Increased coagulation factor VIII, IX, XI and XII activities in non-alcoholic fatty liver disease

被引:98
作者
Kotronen, Anna [1 ,2 ]
Joutsi-Korhonen, Lotta [3 ,4 ]
Sevastianova, Ksenia [2 ]
Bergholm, Robert [2 ]
Hakkarainen, Antti [5 ]
Pietilainen, Kirsi H. [6 ,7 ]
Lundbom, Nina [5 ]
Rissanen, Aila [3 ,7 ]
Lassila, Riitta [4 ]
Yki-Jarvinen, Hannele
机构
[1] Univ Helsinki, Dept Med, Div Diabet, HUCH, FIN-00029 Helsinki, Finland
[2] Minerva Med Res Inst, Helsinki, Finland
[3] Helsinki Univ Hosp, Coagulat Disorders Unit, HUSLAB Lab Serv, Dept Hematol, Helsinki, Finland
[4] Helsinki Univ Hosp, Coagulat Disorders Unit, HUSLAB Lab Serv, Dept Clin Chem, Helsinki, Finland
[5] Univ Helsinki, Helsinki Med Imaging Ctr, FIN-00029 Helsinki, Finland
[6] Univ Helsinki, Dept Publ Hlth, Finnish Twin Cohort Study, FIN-00029 Helsinki, Finland
[7] Univ Helsinki, Dept Psychiat, Obes Res Unit, FIN-00029 Helsinki, Finland
基金
芬兰科学院;
关键词
activated partial thromboplastin time; coagulation factor VIII; IX; XI; XII; fibrinogen; insulin resistance; metabolic syndrome; obesity; prothrombin time; proton magnetic resonance spectroscopy; von Willebrand factor; CARDIOVASCULAR RISK-FACTORS; CLOTTING FACTOR LEVELS; HEPATIC STEATOSIS; MYOCARDIAL-INFARCTION; METABOLIC SYNDROME; VENOUS THROMBOEMBOLISM; THROMBUS PROPAGATION; INSULIN-RESISTANCE; HEMOSTATIC FACTORS; TISSUE FACTOR;
D O I
10.1111/j.1478-3231.2010.02375.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aims Obesity and the metabolic syndrome are established risk factors of venous thromboembolism. As most coagulation factors are produced exclusively by the liver and non-alcoholic fatty liver disease (NAFLD) is tightly related to metabolic disorders, we aimed at studying the association of liver fat with various coagulation factor activities. Methods Plasma prothrombin (PT) and activated partial thromboplastin time, activities of vWF:RCo, FVII, FVIII, FIX, FXI, FXII, FXIII, fibrinogen and D-dimer concentrations were measured in 54 subjects with and 44 without NAFLD diagnosed by proton magnetic resonance spectroscopy. Subjects were recruited retrospectively for metabolic studies in our laboratory. The body composition and features of insulin resistance were measured in all subjects. Results FVIII (107 +/- 30 vs. 84 +/- 22%, P < 0.001), FIX (110 +/- 14 vs. 94 +/- 16%, P < 0.001), FXI (109 +/- 16 vs. 96 +/- 19%, P=0.001) and FXII (113 +/- 21 vs. 99 +/- 32%, P=0.002) activities were consistently elevated in subjects with as compared with those without NAFLD. Liver fat percentage was positively related to FVIII (r=0.28, P=0.005), FIX (r=0.36, P=0.0003), FXI (r=0.29, P=0.004) and FXII (r=0.30, P=0.003) activities, again independent of age, gender and body mass index (BMI). PT%, vWF:RCo activity and fibrinogen were higher in subjects with as compared with those without NAFLD, but this difference disappeared after adjusting for age, gender and BMI. Conclusion FVIII, FIX, FXI and FXII activities are increased in human NAFLD and correlate with the features of insulin resistance. The relationships between NAFLD and these coagulation factors are independent of age, gender and BMI, suggesting that the fatty liver can contribute to the risk of thrombosis.
引用
收藏
页码:176 / 183
页数:8
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