Brophy Donald F, Martin Rika J, Gehr Todd Wb, Carr Marcus E
Department of Pharmacy Practice, Virginia Commonwealth University/Medical College of Virginia Campus (VCU/MCV), Richmond, VA, USA.
Thromb J. 2005 Mar 29;3(1):3. doi: 10.1186/1477-9560-3-3.
It is well described that diabetes mellitus is a hypercoagulable state. It is also known that patients with renal dysfunction have impaired platelet aggregation and function. It is not well described how renal dysfunction affects the hypercoagulability associated with diabetes. This post-hoc sub-group analysis compares platelet function, clot structure and thrombin generation time at baseline, and following enoxaparin exposure in three groups of subjects. METHODS: 30 total subjects were evaluated in the three groups: Group I: normal controls (n = 10), Group II: subjects with renal dysfunction but without diabetes (n = 13), and Group III: subjects with concomitant diabetes and renal dysfunction (n = 7). For each subject, platelet contractile force (PCF), clot elastic modulus (CEM) and thrombin generation time (TGT) were simultaneously measured in whole blood at baseline, and following increasing enoxaparin antifactor Xa activity exposure. The group means for each parameter were determined and compared using one-way analysis of variance, with post-hoc Tukey-Kramer test. RESULTS: At baseline, subjects in Group III (diabetics with concomitant renal dysfunction) display significantly enhanced platelet activity, as measured by PCF (p = 0.003) and CEM (p = 0.03), relative to the non-diabetic Groups I and II. Subjects in Group II (renal dysfunction without diabetes) had significantly prolonged TGT values relative to controls when the antifactor Xa activity concentration reached 0.5 (p = 0.007), 1.0 (p = 0.005) and 3.0 IU/mL (p < 0.0001), respectively. There were no differences between Group II and Group III with respect to TGT at these antifactor Xa activity concentrations. When the antifactor Xa activity concentration reached 3.0 IU/mL, Groups II and III formed significantly less rigid blood clots (CEM p = 0.003) and also trended toward reduced PCF (p = 0.06) relative to Group I. CONCLUSION: This hypothesis-generating sub-group analysis suggests that at baseline, patients with concomitant diabetes and renal dysfunction have significantly enhanced platelet activity (PCF), and form more rigid blood clots (CEM) compared to controls and subjects with renal dysfunction but no diabetes. This may suggest that the presence of renal dysfunction does not ameliorate the hypercoagulable state associated with diabetes. Secondly, it appears that subjects with renal dysfunction but without diabetes have an enhanced response to enoxaparin relative to controls.
糖尿病是一种高凝状态,这已被充分描述。肾功能不全患者的血小板聚集和功能受损也为人所知。但肾功能不全如何影响与糖尿病相关的高凝状态,目前尚无充分描述。这项事后亚组分析比较了三组受试者在基线时以及接受依诺肝素治疗后的血小板功能、血凝块结构和凝血酶生成时间。
共30名受试者被分为三组进行评估:第一组:正常对照组(n = 10);第二组:肾功能不全但无糖尿病的受试者(n = 13);第三组:合并糖尿病和肾功能不全的受试者(n = 7)。对每位受试者,在基线时以及依诺肝素抗Xa因子活性增加后,同时在全血中测量血小板收缩力(PCF)、血凝块弹性模量(CEM)和凝血酶生成时间(TGT)。使用单因素方差分析确定并比较每组各参数的均值,并进行事后Tukey-Kramer检验。
在基线时,与非糖尿病的第一组和第二组相比,第三组(合并糖尿病和肾功能不全的患者)的血小板活性显著增强,通过PCF(p = 0.003)和CEM(p = 0.03)测量。当抗Xa因子活性浓度分别达到0.5(p = 0.007)、1.0(p = 0.005)和3.0 IU/mL(p < 0.0001)时,第二组(肾功能不全但无糖尿病)的受试者相对于对照组的TGT值显著延长。在这些抗Xa因子活性浓度下,第二组和第三组在TGT方面没有差异。当抗Xa因子活性浓度达到3.0 IU/mL时,相对于第一组,第二组和第三组形成的血凝块硬度显著降低(CEM p = 0.003),PCF也有降低趋势(p = 0.06)。
这项产生假设的亚组分析表明,在基线时,合并糖尿病和肾功能不全的患者与对照组以及肾功能不全但无糖尿病的受试者相比,血小板活性显著增强(PCF),形成的血凝块更硬(CEM)。这可能表明肾功能不全并未改善与糖尿病相关的高凝状态。其次,肾功能不全但无糖尿病的受试者相对于对照组,对依诺肝素的反应增强。