Obesity

Visceral adipose tissue is an independent predictor and mediator of the progression of coronary calcification: a prospective sub-analysis of the GEA study

Cardiovasc DiabetolPublished Prospective cohort study

Authors' conclusion

This study supports the hypothesis that VAT is a mediator of the risk conferred by subcutaneous adipose tissue dysfunction. METS-VF is an efficient clinical surrogate that could facilitate the identification of at-risk adiposity subjects in daily clinical practice.

Study context

Population
Adults (53 ± 9 years, 53% women) with coronary artery calcium (CAC) quantified by computed tomography (CT) at baseline and after 5 years
Participants
862 adults
Outcome
CAC progression
Follow-up
5 years
Methodological detailssub-analysis of the GEA study, adjusted Cox proportional hazard models, mediation and interaction models
  • Sub-analysis of the GEA study
  • Adjusted Cox proportional hazard models
  • Mediation and interaction models

Main finding

As reported in the abstract

Predictors of CAC progression

Visceral adipose tissue (VAT) independently predicted CAC progression

HR 1.004

95% CI 1.001–1.007p < 0.01

METS-VF independently predicted CAC progression

HR 1.001

95% CI 1.0–1.001p < 0.05

Incidence of CAC progression per 1000 person-years

30.2

95% CI 25.3–35.8

Observational data: associations, not effects.

Further findings

VAT-associated CAC progression risk by ASCVD risk

Evident among low-risk ASCVD subjects, attenuated among medium-high-risk subjects

Mediation by VAT of the effect of insulin resistance (IR) with adipose tissue dysfunction on CAC progression

Proportion mediated by VAT
51.8% (95% CI 44.5-58.8%)

Original publication

Visceral adipose tissue is an independent predictor and mediator of the progression of coronary calcification: a prospective sub-analysis of the GEA study. Cardiovasc Diabetol. Published 3 April 2023. doi:10.1186/s12933-023-01807-6

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.