Effect of linagliptin plus insulin in comparison to insulin alone on metabolic control and prognosis in hospitalized patients with SARS-CoV-2 infection

Rodolfo Guardado-Mendoza, Miguel Angel Garcia-Magaña, Liz Jovanna Martínez-Navarro, Hilda Elizabeth Macías-Cervantes, Rodolfo Aguilar-Guerrero, Erick L Suárez-Pérez, Alberto Aguilar-García, Rodolfo Guardado-Mendoza, Miguel Angel Garcia-Magaña, Liz Jovanna Martínez-Navarro, Hilda Elizabeth Macías-Cervantes, Rodolfo Aguilar-Guerrero, Erick L Suárez-Pérez, Alberto Aguilar-García

Abstract

To evaluate the effect of the combination of linagliptin and insulin on metabolic control and prognosis in hospitalized patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and hyperglycemia. A parallel double-blind randomized clinical trial including hospitalized patients with SARS-CoV-2 infection and hyperglycemia, randomized to receive 5 mg linagliptin + insulin (LI group) or insulin alone (I group) was performed. The main outcomes were the need for assisted mechanical ventilation and glucose levels during hospitalization. Subjects were screened for eligibility at hospital admission if they were not with assisted mechanical ventilation and presented hyperglycemia, and a total of 73 patients with SARS-CoV-2 infection and hyperglycemia were randomized to the LI group (n = 35) or I group (n = 38). The average hospital stay was 12 ± 1 vs 10 ± 1 days for the I and LI groups, respectively (p = 0.343). There were no baseline clinical differences between the study groups, but the percentage of males was higher in the LI group (26 vs 18, p = 0.030). The improvements in fasting and postprandial glucose levels were better in the LI group that the I group (122 ± 7 vs 149 ± 10, p = 0.033; and 137 ± 7 vs 173 ± 12, p = 0.017, respectively), and insulin requirements tended to be lower in the LI group than the I group. Three patients in the LI group and 12 in the I group required assisted mechanical ventilation (HR 0.258, CI 95% 0.092-0.719, p = 0.009); 2 patients in the LI group and 6 in the I group died after a follow-up of 30 days (p = 0.139). No major side effects were observed. The combination of linagliptin and insulin in hospitalized patients with SARS-CoV-2 infection and hyperglycemia reduced the relative risk of assisted mechanical ventilation by 74% and improved better pre and postprandial glucose levels with lower insulin requirements, and no higher risk of hypoglycemia.This study is registered at clinicaltrials.gov, number NCT04542213 on 09/03/2020.

Conflict of interest statement

The authors declare no competing interests.

© 2022. The Author(s).

Figures

Figure 1
Figure 1
Study profile.
Figure 2
Figure 2
Incidence of assisted mechanical ventilation (A), and Kaplan–Meier analysis for assisted mechanical ventilation-free between the study groups (B).
Figure 3
Figure 3
Pre- and postprandial glucose levels during the first 5 days of hospitalization between the study groups. *p LI group; †p < 0.05 vs day 1 in I group; ‡p < 0.05 for comparison between groups in the change from day 1.
Figure 4
Figure 4
Total (A), basal (B), and prandial (C) insulin requirements between the study groups. *p < 0.05 vs day 1 in LI group; †p < 0.05 vs day 1 in I group.

