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本文引用的文献

1
Regarding the article: Hepatic ischemia/reperfusion injury is diminished by atorvastatin in Wistar rats.关于这篇文章:阿托伐他汀可减轻Wistar大鼠的肝脏缺血/再灌注损伤。
Arch Med Res. 2014 Jul;45(5):439-40. doi: 10.1016/j.arcmed.2014.06.002. Epub 2014 Jun 14.
2
Effects of statins on serum n-3 to n-6 polyunsaturated fatty acid ratios in patients with coronary artery disease.他汀类药物对冠心病患者血清 n-3 至 n-6 多不饱和脂肪酸比值的影响。
J Cardiovasc Pharmacol Ther. 2013 Jul;18(4):320-6. doi: 10.1177/1074248412473202. Epub 2013 Jan 15.
3
Effects of serum n-3 to n-6 polyunsaturated fatty acids ratios on coronary atherosclerosis in statin-treated patients with coronary artery disease.血清 n-3 至 n-6 多不饱和脂肪酸比值对冠心病合并他汀类药物治疗患者冠状动脉粥样硬化的影响。
Am J Cardiol. 2013 Jan 1;111(1):6-11. doi: 10.1016/j.amjcard.2012.08.038. Epub 2012 Oct 2.
4
Effects of lipid-lowering therapy with strong statin on serum polyunsaturated fatty acid levels in patients with coronary artery disease.强效他汀类药物降脂治疗对冠心病患者血清多不饱和脂肪酸水平的影响。
Heart Vessels. 2013 Jan;28(1):34-8. doi: 10.1007/s00380-011-0213-6. Epub 2011 Dec 21.
5
Beneficial actions of statins in the reduction of atrial fibrillation and stabilization and regression of coronary plaques: but how and why?他汀类药物在减少心房颤动以及冠状动脉斑块的稳定和消退方面的有益作用:但具体方式和原因是什么呢?
Circ J. 2011;75(1):224-5; author reply 226. doi: 10.1253/circj.cj-10-0939. Epub 2010 Nov 7.
6
HDL cholesterol and residual risk of first cardiovascular events after treatment with potent statin therapy: an analysis from the JUPITER trial.强效他汀类药物治疗后首次心血管事件残余风险的高密度脂蛋白胆固醇:来自 JUPITER 试验的分析。
Lancet. 2010 Jul 31;376(9738):333-9. doi: 10.1016/S0140-6736(10)60713-1. Epub 2010 Jul 23.
7
Incremental effects of eicosapentaenoic acid on cardiovascular events in statin-treated patients with coronary artery disease.二十碳五烯酸对接受他汀类药物治疗的冠心病患者心血管事件的增量影响。
Circ J. 2009 Jul;73(7):1283-90. doi: 10.1253/circj.cj-08-1197. Epub 2009 May 8.
8
Effects of EPA on coronary artery disease in hypercholesterolemic patients with multiple risk factors: sub-analysis of primary prevention cases from the Japan EPA Lipid Intervention Study (JELIS).二十碳五烯酸对具有多种危险因素的高胆固醇血症患者冠心病的影响:日本二十碳五烯酸脂质干预研究(JELIS)中一级预防病例的亚组分析。
Atherosclerosis. 2008 Sep;200(1):135-40. doi: 10.1016/j.atherosclerosis.2008.06.003. Epub 2008 Jun 19.
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Proposed guidelines for hypertriglyceridemia in Japan with non-HDL cholesterol as the second target.以非高密度脂蛋白胆固醇为次要目标的日本高甘油三酯血症拟议指南。
J Atheroscler Thromb. 2008 Jun;15(3):116-21. doi: 10.5551/jat.e560.
10
Pitavastatin: efficacy and safety in intensive lipid lowering.匹伐他汀:强化降脂治疗中的疗效与安全性
Expert Opin Pharmacother. 2007 Oct;8(14):2315-27. doi: 10.1517/14656566.8.14.2315.

他汀类药物治疗会改变血脂异常患者血清中n-3与n-6多不饱和脂肪酸的比例。

Statin treatment alters serum n-3 to n-6 polyunsaturated fatty acids ratio in patients with dyslipidemia.

作者信息

Nozue Tsuyoshi, Michishita Ichiro

机构信息

Division of Cardiology, Department of Internal Medicine, Yokohama Sakae Kyosai Hospital, Federation of National Public Service Personnel Mutual Associations, 132 Katsura-cho, Sakae-ku, Yokohama, 247-8581, Japan.

出版信息

Lipids Health Dis. 2015 Jul 7;14:67. doi: 10.1186/s12944-015-0066-6.

DOI:10.1186/s12944-015-0066-6
PMID:26149129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4492075/
Abstract

BACKGROUND

The effects of statins on serum n-3 to n-6 polyunsaturated fatty acids (PUFAs) levels have not been fully evaluated. We examined the effects of two types of statins (rosuvastatin and pitavastatin) on serum PUFAs levels and their ratios in patients with dyslipidemia.

FINDINGS

A total of 46 patients who were not receiving lipid-lowering therapy were randomly assigned to receive either 2.5 mg/day of rosuvastatin or 2 mg/day of pitavastatin. Serum PUFAs levels were measured at baseline, at 4 weeks, and at 12 weeks. Rosuvastatin was used to treat 23 patients, and the remaining 23 patients were treated using pitavastatin. Serum docosahexaenoic acid (DHA) levels decreased significantly at 12 weeks in both groups (rosuvastatin: from 169.6 to 136.3 μg/mL, p = 0.006; pitavastatin: from 188.6 to 153.9 μg/mL, p = 0.03). However, serum levels of eicosapentaenoic acid (EPA) and arachidonic acid (AA) did not change. In addition, the EPA/AA ratio did not change, whereas the DHA/AA ratio decreased significantly at 12 weeks in both groups (rosuvastatin: from 0.99 to 0.80, p = 0.01; pitavastatin: from 1.14 to 0.91, p = 0.003). No adverse events were observed during the study period.

CONCLUSIONS

In this small, open-label, pilot study, rosuvastatin and pitavastatin decreased serum DHA levels and the DHA/AA ratio in patients with dyslipidemia.

摘要

背景

他汀类药物对血清n-3至n-6多不饱和脂肪酸(PUFA)水平的影响尚未得到充分评估。我们研究了两种他汀类药物(瑞舒伐他汀和匹伐他汀)对血脂异常患者血清PUFA水平及其比值的影响。

研究结果

共有46名未接受降脂治疗的患者被随机分配接受每日2.5毫克瑞舒伐他汀或每日2毫克匹伐他汀治疗。在基线、4周和12周时测量血清PUFA水平。23名患者使用瑞舒伐他汀治疗,其余23名患者使用匹伐他汀治疗。两组患者在12周时血清二十二碳六烯酸(DHA)水平均显著下降(瑞舒伐他汀组:从169.6微克/毫升降至136.3微克/毫升,p = 0.006;匹伐他汀组:从188.6微克/毫升降至153.9微克/毫升,p = 0.03)。然而,血清二十碳五烯酸(EPA)和花生四烯酸(AA)水平未发生变化。此外,EPA/AA比值未改变,而两组患者在12周时DHA/AA比值均显著下降(瑞舒伐他汀组:从0.99降至0.80,p = 0.01;匹伐他汀组:从1.14降至0.91,p = 0.003)。在研究期间未观察到不良事件。

结论

在这项小型、开放标签的试点研究中,瑞舒伐他汀和匹伐他汀降低了血脂异常患者的血清DHA水平和DHA/AA比值。