Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Combined Impact of Cardiorespiratory Fitness and Visceral Adiposity on Metabolic Syndrome in Overweight and Obese Adults in Korea

Combined Impact of Cardiorespiratory Fitness and Visceral Adiposity on Metabolic Syndrome in Overweight and Obese Adults in Korea

  • Sue Kim, 
  • Ji-Young Kim, 
  • Duk-Chul Lee, 
  • Hye-Sun Lee, 
  • Ji-Won Lee, 
  • Justin Y. Jeon
PLOS
x

Abstract

Background

Obesity, especially visceral obesity, is known to be an important correlate for cardiovascular disease and increased mortality. On the other hand, high cardiorespiratory fitness is suggested to be an effective contributor for reducing this risk. This study was conducted to determine the combined impact of cardiorespiratory fitness and visceral adiposity, otherwise known as fitness and fatness, on metabolic syndrome in overweight and obese adults.

Methods

A total of 232 overweight and obese individuals were grouped into four subtypes according to their fitness level. This was measured by recovery heart rate from a step test in addition to visceral adiposity defined as the visceral adipose tissue area to subcutaneous adipose tissue area ratio (VAT/SAT ratio). Associations of fitness and visceral fatness were analyzed in comparison with the prevalence of metabolic syndrome.

Results

The high visceral fat and low fitness group had the highest prevalence of metabolic syndrome [Odds Ratio (OR) 5.02; 95% Confidence Interval (CI) 1.85–13.61] compared with the reference group, which was the low visceral adiposity and high fitness group, after adjustments for confounding factors. Viscerally lean but unfit subjects were associated with a higher prevalence of metabolic syndrome than more viscerally obese but fit subjects (OR 3.42; 95% CI 1.27–9.19, and OR 2.70; 95% CI 1.01–7.25, respectively).

Conclusions

Our study shows that visceral obesity and fitness levels are cumulatively associated with a higher prevalence of metabolic syndrome in healthy overweight and obese adults. This suggests that cardiorespiratory fitness is a significant modifier in the relation of visceral adiposity to adverse metabolic outcomes in overweight and obese individuals.

Introduction

Obesity is a major cause of metabolic dysregulation and leads to increased morbidity and mortality; therefore, it is a significant health concern worldwide [1], [2]. Among obese characteristics, the accumulation of abdominal visceral adiposity has been shown to be strongly associated with a cluster of metabolic abnormalities and contributes to insulin resistance and metabolic syndrome [3], [4]. Furthermore, visceral adiposity is an independent risk factor for cardiovascular diseases, such as hypertension and diabetes, irrespective of total body fat [5], [6].

On the other hand, increased energy expenditure through physical activity prevents individuals from developing obesity and its related risks of metabolic abnormalities [7], [8]. Cardiorespiratory fitness, or aerobic fitness, refers to the ability of circulatory and respiratory function to supply oxygen to muscles and other organs during sustained physical activity without tiring out [9]. Increased cardiorespiratory fitness is known to reduce the risk of cardiometabolic diseases and can be estimated with recovery heart rate after exercise quantified as the indicator for physical fitness level [10], [11]. Recent studies demonstrate that a greater level of measured recovery heart rate is associated with an increased risk for metabolic syndrome as well as cardiovascular diseases and all-cause mortality [12][14].

The effects of obesity and fitness as unfavorable and favorable contributors to the risk of developing cardiometabolic diseases have become of clinical interest. Indeed, some studies exploring the combination of fitness and fatness on metabolic disturbance and mortality have shown that fitness was a powerful modifier of this association [15], [16]. Moreover, overweight but physically active individuals were shown to have an equivalent or even lower risk of death than lean but inactive individuals [17], [18]. However, although central visceral adiposity is a critical determinant of metabolic profiles in obesity, little is known about visceral adiposity, cardiorespiratory fitness, and their combined impact on metabolic profiles in overweight and obese subjects.

