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首页> 外文期刊>Medical science monitor : >Do elevated plasma prothrombin levels correspond to genetic variation in the 3'-untranslated region of the prothrombin gene in type 2 diabetic patients? - preliminary report
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Do elevated plasma prothrombin levels correspond to genetic variation in the 3'-untranslated region of the prothrombin gene in type 2 diabetic patients? - preliminary report

机译:2型糖尿病患者血浆凝血酶原水平升高是否对应于凝血酶原基因3'-非翻译区的遗传变异? - 初步报告

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Background:Numerous coagulation abnormalities resulting in a state of acquired thrombophilia have been demonstrated in the patients suffering from diabetes mellitus. Diabetes itself, however, is known to constitute an additional independent risk factor in the development of vascular complications. Recently, occasional reports pointed to the possible correlation between the genetic polymorphism 20210G/A in 3'-untranslated region in prothrombin gene and the elevated prothrombin level in blood plasma, particularly in the cases of familial thrombophilia. Our aim was to verify the hypothesis whether the elevated plasma prothrombin levels in some patients might correspond to the genetic variation in the 3'-untranslated region of the prothrombin gene in patients with type 2 diabetes mellitus.Results: We revealed that the averaged plasma level of prothrombin fragment F1+2 in an overall group of 128 type 2 diabetic patients was not significantly different compared to controls (2.93&plusm;2.40 nmol/l vs. 2.21&plusm;1.83 nmol/l); in selected patients (16%), however, the level of F1+2 was vastly increased (7.70&plusm;1.83 nmol/l), although these patients showed no evident clinical symptoms of vascular disease. The frequency of the genetic polymorphism 20210G/A in 3'-untranslated region in prothrombin gene in the examined group of diabetic subjects (1.3%) was not significantly higher compared to the group of control individuals and did not correspond to the increased F1+2 plasma levels: all the diabetic patients with the markedly increased levels of F1+2, were wild type homozygotes 20210G/G.Conclusions: Overall, we conclude that the genetic polymorphism 20210G/A in 3'-untranslated region in prothrombin gene is not evidently associated with the increased plasma thrombin generation in the examined group of diabetic patients. Other, yet undefined, compounding factors might underlie the accelerated thrombogenesis occurring in some patients with diabetes mellitus.
机译:背景:在患有糖尿病的患者中已证实大量凝血异常导致获得性血栓形成状态。然而,已知糖尿病本身在血管并发症的发展中构成另外的独立危险因素。最近,偶有报道指出凝血酶原基因3'-非翻译区的遗传多态性20210G / A与血浆中凝血酶原水平升高之间可能存在相关性,特别是在家族性血友病患者中。我们的目的是验证以下假设:某些患者血浆中凝血酶原水平升高是否可能与2型糖尿病患者中凝血酶原基因3'非翻译区的遗传变异相对应。结果:我们揭示了平均血浆水平在总共128例2型糖尿病患者中,凝血酶原片段F1 + 2的含量与对照组相比无显着差异(2.93 + 2.40 nmol / l与2.21 + 1.83 nmol / l);在某些患者中(16%),尽管这些患者没有明显的血管疾病临床症状,但F1 + 2的水平却大大增加(7.70 +1.83 nmol / l)。在糖尿病受试者组(1.3%)中,凝血酶原基因3'-非翻译区的遗传多态性20210G / A的频率与对照组相比没有显着更高,并且与F1 +的增加不相符。 2血浆水平:所有F1 + 2水平明显升高的糖尿病患者均为野生型纯合子20210G / G。结论:总体而言,我们得出结论,凝血酶原基因3'-非翻译区的遗传多态性20210G / A不是显然与所检查的糖尿病患者组中血浆凝血酶产生增加有关。其他尚未确定的复合因素可能是某些糖尿病患者中加速血栓形成的基础。

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