Preview

Messenger of ANESTHESIOLOGY AND RESUSCITATION

Advanced search

PREDICTORS OF HYPOXIC ISCHEMIC ENCEPHALOPATHY IN NEWBORNS

https://doi.org/10.21292/2078-5658-2017-14-4-16-22

Abstract

Goal of the study: to study the level of markers of the system fetal inflammatory response and endothelial dysfunction in the umbilical blood of full-term newborns survived after intranatal asphyxia. Materials and methods. Group 1 included 12 full-term newborns who were born with 5 and less Apgar scores for the 1st minute, and Group 2 included 12 children with a normal course of the early neonatal period. The levels of interleukin-8 (IL-8), interleukin-10 (IL-10), C-reactive protein (CRP), soluble form of E-selectin (sE-selectin) and intercellular adhesion molecule-1 (sICAM-1) in umbilical blood were tested. Results. Mothers of newborns from Group 1 demonstrated inflammatory changes in placenta compared to Group 2 (60 and 8%, p = 0.018) as well as higher levels of CRP (961 [520; 1 096] and 43 [33; 71] ng/ml, p < 0.06), IL-8 (153 [53; 323] and 28 [22; 42] pg/ml, p = 0.001), IL-10 (12.3 [7.5; 43.5] and 2.5 [1.9; 5.0] pg/ml, p < 0.001), and sICAM-1 (40 [33; 45] and 18 [17; 21] ng/ml, p < 0.06), which correlated to the inflammatory changes in placenta (r = 0.812, p = 0.028; r = 0.534, p < 0.001; r = 0.492, p = 0.034; r = 0.688, p = 0.089 for CRP, IL-8, IL-10 and sICAM-1 respectively). It was also found that Apgar score had negative correlation with IL-8 level (r = -0.453, p = 0.04 and r = -0.565, p = 0.008 on the 1st and 5th minutes respectively); IL-10 (r = -0.711, p < 0.001 и r = -0.727, p < 0.001 on the 1st and 5th minutes respectively), and sICAM-1 (r = -0.796, p = 0.013 и r = -0.904, p = 0.002 on the 1st and 5th minutes respectively). Conclusions. The system fetal inflammatory response and endothelial dysfunction related to it may predetermine the development of hypoxic ischemic encephalopathy and reduce the efficiency of treatment interventions.

 

About the Authors

V. A. Sergeeva
Kursk State Medical University, Kursk; Regional Perinatal Center, Kursk
Russian Federation
Doctor of Medical Sciences, Professor of Anesthesiology and Intensive Care Department


Yu. S. Aleksandrovich
St. Petersburg State Pediatric Medical University, St. Petersburg
Russian Federation
Doctor of Medical Sciences, Professor, Head of Anesthesiology, Intensive Care and Emergency Pediatrics Department within Professional Development Unit


N. S. Petrenkova
Kursk State Medical University, Kursk; Regional Perinatal Center, Kursk
Russian Federation
Post Graduate Student of Anesthesiology and Intensive Care Department of Professional Development Faculty


References

1. Glukhovets B.I., Glukhovets N.G. Patologiya posleda. [Pathologic secundines]. St. Petersburg, GRAAL Publ., 2002, 446 p.

2. Disfunktsiya endoteliya. Prichiny, mekhanizmy, farmakologicheskaya korrektsiya. [Endothelial dysfunction. Causes, mechanisms, pharmacological management]. Ed. by N.N. Petrischev, St. Petersburg, Izdatelstvo SPbGMU Publ., 2003, 184 p.

3. Sergeeva V.А., Nesterenko S.N., Shabalov N.P. et al. Testing cytokine blood profile in newborns with lethal outcomes accompanied with system inflammatory response. Ross. Med. Journal, 2011, no. 5, pp. 39-43. (In Russ.)

4. Sergeeva V.А., Shabalov N.N., Аleksandrovich Yu.S. et al. Impact of fetal inflammatory response on the post-natal adaptation of newborns. Ros. Med.-Biologichesky Vestnik Im. Akad. I.P. Pavlova, 2010, no. 4, pp. 34-45. (In Russ.)

5. Alvarez-Diaz A., Hilario E. Hypoxic-ischemic injury in the immature brain – key vascular and cellular players. Neonatology, 2007, vol. 92, pp. 227-235.

6. Bartha A.I., Foster-Barber A., Miller S.P. et al. Neonatal encephalopathy: association of cytokines with MR spectroscopy and outcome. Pediatric Research, 2004, vol. 56, no. 6, pp. 960-966.

7. Brandon J.D., Cesar R., Wing M. et al. Neuroprotective strategies after neonatal hypoxic ischemic encephalopathy. Int. J. Mol. Sci., 2015, vol. 16, pp. 22368-22401.

8. Caringo A., Tesoriero L., Cayabyab R. et al. Constitutine IL-10 expression by lung inflammatory cells and risk for bronchopulmonary dysplasia. Pediatr. Res., 2007, vol. 61, pp. 197-202.

9. Covert R., Kohn J., Yousefzadef D. et al. Thalamostriate vasculopathy in neonates in the MagNET trial: association with placental funicitis and intraventricular hemorrhage. Pediatr. Res., 1999, vol. 45, no. 4, pp. 192A.

