Treatment with a DPP-4 inhibitor at time of hospital admission for COVID-19 is not associated with improved clinical outcomes: data from the COVID-PREDICT cohort study in The Netherlands

Journal of Diabetes & Metabolic Disorders - Tập 20 - Trang 1155-1160 - 2021
Rick I. Meijer1, Trynke Hoekstra2, Niels C. Gritters van den Oever3, Suat Simsek4,5, Joop P. van den Bergh6, Renée A. Douma7, Auke C. Reidinga8, Hazra S. Moeniralam9, Tom Dormans10, Mark M. Smits5,11
1Department of Internal Medicine, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands
2Department of Health Sciences and Amsterdam Public Health Research Institute, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands
3Department of Intensive Care Medicine, Treant Zorggroep Emmen, Emmen, The Netherlands
4Department of Internal Medicine, Northwest Clinics, Alkmaar, The Netherlands
5Department of Internal Medicine, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands
6Department of Internal Medicine, Viecuri, Venlo, The Netherlands
7Department of Internal Medicine, Flevohospital, Almere, The Netherlands
8Department of Intensive Care Medicine, Martini Hospital, Groningen, The Netherlands
9Department of Internal Medicine, St. Antonius Hospital, Nieuwegein, The Netherlands
10Department of Intensive Care Medicine, Zuyderland Hospital, Heerlen, The Netherlands
11Diabetes Center, Department of Internal Medicine, Amsterdam University Medical Center, Location Vumc, Amsterdam, Netherlands

Tóm tắt

Inhibition of dipeptidyl peptidase (DPP-)4 could reduce coronavirus disease 2019 (COVID-19) severity by reducing inflammation and enhancing tissue repair beyond glucose lowering. We aimed to assess this in a prospective cohort study. We studied in 565 patients with type 2 diabetes in the CovidPredict Clinical Course Cohort whether use of a DPP-4 inhibitor prior to hospital admission due to COVID-19 was associated with improved clinical outcomes. Using crude analyses and propensity score matching (on age, sex and BMI), 28 patients using a DPP-4 inhibitor were identified and compared to non-users. No differences were found in the primary outcome mortality (matched-analysis = odds-ratio: 0,94 [95% confidence interval: 0,69 – 1,28], p-value: 0,689) or any of the secondary outcomes (ICU admission, invasive ventilation, thrombotic events or infectious complications). Additional analyses comparing users of DPP-4 inhibitors with subgroups of non-users (subgroup 1: users of metformin and sulphonylurea; subgroup 2: users of any insulin combination), allowing to correct for diabetes severity, did not yield different results. We conclude that outpatient use of a DPP-4 inhibitor does not affect the clinical outcomes of patients with type 2 diabetes who are hospitalized because of COVID-19 infection.

Tài liệu tham khảo

Bode B, Garrett V, Messler J, et al. Glycemic characteristics and clinical outcomes of COVID-19 patients hospitalized in the United States. J Diabetes Sci Technol. 2020;14(4):813–21. Apicella M, Campopiano MC, Mantuano M, et al. COVID-19 in people with diabetes: understanding the reasons for worse outcomes. Lancet Diabetes Endocrinol. 2020;8(9):782–92. Sathish T, Cao Y. What is the role of admission HbA1c in managing COVID-19 patients? J Diabetes. 2021;13(3):273–5. Sathish T, Mello GT, Cao Y. Is newly diagnosed diabetes a stronger risk factor than pre-existing diabetes for COVID -19 severity? J Diabetes. 2021;13(2):177–8. Eleftheriou P, Amanatidou D, Petrou A, Geronikaki A. In silico evaluation of the effectivity of approved protease Inhibitors against the main protease of the novel SARS-CoV-2 virus. Molecules. 2020;25(11):2529. Shinjo T, Nakatsu Y, Iwashita M, et al. DPP-IV inhibitor anagliptin exerts anti-inflammatory effects on macrophages, adipocytes, and mouse livers by suppressing NF-κB activation. Am J Physiol Endocrinol Metab. 2015;309(3):E214–23. Kawasaki T, Chen W, Htwe YM, Tatsumi K, Dudek SM. DPP4 inhibition by sitagliptin attenuates LPS-induced lung injury in mice. Am J Physiol Cell Mol Physiol. 2018;315(5):L834–45. Tang Y, liu J, zhang d, et al. cytokine storm in covid-19: the current evidence and treatment Strategies. Front Immunol. 2020;11:1708. Zhong J, Rajagopalan S. Dipeptidyl peptidase-4 regulation of SDF-1/CXCR4 axis: implications for cardiovascular disease. Front Immunol. 2015;6:477. Solerte SB, D’Addio F, Trevisan R, et al. Sitagliptin treatment at the time of hospitalization was associated with reduced mortality in patients with type 2 diabetes and covid-19: a multicenter case-control retrospective observational study. Diabetes Care. 2020;43(12):2999–3006. Prokop M, Van Everdingen W, Van Rees VT, et al. CO-RADS: A Categorical CT Assessment Scheme for Patients Suspected of Having COVID-19-Definition and Evaluation. Radiology. 2020;296(2):E97-104. teffects psmatch - propensity score matching. Stata Manuals v13. Rakhmat II, Kusmala YY, Handayani DR, et al. Dipeptidyl peptidase-4 (DPP-4) inhibitor and mortality in coronavirus disease 2019 (COVID-19) – a systematic review, meta-analysis, and meta-regression. Diabetes Metab Syndr Clin Res Rev. 2021;15(3):777–82. Hariyanto TI, Kurniawan A. Dipeptidyl peptidase 4 (DPP4) inhibitor and outcome from coronavirus disease 2019 (COVID-19) in diabetic patients: a systematic review, meta-analysis, and meta-regression. J Diabetes Metab Disord. 2021. Dalan R, Ang LW, Tan WYT, et al. The association of hypertension and diabetes pharmacotherapy with COVID-19 severity and immune signatures: an observational study. Eur Hear J Cardiovasc Pharmacother. 2021;7(3):e48-51.