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dc.contributor.authorAzizallah Dehghan
dc.contributor.authorLeila Jahangiry
dc.contributor.authorRozhan Khezri
dc.contributor.authorAlireza Jafari
dc.contributor.authorBabak Pezeshki
dc.contributor.authorFatemeh Rezaei
dc.contributor.authorDagfinn Aune
dc.contributor.otherNoncommunicable Diseases Research Center, Fasa University of Medical Sciences
dc.contributor.otherRoad Traffic Injury Research Center, Tabriz Health Services Management Research Center, Tabriz University of Medical Sciences
dc.contributor.otherStudent Research Committee, Iran University of Medical Sciences
dc.contributor.otherDepartment of Health Education and Health Promotion, School of Health, Social Development and Health Promotion Research Center, Gonabad University of Medical Sciences
dc.contributor.otherNoncommunicable Diseases Research Center, Fasa University of Medical Sciences
dc.contributor.otherResearch Center for Social Determinants of Health, Jahrom University of Medical Sciences
dc.contributor.otherDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London
dc.date.accessioned2024-06-30T11:24:12Z
dc.date.accessioned2025-10-08T08:27:26Z
dc.date.available2025-10-08T08:27:26Z
dc.date.issued01-06-2024
dc.identifier.urihttp://digilib.fisipol.ugm.ac.id/repo/handle/15717717/35957
dc.description.abstractAbstract Background Metabolic syndrome (MetS) is a cluster of risk factors and the Framingham risk score (FRS) is a useful metric for measuring the 10-year cardiovascular disease (CVD) risk of the population. The present study aimed to determine the 10-year risk of cardiovascular disease using the Framingham risk score in people with and without MetS in a large Iranian cohort study. Methods This cross-sectional study was done using the Fasa cohort. Participants aged ≥ 35 years old were recruited to the study from 2015 to 2016. The FRS was calculated using age, sex, current smoking, diabetes, systolic blood pressure (SBP), total cholesterol, and high-density lipoprotein (HDL) cholesterol. MetS was defined as the presence of three or more of the MetS risk factors including triglyceride (TG) level ≥ 150 mg dl− 1, HDL level < 40 mg dl− 1 in men and < 50 mg dl− 1 in women, systolic/diastolic blood pressure ≥ 130/≥85 mmHg or using medicine for hypertension, fasting blood sugar (FBS) level ≥ 100 mg dl− 1 or using diabetes medication and abdominal obesity considered as waist circumference (WC) ≥ 88 cm for women and ≥ 102 cm for men. Multiple logistic regressions were applied to estimate the 10- year CVD risk among people with and without MetS. Results Of 8949 participants, 1928 people (21.6%) had MetS. The mean age of the participants with and without Mets was 50.4 ± 9.2 years and 46.9 ± 9.1 years respectively. In total 15.3% of participants with MetS and 8.0% of participants without MetS were in the high-risk category of 10-year CVD risk. Among participants with MetS gender, TG, SBP, FBS and in people without MetS gender, TG, SBP, FBS, and HDL showed strong associations with the predicted 10-year CVD risk. Conclusion Male sex and increased SBP, TG, and FBS parameters were strongly associated with increased 10-year risk of CVD in people with and without MetS. In people without MetS, reduced HDL-cholestrol was strongly associated with increased 10-year risk of CVD. The recognition of participant’s TG, blood pressure (BP), FBS and planning appropriate lifestyle interventions related to these characteristics is an important step towards prevention of CVD.
dc.language.isoEN
dc.publisherBMC
dc.subject.lccDiseases of the endocrine glands. Clinical endocrinology
dc.titleFramingham risk scores for determination the 10-year risk of cardiovascular disease in participants with and without the metabolic syndrome: results of the Fasa Persian cohort study
dc.typeArticle
dc.description.keywordsCardiovascular disease
dc.description.keywords10-year risk
dc.description.keywordsFramingham risk score
dc.description.keywordsMetabolic syndrome
dc.description.pages1-9
dc.description.doi10.1186/s12902-024-01621-5
dc.title.journalBMC Endocrine Disorders
dc.identifier.e-issn1472-6823
dc.identifier.oai44376947e0224f44ad9030a75d2a6cf6
dc.journal.infoVolume 24, Issue 1


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