首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: A randomized trial. Arterial Disease Multiple Intervention Trial.
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Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: A randomized trial. Arterial Disease Multiple Intervention Trial.

机译:烟酸对糖尿病和周围动脉疾病患者脂质和脂蛋白水平及血糖控制的影响:ADMIT研究:一项随机试验。动脉疾病多重干预试验。

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CONTEXT: Although niacin increases low levels of high-density lipoprotein cholesterol (HDL-C), which frequently accompany diabetes, current guidelines do not recommend use of niacin in patients with diabetes because of concerns about adverse effects on glycemic control; however, this is based on limited clinical data. OBJECTIVE: To determine the efficacy and safety of lipid-modifying dosages of niacin in patients with diabetes. DESIGN AND SETTING: Prospective, randomized placebo-controlled clinical trial conducted in 6 clinical centers from August 1993 to December 1995. PARTICIPANTS: A total of 468 participants, including 125 with diabetes, who had diagnosed peripheral arterial disease. INTERVENTIONS: After an active run-in period, participants were randomly assigned to receive niacin (crystalline nicotinic acid), 3000 mg/d or maximum tolerated dosage (n = 64 with diabetes; n = 173 without diabetes), or placebo (n = 61 with diabetes; n = 170 without diabetes) for up to 60 weeks (12-week active run-in and 48-week double-blind). MAIN OUTCOME MEASURES: Plasma lipoprotein, glucose, hemoglobin A(1c) (HbA(1c)), alanine aminotransferase, and uric acid levels; hypoglycemic drug use; compliance; and adverse events, in patients with diabetes vs without who were receiving niacin vs placebo. RESULTS: Niacin use significantly increased HDL-C by 29% and 29% and decreased triglycerides by 23% and 28% and low-density lipoprotein cholesterol (LDL-C) by 8% and 9%, respectively, in participants with and without diabetes (P<.001 for niacin vs placebo for all). Corresponding changes in participants receiving placebo were increases of 0% and 2% in HDL-C and increases of 7% and 0% in triglycerides, and increases of 1% and 1% in LDL-C. Glucose levels were modestly increased by niacin (8.7 and 6.3 mg/dL [0.4 and 0.3 mmol/L]; P =.04 and P<.001) in participants with and without diabetes, respectively. Levels of HbA(1c) were unchanged from baseline to follow-up in participants with diabetes treated with niacin. In participants with diabetes treated with placebo, HbA(1c) decreased by 0.3% (P =.04 for difference). There were no significant differences in niacin discontinuation, niacin dosage, or hypoglycemic therapy in participants with diabetes assigned to niacin vs placebo. CONCLUSIONS: Our study suggests that lipid-modifying dosages of niacin can be safely used in patients with diabetes and that niacin therapy may be considered as an alternative to statin drugs or fibrates for patients with diabetes in whom these agents are not tolerated or fail to sufficiently correct hypertriglyceridemia or low HDL-C levels. JAMA. 2000;284:1263-1270
机译:背景:尽管烟酸会增加糖尿病常伴有的低密度高密度脂蛋白胆固醇(HDL-C)水平,但由于担心对血糖控制有不良影响,目前的指南不建议在烟酒患者中使用烟酸。但是,这是基于有限的临床数据。目的:确定烟酸调脂剂量对糖尿病患者的疗效和安全性。设计与地点:从1993年8月至1995年12月在6个临床中心进行的前瞻性,随机安慰剂对照临床试验。参与者:共有468名参与者(包括125名患有糖尿病)被诊断为外周动脉疾病。干预:在积极的磨合期后,参与者被随机分配接受烟酸(结晶烟酸),3000 mg / d或最大耐受剂量(糖尿病患者为n = 64;糖尿病患者为n = 173)或安慰剂(n = 61例患有糖尿病; n = 170例无糖尿病),长达60周(12周主动磨合和48周双盲)。主要观察指标:血浆脂蛋白,葡萄糖,血红蛋白A(1c)(HbA(1c)),丙氨酸转氨酶和尿酸水平。降糖药物使用;遵守;和不良事件,糖尿病患者与未接受烟酸与安慰剂的患者之间。结果:在患有糖尿病和无糖尿病的参与者中,烟酸的使用分别使HDL-C显着增加29%和29%,并使甘油三酸酯减少23%和28%以及低密度脂蛋白胆固醇(LDL-C)分别减少8%和9% (烟酸与安慰剂的P均<0.001)。接受安慰剂的参与者的相应变化是,HDL-C分别增加0%和2%,甘油三酸酯增加7%和0%,LDL-C增加1%和1%。烟酸分别使患有和不患有糖尿病的参与者的烟酸水平分别升高(8.7和6.3 mg / dL [0.4和0.3 mmol / L]; P = .04和P <.001)。从基线到接受烟酸治疗的糖尿病患者的随访,HbA(1c)水平均保持不变。在接受安慰剂治疗的糖尿病患者中,HbA(1c)降低了0.3%(差异P = 0.04)。分配给烟酸与安慰剂的糖尿病参与者的烟酸停药,烟酸剂量或降糖治疗无显着差异。结论:我们的研究表明,糖尿病患者可以安全地使用改变烟酸的脂质剂量,对于那些不能耐受或不能充分耐受的糖尿病患者,烟酸治疗可以被认为是他汀类药物或贝特类药物的替代品纠正高甘油三酸酯血症或低HDL-C水平。贾玛2000; 284:1263-1270

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