Sex Factors in the Metabolic Syndrome as a Predictor of Cardiovascular Disease.
10.3803/EnM.2014.29.4.522
- Author:
Sunghwan SUH
1
;
Jongha BAEK
;
Ji Cheol BAE
;
Kyoung Nyoun KIM
;
Mi Kyoung PARK
;
Duk Kyu KIM
;
Nam H CHO
;
Moon Kyu LEE
Author Information
1. Division of Endocrinology and Metabolism, Department of Internal Medicine, Dong-A Medical Center, Dong-A University College of Medicine, Busan, Korea.
- Publication Type:Original Article
- Keywords:
Cardiovascular diseases;
Metabolic syndrome;
Coronary disease;
Stroke;
Sex
- MeSH:
Cardiovascular Diseases*;
Coronary Disease;
Female;
Genome;
Humans;
Hypertension;
Male;
Obesity, Abdominal;
Prevalence;
Risk Factors;
Sex Factors*;
Stroke
- From:Endocrinology and Metabolism
2014;29(4):522-529
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Metabolic syndrome (MetS) is a condition characterized by a cluster of metabolic disorders and is associated with increased risk of cardiovascular disease (CVD). This study analyzed data from the Korean Health and Genome Study to examine the impact of MetS on CVD. METHODS: A total of 8,898 subjects (4,241 males and 4,657 females), 40 to 69 years of age, were enrolled and evaluated for the development of new onset CVD from 2001 to 2012 (median 8.1 years of follow-up). RESULTS: The prevalence of MetS at baseline was 22.0% (932/4,241) and 29.7% (1,383/4,657) in males and females, respectively. MetS was associated with increased risk of coronary heart disease (CHD; hazard ratio [HR], 1.818; 95% confidence interval [CI], 1.312 to 2.520 in males; HR, 1.789; 95% CI, 1.332 to 2.404 in females) and CVD (HR, 1.689; 95% CI, 1.295 to 2.204 in males; HR, 1.686; 95% CI, 1.007 to 2.192 in females). Specifically, MetS was associated with risk of future stroke in females only (HR, 1.486; 95% CI, 1.007 to 2.192). Among MetS components, abdominal obesity and hypertension were independent predictors of both CHD and CVD. In addition, a higher number of MetS components correlated with higher CVD risk. CONCLUSION: MetS is a significant risk factor for the development of CVD although its impact varies between sexes.