References

    1. Hamming I, et al. Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis. J. Pathol. 2004;203:631–637. doi: 10.1002/path.1570.
    1. Feng W, Zong W, Wang F, Ju S. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A review. Mol. Cancer. 2020;19:100. doi: 10.1186/s12943-020-01218-1.
    1. DeFronzo RA. Pathogenesis of type 2 diabetes mellitus. Med. Clin. N. Am. 2004;88:787–835. doi: 10.1016/j.mcna.2004.04.013.
    1. Allard R, Leclerc P, Tremblay C, Tannenbaum TN. Diabetes and the severity of pandemic influenza A (H1N1) infection. Diabetes Care. 2010;33:1491–1493. doi: 10.2337/dc09-2215.
    1. Cariou B, et al. Phenotypic characteristics and prognosis of inpatients with COVID-19 and diabetes: The CORONADO study. Diabetologia. 2020 doi: 10.1007/s00125-020-05180-x.
    1. Fadini GP, Morieri ML, Longato E, Avogaro A. Prevalence and impact of diabetes among people infected with SARS-CoV-2. J. Endocrinol. Investig. 2020;43:867–869. doi: 10.1007/s40618-020-01236-2.
    1. Grasselli G, et al. Baseline characteristics and outcomes of 1591 patients infected with SARS-CoV-2 admitted to ICUs of the lombardy region, Italy. JAMA. 2020 doi: 10.1001/jama.2020.5394.
    1. Guan WJ, et al. Comorbidity and its impact on 1590 patients with COVID-19 in China: A nationwide analysis. Eur. Respir. J. 2020 doi: 10.1183/13993003.00547-2020.
    1. Guan WJ, et al. Clinical characteristics of coronavirus disease 2019 in China. N. Engl. J. Med. 2020;382:1708–1720. doi: 10.1056/NEJMoa2002032.
    1. Guan WJ, Zhong NS. Clinical characteristics of Covid-19 in China. Reply. N. Engl. J. Med. 2020;382:1861–1862. doi: 10.1056/NEJMc2005203.
    1. Chen Y, et al. Clinical characteristics and outcomes of patients with diabetes and COVID-19 in association with glucose-lowering medication. Diabetes Care. 2020;43:1399–1407. doi: 10.2337/dc20-0660.
    1. Codo AC, et al. Elevated glucose levels favor SARS-CoV-2 infection and monocyte response through a HIF-1alpha/glycolysis-dependent axis. Cell Metab. 2020;32:498–499. doi: 10.1016/j.cmet.2020.07.015.
    1. Lim S, Bae JH, Kwon HS, Nauck MA. COVID-19 and diabetes mellitus: From pathophysiology to clinical management. Nat. Rev. Endocrinol. 2021;17:11–30. doi: 10.1038/s41574-020-00435-4.
    1. McAlister FA, et al. The relation between hyperglycemia and outcomes in 2,471 patients admitted to the hospital with community-acquired pneumonia. Diabetes Care. 2005;28:810–815. doi: 10.2337/diacare.28.4.810.
    1. Coppelli A, et al. Hyperglycemia at hospital admission is associated with severity of the prognosis in patients hospitalized for COVID-19: The Pisa COVID-19 study. Diabetes Care. 2020;43:2345–2348. doi: 10.2337/dc20-1380.
    1. Guardado-Mendoza R, et al. Linagliptin plus insulin for hyperglycemia immediately after renal transplantation: A comparative study. Diabetes Res. Clin. Pract. 2019;156:107864. doi: 10.1016/j.diabres.2019.107864.
    1. Broxmeyer HE, Capitano M, Campbell TB, Hangoc G, Cooper S. Modulation of hematopoietic chemokine effects in vitro and in vivo by DPP-4/CD26. Stem Cells Dev. 2016;25:575–585. doi: 10.1089/scd.2016.0026.
    1. Mulvihill EE, Drucker DJ. Pharmacology, physiology, and mechanisms of action of dipeptidyl peptidase-4 inhibitors. Endocr. Rev. 2014;35:992–1019. doi: 10.1210/er.2014-1035.
