Evidence map›Paper›PMID 34042254›Full record

ArticleAmerican journal of medical genetics. Part A2021

TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study.

Bradley Bowles, Alejandro Ferrer, Carla J Nishimura, Filippo Pinto E Vairo, Tristan Rey, Bruno Leheup, Jennifer Sullivan, Kelly Schoch, Nicholas Stong, Emanuele Agolini and 22 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02450851 (Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 26% 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.

NCT02450851 recruitingnot on this map

Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network

TypeobservationalSponsorNational Human Genome Research Institute (NHGRI)Ran2015 to 2028Enrolled20,000ConditionsGenetic Disease
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  6. Novel compound heterozygous variants in thePediatric investigation · 2024
    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

32 authors at 11 institutions in 5 countries.

Bradley BowlesCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-9468-3284
Alejandro FerrerCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-4883-3023
Carla J NishimuraMolecular Otolaryngology and Renal Research Laboratories, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
Filippo Pinto E VairoCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Tristan ReyFaculté de Chirurgie Dentaire, Université de Strasbourg, Strasbourg, France.
Bruno LeheupDépartement de Médecine Infantile, CHRU de Nancy, Nancy, France.
Jennifer SullivanDepartment of Pediatrics, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-8782-2183
Kelly SchochDepartment of Pediatrics, Duke University, Durham, North Carolina, USA.
Nicholas StongInstitute for Genomic Medicine, Columbia University, New York, New York, USA.
Emanuele AgoliniLaboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0001-6543-6225
Dario CocciadiferroLaboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Abigail WilliamsDepartment of Pediatrics, East Tennessee Children's Hospital, Knoxville, Tennessee, USA.
Alex CummingsDepartment of Pediatrics, East Tennessee Children's Hospital, Knoxville, Tennessee, USA.
Sara LoddoLaboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-8837-3519
Silvia GenoveseLaboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-5514-5018
Chelsea RoadhouseDepartment of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Kirsty McWalterGeneDx Inc., Gaithersburg, Maryland, USA.
Undiagnosed Diseases Network
Ingrid M WentzensenGeneDx Inc., Gaithersburg, Maryland, USA.
Chumei LiDepartment of Pediatrics, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0002-4207-6914
Dusica Babovic-VuksanovicCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Brendan C LanpherCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Maria Lisa DenticiGenetics and Rare Diseases Research Division, Molecular Genetics and Functional Genomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-9505-5906
Arun AnkalaEGL Genetics LLC, Tucker, Georgia, USA.ORCID 0000-0002-6373-9916
J Austin HammDepartment of Pediatrics, East Tennessee Children's Hospital, Knoxville, Tennessee, USA.
Bruno DallapiccolaGenetics and Rare Diseases Research Division, Molecular Genetics and Functional Genomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Francesca Clementina RadioGenetics and Rare Diseases Research Division, Molecular Genetics and Functional Genomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0003-1993-8018
Vandana ShashiDepartment of Pediatrics, Duke University, Durham, North Carolina, USA.
Benedicte GérardLaboratoires de Diagnostic génétique, Pôle de Biologie, Hôpitaux Universitaires de Strasbourg, Institut de Génétique Médicale d'Alsace, Strasbourg, France.
Agnes Bloch-ZupanFaculté de Chirurgie Dentaire, Université de Strasbourg, Strasbourg, France.ORCID 0000-0002-6511-2615
Richard J SmithMolecular Otolaryngology and Renal Research Laboratories, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
Eric W KleeCenter for Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Clinic · USBambino Gesù Children's Hospital · ITDuke University · USUniversity of Iowa · USCentre National de la Recherche Scientifique · FREmory University · USMcMaster University · CABristol-Myers Squibb (Germany) · DECentre Hospitalier Régional et Universitaire de Nancy · FREast Tennessee Children's Hospital · USUW Health University Hospital · US

Funding

An integrated and diverse genomic medicine program for undiagnosed diseasesU01HG007672 · NHGRI · DUKE UNIVERSITY · PI SHASHI, VANDANA · 2014 to 2022
$13.4M
NONSYNDROMIC HEARING LOSS--A COLLABORATIVE STUDYR01DC002842 · NIDCD · UNIVERSITY OF IOWA · PI SMITH, RICHARD J.H. · 1996 to 2024
$12.7M
Optimizing Genetic Testing for Deafness for Clinical DiagnosticsR01DC012049 · NIDCD · UNIVERSITY OF IOWA · PI TERRY A BRAUN, Thomas L. Casavant · 2011 to 2026
$8.7M
NHGRI NIH HHS U01 HG007672NIDCD NIH HHS R01 DC002842NIDCD NIH HHS R01 DC012049
6 · The paper itself

Abstract

Biallelic loss-of-function variants in the thrombospondin-type laminin G domain and epilepsy-associated repeats (TSPEAR) gene have recently been associated with ectodermal dysplasia and hearing loss. The first reports describing a TSPEAR disease association identified this gene is a cause of nonsyndromic hearing loss, but subsequent reports involving additional affected families have questioned this evidence and suggested a stronger association with ectodermal dysplasia. To clarify genotype-phenotype associations for TSPEAR variants, we characterized 13 individuals with biallelic TSPEAR variants. Individuals underwent either exome sequencing or panel-based genetic testing. Nearly all of these newly reported individuals (11/13) have phenotypes that include tooth agenesis or ectodermal dysplasia, while three newly reported individuals have hearing loss. Of the individuals displaying hearing loss, all have additional variants in other hearing-loss-associated genes, specifically TMPRSS3, GJB2, and GJB6, that present competing candidates for their hearing loss phenotype. When presented alongside previous reports, the overall evidence supports the association of TSPEAR variants with ectodermal dysplasia and tooth agenesis features but creates significant doubt as to whether TSPEAR variants are a monogenic cause of hearing loss. Further functional evidence is needed to evaluate this phenotypic association.

Indexed as

Genetic VariationPhenotypeAllelesAmino Acid SubstitutionAnodontiaCohort StudiesEctodermal DysplasiaFemaleGenetic Association StudiesGenetic LociHumansMaleMutationPedigreeProteinsRadiographyProteinsTSPEAR protein, humanautosomal recessive deafnessectodermal dysplasiahearing losstooth agenesisTSPEAR

Identifiers

PMID34042254
PMCPMC8361973
OpenAlexW3165039645

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.