Work

Integrative Genomic Analyses Identify Collagen Type XXI Alpha 1 Chain and ENPEP‐Fibroblast Growth Factor 5 Regulatory Pathways for Blood Pressure Variation in East Asian People

Year: 2026

Type: article

Abstract: Background Hypertension is a highly heritable cardiovascular disorder and a major determinant of cardiometabolic disease, including diabetes. However, the regulatory genes and tissue-specific mechanisms underlying blood pressure variations remain incompletely understood. Methods Leveraging a well-characterized prospective population-based cohort comprised of 27,308 participants from the Singapore Chinese Health Study (SCHS), we evaluated genome-wide genetic associations for five blood pressure traits: hypertension status, systolic blood pressure, diastolic blood pressure, mean arterial pressure (MAP) and pulse pressure (PP). Additionally, we conducted a transcriptome-wide association study (TWAS), integrating gene expression data from 49 tissues, followed by colocalization and fine-mapping to prioritize regulatory genes. Association of identified variants with incident diabetes was additionally evaluated in the longitudinal data. Results We validated 10 blood pressure loci ( P between 1.64 x 10 -20 – 4.10 x 10 -8 ) and identified an East-Asian specific splice donor variant at the COL21A1 gene associated with PP (rs149344559, P = 6.78 × 10 -10 ). Integrative analyses prioritized FGF5 in kidney cortex and ENPEP in pituitary tissue as candidate regulatory genes. The blood pressure-lowering allele at ENPEP (T allele, rs1879056) was associated with reduced risk of incident diabetes. Mediation analysis demonstrated that approximately 21% of the genetic association with diabetes was mediated through MAP (P indirect-effect = 2 x 10 -16 ). Conclusion This study refines genetic predispositions for blood pressure among East-Asians. We further delineate tissue-specific regulatory pathways underlying blood pressure variations and identify ENPEP -mediated dysfunctions linking blood pressure genetics to diabetes risk, underscoring integrated disease mechanisms.

Source: Journal of the American Heart Association

DOI: 10.1161/jaha.126.052309