rs11776713 - PURG

Magnitude 2.2 · 1 study on file

Reported associations

  • Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease. - Nature medicine (2019) · Karlsson T, Rask-Andersen M, Pan G, Höglund J, Wadelius C, Ek WE, Johansson Å · PubMed 31501611

    Visceral adipose tissue (VAT)-fat stored around the internal organs-has been suggested as an independent risk factor for cardiovascular and metabolic disease , as well as all-cause, cardiovascular-specific and cancer-specific mortality . Yet, the contribution of genetics to VAT, as well as its disease-related effects, are largely unexplored due to the requirement for advanced imaging technologies to accurately measure VAT. Here, we develop sex-stratified, nonlinear prediction models (coefficient of determination = 0.76; typical 95% confidence interval (CI) = 0.74-0.78) for VAT mass using the UK Biobank cohort. We performed a genome-wide association study for predicted VAT mass and identified 102 novel visceral adiposity loci. Predicted VAT mass was associated with increased risk


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Lifestyle context

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

Screening

  • visceral adipose tissue accumulation Moderate

    rs11776713 C allele associates with increased predicted visceral adiposity (n=325153, p=1e-9), a cardiometabolic risk factor.

    Measure waist circumference annually; consider imaging to quantify visceral adiposity.