Key result
Obesity is linked to ~2.4-fold higher incident CAD risk, partially mediated by inflammatory markers.
Why the study?
It was unknown to what extent the effect of body mass index on coronary artery disease risk is mediated by chronic inflammation.
Does overweight and obesity increase the risk of incident coronary artery disease, and is this effect mediated by chronic inflammation in adults?
Cohort (n=1,416)
Yes
Does overweight and obesity increase the risk of incident coronary artery disease, and is this effect mediated by chronic inflammation in adults?
Hazard Ratio: 2.43 (95% CI 2.03–2.88)
Chronic inflammation (measured by CRP and PAI-1 levels) partially mediates the increased risk of incident coronary artery disease observed in overweight and obese individuals.
Obesity-CAD link may involve CRP/PAI-1 mediation; leaves open whether targeting inflammation alters outcomes pending trials.
BACKGROUND AND AIMS: It is well known that being overweight or obese is a risk factor for coronary artery disease (CAD). At the same time, belonging to these categories indirectly influences other risk factors like hypertension, diabetes or dyslipidemia also through a chronic inflammation condition. The aim of this study was to establish to which extent the effect of body mass index (BMI) on CAD risk can be explained by the chronic inflammation degree, using a statistical mediation model. METHODS AND RESULTS: The present study used data from EPICOR, the cardiovascular branch of the EPIC Italy (European Investigation into Cancer and Nutrition) study. We employed a case-cohort design including 1416 participants with 622 incident CAD cases (major coronary events, myocardial infarction). Acute phase reactant C-reactive protein (CRP) and Plasminogen Activator Inhibitor-1 (PAI-1), were measured at baseline. A mediation analysis was performed to establish to which extent the effect of BMI on CAD risk can be explained by the inflammation degree expressed by the levels of both CRP and PAI-1. Using a fully adjusted survival model individuals in the second and third BMI categories had increased hazard ratios for CAD compared to the first BMI category. Mediation analysis revealed significant direct and indirect effects of BMI on CAD risk through inflammation, and results were consistent across gender and with waist-to-hip ratio analyses. CONCLUSION: Chronic inflammation might explain part of the increased risk of CAD due to more or less severe excess weight, in a robust statistical mediation model.
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Giraudo et al. (2024) conducted a cohort in Coronary artery disease (n=1,416). Obesity (BMI > 30 kg/m²) vs. Normal weight (BMI < 25 kg/m²) was evaluated on Incident coronary artery disease (major coronary events, myocardial infarction) (HR 2.43, 95% CI 2.03-2.88). Obesity was associated with an increased risk of incident coronary artery disease compared to normal weight (HR 2.43), an effect that was partially mediated by chronic inflammation markers CRP and PAI-1.
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