We hypothesized that overweight and obese adults with high visceral adiposity and low fitness level would have high prevalence of metabolic syndrome, and furthermore, the combination of the two factors would be related to the magnitude of the association on the prevalence of metabolic syndrome. Therefore, this study was conducted to investigate the combined impact of visceral obesity and cardiorespiratory fitness on metabolic syndrome in overweight and obese adults as determined by abdominal computed tomography (CT) scan measurement and heart rate recovery after exercise.

Materials and Methods

Ethics Statement

All subjects participated in the study voluntarily, and written informed consent was obtained from each participant. The study complied with the Declaration of Helsinki and was approved by the Institutional Review Board of Severance Hospital.

Study participants

A total of 232 men and women participated in this substudy of the Korean Physical Activity and Obesity (K-POP) study, which is an ongoing study designed to examine physical fitness and metabolic markers of overweight and obese adults in Seoul, Korea. The participants were recruited from the visitors to the obesity clinic in the department of family medicine at Severance Hospital from January 2010 to March 2013.

Being overweight was defined as having a body mass index (BMI) ≥ 23 kg/m2, and obesity was defined as having a BMI ≥ 25 kg/m2, following Asian-pacific population specific BMI criteria by World Health Organization expert consultation [19]. Only healthy subjects aged 18 to 70 years without underlying medical conditions were included in this study, such that those with histories of hypertension, diabetes, dyslipidemia, chronic liver disease or other cardiovascular diseases were excluded. Those with medications that can affect cardiometabolic function, including anti-hypertensives, hypoglycemic agents, or anti-obesity drugs, were also excluded from the study. Participants who were not able to fulfill the cardiorespiratory fitness evaluation due to their physical or psychological conditions were likewise excluded.

Clinical and anthropometric evaluation

Data on past and current medical conditions and medications were collected from medical records. BMI was calculated as weight divided by height squared. Body weight was measured to the nearest 0.1 kg with an electronic scale, and height was measured to the nearest 0.1 cm with a stadiometer. Waist circumference was measured midway between the lowest rib and the iliac crest in the standing position. Blood pressure was measured two times by mercury sphygmomanometer after at least 10-min seated rest, and the average of the two measurements was recorded. Mean blood pressure was calculated based on this measurement. Lifestyle factors such as smoking status, alcohol consumption, and physical activity status were provided by participants through questionnaires. Smoking status was considered “yes” if the subjects reported themselves as a current smoker. Alcohol consumption was defined as a positive factor if alcohol consumption was 72 g or more per week. Physical activity status was analyzed from a participant’s overall energy expenditure calculated in metabolic equivalents hour (MET-h) per week from information acquired through the Korean version of the International Physical Activity Questionnaire (IPAQ) [20].

Abdominal adipose tissue area was quantified by CT (Tomoscan 350; Philips, Mahwah, NJ, USA). Specifically, a 10-mm CT slice scan was acquired at the L4–L5 level with subjects in the supine position in order to measure the total abdominal tissue (TAT) and visceral adipose tissue (VAT) area. VAT was quantified by delineating the intra-abdominal cavity at the internal aspect of the abdominal and oblique muscle walls surrounding the cavity and the posterior aspect of the vertebral body. The subcutaneous adipose tissue (SAT) area was calculated by subtracting the VAT area from the TAT area. The coefficients of variation for inter- and intra-observer reproducibility for VAT were 1.4% and 0.5%, respectively.

Biochemical analyses

Biochemical analyses were performed on blood samples collected after overnight fasting (>12 hrs). Serum levels of fasting glucose, total cholesterol, triglycerides, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and high-sensitivity C-reactive protein were measured with the Hitachi 7600 Automatic analyzer (High-Technologies Corporation, Hitachi, Tokyo, Japan). Fasting insulin was measured by electrochemiluminescence immunoassay using an Elecsys 2010 (Roche, Indianapolis, IN, USA), and insulin resistance was estimated using the homeostasis model assessment of insulin resistance (HOMA-IR) index [Insulin (mUl/L) × fasting glucose (mg/dl)/405] [21].

