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International Journal of Endocrinology
Volume 2013 (2013), Article ID 740419, 7 pages
Different Impacts of Metabolic Syndrome Components on Insulin Resistance in Type 2 Diabetes
1Institute of Traditional Medicine, National Yang-Ming University, Taipei 112, Taiwan
2Linsen (Chinese Medicine) Branch, Taipei City Hospital, Taipei, Taiwan
Received 10 September 2012; Accepted 14 January 2013
Academic Editor: Atheline Major-Pedersen
Copyright © 2013 Chung-Hua Hsu. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Objective. To examine the different impacts of MS components on insulin resistance in type 2 diabetes. Methods. A number of subjects (144) who met the criteria of (1) age between 30 and 75 years, (2) had type 2 diabetes for more than one year, and (3) taking gliclazide and metformin for more than 6 months were enrolled. All subjects were assigned to one of the four HOMA index categories. The HOMA index quartile 4 denotes the highest insulin resistance. The main outcome evaluated is the odds ratios (ORs) of different MS components on HOMA index quartile 4. The characteristics in HOMA index quartiles and groups of nonmetabolic syndrome (NMS; number of components < 2), metabolic syndrome A (MSA; number of components = 2), and metabolic syndrome B (MSB; number of components > 2) were also evaluated. Results. The results showed that both MSA and MSB groups had higher ORs (5.9 and 13.8 times, resp.) than the NMS group; and that subjects with large waist circumference (LWC) and high triglyceride (HTG) level have higher ORs (6.1 and 2.6 times, resp.) in developing higher insulin resistance than normal control subjects. Conclusion. Type 2 diabetic patients with greater number of MS components have higher ORs in developing increased insulin resistance.
Insulin resistance is an important pathogenic factor in type 2 diabetic patients. Increased insulin resistance in type 2 diabetes is known to cause high risk in developing cardiovascular disease (CVD) [1–3]. Metabolic syndrome (MS) is an important cluster of metabolic abnormalities associated with insulin resistance and CVD [4, 5]. Despite the different definitions of MS proposed, high fasting plasma glucose level is one of the MS components [6, 7]. A high prevalence (35%–60%, depending on ethnicity, gender, and definition) of MS was found among type 2 diabetic patients [8–15]. Many studies have reported insulin resistance as the key pathogenic factor for the development of hyperlipidemia, glucose intolerance, hypertension, and obesity, all of which are MS components [16–23], while insulin resistance is not [6, 7]. Hence, the relationship between the components of MS and insulin resistance in type 2 diabetes merits further investigation.
Different severities or conditions of type 2 diabetes might lead to different degrees of insulin resistance. To understand the different impacts of MS components on insulin resistance in type 2 diabetes, and to avoid undetectable confounders and bias, this study enrolled subjects from a Chinese adult homogenous cohort aged between 30–75 years, who have had type 2 diabetes for more than one year and have been taking gliclazide and metformin for more than six months.
We hypothesized that there would be different impacts of MS components on insulin resistance among type 2 diabetes after controlling for other factors in the homogenous diabetes cohort. This study also compared the characteristics among different numbers of MS components in this cohort.
2. Research Design and Method
2.1. Study Population
The trial was conducted from July 2005 through June 2006 in Taipei Hospital, Taiwan. A total of 1356 registered diabetic patients were screened and 186 met the following criteria: (1) age between 30 and 75 years old, (2) being Chinese, (3) having been type 2 diabetes for more than one year, and (4) having been taking gliclazide and metformin for more than six months without taking other antidiabetic medication or insulin injection. The exclusion criteria include (1) GOT, GPT >80 U/L, serum creatinine >2.0 mg/dL, (2) lactation or pregnancy, (3) heart failure with New York Heart Association (NYHA) class >I, acute myocardial infarction, stroke, and that caused disabilities, and (4) any other conditions not suitable for trial as evaluated by the physician. After giving extensive oral and written information, a written informed consent form was obtained from the subjects before commencing any study-related activity. Finally, 144 subjects were enrolled in the study. The protocol was approved by the Human Ethics Committee of Taipei Hospital.
2.2. MS Components
According to ATP III Asian (Chinese) definition, the components of MS are (1) large waist circumference (LWC) ≥80 cm in female and ≥90 cm in male, (2) high triglyceride (HTG) ≥150 mg/dL, (3) low HDL-cholesterol (LHDL) <40 mg in male and <50 mg in female, and (4) high blood pressure (HBP) ≥130/85 mg or on medication [6, 7].
