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

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL
Pragmatic and Observational Research Pub Date : 2017-12-01 eCollection Date: 2017-01-01 DOI:10.2147/POR.S144018
Gene Colice, David Price, Maria Gerhardsson de Verdier, Karma Rabon-Stith, Christopher Ambrose, Katherine Cappell, Debra E Irwin, Paul Juneau, Anna Vlahiotis
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引用次数: 18

Abstract

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.

Abstract Image

Abstract Image

DPP-4抑制剂对哮喘控制的影响:一项评估潜在病理生理关系的行政数据库研究。
理由:DPP-4可能调节与哮喘有关的免疫通路。评估DPP-4抑制剂(DPP-4i)的使用是否会影响哮喘控制在临床上具有重要意义,因为DPP-4i在2型糖尿病管理(T2DM)中的使用正在增加。本研究评估了DPP-4i使用与哮喘控制之间的关系。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)以及医疗保险补充和福利协调(医疗保险补充)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,随访患者12个月的哮喘相关结果。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,无口服皮质类固醇(OCS)处方;整体哮喘控制(RDAC标准加上有限的短效受体激动剂使用);治疗稳定性(RDAC标准加上吸入皮质类固醇剂量未增加≥50%或添加其他哮喘治疗);严重哮喘加重率(哮喘相关住院、急诊室就诊或OCS急性治疗)。使用多变量逻辑回归和广义线性模型对两个匹配队列(DPP-4i与非DPP-4i启动者)进行比较。协变量包括与哮喘和2型糖尿病相关的基线人口统计学和临床特征。结果:经调整后达到RDAC的几率(优势比[OR]: 1.05;95% CI: 0.964 ~ 1.147),总体哮喘控制(OR: 1.04;95% CI: 0.956 ~ 1.135),治疗稳定性(OR: 1.04;95% CI: 0.949 ~ 1.115)在DPP-4i组和非DPP-4i组之间没有差异。在开始抗糖尿病治疗后的12个月内,各组间的严重哮喘加重率没有差异(平均= 0.32对0.34次加重/受试者年);p = 0.064)。结论:DPP-4i与非DPP-4i抗糖尿病药物患者哮喘控制相似,提示DPP-4i的使用与哮喘控制无关联。
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来源期刊
Pragmatic and Observational Research
Pragmatic and Observational Research MEDICINE, GENERAL & INTERNAL-
自引率
0.00%
发文量
11
期刊介绍: Pragmatic and Observational Research is an international, peer-reviewed, open-access journal that publishes data from studies designed to closely reflect medical interventions in real-world clinical practice, providing insights beyond classical randomized controlled trials (RCTs). While RCTs maximize internal validity for cause-and-effect relationships, they often represent only specific patient groups. This journal aims to complement such studies by providing data that better mirrors real-world patients and the usage of medicines, thus informing guidelines and enhancing the applicability of research findings across diverse patient populations encountered in everyday clinical practice.
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