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DPP4 inhibitors and respiratory infection, a systematic review and meta-analysis of the CardioVascular Outcomes Trials conducted before the pandemic and implications for the management of diabetes during COVID-19
Guillaume Grenet; Samia Mekhaldi; Sabine MAINBOURG; Marine AUFFRET; Catherine Cornu; Jean-Luc Cracowski; Francois Gueyffier; Jean-Christophe Lega; Michel CUCHERAT.
Affiliation
  • Guillaume Grenet; Hospices Civils de Lyon
  • Samia Mekhaldi; Universite de Lyon, Universite Lyon 1, CNRS, Laboratoire de Biometrie et Biologie Evolutive UMR 5558, F-69622 Villeurbanne, France
  • Sabine MAINBOURG; Hospices Civils de Lyon, Hopital Lyon Sud, Service de Medecine Interne et Vasculaire, Lyon, France
  • Marine AUFFRET; Hospices Civils de Lyon, Pole Sante Publique, Service hospitalo-universitaire de pharmacotoxicologie, Lyon, France
  • Catherine Cornu; CIC1407 INSERM, Hospices Civils de Lyon, Lyon, France
  • Jean-Luc Cracowski; Univ. Grenoble Alpes, INSERM, HP2, and centre regional de pharmacovigilance de Grenoble, F-38000 Grenoble, France
  • Francois Gueyffier; Universite de Lyon, Universite Lyon 1, CNRS, Laboratoire de Biometrie et Biologie Evolutive UMR 5558, F-69622 Villeurbanne, France
  • Jean-Christophe Lega; Hospices Civils de Lyon, Hopital Lyon Sud, Service de Medecine Interne et Vasculaire, Lyon, France
  • Michel CUCHERAT; Universite de Lyon, Universite Lyon 1, CNRS, Laboratoire de Biometrie et Biologie Evolutive UMR 5558, F-69622 Villeurbanne, France
Preprint in English | medRxiv | ID: ppmedrxiv-20163386
ABSTRACT
BackgroundAssociation between DPP4 inhibitors and respiratory infection remains unclear. CardioVascular Outcomes Trials (CVOTs) conducted before the COVID-19 pandemic are available. We aimed to estimate the effect of DPP4 inhibitors on the risk of respiratory infections. MethodsWe updated a previous systematic review and meta-analysis, searching for CVOTs assessing a DPP4 inhibitor in patients with type 2 diabetes mellitus. We focused on placebo-controlled CVOTs. Our primary outcome was any respiratory infection. We added a sensitivity analysis integrating non-CVOTs and active-controlled CVOTs. FindingsWe included 47 714 patients in five placebo-controlled CVOTs. Median follow-up ranged from 1{middle dot}5 years to 3 years. 4 369 events of overall respiratory infection were reported (rate of 9{middle dot}2%). DPP4 inhibitors were not associated with a different risk compared to placebo (RR = 0{middle dot}99 [95% CI 0{middle dot}93; 1{middle dot}04]). The sensitivity analysis integrating the non-CVOTs studies and the active-controlled CVOT reached 11 349 events among 82 644 participants (rate of 13{middle dot}7%). DPP4 inhibitors were not associated with a different risk of overall respiratory infection (RR = 1{middle dot}00 [95% CI 0{middle dot}97; 1{middle dot}03]). InterpretationOur up-dated meta-analysis provides the most powerful and least biased estimation of the association of DPP4 inhibitors and the risk of overall (non COVID-19) respiratory infection. We did not find any effect of the DPP4 inhibitors on the risk of respiratory infection. Our results support the recently published practical recommendations for the management of diabetes in patients with COVID-19, suggesting that DPP4 inhibitors should not be discontinued regarding the COVID-19 pandemic. FundingNo source of funding Panel Research in contextO_ST_ABSEvidence before this studyC_ST_ABSFrom before the COVID19 pandemic, respiratory infections are considered potential adverse effects of DPP4 inhibitors. Randomized trials assessing DPP4 inhibitors in patients with type 2 diabetes (T2D), their meta-analyses and pharmacovigilance studies reported conflicting results. Since the last meta-analyses assessing the risk of infections with DPP4 inhibitors, powerful cardiovascular outcomes randomized trials (CVOTs) became available. Recent practical recommendations for the management of diabetes during COVID-19 suggested that DPP4 inhibitors could be continued. We updated our previous meta-analysis of CVOTs and focused to the overall risk of respiratory infection associated with DPP4 inhibitors. We searched for published and unpublished CVOTs in Medline, the Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov, up to January 27, 2020, using key word as "diabetes mellitus", "hypoglycemic agents", "glucose control", "randomized controlled trial", "cardiovascular diseases". Added value of this studyWe included CVOTs comparing a DPP4 inhibitor versus placebo, in people with T2D, and analysed the risk of respiratory infection with DPP4 inhibitors. We focused on placebo-controlled CVOTs to avoid the pitfalls of small study effect and heterogeneous comparators. We added a sensitivity analysis integrating non-CVOTs and non-placebo CVOTs to challenge our results and to increase the statistical power. Our meta-analysis provides the most powerful and least biased estimation of the association of DPP4 inhibitors and the risk of overall (non COVID-19) respiratory infection. Our analyses integrated 11 349 events of any respiratory infections through 82 644 patients from randomized trials. Our results did not find any association between DPP4 inhibitors use and risk of non-COVID respiratory infections. Implications of all the available evidenceThe current COVID-19 pandemic has raised some questions about pros and cons of certain cardiovascular drugs. Our results support the recent practical recommendations for the management of diabetes in patients with COVID-19, suggesting that DPP4 inhibitors should not be discontinued regarding the COVID-19 pandemic.
License
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Prognostic study / Rct / Review / Systematic review Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Experimental_studies / Prognostic study / Rct / Review / Systematic review Language: English Year: 2020 Document type: Preprint
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