2.3. Definition Groups of Non-MS (NMS), MS A (MSA), and MS B (MSB)
Subjects with a number of MS components <2 were classified as the NMS group, those with a number of MS components =2 were grouped under MSA, and those with a number of MS components >2 were grouped under MSB.
Homeostasis model assessment for insulin resistance (HOMA index) (fasting glucose (mmol/L) × fasting insulin (UI/L)/22.5) was employed for evaluating insulin resistance [24, 25]. All subjects were assigned to one of the HOMA index categories according to the following quartiles: quartile 1 (<25%), quartile 2 (25%–49%), quartile 3 (50%–75%), and quartile 4 (>75%) for further assessment and comparison. The HOMA index quartile 4 denotes the highest insulin resistance. The main outcome evaluated is the ORs of different MS components on HOMA index quartile 4, which were assessed using multiple logistic regression analysis. The characteristics in HOMA index quartiles and groups of NMS, MSA, and MSB were also evaluated.
Anthropometric measurements including blood pressure, fasting glucose, HbA1C, insulin, adiponectin and triglyceride, cholesterol, cholesterol-HDL (HDL), and cholesterol-LDL (LDL) were taken. Waist circumference (WC) was measured midway between the lateral lower rib margin and the iliac crest, while hip circumference (HC) was measured at the levels of the major trochanters through the pubic symphysis. Height was measured with a wall-mounted stadiometer to the nearest 0.1 cm, weight was measured on a calibrated balance beam scale to the nearest 0.1 kg, and BMI was calculated (BMI = body weight/height (kg/m2)). A mercury sphygmomanometer with standard cuff was employed to measure the indirect auscultatory arterial blood pressure taken from the right arm with subjects in seated position.
All measurements were made at 0800–0900 after an overnight fast using standardized methods. A sample of whole blood was drawn and centrifuged at 4°C, and a 1-mL aliquot of serum was rapidly frozen (−80°C) for subsequent hormone analysis. The plasma adiponectin concentration was measured by a radioimmunoassay kit (Linco Research, Inc., St. Charles, MO, USA). This kit employs the double-antibody/polyethylene glycol technique using 125I-lableled adiponectin and a multispecies adiponectin rabbit antiserum. Plasma insulin levels were measured using a commercially available radioimmunoassay (Linco Research Inc.). The intra- and interassay coefficients of variation were 3.1% and 4.9%, respectively. The limit of sensitivity is 0.5 ng/mL.
2.5. Statistical Analysis
One-way analysis of variance (ANOVA) and linear trend test were employed to evaluate the trend among the HOMA index quartile groups and among groups of NMS, MSA, and MSB. Chi-square test was used for comparison of gender (male/female), family history of type 2 diabetes, and the percentage of MS component among groups. Multiple logistic regression analysis was employed for analysis among different MS components and groups of NMS, MSA, and MSB on the highest HOMA insulin resistance index quartile 4, with other factors adjusted. All values were two-tailed and α level of significance was set at 0.05. The data were analyzed with SPSS software (version 11.5).
Among the 1356 screened patients, 186 met the inclusion criteria and 144 (77.4%) agreed to participate. There are 79 females (age years) and 65 males (age years). There is no significant gender difference in means of age, BMI, WC, blood pressure, HbA1C, fasting glucose, cholesterol, triglycerol, insulin, HOMA index, aminotransferases alanine, aminotransferases aspartate, and creatinine.
3.2. Comparison among Quartiles of HOMA Index
Table 1 displays the comparison of characteristics among quartiles of HOMA index categories. As can be seen, the means of HOMA index quartile 4 and all the subjects are 9.3 (3.2) and 4.8 (3.3). Results of linear trend test show significant difference in %LWC (), %HTN (), %HTG (), BMI (), WC (), HC (), diastolic blood pressure (), fasting glucose (), HbA1C (), adiponectin level (), triglyceride level (), and cholesterol level (), but no statistical difference in family history of type 2 diabetes, gender ratio, %LHDL, and dose of metformin and gliclazide taken among quartiles of HOMA index.
3.3. Comparison among NMS, MSA, and MSB Groups
Table 2 displays the demographic and biochemical characteristics among the NMS, MSA, and MSB groups. As can be seen, 64.6% of the subjects met the ATP III Asian (Chinese) definition of having MS (MSA 36.2% and MSB 28.5%). Results of linear trend test show significant difference in means of HOMA index, BMI, WC, HC, blood pressure, percentage of all MS components, and insulin level (all the above having ), but no statistical difference in family history of type 2 diabetes, HbA1C, and dose of metformin and gliclazide taken among the three groups.
