Bradykinin and Galectin-3 in Survived and Deceased Patients with COVID-19 Pneumonia: An Increasingly Promising Biochemical Target.


Journal

Oxidative medicine and cellular longevity
ISSN: 1942-0994
Titre abrégé: Oxid Med Cell Longev
Pays: United States
ID NLM: 101479826

Informations de publication

Date de publication:
2022
Historique:
received: 06 06 2022
revised: 13 08 2022
accepted: 07 10 2022
entrez: 7 11 2022
pubmed: 8 11 2022
medline: 9 11 2022
Statut: epublish

Résumé

There are still no definite curative or preventive strategies for COVID-19 disease. It is crucial to fully comprehend the pathogenesis of COVID-19 infection so that we can develop expedient pharmacological protocols. While the impact of cytokine storm on COVID-19 severity has been one of the most tested hypotheses, the role of bradykinin and various other oxidative stress markers has been relatively under-researched. Their levels can be determined immediately after a hospital admission so they could be used as early predictors of the further development of the disease. The study aims at evaluating the possibility of using bradykinin and galectin-3 levels as early predictors that COVID-19 disease will progress into a severe case. The patients who passed away were predominantly older men with comorbidities. We recorded higher CT scores in the deceased patients and the significantly higher levels of urea, creatinine, CK, troponine, CRP, and other laboratory markers. They stayed at the ICU unit longer and required mechanical ventilation more frequently than the patients who survived. On the other hand, no differences were recorded in the time periods passing from the onset of the systems to the hospital admissions. Finally, we can highlight several independent predictors of mortality in patients with COVID-19 pneumonia, including the following: (1) patients who are 50 or more years old, (2) with in-hospital stays are longer that 4 days, (3) bradykinin levels surpass 220000 pg/ml, (4) D-dimer, creatinine, and CRP are elevated, and (5) comorbidities were present (such as hypertension and diabetes). The present study strongly supports the bradykinin storm hypothesis. Since elevated bradykinin levels have been found in most COVID-19 cases with fatal outcomes, the future therapeutical strategies for COVID-19 have to be focused on reducing bradykinin serum concentrations.

Identifiants

pubmed: 36338343
doi: 10.1155/2022/7920915
pmc: PMC9633192
doi:

Substances chimiques

Bradykinin S8TIM42R2W
Galectin 3 0
Creatinine AYI8EX34EU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7920915

Informations de copyright

Copyright © 2022 Tamara Nikolic Turnic et al.

Déclaration de conflit d'intérêts

The authors declare that they have no conflicts of interest.

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Auteurs

Tamara Nikolic Turnic (TN)

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Serbia.
N.A.Semashko Public Health and Healthcare Department, F.F. Erismann Institute of Public Health, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Viseslav Popadic (V)

University Clinical Hospital Center Bežanijska kosa, Belgrade, Serbia.

Slobodan Klasnja (S)

University Clinical Hospital Center Bežanijska kosa, Belgrade, Serbia.

Ana Sekulic (A)

University Clinical Hospital Center Bežanijska kosa, Belgrade, Serbia.

Novica Nikolic (N)

University Clinical Hospital Center Bežanijska kosa, Belgrade, Serbia.

Vladimir Zivkovic (V)

Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Serbia.
Department of Pharmacology, 1st Moscow State Medical, University IM Sechenov, Trubetskaya street 8, str. 2, 119991 Moscow, Russia.

Nevena Jeremic (N)

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Serbia.
I.M. Shechenov First Moscow State Medical University (Sechenov University), 8-2 Trubetskaya st., Moscow, Russia.

Marijana Andjic (M)

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Serbia.

Nevena Draginic (N)

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Serbia.

Ivan Srejovic (I)

Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Serbia.
Department of Pharmacology, 1st Moscow State Medical, University IM Sechenov, Trubetskaya street 8, str. 2, 119991 Moscow, Russia.

Jovana Jeremic (J)

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Serbia.

Marija Zdravkovic (M)

University Clinical Hospital Center Bežanijska kosa, Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Vladimir Jakovljevic (V)

Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Serbia.
Department of Human Pathology, 1st Moscow State Medical, University IM Sechenov, Trubetskaya street 8, str. 2, 119991 Moscow, Russia.

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