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吸入性皮质类固醇与糖尿病发病和进展的风险。

Inhaled corticosteroids and the risks of diabetes onset and progression.

机构信息

Lady Davis Research Institute, Jewish General Hospital, Montreal, Quebec, Canada.

出版信息

Am J Med. 2010 Nov;123(11):1001-6. doi: 10.1016/j.amjmed.2010.06.019. Epub 2010 Oct 1.

Abstract

BACKGROUND

Systemic corticosteroids are known to increase diabetes risk, but the effects of high-dose inhaled corticosteroids are unknown. We assessed whether the use and dose of inhaled corticosteroids increase the risk of diabetes onset and progression.

METHODS

We formed a new-user cohort of patients treated for respiratory disease during 1990-2005, identified using the Quebec health insurance databases and followed through 2007 or until diabetes onset. The subcohort treated with oral hypoglycemics was followed until diabetes progression. A nested case-control analysis was used to estimate the rate ratios of diabetes onset and progression associated with current inhaled corticosteroid use, adjusted for age, sex, respiratory disease severity, and co-morbidity.

RESULTS

The cohort included 388,584 patients, of whom 30,167 had diabetes onset during 5.5 years of follow-up (incidence rate 14.2/1000/year), and 2099 subsequently progressed from oral hypoglycemic treatment to insulin (incidence rate 19.8/1000/year). Current use of inhaled corticosteroids was associated with a 34% increase in the rate of diabetes (rate ratio [RR] 1.34; 95% confidence interval [CI], 1.29-1.39) and in the rate of diabetes progression (RR 1.34; 95% CI, 1.17-1.53). The risk increases were greatest with the highest inhaled corticosteroid doses, equivalent to fluticasone 1000 μg per day or more (RR 1.64; 95% CI, 1.52-1.76 and RR 1.54; 95% CI, 1.18-2.02; respectively).

CONCLUSIONS

In patients with respiratory disease, inhaled corticosteroid use is associated with modest increases in the risks of diabetes onset and diabetes progression. The risks are more pronounced at the higher doses currently prescribed in the treatment of chronic obstructive pulmonary disease.

摘要

背景

已知全身皮质类固醇会增加糖尿病风险,但高剂量吸入皮质类固醇的影响尚不清楚。我们评估了吸入皮质类固醇的使用和剂量是否会增加糖尿病发病和进展的风险。

方法

我们建立了一个新的使用者队列,队列中的患者在 1990-2005 年间因呼吸疾病接受治疗,通过魁北克省健康保险数据库识别,并随访至 2007 年或直至糖尿病发病。使用口服降糖药治疗的亚队列则随访至糖尿病进展。采用巢式病例对照分析来估计与当前吸入皮质类固醇使用相关的糖尿病发病和进展的率比,调整年龄、性别、呼吸疾病严重程度和合并症。

结果

该队列包括 388584 名患者,其中 30167 名患者在 5.5 年的随访中发生糖尿病(发病率为 14.2/1000/年),2099 名患者随后从口服降糖药物治疗进展为胰岛素治疗(发病率为 19.8/1000/年)。当前使用吸入皮质类固醇与糖尿病发病率增加 34%相关(发病率比 [RR] 1.34;95%置信区间 [CI],1.29-1.39)和糖尿病进展率增加相关(RR 1.34;95% CI,1.17-1.53)。使用最高剂量的吸入皮质类固醇时,风险增加最大,相当于氟替卡松每天 1000μg 或更高(RR 1.64;95% CI,1.52-1.76 和 RR 1.54;95% CI,1.18-2.02)。

结论

在患有呼吸疾病的患者中,吸入皮质类固醇的使用与糖尿病发病和糖尿病进展的风险适度增加相关。在目前用于治疗慢性阻塞性肺疾病的较高剂量下,风险更为明显。

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