Evidence map›Paper›PMID 31001105›Full record

ArticleFrontiers in aging neuroscience2019

5XFAD Mice Show Early Onset Gap Detection Deficits.

Katherine Kaylegian, Amanda J Stebritz, Aldis P Weible, Michael Wehr

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

4 authors.

Katherine KaylegianDepartment of Psychology, Institute of Neuroscience, University of Oregon, Eugene, OR, United States.
Amanda J StebritzDepartment of Psychology, Institute of Neuroscience, University of Oregon, Eugene, OR, United States.
Aldis P WeibleDepartment of Psychology, Institute of Neuroscience, University of Oregon, Eugene, OR, United States.
Michael WehrDepartment of Psychology, Institute of Neuroscience, University of Oregon, Eugene, OR, United States.

Funding

Circuit mechanisms underlying temporal processing in auditory cortexR01DC015828 · NIDCD · UNIVERSITY OF OREGON · PI WEHR, MICHAEL · 2017 to 2021
$2.9M
NIDCD NIH HHS R01 DC015828
6 · The paper itself

Abstract

Alzheimer's patients show auditory temporal processing deficits very early in disease progression, before the onset of major cognitive impairments. In addition to potentially contributing to speech perception and communication deficits in patients, this also represents a potential early biomarker for Alzheimer's. For this reason, tests of temporal processing such as gap detection have been proposed as an early diagnosis tool. For a biomarker such as gap detection deficits to have maximum clinical value, it is important to understand what underlying neuropathology it reflects. For example, temporal processing deficits could arise from alterations at cortical, midbrain, or brainstem levels. Mouse models of Alzheimer's disease can provide the ability to reveal in detail the molecular and circuit pathology underlying disease symptoms. Here we tested whether 5XFAD mice, a leading Alzheimer's mouse model, exhibit impaired temporal processing. We found that 5XFAD mice showed robust gap detection deficits. Gap detection deficits were first detectable at about 2 months of age and became progressively worse, especially for males and for longer gap durations. We conclude that 5XFAD mice are well-suited to serve as a model for understanding the circuit mechanisms that contribute to Alzheimer's-related gap detection deficits.

Indexed as

acoustic startle responseAlzheimer'sauditory processinggap detectionmouse model

Identifiers

PMID31001105
PMCPMC6454034

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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.