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The effect of DPP-4 inhibitors on asthma control: an administrative database study to evaluate a potential pathophysiological relationship

机译:DPP-4抑制剂对哮喘控制的作用:一项行政数据库研究,以评估潜在的病理生理关系

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Rationale: DPP-4 may regulate immunological pathways implicated in asthma. Assessing whether DPP-4 inhibitor (DPP-4i) use might affect asthma control is clinically important because DPP-4i use in type 2 diabetes mellitus management (T2DM) is increasing. This study evaluated associations between DPP-4i use and asthma control. Methods: This was a retrospective, observational, matched cohort study using administrative claims in the MarketScan? Commercial Claims and Encounters (Commercial) and Medicare Supplemental and Coordination of Benefits (Medicare Supplemental) databases. Adult asthma patients initiating an oral DPP-4i or a non-DPP-4i between November 1, 2006 and March 31, 2014 were included. Patients were followed for asthma-related outcomes for 12 months after initiation of the antidiabetes medication. Outcomes included risk-domain asthma control (RDAC), defined as no asthma hospitalizations, no lower respiratory tract infections, and no oral corticosteroid (OCS) prescriptions; overall asthma control (RDAC criteria plus limited short-acting beta agonist use); treatment stability (RDAC criteria plus no increase of ≥50% in inhaled corticosteroid dose or addition of other asthma therapy); and severe asthma exacerbation rates (asthma-related hospitalizations, emergency room visits, or acute treatments with OCS). Comparisons were made between two matched cohorts (DPP-4i vs. non-DPP-4i initiators) using multivariable logistic regression and generalized linear modeling. Covariates included baseline demographic and clinical characteristics related to asthma and T2DM. Results: The adjusted odds of achieving RDAC (odds ratio [OR]: 1.05; 95% CI: 0.964 to 1.147), overall asthma control (OR: 1.04; 95% CI: 0.956 to 1.135), and treatment stability (OR: 1.04; 95% CI: 0.949 to 1.115) did not differ between the DPP-4i and non-DPP-4i cohorts. A difference was not found between cohorts in severe asthma exacerbation rates during the 12 months following initiation of antidiabetes treatment (mean = 0.32 vs. 0.34 exacerbations per subject-year, respectively; p =0.064). Conclusion: Asthma control was similar between patients initiating DPP-4i and non-DPP-4i antidiabetes medications, suggesting no association between DPP-4i use and asthma control.
机译:理由:DPP-4可能调节与哮喘有关的免疫途径。在临床上评估DPP-4抑制剂(DPP-4i)的使用是否会影响哮喘的控制具有重要的临床意义,因为在2型糖尿病管理(T2DM)中DPP-4i的使用正在增加。这项研究评估了DPP-4i使用与哮喘控制之间的关联。方法:这是一项回顾性,观察性,匹配队列研究,使用MarketScan ?商业索赔和遭遇(商业)和Medicare补充与利益协调(Medicare补充)数据库中的行政索赔。纳入了2006年11月1日至2014年3月31日期间开始口服DPP-4i或非DPP-4i的成年哮喘患者。在开始抗糖尿病药物治疗后的12个月,随访患者的哮喘相关结局。结果包括风险域哮喘控制(RDAC),定义为无哮喘住院,无下呼吸道感染,无口服糖皮质激素(OCS)处方;总体哮喘控制(RDAC标准加上有限的短效β受体激动剂使用);治疗稳定性(RDAC标准,加上皮质类固醇吸入剂量的增加或其他哮喘治疗的增加不超过50%);和严重的哮喘急性发作率(与哮喘有关的住院,急诊就诊或使用OCS进行的急性治疗)。使用多变量logistic回归和广义线性建模对两个匹配的队列(DPP-4i与非DPP-4i发起者)进行了比较。协变量包括与哮喘和T2DM相关的基线人口统计学和临床​​特征。结果:获得RDAC的调整后几率(赔率[OR]:1.05; 95%CI:0.964至1.147),总体哮喘控制(OR:1.04; 95%CI:0.956至1.135)和治疗稳定性(OR:1.04) ; 95%CI:0.949至1.115)在DPP-4i和非DPP-4i组之间没有差异。在开始抗糖尿病治疗后的12个月中,严重哮喘加重率的队列之间未发现差异(分别为每受试者年0.32 vs.0.34加重; p = 0.064)。结论:开始使用DPP-4i和非DPP-4i抗糖尿病药物的患者的哮喘控制相似,这表明DPP-4i的使用与哮喘控制之间没有关联。

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