10. Davidson D., Miskolci V., Clark D.C. et al. Interleukin-10 production after pro-inflammatory stimulation of neutrophils and monocytic cells of the newborn. Comparision to exogenous interleukin-10 and dexamethason levels needed to inhibit chemokine release. Neonatology, 2007, vol. 92, no. 2, pp. 127-133.

11. Debeaux A. C., Maingay J.P., Ross J.A. et al. Interleukin-4 and interleukin-10 increase endotoxin-stimulated human umbilical vein endothelial cell interleukin-8 release. J. Interferon Cytokine Res., 1995, vol. 15, pp. 441-445.

12. Fudong L., Louise D. Mccullough. Inflammatory responses in hypoxic ischemic encephalopathy. Acta Pharmacologica Sinica, 2013, vol. 34, pp. 1121-1130.

13. Grua A.J., Reis A., Buggle F. et al. Monocyte function and plasma levels of interleukin-8 in acute ischemic stroke. J. Neurol. Sci., 2001, vol. 192, pp. 41-47.

14. Haque K.N. Definitions of blood stream infection in the newborn. Pediatr. Crit. Care Med., 2005, vol. 6, pp. 545-549.

15. Jing L., Ying H.C., Hang F.M. et al. The Role and Mechanisms of IL-6, IL-8 and TNF-a for regulating cerebral hemodynamics in term infants with hypoxic-ischemic encephalopathy. J. Turkish-German Gynecol Assoc., 2007, vol. 8, no. 1, pp. 63-66.

16. Lee S.E., Romero R., Kim C.J. et al. Funisitis in term pregnancy is associated with microbial invasion of the amniotic cavity and intra-amniotic inflammation. J. Matern. Fetal Neonatal Med., 2006, vol. 19, no. 11, pp. 693-697.

17. McAdams R., Juul S.E. The role of cytokines and inflammatory cells in perinatal brain injury. Hindawi Publishing Corporation. Neurology Research International, vol. 2012, Article ID 561494, 15 pages doi:10.1155/2012/56149.

18. Mittendorf R., Montag A.G., MacMillan W. et al. Components of the systemic fetal inflammatory response syndrome as predictors of impaired neurologic outcomes in children. Am. J. Obstet. Gynecol., 2003, vol. 18, pp. 1438-1446.

19. Mukaida N., Matsumoto T., Yokoi K. et al. Inhibition of neutrophil-mediated acute inflammation injury by an antibody against interleukin-8. Inflamm Res., 1998, vol. 47, suppl. 3, pp. 151-157.

20. Naccasha N., Hinson R., Montag A. et al. Association between funicitis and elevated interleukin-6 in cord blood. Obstet. Gynecol., 2001, vol. 97, pp. 220-224.

21. O’Callaghan E., Sharm P., Takei N. et al. Schizophrenia after prenatal exposure to 1957 A2 influenza epidemic. Lancet, 1991, vol. 337, pp. 1248.

22. Paananen R., Husa A.K., Vuolteenaho R. et al. Blood cytokines during perinatal period in very preterm infants: relationship of inflammatory response and bronchopulmonary dysplasia. J. Pediatr., 2009, vol. 154, no. 1, pp. 39−43e3.

23. Pacora P., Chaiworapongsa T., Maymon E. et al. Funicitis and chorionic vasculitis: the histological counterpart of the fetal inflammatory response syndrome. J. Maternal-Fetal Neonat. Med., 2002, vol. 11, pp. 18-25.

24. Romero R., Mazor M. Infection and preterm labor. Clin. Obstet. Gynecol., 1988, vol. 31, pp. 553-584.

25. Shervin C., Broadbent R., Young S. et al. Utility of interleukin-12 and interlrukin-10 in comparision with other cytokines and acute-phase reactants in the diagnosis of neonatal sepsis. Am. J. Perinatol., 2008, vol. 25, no. 10, pp. 629-636.

26. Vintzeleos A., Campbell W., Nochimson D. et al. The fetal biophysical profile in patients with premature rupture of membranes – an early predictor of fetal infection. Am. J. Obstet. Gynecol., 1985, vol. 152, no. 5, pp. 510-516.

27. Whalen M.J., Doughty L.A., Carlos T.M. et al. Intracellular adhesion molecule-1 and vascular cell adhesion molecule-1 are increased in the plasma of children with sepsis-induced multiple organ failure. Crit. Care Med., 2000, vol. 28, no. 7, pp. 2600-2607.

28. Wintermark P., Boyd T., Gregas M.C. et al. Placental pathology in asphyxiated newborns meeting the criteria for therapeutic hypothermia. J. Obstet. Gynecol., 2010, 203, no. 6, pp. 579.e1−9.

29. Yoon B.H., Romero R., Park J.S. et al. Fetal exposure to an intra-amniotic inflammation and the development of cerebral palsy at the age of three years. Am. J. Obstetrics and Gynecology, 2000, vol. 182, no. 3, pp. 675-681.


Review

For citations:


Sergeeva V.A., Aleksandrovich Yu.S., Petrenkova N.S. PREDICTORS OF HYPOXIC ISCHEMIC ENCEPHALOPATHY IN NEWBORNS. Messenger of ANESTHESIOLOGY AND RESUSCITATION. 2017;14(4):16-22. (In Russ.) https://doi.org/10.21292/2078-5658-2017-14-4-16-22



Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2078-5658 (Print)
ISSN 2541-8653 (Online)