Evidence map›Paper›PMID 39699839›Full record

ArticleCerebellum (London, England)2024

Uneven Distribution of Purkinje Cell Injury in the Cerebellar Vermis of Term Neonates with Hypoxic-Ischemic Encephalopathy.

Kim V Annink, Ilona C E van Leeuwen, Nina A Smeets, Lianne A J Peeters, Niek E van der Aa, Thomas Alderliesten, Floris Groenendaal, Reint K Jellema, Cora H A Nijboer, Peter G J Nikkels and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Kim V AnninkDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Ilona C E van LeeuwenDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Nina A SmeetsDepartment of Development and Origin of Disease (DDOD), UMC Utrecht Brain Center, University Utrecht, Utrecht, the Netherlands.
Lianne A J PeetersDepartment of Development and Origin of Disease (DDOD), UMC Utrecht Brain Center, University Utrecht, Utrecht, the Netherlands.
Niek E van der AaDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Thomas AlderliestenDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Floris GroenendaalDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Reint K JellemaDepartment of Neonatology, Maastricht University Medical Center, Maastricht, the Netherlands.
Cora H A NijboerDepartment of Development and Origin of Disease (DDOD), UMC Utrecht Brain Center, University Utrecht, Utrecht, the Netherlands.
Peter G J NikkelsDepartment of Pathology, University Medical Center Utrecht, University Utrecht, Utrecht, the Netherlands.
Martin LammensDepartment of Pathology, Antwerp University Hospital, Edegem, Belgium.
Manon J N L BendersDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Freek E HoebeekDepartment of Development and Origin of Disease (DDOD), UMC Utrecht Brain Center, University Utrecht, Utrecht, the Netherlands.
Jeroen DudinkDepartment of Neonatology, UMC Utrecht Brain Center, University Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands. j.dudink@umcutrecht.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In term neonates with hypoxic-ischemic encephalopathy (HIE), cerebellar injury is becoming more and more acknowledged. Animal studies demonstrated that Purkinje cells (PCs) are especially vulnerable for hypoxic-ischemic injury. In neonates, however, the extent and pattern of PC injury has not been investigated. The aim of this study was to characterize the morphology and distribution of PCs in the cerebellar vermis of term born neonates with HIE. Twenty-two term born neonates with severe HIE, several of which received therapeutic hypothermia, who underwent post-mortem autopsy of the brain including cerebellar vermis within three to five days after birth were included. Haematoxylin & Eosin (H&E) stained sections of the vermis were used to determine total PC count and morphology (normal, abnormal or non-classified) at the bases and crowns of the folia and of the lobules in both the anterior and posterior lobes. Differences in PC count and PC morphology between the anterior and posterior lobe and between the bases and crowns were compared. The total number of PCs was significantly higher at the crowns compared to the bases (p < 0.001) irrespective of the precise location. Besides, PCs at the bases more often had an abnormal morphology. Also, a significant difference between the injury in the anterior and posterior lobe was observed, notably at specific microscopic locations with more abnormal PCs in the posterior lobe. The number of PCs scored as abnormal was increased in the bases compared to the crowns, which might resemble supratentorial ulegyria.

Indexed as

Cerebellar VermisHypoxia-Ischemia, BrainPurkinje CellsCell CountFemaleHumansInfant, NewbornMaleCerebellumHypoxic-ischemic encephalopathyPurkinje cellsUlegyria

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.