Evidence map›Paper›PMID 32462407›Full record

Observational studyNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2020

Finding Suitable Clinical Endpoints for a Potential Treatment of a Rare Genetic Disease: the Case of ARID1B.

Matthijs D Kruizinga, Rob G J A Zuiker, Elif Sali, Marieke L de Kam, Robert J Doll, Geert Jan Groeneveld, Gijs W E Santen, Adam F Cohen

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Clonazepam repurposing inJournal of medical genetics · 2025
    Trial
  3. Article
  4. Review
  5. Pleiotropic effects of a high confidence Autism Spectrum Disorder gene,Neurobiology of sleep and circadian rhythms · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Article
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

8 authors at 2 institutions in 1 country.

Matthijs D KruizingaCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands. mkruizinga@chdr.nl.ORCID http://orcid.org/0000-0002-2054-2187
Rob G J A ZuikerCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Elif SaliCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Marieke L de KamCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Robert J DollCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Geert Jan GroeneveldCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Gijs W E SantenDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands.
Adam F CohenCentre for Human Drug Research, Zernikedreef 8, 2333 CL, Leiden, the Netherlands.
Centre for Human Drug Research · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a lack of reliable, repeatable, and non-invasive clinical endpoints when investigating treatments for intellectual disability (ID). The aim of this study is to explore a novel approach towards developing new endpoints for neurodevelopmental disorders, in this case for ARID1B-related ID. In this study, twelve subjects with ARID1B-related ID and twelve age-matched controls were included in this observational case-control study. Subjects performed a battery of non-invasive neurobehavioral and neurophysiological assessments on two study days. Test domains included cognition, executive functioning, and eye tracking. Furthermore, several electrophysiological assessments were performed. Subjects wore a smartwatch (Withings® Steel HR) for 6 days. Tests were systematically assessed regarding tolerability, variability, repeatability, difference with control group, and correlation with traditional endpoints. Animal fluency, adaptive tracking, body sway, and smooth pursuit eye movements were assessed as fit-for-purpose regarding all criteria, while physical activity, heart rate, and sleep parameters show promise as well. The event-related potential waveform of the passive oddball and visual evoked potential tasks showed discriminatory ability, but EEG assessments were perceived as extremely burdensome. This approach successfully identified fit-for-purpose candidate endpoints for ARID1B-related ID and possibly for other neurodevelopmental disorders. Next, results could be replicated in different ID populations or the assessments could be included as exploratory endpoint in interventional trials in ARID1B-related ID.

Indexed as

AdolescentAdultAnimalsCase-Control StudiesChildChild, PreschoolDNA-Binding ProteinsEndpoint DeterminationEvoked Potentials, VisualExecutive FunctionFemaleGenetic VariationHumansIntellectual DisabilityMalePhotic StimulationARID1B protein, humanDNA-Binding ProteinsTranscription FactorsARID1BBiomarkersCognitionElectrophysiologyEndpointExecutive functioningEye tracking

Identifiers

PMID32462407
PMCPMC7609730
OpenAlexW3030878734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.