Evidence map›Paper›PMID 37239215›Full record

ArticleBrain sciences2023

Emergence of Treadmill Running Ability and Quantitative Assessment of Gait Dynamics in Young Ts65Dn Mice: A Mouse Model for Down Syndrome.

Jonah J Scott-McKean, Ryan Jones, Mark W Johnson, Joyce Mier, Ines A Basten, Melissa R Stasko, Alberto C S Costa

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

7 authors at 2 institutions in 1 country.

Jonah J Scott-McKeanDepartment of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH 44106-6090, USA.
Ryan JonesCollege of Medicine and Life Sciences, The University of Toledo, Toledo, OH 43606-3390, USA.
Mark W JohnsonDepartment of Pediatrics, Case Western Reserve University, Cleveland, OH 44106-6090, USA.ORCID 0009-0001-3958-6163
Joyce MierPhysical Therapy Program, University of Wisconsin, Madison, WI 53706-1532, USA.ORCID 0009-0008-8776-0120
Ines A BastenPsychiatric Hospital Asster, 3800 Sint-Truiden, Belgium.
Melissa R StaskoDepartment of Pediatrics, Case Western Reserve University, Cleveland, OH 44106-6090, USA.ORCID 0000-0003-1412-0727
Alberto C S CostaDepartment of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH 44106-6090, USA.ORCID 0000-0002-7855-1190
Case Western Reserve University · USUniversity of Wisconsin–Madison · US

Funding

Alana's Foundation 124124
6 · The paper itself

Abstract

Down syndrome (DS), which results from the complete or partial trisomy of chromosome 21 (trisomy-21), is the most common genetically defined cause of intellectual disability. Trisomy-21 also produces, or is associated with, many neurodevelopmental phenotypes and neurological comorbidities, including delays and deficits in fine and gross motor development. The Ts65Dn mouse is the most studied animal model for DS and displays the largest known subset of DS-like phenotypes. To date, however, only a small number of developmental phenotypes have been quantitatively defined in these animals. Here, we used a commercially available high-speed, video-based system to record and analyze the gait of Ts65Dn and euploid control mice. Longitudinal treadmill recordings were performed from p17 to p35. One of the main findings was the detection of genotype- and sex-dependent developmental delays in the emergence of consistent, progressive-intensity gait in Ts65Dn mice when compared to control mice. Gait dynamic analysis showed wider normalized front and hind stances in Ts65Dn mice compared to control mice, which may reflect deficits in dynamic postural balance. Ts65Dn mice also displayed statistically significant differences in the variability in several normalized gait measures, which were indicative of deficits in precise motor control in generating gait.

Indexed as

balancedown syndromemotor controlneurodevelopmenttrisomy 21Ts65Dn mouse

Identifiers

PMID37239215
PMCPMC10216633
OpenAlexW4367627388

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.