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首页> 外文期刊>Atherosclerosis >Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and cardiovascular risk and efficacy of atorvastatin among subjects with diabetes on dialysis: The 4D study
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Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and cardiovascular risk and efficacy of atorvastatin among subjects with diabetes on dialysis: The 4D study

机译:透析对象中驱动蛋白样蛋白6的Trp719Arg多态性与心血管疾病风险和阿托伐他汀疗效之间缺乏关联:4D研究

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Aims: We investigated whether KIF6 Trp719Arg genotypes affect cardiovascular outcomes and efficacy of statin therapy in patients with type 2 diabetes mellitus undergoing hemodialysis. Methods and results: We conducted a post hoc analysis of the 4D-study, a randomized trial including 1255 patients. Patients were randomly assigned to double-blind treatment with either 20. mg of atorvastatin (n= 619) or placebo (n= 636) once daily and followed for 4 years (median). DNA was available for 1232 patients and we assessed KIF6 Trp719Arg genotypes by PCR and subsequent restriction digest. Carriers of the Arg719 allele showed no increased prevalence of cardiovascular disease. The incidence of cardiac death, MI, and stroke did not differ across KIF6 genotypes, irrespective of whether the patients were treated with atorvastatin or not. Conclusion: In patients with type 2 diabetes mellitus on hemodialysis, KIF6 Trp719Arg genotypes were not associated with adverse cardiovascular outcomes during follow-up or with the efficacy of atorvastatin therapy.
机译:目的:我们调查了KIF6 Trp719Arg基因型是否影响接受血液透析的2型糖尿病患者的心血管结果和他汀类药物治疗的疗效。方法和结果:我们对4D研究进行了事后分析,该研究包括1255名患者,是一项随机试验。患者被随机分配接受每日一次20 mg阿托伐他汀(n = 619)或安慰剂(n = 636)的双盲治疗,并随访4年(中位)。 DNA可用于1232位患者,我们通过PCR和随后的限制性酶切消化评估了KIF6 Trp719Arg基因型。 Arg719等位基因携带者未显示心血管疾病的患病率增加。不论患者是否接受阿托伐他汀治疗,不同KIF6基因型的心源性死亡,心梗和中风发生率均无差异。结论:在接受血液透析的2型糖尿病患者中,KIF6 Trp719Arg基因型与随访期间不良的心血管预后或阿托伐他汀治疗的疗效无关。

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