Do inflammation and procoagulation biomarkers contribute to the metabolic syndrome cluster?
2007

Inflammation and Procoagulation Biomarkers in Metabolic Syndrome

Sample size: 2762 publication 10 minutes Evidence: high

Author Information

Author(s): Kraja Aldi T, Province Michael A, Arnett Donna, Wagenknecht Lynne, Tang Weihong, Hopkins Paul N, Djoussé Luc, Borecki Ingrid B

Primary Institution: Washington University School of Medicine

Hypothesis

Do inflammation and procoagulation biomarkers contribute to the metabolic syndrome cluster?

Conclusion

PAI1 is an important risk factor for MetS, correlating significantly with most variables studied and demonstrating the greatest relative odds among the biomarkers.

Supporting Evidence

  • Subjects in the top 75% quartile for PAI1 had a 6.9 greater odds of being classified with MetS.
  • Significant associations were found for MCP1, CRP, IL6, sICAM1, and fibrinogen with respect to MetS.
  • PAI1 correlated significantly with all obesity and dyslipidemia variables.
  • CRP had a high correlation with serum amyloid A and IL6.

Takeaway

This study found that certain proteins in the blood can help predict if someone has metabolic syndrome, which is a group of health problems that increase the risk of heart disease and diabetes.

Methodology

The study analyzed ten conventional MetS risk variables and ten biomarkers using correlations, factor analysis, hexagonal binning, and regression in the Family Heart Study.

Potential Biases

Participants using anti-hyperlipidemics may have confounded the results, as these medications affect biomarker concentrations.

Limitations

The study only included 10 biomarkers, and the sample size for some biomarker assays was smaller due to cost constraints.

Participant Demographics

The study included 2762 participants, primarily white, with a mean age of 57 years and 55% females.

Statistical Information

P-Value

p < 0.0001

Confidence Interval

[4.2–11.2]

Statistical Significance

p < 0.0001

Digital Object Identifier (DOI)

10.1186/1743-7075-4-28

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