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. 2023 Winter;17(1):99-110.
doi: 10.22037/ijcn.v17i2.38561. Epub 2023 Jan 1.

Comparison of new biomarkers in the diagnosis of perinatal asphyxia

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Comparison of new biomarkers in the diagnosis of perinatal asphyxia

Hassan Boskabadi et al. Iran J Child Neurol. 2023 Winter.

Abstract

Objectives: Precise and early diagnosis of neonatal asphyxia may improve outcomes. Recent studies aim to identify diagnostic biomarkers in neonates at risk for brain damage. The current study was designed to evaluate the diagnostic value of new biomarkers for neonatal asphyxia.

Materials & methods: This prospective study was conducted with an available sampling of infants upper 35 weeks of gestational age, including neonates with asphyxia (case group) and healthy controls, 2014-2022, in Ghaem Hospital, Mashhad, Iran. Data collection was performed utilizing a researcher-made questionnaire, including maternal and neonatal characteristics, as well as clinical and laboratory evaluation. Serum umbilical cord levels of interleukin-6 (IL6), interleukin-1-beta (IL- 1β), pro-oxidant-antioxidant balance (PAB), and heat shock protein-70 (HSP70), as well as nucleated red blood cells count (NRBC), were determined. Data were analyzed by t-test, Chi-square, receiver operating characteristic (ROC), and regression models.

Results: The differences in variables IL6, IL1β, PAB, NRBC/100WBC, and HSP70 were statistically significant between the two groups (in all cases, P<0.0001). In the diagnosis of asphyxia, the most sensitive marker (89%) was IL1β more than 2.39 pg/ml and HSP 70 upper than 0.23 ng/ml, while IL6 was higher than 9pg/ml, determined as the most specific marker (85%). Furthermore, a combination of HSP + PAB and IL6 + lL1b + PAB + NRBC/100WBC possesses the prediction power of 93.2% and 87.3%, respectively, for diagnosing asphyxia.

Conclusion: According to data analysis, the combination of new biochemical markers (NRBC count, IL6, IL1β, PAB, and HSP 70) could be a reliable marker for diagnosing infants with asphyxia.

Keywords: Heat shock protein; Interleukin-1β; Interleukin-6; Neonatal asphyxia; Pro-oxidant-antioxidant balance; nucleated red blood cells count.

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Conflict of interest statement

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References

    1. Fattuoni C, Palmas F, Noto A, Fanos V, Barberini L. Perinatal Asphyxia: A Review from a Metabolomics Perspective. Molecules. 2015;20:7000–7016. - PMC - PubMed
    1. Derganc M, Osredkar D. HYPOXIC-ISCHEMIC BRAIN INJURY IN THE NEONATALPERIOD–CURRENT CONCEPTS, NOVEL DIAGNOSTICAPPROACHES AND NEUROPROTECTIVE STRATEGIES*. Zdravniški Vestnik. 2008;77(SUPPII)=)
    1. Miller SP, Ramaswamy V, Michelson D, Barkovich AJ, Holshouser B, Wycliffe N, et al. Patterns of brain injury in term neonatal encephalopathy. The Journal of pediatrics. 2005;146:453–460. - PubMed
    1. Douglas-Escobar M, Weiss MD. Biomarkers of brain injury in the premature infant. Frontiers in neurology. 2012:3. - PMC - PubMed
    1. Naithani M, Simalti AK. Biochemical markers in perinatal asphyxia. Journal of Nepal Paediatric Society. 2011;31:151–156.

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