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Influence of lipid metabolism disorders on venous thrombosis risk

机译:脂质代谢紊乱对静脉血栓形成风险的影响

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Background: To investigate the influence of lipid metabolism disorders on the risk of deep vein thrombosis. Methods: A total of 200 subjects participated in the study, 100 of whom experienced DVT with or without PTE, and 100 healthy subjects representing the control group. We classified patients and controls in terms of serum concentrations of chylomicrons, LDL, IDL, VLDL, and HDL particles, as those with or without hyperlipoproteinemia and in terms of serum Lp (a) lipoprotein levels, as those with hyperLp (a) lipoproteinemia (serum Lp (a) values &0.3 g/L) and those without hyperLp (a) lipoproteinemia (serum Lp (a) values &0.3 g/L). Based on the modified and supplemented Fredrickson classification, participants with verified existences of hyperlipoproteinemia were classified into subgroups based on the type of hyperlipoproteinemia. Unconditional logistic regression was used to calculate ORs with 95% CIS as a measure of the relative risks for venous thrombosis in participants with hyperlipoproteinemia compared with those without hyperlipoproteinemia. The analysis was adjusted for all potential confounders (age, sex, obesity) related to the functionality of the lipid metabolism, and at the same time, may have an impact on the risk of venous thrombosis. Results: The results of the comparison of the mean values of individual lipid status parameters between the patient group and the control group clearly indicate higher concentrations of total cholesterol (5.93 mmol/L vs. 5.52 mmol/L), total triglycerides (1.58 mmol/L vs. 1.50 mmol/L), and LDL-cholesterol (3.83 mmol/L vs. 3.44 mmol/L) in the patient group relative to the control group, with a statistically significant difference observed only in the case of LDL-cholesterol concentrations. We have found that type IIa hyperlipoproteinemia is associated with a nearly double increased risk for deep vein thrombosis (OR 1.99; Cl 1.01-3.90), while type IIb, IV, or hyperLp (a) lipoproteinemia did not influence the risk (OR 1.22; 95% Cl 0.79-1.84; OR 0.89; 95% Cl 0.52-1.54 OR 1.85; 95% CI 0.84-4.04). Conclusions: Hypercholesterolemia doubles the risk of deep vein thrombosis development.
机译:背景:探讨脂质代谢障碍对深静脉血栓形成风险的影响。方法:共有200名科目参加了这项研究,其中100名有人经历过或没有PTE的DVT,以及100个具有代表对照组的健康受试者。在血清浓度的乳清微粒,LDL,IDL,VLDL和HDL颗粒方面分类患者和对照,作为有或没有高脂蛋白血症的那些,并且在血清LP(A)脂蛋白水平方面,作为具有HyperLp(A)脂蛋白血症(血清LP(a)值& 0.3 g / l)和没有血清液(a)脂蛋白血症的那些(血清Lp(a)值& 0.3 g / l)。基于修改和补充的FredRickson分类,基于高脂蛋白血症的类型分类为核蛋白血症的核查存在的参与者。无条件的逻辑回归用于计算或在与没有高脂蛋白血症的那些相比,以95%CIS计算出95%CIS作为静脉血栓血症的静脉血栓形成的相对风险的衡量标准。对与脂质代谢功能相关的所有潜在混淆(年龄,性别,肥胖)进行调整分析,同时可能对静脉血栓形成的风险产生影响。结果:患者组和对照组各种脂质状态参数的平均值的比较结果清楚地表明了更高浓度的总胆固醇(5.93mmol / L与5.52mmol / L),总甘油三酯(1.58mmol / LDL-胆固醇(3.83mmol / L vs.3.44mmol / L)相对于对照组,只有在LDL-胆固醇浓度的情况下观察到统计学上显着的差异。我们发现IIA型高氧化蛋白血症与深静脉血栓形成的几乎增加了几乎双重增加的风险(或1.99; Cl 1.01-3.90),而IIB型,IV或HyperLP(A)脂蛋白血症的脂蛋白血症不影响风险(或1.22; 95%Cl 0.79-1.84;或0.89; 95%Cl 0.52-1.54或1.85; 95%CI 0.84-4.04)。结论:高胆固醇血症使静脉血栓形成发育的风险加倍。

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