Key result
Genome-wide association analyses in East Asian populations revealed significant genetic correlations between myocardial infarction and systolic blood pressure (rg = 0.35) and between heart failure and diastolic blood pressure (rg = 0.54).
Why the study?
The shared genetic architecture across CVDs and related cardiometabolic traits remains underexplored, particularly in East Asian populations.
Observational (n=92,615)
Yes
Effect estimate: rg = 0.54
p-value: p=9.84 × 10-9
The study identifies shared genetic determinants and novel pleiotropic loci connecting cardiovascular diseases and cardiometabolic traits in East Asian populations, highlighting tissue-specific regulatory patterns.
Hypothesis-generating for shared CVD loci in East Asians; leaves open clinical utility for risk prediction or therapy.
Introduction Cardiovascular diseases (CVDs), including myocardial infarction (MI), heart failure (HF), atrial fibrillation (AF), and arrhythmia, are major contributors to global mortality and often share overlapping risk factors and pathophysiological mechanisms. While genome-wide association studies (GWAS) have identified many loci for individual CVDs, the shared genetic architecture across related traits—particularly in East Asian populations—remains underexplored. Materials and methods We integrated large-scale GWAS summary statistics from East Asian populations to perform genome-wide and local genetic correlation analyses across four CVD phenotypes and five cardiometabolic traits (blood pressure and lipid levels). Using stratified LD score regression, we assessed tissue-specific heritability enrichment. Multi-trait analysis of GWAS (MTAG) was then employed to identify pleiotropic loci associated with multiple traits, with functional annotation and expression quantitative trait loci (eQTL) data used to explore biological relevance. Results We observed extensive genetic correlations among CVDs and between CVDs and cardiometabolic traits, with HF showing the strongest connections to both MI and arrhythmia. Notable genome-wide correlations were found between MI and SBP (rg = 0.35, P = 1.59 × 10 −14 ) and between HF and DBP (rg = 0.54, P = 9.84 × 10 −9 ). Stratified heritability analyses revealed significant enrichment in heart and arterial tissues, highlighting the relevance of cardiovascular-specific regulatory elements. MTAG identified several pleiotropic loci, including established genes such as APOB and MC4R , and novel East Asian-enriched signals such as QSOX2 and GUCY1A1 / GUCY1B1 . Functional data indicated that QSOX2 variants regulate gene expression in arterial and cardiac tissues, implicating redox regulation in HF and hypertension pathogenesis. Conclusion Our findings provide comprehensive insight into the shared genetic determinants of cardiovascular and metabolic diseases in East Asian populations. The identification of pleiotropic and ancestry-specific loci, along with tissue-specific regulatory patterns, underscores the need for integrative multi-trait and population-informed approaches in cardiovascular genetics and risk prediction.
No takes yet. Share an insight, caveat, or question.
Zhong et al. (2025) conducted an observational in Cardiovascular diseases and cardiometabolic traits (n=92,615). Genetic variants (pleiotropic loci) vs. Reference alleles was evaluated on Genome-wide genetic correlation between heart failure and diastolic blood pressure (rg = 0.54, p=9.84 × 10-9). Genome-wide association analyses in East Asian populations revealed significant genetic correlations between myocardial infarction and systolic blood pressure (rg = 0.35) and between heart failure and diastolic blood pressure (rg = 0.54).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: