Purpose of the study. The aim of the study is to identify the diagnostic capability of biomarkers – Nitric Oxide (NO), Erythropoietin (EPO) and Calcium ion (Са+2) in differentiating NEC from Sepsis in full-term newborns. Material/patients. A prospective case-control study was conducted in the intensive care and in the full-term neonatal pathology units of the Scientific Research Institute of Pediatrics named after K.Y. Farajova – Baku, Azerbaijan. The study included infants with a gestational age of 37≤ weeks. Demographic and clinical data were collected from patients with abdominal and systemic symptoms, associated with NEC. To conduct differential diagnosis of NEC from NEC + Sepsis, we chose NO, EPO and Ca+2 as potential biomarkers. ROC-curve analysis was used to calculate the diagnostic capability of these biomarkers. Results. We examined 100 full-term sick newborns with NEC. The weight of the children ranged between 2500 and 4400 grams. The levels of NO, EPO and Ca+2 were determined in the blood of all newborns in our sample. Elevated levels of NO, EPO and decreased levels of Ca+2 were observed in 83 patients. Whereas in 17 patients with NEC + Sepsis, that is, with septic complication of the disease, the test results obtained were opposite to those of the other group (p <0.001). Levels of NO in the patients with septic complication were even lower than the patients diagnosed with NEC I. Conclusions. Therefore, NO can be used as a biomarker for differential diagnosis of NEC from Sepsis.
Ahle M, Drott P, Elfvin A, Andersson RE. Maternal, fetal and perinatal factors associated with necrotizing enterocolitis in Sweden. A national case-control study. PLoS One. 2018; 13(3):e0194352. doi:10.1371/journal.pone.0194352
Gephart SM.,Wetzel C., Krisman B. Prevention and early recognition of necrotizing enterocolitis, a tale of two tools. Adv Neonatal Care: official journal of the National Association of Neonatal Nurses. 2014 V 14 (3). P. 201-210. DOI: 10.1097ANC.00000000000000063.
Markel T.A., Engelstad H., Poindexter B.B. Predicting disease severity of necrotizing enterocolitis: how to identify infants for novel therapies. J Clin Neonatal. 2014 Jan; 3(1): 1-9. Doi: 10.41032249-4847. 128717.
Li QY, An Y, Liu L, et al. Differences in the Clinical Characteristics of Early- and Late-Onset Necrotizing Enterocolitis in Full-Term Infants: A Retrospective Case-Control Study. Sci Rep. 2017; 7: 43042. Published 2017 Feb 17. doi:10.1038/srep43042
Khalid N. Necrotizing enterocolitis – some things old and some things new: A comprehensive review. 2016, Vol. 5issue:2P: 79-90.
Маммадова Т.А. Факторы риска некротического энтероколита у доношенных новорожденных. Международный журнал прикладных и фундаментальных исследований. 2020. № 6. С. 45-49. URL: http://applied-research.ru/ru/article/view?id=13087 (дата обращения: 04.09.2020).
Cokic BB, Cokic VP, Suresh S, Wirt S, Noguchi CT. Nitric oxide and hypoxia stimulate erythropoietin receptor via MAPK kinase in endothelial cells. Microvasc Res. 2014; 92:34-40. doi:10.1016/j.mvr.2014.01.009
Watkins D.J., Besner G.E. The Role of the Intestinal Microcirculation in Necrotizing Enterocolitis. Semin Pediatr Surg. 2013. V 22 (2). P. 83-87. Doi: 10.1053/j.sempedsurg.2013.01.004
N.A. Drucker, A.R. Jensen, Jan P Te Winkel, M.J. Ferkowicz, T.A. Markel. Loss of endothelial nitric oxide synthase exacerbates intestinal and lung injury in experimental necrotizing enterocolitis. J Pediatr Surg. 2018; 53(6): 1208-1214. Doi:10.1016/j.jpedsurg.2018.02.087. Epub 2018 Mar 8.
Dzik J.M., Dobrzanska A., Gruszfeld D., Walajtys-Rode E. Nitric oxide metabolitis in the urine of full-term and preterm infants. Pediatrics International: Official Journal of the Japan Pediatric Society. 2002. V. 44(4). P. 368-375.