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Do obese but metabolically normal women differ in intra-abdominal fat and physical activity levels from those with the expected metabolic abnormalities? A cross-sectional study
© Hayes et al; licensee BioMed Central Ltd. 2010
Received: 22 June 2010
Accepted: 24 November 2010
Published: 24 November 2010
Obesity remains a major public health problem, associated with a cluster of metabolic abnormalities. However, individuals exist who are very obese but have normal metabolic parameters. The aim of this study was to determine to what extent differences in metabolic health in very obese women are explained by differences in body fat distribution, insulin resistance and level of physical activity.
This was a cross-sectional pilot study of 39 obese women (age: 28-64 yrs, BMI: 31-67 kg/m2) recruited from community settings. Women were defined as 'metabolically normal' on the basis of blood glucose, lipids and blood pressure. Magnetic Resonance Imaging was used to determine body fat distribution. Detailed lifestyle and metabolic profiles of participants were obtained.
Women with a healthy metabolic profile had lower intra-abdominal fat volume (geometric mean 4.78 l [95% CIs 3.99-5.73] vs 6.96 l [5.82-8.32]) and less insulin resistance (HOMA 3.41 [2.62-4.44] vs 6.67 [5.02-8.86]) than those with an abnormality. The groups did not differ in abdominal subcutaneous fat volume (19.6 l [16.9-22.7] vs 20.6 [17.6-23.9]). A higher proportion of those with a healthy compared to a less healthy metabolic profile met current physical activity guidelines (70% [95% CIs 55.8-84.2] vs 25% [11.6-38.4]). Intra-abdominal fat, insulin resistance and physical activity make independent contributions to metabolic status in very obese women, but explain only around a third of the variance.
A sub-group of women exists who are metabolically normal despite being very obese. Differences in fat distribution, insulin resistance, and physical activity level are associated with metabolic differences in these women, but account only partially for these differences. Future work should focus on strategies to identify those obese individuals most at risk of the negative metabolic consequences of obesity and on identifying other factors that contribute to metabolic status in obese individuals.
The health consequences of obesity are well established. Obese individuals are at greater risk of cardiovascular disease[1, 2], largely through the association of obesity with dyslipidaemia, hypertension, glucose intolerance and diabetes. It is well known that individuals who are not obese can develop these metabolic abnormalities[4, 5]. What has been less widely appreciated until recently is that a subset of obese individuals remains free of any of these metabolic abnormalities. Current data suggest that 20-30% of obese individuals appear to maintain a favourable metabolic profile, more usually associated with lean individuals[6, 7]. Such individuals have been termed 'metabolically normal obese', 'metabolically healthy but obese', 'obese metabolically normal' or described as having metabolically benign obesity or uncomplicated obesity
The mechanisms through which obesity exerts its effect on metabolic disorders remain to be fully explained, but considerable interest has focused on the role of body fat distribution. Vague first identified android (upper-body or abdominal) obesity as being associated with diabetes and atherosclerosis over 50 years ago . Individuals with higher levels of central adiposity are at greater risk of developing lipid and glucose abnormalities than those with fat distributed more peripherally [14, 15]. Compelling evidence now exists to suggest that excess intra-abdominal (visceral) fat in particular confers an increased risk of developing a metabolic disorder[16, 17].
An increasing body of work exists to suggest that poor metabolic health associated with obesity is mediated by physical activity. Several studies have demonstrated that higher physical activity and/or cardiorespiratory fitness is associated with more favourable metabolic health even among obese individuals[7, 18–22].
Several recent studies have identified factors that are associated with high insulin sensitivity and a favourable metabolic profile in obese individuals. Although standard criteria to define the metabolically healthy obese (MHO) individual are lacking, studies have suggested that both lower intra-abdominal fat (IAF)[8, 23] and higher physical activity level are associated with a more healthy metabolic profile in obese individuals.
However, data on the association of directly measured IAF and other cardiovascular risk factors with metabolic health in the very obese (BMI ≥ 35) are scarce. Most work in this field has focused on the overweight and modestly obese (BMI 25-34)[11, 25].
This paper presents a pilot study that arose from the clinical observation that a substantial minority of individuals referred to a metabolic clinic for the management of severe obesity had a healthy metabolic profile. Our aim was to determine to what extent differences in metabolic health in very obese (class II and class III obesity) women are explained by differences in body fat distribution, insulin resistance and level of physical activity.
