Impact of atorvastatin and omega-3 ethyl esters 90 on plasma plant sterol concentrations and cholesterol synthesis in type 2 diabetes: A randomised placebo controlled factorial trial

阿托伐他汀 内科学 胆固醇 安慰剂 羊毛甾醇 他汀类 糖尿病 内分泌学 2型糖尿病 甾醇 医学 化学 病理 替代医学
作者
H. A. W. Neil,Uta Ceglarek,Joachim Thiery,Sanjoy K. Paul,Andrew Farmer,Rury R. Holman
出处
期刊:Atherosclerosis [Elsevier]
卷期号:213 (2): 512-517 被引量:24
标识
DOI:10.1016/j.atherosclerosis.2010.09.013
摘要

Objective To determine the effects of statin treatment and omega-3 polyunsaturated fatty acid supplementation on plasma plant sterol concentrations and cholesterol synthesis in patients with type 2 diabetes. Methods Plant sterol concentrations and lanosterol (a marker of cholesterol synthesis) were measured using a high sensitivity assay to assess the effect of double-blind daily treatment for 4 months with atorvastatin 20 mg or placebo and, in a 2 × 2 factorial design, omega-3 ethyl esters 90 2 g or placebo. Results 658 patients were included in a per protocol analysis. The 4 treatment groups had similar mean [SD] age (63.5 years [11.7]), HbA1c (6.9% [1.1]) and diabetes duration (median 4 years [inter-quartile range 2, 8]). Atorvastatin treatment alone reduced low density lipoprotein (LDL) cholesterol by 1.4 mmol/l (44%, p < 0.001), triglycerides by 0.3 mmol/l (20%, p < 0.0001) and lanosterol by 0.36 μmol/l (72%, p < 0.001). There was no significant placebo adjusted change in median [95% confidence intervals] total plant sterol concentrations (−0.77 μmol/l [inter-quartile range −2.13, 0.59]), although they were increased significantly with omega-3-acid EE90 treatment (3.23 μmol/l [1.28, 5.17]). There was a 27% smaller reduction in LDL cholesterol with atorvastatin treatment in low cholesterol synthesisers with high absorption, defined by changes at or above the median lanosterol and campesterol levels, respectively, compared with the obverse group (difference 0.42 mmol/l [0.21, 0.62]). Conclusion Treatment with atorvastatin in type 2 diabetes did not change median total plasma plant sterol concentrations, but LDL cholesterol was reduced most efficaciously in high cholesterol synthesisers with low intestinal cholesterol absorption. Clinical trial registration information Current controlled trials number ISRCTN: 76737502 (http://isrctn.org).
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