3.4. Odds Ratio of Multiple Logistic Regression on HOMA Index Quartile 4 (The Highest Insulin Resistance)
Table 3 shows the ORs of different MS groups, gender, family history of type 2 diabetes, different BMI categories, and HbA1C groups on the highest HOMA index group (quartile 4), after adjustment of age, gender, family history of type 2 diabetes, and dose of metformin and gliclazide taken. The results showed that both MSA and MSB groups had higher ORs (5.9 and 13.8 times, resp.) than the NMS group, obese subjects (BMI ≥ 27) had higher ORs (2.8 times) than nonobese subjects, and high HbA1C subjects (>9.0) had higher ORs (3.6 times) than control groups in developing higher HOMA index. Table 4 shows the ORs of different MS components (LWC, HTN, HTG, and LHDL), gender, family history of type 2 diabetes, different BMI categories, and HbA1C groups on the poor HOMA index group (quartile 4), after adjusting the age and dose of metformin and gliclazide taken. Significant difference can be seen in subjects with LWC, HTG, and high HbA1C having higher ORs, but not those with HTN and LHDL.
Our initial findings evidenced different impacts of MS components on insulin resistance in type 2 diabetes. Subjects with LWC and HTG have higher ORs (6.1 and 2.6 times, resp.) in developing higher insulin resistance than subjects with normal WC and TG. The results also reveal that subjects with greater number of MS components have higher ORs in developing higher insulin resistance than the NMS group in this type 2 diabetic cohort.
Different severity or condition of type 2 diabetes might result in different insulin resistance, and taking different oral hypoglycemia agents might also influence insulin sensitivity [26–29]. Hence, we enrolled a homogenous adult Chinese cohort of 30–75 years old with type 2 diabetes for more than one year and having been taking gliclazide and metformin for more than six months to avoid undetectable confounders and bias.
Reaven reported insulin resistance as the central pathophysiological feature of the cluster of metabolic abnormalities, which has been associated with MS in many subsequent reports . Many evidences also support the association between insulin resistance and vascular disease, and this has led to wide acceptance of the clustering of hyperlipidemia, glucose intolerance, hypertension, and obesity, all of which are MS components [30, 31]. Since there is still intense controversies among the definition of metabolic syndrome by ATPIII and its value as a CVD risk marker , we tried to figure out different impacts of the clustering MS components on insulin resistance of type 2 diabetic patients which has been proven to cause elevated risk of atherosclerosis .
Our results have reconfirmed the strong positive relationship between HOMA index and WC, BMI, HC, HbA1C, yes % of LWC, HTN HTG, and serum levels of glucose, triglyceride, and cholesterol (Table 1). All the above variables are the risk factors of developing complications in type 2 diabetes. It is interesting that yes % of LHDL, although being an MS component, shows no statistical significance in the trend test. The data have also demonstrated a negative relationship between the level of adiponectin and HOMA index in this homogenous type 2 diabetes cohort. Many studies have reported that adiponectin has both antiatherogenic and antidiabetic properties [34–36]. Previous research has shown that adiponectin levels are significantly lower in type 2 diabetes [3, 37, 38]. Subjects with hypoadiponectin level might have higher risk of developing cardiovascular disease [39, 40]. Adiponectin levels are positively correlated with insulin sensitivity and negatively with insulin resistance [34, 36, 40]. The findings in this study support that high HOMA index of type 2 diabetes has lower adiponectin level, which might lead to higher risk of developing cardiovascular disease in the future.
Our data also revealed that both MSA and MSB groups have higher ORs in developing higher insulin resistance than the NMS group in this type 2 diabetes cohort. Moreover, subjects with greater number of MS components have higher ORs in developing higher insulin resistance (Table 3). Although insulin resistance is not an MS component, the above finding has reconfirmed the association between insulin resistance and the number of MS components in type 2 diabetes, which corresponds to the observation of Hsieh et al. in the early onset DM population . We have a reason to believe that the greater the number of MS components in type 2 diabetes, the higher the risk in developing increased insulin resistance will be, and both of them lead to higher risk of CVD.
