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Decoding blood fatty acids in Crimean-Congo hemorrhagic fever
Serkan Bolat1, Seyit Ali Büyüktuna2, Serra İlayda Yerlitaş3
1Department of Medical Biochemistry, Sivas Cumhuriyet University School of Medicine, Sivas, Türkiye.
Metabolomics : Official Journal of the Metabolomic Society
|August 29, 2025
Summary
Fatty acid profiles, particularly elevated omega-6/omega-3 ratios, indicate Crimean-Congo hemorrhagic fever severity. These findings may aid in developing biomarkers and targeted therapies for this dangerous viral illness.
Area of Science:
- Biochemistry
- Virology
- Clinical Medicine
Background:
- Fatty acids (FAs) are crucial for cellular functions, metabolism, and inflammation.
- Crimean-Congo hemorrhagic fever (CCHF) is a severe viral illness with high mortality rates.
Purpose of the Study:
- Investigate fatty acid profiles in CCHF patients.
- Identify potential FA biomarkers for disease progression and severity.
- Explore FA alterations in CCHF pathogenesis.
Main Methods:
- Analyzed FA concentrations in 190 participants (115 CCHF-positive, 30 CCHF-negative, 45 healthy controls) using gas chromatography‒mass spectrometry (GC-MS).
- Performed pathway analysis to identify disruptions in FA metabolism.
- Utilized Cox regression to determine FAs associated with prognosis.
Main Results:
- Significant differences in FA levels were observed between CCHF cases and controls.
- Severe CCHF cases exhibited distinct FA profiles, including higher omega-6/omega-3 and linoleic acid/dihomo-γ-linolenic acid (LA/DGLA) ratios, correlated with inflammatory markers (IL-6, D-dimer).
- Key prognostic FAs identified include myristic acid, phytanic acid, linoleic acid, gamma-linolenic acid, alpha-linolenic acid, oleic acid, behenic acid, cerotic acid, LA/DGLA, omega-6, omega-9, and the omega-6/omega-3 ratio. Affected pathways include unsaturated fatty acid biosynthesis and arachidonic acid metabolism.
Conclusions:
- Significant alterations in FA metabolism and laboratory markers are evident in CCHF.
- These findings offer insights into CCHF pathophysiology.
- Potential for developing targeted therapeutic strategies based on FA alterations.
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