- Open Access
Metabolic syndrome as an indicator of high cardiovascular risk in patients with diabetes: Analyses based on Korea National Health and Nutrition Examination Survey (KNHANES) 2008
Diabetology & Metabolic Syndrome volume 6, Article number: 98 (2014)
Patients with either diabetes mellitus (DM) or metabolic syndrome (MS) are recognized as a high risk group for cardiovascular disease (CVD). Several studies have demonstrated the clinical value of MS for predicting additional CVD risk in the DM population, although the clinical significance remains debatable.
We used the Korea National Health and Nutrition Examination Survey (KNHANES) 2008, which is the national representative database. We classified the KNHANES subjects based on MS and glucose tolerance status, and compared clinical characteristics and future CVD risk among the subgroups.
A total of 796 of the 4314 subjects were diagnosed with MS. Their clinical characteristics were significantly different from patients without MS. Prevalence of DM was 9.5% in subjects with MS, but only 1.1% in subjects without MS. In addition, there was no MS in 30.9% of total DM patients who were enrolled in this study. For the normal and impaired fasting glucose subgroups, the prevalence of moderate (5–10%) and high (>10%) CVD risk was significantly higher in patients with MS than in patients without MS (p < 0.001). However, in the DM subgroup, even after multiple adjustments, there were no differences in clinical characteristics or in the prevalence of moderate to high CVD risk according to MS status. That said, LDL cholesterol in the DM group without MS was significantly higher than in the DM group with MS (p = 0.010).
The efficacy of MS as a screening tool for high CVD risk may be limited in DM patients, and conventional risk factors such as LDL may be more important.
The term “metabolic syndrome” (MS) refers to a cluster of metabolic risk factors that accelerate the development of cardiovascular disease (CVD). Since Reaven described “syndrome X” in 1988, several expert groups have endeavored to identify diagnostic criteria that will more easily identify patients with multiple risk factors for MS. The most widely recognized metabolic risk factors consist of abdominal obesity; atherogenic dyslipidemia such as elevated triglycerides (TG), apolipoprotein B-containing lipoproteins and low levels of high-density lipoprotein (HDL) cholesterol; elevated blood pressure and glucose levels; and prothrombotic and proinflammatory states[1, 4, 5]. The mechanism of interaction among these metabolic risk factors is not completely understood. However, these factors appear to be associated with metabolic susceptibility (e.g. insulin signaling defects, adipose tissue disorder, mitochondrial dysfunction, endocrine dysfunction, ethnic variations, aging, and drugs), and people who have metabolic susceptibility usually manifest insulin resistance.
According to a recent meta-analysis, the risk of CVD in MS subjects is approximately double that of non-MS subjects[4, 7]. Therefore, aggressive interventional strategies for CVD prevention should be initiated earlier in MS subjects. However, there is still debate regarding the value of MS as an additive risk factor for CVD in those who have already been diagnosed with diabetes or have a prediabetic conditions, such as impaired fasting glucose (IFG).
Our aim in this study was to investigate the association of MS and future CVD risk based on glucose tolerance status. Furthermore, we attempted to identify practical methods for screening diabetes patients who are at high risk for CVD using the nationally representative Korean population data base, the Korea National Health and Nutrition Examination Survey (KNHANES) of 2008.
KNHANES is a nationwide, population-based, and cross-sectionally designed health survey conducted by the Korea Centers for Disease Control and Prevention. After the first KNHANES was conducted in 1998, the second, third, and fourth surveys were conducted in 2001, 2005, and 2007–2009, respectively.
We utilized the KNHANES 2008 data in this study. KNHANES 2008 was conducted from January to December 2008. The subject population included all households recorded in the 2005 Population and Housing Census in Korea. Relevant households were randomly selected through stratified and multistage probability sampling. As rolling survey methods were used for sampling, the sample for each year was a probability sample representing all parts of the country.
Subjects aged 20 years and older were selected from the KNHANES 2008 sample (n = 6,123). Of these 6,123 subjects, individuals taking medication for hypertension, Diabetes Mellitus, or dyslipidemia (n = 1,303) were excluded to eliminate the potential effect of medication on MS status, as were those with insufficient data to diagnose MS (n =197). Subjects who had a chronic disease including any type of cancer, viral hepatitis carrier, liver cirrhosis, current tuberculosis, chronic obstructive lung disease, renal failure, myocardial infarction, angina or stroke were also excluded (n = 168). Subjects lacking sufficient demographic data, including age, sex, body mass index (BMI), physical activity, smoking and drinking history, income level, education level, residential district and occupation were also excluded (n = 141). All subjects included in the study had blood sample data. A total of 4,314 subjects were enrolled in this study.