Participants in this study were 39 very obese women (median BMI 39.6 kg/m2), aged 28-64 years and of Caucasian origin. The women were recruited from a number of sources, including an obesity clinic, dieticians and from responding to a press release. Participants were defined as 'metabolically healthy' (MHO) if they had a fasting plasma glucose less than 6.1 mmol/l-1, a 2-hour post 75 g glucose challenge plasma glucose less than 7.8 mmol/l-1, fasting triglycerides less than 2.2 mmol/l-1, HDL cholesterol greater than 1.1 mmol/l-1and blood pressure < 160/95 mmHg (n = 20). Participants not meeting these criteria were defined as 'metabolically abnormal' (MetAb). At the time this study was planned there was a lack of consensus on appropriate cut points for metabolic abnormalities, and for example, no internationally agreed definition of the metabolic syndrome. Our approach to defining MHO was therefore somewhat pragmatic, combining WHO cut points for glucose with cut points recommended locally and used in care for people with diabetes and treatment within the obesity service for lipids and blood pressure. Nineteen women (9 MHO and 10 MetAb) were postmenopausal; four (1 MHO; 3 MetAb) were currently using HRT.
Ethical approval for the study was obtained from the Joint Ethics Committee of Newcastle and North Tyneside Health Authority and the Newcastle Universities. Participants provided written consent for their participation.
Assessment of body fat distribution
Body fat was assessed using magnetic resonance imaging (MRI). Images were acquired on a Philips Intera 1.5 T MRI system and rapid T1-weighted spin-echo sequence with repetition time = 36 ms, echo time = 14 ms, flip angle 120°, field of view = 60 cm, 256 × 256 matrix and phase-conjugate symmetry. Participants were scanned from the lower sternum to the mid thigh, by acquiring 10 mm thick transverse images with 30 mm gaps between slices, as they lay in a supine position.
The volume of IAF and SCF fat compartments were determined based on the method of Thomas. The MR images were transferred from the scanner to a PC for analysis with custom written software. Fat appears as a bright, high-intensity signal against a lower signal from other tissues. Total fat content was determined in the following fashion for each slice in the image. To automatically locate the outside of the torso, the software examines pixels starting at the posterior left of the image, and moving diagonally inwards, until two adjacent pixels brighter than 1/3 of the maximum signal intensity are found. A threshold value is determined from the sharpest edge in a 5 × 5 pixel neighbourhood of this point, and a contour around the torso automatically generated using this threshold. The mean (Mc) and standard deviation (SDc) of the pixels along this contour are determined and a final threshold Tf is set as Tf = Mc - SDc.
A new contour around the outside of the torso is automatically generated using this threshold, and those pixels with an intensity brighter than Tf are designated as fat. The images were manually checked, and the contour, and/or threshold level could be adjusted as necessary. Each slice was reviewed manually to delete unwanted voxels associated with, for example, bone marrow and some stomach contents which give high intensity signals in the images. The total fat volume was then determined by multiplying the number of pixels brighter than the threshold Tf by the pixel size and sum of slice thickness and slice gap.
Abdominal adipose tissue was defined as fat found in the slices from the femoral heads to the top of the liver or base of the lungs. Subcutaneous fat in this region was identified as SCF. Fat that was within the peritoneum was identified as IAF. To determine the IAF content, a region encompassing the viscera was drawn manually by an operator using a computer mouse. The IAF volume was determined by multiplying the number of pixels brighter than the threshold Tf in this region by the pixel size and sum of slice thickness and slice gap. The subcutaneous fat volume was determined by subtracting the intra-abdominal fat volume from the total fat volume. A measure of thigh fat was made by calculating the fat area in one slice of one leg taken 80 mm (2 slices) below the femoral heads slice.
Height was measured without shoes to the nearest 5 mm, with the head positioned so that the eye and the external auditory meatus were level. Weight was measured to the nearest 100 g with the subject lightly clothed. Waist circumference was measured, with the waist unclothed and hip circumference over the subject's underwear, to the nearest centimetre at the midpoint between the lower costal margin and the superior iliac crest, and the hips over the greater trochanters. Sagittal diameter was measured using an abdominal caliper as the distance between the highest point of the abdomen and the examination table with the participant lying supine. Body Mass Index (BMI) was calculated as weight (kg)/[height(m)2].
