Itraconazole alters the pharmacokinetics of atorvastatin to a greater extent than either cerivastatin or pravastatin

西伐他汀 最大值 普伐他汀 阿托伐他汀 药理学 药代动力学 伊曲康唑 化学 药物相互作用 CYP3A4型 医学 胆固醇 细胞色素P450 新陈代谢 生物化学 抗真菌 皮肤病科
作者
A. Mazzu
出处
期刊:Clinical Pharmacology & Therapeutics [Wiley]
卷期号:68 (4): 391-400 被引量:135
标识
DOI:10.1067/mcp.2000.110537
摘要

Background 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) are metabolized by distinct pathways that may alter the extent of drug-drug interactions. Cerivastatin is metabolized by cytochrome P450 (CYP)3A4 and CYP2C8. Atorvastatin is metabolized solely by CYP3A4, and pravastatin metabolism is not well defined. Coadministration of higher doses of these statins with CYP3A4 inhibitors has the potential for eliciting adverse drug-drug interactions. Objective To determine the comparative effect of itraconazole, a potent CYP3A4 inhibitor, on the pharmacokinetics of cerivastatin, atorvastatin, and pravastatin. Methods In this single-site, randomized, three-way crossover, open-labeled study, healthy subjects (n = 18) received single doses of cerivastatin 0.8 mg, atorvastatin 20 mg, or pravastatin 40 mg without and with itraconazole 200 mg. Pharmacokinetic parameters [AUC(0-∞), AUC(0-tn), peak concentration (Cmax), time to reach Cmax (tmax), and half-life (t½)] were determined for parent statins and major metabolites. Results Concomitant cerivastatin/itraconazole treatment produced small elevations in the cerivastatin AUC(0-∞), Cmax, and t½ (27%, 25%, and 19%, respectively; P < .05 versus cerivastatin alone). Itraconazole coadministration produced similar changes in pravastatin pharmacokinetics [AUC elevated 51% (P < .05 versus pravastatin alone), 24% (Cmax), and 23% (t½), respectively]. However, itraconazole dramatically increased atorvastatin AUC (150%), Cmax (38%), and t½ (30%) (P < .05). The elevation in atorvastatin AUC was significantly greater than that of cerivastatin (P < .005) or pravastatin (P < .005). Conclusion Itraconazole markedly elevated atorvastatin plasma levels (2.5-fold) after 20 mg dosing, suggesting that concomitant itraconazole/atorvastatin therapy be carefully considered. Itraconazole produced modest elevations in the plasma levels of cerivastatin 0.8 mg or pravastatin 40 mg (1.3-fold and 1.5-fold, respectively), indicating that combination treatment with itraconazole with cerivastatin or pravastatin may be preferable. (Clin Pharmacol Ther 2000;68:391-400.) Clinical Pharmacology & Therapeutics (2000) 68, 391–400; doi: 10.1067/mcp.2000.110537

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
1秒前
1秒前
zz6532应助zxh_采纳,获得10
1秒前
asdfghjkl完成签到,获得积分10
1秒前
lizishu应助油菜的星星采纳,获得10
1秒前
celina完成签到,获得积分10
2秒前
Rue完成签到,获得积分10
2秒前
3秒前
4秒前
4秒前
Jiachenchen发布了新的文献求助10
4秒前
乐乐应助活力易蓉采纳,获得10
4秒前
完美世界应助Wcy采纳,获得10
4秒前
柚子发布了新的文献求助10
5秒前
九思发布了新的文献求助10
5秒前
九城发布了新的文献求助10
5秒前
6秒前
欢呼妙菱发布了新的文献求助10
6秒前
英俊的铭应助chenwen采纳,获得150
6秒前
龙龙龙发布了新的文献求助10
7秒前
瑾瑜玉发布了新的文献求助10
7秒前
受伤冰菱完成签到,获得积分10
7秒前
7秒前
8秒前
瘾9发布了新的文献求助10
8秒前
9秒前
建国发布了新的文献求助10
10秒前
10秒前
11秒前
11秒前
aka发布了新的文献求助10
12秒前
思源应助SCUTXieYijia采纳,获得10
12秒前
bcsunny2022发布了新的文献求助10
13秒前
梁其杰完成签到,获得积分10
13秒前
星辰大海应助Wcy采纳,获得10
13秒前
科研通AI2S应助好天气采纳,获得10
14秒前
lucky小蘑菇完成签到,获得积分10
15秒前
内向蜜蜂发布了新的文献求助10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Organic Reactions, Volume 116 1500
VALIDATION OF THE TAYLOR, ALAMEL AND VPSC MODELS FOR PLASTIC ANISOTROPY MODELING OF SHEET METALS 1000
Geist der Kunst und Kultur 1000
Middleton's Allergy Principles and Practice 10th Edition(Middleton's Allergy 2-Volume Set, 10th Edition) 1000
Resistance Spot Welding Dataset for Automobile Body-in-White Quality Analysis 748
日本現代怪異事典 副読本 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7403660
求助须知:如何正确求助?哪些是违规求助? 9008343
关于积分的说明 19181654
捐赠科研通 7037248
什么是DOI,文献DOI怎么找? 3231634
关于科研通互助平台的介绍 2393892
邀请新用户注册赠送积分活动 2213457