The subjects were divided according to presence of MS and glucose tolerance status. The Modified National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATP III) criteria were adopted and MS was diagnosed if a subject met three or more of the following five factors: elevated waist circumference, TG ≥150 mg/dL, HDL cholesterol <40 mg/dL in males and <50 mg/dL in females, systolic blood pressure ≥130 mmHg and/or diastolic ≥85 mmHg, and fasting glucose ≥100 mg/dL. However, the criterion of waist circumference measurement was selected based on the Korean Society for the Study of Obesity criteria, as ≥90 cm in males and ≥85 cm in females. The ten-year CVD risk of subjects was also analyzed by age, smoking status, total cholesterol, HDL cholesterol, and systolic blood pressure using the Framingham risk score[11, 12]. Based on these risk criteria, subjects were classified into low (<5%), moderate (5 to <10%) and high-risk (≥10%) groups. Glucose tolerance status was subdivided into normal fasting glucose (NFG), impaired fasting glucose (IFG) and DM based on the fasting plasma glucose concentration and the diagnostic criteria of the American Diabetes Association. Current smokers were defined as those who had smoked more than five packs of cigarettes during their lifetime and were smoking at the time of the survey. All other subjects were defined as non-smokers. Regular alcohol drinkers were those who currently drank alcohol more than one glass per month regardless of alcohol types, and all others were defined as non-drinkers. The sixteen residential areas of the KNHANES were classified into urban or rural areas. Household income was divided into quartiles. Educational status was categorized as none, elementary school, middle school, high school, or college or higher. Occupation was divided into seven groups: group 1, managers, professionals, technicians and associate professionals; group 2, clerical support workers; group 3, service and sales workers; group 4, skilled agricultural, forestry and fishery workers; group 5, craft and related trades workers, plant and machine operators, and assemblers; group 6, elementary occupations; group 7, housewife, student, and unemployed, based on the 6th Korean Standard Classification of Occupations from the Korean National Statistical Office, which was created by following the International Standard Classification of Occupations of the International Labor Organization. Physical activity of the subjects was categorized according to their participation in recreational physical activity during the week prior to the survey.
Samples from all subjects were collected after a >8 hour period of fasting. Specimens were immediately transported to the central laboratory (NeoDIN Medical Institute, Seoul, Korea) where they were analyzed within 24 hours. Biochemical measurements, including total cholesterol, TG, HDL cholesterol, blood urea nitrogen (BUN), creatinine, aspartate aminotransferase (AST), alanine aminotransferase (ALT) and fasting plasma glucose concentration were analyzed using an automated analyzer (Hitachi Automatic Analyzer 7600; Tokyo, Japan) with enzymatic assays. HDL cholesterol was evaluated using standard samples as equivalents between the KNHANES central laboratory and the U.S. Centers for Disease Control and Prevention to produce an accurate lipid profile. The differences between the two laboratories were adjusted for by Passing–Bablok regression. LDL cholesterol levels were calculated using the Friedewald equation. Instead of apolipoprotein, which is typically difficult to analyze in a clinical setting, non-HDL cholesterol was analyzed as a potential predictor of CVD risk in the presence of high serum TG common in subjects with DM[17, 18]. Non-HDL cholesterol was calculated as total cholesterol concentration minus HDL cholesterol. The non-HDL/HDL ratio was divided into tertiles to compare trends of prevalence of IFG and DM in both MS and non-MS subjects. Serum insulin concentration was measured using a gamma counter (1470 Wizard, Perkin Elmer, Turku, Finland) and an immunoradiometric assay (Biosource, Nivelles, Belgium). An updated homeostasis model assessment (HOMA2) method was employed to assess β-cell insulin secretion capacity (HOMA2%B) and insulin sensitivity (HOMA2%S) in fasting plasma glucose and fasting serum insulin[19, 20]. The HOMA2 method, a computerized improvement on the standard HOMA method, reflects a more accurate insulin secretion capacity and insulin resistance than the previous HOMA method[19, 20].
