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Crimean-Congo Hemorrhagic Fever Disease: Relationship Between Clinical Course and Apoptosis
Mehmet Samet Demirel1, Çigdem Kader1, Emine Yeşilyurt2
1Department of Infectious Diseases and Clinical Microbiology, Yozgat Bozok University School of Medicine, Yozgat, Türkiye.
Crimean-Congo hemorrhagic fever (CCHF) severity is linked to apoptosis biomarkers. Elevated clusterin and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) in acute phases indicate severe disease, aiding early clinical management.
Area of Science:
- Virology
- Immunology
- Pathogenesis
Background:
- Crimean-Congo hemorrhagic fever (CCHF) is a severe zoonotic illness.
- Understanding CCHF pathogenesis is crucial for patient outcomes.
Purpose of the Study:
- To evaluate apoptosis biomarkers in mild vs. severe CCHF.
- To correlate biomarker levels with CCHF disease severity.
Main Methods:
- Adult CCHF patients categorized into mild and severe groups.
- Apoptosis markers (clusterin, TRAIL, caspase-8, cytochrome C, Apaf-1) measured via ELISA.
- Biomarker levels assessed during acute and convalescent phases.
Main Results:
- TRAIL levels were higher in the acute phase for both mild and severe CCHF.
- During the acute phase, severe CCHF showed higher clusterin, TRAIL, caspase-8, and Apaf-1.
- TRAIL levels remained significantly higher in severe CCHF during convalescence.
Conclusions:
- Apoptosis proteins are integral to CCHF pathogenesis.
- Clusterin and TRAIL show potential as indicators of CCHF severity.
- Early detection of these biomarkers may improve clinical management of severe CCHF.
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