Participants attended for screening after an overnight fast. Participants followed their usual diet and physical activity pattern prior to screening. Fasting blood samples were taken on arrival at the clinic. Participants then took a standard oral glucose tolerance test. A venous blood was taken after 30 minutes and 2 hours. Plasma was separated by centrifugation within an hour (after refrigeration of the sample). Serum insulin levels were measured by an enzyme linked immunosorbent assay (ELISA; Dako Ltd, Ely, UK). Plasma glucose concentrations were measured on a Yellow Springs Analyser (YSI Stat Plus 2300; Yellow Springs Instruments, Farnborough, UK). Insulin resistance (HOMA-IR) was estimated using the Homeostasis Model Assessment, based on fasting insulin and glucose.
Serum triglycerides were measured by a lipase/glycerol kinase method on a Cobas Bio centrifugal analyser (Roche Products Ltd, Welwyn, UK) using a commercial kit (Sigma Diagnostics, Poole, UK). Serum HDL cholesterol was estimated by measuring the supernatant cholesterol concentration after precipitation of apolipoprotein B containing lipoproteins with heparin and manganese. LDL cholesterol was estimated using the Friedwald formula. Non-esterfied fatty acid (NEFA) was measured by a WAKO cabas analyser.
Blood pressure was measured twice in the right arm using an automated blood pressure monitor (Omron M5-I) and a large cuff (for arm circumference 32-42 cm). The mean measurement was used in analysis.
Current level of physical activity was assessed by an interviewer-administered questionnaire, based on the Modifiable Activity Questionnaire, and by the use of a pedometer (Yamax Digiwalker SW-200). The Modifiable Activity Questionnaire collects information on leisure time, occupational and transportation (walking or cycling) physical activity. The amount of leisure time, occupational and transportation physical activity undertaken was recorded and assigned a metabolic equivalent score (MET; 1 MET = 3.5 ml O2 uptake per kg/min) according to the Compendium of Physical Activities. The reported daily average time spent in leisure time activities, occupational activities (including sitting) and walking or cycling for transport was summed and total energy expenditure was computed assuming that time not reported (i.e. 24 hours minus the sum of the hours reported) was spent at rest and assigned a MET score of 1. In addition participants were categorised according to whether or not they met the current UK recommendation for the level of physical activity required to provide health benefits (at least 30 minutes of moderate activity on at least 5 occasions per week).
Participants wore the pedometer for four days (1 weekend day and 3 weekdays). A daily mean number of steps walked was calculated.
All data analyses were performed using SPSS version 11.0. Measures of central tendency and variability are presented for anthropometric and biochemical data. Variables were log transformed where appropriate and geometric means with 95% confidence intervals are presented. Where variable distributions were not normalised by log transformation medians and inter-quartile ranges are presented. Independent samples t-tests or Mann-Whitney tests were used to compare means or medians between cases and controls as appropriate. Pearson correlations were calculated to evaluate the relationship between IAF and SCF and glucose, lipids and blood pressure. Multivariable logistic regression was used to identify determinants of MHO status. Odds ratios (OR) and corresponding 95% confidence intervals (CIs) are reported. The amount of variance explained by independent variables in logistic regression analysis was calculated as the difference in deviance between the null model and the model with the independent variable divided by the deviance in the null model. A p value < 0.05 was considered statistically significant.
Body fat distribution and metabolic status
Fasting glucose (mmol/l-1)a
2-hour glucose (mmol/l-1)b
HDL cholesterol (mmol/l-1)
Systolic BP (mmHg)b
Body Mass Index (kg/m2)a
Age (yrs) c
Correlations of fat volumes with fasting and postload glucose, triglycerides, HDL, blood pressure and HOMA-IR
Fasting glucose (mmol/l-1)
2-hour glucose (mmol/l-1)
HDL cholesterol (mmol/l-1)
Self-reported and pedometer recorded physical activity
Steps per day (pedometer)a
DEE Past year leisure (Kcal)b
DEE Past week leisure (Kcal)b
DEE Past year occupational (Kcal)b
DEE Past week occupational (Kcal)b
Total DEE Past year (Kcal)a
Total DEE Past week (Kcal)a
Moderate activity × 5 per week
Although the groups did not differ significantly in terms of their self-reported total energy expenditure there was a significant difference between the groups in the proportion of participants reporting meeting current guidelines for the level of physical activity required to have an impact on health. Seventy per cent of the MHO group reported participating in at least 30 minutes of moderate physical activity on at least 5 occasions per week (the current UK Government guideline ), compared to 25% of the MetAb group (p = 0.010).