All data are expressed as either numbers with proportions for categorical variables or as means ± SD for numerical variables. Student’s t-tests were used for the comparison of continuous variables and Pearson's Chi-square tests(χ2-test) were used for the comparison of categorical variables of demographic and clinical characteristics between MS subjects and non-MS subjects. The study population was subdivided into NFG, IFG and DM groups and the prevalence of MS based on glucose tolerance status was analyzed by χ2-test. In those subgroups, demographic and clinical characteristics and CVD risk were analyzed according to the presence of MS by independent sample t-test and χ2-test. Odds ratios (ORs) and 95% confidence intervals (CIs) for the prevalence of MS according to CVD risk were estimated by logistic regression.
Statistical analyses were conducted using Predictive Analytics Software (PASW; version 18.0) (SPSS, Inc., Chicago, IL, USA). P-values less than 0.05 were considered statistically significant.
Because this study analyzed publicly available data sets, it was exempt from Institutional Review Board approval.
A total of 4,314 subjects were included for analysis in this study. Subjects with MS and those who were classified as non-MS accounted for 18.5% (n = 796) and 81.5% (n = 3,518), respectively, of the total study population (Additional file1: Table S1). Mean age, BMI, percentage of males and current smokers were significantly higher in the MS group than in the non-MS group (p < 0.001). When compared with MS subjects, non-MS subjects tended to live in urban areas (p = 0.041), had a higher household income (p < 0.001), and were more educated (p < 0.001). Occupations were also significantly different between the study groups (p = 0.002). Biochemical parameters, including BUN (p < 0.001), creatinine (p < 0.001), AST (p < 0.001), and ALT (p < 0.001) were all significantly higher in MS subjects than in non-MS subjects.
The prevalence of glucose tolerance status and MS
The prevalence of NFG, IFG and DM in the study sample were 78.6% (n = 3,392), 18.8% (n = 812), and 2.5% (n = 110) respectively. However, there were significant differences in the prevalence of each glucose tolerance status according to MS status (Figure 1). Prevalence of NFG, IFG, and DM in MS subjects was 40.3%, 50.1%, and 9.5% respectively, whereas the prevalence was 87.3%, 11.7%, and 1.0%, respectively, in non-MS subjects (p < 0.001). There was a significantly lower prevalence of DM in non-MS subjects, although non-MS subjects comprised 30.9% of the DM subgroup.
Clinical characteristics according to glucose tolerance status and MS
When comparing subjects by their glucose tolerance status, there were significant differences in clinical variables between MS subjects and non-MS subjects in the NFG and IFG subgroups (Table 1). However, there were no significant differences except for the NCEP-ATP III diagnostic criteria of MS between the MS subjects and non-MS subjects in the DM subgroup. In fact, in the DM subgroup, LDL cholesterol, which is an established risk factor for cardiovascular disease, was significantly higher in non-MS subjects than in MS subjects.
Risk of a cardiovascular event according to glucose tolerance status and MS
Ten-year CVD event risk was estimated by the Framingham risk score and compared according to glucose tolerance and MS status (Figure 2). Subjects diagnosed with MS had a higher prevalence of moderate (5 to <10%) and high (≥10%) CVD risk than non-MS subjects in the NFG and IFG subgroups (p < 0.001). However, in the DM subgroup, the presence of MS was not associated with the prevalence of moderate or high CVD risk (p = 0.649). We also analyzed odds ratios for MS prevalence in moderate or high CVD risk subjects by glucose tolerance status, and found that ORs for MS prevalence in moderate or high CVD risk subjects in the DM subgroup were not significant even after multiple adjustments (Table 2).
Metabolic syndrome and DM are the most well-known CVD risk factors and are used as a measure of CVD risk in many studies. The pathophysiology of MS is not completely understood, but since insulin resistance is known to be a representative pathophysiological factor, many studies have focused on the relationship between DM and MS. The prevalence of DM risk for patients with MS (diagnosed per NCEP criteria) was 2.99 times higher than patient without MS (95% CI 1.96–4.57) (P for heterogeneity < 0.001). Approximately 60-70% of DM patients have MS[23, 24]. Previous research indicates that DM and MS are independent CVD risk factors but it is still unclear whether MS is useful as a predictor of CVD risk in subjects with DM[24, 25].
