 7695 participants were included (mean age: 49.2 years; 50.4% men, median follow-up: 19.1 years). In the fully adjusted model, participants in the highest quartile (Q4) of apoB/apoA-I had a significantly greater risk for cancer mortality (hazard ratio (HR): 1.40; 95% confidence interval (CI): 1.25-1.93) compared with those in the first quartile (Q1) In the same model, a positive and significant association between apoB levels and cancer mortality was observed for individuals in Q3 (HR: 1.12; 95% CI: 1.09-1.16) and Q4 (HR: 1.17; 95% CI: 1.09-1.25) compared with those in Q1. When CRP levels were added in the analysis, the apoB/apoA-I ratio, but not apoB levels, remained significantly related to cancer mortality (Q4 = HR: 1.17; 95% CI: 1.09-1.25). In contrast, CRP levels were not able to predict cancer death after correction for apoB/apoA-I ratio.
In a large representative sample of the US adult population, the apoB/apoA-I ratio and apoB levels significantly predicted cancer mortality, independently of several cardiometabolic risk factors. The predictive value of apoB/apoA-I, but not apoB levels, remained significant after taking into account CRP, whereas CRP was not associated with cancer mortality after adjustment for apoB/apoA-I ratio. If further evidence supports our findings, apoA-I and apoB measurements could be considered in general healthcare policies.
关于载脂蛋白与癌症死亡率之间的联系,目前缺乏证据。通过使用两个具有全国代表性的美国成年人样本,我们前瞻性地评估了载脂蛋白B(apoB)水平和apoB/apoA-I比值与癌症死亡率之间的关联。我们还研究了C反应蛋白(CRP)在这些关联中的作用。
纳入参加第三次全国健康和营养检查调查(NHANES III,1988 - 1994年)以及连续的NHANES(2005 - 2010年)且年龄≥20岁,并随访至2011年12月31日的成年人进行分析。应用多重Cox回归来评估感兴趣的变量与癌症死亡率之间的关联。
总体而言,共纳入7695名参与者(平均年龄:49.2岁;男性占50.4%,中位随访时间:19.1年)。在完全调整模型中,与处于第一四分位数(Q1)的参与者相比,apoB/apoA-I处于最高四分位数(Q4)的参与者癌症死亡风险显著更高(风险比(HR):1.40;95%置信区间(CI):1.25 - 1.93)。在同一模型中,与Q1的个体相比,Q3(HR:1.12;95% CI:1.09 - 1.16)和Q4(HR:1.17;95% CI:1.09 - 1.25)的个体中观察到apoB水平与癌症死亡率呈正相关且具有统计学意义。当在分析中加入CRP水平时,apoB/apoA-I比值而非apoB水平仍与癌症死亡率显著相关(Q4 = HR:1.17;95% CI:1.09 - 1.25)。相比之下,在对apoB/apoA-I比值进行校正后,CRP水平无法预测癌症死亡。
在一个具有全国代表性的美国成年人群大样本中,apoB/apoA-I比值和apoB水平显著预测癌症死亡率,独立于多种心血管代谢危险因素。在考虑CRP后,apoB/apoA-I的预测价值仍然显著,而apoB水平则不然,而在对apoB/apoA-I比值进行调整后,CRP与癌症死亡率无关。如果进一步的证据支持我们的发现,那么在一般医疗保健政策中可以考虑检测apoA-I和apoB。