期刊文献+

以特发型下肢深静脉血栓为模式疾病研究下肢深静脉血栓形成的价值 被引量:5

Using idiopathic lower extremity deep venous thrombosis as a model disease for research into lower extremity deep venous thrombosis
原文传递
导出
摘要 目的:探讨以特发型下肢深静脉血栓(IDVT)为模式疾病,研究下肢深静脉血栓(DVT)的发病机制及遗传因素的可行性。方法:随机选择IDVT患者(病例组)与健康体检者(对照组)各120例,比较两组人口学资料、血流动力学、血常规、血生化及凝血功能等指标。结果:两组年龄与性别组成差异无统计学意义(均P>0.05),与对照组比较,病例组的股、腘静脉流速降低,股、腘静脉内径增大(均P<0.05);红细胞计数及血红蛋白含量降低,白细胞及血小板计数升高(均P<0.05);白蛋白含量降低,谷草转氨酶与肌酐含量升高(均P<0.05);红细胞沉降率、凝血酶原时间、纤维蛋白原含量及活化部分凝血活酶时间升高,而凝血酶时间减少,差异均有统计学意义(均P<0.05)。结论:下肢IDVT混杂因素少,均衡性好,是进行下肢DVT临床及遗传学研究较好的模式疾病。 Objective: To investigate the feasibility of using idiopathic deep venous thrombosis (IDVT) of the lower extremity as a model disease for research into the pathogenesis and genetic factors of lower extremity deep venousthrombosis (DVT). Methods: IDVT patients and healthy subjects undergoing health maintenance examination were randomlyselected as case group and control group, with 120 cases in each group. The demographical data and parameters ofhemodynamics, blood routine, blood biochemistry and clotting function between the two groups were compared. Results: The difference in age and gender composition had no statistical significance between the two groups(both P〉O.O5). In case group compared with control group, the flow velocity in the femoral and popliteal vein was decreased, and the inner diameter of the femoral and popliteal vein was increased; the red blood cell countand hemoglobin content were decreased and the white blood cell and blood platelet count were increased; the albumin level was decreased and aspartate aminotransferase and creatinine level were increased; the erythrocyte sedimentation rate, prothrombin and fibrinogen level and activated partial thromboplastin time were increased and thrombin time was decreased, and all the differences had statistical significance (all P〈0.05).Conclusion: Because of few confounding factors and better equilibrium, lower extremity IDVT is an ideal model disease for clinical and genetic research of lower extremity DVT.
出处 《中国普通外科杂志》 CAS CSCD 北大核心 2014年第6期811-815,共5页 China Journal of General Surgery
基金 云南省科技厅应用基础研究资助项目(2010ZC123)
关键词 静脉血栓形成 病因学 下肢 血流动力学 Venous Thrombosis Lower Extremity Hemodynamics
  • 相关文献

参考文献18

  • 1张小明.血管疾病彩色图谱[M].北京:人民卫生出版社,2003:247. 被引量:3
  • 2Baglin T. What happens after venous thromboembolism?[J]. J Thromb Haemost, 2009, 7(Suppl 1):287-290. 被引量:1
  • 3肖春梅,钟毓东,陈琴,张乃平.下肢深静脉血栓形成的彩色多普勒超声诊断价值[J].西部医学,2010,22(10):1913-1914. 被引量:20
  • 4Labropoulos N, Gasparis AP, Pefanis D, et al. Secondary chronic venous disease progresses faster than primary[J]. J Vasc Surg, 2009, 49(3): 704-710. 被引量:1
  • 5汪忠镐著..汪忠镐血管外科学[M].杭州:浙江科学技术出版社,2010:1568.
  • 6Labropoulos N, Jen J, Jen H, et al. Recurrent deep vein thrombosis: long-term incidence and natural history[J]. Ann Surg, 2010, 251(4):749-753. 被引量:1
  • 7林威,陈群.纤维蛋白原基因多态性研究进展[J].心肺血管病杂志,2009,28(1):58-60. 被引量:11
  • 8Camilleri RS, Cohen H. No association between pulmonary embolism or deep vein thrombosis and the -455G/A β-fibrinogen gene polymorphism[J]. Blood Coagul Fibrinolysis, 2005, 16(3):193-198. 被引量:1
  • 9Fowkes FJ, Price JF, Fowkes FG. Incidence of diagnosed deep vein thrombosis in the general population: systematic review[J]. Eur J Vasc Endovasc Surg, 2003, 25(1):1-5. 被引量:1
  • 10Roumen-Klappe EM, Janssen MC, Van Rossum J, et a1. Inflammation in deep vein thrombosis and the development of post-thrombotic syndrome: a prospective study[J]. J Thromb Haemost, 2009, 7(4):582-587. 被引量:1

二级参考文献50

共引文献104

同被引文献56

  • 1李方超,靳会敏,佟倩.静脉血栓栓塞症患者蛋白C和蛋白S基因单核苷酸多态性分析[J].中国老年学杂志,2014,34(3):859-860. 被引量:3
  • 2何春水,周翔宇,袁丹,陈枫.炎症反应在下肢深静脉血栓形成中的作用[J].中华实验外科杂志,2007,24(2):150-152. 被引量:11
  • 3李玉林.病理学[M].第6版.北京:人民卫生出版社,2008:32-46. 被引量:1
  • 4Siegerink B,Rosendall FR,Aglara A. Genetic variation in fibrinogen:its relationship to fibrinogen levels and the risk of myocardial infarc-tion and ischemic stroke [ J ]. Thromb Haemost, 2009 ,7 (3): 385-390. 被引量:1
  • 5Toshiya M, Ashu S, Erneslo DM. The functional effects of the-455G/A polymorphism on the lL-6-induced expression of the ^-fi-brinogen gene may be due to linkage disequilibrium with other func-tionai polymorphisms[ J]. Immunol Invest,2009,38(3) :311-323. 被引量:1
  • 6Cordell HJ. Detecting gene-gene interactions that underlie human dis-eases [J]. Nat Rev Genet,2009,10(6) :392404. 被引量:1
  • 7Stephens JC, Schneider JA, Tanguay DA , et al. Haplotype variationand linkage disequilibrium in 313 human genes [ J ]. Science, 2001,293(5529):489^93. 被引量:1
  • 8Minelli C ,Thompson JH, Abrams KR,el al. How should we use infor-mation about HWE in the meta-analyses of genetic association stud-ies? [J].Int J Epidemiol, 2008 ,37(1) :136-146. 被引量:1
  • 9Rogers AR, Huff C. Linkage disequilibrium between loci with un-known phase[ J]. Genetics,2009 ,182(3) :839-844. 被引量:1
  • 10YanLiere JM,Rosenberg NA. Mathematical properties of the r2 meas-ure of linkage disequilibrium [ J ]. Theor Popul Biol, 2008 ,74 ( 1 ):130-137. 被引量:1

引证文献5

二级引证文献21

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部