Metabolic syndrome was defined using the criteria proposed by the American Heart Association and the National Heart, Lung, and Blood Institute, with waist circumference criteria modification based on the following World Health Organization-Asian Pacific region criteria for abdominal obesity [19], [22]: (1) a waist circumference ≥90 cm for men and ≥85 cm for women; (2) triglycerides ≥150 mg/dl; (3) serum HDL cholesterol <40 mg/dl for men and <50 mg/dl for women; (4) systolic blood pressure ≥130 mmHg, diastolic blood pressure ≥85 mmHg, or use of anti-hypertensive medication); and (5) fasting glucose ≥100 mg/dl, or insulin or hypoglycemic medication use.

Cardiorespiratory fitness

Cardiorespiratory fitness was evaluated using Tecumseh, a standardized 3-minute step test. Participants performed 24 steps per minute based on the protocol for the Tecumseh step test, maintaining a constant stepping rate on a 20.3 cm-high step for 3 minutes [10], [23]. The participants were aided by an assistant’s demonstration and a metronome cadence for proper stepping technique and constant step maintenance. Heart rates were measured and recorded by a heart rate monitor (Polar-FS3C, USA) attached on the anterior chest wall of the participant. Heart rates were recorded in a seating position 1 minute prior to exercise after at least 5 minutes of resting and 1 minute after the completion of the 3-minute step exercise (1 minute recovery heart rate). The expectation was that participants with greater cardiorespiratory fitness would have lower heart rates at 1 minute post-exercise than those with worse cardiorespiratory fitness [11].

Statistical analyses

To examine the joint impact of visceral fat and fitness level on the prevalence of metabolic syndrome, participants were divided into the following four groups according to the combination of their visceral obesity and fitness level: (1) low visceral fat and high level of fitness, (2) low visceral fat and low level of fitness, (3) high visceral adiposity and high level of fitness, and (4) high visceral adiposity and low level of fitness. Low visceral obesity was defined as having a VAT/SAT ratio measured by CT scan of less than 0.4, and high visceral obesity was defined as having a VAT/SAT ratio ≥ 0.4 [24]. Fitness level was divided into high or low according to the median value (50th percentile) of the distribution.

Data are expressed as means ± standard deviation (SD) or numbers (percentages). Normality of the variables was tested using the Kolmogorov-Smirnov test. The data between the groups were compared with analysis of variance for continuous data or chi-square test for categorical data. Bonferroni’s post hoc tests were performed when significant differences were found to assess the magnitude of the differences.

To test the combined effect of visceral adiposity and fitness level, we tested their interactions with the interaction term for visceral adiposity*fitness level by logistic regression models for metabolic syndrome after adjusting for age and sex.

Multiple logistic regression analyses were performed to estimate the magnitude of the association of the four groups divided according to the combination of visceral adiposity and fitness level combined on the development of metabolic syndrome, after adjusting for age, sex, lifestyle factors (smoking, alcohol, and physical activity status), and BMI. The interaction between visceral adiposity and fitness level was tested at a significance level of 0.15 [25], . Hypothesis testing was two-sided at a significance level of 0.05. Statistical analyses were performed with SPSS (version 20.0; SPSS Inc., Chicago, IL, USA).

Results

Characteristics of the participants divided into the four groups according to visceral adiposity and fitness level are shown in Table 1. The VAT/SAT ratio was approximately 0.28 in the low adiposity groups and 0.65 in the high visceral adiposity groups, and was highest in the high visceral adiposity and low fitness level group. Recovery heart rate after exercise was approximately 81.1 beats per min (bpm) in the high fitness level groups and 105.8 bpm in the low fitness level groups, and was highest in the low visceral adiposity and low fitness level group. In comparison between the groups, the high visceral adiposity groups had a tendency to be older and the low visceral adiposity groups had more males in each of their groups. Notwithstanding having greater visceral adiposity, the high visceral adiposity and high fitness level group had lower parameters of insulin resistance, insulin, and HOMA-IR than did the low visceral adiposity and low fitness level group. There were no differences in lifestyle factors (smoking, alcohol, and physical activity status) between the groups.

thumbnail
Table 1. Clinical characteristics according to visceral adiposity (VAT/SAT ratio) and fitness level (recovery heart rate).

http://dx.doi.org/10.1371/journal.pone.0085742.t001

Visceral adiposity and fitness level were seen to have a significant interaction for the prevalence of metabolic syndrome via the interaction term between the two factors, after adjusting for age and sex (p = 0.138).

