rs11570058 - MYBPC3

Magnitude 2.2 · 1 study on file

Reported associations

  • Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population - Unknown journal (n.d.) · Unknown authors · PubMed 41184235

    ABSTRACT: To understand the genetic basis of heart failure (HF) in the Japanese population, we performed genome-wide association studies (GWASs) comprising 16,251 all-cause HF cases, 4254 HF with reduced ejection fraction (HFrEF) cases, 7154 HF with preserved ejection fraction cases, and 11,122 non-ischemic HF cases among 213,828 individuals and identified five novel loci. A subsequent cross-ancestry meta-analysis and multi-trait analysis of the GWAS data identified 19 novel loci in total, with 31 out of the 76 genome-wide significant loci associated with HFrEF despite its smaller sample size. Among these susceptibility loci, a common non-coding variant in TTN (rs1484116) was associated with reduced cardiac function and worse long-term mortality. We leveraged the HF meta-GWASs along with c


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Discuss with your doctor

  • Non-ischemic heart failure screening plan Moderate

    MYBPC3 rs11570058 A allele is associated with significantly increased non-ischemic heart failure risk in a large genome-wide association study

    Discuss baseline echocardiography and surveillance plan with your cardiologist

Screening

  • Monitor for heart failure symptoms Moderate

    With increased genetic predisposition to non-ischemic heart failure, early symptom recognition allows timely medical intervention

    Report new dyspnea, fatigue, lower extremity edema, or reduced exercise tolerance to your doctor