The finding in Table 4 also showed that groups with higher HbA1C (≥9.0) have higher ORs (3.6 times) in developing higher insulin resistance than the control group. Difference in BMI did not reach statistical significance. This may be because BMI can be fully predicted by waist circumference in this type 2 diabetes cohort. Previous studies have demonstrated that WC can be employed to predict insulin resistance , and some studies showed that WC is a better predictor of risk factors than BMI [43, 44]. Changes in BMI can be due to changes in skeletal muscle rather than body fat, whereas variations in WC are attributed mainly to changes in abdominal fat. Tankó et al. demonstrated that central abdominal fat is positively associated with insulin resistance . According to previous studies, lipid and fatty acids may induce insulin resistance by blunting insulin sensitivity through inhibition of glycolysis at key points . This explains the correlation of obesity, hyperlipidemia, and insulin resistance found in our study. From the results, we have a reason to believe that central obesity, hypertriglyceride, and long-term glucose control are the most important factors associated with insulin resistance in type 2 diabetes.
In conclusion, this study indicates the different impacts of MS components on insulin resistance in type 2 diabetes. Type 2 diabetic patients with greater number of MS components have higher ORs in developing higher insulin resistance. Central obesity and hypertriglyceride are the most important MS components associated with insulin resistance in type 2 diabetes.
|HOMA index:||HOMA insulin resistance index|
|FH:||Family history of type 2 diabetes disease|
|BMI:||Body mass index|
|SBP:||Systolic blood pressure|
|DBP:||Diastolic blood pressure|
|MSA:||Group of metabolic syndrome A|
|MSB:||Group of metabolic syndrome B|
|NMS:||Group of nonmetabolic syndrome|
|LWC:||Large waist circumference|
|LTN:||High blood pressure|
Conflict of Interests
The author declares that he has no conflict of interests.
The author would like to thank all colleagues in Taipei Hospital, Taiwan, for helping with this study. This study was supported by grants from the Taipei Hospital.
- J. Tuomilehto, J. Lindström, J. G. Eriksson et al., “Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance,” New England Journal of Medicine, vol. 344, no. 18, pp. 1343–1350, 2001.
- D. A. Lawlor, G. D. Smith, and S. Ebrahim, “Life course influences on insulin resistance: findings from the British women's heart and health study,” Diabetes Care, vol. 26, no. 1, pp. 97–103, 2003.
- C. Weyer, T. Funahashi, S. Tanaka et al., “Hypoadiponectinemia in obesity and type 2 diabetes: close association with insulin resistance and hyperinsulinemia,” Journal of Clinical Endocrinology and Metabolism, vol. 86, no. 5, pp. 1930–1935, 2001.
- G. M. Reaven, “Role of insulin resistance in human disease,” Diabetes, vol. 37, no. 12, pp. 1595–1607, 1988.
- R. H. Eckel, S. M. Grundy, and P. Z. Zimmet, “The metabolic syndrome,” Lancet, vol. 365, no. 9468, pp. 1415–1428, 2005.
- P. Zimmet, D. Magliano, Y. Matsuzawa, G. Alberti, and J. Shaw, “The metabolic syndrome: a global public health problem and a new definition,” Journal of atherosclerosis and thrombosis., vol. 12, no. 6, pp. 295–300, 2005.
- K. G. M. M. Alberti, P. Zimmet, and J. Shaw, “The metabolic syndrome—a new worldwide definition,” Lancet, vol. 366, no. 9491, pp. 1059–1062, 2005.
- P. Ilanne-Parikka, J. G. Eriksson, J. Lindström et al., “Prevalence of the metabolic syndrome and its components: findings from a Finnish general population sample and the Diabetes Prevention Study cohort,” Diabetes Care, vol. 27, no. 9, pp. 2135–2140, 2004.
- C. M. Alexander, P. B. Landsman, S. M. Teutsch, and S. M. Haffner, “NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among NHANES III participants age 50 years and older,” Diabetes, vol. 52, no. 5, pp. 1210–1214, 2003.
- G. Bruno, F. Merletti, A. Biggeri et al., “Metabolic syndrome as a predictor of all-cause and cardiovascular mortality in type 2 diabetes: the Casale Monferrato study,” Diabetes Care, vol. 27, no. 11, pp. 2689–2694, 2004.
- F. Relimpio, M. A. Martinez-Brocca, A. Leal-Cerro et al., “Variability in the presence of the metabolic syndrome in Type 2 diabetic patients attending a diabetes clinic: influences of age and gender,” Diabetes Research and Clinical Practice, vol. 65, no. 2, pp. 135–142, 2004.
- E. Bonora, G. Targher, G. Formentini et al., “Metabolic syndrome is an independent predictor of cardiovascular disease in type 2 diabetic subjects: prospective data from the verona diabetes complications study,” Diabetic Medicine, vol. 21, no. 1, pp. 52–58, 2004.