Our study classified the subjects into NFG, IFG and DM subgroups according to glucose tolerance status and analyzed the prevalence of MS and its relationship to CVD risk using the Framingham risk score. CVD risk in MS subjects was higher than in non-MS subjects in the NFG and IFG subgroups, but there was no significant difference in CVD risk between MS subjects and non-MS subjects in the DM subgroup. This suggests that MS is a useful CVD risk predictive factor in the NFG and IFG subgroups, but not in the DM subgroup. On the other hand, LDL cholesterol levels in non-MS subjects in the DM subgroup were higher compared with MS subjects in the DM subgroup. This is likely because DM, a strong CVD risk factor, already existed in the DM subgroup, and the impact of DM was stronger than other components included in the MS cluster.
The term metabolic syndrome refers to a cluster of metabolic risk factors that accelerate the development of cardiovascular disease, and there has been controversy surrounding the establishment of MS diagnostic criteria. Some experts explain that the reason why DM is not included in the NCEP-ATP III criteria (which include BMI, waist circumference, high BP, high TG, low HDL, and high fasting glucose) is because CVD risk associated with MS preferentially increases in subjects with DM. This supports the conclusion of our study that DM has a greater impact on CVD risk than other MS components.
The American Heart Association designates Type 2 DM, together with Peripheral Arterial Disease (PAD) and Carotid Artery Disease (CAD), as “Coronary Heart Disease (CHD) risk equivalents”. In DM patients, hyperglycemia works synergistically with other CVD risk factors such as hypertension, dyslipidemia, obesity, reduced physical activity, and cigarette smoking to increase CVD morbidity and mortality. Due to insulin resistance, plasminogen activator inhibitors and fibrinogen increase and the coagulation process is reinforced so that fibrinolysis is hindered. In addition, DM is related to endothelial, vascular, smooth muscle, and platelet dysfunction. A recent study measured circulating endothelial progenitor cells (EPCs) in CHD and CHD risk equivalent (PAD, CAD and Type 2 diabetes mellitus) groups. EPCs play an important role in neovasculogenesis, vascular repair and atherogenic processes. There were more EPCs in subjects with DM than in other disease groups. These results are another evidence that DM has a strong influence on CVD prevalence. Therefore, independent CVD risk factors such as LDL cholesterol, age, gender, cigarette smoking and family history or parameters such as hs-CRP, CD40L, MCP-1, ICAM-1, VCAM-1, and p-selectin might be helpful in determining CVD risks in individuals with DM. New diagnostic tools should be developed to help correctly predict CVD.
Recently Li et al. studied the relationship between the prevalence of MS and non-embolic ischemic stroke according to glucose tolerance status. The results showed that MS prevalence was higher in the stroke group than in the control group. Subjects were then classified according to glucose tolerance status (NGT, IFG or DM) and a multiple logistic regression analysis was performed. This analysis showed that the ORs of ischemic stroke in the MS with DM, MS with IFG and MS with NGT groups were all high (5.70, 2.24 and 2.19, respectively) (p < 0.05). Among them, the odds ratio was the highest in the MS with DM group. Accordingly, they concluded that MS increased ischemic stroke risk, especially in hyperglycemic patients with DM. This contradicts the findings of our study, but this may be due to the fact that they measured blood glucose when a stroke was occurring, and included only acute cerebral stroke patients who visited a university medical center emergency room within 2 hours of the onset of symptoms.
Kim et al. studied the association between inflammatory markers, adipokines (hs-CRP, IL-6, resistin, and adiponectin) and MS score. In addition, they explored whether or not MS score is useful in predicting the risk of coronary artery disease in patients with chest pain who received a coronary angiography, according to DM status. Their study findings were similar to ours. MS score was useful in predicting CAD risk in non-DM patients, and an increased MS score was associated with increased IL-6 and decreased adiponectin. However, MS score was not useful for predicting CAD risk in DM patients, nor there was any consistent relationship between MS scores and bioparameters in DM patients. Their study did not completely exclude medication effects such as the effect of anti-diabetic agents, and their work was conducted on patients who likely had CAD and were treated with coronary angiography. On the other hand, our study avoided selection bias and obtained more objective results because it excluded medication effects, used the Framingham risk score as a CVD risk prediction method, and used KNHANES 2008 data to create a large-scale subject group.
