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Published on: February 25, 2016
C-reactive protein is not correlated with endothelial dysfunction in overweight and obese women
Raphael Ribeiro Sampaio1, Ana Marice Ladeia, Romulo Bagano Meneses
1Bahiana School of Medicine and Public Health, Bahia Foundation for the Development of Sciences, FBDC, Salvador, Bahia, Brazil.
Insights
This study found no link between C-Reactive Protein (CRP) levels and endothelial dysfunction in women with obesity. Increased CRP did not correlate with impaired blood vessel function or BMI in this group.
Area of Science:
- Cardiology
- Endocrinology
- Inflammation Research
Background:
- Obesity is a complex disease with inflammatory patterns, increasing cardiometabolic risk.
- Elevated C-Reactive Protein (CRP) is linked to microscopic endothelial dysfunction.
- Understanding the relationship between CRP and endothelial function in obesity is crucial for risk assessment.
Purpose of the Study:
- To investigate the association between serum CRP levels and endothelial function in women with overweight/obesity.
- To explore the correlation between CRP and anthropometric variables in this population.
- To determine if CRP is a reliable marker for endothelial dysfunction in obese women.
Main Methods:
- Cross-sectional analysis of secondary data from a tertiary education institution's survey.
- Inclusion of 47 non-smoker women with overweight/obesity and available CRP and endothelial function data.
- Endothelial function assessed via reactive hyperemia test (endothelium-dependent vasodilation); statistical analysis using SPSS v.14.
Main Results:
- No significant correlation was found between CRP levels and endothelial dysfunction (rs = 0.08, P = 0.64).
- CRP did not correlate with Body Mass Index (BMI) in the study population.
- No differences in endothelial function or CRP levels were observed between groups using or not using lipid-lowering, antihypertensive, or hypoglycemic medications.
Conclusions:
- The study found no association between C-Reactive Protein (CRP) and flow-mediated dilation (FMD).
- This suggests that CRP-associated endothelial dysfunction may not be severe enough to cause macroscopic changes in vasodilation.
- Further research is needed to clarify the role of CRP in endothelial health within obese populations.
Background:
Obesity is a complex and multifactorial disease, has an inflammatory pattern and is associated with higher cardiometabolic risk. There are recent reports associating an elevated C-Reactive Protein (CRP) with a microscopic endothelial dysfunction. The objective is to evaluate if there is an association between serum levels of CRP and endothelial function in women with overweight/obesity, as well as the correlation between CRP and anthropometric variables.
Methods:
This is a cross-sectional study that analyzed secondary data from patients treated in an institution of tertiary education, as part of the weight excess and cardiometabolic disease survey. The study included patients with overweight/obesity who had CRP and endothelial function tests already made and inserted into the survey database. The endothelial function was evaluated by: reactive hyperemia test (endothelium-dependent vasodilation). All tests were recorded and later analyzed by the same echocardiographer who performed the examination. Statistical analyses were realized in the Statistical Package for the Social Sciences (SPSS) version 14. It was considered statistically significant a P value < 0.05.
Results:
This study included 47, nonsmoker women. with a BMI of 32.37 ± 5.06 kg/m(2), median of CRP of 2.59 mg/L and flow-mediated dilation (FMD) of 8.75% ± 5.22%. There was no correlation between CRP and endothelial dysfunction in this population (rs = 0.08, P = 0.64). No correlation was observed between CRP and BMI. There were no differences of endothelial dysfunction variables and CRP in groups in use or not of medications (Hypolipidemic, antihypertensives and hypoglycemic agents).
Conclusion:
There was no association between CRP and FMD and this can suggest that it is possible that the level of eNOS dysfunction associated with increased CRP is not enough to lead to macroscopic changes and harm vasodilation.
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