- L. A. Costa, L. H. Canani, H. R. K. Lisbôa, G. S. Tres, and J. L. Gross, “Aggregation of features of the metabolic syndrome is associated with increased prevalence of chronic complications in Type 2 diabetes,” Diabetic Medicine, vol. 21, no. 3, pp. 252–255, 2004.
- Y. J. Lee and J. C. R. Tsai, “ACE gene insertion/deletion polymorphism associated with 1998 World Health Organization definition of metabolic syndrome in Chinese type 2 diabetic patients,” Diabetes Care, vol. 25, no. 6, pp. 1002–1008, 2002.
- C. F. Semenkovich, “Insulin resistance and atherosclerosis,” Journal of Clinical Investigation, vol. 116, no. 7, pp. 1813–1822, 2006.
- H. N. Ginsberg, “Review: efficacy and mechanisms of action of statins in the treatment of diabetic dyslipidemia,” The Journal of Clinical Endocrinology & Metabolism, vol. 91, pp. 383–392, 2006.
- M. K. Cavaghan, D. A. Ehrmann, and K. S. Polonsky, “Interactions between insulin resistance and insulin secretion in the development of glucose intolerance,” Journal of Clinical Investigation, vol. 106, no. 3, pp. 329–333, 2000.
- E. Bonora, S. Kiechl, J. Willeit et al., “Prevalence of insulin resistance in metabolic disorders: the Bruneck Study,” Diabetes, vol. 47, no. 10, pp. 1643–1649, 1998.
- E. Ferrannini, G. Buzzigoli, R. Bonadonna et al., “Insulin resistance in essential hypertension,” The New England Journal of Medicine, vol. 370, no. 6, pp. 350–357, 1988.
- E. J. Diamantopoulos, E. Andreadis, G. Tsourous et al., “Insulin resistance and blood pressure circadian variation in an obese hypertensive population,” Clinical and Experimental Hypertension, vol. 28, no. 7, pp. 625–630, 2006.
- Z. T. Bloomgarden, “Inflammation, atherosclerosis, and aspects of insulin action,” Diabetes Care, vol. 28, no. 9, pp. 2312–2319, 2005.
- T. McLaughlin, F. Abbasi, C. Lamendola et al., “Differentiation between obesity and insulin resistance in the association with C-reactive protein,” Circulation, vol. 106, no. 23, pp. 2908–2912, 2002.
- M. Cnop, M. J. Landchild, J. Vidal et al., “The concurrent accumulation of intra-abdominal and subcutaneous fat explains the association between insulin resistance and plasma leptin concentrations: distinct metabolic effects of two fat compartments,” Diabetes, vol. 51, no. 4, pp. 1005–1015, 2002.
- D. R. Matthews, J. P. Hosker, and A. S. Rudenski, “Homeostasis model assessment: insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man,” Diabetologia, vol. 28, no. 7, pp. 412–419, 1985.
- E. Bonora, G. Formentini, F. Calcaterra et al., “HOMA-estimated insulin resistance is an independent predictor of cardiovascular disease in type 2 diabetic subjects: prospective data from the Verona Diabetes Complications Study,” Diabetes Care, vol. 25, no. 7, pp. 1135–1141, 2002.
- J. J. Nolan, B. Ludvik, P. Beerdsen, M. Joyce, and J. Olefsky, “Improvement in glucose tolerance and insulin resistance in obese subjects treated with troglitazone,” New England Journal of Medicine, vol. 331, no. 18, pp. 1188–1193, 1994.
- F. Pistrosch, J. Passauer, S. Fischer, K. Fuecker, M. Hanefeld, and P. Gross, “In type 2 diabetes, rosiglitazone therapy for insulin resistance ameliorates endothelial dysfunction independent of glucose control,” Diabetes Care, vol. 27, no. 2, pp. 484–490, 2004.
- C. J. Bailey, “Treating insulin resistance in type 2 diabetes with metformin and thiazolidinediones,” Diabetes, Obesity and Metabolism, vol. 7, no. 6, pp. 675–691, 2005.
- J. Noble, M. O. Baerlocher, and J. Silverberg, “Management of type 2 diabetes mellitus. Role of thiazolidinediones,” Canadian Family Physician, vol. 51, pp. 683–687, 2005.
- Z. T. Bloomgarden, “Developments in diabetes and insulin resistance,” Diabetes Care, vol. 29, no. 1, pp. 161–167, 2006.
