rs11708647 - PCOLCE2 - HLMR1
Magnitude 2.2 · 1 study on file
Reported associations
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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation - Unknown journal (n.d.) · Unknown authors · PubMed 27841878
ABSTRACT: Longitudinal electronic health records on 99,785 Genetic Epidemiology Research on Adult Health and Aging (GERA) cohort individuals provided 1,342,814 systolic and diastolic blood pressure measurements for a genome-wide association study on long-term average systolic, diastolic, and pulse pressure. We identified 39 novel among 75 significant loci (P≤5×10−8), most replicating in the combined International Consortium for Blood Pressure (ICBP, n=69,396) and UK Biobank (UKB, n=152,081) studies. Combining GERA with ICBP yielded 36 additional novel loci, most replicating in UKB. Combining all three studies (n=321,262) yielded 241 additional genome-wide significant loci, although for these no replication sample was available. All associated loci explained 2.9%/2.5%/3.1% of systolic/
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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cardiovascular risk stratification Moderate
rs11708647 G allele increases pulse pressure via PCOLCE2-mediated vascular remodeling, affecting arterial stiffness and cardiovascular risk
discuss with primary care physician or cardiologist for cardiovascular risk assessment
Screening
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blood pressure and pulse pressure Moderate
rs11708647 G allele is associated with increased pulse pressure, a marker of arterial stiffness, via effects on PCOLCE2 expression in vascular tissue
measure and record pulse pressure (systolic minus diastolic) annually or as recommended by physician