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凝血因子VII和纤维蛋白原水平作为静脉血栓形成的危险因素。一项关于血浆水平和DNA多态性的病例对照研究——莱顿血栓形成倾向研究(LETS)。

Factor VII and fibrinogen levels as risk factors for venous thrombosis. A case-control study of plasma levels and DNA polymorphisms--the Leiden Thrombophilia Study (LETS).

作者信息

Koster T, Rosendaal F R, Reitsma P H, van der Velden P A, Briët E, Vandenbroucke J P

机构信息

Department of Clinical Epidemiology, University Hospital Leiden, The Netherlands.

出版信息

Thromb Haemost. 1994 Jun;71(6):719-22.

PMID:7974338
Abstract

The plasma levels of coagulation factor VII and fibrinogen are well known risk factors for arterial thrombosis. We tested the hypothesis that this association also exists for venous thrombosis. Additionally, MspI and HaeIII polymorphisms in the factor VII and fibrinogen genes have recently been reported to be associated with the concentration of both proteins in the plasma. However, no conclusion could be drawn with respect to an increase or decrease in thrombosis risk. We undertook a population-based case-control study, in which 199 patients with a population-based case-control study, in which 199 patients with a first, objectively confirmed episode of deep vein thrombosis, aged less than 70, and without a known malignant disorder were compared to 199 age- and sex-matched healthy controls, to evaluate the clinical importance of these reported findings. For fibrinogen we found a positive level-related association between the plasma fibrinogen level and thrombotic risk. Subjects with a plasma fibrinogen greater than 5 g/l had an almost 4-fold increase of thrombosis risk. The frequencies of the different HaeIII genotypes were out of balance only for the thrombosis patients, with a deficit of the H1H2 genotype. Possession of an H1H2 genotype was associated with a 40% reduction in thrombosis risk. For factor VII, neither the plasma level nor the MspI genotypes were related to deep vein thrombosis, although possession of a M2 allele was clearly associated with significantly lower factor VII levels. The frequencies of the MspI-genotypes were the same for patients and control subjects and exhibited Hardy-Weinberg equilibrium. (ABSTRACT TRUNCATED AT 250 WORDS)

摘要

凝血因子VII和纤维蛋白原的血浆水平是动脉血栓形成的众所周知的危险因素。我们检验了这种关联在静脉血栓形成中也存在的假设。此外,最近有报道称,因子VII和纤维蛋白原基因中的MspI和HaeIII多态性与血浆中这两种蛋白质的浓度相关。然而,关于血栓形成风险的增加或降低,尚未得出结论。我们进行了一项基于人群的病例对照研究,将199例年龄小于70岁、首次客观确诊为深静脉血栓形成且无已知恶性疾病的患者,与199例年龄和性别匹配的健康对照进行比较,以评估这些报道结果的临床重要性。对于纤维蛋白原,我们发现血浆纤维蛋白原水平与血栓形成风险之间存在正相关。血浆纤维蛋白原大于5 g/l的受试者血栓形成风险几乎增加了4倍。仅在血栓形成患者中,不同HaeIII基因型的频率失衡,H1H2基因型缺失。拥有H1H2基因型与血栓形成风险降低40%相关。对于因子VII,血浆水平和MspI基因型均与深静脉血栓形成无关,尽管拥有M2等位基因显然与因子VII水平显著降低相关。患者和对照受试者的MspI基因型频率相同,且呈现哈迪-温伯格平衡。(摘要截短于250字)

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