This study has several limitations. The first issue is that it is unclear if the Framingham risk score will be an appropriate risk prediction factor for CVD prevalence in the future. In fact, some researchers believe that the Framingham risk score underestimates CVD risk in specific age and gender groups[32, 33]. In addition, more precise methods are available to measure CVD risk, such as the coronary artery calcium score by computed tomography and carotid intima-media thickness by ultrasonography. However, the Framingham risk score is still recognized as a reliable predictor of CVD risk and continues to be used frequently in clinical settings. Carotid intima-media thickness by ultrasonography or coronary artery calcium score by computed tomography (CT) for the purpose of screening is costly, and also may result in unnecessary exposure to contrast media. Another limitation of this study is the cross-sectional design. Therefore, the results of this study cannot provide long-term information about the relationship between MS and CVD risk. Thus, future studies should be long-term and retrospective or prospective in nature. Finally, this study is not widely applicable because it was conducted on Korean subjects only. There are many genetic and lifestyle differences between ethnicities that can greatly impact MS components. Therefore, future studies of replication should include individuals of various ethnic backgrounds.
However, the results of this study are more objective than similarly scaled studies due to the use of national representative epidemiological data, KNHANES, which is collected through strict quality control. Using the KNHANES 2008 database made it possible to gather socioeconomic variables and control and adjust for the effect of these variables on study results. Hence, the results of this study are relatively accurate and detailed analyses were possible.
In addition, our study segmented groups according to glucose tolerance status. This is important because it was possible to independently classify prediabetes patients into the NGT, IGT and DM group according to glucose tolerance status rather than simply creating a DM and a non-DM group. Also, considering that high fasting glucose is an MS component, it is impossible to completely exclude the influence of hyperglycemia on CVD risk in the MS group. However, we could control the influence of hyperglycemia by dividing the MS group according to glucose tolerance status. And we focused on other MS components except high fasting glucose.
In conclusion, MS is not a useful tool for screening CVD risk in DM patients, but may be applicable in NFG or IFG patients. Currently, stress tests such as exercise or adenosine stress SPECT radionuclide myocardial perfusion imaging (rMPI), dobutamine-atropine stress echocardiography and coronary angiography, noninvasive CT coronary angiogram or cardiac magnetic resonance imaging (MRI) techniques have used for screening of cardiovascular disease in DM patients. However, these tests are too invasive, expensive and not accessible. Also, patients could be exposed to radiation and contrast media. Instead, conventional risk factors such as age, gender, cigarette smoking, family history, LDL cholesterol, and inflammation markers may be more important when predicting CVD risk in DM patients. Therefore, MS can be a good tool for non-DM patients, while it is necessary to further study and develop new tools and criteria for risk prediction in DM patients.
Korea National Health and Nutrition Examination Survey
Normal fasting glucose
Impaired glucose tolerance
High density lipoprotein
Low density lipoprotein
Updated homeostasis model assessment for β-cell insulin secretion
Updated homeostasis model assessment for insulin sensitivity.
Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, Gordon DJ, Krauss RM, Savage PJ, Smith SC, Spertus JA, Costa F: Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation. 2005, 112: 2735-2752. 10.1161/CIRCULATIONAHA.105.169404.
Reaven GM: Banting lecture 1988. Role of insulin resistance in human disease. Diabetes. 1988, 37: 1595-1607. 10.2337/diab.37.12.1595.
Alberti KG, Zimmet P, Shaw J: The metabolic syndrome–a new worldwide definition. Lancet. 2005, 366: 1059-1062. 10.1016/S0140-6736(05)67402-8.
Grundy SM: Metabolic syndrome pandemic. Arterioscler Thromb Vasc Biol. 2008, 28: 629-636. 10.1161/ATVBAHA.107.151092.
Expert Panel on Detection E: Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA: J Am Med Assoc. 2001, 285: 2486-2497. 10.1001/jama.285.19.2486.
Grundy SM: Metabolic syndrome: a multiplex cardiovascular risk factor. J Clin Endocrinol Metab. 2007, 92: 399-404. 10.1210/jc.2006-0513.
