首页> 外文期刊>Journal of diabetes and its complications >Thrombin-activatable fibrinolysis inhibitor activity and global fibrinolytic capacity in Type 1 diabetes: evidence for normal fibrinolytic state.
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Thrombin-activatable fibrinolysis inhibitor activity and global fibrinolytic capacity in Type 1 diabetes: evidence for normal fibrinolytic state.

机译:1型糖尿病的凝血酶激活性纤溶抑制剂活性和整体纤溶能力:正常纤溶状态的证据。

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Hypofibrinolysis is a state that is commonly observed in type 2 diabetic patients, a finding also possibly related to obesity and insulin resistance. There is little information, however, regarding the status of fibrinolytic system in Type 1 diabetes, in particular as reflected by thrombin-activatable fibrinolysis inhibitor (TAFI) activity and global fibrinolytic capacity (GFC). To provide information in this respect, 30 Type 1 diabetic patients (median age=16) and 28 healthy controls (median age=14) were enrolled in this study. The median duration of diabetes was 7 years, and median HbA(1c) was 8.85% (range: 5.5-11.9%) in the diabetic group. None of the patients had macrovascular complications. Microvascular complications were present in a total of eight patients (nephropathy: n=5; retinopathy: n=3). A comparison of the TAFI activity between the patient (median 84.9, range: 71.5-103.3%) and the control groups (median=83.3, range: 63.7-97.4%) yielded no statistically significant difference (P=.950). Similarly, GFC was comparable between the two groups (median=8.22, range: 0.72-22.38 microg/ml, and median=13.32, range: 3.0-23.22 microg/ml, respectively, in the diabetic and control groups, P=.086). TAFI activity did not significantly correlate with age, albumin excretion, fasting plasma glucose, HbA(1c), D-dimer, and fibrinogen by Spearman rank correlation test. There was as a significant inverse correlation between GFC and TAFI activity (r=-.414, P=.006). Contrary to the previous observations in Type 2 diabetes, our data suggest that fibrinolytic activity is not adversely affected by Type 1 diabetes, and it has no relationship with the degree of metabolic control.
机译:低纤维蛋白溶解是在2型糖尿病患者中常见的一种状态,这一发现也可能与肥胖和胰岛素抵抗有关。然而,关于纤溶系统在1型糖尿病中的状态的信息很少,特别是通过凝血酶激活的纤溶抑制剂(TAFI)活性和整体纤溶能力(GFC)反映出来的信息。为了提供这方面的信息,该研究招募了30位1型糖尿病患者(中位年龄= 16)和28位健康对照(中位年龄= 14)。糖尿病组的中位病程为7年,HbA(1c)的中位值为8.85%(范围:5.5-11.9%)。所有患者均无大血管并发症。共有八名患者出现微血管并发症(肾病:n = 5;视网膜病:n = 3)。患者(中位数84.9,范围:71.5-103.3%)和对照组(中位数= 83.3,范围:63.7-97.4%)之间TAFI活性的比较没有统计学上的显着差异(P = .950)。同样,在糖尿病组和对照组中,两组之间的GFC相当(中位数= 8.22,范围:0.72-22.38 microg / ml,中位数= 13.23,范围:3.0-23.22 microg / ml,P = .086 )。通过Spearman秩相关检验,TAFI活性与年龄,白蛋白排泄,空腹血糖,HbA(1c),D-二聚体和纤维蛋白原没有显着相关。 GFC和TAFI活性之间存在显着的负相关关系(r =-。414,P = .006)。与先前在2型糖尿病中的观察结果相反,我们的数据表明纤溶活性不受1型糖尿病的不利影响,并且与代谢控制的程度无关。

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