• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在临床实践中,对于预处理水平超过正常上限三倍的患者,给予 HMG-CoA 还原酶抑制剂后 ALT 水平的变化。

Change in ALT levels after administration of HMG-CoA reductase inhibitors to subjects with pretreatment levels three times the upper normal limit in clinical practice.

机构信息

College of Pharmacy, Sookmyung Women's University, Seoul, Korea.

Department of Industrial and Management Engineering, Pohang University of Science and Technology, Seoul, Korea.

出版信息

Cardiovasc Ther. 2018 Jun;36(3):e12324. doi: 10.1111/1755-5922.12324. Epub 2018 Mar 6.

DOI:10.1111/1755-5922.12324
PMID:29464863
Abstract

AIM

Prescription of statins to patients with chronic liver disease whose alanine transaminase (ALT) is over three times the upper normal limit (UNL) is not recommended. In this study, we attempted to evaluate patients with baseline ALT levels > 3 ×  UNL who were prescribed statins without ethical problems, using electronic medical records.

METHODS

We enrolled subjects with ALT levels > 3 ×  UNL. The patients were divided into three groups consisting of those who had been taking agents affecting liver function (HEPA) and continued to do so after the statin prescription (HepCon), those who had not previously taken HEPA and began doing so after statin prescription (HepNew), and those who had never taken HEPA (HepNo). All ALT levels were determined within 3 months of statins administration, and changes were monitored.

RESULTS

From January 2009 to December 2012, 61 patients with baseline ALT levels > 3 ×  UNL were prescribed statins for the first time. During the 3-month ALT monitoring, levels of the HepCon, HepNew, and HepNo groups decreased by 45 ± 8%, 64 ± 10%, and 42 ± 8%, respectively; however, intergroup differences were not significant (P = .386). All the subjects who were administered statins showed improvement or maintained their ALT levels, except for two subjects, which showed deterioration. However, the ALT levels of the two subjects subsequently remained stable.

CONCLUSION

It is not clear whether it is safe to prescribe statins to patients with ALT > 3 times the UNL. Our study showed that prescription of statins in combination with HEPA did not cause deleterious effects, suggesting that ALT levels > 3 times the UNL do not have harmful effects.

摘要

目的

不建议将他汀类药物开给丙氨酸转氨酶(ALT)超过正常上限(UNL)三倍的慢性肝病患者。在这项研究中,我们试图使用电子病历评估无伦理问题的基线 ALT 水平>3×UNL 并接受他汀类药物治疗的患者。

方法

我们纳入了 ALT 水平>3×UNL 的患者。将患者分为三组:服用影响肝功能药物(HEPA)且在他汀类药物处方后继续服用(HepCon)、未服用过 HEPA 且在服用他汀类药物后开始服用(HepNew)和从未服用过 HEPA(HepNo)的患者。所有 ALT 水平均在他汀类药物给药后 3 个月内确定,并监测变化。

结果

2009 年 1 月至 2012 年 12 月,61 例基线 ALT 水平>3×UNL 的患者首次服用他汀类药物。在 3 个月的 ALT 监测期间,HepCon、HepNew 和 HepNo 组的 ALT 水平分别下降了 45±8%、64±10%和 42±8%;然而,组间差异无统计学意义(P=0.386)。除两名患者出现恶化外,所有接受他汀类药物治疗的患者的 ALT 水平均得到改善或保持稳定。然而,这两名患者的 ALT 水平随后保持稳定。

结论

将他汀类药物开给 ALT 超过 UNL3 倍的患者是否安全尚不清楚。我们的研究表明,在 ALT 水平>3 倍 UNL 时,联合使用他汀类药物和 HEPA 不会产生有害影响,这表明 ALT 水平>3 倍 UNL 不会产生有害影响。

