Serum Catestatin Level as a Stratification Assessment Tool in Non-Critical COVID-19 Patients.


Journal

International journal of environmental research and public health
ISSN: 1660-4601
Titre abrégé: Int J Environ Res Public Health
Pays: Switzerland
ID NLM: 101238455

Informations de publication

Date de publication:
09 01 2023
Historique:
received: 11 12 2022
revised: 01 01 2023
accepted: 05 01 2023
entrez: 21 1 2023
pubmed: 22 1 2023
medline: 25 1 2023
Statut: epublish

Résumé

Introduction: Catestatin (CST) is a peptide with immunomodulatory, anti-inflammatory, and anti-microbial activities. There are only a few studies that have investigated plasma CST levels in COVID-19 patients (mostly in ICU patients). In our work, the aim was to demonstrate serum CST levels and their correlation with clinical outcomes in a group of severe COVID-19 patients admitted to the non-ICU department. Methods: The subjects were 32 patients (25 females, 7 males) admitted to the non-ICU unit for COVID-19 patients. Results: CST levels in our cohort were higher (8.91 ± 7.00) than previously reported CST levels in control subjects. We found a significant positive correlation between serum CST levels and C-reactive protein (r = 0.423, p = 0.008), D-dimers (r = 0.395, p = 0.013), hsTNT (high-sensitivity troponin T) (r = 0.603, p < 0.001), proBNP (N-terminal pro-brain natriuretic peptide) (r = 0.569, p < 0.001), and hospitalization days (r = 0.388, p = 0.014). There was a difference between groups of participants with SOFA <3 (n = 18) and SOFA >=3 (n = 14) in catestatin serum levels (7.25 ± 3.66 vs. 11.05 ± 9.52 ng/mL), but the difference was statistically insignificant (p = 0.065). Conclusion: We considered plasma CST level at hospital admission as a possible tool for early risk assessment in non-critical COVID-19 patients. This study is an attempt to clarify the complex pathophysiological mechanisms present in the development of severe forms of SARS-CoV2 infection.

Identifiants

pubmed: 36673891
pii: ijerph20021136
doi: 10.3390/ijerph20021136
pmc: PMC9858918
pii:
doi:

Substances chimiques

chromogranin A (344-364) 0
RNA, Viral 0
Chromogranin A 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Ivan Jerkovic (I)

Department for Urgent and Intensive Medicine with Clinical Pharmacology and Toxicology, Internal Medicine Clinic, University Hospital Split, University of Split School of Medicine, 21000 Split, Croatia.

Vedran Kovacic (V)

Department for Urgent and Intensive Medicine with Clinical Pharmacology and Toxicology, Internal Medicine Clinic, University Hospital Split, University of Split School of Medicine, 21000 Split, Croatia.

Tina Ticinovic Kurir (T)

Department of Endocrinology, Internal Medicine Clinic, University Hospital Split, University of Split School of Medicine, 21000 Split, Croatia.
Department of Pathophysiology, University of Split School of Medicine, 21000 Split, Croatia.

Josko Bozic (J)

Department of Pathophysiology, University of Split School of Medicine, 21000 Split, Croatia.

Leida Tandara (L)

Department of Medical Laboratory Diagnostics, University Hospital Split, University of Split School of Medicine, 21000 Split, Croatia.

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Classifications MeSH