Literature DB >> 28095379

Diffusion Tensor Imaging Detects Occult Cerebellar Injury in Severe Neonatal Hypoxic-Ischemic Encephalopathy.

Monica E Lemmon1, Matthias W Wagner, Thangamadhan Bosemani, Kathryn A Carson, Frances J Northington, Thierry A G M Huisman, Andrea Poretti.   

Abstract

BACKGROUND: Despite the benefits of whole-body hypothermia therapy, many infants with hypoxic-ischemic encephalopathy (HIE) die or have significant long-term neurodevelopmental impairment. Prospectively identifying neonates at risk of poor outcome is essential but not straightforward. The cerebellum is not classically considered to be a brain region vulnerable to hypoxic-ischemic insults; recent literature suggests, however, that the cerebellum may be involved in neonatal HIE. In this study, we aimed to assess the microstructural integrity of cerebellar and linked supratentorial structures in neonates with HIE compared to neurologically healthy neonatal controls.
METHODS: In this prospective cohort study, we performed a quantitative diffusion tensor imaging (DTI) analysis of the structural pathways of connectivity, which may be affected in neonatal cerebellar injury by measuring fractional anisotropy (FA) and mean diffusivity (MD) within the superior, middle, and inferior cerebellar peduncles, dentate nuclei, and thalami. All magnetic resonance imaging (MRI) studies were grouped into 4 categories of severity based on a qualitative evaluation of conventional and advanced MRI sequences. Multivariable linear regression analysis of cerebellar scalars of patients and controls was performed, controlling for gestational age, age at the time of MRI, and HIE severity. Spearman rank correlation was performed to correlate DTI scalars of the cerebellum and thalami.
RESULTS: Fifty-seven (23 females, 40%) neonates with HIE and 12 (6 females, 50%) neonatal controls were included. There were 8 patients (14%) in HIE severity groups 3 and 4 (injury of the basal ganglia/thalamus and/or cortex). Based on a qualitative analysis of conventional and DTI images, no patients had evidence of cerebellar injury. No significant differences between patients and controls were found in the FA and MD scalars. However, FA values of the middle cerebellar peduncles (0.294 vs. 0.380, p < 0.001) and MD values of the superior cerebellar peduncles (0.920 vs. 1.007 × 10-3 mm/s2, p = 0.001) were significantly lower in patients with evidence of moderate or severe injury on MRI (categories 3 and 4) than in controls. In patients, cerebellar DTI scalars correlated positively with DTI scalars within the thalami.
CONCLUSION: Our results suggest that infants with moderate-to-severe HIE may have occult injury of cerebellar white-matter tracts, which is not detectable by the qualitative analysis of neuroimaging data alone. Cerebellar DTI scalars correlate with thalamic measures, highlighting that cerebellar injury is unlikely to occur in isolation and may reflect the severity of HIE. The impact of concomitant cerebellar injury in HIE on long-term neurodevelopmental outcome warrants further study.
© 2017 S. Karger AG, Basel.

Entities:  

Keywords:  Diffusion tensor imaging; Hypoxic-ischemic encephalopathy; Magnetic resonance imaging; Neonatal cerebellum

Mesh:

Year:  2017        PMID: 28095379      PMCID: PMC5607011          DOI: 10.1159/000454856

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  29 in total

1.  Predictive value of neonatal MRI showing no or minor degrees of brain injury after hypothermia.

Authors:  Nancy Rollins; Timothy Booth; Michael C Morriss; Pablo Sanchez; Roy Heyne; Lina Chalak
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2.  Involvement of the anterior lobe of the cerebellar vermis in perinatal profound hypoxia.

Authors:  D J A Connolly; E Widjaja; P D Griffiths
Journal:  AJNR Am J Neuroradiol       Date:  2007-01       Impact factor: 3.825

3.  An improved survival model of hypoxia/ischaemia in the piglet suitable for neuroprotection studies.

Authors:  K A Foster; P B Colditz; B E Lingwood; C Burke; K R Dunster; M S Roberts
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5.  Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy.