Contribution of body fat distribution and physical activity to metabolic status
Logistic regression analysis to identify determinants of being MetAb
All abdominal fat
IAF + SCF
IAF, SCF + BMI
IAF, SCF, BMI + waist
IAF + HOMA-IR
IAF + Physically active
IAF + HOMA-IR + Physically active
Meeting current UK Government guidelines for physical activity participation was negatively associated with being MetAb (OR for meeting the guidelines = 0.14, 95% CIs 0.04-0.58, p-0.006) and explained 15.2% of the variance. When IAF and physical activity were included in the same model the effect of both was attenuated only slightly. When HOMA was added to the model HOMA and physical activity remained independent predictors, together explaining 38.2% of the variance, but IAF was no longer a statistically significant predictor (p = 0.077), although it did contribute to the explanatory power of the model.
We have demonstrated in this study of very obese women that lower intra-abdominal fat volume, less insulin resistance and higher level of physical activity are factors that influence metabolic function beneficially. The results of multivariable modelling suggest that each makes an independent contribution to the risk of having a metabolic abnormality, suggesting that the impact of physical activity on metabolic health is independent of its effect on IAF and that IAF itself makes an independent contribution and does not only operate via insulin resistance. Our findings support a growing body of evidence that individuals exist who are very obese (in this study median BMI of 39.6) but remain metabolically normal.
However, together IAF, HOMA-IR and meeting current guidelines for participation in physical activity accounted for only a little over a third of the risk of having a glucose, lipid or blood pressure abnormality in this group of women. Much of the variance in metabolic status in these women remains unexplained by the variables considered here.
In contrast to other studies[15, 32, 33] we did not find an association between abdominal SCF and presence of a metabolic abnormality. Although the MHO and MetAb groups did not differ in volume of total abdominal SCF, differences may exist in deep and superficial subcutaneous fat depots, which were not examined in this study. Alternatively, in this very obese population SCF may play a less important role in the metabolic complications of adiposity than in less obese groups.
Characteristics of IAF that support its importance in terms of metabolic health, including the lower sensitivity of IAF to the anti-lipolytic effect of insulin, greater sensitivity to the lipolytic effect of catecholamines and role as a source of cytokines have been well documented [5, 34].
It has also been suggested that an excess of IAF may act as a marker for an impairment in an individual's ability to store fat in the subcutaneous depot or to utilise it efficiently within mitochondria . This suggests that the MHO women in this study are better able to store fat appropriately than those with a metabolic abnormality who store excess energy as IAF, and also potentially in skeletal muscle and the liver.
Insulin resistance, as estimated by HOMA, was an independent predictor of metabolic status, and explained a comparable amount of the variance to IAF. It should be noted, however, that it was to be expected that the MHO women would have lower HOMA values as normal glycaemic control, a component of HOMA, was part of the definition of MHO.
It was surprising that neither IAF nor SCF were significantly correlated with insulin resistance in this study. This could be attributed to the use of HOMA-IR as a proxy for insulin resistance in this study. Although HOMA-IR and the euglycaemic hyperinsulinaemic glucose clamp procedure have a good correlation in larger studies (0.6-0.88) HOMA-IR may have less utility in a small study. Furthermore, HOMA-IR is closely correlated with fasting insulin and other investigators have reported no association or a weak association between fasting insulin and/or glucose and IAF[37, 38] even when a significant relationship between glucose disposal and IAF exists.
The participants in this study, and especially those with normal metabolic function, reported higher levels of physical activity than have been reported in other studies, including, for example, the Health Survey for England 2008, which reported only 19% of obese women meet the current guideline. The difficulties associated with collecting data on physical activity level have long been acknowledged. However, there is no reason to believe that the MHO and MetAb groups would have reported their physical activity habits systematically differently, and as the focus of the study was on differences between the two groups, this does not present a major threat to the validity of these data. Nevertheless it would be desirable in future work to have a more sophisticated measure of physical activity using an accelerometer and/or heart rate monitoring to provide more precise information on how energy expenditure and physical activity duration and intensity differ between those who maintain normal metabolic function and those who develop an abnormality.
