Framingham risk score for estimation of 10-years of cardiovascular diseases risk in patients with metabolic syndrome
- PMID: 29132438
- PMCID: PMC5682637
- DOI: 10.1186/s41043-017-0114-0
Framingham risk score for estimation of 10-years of cardiovascular diseases risk in patients with metabolic syndrome
Abstract
Background: There are a few studies evaluating the predictive value of Framingham risk score (FRS) for cardiovascular disease (CVD) risk assessment in patients with metabolic syndrome in Iran. Because of the emerging high prevalence of CVD among Iranian population, it is important to predict its risk among populations with potential predictive tools. Therefore, the aim of the current study is to evaluate the FRS and its determinants in patients with metabolic syndrome.
Methods: In the current cross-sectional study, 160 patients with metabolic syndrome diagnosed according to the National Cholesterol Education Adult Treatment Panel (ATP) III criteria were enrolled. The FRS was calculated using a computer program by a previously suggested algorithm.
Results: Totally, 77.5, 16.3, and 6.3% of patients with metabolic syndrome were at low, intermediate, and high risk of CVD according to FRS categorization. The highest prevalence of all of metabolic syndrome components were in low CVD risk according to the FRS grouping (P < 0.05), while the lowest prevalence of these components was in high CVD risk group (P < 0.05). According to multiple logistic regression analysis, high systolic blood pressure (SBP) and fasting serum glucose (FSG) were potent determinants of intermediate and high risk CVD risk of FRS scoring compared with low risk group (P < 0.05).
Conclusion: In the current study, significant associations between components of metabolic syndrome and different FRS categorization among patients with metabolic syndrome were identified. High SBP and FSG were associated with meaningfully increased risk of CVD compared with other parameters.
Trial registrations: The study is not a trial; the registration number is not applicable.
Keywords: Cardiovascular disease; Framingham risk score; Metabolic syndrome.
Conflict of interest statement
Competing interest
The authors declare that they have no competing interests.
Ethics approval and consent to participate
The protocol of the current study has been approved by the ethics committee of Tehran University of Medical Sciences (97/130/1736) and Ethics committee of Tabriz University of Medical Sciences (5/92/1228), and written informed consent was obtained from all of the participant’s prior participation in the study.
Consent for publication
All of the authors have read and approved the article draft and were in agreement of article submission.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figures
References
-
- Grundy SM, Brewer HB, Cleeman JI, Smith SC, Lenfant C. Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition. Circulation. 2004;109(3):433–438. doi: 10.1161/01.CIR.0000111245.75752.C6. - DOI - PubMed
-
- Malik S, Wong ND, Franklin SS, Kamath TV, Gilbert JL, Pio JR, Williams GR. Impact of the metabolic syndrome on mortality from coronary heart disease, cardiovascular disease, and all causes in United States adults. Circulation. 2004;110(10):1245–1250. doi: 10.1161/01.CIR.0000140677.20606.0E. - DOI - PubMed
-
- Khaki Khatibi F, Yaghoubi A, Zarghami N, Rahbani M, Babaie H. Evaluation of hs-CRP, antioxidant markers and MDA in patients of coronary artery disease (CAD) containing non-smokers and non-diabetics. J Cardiovasc Thorac Res. 2011;2(4):13–18.
-
- Pezeshkian M, Darbin A, Rashidi MR, Vatankhah A, Golmohammadi Z, Afrasiabi A, et al. The effect of atherogenic diet with or without enzyme inhibitors on the incidence and progress of atherosclerosis in rabbits. J Cardiovasc Thorac Res. 2011;3(1):7–10.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
