首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Randomized placebo-controlled trial assessing a treatment strategy consisting of pravastatin, vitamin E, and homocysteine lowering on plasma asymmetric dimethylarginine concentration in mild to moderate CKD.
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Randomized placebo-controlled trial assessing a treatment strategy consisting of pravastatin, vitamin E, and homocysteine lowering on plasma asymmetric dimethylarginine concentration in mild to moderate CKD.

机译:随机安慰剂对照试验评估了由普伐他汀,维生素E和高半胱氨酸降低轻度至中度CKD患者血浆不对称二甲基精氨酸浓度组成的治疗策略。

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BACKGROUND: Chronic kidney disease (CKD) is associated with an increased incidence of cardiovascular disease (CVD). The Anti-oxidant Therapy In Chronic Renal Insufficiency (ATIC) Study showed that a multistep treatment strategy improved carotid intima-media thickness, endothelial function, and microalbuminuria in patients with stages 2 to 4 CKD. Increased plasma concentrations of asymmetric dimethylarginine (ADMA), an endogenous inhibitor of nitric oxide synthase, have been linked to greater CVD risk in patients with CKD. The aim of this study is to assess effects of the multistep intervention on plasma ADMA concentrations in the ATIC Study. STUDY DESIGN: Secondary analysis of a randomized double-blind placebo-controlled trial. SETTING & PARTICIPANTS: 93 patients with creatinine clearance of 15 to 70 mL/min/1.73 m(2) (according to the Cockcroft-Gault equation) from 7 outpatient clinics in Amsterdam, The Netherlands. INTERVENTION: The treatment group received sequential treatment consisting of pravastatin, 40 mg/d. After 6 months, vitamin E, 300 mg/d, was added, and after another 6 months, homocysteine-lowering therapy (folic acid, 5 mg/d; pyridoxine, 100 mg/d; and vitamin B(12), 1 mg/d, all in 1 tablet) were added and continued for another year. The control group received matching placebos. OUTCOME & MEASURES: Plasma ADMA levels. RESULTS: 36 participants (77%) in the treatment group and 38 (83%) in the placebo group completed the study. Mean ADMA and symmetric dimethylarginine concentrations in the total study population were 0.53 +/- 0.07 (SD) and 1.14 +/- 0.46 mumol/L, respectively. After 24 months, there was no overall effect of the treatment strategy on ADMA concentrations (beta = -0.006; P = 0.27). Analysis of separate treatment effects suggested that vitamin E significantly decreased ADMA levels by 4% in the treatment group compared with the placebo group (multiple adjusted P = 0.02). LIMITATIONS: The study was a secondary analysis, power calculation was based on the primary end point of carotid intima-media thickness, mean plasma ADMA levels were relatively low. CONCLUSION: Overall, a multistep treatment strategy consisting of pravastatin, vitamin E, and B vitamins had no effect on plasma ADMA levels in a stage 2 to 4 CKD population. This suggests that the beneficial effects of the intervention were not mediated by changes in ADMA levels. Possible ADMA-lowering effects of vitamin E deserve further attention.
机译:背景:慢性肾脏疾病(CKD)与心血管疾病(CVD)的发生率增加相关。慢性肾功能不全(ATIC)的抗氧化治疗研究表明,多步治疗策略可改善CKD 2至4期患者的颈动脉内膜中层厚度,内皮功能和微量白蛋白尿。血浆中不对称二甲基精氨酸(ADMA)(一氧化氮合酶的内源性抑制剂)的浓度升高与CKD患者的CVD风险增加有关。这项研究的目的是评估ATIC研究中多步干预对血浆ADMA浓度的影响。研究设计:一项随机双盲安慰剂对照试验的二级分析。地点和参与者:来自荷兰阿姆斯特丹7家门诊的93例肌酐清除率在15至70 mL / min / 1.73 m(2)(根据Cockcroft-Gault方程)的患者。干预:治疗组接受了普伐他汀40毫克/天的序贯治疗。 6个月后,添加300毫克/天的维生素E,另外6个月后,降低同型半胱氨酸的疗法(叶酸5毫克/天;吡ido醇100毫克/天;维生素B(12)1毫克/ d,全部合计1片),并持续一年。对照组接受匹配的安慰剂。结果与措施:血浆ADMA水平。结果:治疗组36名参与者(77%)和安慰剂组38名(83%)完成了研究。总研究人群中的平均ADMA和对称二甲基精氨酸浓度分别为0.53 +/- 0.07(SD)和1.14 +/- 0.46 mumol / L。 24个月后,治疗策略对ADMA浓度没有总体影响(β= -0.006; P = 0.27)。对单独治疗效果的分析表明,与安慰剂组相比,治疗组中的维生素E可使ADMA水平显着降低了4%(多次调整P = 0.02)。局限性:该研究是次要分析,功率计算基于颈动脉内膜中层厚度的主要终点,平均血浆ADMA水平相对较低。结论:总体而言,由普伐他汀,维生素E和B维生素组成的多步治疗策略对2-4岁CKD人群的血浆ADMA水平没有影响。这表明干预的有益作用不是由ADMA水平的变化介导的。维生素E可能降低ADMA的作用值得进一步关注。

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