Our results could have important public health and clinical significance. Despite widespread awareness of the negative consequences of excess adiposity and efforts to redress or at least halt the rise in obesity, its prevalence continues to increase. Not all obese individuals have the glucose, lipid and blood pressure abnormalities usually associated with obesity. This suggests that there is a need for a different approach to the problem, which focuses on those most at risk of developing the ill health consequences of obesity and who should be targeted for intervention. The findings of this pilot study suggest that IAF accumulation, insulin resistance and lack of physical activity each have an independent role to play in identifying those most at risk of the negative metabolic health consequences of obesity. Future work should focus on strategies to identify individuals most likely to benefit from intervention, for example, by encouraging the routine use of established simple methods, including the measurement of waist circumference and the use of dual energy X-ray absorptiometry (DXA) where available, to identify those likely to have high levels of IAF. In addition work is needed to identify factors that drive deposition of fat in the visceral depot. Many determinants of IAF accumulation have been proposed, including genes , smoking  and psychological stress , but the contribution of these putative determinants has yet to be fully elucidated.
It has been suggested that some of the previous research linking obesity to poor health and mortality has failed to take account adequately of physical activity or physical fitness  and the relative contributions of fitness and fatness to the development of CVD and its associated risk factors is still debated . Data from this study support an increasing body of work that physical activity is important in terms of being metabolically healthy, independently of adiposity. This supports a move away from a focus primarily on weight loss to reduce CVD and diabetes risk and towards promoting increased physical activity and cardiorespiratory fitness  both for the beneficial effects on health it confers independently of weight loss and its role as an important weight management tool.
As discussed above, the factors that we identify explain only a relatively small amount of the risk of having a metabolic abnormality in these very obese women. Future work should focus on identifying other contributory factors. One putative risk factor for poor metabolic health is accumulation of fat in the liver. High liver fat content leads to raised very low density lipoprotein levels and is associated with dysglycaemia[47, 48]. The possibility that the women who had a metabolic abnormality in this study had high liver fat content is consistent with the suggestion that these women are impaired in their ability to store fat appropriately in the subcutaneous depot. In addition an association between liver fat and habitual physical activity has been observed, which is consistent with our findings. Other factors worthy of consideration include aspects of diet  and duration of or age at onset of obesity.
Strengths of this study include the detailed metabolic assessments and the accurate assessment of body fat distribution that were undertaken on each of the participants. The small number of participants in this study, which arose from clinical observations and is intended as a pilot study to inform future work, and the relatively weak measures of physical activity and insulin resistance that were used for pragmatic reasons mean that the strength of reported associations may have been underestimated, but nevertheless the substantial amount of variance in metabolic status that remains unexplained suggests that other factors remain to be identified.
In summary, our results confirm that individuals exist who are obese but do not appear to suffer the negative metabolic consequences of obesity. Lower levels of intra-abdominal fat, less insulin resistance and higher levels of physical activity are all associated with better metabolic health even in very obese individuals. These findings could be used to guide strategies to identify those obese individuals most at risk of the negative metabolic consequences of obesity. Intra-abdominal fat, insulin resistance and physical activity together account for only around a third of the risk of having a metabolic abnormality in obese women. Future work should aim to identify other contributory factors.
This work was funded by a grant from the Newcastle Healthcare Charity. The authors wish to thank the participants for the time and effort they put into the study. We also wish to acknowledge the contribution made by Philip English (radiographer), Elaine Farrell (phlebotomist), Pauline Collins, Jean Gerrard, Jan Gebbie, Wendy Hicks (SWiMS), Kate Hesketh (dietician) and Heather Gilbert (laboratory technician).
