Lower plasma creatinine and urine albumin in individuals at increased risk of type 2 diabetes with factor v leiden mutation.

ISRN endocrinology Pub Date : 2014-03-04 eCollection Date: 2014-01-01 DOI:10.1155/2014/530830
Andreas Peter, Andreas Fritsche, Fausto Machicao, Peter P Nawroth, Hans-Ulrich Häring, Berend Isermann
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引用次数: 7

Abstract

The factor V Leiden (FVL) mutation is the most frequent genetic cause of venous thrombosis in Caucasians. However, protective effects have been suggested to balance the disadvantages. We have recently observed protective effects of FVL mutation on experimental diabetic nephropathy in mice as well as an association with reduced albuminuria in two human cohorts of diabetic patients. In the present study we aimed to reevaluate these findings in an independent, larger cohort of 1905 Caucasians at risk of developing type 2 diabetes and extend possible associations to earlier disease stages of nephropathy. Carriers of FVL mutation had a significantly lower urine albumin excretion (P = 0.03) and tended to have lower plasma creatinine concentrations (P = 0.07). The difference in plasma creatinine concentrations was significant after adjustment for the influencing factors: age, gender, and lean body mass (P = 0.048). These observations at a very early "disease" stage are an important extension of previous findings and suggest that modification of glomerular dysfunction by FVL mutation is relevant during very early stages of diabetic nephropathy. This makes the underlying mechanism an interesting therapeutic target and raises the question whether FVL mutation may also exert protective effects in other glomerulopathies.

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2型糖尿病伴因子v leen突变风险增高者血浆肌酐和尿白蛋白降低
因子V Leiden (FVL)突变是白种人静脉血栓形成最常见的遗传原因。然而,有人建议保护作用来平衡其缺点。我们最近观察到FVL突变对小鼠实验性糖尿病肾病的保护作用,以及与两组糖尿病患者蛋白尿减少的关联。在目前的研究中,我们的目的是在一个独立的、更大的队列中重新评估这些发现,该队列包括1905名有发生2型糖尿病风险的高加索人,并将可能的关联扩展到肾病的早期疾病阶段。FVL突变携带者尿白蛋白排泄量显著降低(P = 0.03),血浆肌酐浓度显著降低(P = 0.07)。在校正影响因素:年龄、性别和瘦体重后,血浆肌酐浓度的差异有统计学意义(P = 0.048)。这些在非常早期“疾病”阶段的观察结果是对先前研究结果的重要延伸,并表明FVL突变对肾小球功能障碍的改变与糖尿病肾病的早期阶段有关。这使得其潜在机制成为一个有趣的治疗靶点,并提出了FVL突变是否也可能在其他肾小球疾病中发挥保护作用的问题。
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