Sarafidis Panteleimon A, Lasaridis Anastasios N, Nilsson Peter M, Mouslech Tzant F, Hitoglou-Makedou Areti D, Stafylas Panagiotis C, Kazakos Kiriakos A, Yovos John G, Tourkantonis Achilleas A
1st Department of Medicine, AHEPA University Hospital, Aristotle University, 54636 Thessaloniki, Greece.
Metabolism. 2005 Sep;54(9):1236-42. doi: 10.1016/j.metabol.2005.04.010.
Thiazolidinediones are antidiabetic agents that decrease insulin resistance. Emerging evidence indicates that they present beneficial effects for the vasculature beyond glycemic control. The aim of this open-label observational study was to determine the effect of the thiazolidinedione rosiglitazone on novel cardiovascular risk factors, namely, lipoprotein(a) [Lp(a)], C-reactive protein (CRP), homocysteine, and fibrinogen in patients with type 2 diabetes and hypertension. A total of 40 type 2 diabetic patients already on treatment with 15 mg of glibenclamide daily and with poorly controlled or newly diagnosed hypertension were included in the study. Twenty of them received 4 mg of rosiglitazone daily as added-on therapy, whereas the rest remained on the preexisting antidiabetic treatment for 26 weeks. At baseline and the end of the study, subjects gave blood tests for the determination of Lp(a), CRP, homocysteine, fibrinogen, serum lipids, apolipoprotein (apo) A-I, and apo B. At the end of the study, rosiglitazone treatment was associated with significant reductions in Lp(a) (10.5 [8.9-54.1] to 9.8 [8.0-42.0] mg/dL, P<.05) and CRP levels (0.33 [0.07-2.05] to 0.25 [0.05-1.84] mg/dL, P<.05) vs baseline. Homocysteine levels were not affected but plasma fibrinogen presented a significant increase (303.5+/-75.1 to 387.5+/-70.4 mg/dL, P<.01) with rosiglitazone. Although no significant changes were observed in the rosiglitazone group for triglycerides, total cholesterol, high-density lipoprotein cholesterol, and low-density lipoprotein (LDL) cholesterol, both apo A-I and apo B presented small significant reductions and the LDL-apo B ratio was significantly increased. None of the above parameters were changed in the control group. In conclusion, rosiglitazone treatment had a beneficial impact on Lp(a), CRP, and LDL particles' lipid content in type 2 diabetic hypertensive patients but not on homocysteine and fibrinogen. The overall effect of rosiglitazone on cardiovascular risk factors seems positive but must be further evaluated.
噻唑烷二酮类药物是降低胰岛素抵抗的抗糖尿病药物。新出现的证据表明,它们除了控制血糖外,还对脉管系统有有益作用。这项开放标签观察性研究的目的是确定噻唑烷二酮类药物罗格列酮对2型糖尿病合并高血压患者的新型心血管危险因素,即脂蛋白(a)[Lp(a)]、C反应蛋白(CRP)、同型半胱氨酸和纤维蛋白原的影响。共有40例已接受每日15毫克格列本脲治疗且血糖控制不佳或新诊断为高血压的2型糖尿病患者纳入该研究。其中20例患者每日加用4毫克罗格列酮治疗,其余患者继续原有的抗糖尿病治疗26周。在基线期和研究结束时,受试者接受血液检测以测定Lp(a)、CRP、同型半胱氨酸、纤维蛋白原、血脂、载脂蛋白(apo)A-I和apo B。研究结束时,与基线相比,罗格列酮治疗使Lp(a)水平显著降低(从10.5[8.9 - 54.1]降至9.8[8.0 - 42.0]毫克/分升,P<0.05),CRP水平也显著降低(从0.33[0.07 - 2.05]降至0.25[0.05 - 1.84]毫克/分升,P<0.05)。同型半胱氨酸水平未受影响,但罗格列酮使血浆纤维蛋白原显著升高(从303.5±75.1升至387.5±70.4毫克/分升,P<0.01)。虽然罗格列酮组的甘油三酯、总胆固醇、高密度脂蛋白胆固醇和低密度脂蛋白(LDL)胆固醇未见显著变化,但apo A-I和apo B均有小幅显著降低,且LDL-apo B比值显著升高。对照组上述参数均未改变。总之,罗格列酮治疗对2型糖尿病合并高血压患者的Lp(a)、CRP和LDL颗粒的脂质含量有有益影响,但对同型半胱氨酸和纤维蛋白原无影响。罗格列酮对心血管危险因素的总体影响似乎是积极的,但必须进一步评估。