Journals / Turkish Journal of Medical Sciences / 2021 / Cilt: 51 - Sayı: 3

A sensitive indicator for the severity of COVID-19: thiol

Pages
921–928
Publication Date
2022-11-06
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

This outcome highlights that thiols could be an impressible biomarker for predicting of the severity of COVID-19.Key words: COVID-19, inflammation, immune response, severity, thiol

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background/aim: Thiol status is a good reflector of the cellular redox and have vital roles in various cellular signaling pathways.
📊
Key Findings & Data:The purpose of the study was to investigate thiol status in patients with SARS-CoV-2 infection.
💡
Conclusion & Impact:This outcome highlights that thiols could be an impressible biomarker for predicting of the severity of COVID-19.Key words: COVID-19, inflammation, immune response, severity, thiol
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: Thiol status is a good reflector of the cellular redox and have vital roles in various cellular signaling pathways. The purpose of the study was to investigate thiol status in patients with SARS-CoV-2 infection. Materials and methods: A total of 587 subjects (517 patients/70 healthy controls) were enrolled in the study.The patients were categorized into the groups regarding to the severity of disease (mild, moderate, severe, and critical).Thiol status of all groups were compared. Results: The patients had significantly diminished thiol levels compared to controls. Thiol levels were gradually decreased as the severity of the disease increased. Logistic regression analyses identified that thiol concentrations were an independent risk factor for the disease severity in each phase (mild group OR 0.975, 95%CI 0.965-0.986; moderate group, OR 0.964, 95%CI 0.953-0.976; severe group OR 0.953, 95%CI 0.941-0.965; critical group OR 0.947, 95%CI 0.935-0.960).Thiol test exhibited the largest area under the curve at 0.949, with the highest sensitivity (98.6%) and specificity (80.4%). Conclusions: Depleted thiol status was observed in SARS-CoV-2 infection. Decline of the thiol levels by degrees while the severity of infection increased was closely related to the progression of the disease. This outcome highlights that thiols could be an impressible biomarker for predicting of the severity of COVID-19.Key words: COVID-19, inflammation, immune response, severity, thiol

🔖

Cite This Article

OĞUZ, E. F., EREN, F., AKKUŞ, M. S., ATEŞ, İ., EREL, Ö., NEŞELİOĞLU, S., GÜNER, R. (2022). A sensitive indicator for the severity of COVID-19: thiol. Turkish Journal of Medical Sciences, Cilt: 51 - Sayı: 3, 921–928. https://ajindex.com/articles/609442

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Pascarella G, Strumia A, Piliego C, Bruno F, Del Buono R et al. COVID-19 diagnosis and management: a comprehensive review. Journal of Internal Medicine 2020
  2. 288 (2): 192-206. doi: 10.1111/joim.13091 2. Petersen E, Koopmans M, Go U, Hamer DH, Petrosillo N et al. Comparing SARS-CoV-2 with SARS-CoV and influenza pandemics. The Lancet Infectious Diseases 2020
  3. 20 (9): e238-e244. doi: 10.1016/S1473-3099(20)30484-9 3. Tay MZ, Poh CM, Rénia L, MacAry PA, Ng LFP. The trinity of COVID-19: immunity, inflammation, and intervention. Nature Reviews Immunology 2020
  4. 20 (6): 363-374. doi: 10.1038/s41577-020-0311-8 4. García LF. Immune response, inflammation, and the clinical spectrum of COVID-19. Frontiers in Immunology 2020
  5. doi: 10.3389/fimmu.2020.01441 5. Paces J, Strizova Z, Smrz D, Cerny J. COVID-19 and the immune system. Physiological Research 2020
  6. 69 (3): 379-388. doi: 10.33549/physiolres.934492 6. Maggi E, Canonica WG, Moretta L. COVID-19: unanswered questions on immune response and pathogenesis. The Journal of Allergy and Clinical Immunology 2020
  7. 146 (1): 18-22. doi: 10.1016/j.jaci.2020.05.001 7. Zhand S, Saghaeian Jazi M, Mohammadi S, Rasekhi RT, Rostamian G et al. COVID-19: the immune responses and clinical therapy candidates. International Journal of Molecular Sciences 2020
  8. 21 (15): 5559. doi: 10.3390/ijms21155559 8. Merad M, Martin JC. Pathological inflammation in patients with COVID-19: a key role for monocytes and macrophages. Nature Reviews Immunology 2020
  9. 20 (6): 355-362. doi: 10.1038/s41577-020-0331-4 9. Mahmudpour M, Roozbeh J, Keshavarz M, Farrokhi S, Nabipour I. COVID-19 cytokine storm: the anger of inflammation. Cytokine 2020
  10. 15515. doi: 10.1016/j. cyto.2020.155151 10. Erel O, Neselioglu S. A novel and automated assay for thiol/ disulphide homeostasis. Clinical Biochemistry 2014
  11. 47 (18): 326-332. doi: 10.1016/j.clinbiochem.2014.09.026 11. Moriarty-Craige SE, Jones DP. Extracellular thiols and thiol/ disulfide redox in metabolism. Annual Review of Nutrition 2004
  12. doi: 10.1146/annurev.nutr.24.012003.132208 12. Rodosskaia NK, Chernousova GM. Immune system and thiols: some peculiarities of thiol exchange. Comparative Immunology Microbiology and Infectious Diseases 2010
  13. 33 (1): 65-71. doi: 10.1016/j.cimid.2008.08.001 13. Rahman I, Biswas SK, Jimenez LA, Torres M, Forman HJ. Glutathione, stress responses, and redox signaling in lung inflammation. Antioxidants & Redox Signaling 2005
  14. 7 (1-2): 42-59. doi: 10.1089/ars.20