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吸入性皮质类固醇治疗的哮喘或 COPD 患者新发糖尿病的风险。

Risk of new onset diabetes mellitus in patients with asthma or COPD taking inhaled corticosteroids.

机构信息

Firestone Institute of Respiratory Health, Michael G DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.

出版信息

Respir Med. 2012 Nov;106(11):1487-93. doi: 10.1016/j.rmed.2012.07.011. Epub 2012 Aug 15.

Abstract

BACKGROUND

A recent case-controlled study reported an increased risk of diabetes mellitus in patients treated with inhaled corticosteroids for asthma or COPD, versus age-matched controls.

OBJECTIVE

The purpose of the current study was to evaluate whether there was an increased risk of new onset diabetes mellitus or hyperglycaemia among patients with asthma or COPD treated with inhaled corticosteroids.

METHODS

A retrospective analysis evaluated all double-blind, placebo-controlled, trials in patients ≥4 years of age involving budesonide or budesonide/formoterol in asthma (26 trials; budesonide: n = 9067; placebo: n = 5926), and in COPD (8 trials; budesonide: n = 4616; non-ICS: n = 3643). A secondary dataset evaluated all double-blind, controlled trials in asthma involving the use of inhaled corticosteroids (60 trials; budesonide: n = 33,496; fluticasone: n = 2773).

RESULTS

In the primary asthma dataset, the occurrence of diabetes mellitus/hyperglycaemia adverse events (AEs) was 0.13% for budesonide and 0.13% for placebo (HR 0.98 [95% CI: 0.38-2.50], p = 0.96) and serious adverse events (SAEs) was 0% for budesonide and 0.05% for placebo. In the secondary dataset, the occurrence of diabetes/hyperglycaemia as AE and SAE was 0.19% and 0.03%, respectively. In the COPD dataset, the occurrence of diabetes mellitus/hyperglycaemia AEs was 1.3% for budesonide and 1.2% for non-ICS (HR 0.99 [95% CI: 0.67-1.46], p = 0.96) and SAEs was 0.1% for budesonide and 0.03% for non-ICS.

CONCLUSION AND CLINICAL RELEVANCE

Treatment with inhaled corticosteroids in patients with asthma or COPD was not associated with increased risk of new onset diabetes mellitus or hyperglycaemia.

摘要

背景

最近一项病例对照研究报告称,与年龄匹配的对照组相比,接受吸入皮质类固醇治疗哮喘或 COPD 的患者发生糖尿病的风险增加。

目的

本研究的目的是评估哮喘或 COPD 患者接受吸入皮质类固醇治疗是否会增加新发糖尿病或高血糖的风险。

方法

回顾性分析评估了所有年龄≥4 岁的患者的双盲、安慰剂对照试验,涉及布地奈德或布地奈德/福莫特罗治疗哮喘(26 项试验;布地奈德:n=9067;安慰剂:n=5926),以及 COPD(8 项试验;布地奈德:n=4616;非 ICS:n=3643)。二次数据集评估了所有涉及使用吸入皮质类固醇治疗哮喘的双盲对照试验(60 项试验;布地奈德:n=33496;氟替卡松:n=2773)。

结果

在主要哮喘数据集中,布地奈德组和安慰剂组糖尿病/高血糖不良事件(AE)的发生率分别为 0.13%和 0.13%(HR 0.98[95%CI:0.38-2.50],p=0.96),严重不良事件(SAE)的发生率分别为 0%和 0.05%。在二次数据集,AE 和 SAE 中糖尿病/高血糖的发生率分别为 0.19%和 0.03%。在 COPD 数据集中,布地奈德组和非 ICS 组糖尿病/高血糖 AE 的发生率分别为 1.3%和 1.2%(HR 0.99[95%CI:0.67-1.46],p=0.96),SAE 的发生率分别为 0.1%和 0.03%。

结论和临床相关性

在哮喘或 COPD 患者中使用吸入皮质类固醇治疗与新发糖尿病或高血糖风险增加无关。

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