Intestinal Fatty Acid Binding Protein (I-FABP) as a Prognostic Marker in Critically Ill COVID-19 Patients.
Maciej TyszkoMałgorzata Lipińska-GedigaAnna Lemańska-PerekKatarzyna KobylińskaWaldemar GozdzikBarbara AdamikPublished in: Pathogens (Basel, Switzerland) (2022)
Gastrointestinal symptoms are common in critically ill COVID-19 patients. There is currently no generally recognized method of assessing gastrointestinal injury in unconscious or sedated intensive care unit (ICU) patients. I-FABP (intestinal fatty acid binding protein) and citrulline have previously been studied as potential biomarkers of enterocyte damage in various gastrointestinal tract diseases, and changes in the levels of these markers may reflect intestinal wall damage in COVID-19. Patients with critical COVID-19, with diagnosed sepsis, or septic shock requiring ICU treatment were included in the study. Blood samples for citrulline and I-FABP were taken daily from day 1 to 5. I-FABP levels were significantly higher in patients who eventually died from COVID-19 than in survivors, and the optimal I-FABP cut-off point for predicting 28-day mortality was 668.57 pg/mL (sensitivity 0.739, specificity 0.765). Plasma levels of I-FABP, but not citrulline, were associated with significantly higher mortality and appeared to be a predictor of poor outcome in multivariate logistic regression analysis. In conclusion, I-FABP seems to be an effective prognostic marker in critically ill COVID-19 patients. Assessing mortality risk based on intestinal markers may be helpful in making clinical decisions regarding the management of intestinal injury, imaging diagnostics, and potential surgical interventions.
Keyphrases
- binding protein
- sars cov
- intensive care unit
- coronavirus disease
- septic shock
- fatty acid
- physical activity
- end stage renal disease
- oxidative stress
- mechanical ventilation
- high resolution
- newly diagnosed
- cardiovascular events
- respiratory syndrome coronavirus
- ejection fraction
- acute kidney injury
- young adults
- coronary artery disease
- acute respiratory distress syndrome
- combination therapy
- sleep quality
- patient reported
- mass spectrometry
- solid state