Serum Humanin in Pediatric Septic Shock Associated Multiple Organ Dysfunction Syndrome

Abstract

Abstract Background Multiple organ dysfunction syndrome (MODS) disproportionately contributes to pediatric sepsis morbidity. Humanin (HN) is a small peptide encoded by mitochondrial DNA and thought to exert cytoprotective effects in endothelial cells and platelets. We sought to test the association between serum HN (sHN) concentrations and MODS in a prospectively enrolled cohort of pediatric septic shock. Methods Human MT-RNR2 ELISA was used to determine sHN concentrations on day 1 and 3. The primary outcome was thrombocytopenia associated multi-organ failure (TAMOF). Secondary outcomes included individual organ dysfunctions on day 7. Associations across pediatric sepsis biomarker (PERSEVERE) based mortality risk strata and correlation with platelet and markers endothelial activation were tested. Results 140 subjects were included in this cohort, of whom 39 had TAMOF phenotype. Concentration of sHN was higher on day 1 relative to day 3, and among those with TAMOF phenotype in comparison to those without. Although, the association between sHN and TAMOF phenotype was not significant after adjusting for age and PRISM-III score in multivariate models, we identified that sHN was independently associated with presence of day 7 sepsis-associated acute kidney injury (SA-AKI) (p = 0.032). Further, sHN was higher among those with high PERSEVERE-mortality risk strata and correlated with platelet counts and several markers of endothelial activation. Conclusion Among children with septic shock, sHN concentrations were higher among patients with TAMOF phenotype and independently associated with persistent SA-AKI. Pending further validation and rigorous mechanistic studies, interventions aimed at restoring humanin may have therapeutic implications in recovery of organ function among critically ill patients.