- Eckel RH: Obesity and heart disease: A statement for healthcare professionals from the Nutrition Committee, American Heart Association. Circulation. 1997, 4: 3248-3250.View ArticleGoogle Scholar
- Grundy SM: Primary prevention of coronary heart disease: integrating risk assessment with intervention. Circulation. 1999, 100 (9): 988-998.View ArticlePubMedGoogle Scholar
- Abate N: Obesity and cardiovascular disease - Pathogenetic role of the metabolic syndrome and therapeutic implications (Review, English). Journal Of Diabetes And Its Complications. 2000, 14 (3): 154-174. 10.1016/S1056-8727(00)00067-2.View ArticlePubMedGoogle Scholar
- Conus F, Rabasa-Lhoret R, Peronnet F: Characteristics of metabolically obese normal-weight (MONW) subjects. Applied Physiology, Nutrition, & Metabolism. 2007, 32 (1): 4-12.View ArticleGoogle Scholar
- Ruderman N, Chisholm D, Pi-Sunyer X, Schneider S: The Metabolically Obese, Normal-Weight Individual Revisited. Diabetes. 1998, 47 (5): 699-713. 10.2337/diabetes.47.5.699.View ArticlePubMedGoogle Scholar
- Karelis AD, St-Pierre DH, Conus F, Rabasa-Lhoret R, Poehlman ET: Metabolic and body composition factors in subgroups of obesity: what do we know?. Journal of Clinical Endocrinology & Metabolism. 2004, 89 (6): 2569-2575.View ArticleGoogle Scholar
- Wildman RP, Muntner P, Reynolds K, McGinn AP, Rajpathak S, Wylie-Rosett J, Sowers MR: The obese without cardiometabolic risk factor clustering and the normal weight with cardiometabolic risk factor clustering: prevalence and correlates of 2 phenotypes among the US population (NHANES 1999-2004). Archives of Internal Medicine. 2008, 168: 1617-1624. 10.1001/archinte.168.15.1617.View ArticlePubMedGoogle Scholar
- Brochu M, Tchernof A, Dionne IJ, Sites CK, Eltabbakh GH, Sims EA, Poehlman ET: What are the physical characteristics associated with a normal metabolic profile despite a high level of obesity in postmenopausal women?. Journal of Clinical Endocrinology & Metabolism. 2001, 86 (3): 1020-1025.Google Scholar
- Karelis AD, Brochu M, Rabasa-Lhoret R: Can we identify metabolically healthy but obese individuals (MHO)?. Diabetes & Metabolism. 2004, 30 (6): 569-572.View ArticleGoogle Scholar
- Sims EAH: Are there persons who are obese but metabolically healthy?. Metabolism. 2001, 50 (12): 1499-1504. 10.1053/meta.2001.27213.View ArticlePubMedGoogle Scholar
- Stefan N, Kantartzis K, Machann J, Schick F, Thamer C, Rittig K, Balletshofer B, Machicao F, Fritsche A, Haring HU: Identification and characterization of metabolically benign obesity in humans. Archives of Internal Medicine. 2008, 168 (15): 1609-1616. 10.1001/archinte.168.15.1609.View ArticlePubMedGoogle Scholar
- Iacobellis G, Ribaudo MC, Zappaterreno A, Iannucci CV, Leonetti F, Iacobellis G, Ribaudo MC, Zappaterreno A, Iannucci CV, Leonetti F: Prevalence of uncomplicated obesity in an Italian obese population. Obesity Research. 2005, 13 (6): 1116-1122. 10.1038/oby.2005.130.View ArticlePubMedGoogle Scholar
- Vague J: The degree of masculine differentiation of obesities: A factor determining predisposition to diabetes, atherosclerosis, gout and uric calculus disease. American Journal of Clinical Nutrition. 1956, 4: 20-34.PubMedGoogle Scholar
- Kissebah AH, Krakower GR: Regional adiposity and morbidity. Physiological Reviews. 1994, 74 (4): 761-811.PubMedGoogle Scholar
- Snijder MB, Visser M, Dekker J, Goodpaster BH, Harris TB, Kritchevsky SB, et al: Low subcutaneous thigh fat is a risk factor for unfavourable glucose and lipid levels, independently of high abdominal fat. The Health ABC Study. Diabetologia. 2005, 48: 301-308. 10.1007/s00125-004-1637-7.View ArticlePubMedGoogle Scholar
- Despres JP: Is visceral obesity the cause of the metabolic syndrome?. Annals of Medicine. 2006, 38 (1): 52-63. 10.1080/07853890500383895.View ArticlePubMedGoogle Scholar
- Fox CS, Massaro JM, Hoffmann U, Pou KM, Maurovich-Horvat P, Liu C-Y, Vasan RS, Murabito JM, Meigs JB, Cupples LA, et al: Abdominal visceral and subcutaneous adipose tissue compartments: association with metabolic risk factors in the Framingham Heart Study. Circulation. 2007, 116 (1): 39-48. 10.1161/CIRCULATIONAHA.106.675355.View ArticlePubMedGoogle Scholar