- S. E. Shoelson, J. Lee, and A. B. Goldfine, “Inflammation and insulin resistance.,” The Journal of Clinical Investigation, vol. 116, pp. 1793–1801, 2006.
- R. Kahn, J. Buse, E. Ferrannini, and M. Stern, “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, vol. 28, no. 9, pp. 2289–2304, 2005.
- A. Festa, R. D'Agostino Jr., G. Howard, L. Mykkänen, R. P. Tracy, and S. M. Haffner, “Chronic subclinical inflammation as part of the insulin resistance syndrome: the insulin resistance atherosclerosis study (IRAS),” Circulation, vol. 102, no. 1, pp. 42–47, 2000.
- M. B. Schulze, I. Shai, E. B. Rimm, T. Li, N. Rifai, and F. B. Hu, “Adiponectin and future coronary heart disease events among men with type 2 diabetes,” Diabetes, vol. 54, no. 2, pp. 534–539, 2005.
- M. S. Farvid, T. W. K. Ng, D. C. Chan, P. H. R. Barrett, and G. F. Watts, “Association of adiponectin and resistin with adipose tissue compartments, insulin resistance and dyslipidaemia,” Diabetes, Obesity and Metabolism, vol. 7, no. 4, pp. 406–413, 2005.
- J. P. Whitehead, A. A. Richards, I. J. Hickman, G. A. Macdonald, and J. B. Prins, “Adiponectin—a key adipokine in the metabolic syndrome,” Diabetes, Obesity and Metabolism, vol. 8, no. 3, pp. 264–280, 2006.
- F. Jaleel, A. Jaleel, J. Aftab, and M. A. Rahman, “Relationship between adiponectin, glycemic control and blood lipids in diabetic type 2 postmenopausal women with and without complication of ischemic heart disease,” Clinica Chimica Acta, vol. 370, no. 1-2, pp. 76–81, 2006.
- K. Hotta, T. Funahashi, and Y. Arita, “et al. Plasma concentractions of a ovel, adipose-specific protein, adiponectin, in type 2 diabetic patients,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 20, pp. 1595–1599, 2000.
- M. B. Schulze, E. B. Rimm, I. Shai, N. Rifai, and F. B. Hu, “Relationship between adiponectin and glycemic control, blood lipids, and inflammatory markers in men with type 2 diabetes,” Diabetes Care, vol. 27, no. 7, pp. 1680–1687, 2004.
- G. K. Shetty, P. A. Economides, E. S. Horton, C. S. Mantzoros, and A. Veves, “Circulating adiponectin and resistin levels in relation to metabolic factors, inflammatory markers, and vascular reactivity in diabetic patients and subjects at risk for diabetes,” Diabetes Care, vol. 27, no. 10, pp. 2450–2457, 2004.
- C. H. Hsieh, C. Z. Wu, F. C. Hsiao et al., “The impact of metabolic syndrome on insulin sensitivity, glucose sensitivity, and acute insulin response after glucose load in early-onset type 2 diabetes mellitus: Taiwan Early-Onset Type 2 Diabetes Cohort Study,” Metabolism: Clinical and Experimental, vol. 57, no. 11, pp. 1615–1621, 2008.
- H. Wahrenberg, K. Hertel, B. M. Leijonhufvud, L. G. Persson, E. Toft, and P. Arner, “Use of waist circumference to predict insulin resistance: retrospective study,” British Medical Journal, vol. 330, no. 7504, pp. 1363–1364, 2005.
- B. A. Reeder, A. Senthilselvan, J. P. Després et al., “The association of cardiovascular disease risk factors with abdominal obesity in Canada,” Canadian Medical Association Journal, vol. 157, supplement 1, pp. S39–S45, 1997.
- M. C. Pouliot, J. P. Despres, S. Lemieux et al., “Waist circumference and abdominal sagittal diameter: best simple anthropometric indexes of abdominal visceral adipose tissue accumulation and related cardiovascular risk in men and women,” American Journal of Cardiology, vol. 73, no. 7, pp. 460–468, 1994.
- L. B. Tankó, Y. Z. Bagger, P. Alexandersen, P. J. Larsen, and C. Christiansen, “Peripheral adiposity exhibits an independent dominant antiatherogenic effect in elderly women,” Circulation, vol. 107, no. 12, pp. 1626–1631, 2003.
- V. T. Samuel, K. F. Petersen, and G. I. Shulman, “Lipid-induced insulin resistance: unravelling the mechanism,” The Lancet, vol. 375, no. 9733, pp. 2267–2277, 2010.