Low Levels of Serum Paraoxonase Activities are Characteristic of Metabolic Syndrome and May Influence the Metabolic-Syndrome-Related Risk of Coronary Artery Disease
2012

Low Levels of Serum Paraoxonase Activities and Metabolic Syndrome's Impact on Coronary Artery Disease Risk

Sample size: 293 publication 10 minutes Evidence: moderate

Author Information

Author(s): Martinelli Nicola, Micaglio Roberta, Consoli Letizia, Guarini Patrizia, Grison Elisa, Pizzolo Francesca, Friso Simonetta, Trabetti Elisabetta, Pignatti Pier Franco, Corrocher Roberto, Olivieri Oliviero, Girelli Domenico

Primary Institution: University of Verona

Hypothesis

Low paraoxonase (PON1) activities are characteristic of metabolic syndrome and may influence the risk of coronary artery disease.

Conclusion

The study found that low PON1 concentrations are typical in metabolic syndrome and may modulate the risk of coronary artery disease.

Supporting Evidence

  • Subjects with metabolic syndrome had lower PON1 activities.
  • Low DEPCyMCase activity was significantly associated with increased coronary artery disease risk.
  • DEPCyMCase activity remained a significant predictor of metabolic syndrome independent of HDL levels.

Takeaway

People with metabolic syndrome have lower levels of a protective enzyme called paraoxonase, which may increase their risk of heart disease.

Methodology

The study evaluated PON1 activities in 293 subjects with or without metabolic syndrome and coronary artery disease using various biochemical assays.

Potential Biases

Potential bias due to the retrospective nature of the study and the small number of enrolled subjects.

Limitations

The study's retrospective design, small sample size, and lack of some clinical data such as waist circumference are limitations.

Participant Demographics

Participants were from Northern Italy, with a mix of those diagnosed with metabolic syndrome and coronary artery disease.

Statistical Information

P-Value

1.58 × 10−5

Confidence Interval

95% CI 1.44–13.10

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1155/2012/231502

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication