Evidence map›Paper›PMID 23555729›Full record

ArticlePloS one2013

Etiology and audiological outcomes at 3 years for 364 children in Australia.

Hans-Henrik M Dahl, Teresa Y C Ching, Wendy Hutchison, Sanna Hou, Mark Seeto, Jessica Sjahalam-King

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 65 citations in OpenAlex.

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  11. Molecular diagnosis ofIntractable & rare diseases research · 2021
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  13. Etiology of Prelingual Hearing Loss in the Universal Newborn Hearing Screening Era: A Scoping Review.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2020
    Article
  14. Should You Follow the Better-Hearing Ear for Congenital Cytomegalovirus Infection and Isolated Sensorineural Hearing Loss?Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2020
    Article
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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

6 authors at 4 institutions in 1 country.

Hans-Henrik M DahlMurdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Australia.
Teresa Y C Ching
Wendy Hutchison
Sanna Hou
Mark Seeto
Jessica Sjahalam-King
Australian Hearing · AUNational Acoustic Laboratories · AUMurdoch Children's Research Institute · AURoyal Children's Hospital · AU

Funding

Longitudinal outcomes of hearing-impaired children: early vs later interventionR01DC008080 · NIDCD · AUSTRALIAN HEARING SERVICES · PI EASWAR, VIJAYALAKSHMI · 2007 to 2023
$4.6M
NIDCD NIH HHS R01 DC008080NIDCD NIH HHS R01DC008080
6 · The paper itself

Abstract

Hearing loss is an etiologically heterogeneous trait with differences in the age of onset, severity and site of lesion. It is caused by a combination of genetic and/or environmental factors. A longitudinal study to examine the efficacy of early intervention for improving child outcomes is ongoing in Australia. To determine the cause of hearing loss in these children we undertook molecular testing of perinatal "Guthrie" blood spots of children whose hearing loss was either detected via newborn hearing screening or detected later in infancy. We analyzed the GJB2 and SLC26A4 genes for the presence of mutations, screened for the mitochondrial DNA (mtDNA) A1555G mutation, and screened for congenital CMV infection in DNA isolated from dried newborn blood spots. Results were obtained from 364 children. We established etiology for 60% of children. One or two known GJB2 mutations were present in 82 children. Twenty-four children had one or two known SLC26A4 mutations. GJB2 or SLC26A4 changes with unknown consequences on hearing were found in 32 children. The A1555G mutation was found in one child, and CMV infection was detected in 28 children. Auditory neuropathy spectrum disorder was confirmed in 26 children whose DNA evaluations were negative. A secondary objective was to investigate the relationship between etiology and audiological outcomes over the first 3 years of life. Regression analysis was used to investigate the relationship between hearing levels and etiology. Data analysis does not support the existence of differential effects of etiology on degree of hearing loss or on progressiveness of hearing loss.

Indexed as

AudiologyAustraliaChild, PreschoolConnexin 26ConnexinsDisease ProgressionHearing LossHumansInfantInfant, NewbornMutationPrognosisConnexin 26ConnexinsGJB2 protein, human

Identifiers

PMID23555729
PMCPMC3610796
OpenAlexW2030444807

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.