Across the four groups in regards to the association with the prevalence of metabolic syndrome, and with the most favorable group defined by low visceral adiposity and high fitness as the reference, subjects with a high visceral fat and low fitness level were associated with the highest prevalence of metabolic syndrome among all other groups (OR: 5.02, 95% CI: 1.85–13.61), after adjustment for age, sex, smoking, alcohol, physical activity status, and BMI. Furthermore, low visceral adiposity but low fitness level had a significantly higher OR for the development of metabolic syndrome than did high visceral adiposity but high fitness level, after adjustment for the covariates (OR 3.42, 95% CI: 1.27–9.19 and OR 2.70, 95% CI: 1.01–7.25, respectively) (Figure 1).

thumbnail
Figure 1. Odds ratio for metabolic syndrome according to visceral adiposity(VAT/SAT ratio) and fitness level(recovery heart rate).

Adjusted odds ratio: adjusted for age, sex, smoking, alcohol, physical activity status, and body mass index. *p< 0.05, **p<0.01, calculated by multiple logistic regression analyses.

http://dx.doi.org/10.1371/journal.pone.0085742.g001

Discussion

The objective of this study was to evaluate the joint impact of cardiorespiratory fitness and visceral adiposity on metabolic syndrome in overweight and obese adults. Our results showed that high visceral adiposity and low fitness level were cumulatively associated with metabolic syndrome. Furthermore, viscerally lean but unfit subjects were found to have a greater odds for developing metabolic syndrome than viscerally obese but highly fit individuals. These results indicate that the cardiorespiratory fitness level can alter the associations between visceral obesity and metabolic syndrome and is an important factor for reducing metabolic risk factors in overweight and obese adults.

Excessive visceral adipose tissue accumulation is one of the most important contributors to the clustering of adverse cardiometabolic profiles and metabolic syndrome that are associated with being overweight and obese [27]. Recent studies reveal that the characteristic of high visceral fat storage is a part of dysfunctional SAT expansion that leads to the functional loss of SAT as an energy deposit, resulting in ectopic fat deposition predominantly in abdominal visceral adipose tissue, liver, and skeletal muscle, and thus promoting insulin resistance [28], [29]. The concept of the VAT/SAT ratio measurement has therefore been suggested to better represent visceral fat with metabolic abnormalities, reflecting relative distribution of abdominal adipose tissue [24], [30], [31]. Indeed, the VAT/SAT ratio has been reported to have associations with metabolic syndrome, hypertension, and diabetes independent of total visceral fat volume, and with glucose intolerance, insulin resistance, and dyslipidemia [31], [32].

Cardiorespiratory fitness and metabolic syndrome may be related to the fact that unfit subjects are likely to have a high VAT [33]. Moreover, cardiorespiratory fitness is known to counteract the deleterious action of visceral adiposity [34]. In several studies, fitness level was shown to have an impact on modulating cardiovascular diseases such as diabetes as well as on mortality among overweight and obese individuals [35], [36]. While visceral fat leads to greater release of deleterious cytokines and adipokines, improving fitness leads to a greater responsiveness to advantageous adipokines and cytokines, such as leptin, adiponectin, and interleukin (IL)-10 37,38. This adaptive change in sensitivity and metabolism concurrently decreases the release of unfavorable pro-inflammatory adipokines and cytokines, such as resistin, tumor necrosis factor-α, IL-6, retinol binding protein-4, etc [39]. Additionally, the increase in fat-free lean mass and decrease in resting cortisol levels through physical exercise are demonstrated to be associated with metabolic improvements [27], [38]. As a result, fitness and fatness combine to define one’s overall health status through fitness regulating metabolic adaptations and metabolic flexibility of the viscerally obese condition. In this study, fitness was demonstrated to be a modifier of the association between visceral obesity and the prevalence of metabolic syndrome.

