Effect of thyroid hormone status and concomitant medication on statin induced adverse effects in hyperlipidemic patients.

E. Berta, M. Harangi, N. Zsíros, Endre V. Nagy, G. Paragh, M. Bodor
{"title":"Effect of thyroid hormone status and concomitant medication on statin induced adverse effects in hyperlipidemic patients.","authors":"E. Berta, M. Harangi, N. Zsíros, Endre V. Nagy, G. Paragh, M. Bodor","doi":"10.1691/PH.2014.3909R","DOIUrl":null,"url":null,"abstract":"Statins are effective treatment for the prevention of cardiovascular diseases and used extensively worldwide. However, adverse effects induced by statins are the major barrier of maximalizing cardiovascular risk reduction. Hypothyroidism and administration of drugs metabolized on the same cytochrome P450 (CYPP450) pathways where statin biotransformation occurs represent a significant risk factor for statin induced adverse effects including myopathy. Simvastatin, atorvastatin and lovastatin are metabolized by CYP3A4, fluvastatin by CYP2C9, while rosuvastatin by CYP2C9 and 2C19. We investigated the levels of the free thyroid hormones and CYP metabolism of concomitant medication in 101 hyperlipidemic patients (age 61.3 +/- 9.9 ys) with statin induced adverse effects including myopathy (56 cases; 55.4%), hepatopathy (39 cases; 38.6%) and gastrointestinal adverse effects (24 cases; 23.8%). Abnormal thyroid hormone levels were found in 5 patients (4.95%); clinical hypothyroidism in 2 and hyperthyroidism in 3 cases. 11 patients had a positive history for hypothyroidism (10.9%). Myopathy occured in one patient with hypothyroidism and two patients with hyperthyroidism. There were no significant differences in the TSH, fT4 and fT3 levels between patients with statin induced myopathy and patients with other types of adverse effects. 78 patients (77.2%) were administered drugs metabolized by CYP isoforms also used by statins (3A4: 66 cases (65.3%); 2C9: 67 cases (66.3%); 2C19: 54 cases (53.5%)). Patients with myopathy took significantly more drugs metabolized by CYP3A4 compared to patients with other types of adverse effects (p < 0.05). More myopathy cases were found in patients on simvastatin treatment (52% vs. 38%, ns.), while significantly less patients with myopathy were on fluvastatin treatment (13% vs. 33%, p < 0.05) compared to patients with other types of statin induced adverse effects. Both abnormal thyroid hormone status and administration of drugs metabolized by CYP3A4, 2C9 and 2C19 are common in our patients with statin induced adverse effects. Normalizing the thyroid hormone status and optimizing of the concomitant medication may reduce the risk of statin induced adverse effects.","PeriodicalId":86039,"journal":{"name":"Die Pharmazie. Beihefte","volume":"332 1","pages":"420-3"},"PeriodicalIF":0.0000,"publicationDate":"2014-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Die Pharmazie. Beihefte","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1691/PH.2014.3909R","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15

Abstract

Statins are effective treatment for the prevention of cardiovascular diseases and used extensively worldwide. However, adverse effects induced by statins are the major barrier of maximalizing cardiovascular risk reduction. Hypothyroidism and administration of drugs metabolized on the same cytochrome P450 (CYPP450) pathways where statin biotransformation occurs represent a significant risk factor for statin induced adverse effects including myopathy. Simvastatin, atorvastatin and lovastatin are metabolized by CYP3A4, fluvastatin by CYP2C9, while rosuvastatin by CYP2C9 and 2C19. We investigated the levels of the free thyroid hormones and CYP metabolism of concomitant medication in 101 hyperlipidemic patients (age 61.3 +/- 9.9 ys) with statin induced adverse effects including myopathy (56 cases; 55.4%), hepatopathy (39 cases; 38.6%) and gastrointestinal adverse effects (24 cases; 23.8%). Abnormal thyroid hormone levels were found in 5 patients (4.95%); clinical hypothyroidism in 2 and hyperthyroidism in 3 cases. 11 patients had a positive history for hypothyroidism (10.9%). Myopathy occured in one patient with hypothyroidism and two patients with hyperthyroidism. There were no significant differences in the TSH, fT4 and fT3 levels between patients with statin induced myopathy and patients with other types of adverse effects. 78 patients (77.2%) were administered drugs metabolized by CYP isoforms also used by statins (3A4: 66 cases (65.3%); 2C9: 67 cases (66.3%); 2C19: 54 cases (53.5%)). Patients with myopathy took significantly more drugs metabolized by CYP3A4 compared to patients with other types of adverse effects (p < 0.05). More myopathy cases were found in patients on simvastatin treatment (52% vs. 38%, ns.), while significantly less patients with myopathy were on fluvastatin treatment (13% vs. 33%, p < 0.05) compared to patients with other types of statin induced adverse effects. Both abnormal thyroid hormone status and administration of drugs metabolized by CYP3A4, 2C9 and 2C19 are common in our patients with statin induced adverse effects. Normalizing the thyroid hormone status and optimizing of the concomitant medication may reduce the risk of statin induced adverse effects.
甲状腺激素状态及联合用药对高脂血症患者他汀类药物不良反应的影响。
他汀类药物是预防心血管疾病的有效药物,在世界范围内得到广泛应用。然而,他汀类药物引起的不良反应是最大限度降低心血管风险的主要障碍。甲状腺功能减退和在他汀类药物生物转化发生的相同细胞色素P450 (CYPP450)途径上代谢的药物管理是他汀类药物诱导的不良反应(包括肌病)的重要危险因素。辛伐他汀、阿托伐他汀和洛伐他汀通过CYP3A4代谢,氟伐他汀通过CYP2C9代谢,瑞舒伐他汀通过CYP2C9和2C19代谢。我们研究了101例伴有他汀类药物不良反应的高脂血症患者(年龄61.3 +/- 9.9岁)的游离甲状腺激素水平和伴随用药的CYP代谢,包括肌病(56例;55.4%),肝病39例;38.6%)和胃肠道不良反应(24例;23.8%)。甲状腺激素异常5例(4.95%);临床甲状腺功能减退2例,甲状腺功能亢进3例。甲状腺功能减退病史阳性11例(10.9%)。1例甲状腺功能减退患者和2例甲状腺功能亢进患者发生肌病。他汀类药物引起的肌病患者与其他不良反应患者的TSH、fT4、fT3水平无显著差异。78例(77.2%)患者给予他汀类药物也使用CYP亚型代谢的药物(3A4: 66例(65.3%);2C9: 67例(66.3%);2C19: 54例(53.5%))。肌病患者CYP3A4代谢药物用量明显高于其他不良反应类型患者(p < 0.05)。与其他类型的他汀类药物引起的不良反应相比,接受辛伐他汀治疗的患者中肌病病例较多(52%对38%,ns.),而接受氟伐他汀治疗的肌病患者明显较少(13%对33%,p < 0.05)。甲状腺激素异常和服用CYP3A4、2C9和2C19代谢药物在他汀类药物不良反应患者中很常见。使甲状腺激素状态正常化并优化伴随用药可降低他汀类药物引起的不良反应的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信