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Record W4410597258 · doi:10.1016/j.ajhg.2025.04.016

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

2025· article· en· W4410597258 on OpenAlexafffund
Michele Nicastro, Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir, Vinicius Tragante, Lukáš Mach, Alex V. Postma, Elisabeth M. Lodder, Karel van Duijvenboden, Rob Zwart, Leander Beekman, Lingshuang Wu, Sean J. Jurgens, Paul A. van der Zwaag, Mariëlle Alders, Mona Allouba, Yasmine Aguib, José L. Santomé, David de Uña, Lorenzo Monserrat, Antonio M. A. Miranda, Kazumasa Kanemaru, James Cranley, Ingeborg E. van Zeggeren, Eleonora Aronica, Michela Ripolone, Simona Zanotti, Garðar Sveinbjörnsson, Erna V. Ivarsdottir, Hilma Hólm, Daníel F. Guðbjartsson, Ástrós Skúladóttir, Lincoln Nadauld, Kirk U. Knowlton, Sisse Rye Ostrowski, Erik Sørensen, Ole Birger Pedersen, Jonas Ghouse, Søren A Rand, Henning Bundgaard, Henrik Ullum, Christian Erikstrup, Bitten Aagaard, Mie Topholm Bruun, Mette Christiansen, Henrik Kjærulf Jensen, Deanna Alexis Carere, Christopher T. Cummings, Kristen Fishler, Pernille Mathiesen Tørring, Klaus Brusgaard, Trine Juul, Lotte Saaby, Bo Gregers Winkel, Jens Mogensen, Francesco Fortunato, Giacomo P. Comi, Dario Ronchi, J. Peter van Tintelen, Michela Noseda, Michael V. Airola, Imke Christiaans, Arthur A.M. Wilde, Ronald Wilders, Sally‐Ann B. Clur, Arie O. Verkerk, Connie R. Bezzina, Najim Lahrouchi

Bibliographic record

VenueThe American Journal of Human Genetics · 2025
Typearticle
Languageen
FieldMedicine
TopicCardiomyopathy and Myosin Studies
Canadian institutionsUniversité de MontréalMontreal Heart Institute
FundersMinistero dell'Università e della RicercaMinistero della SaluteNIHR Imperial Biomedical Research CentreZonMwNational Institutes of HealthCanada Research ChairsNational Institute of General Medical SciencesUniversité Nice Sophia AntipolisNational Institute for Health and Care ResearchBritish Society for Heart FailureDeutsches Zentrum für Herz-KreislaufforschungRosetrees TrustDipartimenti di EccellenzaMinistero dell’Istruzione, dell’Università e della RicercaBritish Heart FoundationNederlandse Organisatie voor Wetenschappelijk OnderzoekWellcome TrustUniversità degli Studi di MilanoHartstichtingAmerican Heart Association
KeywordsGene knockdownAlleleSick sinus syndromeHypertrophic cardiomyopathyBiologyPhenotypeGeneticsPopulationCardiomyopathyInternal medicineMedicineGeneHeart failure

Abstract

fetched live from OpenAlex

POPDC2 encodes the Popeye domain-containing protein 2, which has an important role in cardiac pacemaking and conduction, due in part to its cyclic AMP (cAMP)-dependent binding and regulation of TREK-1 potassium channels. Loss of Popdc2 in mice results in sinus pauses and bradycardia, and morpholino-mediated knockdown of popdc2 in zebrafish results in atrioventricular (AV) block. We identified bi-allelic variants in POPDC2 in four families with a phenotypic spectrum consisting of sinus node dysfunction, AV conduction defects, and hypertrophic cardiomyopathy. Using homology modeling, we show that the identified variants are predicted to diminish the ability of POPDC2 to bind cAMP. In in vitro electrophysiological studies, we demonstrated that, in contrast with wild-type POPDC2, variants found in affected individuals failed to increase TREK-1 current density. While muscle biopsy of an affected individual did not show clear myopathic disease, it showed significantly reduced abundance of both POPDC1 and POPDC2, suggesting that stability and/or membrane trafficking of the POPDC1-POPDC2 complex is impaired by pathogenic variants in either protein. Single-cell RNA sequencing from human hearts demonstrated that co-expression of POPDC1 and POPDC2 was most prevalent in AV node, AV node pacemaker, and AV bundle cells. Using population-level genetic data of more than 1 million individuals, we show that none of the familial variants were associated with clinical outcomes in heterozygous state, suggesting that heterozygous family members are unlikely to develop clinical manifestations and therefore might not necessitate clinical follow-up. Our findings provide evidence for bi-allelic variants in POPDC2 causing a Mendelian autosomal recessive cardiac syndrome.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0020.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0030.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.019
GPT teacher head0.286
Teacher spread0.267 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2025
Admission routes2
Has abstractyes

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