Reduction in insulin resistance is known to be one of the primary metabolic adaptations of fitness, which leads to improvement in insulin sensitivity and glucose tolerance for skeletal muscle and throughout the body [34], [40]. Increased expression of glucose transporter-4 protein and upregulation of glucose from enhanced skeletal muscle mitochondria enzyme activity may explain the link between cardiorespiratory fitness and improved insulin resistance [41], [42]. Our results also demonstrate that fasting serum insulin levels and the insulin resistance marker HOMA-IR were lower in the high fitness group than the low fitness group despite the high fitness group having a higher visceral adiposity.

Only a few studies have explored the combined effect of visceral adiposity and cardiorespiratory fitness on metabolic outcomes or mortality. For instance, hypertensive patients with abdominal obesity (higher waist circumference) but a high degree of fitness were shown to have lower cardiovascular disease and all-cause death than were those with normal abdominal obesity but a low level of fitness [43]. In patients with cardiovascular disease, subjects with a high waist-to-hip ratio (WHR) and a high fitness level had a lower hazards ratio for mortality than those with a low WHR and a low fitness level [44]. Our study had results in accordance with these prior studies, but was strengthened by an accurate CT measurement of visceral adiposity and by using the criteria of VAT/SAT ratio. Additionally, Rheaume et al. suggested that changes in both visceral fat accumulation and cardiorespiratory fitness were associated with changes in metabolic syndrome components and that the two factors are both important for the maintenance of healthy cardiometabolic risk profiles, which is consistent with the results from our study [45]. Here, we compared these associations for individuals by stratifying their central adiposity by fitness level, permitting more rigorous analyses of combined subgroups than adjustment for either variable alone [43].

There were some limitations to our study. The directionality and causality of the results of cross-sectional analyses could not be determined with certainty. The 3-minute step test was used to measure fitness level instead of a direct measure of maximal oxygen uptake (VO2 max). However, the correlation between the 3-minute step test results and VO2 max has been validated in many studies so far, and the 3 minute step test is known to be a relatively quick and easy method used in clinical settings and in epidemiologic studies since the early 20th century [46], [47]. Also, the HOMA-IR index was used instead of direct measurement for the representation of insulin resistance. Nonetheless, HOMA-IR has been validated as a reliable and clinically useful marker for assessing beta-cell function and insulin resistance [48]. Finally, as the sample was composed of more young to middle-aged adults, it may be difficult to generalize the data and results to older populations with a greater tendency toward higher visceral adiposity accumulation. Further studies are warranted to clearly identify the combined effect of fitness and visceral fatness to metabolic characteristics in an older and larger population.

Conclusions

In conclusion, visceral obesity and fitness level are cumulatively associated with the prevalence of metabolic syndrome in healthy overweight and obese adults. This suggests that cardiorespiratory fitness is a significant modifier of the relation between visceral adiposity and adverse metabolic outcomes, and the effects of improvement in fitness can be an important target for maintenance of the overall healthy metabolic characteristics in overweight and obese individuals.

Author Contributions

Conceived and designed the experiments: SK JYK JWL JYJ. Performed the experiments: SK JYK JWL JYJ. Analyzed the data: SK DCL HSL. Contributed reagents/materials/analysis tools: DCL JWL JYJ. Wrote the paper: SK JYK.