    1. Defronzo RA. Banting lecture. From the triumvirate to the ominous octet: A new paradigm for the treatment of type 2 diabetes mellitus. Diabetes. 2009;58:773–795. doi: 10.2337/db09-9028.
    1. Guardado-Mendoza R, et al. The combination of linagliptin, metformin and lifestyle modification to prevent type 2 diabetes (PRELLIM). A randomized clinical trial. Metabolism. 2020;104:154054. doi: 10.1016/j.metabol.2019.154054.
    1. McGuire DK, et al. Linagliptin effects on heart failure and related outcomes in individuals with type 2 diabetes mellitus at high cardiovascular and renal risk in CARMELINA. Circulation. 2019;139:351–361. doi: 10.1161/CIRCULATIONAHA.118.038352.
    1. Rosenstock J, et al. Effect of linagliptin vs placebo on major cardiovascular events in adults with type 2 diabetes and high cardiovascular and renal risk: The CARMELINA randomized clinical trial. JAMA. 2019;321:69–79. doi: 10.1001/jama.2018.18269.
    1. Meyerholz DK, Lambertz AM, McCray PB., Jr Dipeptidyl peptidase 4 distribution in the human respiratory tract: Implications for the middle east respiratory syndrome. Am. J. Pathol. 2016;186:78–86. doi: 10.1016/j.ajpath.2015.09.014.
    1. Ploquin MJ, et al. Systemic DPP4 activity is reduced during primary HIV-1 infection and is associated with intestinal RORC(+) CD4(+) cell levels: A surrogate marker candidate of HIV-induced intestinal damage. J. Int. AIDS Soc. 2018;21:e25144. doi: 10.1002/jia2.25144.
    1. Seys LJM, et al. DPP4, the middle east respiratory syndrome coronavirus receptor, is upregulated in lungs of smokers and chronic obstructive pulmonary disease patients. Clin. Infect. Dis. 2018;66:45–53. doi: 10.1093/cid/cix741.
    1. Craddy P, Palin HJ, Johnson KI. Comparative effectiveness of dipeptidylpeptidase-4 inhibitors in type 2 diabetes: A systematic review and mixed treatment comparison. Diabetes Ther. 2014 doi: 10.1007/s13300-014-0061-3.
    1. Deacon CF. Dipeptidyl peptidase-4 inhibitors in the treatment of type 2 diabetes: A comparative review. Diabetes Obes. Metab. 2011;13:7–18. doi: 10.1111/j.1463-1326.2010.01306.x.
    1. Del Prato S, et al. Efficacy and safety of linagliptin in subjects with type 2 diabetes mellitus and poor glycemic control: Pooled analysis of data from three placebo-controlled phase III trials. J. Diabetes Complic. 2013;27:274–279. doi: 10.1016/j.jdiacomp.2012.11.008.
    1. Gross JL, et al. A novel model-based meta-analysis to indirectly estimate the comparative efficacy of two medications: An example using DPP-4 inhibitors, sitagliptin and linagliptin, in treatment of type 2 diabetes mellitus. BMJ Open. 2013 doi: 10.1136/bmjopen-2012-001844.
    1. Karagiannis T, Paschos P, Paletas K, Matthews DR, Tsapas A. Dipeptidyl peptidase-4 inhibitors for treatment of type 2 diabetes mellitus in the clinical setting: Systematic review and meta-analysis. BMJ. 2012;344:e1369. doi: 10.1136/bmj.e1369.
    1. Raj VS, et al. Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature. 2013;495:251–254. doi: 10.1038/nature12005.
    1. Cockrell AS, et al. Mouse dipeptidyl peptidase 4 is not a functional receptor for Middle East respiratory syndrome coronavirus infection. J. Virol. 2014;88:5195–5199. doi: 10.1128/JVI.03764-13.
    1. Kleine-Weber H, et al. Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus. Emerg. Microbes Infect. 2020;9:155–168. doi: 10.1080/22221751.2020.1713705.
