Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing 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.
Hiroko MorisakiDepartment of Medical Genetics Sakakibara Heart Institute Tokyo Japan.ORCID 0000-0002-6956-6374
Atsushi SuzukiDepartment of Cardiology Tokyo Women's Medical University Tokyo Japan.
Takeshi KashimuraDepartment of Cardiovascular Medicine Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.
Shouji MatsushimaDepartment of Cardiovascular Medicine, Faculty of Medical Sciences Kyushu University Fukuoka Japan.ORCID 0000-0001-9774-4513
Keiko GotoDepartment of Cardiovascular Biology and Medicine Juntendo University Graduate School of Medicine Tokyo Japan.ORCID 0000-0001-6684-3332
Masahiro WanezakiDepartment of Cardiology, Pulmonology, and Nephrology Yamagata University Faculty of Medicine Yamagata Japan.ORCID 0000-0001-7893-336X
Ryo AbeDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0002-3922-6029
Takanobu YamadaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0002-8258-4219
Takashige TobitaDepartment of Cardiology Tokyo Women's Medical University Tokyo Japan.
Manami KatohDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0001-5634-9170
Toshiyuki KoDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0002-9043-064X
Masamichi ItoDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0001-6945-3137
Junichi IshidaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0001-9703-9419
Eisuke AmiyaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0003-2810-8040
Masaru HatanoDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0003-2135-3625
Norifumi TakedaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0003-4818-3347
Hiroyuki MoritaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.
Masafumi WatanabeDepartment of Cardiology, Pulmonology, and Nephrology Yamagata University Faculty of Medicine Yamagata Japan.ORCID 0000-0002-8672-7483
Tohru MinaminoDepartment of Cardiovascular Biology and Medicine Juntendo University Graduate School of Medicine Tokyo Japan.ORCID 0000-0003-1627-6151
Junichi YamaguchiDepartment of Cardiology Tokyo Women's Medical University Tokyo Japan.ORCID 0000-0003-0967-0978
Takayuki InomataDepartment of Cardiovascular Medicine Niigata University Graduate School of Medical and Dental Sciences Niigata Japan.ORCID 0009-0007-4009-2359
Hiroyuki TsutsuiDepartment of Cardiovascular Medicine, Faculty of Medical Sciences Kyushu University Fukuoka Japan.
Morimasa TakayamaDepartment of Cardiology Sakakibara Heart Institute Tokyo Japan.ORCID 0000-0001-5736-0064
Hiroaki KitaokaDepartment of Cardiology and Geriatrics, Kochi Medical School Kochi University Kochi Japan.ORCID 0000-0003-0529-7125
Norihiko TakedaDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0003-1023-6116
Issei KomuroDepartment of Frontier Cardiovascular Science The University of Tokyo Graduate School of Medicine Tokyo Japan.ORCID 0000-0002-0714-7182
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
backgroundIn patients with hypertrophic cardiomyopathy (HCM), genetic testing is crucial for cascade screening and risk stratification. However, it remains limited by financial and logistical constraints, necessitating prioritization. The Mayo HCM Genotype Predictor Score, based on clinical and echocardiographic variables, estimates genotype positivity with acceptable performance. Although sarcomeric variants are also associated with electrophysiological abnormalities, ECG parameters were not incorporated into this model. This study aimed to enhance genotype prediction in HCM by integrating ECG parameters.
methodsWe retrospectively analyzed 466 patients with HCM from a Japanese multicenter cohort. Genotype positivity was defined as harboring pathogenic/likely pathogenic variants in sarcomere-encoding genes. Candidate ECG variables were selected via multivariable logistic regression with bootstrap aggregation. A point-based novel score was developed and internally validated using cross-validation. Model performance was assessed by the area under the receiver operating characteristic curve and Akaike's information criterion.
resultsGenotype-positive patients (30.3%) more frequently exhibited atrial fibrillation, intraventricular conduction disturbance, lower prevalence of high voltage, and abnormal T-wave inversion in precordial leads than genotype-negative patients and thus were incorporated into the novel Mayo-ECG score. This score stratified genotype positivity from 7.1% (score ≤-1) to 91.4% (score ≥4), and its discriminative performance (area under the receiver operating characteristic curve, 0.81 [95% CI, 0.77-0.85]) outperformed the Mayo score (area under the receiver operating characteristic curve, 0.76 [95% CI, 0.71-0.81];
conclusionsThe Mayo-ECG improves genotype prediction, outperforming the conventional model. Given its simplicity, this model has the potential to prioritize genetic testing in HCM.
Indexed as
Cardiomyopathy, HypertrophicElectrocardiographyAdultAgedFemaleGenetic Predisposition to DiseaseGenetic TestingGenotypeHumansJapanMaleMiddle AgedPhenotypePredictive Value of TestsRetrospective StudiesRisk AssessmentECGgenotypegenotype predictionhypertrophic cardiomyopathy
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.
Integrating ECG Into the Mayo Score Enhances Genotype Prediction in Hypertrophic Cardiomyopathy. · full record | OpenQuestion