Radiologic diagnostics in complex estimation of the features of neuroplasticity in preterm newborns with extremely low birth weight

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Abstract

Patterns of neuroplasticity and cerebral maturation in preterm neonate can be assessed by MRI and cranial ultrasound. The score system of brain maturation includes the account of germinal matrix (GM) regression by MRI. The GM regression can be considered as pattern of neuroplasticity. There have been investigated the changes of neuroplasticity pattern or GM regression in preterm neonates with extremely low birth weight (ELBW) without intragerminal/intraventricular hemorrhages (n = 21). It is believe that the main causes of impair of GM are the intragerminal hemorrhages and hypoxia. The methods of study were cranial ultrasound (CU) and MRI. The measurement of GM was carried out by CU in anterior horn of the lateral ventricles of neonates in the study group (25-29 weeks). It was detected the GM regression in preterm neonates with increasing age, and complete GM regression to 30 week. MRI has been performed in 15 neonates from the study group on 27-38 weeks age with using the common pulse sequences – T1 WI, T2 WI and Flair. GM was detected by MRI up to 34 weeks inclusive by using the additional pulse sequence – DWI. By using common pulse sequences the GM was visualized up to 32 weeks age. Furthermore there has been pathological examination of GM in anterior horn of lateral ventricle in dead neonates from the study group (n = 3). We revealed the thickness reduction of GM in the lateral ventricles with increasing age of the dead neonates. Also we identified the delay of the GM reduction in two dead neonates 36-38 weeks age (post conceptual age) what may indicate the disorder of neuroplasticity in those preterm neonates. The performed study showed the capability of CU and MRI in examination of neuroplasticity in preterm neonates.

About the authors

Tat'yana V. Melashenko

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Author for correspondence.
Email: Radiology@mail.ru

MD, PhD, Neurologist of Neonatal Intensive Care Unit

Russian Federation, Saint Petersburg

Alexey I. Tashilkin

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

Assistant of the Department of Medical Biophysics, radiologist of the Department of Radiology

Russian Federation, Saint Petersburg

Tatiana A. Narkevich

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

Assistant, Department of Pathological Anatomy with the Course of Forensic Medicine

Russian Federation, Saint Petersburg

Aleksandr V. Pozdnyakov

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

MD, PhD, Dr Med Sci, Professor, Head of Department of Radiology, Head of the Department of Medical Biophysics

Russian Federation, Saint Petersburg

Olga L. Krasnogorskaya

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

MD, PhD, Associate Professor of the Department of Pathological Anatomy with the Course of Forensic Medicine

Russian Federation, Saint Petersburg

Ruslan A. Nasyrov

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

MD, PhD, Dr Med Sci, Professor, Head of the Department of Pathological Anatomy with the Course of Forensic Medicine

Russian Federation, Saint Petersburg

Dmitry O. Ivanov

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: Radiology@mail.ru

MD, PhD, Dr Med Sci, Professor, Rector

Russian Federation, Saint Petersburg

Viktor S. Lvov

St. Petersburg State Pediatric Medical University, Ministry of Healthcare of the Russian Federation