Authors:  Seetha Shankaran; Abbot R Laptook; Richard A Ehrenkranz; Jon E Tyson; Scott A McDonald; Edward F Donovan; Avroy A Fanaroff; W Kenneth Poole; Linda L Wright; Rosemary D Higgins; Neil N Finer; Waldemar A Carlo; Shahnaz Duara; William Oh; C Michael Cotten; David K Stevenson; Barbara J Stoll; James A Lemons; Ronnie Guillet; Alan H Jobe
Journal:  N Engl J Med       Date:  2005-10-13       Impact factor: 91.245

Review 6.  Prognostic tests in term neonates with hypoxic-ischemic encephalopathy: a systematic review.

Authors:  Henriette van Laerhoven; Timo R de Haan; Martin Offringa; Bart Post; Johanna H van der Lee
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7.  Temporal evolution of neuropathologic changes in an immature rat model of cerebral hypoxia: a light microscopic study.

Authors:  J Towfighi; N Zec; J Yager; C Housman; R C Vannucci
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8.  Antemortem cranial MRI compared with postmortem histopathologic examination of the brain in term infants with neonatal encephalopathy following perinatal asphyxia.

Authors:  Thomas Alderliesten; Peter G J Nikkels; Manon J N L Benders; Linda S de Vries; Floris Groenendaal
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9.  Perinatal asphyxia: MR findings in the first 10 days.

Authors:  A J Barkovich; K Westmark; C Partridge; A Sola; D M Ferriero
Journal:  AJNR Am J Neuroradiol       Date:  1995-03       Impact factor: 3.825

10.  Hypoxia-ischemia and therapeutic hypothermia in the neonatal mouse brain--a longitudinal study.

Authors:  Jennifer C Burnsed; Raul Chavez-Valdez; Mir Shanaz Hossain; Kalpashri Kesavan; Lee J Martin; Jiangyang Zhang; Frances J Northington
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  14 in total

1.  Cerebral Autoregulation and Conventional and Diffusion Tensor Imaging Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy.

Authors:  Melisa Carrasco; Jamie Perin; Jacky M Jennings; Charlamaine Parkinson; Maureen M Gilmore; Raul Chavez-Valdez; An N Massaro; Raymond C Koehler; Frances J Northington; Aylin Tekes; Jennifer K Lee
Journal:  Pediatr Neurol       Date:  2018-04-02       Impact factor: 3.372

Review 2.  The Applicability of Amide Proton Transfer Imaging in the Nervous System: Focus on Hypoxic-Ischemic Encephalopathy in the Neonate.

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3.  Ultrasound Predicts White Matter Integrity after Hypothermia Therapy in Neonatal Hypoxic-Ischemic Injury.

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Review 4.  Challenges in pediatric neuroimaging.

Authors:  Matthew J Barkovich; Yi Li; Rahul S Desikan; A James Barkovich; Duan Xu
Journal:  Neuroimage       Date:  2018-04-22       Impact factor: 6.556

5.  The Role of Diffusion Tensor Imaging in Detecting Hippocampal Injury Following Neonatal Hypoxic-Ischemic Encephalopathy.

Authors:  Jacqueline Salas; Nihaal Reddy; Emanuele Orru; Kathryn A Carson; Raul Chavez-Valdez; Vera Joanna Burton; Carl E Stafstrom; Frances J Northington; Thierry A G M Huisman
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6.  Neonatal hypoxia ischemia redistributes L1 cell adhesion molecule into rat cerebellar lipid rafts.

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Review 7.  Neuroimaging in the term newborn with neonatal encephalopathy.

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Review 8.  Contrast-enhanced ultrasound of the pediatric brain.

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9.  Thermal Index for early non-invasive assessment of brain injury in newborns treated with therapeutic hypothermia: preliminary report.

Authors:  W Walas; A Mączko; Z Halaba; M Bekiesińska-Figatowska; I Miechowicz; D Bandoła; Z Ostrowski; M Rojczyk; A J Nowak
Journal:  Sci Rep       Date:  2021-06-15       Impact factor: 4.379

10.  Comparison of fractional anisotropy and apparent diffusion coefficient among hypoxic ischemic encephalopathy stages 1, 2, and 3 and with nonasphyxiated newborns in 18 areas of brain.

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Journal:  Indian J Radiol Imaging       Date:  2017 Oct-Dec
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