Alexandre Tavartkiladze, Gaiane Simonia, Dinara Kasradze, Nana Okrostsvaridze, Pati Revazishvili, Maia Maisuradze, Irine Andronikashvili, Givi Tavartkiladze, George Dundua, David Egiazarov, Shota Gabadadze, Tatia Potskhoraia, Tamar Japaridze and Tamaz Mamukishvili
Objective: This study aims to evaluate the biochemical and clinical parameters in patients exhibiting symptoms of probable post-COVID syndrome, including general weakness, musculoskeletal pain, severe dyslipidemia, functional nervous system changes, increased oncological disease frequency, and arterial hypertension.
Methods: A total of 102 patients with a history of COVID-19 infection and the aforementioned symptom complex were included in the study. Blood plasma and urine samples were analyzed for melatonin, melatonin sulfate, serotonin, TNFalpha, interleukin-6, interleukin-8, serum amyloid A, BNP, squalene, homocysteine, endothelin, and prostacyclin. The results were compared with a control group of 70 practically healthy patients of the same age group (23-77 years old) who did not exhibit these symptoms.
Results: The study found significant alterations in various biochemical parameters in the patient group compared to the control group. Key findings include a sharp decrease in melatonin (15.4 ± 2.1 ng/mL vs. 40.2 ± 3.2 ng/mL) and melatonin sulfate (45.3 ± 5.6 μg/24h vs. 130.4 ± 7.1 μg/24h), moderate decreases in serotonin (120.4 ± 10.5 ng/mL vs. 190.7 ± 12.3 ng/mL), and increases in TNF-alpha (8.2 ± 1.4 pg/mL vs. 3.6 ± 0.9 pg/mL), interleukin-6 (75.3 ± 6.8 pg/mL vs. 6.2 ± 0.7 pg/mL), interleukin-8 (20.4 ± 2.1 pg/mL vs. 8.5 ± 1.0 pg/mL), serum amyloid A (15.7 ± 3.2 μg/mL vs. 5.6 ± 1.3 μg/mL), BNP (90.5 ± 12.7 pg/mL vs. 30.3 ± 5.2 pg/mL), and homocysteine (25.4 ± 3.6 μmol/L vs. 10.5 ± 1.7 μmol/L). Additionally, a sharp decrease in squalene (1.2 ± 0.3 μg/mL vs. 6.8 ± 1.0 μg/mL) and moderate increases in endothelin (4.8 ± 0.6 pg/ mL vs. 2.3 ± 0.5 pg/mL) and prostacyclin (120.3 ± 15.6 pg/mL vs. 45.7 ± 6.4 pg/mL) were observed.
Conclusion: The biochemical imbalances observed in the post-COVID syndrome patients suggest a multifaceted impact on metabolic and inflammatory pathways, potentially contributing to the observed symptomatology. Further research is needed to explore targeted therapeutic interventions.