Literature DB >> 33604320

Pathophysiology of Cerebral Hyperperfusion in Term Neonates With Hypoxic-Ischemic Encephalopathy: A Systematic Review for Future Research.

Dianne G Kleuskens1, Filipe Gonçalves Costa1, Kim V Annink1, Agnes van den Hoogen1, Thomas Alderliesten1, Floris Groenendaal1, Manon J N Benders1, Jeroen Dudink1.   

Abstract

Worldwide neonatal hypoxic-ischemic encephalopathy (HIE) is a common cause of mortality and neurologic disability, despite the implementation of therapeutic hypothermia treatment. Advances toward new neuroprotective interventions have been limited by incomplete knowledge about secondary injurious processes such as cerebral hyperperfusion commonly observed during the first 1-5 days after asphyxia. Cerebral hyperperfusion is correlated with adverse neurodevelopmental outcome and it is a process that remains poorly understood. In order to provide an overview of the existing knowledge on the pathophysiology and highlight the gaps in current understanding of cerebral hyperperfusion in term animals and neonates with HIE, we performed a systematic research. We included papers scoping for study design, population, number of participants, study technique and relevant findings. Methodological quality was assessed using the checklist for cohort studies from The Joanna Briggs Institute. Out of 2,690 results, 34 studies were included in the final review-all prospective cohort studies. There were 14 studies of high, 17 moderate and 3 of low methodological quality. Data from the literature were analyzed in two main subjects: (1) Hemodynamic Changes subdivided into macro- and microscopic hemodynamic changes, and (2) Endogenous Pathways which was subdivided into N-methyl-D-aspartate/Mitogen activated protein kinase (NDMA/MAPK), Nitric Oxide (NO), prostanoids and other endogenous studies. Cerebral hyperperfusion in term neonates with HIE was found to be present 10-30 min after the hypoxic-ischemic event and was still present around day 10 and up to 1 month after birth. Cerebral hyperperfusion was also characterized by angiogenesis and cerebral vasodilation. Additionally, cerebral vasodilation was mediated by endogenous pathways such as MAPK through urokinase Plasminogen Activator (uPA), by neuronal NO synthase following NMDA and by prostanoid synthesis. Future research should elucidate the precise role of NMDA, MAPK and prostanoids in cerebral hyperperfusion. Moreover, research should focus on possible interventions and the effect of hypothermia on hyperperfusion. These findings should be taken into account simultaneously with brain imagining techniques, becoming a valuable asset in assessing the impact in neurodevelopmental outcome.
Copyright © 2021 Kleuskens, Gonçalves Costa, Annink, van den Hoogen, Alderliesten, Groenendaal, Benders and Dudink.

Entities:  

Keywords:  cerebral hyperperfusion; cerebral vasodilation; hyperemia; hypoxic-ischemic encephalopathy (HIE); neonatal encephalopathy; perinatal hypoxia-ischemia

Year:  2021        PMID: 33604320      PMCID: PMC7884860          DOI: 10.3389/fped.2021.631258

Source DB:  PubMed          Journal:  Front Pediatr        ISSN: 2296-2360            Impact factor:   3.418


  48 in total

1.  Role of prostanoids in cerebrovascular responses to asphyxia and reventilation in newborn pigs.

Authors:  M Pourcyrous; C Leffler; D Busija
Journal:  Am J Physiol       Date:  1990-09

2.  Hemodynamic Changes During Rewarming Phase of Whole-Body Hypothermia Therapy in Neonates with Hypoxic-Ischemic Encephalopathy.

Authors:  Tai-Wei Wu; Benita Tamrazi; Sadaf Soleymani; Istvan Seri; Shahab Noori
Journal:  J Pediatr       Date:  2018-03-20       Impact factor: 4.406

3.  In vivo Monitoring of Cerebral Hemodynamics in the Immature Rat: Effects of Hypoxia-Ischemia and Hypothermia.

Authors:  Erin M Buckley; Shyama D Patel; Benjamin F Miller; Maria Angela Franceschini; Susan J Vannucci
Journal:  Dev Neurosci       Date:  2015-05-23       Impact factor: 2.984

4.  Brain perfusion in asphyxiated newborns treated with therapeutic hypothermia.

Authors:  P Wintermark; A Hansen; M C Gregas; J Soul; M Labrecque; R L Robertson; S K Warfield
Journal:  AJNR Am J Neuroradiol       Date:  2011-10-06       Impact factor: 3.825

Review 5.  Cell therapy for neonatal hypoxia-ischemia and cerebral palsy.

Authors:  Laura Bennet; Sidhartha Tan; Lotte Van den Heuij; Matthew Derrick; Floris Groenendaal; Frank van Bel; Sandra Juul; Stephen A Back; Frances Northington; Nicola J Robertson; Carina Mallard; Alistair Jan Gunn
Journal:  Ann Neurol       Date:  2012-05       Impact factor: 10.422

6.  Delayed ("secondary") cerebral energy failure after acute hypoxia-ischemia in the newborn piglet: continuous 48-hour studies by phosphorus magnetic resonance spectroscopy.

Authors:  A Lorek; Y Takei; E B Cady; J S Wyatt; J Penrice; A D Edwards; D Peebles; M Wylezinska; H Owen-Reece; V Kirkbride
Journal:  Pediatr Res       Date:  1994-12       Impact factor: 3.756

7.  Comparison of cerebrocortical microvascular effects of different hypoxic-ischemic insults in piglets: a laser-speckle imaging study.

Authors:  F Domoki; D Zolei-Szenasi; O Olah; V Toth-Szuki; J Nemeth; B Hopp; F Bari; T Smausz
Journal:  J Physiol Pharmacol       Date:  2014-08       Impact factor: 3.011

8.  Cerebral ischemia alters cerebral microvascular reactivity in newborn pigs.

Authors:  C W Leffler; D G Beasley; D W Busija
Journal:  Am J Physiol       Date:  1989-07

9.  Inhibition of integrin alphavbeta3 prevents urokinase plasminogen activator-mediated impairment of cerebrovasodilation after cerebral hypoxia/ischemia.

Authors:  J Willis Kiessling; Douglas B Cines; Abd Al-Roof Higazi; William M Armstead
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-01-23       Impact factor: 4.733

10.  PAI-1-derived peptide EEIIMD prevents hypoxia/ischemia-induced aggravation of endothelin- and thromboxane-induced cerebrovasoconstriction.

Authors:  William M Armstead; John Riley; Douglas B Cines; Abd Al-Roof Higazi
Journal:  Neurocrit Care       Date:  2014-02       Impact factor: 3.210

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  2 in total

1.  Cerebral perfusion changes of the basal ganglia and thalami in full-term neonates with hypoxic-ischaemic encephalopathy: a three-dimensional pseudo continuous arterial spin labelling perfusion magnetic resonance imaging study.

Authors:  Jibin Cao; Yongnan Mu; Xiaohan Xu; Huanhuan Li; Zequn Liu; Meiling Cao; Peng Wang; Wenge Sun; Lingling Cui
Journal:  Pediatr Radiol       Date:  2022-03-31

Review 2.  Magnetic Resonance Imaging in (Near-)Term Infants with Hypoxic-Ischemic Encephalopathy.

Authors:  Corline E J Parmentier; Linda S de Vries; Floris Groenendaal
Journal:  Diagnostics (Basel)       Date:  2022-03-06
  2 in total

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