References

  1. 1. Pischon T, Boeing H, Hoffmann K, Bergmann M, Schulze MB, et al. (2008) General and abdominal adiposity and risk of death in Europe. N Engl J Med 359: 2105–2120. doi: 10.1056/nejmoa0801891
  2. 2. Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F, et al. (2003) Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001. JAMA 289: 76–79. doi: 10.1001/jama.289.1.76
  3. 3. Bjorntorp P (1997) Body fat distribution, insulin resistance, and metabolic diseases. Nutrition 13: 795–803. doi: 10.1016/s0899-9007(97)00191-3
  4. 4. Despres JP (2006) Is visceral obesity the cause of the metabolic syndrome? Ann Med 38: 52–63. doi: 10.1080/07853890500383895
  5. 5. Mathieu P, Poirier P, Pibarot P, Lemieux I, Despres JP (2009) Visceral obesity: the link among inflammation, hypertension, and cardiovascular disease. Hypertension 53: 577–584. doi: 10.1161/hypertensionaha.108.110320
  6. 6. Liu J, Fox CS, Hickson DA, May WD, Hairston KG, et al. (2010) Impact of abdominal visceral and subcutaneous adipose tissue on cardiometabolic risk factors: the Jackson Heart Study. J Clin Endocrinol Metab 95: 5419–5426. doi: 10.1210/jc.2010-1378
  7. 7. Katzmarzyk PT, Church TS, Blair SN (2004) Cardiorespiratory fitness attenuates the effects of the metabolic syndrome on all-cause and cardiovascular disease mortality in men. Arch Intern Med 164: 1092–1097. doi: 10.1001/archinte.164.10.1092
  8. 8. LaMonte MJ, Barlow CE, Jurca R, Kampert JB, Church TS, et al. (2005) Cardiorespiratory fitness is inversely associated with the incidence of metabolic syndrome: a prospective study of men and women. Circulation 112: 505–512. doi: 10.1161/circulationaha.104.503805
  9. 9. Steele RM, Brage S, Corder K, Wareham NJ, Ekelund U (2008) Physical activity, cardiorespiratory fitness, and the metabolic syndrome in youth. J Appl Physiol 105: 342–351. doi: 10.1152/japplphysiol.00072.2008
  10. 10. McArdle WD (2000) Essentials of Exercise Physiology. USA: Lipincott Williams and Wilkins.
  11. 11. Siconolfi SF, Garber CE, Lasater TM, Carleton RA (1985) A simple, valid step test for estimating maximal oxygen uptake in epidemiologic studies. Am J Epidemiol 121: 382–390.
  12. 12. Nilsson G, Hedberg P, Jonason T, Lonnberg I, Ohrvik J (2007) Heart rate recovery is more strongly associated with the metabolic syndrome, waist circumference, and insulin sensitivity in women than in men among the elderly in the general population. Am Heart J 154: 460 e461–467.
  13. 13. Morshedi-Meibodi A, Larson MG, Levy D, O'Donnell CJ, Vasan RS (2002) Heart rate recovery after treadmill exercise testing and risk of cardiovascular disease events (The Framingham Heart Study). Am J Cardiol 90: 848–852. doi: 10.1016/s0002-9149(02)02706-6
  14. 14. Shishehbor MH, Litaker D, Pothier CE, Lauer MS (2006) Association of socioeconomic status with functional capacity, heart rate recovery, and all-cause mortality. JAMA 295: 784–792. doi: 10.1001/jama.295.7.784
  15. 15. Sui X, LaMonte MJ, Laditka JN, Hardin JW, Chase N, et al. (2007) Cardiorespiratory fitness and adiposity as mortality predictors in older adults. JAMA 298: 2507–2516. doi: 10.1001/jama.298.21.2507
  16. 16. Stevens J, Evenson KR, Thomas O, Cai J, Thomas R (2004) Associations of fitness and fatness with mortality in Russian and American men in the lipids research clinics study. Int J Obes Relat Metab Disord 28: 1463–1470. doi: 10.1038/sj.ijo.0802770
