Evidence map›Paper›PMID 37573959›Full record

ArticlePhysiology & behavior2023

Ultrasonic vocalization phenotypes in the Ts65Dn and Dp(16)1Yey mouse models of Down syndrome.

Tiffany J Glass, Charles Lenell, Erin H Fisher, Qiuyu Yang, Nadine P Connor

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Tiffany J GlassDepartment of Surgery, Division of Otolaryngology, University of Wisconsin, Madison, WI, USA. Electronic address: glass@surgery.wisc.edu.
Charles LenellDepartment of Communication Sciences and Disorders, University of Northern Colorado, Greeley, CO, USA.
Erin H FisherDepartment of Surgery, Division of Otolaryngology, University of Wisconsin, Madison, WI, USA.
Qiuyu YangDepartment of Surgery, Statistical Analysis and Research Programming Core, University of Wisconsin, Madison, WI, USA.
Nadine P ConnorDepartment of Surgery, Division of Otolaryngology, University of Wisconsin, Madison, WI, USA; Department of Communication Sciences and Disorders, University of Wisconsin, Madison, WI, USA.
University of Wisconsin–Madison · US

Funding

Mechanisms of Down syndrome-associated swallowing dysfunction in mouse modelsR01DC019735 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI NADINE P CONNOR, Tiffany Glass · 2022 to 2026
$3.4M
Bioenergetic Mechanisms of Tongue Muscle FatigueR01DC018071 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI CONNOR, NADINE P · 2019 to 2023
$2.5M
Tongue maturation deficits in a mouse model of Down syndromeR01HD104640 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI GLASS, TIFFANY · 2021 to 2025
$2.4M
Study of Head and Neck Muscular Disruption in Mouse Models of Down SyndromeF32DC014885 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI GLASS, TIFFANY · 2016 to 2016
$59k
Effects of Primary Sex Hormones and Hormone Receptors on the Vocal MechanismF32DC020093 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI LUNARIS, CHARLIE LENELL · 2021 to 2021
$48k
NICHD NIH HHS R01 HD104640NIDCD NIH HHS F32 DC014885NIDCD NIH HHS F32 DC020093NIDCD NIH HHS R01 DC018071NIDCD NIH HHS R01 DC019735
6 · The paper itself

Abstract

Down syndrome (DS) is a developmental disorder associated with a high incidence of challenges in vocal communication. DS can involve medical co-morbidities and structural social factors that may impact communication outcomes, which can present difficulties for the study of vocal communication challenges. Mouse models of DS may be used to study vocal communication differences associated with this syndrome and allow for greater control and consistency of environmental factors. Prior work has demonstrated differences in ultrasonic vocalization (USV) of the Ts65Dn mouse model of DS at a young adult age, however it is not known how USV characteristics are manifested at mature ages. Given that the aging process and age-related co-morbidities may also impact communication in DS, addressing this gap in knowledge may be of value for efforts to understand communication difficulties in DS across the lifespan. The current study hypothesized that the Ts65Dn and Dp(16)1Yey mouse models of DS would demonstrate differences in multiple measures of USV communication at a mature adult age of 5 months.

methodsTs65Dn mice (n = 16) and euploid controls (n = 19), as well as Dp(16)1Yey mice (n = 20) and wild-type controls (n = 22), were evaluated at 5 months of age for USV production using a mating paradigm. Video footage of USV sessions were analyzed to quantify social behaviors of male mice during USV testing sessions. USV recordings were analyzed using Deepsqueak software to identify 10 vocalization types, which were quantified for 11 acoustic measures.

resultsTs65Dn, but not Dp(16)1Yey, showed significantly lower proportions of USVs classified as Step Up, Short, and Frequency Steps, and significantly higher proportions of USVs classified as Inverted U, than euploid controls. Both Ts65Dn and Dp(16)1Yey groups had significantly greater values for power and tonality for USVs than respective control groups. While Ts65Dn showed lower frequencies than controls, Dp(16)1Yey showed higher frequencies than controls. Finally, Ts65Dn showed reductions in a measure of complexity for some call types. No significant differences between genotype groups were identified in analysis of behaviors during testing sessions.

conclusionWhile both Ts65Dn and Dp(16)1Yey show significant differences in USV measures at 5 months of age, of the two models, Ts65Dn shows a relatively greater numbers of differences. Characterization of communication phenotypes in mouse models of DS may be helpful in laying the foundation for future translational advances in the area of communication difficulties associated with DS.

Indexed as

Down SyndromeAnimalsDisease Models, AnimalMaleMicePhenotypeUltrasonicsVocalization, AnimalDown syndromeDp(16)1YeyMouseTs65DnUltrasonic vocalizationUSV

Identifiers

PMID37573959
PMCPMC10592033
OpenAlexW4385753490

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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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.