相似文献

1
Change in ALT levels after administration of HMG-CoA reductase inhibitors to subjects with pretreatment levels three times the upper normal limit in clinical practice.在临床实践中,对于预处理水平超过正常上限三倍的患者,给予 HMG-CoA 还原酶抑制剂后 ALT 水平的变化。
Cardiovasc Ther. 2018 Jun;36(3):e12324. doi: 10.1111/1755-5922.12324. Epub 2018 Mar 6.
2
Statin-related aminotransferase elevation according to baseline aminotransferases level in real practice in Korea.韩国实际临床中他汀类药物相关转氨酶升高与基线转氨酶水平的关系
J Clin Pharm Ther. 2016 Jun;41(3):266-72. doi: 10.1111/jcpt.12377. Epub 2016 Mar 25.
3
Statin therapy and serum transaminases among a cohort of HCV-infected veterans.他汀类药物治疗与 HCV 感染退伍军人队列中的血清转氨酶。
Dig Dis Sci. 2010 Jan;55(1):190-5. doi: 10.1007/s10620-009-0959-1.
4
Effectiveness and hepatotoxicity of statins in men seropositive for hepatitis C virus.他汀类药物对丙型肝炎病毒血清学阳性男性的有效性及肝毒性
Pharmacotherapy. 2007 Jun;27(6):845-51. doi: 10.1592/phco.27.6.845.
5
Effects of statins on the liver: clinical analysis of patients with ischemic stroke.他汀类药物对肝脏的影响:缺血性脑卒中患者的临床分析。
Chin Med J (Engl). 2011 Mar;124(6):897-900.
6
Monitoring statin safety in primary care.在基层医疗中监测他汀类药物的安全性。
Pharmacoepidemiol Drug Saf. 2007 Jun;16(6):652-7. doi: 10.1002/pds.1361.
7
Hepatotoxicity of Statins as Determined by Serum Alanine Aminotransferase in a Pediatric Cohort With Dyslipidemia.他汀类药物肝毒性在伴有血脂异常的儿科队列中通过血清丙氨酸氨基转移酶来确定。
J Pediatr Gastroenterol Nutr. 2019 Feb;68(2):175-181. doi: 10.1097/MPG.0000000000002174.
8
Should high creatine kinase discourage the initiation or continuance of statins for the treatment of hypercholesterolemia?高肌酸激酶是否应阻止使用他汀类药物启动或继续治疗高胆固醇血症?
Metabolism. 2009 Feb;58(2):233-8. doi: 10.1016/j.metabol.2008.09.019.
9
Evaluation of short-term safety and efficacy of HMG-CoA reductase inhibitors in hypercholesterolemic patients with elevated serum alanine transaminase concentrations: PITCH study (PITavastatin versus atorvastatin to evaluate the effect on patients with hypercholesterolemia and mild to moderate hepatic damage).评价高胆固醇血症患者血清丙氨酸氨基转移酶浓度升高时使用 HMG-CoA 还原酶抑制剂的短期安全性和疗效:PITCH 研究(普伐他汀与阿托伐他汀评价对高胆固醇血症合并轻中度肝损伤患者的疗效)。
J Clin Lipidol. 2012 Jul-Aug;6(4):340-51. doi: 10.1016/j.jacl.2012.01.009. Epub 2012 Feb 4.
10
Reducing liver function tests for statin monitoring: an observational comparison of two clinical commissioning groups.减少用于他汀类药物监测的肝功能检查:两个临床委托组的观察性比较
Br J Gen Pract. 2017 Mar;67(656):e194-e200. doi: 10.3399/bjgp17X689365. Epub 2017 Jan 30.

引用本文的文献

1
Understanding and Utilizing Claim Data from the Korean National Health Insurance Service (NHIS) and Health Insurance Review & Assessment (HIRA) Database for Research.理解并利用韩国国民健康保险服务(NHIS)和健康保险审查与评估(HIRA)数据库中的理赔数据进行研究。
J Lipid Atheroscler. 2022 May;11(2):103-110. doi: 10.12997/jla.2022.11.2.103. Epub 2021 Nov 26.
2
Decision-Making in Artificial Intelligence: Is It Always Correct?人工智能中的决策:它总是正确的吗?
J Korean Med Sci. 2020 Jan 6;35(1):e1. doi: 10.3346/jkms.2020.35.e1.