  17. 17. Lee CD, Blair SN, Jackson AS (1999) Cardiorespiratory fitness, body composition, and all-cause and cardiovascular disease mortality in men. Am J Clin Nutr 69: 373–380.
  18. 18. Lee DC, Sui X, Artero EG, Lee IM, Church TS, et al. (2011) Long-term effects of changes in cardiorespiratory fitness and body mass index on all-cause and cardiovascular disease mortality in men: the Aerobics Center Longitudinal Study. Circulation 124: 2483–2490. doi: 10.1161/circulationaha.111.038422
  19. 19. Consultation WHOE (2004) Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet 363: 157–163. doi: 10.1016/s0140-6736(03)15268-3
  20. 20. Hagstromer M, Oja P, Sjostrom M (2006) The International Physical Activity Questionnaire (IPAQ): a study of concurrent and construct validity. Public Health Nutr 9: 755–762. doi: 10.1079/phn2005898
  21. 21. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, et al. (1985) Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 28: 412–419. doi: 10.1007/bf00280883
  22. 22. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, et al. (2005) Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation 112: 2735–2752. doi: 10.1161/circulationaha.105.169404
  23. 23. Jekal Y, Lee MK, Park S, Lee SH, Kim JY, et al. (2010) Association between Obesity and Physical Fitness, and Hemoglobin A1c Level and Metabolic Syndrome in Korean Adults. Korean Diabetes J 34: 182–190. doi: 10.4093/kdj.2010.34.3.182
  24. 24. Fujioka S, Matsuzawa Y, Tokunaga K, Tarui S (1987) Contribution of intra-abdominal fat accumulation to the impairment of glucose and lipid metabolism in human obesity. Metabolism 36: 54–59. doi: 10.1016/0026-0495(87)90063-1
  25. 25. Lentner C (ed) (1982) Geigy Scientific Tables. Basel: Ciba-Geigy Limited.
  26. 26. Lai CL, Gane E, Liaw YF, Hsu CW, Thongsawat S, et al. (2007) Telbivudine versus Lamivudine in Patients with Chronic Hepatitis B. N Engl J Med. 357: 2576–88. doi: 10.1056/nejmoa066422
  27. 27. Tchernof A, Despres JP (2013) Pathophysiology of human visceral obesity: an update. Physiol Rev 93: 359–404. doi: 10.1152/physrev.00033.2011
  28. 28. Heilbronn L, Smith SR, Ravussin E (2004) Failure of fat cell proliferation, mitochondrial function and fat oxidation results in ectopic fat storage, insulin resistance and type II diabetes mellitus. Int J Obes Relat Metab Disord 28 Suppl 4S12–21. doi: 10.1038/sj.ijo.0802853
  29. 29. Despres JP, Lemieux I (2006) Abdominal obesity and metabolic syndrome. Nature 444: 881–887. doi: 10.1038/nature05488
  30. 30. Lee JW, Lee HR, Shim JY, Im JA, Kim SH, et al. (2007) Viscerally obese women with normal body weight have greater brachial-ankle pulse wave velocity than nonviscerally obese women with excessive body weight. Clin Endocrinol (Oxf) 66: 572–578. doi: 10.1111/j.1365-2265.2007.02780.x
  31. 31. Kaess BM, Pedley A, Massaro JM, Murabito J, Hoffmann U, et al. (2012) The ratio of visceral to subcutaneous fat, a metric of body fat distribution, is a unique correlate of cardiometabolic risk. Diabetologia 55: 2622–2630. doi: 10.1007/s00125-012-2639-5
  32. 32. Miyazaki Y, DeFronzo RA (2009) Visceral fat dominant distribution in male type 2 diabetic patients is closely related to hepatic insulin resistance, irrespective of body type. Cardiovasc Diabetol 8: 44. doi: 10.1186/1475-2840-8-44
  33. 33. Arsenault BJ, Lachance D, Lemieux I, Almeras N, Tremblay A, et al. (2007) Visceral adipose tissue accumulation, cardiorespiratory fitness, and features of the metabolic syndrome. Arch Intern Med 167: 1518–1525. doi: 10.1001/archinte.167.14.1518
