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Differential association between metabolic syndrome and coronary artery disease evaluated with cardiac computed tomography according to the presence of diabetes in a symptomatic Korean population

Authors
 Ki-Bum Won  ;  Hyuk-Jae Chang  ;  Jimin Sung  ;  Sanghoon Shin  ;  In-Jeong Cho  ;  Chi-Young Shim  ;  Geu-Ru Hong  ;  Young Jin Kim  ;  Byung-Wook Choi  ;  Namsik Chung 
Citation
 BMC CARDIOVASCULAR DISORDERS, Vol.14(105) : 1-10, 2014 
Journal Title
BMC CARDIOVASCULAR DISORDERS
Issue Date
2014
MeSH
Aged ; Biomarkers/blood ; Chi-Square Distribution ; Coronary Angiography/methods* ; Coronary Artery Disease/diagnostic imaging* ; Coronary Artery Disease/epidemiology* ; Coronary Vessels/diagnostic imaging* ; Cross-Sectional Studies ; Diabetes Mellitus/diagnosis ; Diabetes Mellitus/epidemiology* ; Female ; Humans ; Incidence ; Lipoproteins, HDL/blood ; Logistic Models ; Male ; Metabolic Syndrome/blood ; Metabolic Syndrome/diagnosis ; Metabolic Syndrome/epidemiology* ; Middle Aged ; Multidetector Computed Tomography* ; Multivariate Analysis ; Odds Ratio ; Plaque, Atherosclerotic ; Predictive Value of Tests ; Prevalence ; Republic of Korea/epidemiology ; Risk Factors ; Severity of Illness Index ; Vascular Calcification/diagnostic imaging ; Vascular Calcification/epidemiology
Keywords
Metabolic syndrome ; Diabetes ; Coronary artery disease ; Coronary computed tomographic angiography
Abstract
BACKGROUND:
Metabolic syndrome (MetS) is associated with increased risks of diabetes and coronary artery disease (CAD). Despite the controversial inclusion of established diabetes in MetS, the association between MetS and CAD according to diabetes status has not been elucidated in the Asian population.
METHODS:
We evaluated the association between MetS and CAD using the parameters including any plaque, obstructive plaque, and coronary artery calcium score (CACS) >100 according to diabetes status in 2,869 symptomatic Korean subjects who underwent cardiac computed tomographic angiography.
RESULTS:
The prevalence of MetS was significantly higher in the diabetic subjects than in the non-diabetic subjects (69% vs. 34%, P <0.001). The incidence of any plaque (64% vs. 43%, P <0.001), obstructive plaque (26% vs. 13%, P = 0.006), and CACS >100 (23% vs. 12%, P = 0.012) was significantly higher in diabetic subjects than in non-diabetic subjects. Among the MetS components, decreased high-density lipoprotein level was significantly associated with any plaque (odds ratio [OR] 1.35), obstructive plaque (OR 1.55), and CACS >100 (OR 1.57) in the non-diabetic subjects (P <0.01, respectively). However, none of the MetS components were associated with all the parameters in the diabetic subjects. Multivariate regression analysis revealed that MetS and the number of MetS components (MetSN) were independently associated with any plaque (MetS: OR 1.55, P <0.001; MetSN: OR 1.22, P <0.001), obstructive plaque (MetS: OR 1.52, P = 0.003; MetSN: OR 1.25, P <0.001), and CACS >100 (MetS: OR 1.46, P = 0.015; MetSN: OR 1.21, P = 0.004) only in the non-diabetic subjects, respectively.
CONCLUSIONS:
MetS was independently associated with the presence and severity of CAD only in the non-diabetic subjects among the symptomatic Korean population.
Files in This Item:
T201402932.pdf Download
DOI
10.1186/1471-2261-14-105
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
Yonsei Authors
Kim, Young Jin(김영진) ORCID logo https://orcid.org/0000-0002-6235-6550
Sung, Ji Min(성지민)
Shin, Sang Hoon(신상훈)
Shim, Chi Young(심지영) ORCID logo https://orcid.org/0000-0002-6136-0136
Won, Ki Bum(원기범)
Chang, Hyuk-Jae(장혁재) ORCID logo https://orcid.org/0000-0002-6139-7545
Chung, Nam Sik(정남식)
Cho, In Jeong(조인정)
Choi, Byoung Wook(최병욱) ORCID logo https://orcid.org/0000-0002-8873-5444
Hong, Geu Ru(홍그루) ORCID logo https://orcid.org/0000-0003-4981-3304
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/99638
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