Email: viktorlvov@list.ru

Postgraduate Student of the Department of Medical Biophysics

Russian Federation, Saint Petersburg

References

  1. Гусев У.И., Камчатнов П.Р. Пластичность нервной системы // Журнал неврологии и психиатрии им. С.С. Корсакова. - 2004. - № 3. - С. 73-79. [Gusev UI, Kamchatnov PR. Plastichnost’ nervnoj sistemy. Zhurnal nevrologii i psihiatrii im. S.S. Korsakova. 2004;(3):73-79. (In Russ.)]
  2. Buch K, Podhaizer D, Tsai A, et al. Residual Germinal Matrix Tissue Detected on High- Resolution Ultrasound in Very Premature Neonates. In: Proceedings of the EPOS Congress: ECR2015; 4-8 Mar 2015. Vienna; 2015.
  3. Childs AM, Ramenghi LA, Cornette L, et al. Cerebral maturation in premature infants: quantitative assessment using MR imaging. AJNR Am J Neuroradiol. 2001;22(8):1577-1582.
  4. Counsell SJ, Kennea NL, Herlihy AH, et al. T2 relaxation values in the developing preterm brain. AJNR Am J Neuroradiol. 2003;24(8):1654-1660.
  5. Counsell SJ. Magnetic resonance imaging of preterm brain injury. Arch Dis Child Fetal Neonatal Ed. 2003;88(4):269F-274. doi: 10.1136/fn.88.4.F269.
  6. Deipolyi AR, Mukherjee P, Gill K, et al. Comparing microstructural and macrostructural development of the cerebral cortex in premature newborns: diffusion tensor imaging versus cortical gyration. Neuroimage. 2005;27(3):579-86. doi: 10.1016/j.neuroimage.2005.04.027.
  7. El-Dib M, Massaro AN, Bulas D, Aly H. Neuroimaging and neurodevelopmental outcome of premature infants. Am J Perinatol. 2010;27(10):803-818. doi: 10.1055/s-0030-1254550.
  8. Helwich E, Bekiesinska-Figatowska M, Bokiniec R. Recommendations regarding imaging of the central nervous system in fetuses and neonates. J Ultrason. 2014;14(57):203-216. doi: 10.15557/JoU.2014.0020.
  9. Herculano-Houzel S. Not all brains are made the same: new views on brain scaling in evolution. Brain Behav Evol. 2011;78(1):22-36. doi: 10.1159/000327318.
  10. Lewitus E, Kelava I, Huttner WB. Conical expansion of the outer subventricular zone and the role of neocortical folding in evolution and development. Front Hum Neurosci. 2013;7:424. doi: 10.3389/fnhum.2013.00424.
  11. Matsumoto JA, Gaskin CM, Kreitel KO, et al. MRI atlas Pediatric Brain Maturation and Anatomy. Oxford: Oxford University Press; 2015.
  12. Prager A, Roychowdhury S. Magnetic resonance imaging of the neonatal brain. Indian J Pediatr. 2007;74(2):173-84. doi: 10.1007/s12098-007-0012-3.
  13. Shi Y, Kirwan P, Smith J, et al. Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses. Nat Neurosci. 2012;15(3):477-86, S471. doi: 10.1038/nn.3041.
  14. Vainak N, Calin AM, Fufezan O, et al. Neonatal brain ultrasound - a practical guide for the young Radiologist. In: Proceedings of the EPOS Congress: ECR2014; 6-10 Mar 2014, Vienna. doi: 10.1594/ecr2014/C-0527.
  15. Intracranial hemorrhage: germinal matrix-intraventricular hemorrhage. In: Neurology of the Newborn. 5th ed. Ed. by J.J. Volpe. Philadelphia: Saunders Elsevier; 2008. P. 517-528.

Supplementary files

Supplementary Files
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2. Fig. 1. CUS image of preterm newborn, gestational age 28 wks., frontal scan. Arrows indicate the area of visualization of the germinal matrix

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3. Fig. 2. Study design: 1 – 21 preterm newborns with gestation ages 25-29 weeks; 2 – the findings of cranial ultrasound of 21 preterm newborns with gestation ages 25-29 weeks; 3 – the findings of preterm’s MRI (n = 15) with PCV ages 27-38 weeks

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4. Fig. 3. CUS image of preterm newborn, gestational age 30 weeks, frontal scan. The germinal matrix is not visualized

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5. Fig. 4. MRI of preterm newborn (PCA 28 wks.), DWI, axial plane. Hyperintensive MR-signal from the germinal matrix in the projection of the external parts of lateral ventricles (marked by arrows)

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6. Fig. 5. MRI of preterm newborn (PCA 28 weeks), Т2-WI, axial plane. Arrows mark the areas of the germinal matrix located along the external walls of the lateral ventricles (hypointense MR signal)

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7. Fig. 6. MRI of preterm newborn (PCA 30 weeks), Т1-WI, axial plane. The germinal matrix is visualized in the anterior parts of the lateral ventricles (marked by arrow)

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8. Fig. 7. MRI of preterm newborn (PCA 30 wks.), DWI, axial plane. The germinal matrix is visualized along the external walls of the lateral ventricles (marked by arrows)

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9. Fig. 8. A thin layer of the germinal matrix in a child, PCA 37-38 weeks (hematoxylin-eosin stain, ×100)

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10. Fig. 9. A wide layer of the germinal matrix in a child, PCA 31-32 weeks (hematoxylin-eosin stain, ×100)

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Copyright (c) 2018 Melashenko T.V., Tashilkin A.I., Narkevich T.A., Pozdnyakov A.V., Krasnogorskaya O.L., Nasyrov R.A., Ivanov D.O., Lvov V.S.

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


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