    1. Li K, et al. Middle east respiratory syndrome coronavirus causes multiple organ damage and lethal disease in mice transgenic for human dipeptidyl peptidase 4. J. Infect. Dis. 2016;213:712–722. doi: 10.1093/infdis/jiv499.
    1. Peck KM, et al. Glycosylation of mouse DPP4 plays a role in inhibiting Middle East respiratory syndrome coronavirus infection. J. Virol. 2015;89:4696–4699. doi: 10.1128/JVI.03445-14.
    1. Vankadari N, Wilce JA. Emerging WuHan (COVID-19) coronavirus: Glycan shield and structure prediction of spike glycoprotein and its interaction with human CD26. Emerg. Microbes Infect. 2020;9:601–604. doi: 10.1080/22221751.2020.1739565.
    1. Bassendine MF, Bridge SH, McCaughan GW, Gorrell MD. COVID-19 and comorbidities: A role for dipeptidyl peptidase 4 (DPP4) in disease severity? J. Diabetes. 2020 doi: 10.1111/1753-0407.13052.
    1. Kawasaki T, Chen W, Htwe YM, Tatsumi K, Dudek SM. DPP4 inhibition by sitagliptin attenuates LPS-induced lung injury in mice. Am. J. Physiol. Lung Cell Mol. Physiol. 2018;315:834–845. doi: 10.1152/ajplung.00031.2018.
    1. Soare A, et al. Dipeptidylpeptidase 4 as a marker of activated fibroblasts and a potential target for the treatment of fibrosis in systemic sclerosis. Arthritis Rheumatol. 2020;72:137–149. doi: 10.1002/art.41058.
    1. Beraldo JI, et al. Cardioprotection conferred by sitagliptin is associated with reduced cardiac angiotensin II/angiotensin-(1–7) balance in experimental chronic kidney disease. Int. J. Mol. Sci. 2019;20:1940. doi: 10.3390/ijms20081940.
    1. Kagal UA, Angadi NB, Matule SM. Effect of dipeptidyl peptidase 4 inhibitors on acute and subacute models of inflammation in male Wistar rats: An experimental study. Int. J. Appl. Basic Med. Res. 2017;7:26–31. doi: 10.4103/2229-516X.198516.
    1. Fadini GP, et al. Exposure to DPP-4 inhibitors and COVID-19 among people with type 2 diabetes. A case-control study. Diabetes Obes. Metab. 2020 doi: 10.1111/dom.14097.
    1. Solerte SB, 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 doi: 10.2337/dc20-1521.
    1. Mirani M, et al. Impact of comorbidities and glycemia at admission and dipeptidyl peptidase 4 inhibitors in patients with type 2 diabetes with COVID-19: A case series from an academic hospital in Lombardy, Italy. Diabetes Care. 2020 doi: 10.2337/dc20-1340.
    1. Horby P, et al. Dexamethasone in hospitalized patients with covid-19. N. Engl. J. Med. 2021;384:693–704. doi: 10.1056/NEJMoa2021436.
    1. Cao B, et al. A trial of lopinavir-ritonavir in adults hospitalized with severe covid-19. N. Engl. J. Med. 2020;382:1787–1799. doi: 10.1056/NEJMoa2001282.
    1. Shi Q, et al. Clinical characteristics and risk factors for mortality of COVID-19 patients with diabetes in Wuhan, China: A two-center, retrospective study. Diabetes Care. 2020;43:1382–1391. doi: 10.2337/dc20-0598.
    1. Apicella M, et al. COVID-19 in people with diabetes: Understanding the reasons for worse outcomes. Lancet Diabetes Endocrinol. 2020;8:782–792. doi: 10.1016/S2213-8587(20)30238-2.
    1. Drucker DJ. Coronavirus infections and type 2 diabetes-shared pathways with therapeutic implications. Endocr. Rev. 2020 doi: 10.1210/endrev/bnaa011.
    1. Heise T, et al. Pharmacokinetics, pharmacodynamics and tolerability of multiple oral doses of linagliptin, a dipeptidyl peptidase-4 inhibitor in male type 2 diabetes patients. Diabetes Obes. Metab. 2009;11:786–794. doi: 10.1111/j.1463-1326.2009.01046.x.