- Church TS, Earnest CP, Skinner JS, Blair SN: Effects of different doses of physical activity on cardiorespiratory fitness among sedentary, overweight or obese postmenopausal women with elevated blood pressure: a randomized controlled trial. JAMA. 2007, 297 (19): 2081-2091. 10.1001/jama.297.19.2081.View ArticlePubMedGoogle Scholar
- Hu G, Tuomilehto J, Silventoinen K, Barengo NC, Peltonen M, Jousilahti P: The effects of physical activity and body mass index on cardiovascular, cancer and all-cause mortality among 47 212 middle-aged Finnish men and women. International Journal of Obesity. 2005, 29 (8): 894-902. 10.1038/sj.ijo.0802870.View ArticlePubMedGoogle Scholar
- Jennings CL, Lambert EV, Collins M, Joffe Y, Levitt NS, Goedecke JH, Jennings CL, Lambert EV, Collins M, Joffe Y, et al: Determinants of insulin-resistant phenotypes in normal-weight and obese Black African women. Obesity. 2008, 16 (7): 1602-1609. 10.1038/oby.2008.233.View ArticlePubMedGoogle Scholar
- Sieverdes JC, Sui X, Lee D-C, Church TS, McClain A, Hand GA, Blair SN: Physical activity, cardiorespiratory fi tness and the incidence of type 2 diabetes in a prospective study of men. Br J Sports Med. 2010, 44: 238-244. 10.1136/bjsm.2009.062117.View ArticlePubMedGoogle Scholar
- Sui X, Hooker SP, Lee IM, Church TS, Colabianchi N, Lee C-D, Blair SN: A prospective study of cardiorespiratory fitness and risk of type 2 diabetes in women. Diabetes Care. 2008, 31 (3): 550-555. 10.2337/dc07-1870.View ArticlePubMedGoogle Scholar
- Karelis AD, Faraj M, Bastard JP, St-Pierre DH, Brochu M, Prud'homme D, Rabasa-Lhoret R: The metabolically healthy but obese individual presents a favorable inflammation profile. Journal of Clinical Endocrinology & Metabolism. 2005, 90 (7): 4145-4150.View ArticleGoogle Scholar
- Marchesini G, Melchionda N, Apolone G, Cuzzolaro M, Mannucci E, Corica F, Grossi E, Group QS, Marchesini G, Melchionda N, et al: The metabolic syndrome in treatment-seeking obese persons. Metabolism: Clinical & Experimental. 2004, 53 (4): 435-440.View ArticleGoogle Scholar
- Brochu M, Tchernof A, Dionne IJ, Sites CK, Eltabbakh GH, Sims EA, Poehlman ET: What are the physical characteristics associated with a normal metabolic profile despite a high level of obesity in postmenopausal women?. Journal of Clinical Endocrinology & Metabolism. 2001, 86 (3): 1020-1025.Google Scholar
- Thomas EL, Saeed N, Hajnal JV, Brynes A, Goldstone AP, Frost G, Bell JD: Magnetic resonance imaging of total body fat. Journal of Applied Physiology. 1998, 85 (5): 1778-1785.PubMedGoogle Scholar
- Matthews DR, Hosker JP, Rudenski AS, et al: Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985, 28: 412-419. 10.1007/BF00280883.View ArticlePubMedGoogle Scholar
- Kriska A, Knowler WC, LaPorte RE, Drash AL, Wing RR, Blair SN, Bennett PH, Kuller LH: Development of a questionnaire to examine the relationship between of physical activity and diabetes in Pima Indians. Diabetes Care. 1990, 13 (4): 401-411. 10.2337/diacare.13.4.401.View ArticlePubMedGoogle Scholar
- Ainsworth BE, Haskell WL, Whitt MC, Irwin ML, Swartz AM, Strath SJ, O'Brien WL, Bassett DR, Schmitz KH, Emplaincourt PO, et al: Compendium of physical activities: an update of activity codes and MET intensities. Med Sci Sports Exerc. 2000, 32 (9 Suppl): S498-504.View ArticlePubMedGoogle Scholar
- Department of Health: At least five a week: evidence on the impact of physical activity and its relationship to health. A report from the Chief Medical Officer. 2004, London: Department of Health PublicationsGoogle Scholar
- DeMaris A: Explained Variance in Logistic Regression: A Monte Carlo Study of Proposed Measures. Sociological Methods & Research. 2002, 31: 27-74.View ArticleGoogle Scholar
- Abate N, Garg A, Peshock RM, Stray-Gundersen J, Grundy SM: Relationships of generalized and regional adiposity to insulin sensitivity in men. Journal of Clinical Investigation. 1995, 96 (1): 88-98. 10.1172/JCI118083.View ArticlePubMedPubMed CentralGoogle Scholar
