Prediction of underweight, short stature, and microcephaly based on brain diffusion-weighted imaging sequence in neonates with stage.2 of hypoxic-ischemic encephalopathy: A follow-up study

Abstract

Background: Hypoxic-ischemic encephalopathy (HIE), caused due to reduced oxygenation and brain blood flow, occurs in 1-8 per 1000 live full-term births in developed countries and up to 26 per 1000 live in the developing world. The growth status of survivors of birth HIE has not been evaluated sufficiently.


Objective: This study evaluated, the growth parameters (weight, height, and head circumference) of neonates with Sarnat stage 2 of HIE at 6, 10, and 12 months and its relationship with findings of neonatal brain diffusion-weighted imaging (DWI) sequence.


Materials and Methods: Medical records and growth parameters of 35 neonates with gestational age > 34 wk who were admitted with stage 2 of HIE in Neonatal Intensive Care Unit of Shahid Sadoughi hospital, Yazd, Iran from March 2021-March 2022, and its relationship with neonatal brain DWI sequence finding was evaluated.


Results: 15 girls and 20 boys with a mean birth weight of 2880.3 ± 221.8 gr were evaluated. Conventional magnetic resonance imaging and DWI were found to be abnormal in 6 (17.1%) and 18 neonates (51.4%). The most abnormal finding of DWI was high signal in basal ganglia/thalamus in 9 neonates (25.7%). Abnormal DWI is more frequent in neonates with seizures and low birth weight. Hospital stay days were more prolonged in neonates with abnormal DWI. Microcephaly at 12 months was more frequent in children with abnormal DWI.


Conclusion: In survivors of moderate neonatal HIE, abnormal brain DWI sequence might predict inappropriate head growth, and need close medical and nutritional interventions for growth improvement.


Key words: Hypoxic ischemia encephalopathy, Magnetic resonance imaging, Diffusion weighted imaging, Microcephaly, Underweight.

References
[1] El-Mazary AAM, Nasif KhA, Abdel-Hakeem GL, Sherif T, Farouk E, El-Gezawy EM. Adiponectin, leptin and insulin levels at birth and in early postnatal life in neonates with hypoxic ischemic encephalopathy. J Diabetes Metab Disord 2015; 14: 87.

[2] Groenendaal F, de Vries LS. Fifty years of brain imaging in neonatal encephalopathy following perinatal asphyxia. Pediatr Res 2017; 81: 150–155.

[3] Bano Sh, Chaudhary V, Garga UCh. Neonatal hypoxicischemic encephalopathy: A radiological review. J Pediatr Neurosci 2017; 12: 1–6.

[4] Rana L, Sood D, Chauhan R, Shukla R, Gurnal P, Nautiyal H, et al. MR imaging of hypoxic ischemic encephalopathy - distribution patterns and ADC value correlations. Eur J Radiol Open 2018; 5: 215–220.

[5] Gunn AJ, Thoresen M. Neonatal encephalopathy and hypoxic-ischemic encephalopathy. Handb Clin Neurol 2019; 162: 217–237.

[6] Walas W, Wilinska M, Bekiesinska-Figatowska M, Halaba Z, Smigiel R. Methods for assessing the severity of perinatal asphyxia and early prognostic tools in neonates with hypoxic-ischemic encephalopathy treated with therapeutic hypothermia. Adv Clin Exp Med 2020; 29: 1011–1016.

[7] Cascio A, Ferrand A, Racine E, St-Hilaire M, Sanon PN, Gorgos A, et al. Discussing brain magnetic resonance imaging results for neonates with hypoxic-ischemic encephalopathy treated with hypothermia: A challenge for clinicians and parents. eNeurologicalSci 2022; 29: 100424.

[8] Fallah R, Akhavan Karbasi S, Galalian MT, Dehghani- Firouzabadi R. Comparison of developmental status of 5-year-old singleton children born through assisted and natural conceptions. Iran J Reprod Med 2013; 11: 365–370.

[9] Karimi M, Fallah R, Dehghanpoor A, Mirzaei M. Developmental status of 5-year-old moderate low birth weight children. Brain Dev 2011; 33: 651–655.

[10] Islami Z, Fallah R, Mosavian T, Pahlavanzadeh MR. Growth parameters of NICU admitted low birth weight preterm neonates at corrected ages of 6 and 12 month. Iran J Reprod Med 2012; 10: 459–464.

[11] Ashwal S, Michelson D, Plawner L, Dobyns WB, Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Practice parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology 2009; 73: 887–897.

[12] Shankaran S, Pappas A, McDonald SA, Vohr BR, Hintz SR, Yolton K, et al. Childhood outcomes after hypothermia for neonatal encephalopathy. N Engl J Med 2012; 366: 2085– 2092.

[13] Ristovska S, Stomnaroska O, Danilovski D. Hypoxic ischemic encephalopathy (HIE) in term and preterm infants. Pril 2022; 43: 77–84.

[14] Guillet R, Edwards AD, Thoresen M, Ferriero DM, Gluckman PD, Whitelaw A, et al. Seven- to eight-year follow-up of the CoolCap trial of head cooling for neonatal encephalopathy. Pediatr Res 2012; 71: 205–209.

[15] Preeti S, Kadam A, Kadam S, Vaidya U, Kumar P, Bhagat I, et al. Anthropometric measures as biomarkers of neurodevelopmental outcomes of newborns with moderate to severe hypoxic ischemic encephalopathy. J Neonatal Perinatal Med 2019; 12: 127–134.

[16] Murden S, Borbélyová V, Laštuvka Z, Myslivecek J, Otáhal J, Riljak V. Gender differences involved in the pathophysiology of the perinatal hypoxic-ischemic damage. Physiol Res 2019; 68 (Suppl.): S207-S217.

[17] Russ JB, Simmons R, Glass HC. Neonatal encephalopathy: Beyond hypoxic-ischemic encephalopathy. Neoreviews 2021; 22: e148–e162.

[18] Kwon JM, Guillet R, Shankaran S, Laptook AR, McDonald SA, Ehrenkranz RA, et al. Clinical seizures in neonatal hypoxic-ischemic encephalopathy have no independent impact on neurodevelopmental outcome: Secondary analyses of data from the neonatal research network hypothermia trial. J Child Neurol 2011; 26: 322–328.