Gami AS, Witt BJ, Howard DE, Erwin PJ, Gami LA, Somers VK, Montori VM: Metabolic syndrome and risk of incident cardiovascular events and death: a systematic review and meta-analysis of longitudinal studies. J Am Coll Cardiol. 2007, 49: 403-414. 10.1016/j.jacc.2006.09.032.
Zhang ML, Hou XH, Zhu YX, Lu JX, Peng LP, Gu HL, Jia WP: Metabolic disorders increase the risk to incident cardiovascular disease in middle-aged and elderly Chinese. Biomed Environ Sci. 2012, 25: 38-45.
Alberti KG, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, Fruchart JC, James WP, Loria CM, Smith SC: Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009, 120: 1640-1645. 10.1161/CIRCULATIONAHA.109.192644.
Park HS, Park CY, Oh SW, Yoo HJ: Prevalence of obesity and metabolic syndrome in Korean adults. Obes Rev. 2008, 9: 104-107.
D'Agostino RB, Vasan RS, Pencina MJ, Wolf PA, Cobain M, Massaro JM, Kannel WB: General cardiovascular risk profile for use in primary care: the Framingham Heart Study. Circulation. 2008, 117: 743-753. 10.1161/CIRCULATIONAHA.107.699579.
Wilson PW, D'Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB: Prediction of coronary heart disease using risk factor categories. Circulation. 1998, 97: 1837-1847. 10.1161/01.CIR.97.18.1837.
American DA: Diagnosis and classification of diabetes mellitus. Diabetes Care. 2012, 35 (Suppl 1): S64-S71.
Koh DH, Kim HR, Han SS: The relationship between chronic rhinosinusitis and occupation: the 1998, 2001, and 2005 Korea National health and nutrition examination survey (KNHANES). Am J Ind Med. 2009, 52: 179-184. 10.1002/ajim.20665.
Romain S, Dussert C, Martin PM: Determination of oestrogen receptors: application of the Passing-Bablock linear regression technique for comparison of enzyme immunoassay and radioligand binding assay in 1841 breast cancer tumours. Eur J Cancer. 1991, 27: 715-720. 10.1016/0277-5379(91)90172-A.
Friedewald WT, Levy RI, Fredrickson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972, 18: 499-502.
Gonzalez-Granado LI: Reply: presentations and outcomes of neurosarcoidosis: a study of 54 cases. QJM. 2009, 102: 889-
Pawate S, Moses H, Sriram S: Presentations and outcomes of neurosarcoidosis: a study of 54 cases. QJM. 2009, 102: 449-460. 10.1093/qjmed/hcp042.
Levy JC, Matthews DR, Hermans MP: Correct homeostasis model assessment (HOMA) evaluation uses the computer program. Diabetes Care. 1998, 21: 2191-2192. 10.2337/diacare.21.12.2191.
Wallace TM, Levy JC, Matthews DR: Use and abuse of HOMA modeling. Diabetes Care. 2004, 27: 1487-1495. 10.2337/diacare.27.6.1487.
Hanley AJ, Wagenknecht LE, D'Agostino RB, Zinman B, Haffner SM: Identification of subjects with insulin resistance and beta-cell dysfunction using alternative definitions of the metabolic syndrome. Diabetes. 2003, 52: 2740-2747. 10.2337/diabetes.52.11.2740.
Ford ES: Risks for all-cause mortality, cardiovascular disease, and diabetes associated with the metabolic syndrome: a summary of the evidence. Diabetes Care. 2005, 28: 1769-1778. 10.2337/diacare.28.7.1769.
Osuji CU, Nzerem BA, Dioka CE, Onwubuya EI: Metabolic syndrome in newly diagnosed type 2 diabetes mellitus using NCEP-ATP III, the Nnewi experience. Niger J Clin Pract. 2012, 15: 475-480. 10.4103/1119-3077.104530.
Bruno G, Merletti F, Biggeri A, Bargero G, Ferrero S, Runzo C, Prina Cerai S, Pagano G, Cavallo-Perin P: Metabolic syndrome as a predictor of all-cause and cardiovascular mortality in type 2 diabetes: the Casale Monferrato Study. Diabetes Care. 2004, 27: 2689-2694. 10.2337/diacare.27.11.2689.