- Goodpaster BH, Thaete FL, Simoneau JA, Kelley DE: Subcutaneous abdominal fat and thigh muscle composition predict insulin sensitivity independently of visceral fat. Diabetes. 1997, 46 (10): 1579-1585. 10.2337/diabetes.46.10.1579.View ArticlePubMedGoogle Scholar
- Kershaw EE, Flier JS: Adipose tissue as an endocrine organ. Journal of Clinical Endocrinology & Metabolism. 2004, 89 (6): 2548-2556.View ArticleGoogle Scholar
- Després JP, Lemieux I: Abdominal obesity and metabolic syndrome. Nature. 2006, 444: 881-10.1038/nature05488.View ArticlePubMedGoogle Scholar
- Katz A, Nambi SS, Mather K, Baron AD, Follmann DA, Sullivan G, Quon MJ: Quantitative insulin sensitivity check index: a simple, accurate method for assessing insulin sensitivity in humans. Journal of Clinical Endocrinology & Metabolism. 2000, 85 (7): 2402-2410.View ArticleGoogle Scholar
- Ross R, Freeman J, Hudson R, Janssen I: Abdominal obesity, muscle composition, and insulin resistance in premenopausal women. Journal of Clinical Endocrinology & Metabolism. 2002, 87 (11): 5044-5051.View ArticleGoogle Scholar
- Smith SR, Lovejoy JC, Greenway F, Ryan D, deJonge L, de la Bretonne J, Volafova J, Bray GA: Contributions of total body fat, abdominal subcutaneous adipose tissue compartments, and visceral adipose tissue to the metabolic complications of obesity. Metabolism: Clinical & Experimental. 2001, 50 (4): 425-435.View ArticleGoogle Scholar
- Health Survey for England: Health Survey for England 2006: CVD and risk factors adults, obesity and risk factors children. 2008, The Information Centre, LondonGoogle Scholar
- Kriska AM, Caspersen CJ: Introduction to a collection of physical activity questionnaires. Medicine and Science in Sports and Exercise. 1997, 29: S5-S9.View ArticleGoogle Scholar
- Perusse L, Despres JP, Lemieux S, Rice T, Rao DC, Bouchard C: Familial aggregation of abdominal visceral fat level: results from the Quebec family study. Metabolism: Clinical & Experimental. 1996, 45 (3): 378-382.View ArticleGoogle Scholar
- Samaras K, Campbell LV: The non-genetic determinants of central adiposity. International Journal of Obesity & Related Metabolic Disorders. 1997, 21 (10): 839-845.View ArticleGoogle Scholar
- Bjorntorp P: Do stress reactions cause abdominal obesity and comorbidities?. Obesity Reviews. 2001, 2 (2): 73-86. 10.1046/j.1467-789x.2001.00027.x.View ArticlePubMedGoogle Scholar
- Blair SN, LaMonte MJ: Commentary: current perspectives on obesity and health: black and white, or shades of grey?. International Journal of Epidemiology. 2006, 35 (1): 69-72. 10.1093/ije/dyi259. discussion 81-62View ArticlePubMedGoogle Scholar
- Blair SN, Church TS: The fitness, obesity, and health equation: is physical activity the common denominator?. JAMA. 2004, 292 (10): 1232-1234. 10.1001/jama.292.10.1232.View ArticlePubMedGoogle Scholar
- Campos P, Saguy A, Ernsberger P, Oliver E, Gaesser G: Response: lifestyle not weight should be the primary target. International Journal of Epidemiology. 2006, 35 (1): 81-82. 10.1093/ije/dyi299.View ArticleGoogle Scholar
- Adiels M, Taskinen MR, Packard C, Caslake MJ, Soro-Paavonen A, Westerbacka J, Vehkavaara S, Hakkinen A, Olofsson SO, Yki-Jarvinen H, et al: Overproduction of large VLDL particles is driven by increased liver fat content in man. Diabetologia. 2006, 49 (4): 755-765. 10.1007/s00125-005-0125-z.View ArticlePubMedGoogle Scholar
- Yki-Jarvinen H: Fat in the liver and insulin resistance. Annals of Medicine. 2005, 37 (5): 347-356. 10.1080/07853890510037383.View ArticlePubMedGoogle Scholar
- Perseghin G, Lattuada G, De Cobelli F, Ragogna F, Ntali G, Esposito A, Belloni E, Canu T, Terruzzi I, Scifo P, et al: Habitual physical activity is associated with intrahepatic fat content in humans. Diabetes Care. 2007, 30 (3): 683-688. 10.2337/dc06-2032.View ArticlePubMedGoogle Scholar
- Barnard RJ, Roberts CK, Varon SM, Berger JJ: Diet-induced insulin resistance precedes other aspects of the metabolic syndrome. Journal of Applied Physiology. 1998, 84 (4): 1311-1315.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/10/723/prepub
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