Evidence map›Paper›PMID 33621819›Full record

ArticleEuropean journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society2021

Brain morphological abnormalities in children with cyclin-dependent kinase-like 5 deficiency disorder.

Yingying Tang, Zhong Irene Wang, Shaheera Sarwar, Joon Yul Choi, Shan Wang, Xiaoming Zhang, Sumit Parikh, Ahsan N Moosa, Elia Pestana-Knight

Open access · greenAbstract read
In one paragraph

Article in European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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  4. Review
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

9 authors at 2 institutions in 2 countries.

Yingying TangDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, Sichuan, China; Epilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Zhong Irene WangEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA. Electronic address: wangi2@ccf.org.
Shaheera SarwarNortheast Ohio Medical University, Rootstown, OH, USA; Epilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Joon Yul ChoiEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Shan WangEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Xiaoming ZhangEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Sumit ParikhCenter for Pediatric Neuroscience, Cleveland Clinic, Cleveland, OH, USA.
Ahsan N MoosaEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Elia Pestana-KnightEpilepsy Center, Cleveland Clinic, Cleveland, OH, USA.
Cleveland Clinic · USSichuan University · CN

Funding

MR Fingerprinting for EpilepsyR01NS109439 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI Dan Ma, Zhong Irene Wang · 2019 to 2026
$4.2M
NINDS NIH HHS R01 NS109439
6 · The paper itself

Abstract

backgroundTo quantitatively evaluate the brain MRI morphological abnormalities in patients with cyclin-dependent kinase-like 5 deficiency disorder (CDD) on a group level and longitudinally.

methodsWe performed surface-based MRI analysis on high-resolution T1-weighted images on three CDD patients scanned at age of three years, and compared with 12 age- and gender-matched healthy controls. We further examined the longitudinal morphological changes in one patient with a follow-up of 5 years.

resultsCDD patients presented significant reductions in total intracranial volume, total gray matter (GM) volume and subcortical GM volume compared to controls. For subcortical regions, significant GM volume reductions were seen in the brain stem, bilateral thalamus, bilateral hippocampus, bilateral cerebellum and left amygdala. Although GM volume of cortical mantle did not show statistical differences overall, significant reduction was detected in bilateral parietal, left occipital and right temporal lobes. Cortical thickness exhibited significant decreases in bilateral occipital, parietal and temporal lobes, while surface area did not show any significant differences. Longitudinal follow-up in one patient revealed a monotonic downward trend of relative volume in the majority of brain regions. The relative surface area appeared to gain age-related growth, whereas the relative cortical thickness exhibited a striking progressive decline over time.

conclusionsQuantitative morphology analysis in children with CDD showed global volume loss in the cortex and more notably in the subcortical gray matter, with a progressive trend along with the disease course. Cortical thickness is a more sensitive measure to disclose cortical atrophy and disease progression than surface area.

Indexed as

AtrophyBrainChild, PreschoolDisease ProgressionEpileptic SyndromesFemaleHumansInfantMagnetic Resonance ImagingMaleSpasms, InfantileCDKL5 deficiency disorder (CDD)ChildrenEpileptic encephalopathyMagnetic resonance imaging (MRI)Surface-based analysis

Identifiers

PMID33621819
PMCPMC8026562
OpenAlexW3132071754

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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.