Najarian RM, Sullivan LM, Kannel WB, Wilson PW, D'Agostino RB, Wolf PA: Metabolic syndrome compared with type 2 diabetes mellitus as a risk factor for stroke: the Framingham Offspring Study. Arch Intern Med. 2006, 166: 106-111. 10.1001/archinte.166.1.106.
Kahn R, Buse J, Ferrannini E, Stern M, American Diabetes A: The metabolic syndrome: time for a critical appraisal: joint statement from the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care. 2005, 28: 2289-2304. 10.2337/diacare.28.9.2289.
Harrison's principles of internal medicine: Diabetes Mellitus, Volume 344. 2011, 2985-2986. 18
Liao YF, Feng Y, Chen LL, Zeng TS, Yu F, Hu LJ: Coronary heart disease risk equivalence in diabetes and arterial diseases characterized by endothelial function and endothelial progenitor cell. J Diabetes Complications. 2014, 28: 214-218. 10.1016/j.jdiacomp.2013.09.009.
Liang KW, Lee WJ, Lee WL, Chen YT, Ting CT, Sheu WH: Diabetes exacerbates angiographic coronary lesion progression in subjects with metabolic syndrome independent of CRP levels. Clin Chim Acta; Int J Clin Chem. 2008, 388: 41-45. 10.1016/j.cca.2007.10.003.
Li M, Li Y, Liu J: Metabolic syndrome with hyperglycemia and the risk of ischemic stroke. Yonsei Med J. 2013, 54: 283-287. 10.3349/ymj.2013.54.2.283.
Kim JY, Choi EY, Mun HS, Min PK, Yoon YW, Lee BK, Hong BK, Rim SJ, Kwon HM: Usefulness of metabolic syndrome score in the prediction of angiographic coronary artery disease severity according to the presence of diabetes mellitus: relation with inflammatory markers and adipokines. Cardiovasc Diabetol. 2013, 12: 140-10.1186/1475-2840-12-140.
Rodondi N, Locatelli I, Aujesky D, Butler J, Vittinghoff E, Simonsick E, Satterfield S, Newman AB, Wilson PW, Pletcher MJ, Bauer DC: Framingham risk score and alternatives for prediction of coronary heart disease in older adults. PLoS One. 2012, 7: e34287-10.1371/journal.pone.0034287.
Zomer E, Liew D, Owen A, Magliano DJ, Ademi Z, Reid CM: Cardiovascular risk prediction in a population with the metabolic syndrome: Framingham vs. UKPDS algorithms. Eur J Prev Cardiol. 2014, 21: 384-90. 10.1177/2047487312449307.
Kannel WB, McGee D, Gordon T: A general cardiovascular risk profile: the Framingham Study. Am J Cardiol. 1976, 38: 46-51. 10.1016/0002-9149(76)90061-8.
This study was conducted based on raw data from the Korean National Health and Nutrition Examination Survey (KNHANES) 2008 collected by the Korea Centers for Disease Control and Prevention. This study was supported by a grant (S.Y.R., 2009) from the Korean Diabetes Association.
Korean Diabetes Association.
The authors declare that they have no competing interests.
SYR contributed to the conception and design of the study, wrote the manuscript, researched data, performed the statistical analysis and interpretation of data, and reviewed/edited the manuscript. JKH contributed to the discussion, wrote the manuscript, and reviewed/edited the manuscript. SYP helped research data and drafted the manuscript. JIS contributed to the conception and design of the project, acquired the data, and participated in the discussion. SOC contributed to the conception and design, acquired the data, and participated in the discussion. YSK contributed to the conception and design, participated in the discussion, and reviewed/edited the manuscript. JTW contributed to the conception and design, participated in the discussion, and reviewed/edited the manuscript. All authors read and approved the final manuscript.
Sang Youl Rhee, So Young Park contributed equally to this work.
Electronic supplementary material
About this article
Cite this article
Rhee, S.Y., Park, S.Y., Hwang, J.K. et al. Metabolic syndrome as an indicator of high cardiovascular risk in patients with diabetes: Analyses based on Korea National Health and Nutrition Examination Survey (KNHANES) 2008. Diabetol Metab Syndr 6, 98 (2014) doi:10.1186/1758-5996-6-98
- Metabolic syndrome
- Syndrome X
- Cardiovascular disease
- Framingham risk score
- Diabetes mellitus