    1. Thomas L, et al. (R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylm ethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors. J. Pharmacol. Exp. Ther. 2008;325:175–182. doi: 10.1124/jpet.107.135723.
    1. Forst T, et al. Effects on alpha- and beta-cell function of sequentially adding empagliflozin and linagliptin to therapy in people with type 2 diabetes previously receiving metformin: An exploratory mechanistic study. Diabetes Obes. Metab. 2017;19:489–495. doi: 10.1111/dom.12838.
    1. Qu H, et al. The potential effects of clinical antidiabetic agents on SARS-CoV-2. J. Diabetes. 2021;13:243–252. doi: 10.1111/1753-0407.13135.
    1. Chu C, et al. Comparison of infection risks and clinical outcomes in patients with and without SARS-CoV-2 lung infection under renin-angiotensin-aldosterone system blockade: Systematic review and meta-analysis. Br. J. Clin. Pharmacol. 2021;87:2475–2492. doi: 10.1111/bcp.14660.
    1. Chen L, et al. Association of early-phase in-hospital glycemic fluctuation with mortality in adult patients with coronavirus disease 2019. Diabetes Care. 2021;44:865–873. doi: 10.2337/dc20-0780.
    1. Shen Y, et al. Thresholds of glycemia and the outcomes of COVID-19 complicated with diabetes: A retrospective exploratory study using continuous glucose monitoring. Diabetes Care. 2021;44:976–982. doi: 10.2337/dc20-1448.
    1. Sardu C, et al. Outcomes in patients with hyperglycemia affected by COVID-19: Can we do more on glycemic control? Diabetes Care. 2020;43:1408–1415. doi: 10.2337/dc20-0723.
    1. Yu B, Li C, Sun Y, Wang DW. Insulin treatment is associated with increased mortality in patients with COVID-19 and type 2 diabetes. Cell Metab. 2021;33:65–77. doi: 10.1016/j.cmet.2020.11.014.
    1. Varin EM, et al. Circulating levels of soluble dipeptidyl peptidase-4 are dissociated from inflammation and induced by enzymatic DPP4 inhibition. Cell Metab. 2019;29:320–334. doi: 10.1016/j.cmet.2018.10.001.
    1. Nauck MA, Meier JJ. Reduced COVID-19 mortality with sitagliptin treatment? Weighing the dissemination of potentially lifesaving findings against the assurance of high scientific standards. Diabetes Care. 2020;43:2906–2909. doi: 10.2337/dci20-0062.
    1. Rao PPN, et al. Drug repurposing: Dipeptidyl peptidase IV (DPP4) inhibitors as potential agents to treat SARS-CoV-2 (2019-nCoV) infection. Pharmaceuticals (Basel) 2021 doi: 10.3390/ph14010044.
    1. Arab HH, Eid AH, Mahmoud AM, Senousy MA. Linagliptin mitigates experimental inflammatory bowel disease in rats by targeting inflammatory and redox signaling. Life Sci. 2021;273:119295. doi: 10.1016/j.lfs.2021.119295.
    1. Hasan AA, et al. Mechanisms of GLP-1 receptor-independent renoprotective effects of the dipeptidyl peptidase type 4 inhibitor linagliptin in GLP-1 receptor knockout mice with 5/6 nephrectomy. Kidney Int. 2019;95:1373–1388. doi: 10.1016/j.kint.2019.01.010.
    1. Tsuprykov O, et al. The dipeptidyl peptidase inhibitor linagliptin and the angiotensin II receptor blocker telmisartan show renal benefit by different pathways in rats with 5/6 nephrectomy. Kidney Int. 2016;89:1049–1061. doi: 10.1016/j.kint.2016.01.016.
    1. Yang J, et al. Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: A systematic review and meta-analysis. Int. J. Infect. Dis. 2020;94:91–95. doi: 10.1016/j.ijid.2020.03.017.

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