Association between metabolic syndrome or its components and asymptomatic cardiovascular disease in the RIVANA-study
M J Guembe1, E Toledo, J Barba
1Department of Health Education and Development, Department of Health, Government of Navarra, Pamplona (Navarra), Spain. mguembes@cfnavarra.es
Insights
Metabolic syndrome (MetSd) is linked to asymptomatic cardiovascular disease. However, MetSd may not be superior to individual risk factors like abdominal obesity in identifying cardiovascular risk.
Area of Science:
- Cardiology
- Metabolic Disorders
- Diagnostic Accuracy
Background:
- Metabolic syndrome (MetSd) is a cluster of risk factors associated with increased cardiovascular disease (CVD) risk.
- Asymptomatic cardiovascular disease (ACVD) represents subclinical organ damage that precedes clinical manifestation.
- The predictive value of MetSd versus its individual components for ACVD requires further investigation.
Purpose of the Study:
- To evaluate the association between MetSd and ACVD.
- To compare the discriminatory ability of MetSd and its individual risk factors for prevalent ACVD.
Main Methods:
- 880 community-dwelling subjects underwent physical examination, echocardiography, and carotid artery ultrasound.
- Blood and urine samples were collected for analysis.
- Logistic regression and ROC curve analysis (AUCs) were used to assess associations and discrimination.
Main Results:
- MetSd was independently associated with carotid atherosclerosis, increased left ventricular mass index, and cardiac dysfunction.
- MetSd did not better discriminate carotid intima-media thickness than abdominal obesity or impaired fasting glucose.
- MetSd performed worse than abdominal obesity in discriminating left ventricular mass index in younger males.
Conclusions:
- MetSd is associated with asymptomatic cardiovascular disease.
- Individual components of MetSd may be as effective as the overall syndrome in identifying cardiovascular risk.
Objective:
To assess the association between the metabolic syndrome (MetSd) and asymptomatic cardiovascular disease and determine if the MetSd or its single risk factors perform better in discriminating prevalent asymptomatic cardiovascular disease.
Methods:
A total of 880 community-dwelling subjects (423 with and 457 without MetSd according to ATPIII) underwent a physical examination, an echocardiography and an ultrasound examination of carotid arteries and blood and urine samples were collected. Associations between the subclinical organ damage markers and the MetSd were addressed with non-conditional logistic regression. AUCs of ROCs were used to compare the models' ability to discriminate asymptomatic cardiovascular disease.
Results:
The MetSd was independently associated with carotid subclinical atherosclerosis, increased left ventricular mass index and cardiac dysfunction. The MetSd did not discriminate prevalent increased carotid intima-media thickness better than abdominal obesity and impaired fasting glucose [AUC=0.75 (95% CI: 0.71-0.78) and 0.75 (0.71-0.79), respectively; p=0.55]. The MetSd performed worse than abdominal obesity in discriminating increased left ventricular mass index among males younger than 65 years [AUC=0.66 (95% CI: 0.62-0.69) and 0.69 (0.66-0.73), respectively; p=0.02]. No differences between the ability of MetSd or its components in discriminating increased left ventricular mass index were observed among older men or women. The discrimination ability for microalbuminuria for the MetSd or impaired fasting glucose was not statistically different [AUC=0.67 (95% CI: 0.60-0.74) and 0.69 (0.62-0.76), respectively; p=0.18].
Conclusion:
This study supports the association between the MetSd and asymptomatic cardiovascular disease. The construct of the MetSd might not be better than its single components in addressing cardiovascular risk.
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