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.

Insights

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.
Abstract