Potential Therapeutic Benefits of Metformin Alone and in Combination with Sitagliptin in the Management of Type 2 Diabetes Patients with COVID-19.

SARS-CoV-2 cytokines diabetes mellitus metformin sitagliptin

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
07 Nov 2022
Historique:
received: 13 10 2022
revised: 29 10 2022
accepted: 31 10 2022
entrez: 10 11 2022
pubmed: 11 11 2022
medline: 11 11 2022
Statut: epublish

Résumé

Type 2 diabetes mellitus (T2DM) is a potential risk factor for the development of COVID-19 and is associated with higher severity and mortality rates. T2DM patients are commonly treated with metformin monotherapy or metformin plus sitagliptin. In the present case-control, single-center cohort study, a total number of 112 T2DM patients suffering from COVID-19 and aged 44−62 years old were compared with 78 T2DM patients without COVID-19 and aged 42−56 years old. Both the patient group and the control group were allocated into four groups. Group A: T2DM patients with COVID-19 on metformin treatments plus standard therapy (n = 60); group B: T2DM patients with COVID-19 on metformin plus sitagliptin plus standard therapy (n = 52); group C: T2DM patients without COVID-19 on metformin treatments (n = 40); and group D: T2DM patients without COVID-19 on metformin plus sitagliptin (n = 38). The investigation duration was 2−3 weeks. Anthropometric measurements, serological and biochemical investigations, pulmonary radiological findings, and clinical outcomes were evaluated. Only 101 T2DM patients with COVID-19 continued the study, 71 (70.29%) with mild-moderate COVID-19 and 30 (29.7%) with severe COVID-19 were compared with 78 T2DM patients as a control. Inflammatory biomarkers (C reactive protein, ferritin, and procalcitonin), a lung injury biomarker (lactate dehydrogenase), and a coagulopathy biomarker (D-dimer) were elevated in severe COVID-19 patients compared with mild-moderate COVID-19 (p < 0.05) and T2DM patients (p < 0.05). However, metformin plus sitagliptin was more effective than metformin monotherapy in T2DM patients with COVID-19, as evidenced by the mitigation of oxidative stress, CT scan score, and clinical outcomes. The present study confirmed the protective effects of this combination against the development of COVID-19 severity, as most T2DM COVID-19 patients develop mild-moderate forms. Herein, the combination of metformin and sitagliptin may lead to more beneficial effects than metformin monotherapy.

Identifiants

pubmed: 36355535
pii: ph15111361
doi: 10.3390/ph15111361
pmc: PMC9699540
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Hayder M Al-Kuraishy (HM)

Department of Clinical Pharmacology and Medicine, College of Medicine, AL-Mustansiriyia University, Baghdad 14132, Iraq.

Ali I Al-Gareeb (AI)

Department of Clinical Pharmacology and Medicine, College of Medicine, AL-Mustansiriyia University, Baghdad 14132, Iraq.

Sarah M Albogami (SM)

Department of Biotechnology, College of Science, Taif University, Taif 21944, Saudi Arabia.

Sabatier Jean-Marc (S)

Aix-Marseille Université, Institut de Neurophysiopathologie (INP), CNRS UMR 7051, Faculté des sciences médi-cales et paramédicales, 27 Bd Jean Moulin, 13005 Marseille, France.

Eman Hassan Nadwa (EH)

Department of Pharmacology and Therapeutics, College of Medicine, Jouf University, Sakaka 72345, Saudi Arabia.
Department of Medical Pharmacology, Faculty of Medicine, Cairo University, Cairo 12613, Egypt.

Amin A Hafiz (AA)

Department of Clinical Nutrition, Faculty of Applied Medical Sciences, Umm Al-Qura University, Mecca 24382, Saudi Arabia.

Walaa A Negm (W)

Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta 31527, Egypt.

Marwa Kamal (M)

Clinical Pharmacy Department, Faculty of Pharmacy, Fayoum University, Fayoum 63514, Egypt.

Mohammed Al-Jouboury (M)

Department of Community Medicine and Statistics, College of Medicine, Baghdad University, Baghdad 10071, Iraq.

Engy Elekhnawy (E)

Pharmaceutical Microbiology Department, Faculty of Pharmacy, Tanta University, Tanta 31527, Egypt.

Gaber El-Saber Batiha (GE)

Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour 22511, Egypt.

Michel De Waard (M)

Smartox Biotechnology, 6 Rue des Platanes, 38120 Saint-Egrève, France.
L'institut du thorax, INSERM, CNRS, Université de Nantes, 44007 Nantes, France.
LabEx «Ion Channels, Science & Therapeutics», Université de Nice Sophia-Antipolis, 06560 Valbonne, France.

Classifications MeSH