MétaCan
Menu
Back to cohort
Record W4412679201 · doi:10.1101/2025.07.26.25332081

The contribution of <i>RBM20</i> truncating variants to human cardiomyopathy

2025· preprint· en· W4412679201 on OpenAlexaff
Brendan J. Floyd, Joyce Njoroge, Vikki A. Krysov, Bruna Gomes, Ryan Murtha, Chiaka Aribeana, Douglas Cannie, Eric D. Smith, Alessia Paldino, Emily Brown, Andreas S. Barth, Erkan İlhan, Renee L. Johnson, Julianne Wojciak, Mohamad A. Alkhayat, Sharon Graw, Kristen Medo, Jan Haas, C. Anwar A. Chahal, Kai Fenzl, Lars M. Steinmetz, Michael H. Gollob, Euan A. Ashley, Sharlene M. Day, Daniel P. Judge, Jason Roberts, Vasanth Vedantham, Chad Mao, Diane Fatkin, Neal K. Lakdawala, Matthew R.G. Taylor, Luisa Mestroni, Ardan M. Saguner, Upasana Tayal, Julia Cadrin‐Tourigny, Andrew D. Krahn, Cynthia A. James, Matteo Dal Ferro, Gianfranco Sinagra, Marco Merlo, Anjali Owens, Nosheen Reza, Sara Saberi, Adam Helms, Perry Elliott, Benjamin Meder, Victoria N. Parikh

Bibliographic record

VenuemedRxiv · 2025
Typepreprint
Languageen
FieldMedicine
TopicCardiovascular Effects of Exercise
Canadian institutionsMontreal Heart InstituteMcMaster UniversityMcMaster Children's HospitalHamilton General HospitalUniversity of TorontoUniversity of British Columbia
FundersSchweizerische HerzstiftungCytokineticsSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen ForschungAlexion PharmaceuticalsBaugarten StiftungPfizerNational Institutes of HealthNational Science Foundation
KeywordsMedicineCardiologyInternal medicineEjection fractionDilated cardiomyopathySudden cardiac deathCardiomyopathyHeart failureCohortRestrictive cardiomyopathyPenetranceSudden deathGenetics

Abstract

fetched live from OpenAlex

Abstract Background Genetic diagnosis has become increasingly important to guide clinical decision making for patients with dilated cardiomyopathy (DCM). Disease-causing (P/LP) missense variants in the gene RBM20 cause a highly penetrant arrhythmogenic dilated cardiomyopathy (DCM), but the role of truncating RBM20 variants ( RBM20tvs ) is unclear. Objective Assess the contribution of RBM20tvs to DCM. Methods We assembled an international cohort of DCM patients with RBM20 variants and used data from the genome-first UK Biobank (UKB) to assess the etiologic fraction, natural history and penetrance of RBM20tvs . Results The etiologic fraction of RBM20tvs in arrhythmogenic DCM was modest (0.53[0.32,0.67], p=7.5×10 -5 ). RBM20tv DCM patients presented to referral centers later in life than RBM20 P/LP DCM patients (53±10 vs. 34±18 years, p=4×10 -3 ), and were less likely to have a family history of sudden cardiac arrest (20% vs. 65%, p= 0.046) or cardiomyopathy (20% vs. 78% p=5.4×10 -3 ). There was no significant difference in age- and sex-adjusted incident major heart failure or arrhythmia events between RBM20tv and RBM20 P/LP DCM patients, though sex-adjusted lifetime hazard was reduced in RBM20tv DCM (HR 0.15[0.03,0.66],p=0.009). In UKB, lifetime incidence of cardiomyopathy, heart failure, or major ventricular arrhythmia diagnosis was lower in participants with RBM20tvs than in those with TTNtvs (HR 0.55 [0.36,0.84], p=5.9×10 -3 ). Conclusions RBM20tvs contribute to arrhythmogenic DCM phenotypes, but confer milder disease severity alone than RBM20 P/LP variants, and reduced lifetime disease penetrance compared to TTNtvs . Their potential for additive interactions with other damaging variants should be considered in DCM patients and families.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation 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 score0.474
Threshold uncertainty score0.988

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

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 head0.011
GPT teacher head0.289
Teacher spread0.277 · 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 teacher head, 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

Citations3
Published2025
Admission routes1
Has abstractyes

Explore more

Same venuemedRxivSame topicCardiovascular Effects of ExerciseFrench-language works237,207