Morelli Vânia M, Lijfering Willem M, Bos Mettine H A, Rosendaal Frits R, Cannegieter Suzanne C
Department of Clinical Epidemiology, Leiden University Medical Center, PO Box 9600, 2300 RC, Leiden, The Netherlands.
Department of Clinical and Experimental Oncology, Federal University of São Paulo, São Paulo, Brazil.
Eur J Epidemiol. 2017 Aug;32(8):669-681. doi: 10.1007/s10654-017-0251-1. Epub 2017 May 24.
The relationship between lipid levels and risk of venous thrombosis is not well established. We aimed to assess the association between several lipids and risk of venous thrombosis using data from a population-based case-control study, and to evaluate the underlying mechanism, considering confounding by common risk factors and mediation via hemostatic factors and C-reactive protein. From the Multiple Environmental and Genetic Assessment of risk factors for venous thrombosis (MEGA) study, 2234 patients with a first venous thrombosis and 2873 controls were included. Percentile categories of total/low-density lipoprotein/high-density lipoprotein cholesterol, triglycerides, and apolipoproteins B and A1 were established in controls (<10th, 10th-25th, 25th-75th [reference], 75th-90th, >90th percentile). In age- and sex-adjusted models, decreasing levels of apolipoproteins B and A1 were dose-dependently associated with increased thrombosis risk, with odds ratios of 1.35 (95% confidence interval 1.12-1.62) and 1.50 (95% confidence interval 1.25-1.79) for the lowest category versus the reference category, respectively. The dose-response relation remained with further adjustment for body mass index, estrogen use, statin use, and diabetes. Although apolipoproteins B and A1 were associated with several hemostatic factors and C-reactive protein, none explained the increased risk in mediation analyses. The other lipids were not associated with venous thrombosis risk. In conclusion, decreasing levels of apolipoproteins B and A1 were associated with increased risk of venous thrombosis. Our findings are consistent with experimental data on the anticoagulant properties of apolipoproteins B and A1. These findings need to be confirmed and the underlying mechanism further investigated.
血脂水平与静脉血栓形成风险之间的关系尚未明确确立。我们旨在利用一项基于人群的病例对照研究数据评估几种血脂与静脉血栓形成风险之间的关联,并考虑常见风险因素的混杂作用以及通过止血因子和C反应蛋白的中介作用来评估潜在机制。从静脉血栓形成危险因素的多环境和基因评估(MEGA)研究中,纳入了2234例首次发生静脉血栓的患者和2873例对照。在对照中确定了总胆固醇/低密度脂蛋白/高密度脂蛋白胆固醇、甘油三酯以及载脂蛋白B和A1的百分位数类别(<第10百分位数、第10 - 25百分位数、第25 - 75百分位数[参考]、第75 - 90百分位数、>第90百分位数)。在年龄和性别调整模型中,载脂蛋白B和A1水平降低与血栓形成风险增加呈剂量依赖性相关,最低类别与参考类别相比的比值比分别为1.35(95%置信区间1.12 - 1.62)和1.50(95%置信区间1.25 - 1.79)。在进一步调整体重指数、雌激素使用、他汀类药物使用和糖尿病后,剂量反应关系仍然存在。尽管载脂蛋白B和A1与多种止血因子和C反应蛋白相关,但在中介分析中均未解释风险增加的原因。其他血脂与静脉血栓形成风险无关。总之,载脂蛋白B和A1水平降低与静脉血栓形成风险增加相关。我们的发现与关于载脂蛋白B和A1抗凝特性的实验数据一致。这些发现需要得到证实,其潜在机制有待进一步研究。