  34. 34. Clark JE (2012) An overview of the contribution of fatness and fitness factors, and the role of exercise, in the formation of health status for individuals who are overweight. J Diabetes Metab Disord 11: 19. doi: 10.1186/2251-6581-11-19
  35. 35. McAuley PA, Smith NS, Emerson BT, Myers JN (2012) The obesity paradox and cardiorespiratory fitness. J Obes 2012: 951582. doi: 10.1155/2012/951582
  36. 36. Kelley DE, Goodpaster BH (1999) Effects of physical activity on insulin action and glucose tolerance in obesity. Med Sci Sports Exerc 31: S619–623. doi: 10.1097/00005768-199911001-00021
  37. 37. Nannipieri M, Bonotti A, Anselmino M, Cecchetti F, Madec S, et al. (2007) Pattern of expression of adiponectin receptors in human adipose tissue depots and its relation to the metabolic state. Int J Obes (Lond) 31: 1843–1848. doi: 10.1038/sj.ijo.0803676
  38. 38. Izquierdo M, Ibanez J, Calbet JA, Navarro-Amezqueta I, Gonzalez-Izal M, et al. (2009) Cytokine and hormone responses to resistance training. Eur J Appl Physiol 107: 397–409. doi: 10.1007/s00421-009-1139-x
  39. 39. Jones TE, Basilio JL, Brophy PM, McCammon MR, Hickner RC (2009) Long-term exercise training in overweight adolescents improves plasma peptide YY and resistin. Obesity (Silver Spring) 17: 1189–1195. doi: 10.1038/oby.2009.11
  40. 40. Sieverdes JC, Sui X, Lee DC, Church TS, McClain A, et al. (2010) Physical activity, cardiorespiratory fitness and the incidence of type 2 diabetes in a prospective study of men. Br J Sports Med 44: 238–244. doi: 10.1136/bjsm.2009.062117
  41. 41. Houmard JA, Shinebarger MH, Dolan PL, Leggett-Frazier N, Bruner RK, et al. (1993) Exercise training increases GLUT-4 protein concentration in previously sedentary middle-aged men. Am J Physiol 264: E896–901.
  42. 42. Horowitz JF, Klein S (2000) Lipid metabolism during endurance exercise. Am J Clin Nutr 72: 558S–563S.
  43. 43. McAuley PA, Sui X, Church TS, Hardin JW, Myers JN, et al. (2009) The joint effects of cardiorespiratory fitness and adiposity on mortality risk in men with hypertension. Am J Hypertens 22: 1062–1069.
  44. 44. Goel K, Thomas RJ, Squires RW, Coutinho T, Trejo-Gutierrez JF, et al. (2011) Combined effect of cardiorespiratory fitness and adiposity on mortality in patients with coronary artery disease. Am Heart J 161: 590–597. doi: 10.1016/j.ahj.2010.12.012
  45. 45. Rheaume C, Arsenault BJ, Dumas MP, Perusse L, Tremblay A, et al. (2011) Contributions of cardiorespiratory fitness and visceral adiposity to six-year changes in cardiometabolic risk markers in apparently healthy men and women. J Clin Endocrinol Metab 96: 1462–1468. doi: 10.1210/jc.2010-2432
  46. 46. Wener J, Sandberg AA, Scherlis L, Dvordin J, Master AM (1953) The electrocardiographic response to the standard 2-step exercise test. Can Med Assoc J 68: 368–374.
  47. 47. Santo AS, Golding LA (2003) Predicting maximum oxygen uptake from a modified 3-minute step test. Res Q Exerc Sport 74: 110–115. doi: 10.1080/02701367.2003.10609070
  48. 48. Yokoyama H, Emoto M, Fujiwara S, Motoyama K, Morioka T, et al. (2004) Quantitative insulin sensitivity check index and the reciprocal index of homeostasis model assessment are useful indexes of insulin resistance in type 2 diabetic patients with wide range of fasting plasma glucose. J Clin Endocrinol Metab 89: 1481–1484. doi: 10.1210/jc.2003-031374