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本文引用的文献

1
European Guidelines on cardiovascular disease prevention in clinical practice (version 2012). The Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts).《欧洲临床实践心血管疾病预防指南》(2012年版)。欧洲心脏病学会及其他学会心血管疾病预防临床实践联合工作组第五版(由九个学会的代表及特邀专家组成)。
Eur Heart J. 2012 Jul;33(13):1635-701. doi: 10.1093/eurheartj/ehs092. Epub 2012 May 3.
2
Effect of statins on total cholesterol concentrations and cardiovascular outcomes in patients with diabetes mellitus: a population-based cohort study.他汀类药物对糖尿病患者总胆固醇浓度和心血管结局的影响:基于人群的队列研究。
Eur J Clin Pharmacol. 2012 Aug;68(8):1201-8. doi: 10.1007/s00228-012-1234-5. Epub 2012 Feb 22.
3
Is the use of cholesterol-lowering drugs for the prevention of cardiovascular complications in type 2 diabetics evidence-based? A systematic review.使用降胆固醇药物预防2型糖尿病患者心血管并发症是否有循证依据?一项系统评价。
Rev Recent Clin Trials. 2012 May;7(2):150-7. doi: 10.2174/157488712800100279.
4
Statin use and risk of diabetes mellitus in postmenopausal women in the Women's Health Initiative.女性健康倡议中绝经后女性使用他汀类药物与患糖尿病风险的关系
Arch Intern Med. 2012 Jan 23;172(2):144-52. doi: 10.1001/archinternmed.2011.625. Epub 2012 Jan 9.
5
Risk of incident diabetes with intensive-dose compared with moderate-dose statin therapy: a meta-analysis.与中等剂量他汀类药物治疗相比,强化剂量他汀类药物治疗的新发糖尿病风险:一项荟萃分析。
JAMA. 2011 Jun 22;305(24):2556-64. doi: 10.1001/jama.2011.860.
6
Are statins diabetogenic?他汀类药物会导致糖尿病吗?
Curr Opin Cardiol. 2011 Jul;26(4):342-7. doi: 10.1097/HCO.0b013e3283470359.
7
Balancing the benefits of statins versus a new risk-diabetes.权衡他汀类药物的益处与新出现的糖尿病风险。
Lancet. 2010 Feb 27;375(9716):700-1. doi: 10.1016/S0140-6736(10)60234-6. Epub 2010 Feb 16.
8
Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials.他汀类药物与新发糖尿病风险:随机他汀类药物试验的协作荟萃分析。
Lancet. 2010 Feb 27;375(9716):735-42. doi: 10.1016/S0140-6736(09)61965-6. Epub 2010 Feb 16.
9
Rosuvastatin-associated adverse effects and drug-drug interactions in the clinical setting of dyslipidemia.瑞舒伐他汀在血脂异常临床治疗中的不良反应及药物相互作用。
Am J Cardiovasc Drugs. 2010;10(1):11-28. doi: 10.2165/13168600-000000000-00000.
10
Dose-response analyses using restricted cubic spline functions in public health research.在公共卫生研究中使用受限立方样条函数进行剂量-反应分析。
Stat Med. 2010 Apr 30;29(9):1037-57. doi: 10.1002/sim.3841. Epub 2010 Jan 19.

他汀类药物与初级保健人群中治疗后新发糖尿病的风险。

Statins and risk of treated incident diabetes in a primary care population.

机构信息

Department of Pharmacology, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.

出版信息

Br J Clin Pharmacol. 2013 Apr;75(4):1118-24. doi: 10.1111/j.1365-2125.2012.04403.x.

DOI:10.1111/j.1365-2125.2012.04403.x
PMID:22845189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3612730/
Abstract

AIMS

(i) To examine the incidence of new onset treated diabetes in patients treated with different types of statins and (ii) the relationship between the duration and dose of statins and the subsequent development of new onset treated diabetes.

METHODS

A retrospective cohort study was performed using the Irish Health Services Executive Primary Care Reimbursement Services national pharmacy claims database. Individuals who received any medicines were identified from January 2001 to January 2009 (n = 1 235 671). Patients newly treated with statins from 1 January 2002 to 31 December 2007 were identified (n = 239 628). Cases were identified as individuals newly treated with antidiabetic medication (n = 38 503). Adjusted hazards ratios (HR) with 95% confidence intervals (CI) were calculated to examine the association between statins (any vs. none) and time to new onset treated diabetes using Cox proportional hazard regression. The dose and duration response relationship between statins and new onset treated diabetes was examined using restricted spline functions to assess the linearity of the relationship.

RESULTS

Statin use was associated with an increased risk of new onset treated diabetes (HR = 1.18, 95% CI 1.15, 1.22). Increased risk of new onset treated diabetes was found with rosuvastatin (HR = 1.41, 95% CI 1.31, 1.52), atorvastatin (HR = 1.23, 95% CI 1.19, 1.27) and simvastatin (HR = 1.15, 95% CI 1.05, 1.25). There were statistically significant overall dose and duration effects for all statins, excepting fluvastatin, which only demonstrated a duration effect.

CONCLUSION

An increased risk of new onset treated diabetes was found in those treated with statins showing significant duration and dose effect. Further study is required to confirm this association.

摘要

目的

(i) 研究不同类型的他汀类药物治疗的患者中新发治疗糖尿病的发生率,(ii) 他汀类药物的治疗持续时间和剂量与新发治疗糖尿病之间的关系。

方法

采用爱尔兰卫生服务行政部门初级保健报销服务国家药房报销数据库进行回顾性队列研究。从 2001 年 1 月至 2009 年 1 月(n = 1235671)识别接受任何药物治疗的个体。从 2002 年 1 月 1 日至 2007 年 12 月 31 日识别新开始使用他汀类药物治疗的患者(n = 239628)。病例被确定为新开始使用抗糖尿病药物治疗的个体(n = 38503)。使用 Cox 比例风险回归计算调整后的危险比(HR)和 95%置信区间(CI),以研究他汀类药物(任何 vs. 无)与新发治疗糖尿病之间的关联。使用受限样条函数检查他汀类药物与新发治疗糖尿病之间的剂量和治疗持续时间关系,以评估关系的线性。

结果

他汀类药物的使用与新发治疗糖尿病的风险增加相关(HR = 1.18,95%CI 1.15,1.22)。发现与瑞舒伐他汀(HR = 1.41,95%CI 1.31,1.52)、阿托伐他汀(HR = 1.23,95%CI 1.19,1.27)和辛伐他汀(HR = 1.15,95%CI 1.05,1.25)相关的新发治疗糖尿病风险增加。除氟伐他汀外,所有他汀类药物均显示出统计学上显著的总体剂量和治疗持续时间效应,而氟伐他汀仅显示出治疗持续时间效应。

结论

在接受他汀类药物治疗的患者中发现新发治疗糖尿病的风险增加,且具有显著的治疗持续时间和剂量效应。需要进一步的研究来证实这种关联。