Enhanced insulin sensitivity in successful, long-term weight loss maintainers compared with matched controls with no weight loss history



Weight gain is associated with deterioration in metabolic health, whereas weight loss improves insulin sensitivity. This study assesses the impact of long-term, successfully maintained weight loss and weight-loss relapse on measures of insulin sensitivity and identifies factors that explain variability in insulin sensitivity.


Women (20–45 years) were recruited into four groups: reduced-overweight/obese (RED, n=15); body mass index (BMI)-matched controls (stable low-weight, n=19), BMI27 kg m−2; relapsed-overweight/obese subjects (REL, n=11); and BMI-matched controls (obese stable weight, n=11), BMI27 kg m−2. A 75 g oral glucose tolerance test determined fasting and 2 h plasma glucose and insulin. Homeostatic Model Assessment (HOMA-IR) and insulin sensitivity index (ISI(0,120)) assessed insulin sensitivity. Anthropometric measurements, fasting resting metabolic rate (RMR) and respiratory quotient (RQ) were measured. Questionnaires and dietary intake were recorded, and physical activity was measured using accelerometers.


RED were more insulin sensitive, characterised by lower fasting (P=0.001) and 2 h insulin (P=0.003) levels compared with all other groups. There were no significant differences in dietary intake, sedentary, light and moderate activity, RMR or RQ in the RED compared with the other three groups. % Body weight (BW) lost (P<0.001), % BW regained (P<0.05), body fat %, light activity (P<0.05, only log HOMA), vigorous activity (P<0.05) and RQ (P<0.01) predicted 61.4% and 59.7% of variability in log HOMA and log ISI(0,120), respectively, in multiple linear regression models.


This study showed sustained enhanced insulin sensitivity in successful weight loss maintainers compared with BMI-matched controls with no weight loss history. Weight-loss-relapsed individuals were indistinguishable from controls. Weight loss itself was the strongest predictor of improved insulin sensitivity, whereas weight regain significantly predicted reduced insulin sensitivity. Weight-loss maintenance programs are essential to retaining metabolic benefits acquired through weight loss. Being physically active, reducing sedentary behaviour and, in particular, including small amounts of vigorous physical activity significantly predicted improved insulin sensitivity.


The prevalence of overweight and obesity continues to rise globally, along with associated comorbidities such as type 2 diabetes (T2DM), cardiovascular disease and certain cancers, consequently placing a heavy burden on health care provision.1, 2 This is evident in developed as well as developing countries where obesity is associated with the transition from rural to urban settings.3 Merely being overweight carries a three-fold increased risk of T2DM.4, 5, 6 Insulin influences energy metabolism and storage through its effect on substrate uptake and utilization along with mobilization of stored energy reserves, operating in a way that preferentially favours carbohydrate metabolism, lipid and glycogen synthesis and storage, and protein synthesis.7 In certain populations, long-term weight/body mass index (BMI) gain from early adulthood onwards carries an increased risk for development of T2DM even after adjusting for final BMI, suggesting that weight gain itself is associated with impaired metabolic function.6

Lifestyle factors have a mechanistic role in obesity and disease presentation. Obesity, combined with low levels of physical activity, is associated with intracellular lipid accumulation in the skeletal muscle and liver that impairs insulin signalling, reducing skeletal muscle glucose uptake and utilization, and weakening insulin-mediated inhibition of hepatic glucose production.8, 9, 10, 11, 12 Skeletal muscle alterations in response to exercise improve uptake, utilization and storage of glucose, increasing overall capacity for oxidative metabolism and reducing intramuscular lipid content, thus improving overall skeletal muscle metabolic flexibility.13, 14, 15 Both resistance and aerobic exercise have also repeatedly been shown to reduce intrahepatic lipid content independent of weight loss.16, 17, 18, 19, 20 Regular physical activity is therefore independently associated with improved insulin sensitivity both in the liver and skeletal muscle.

Weight-loss interventions using calorie restriction and/or increased physical activity have shown improvements in insulin sensitivity, with further gains achievable through a combination of both.13, 21, 22, 23, 24, 25, 26 Although some studies show sustained improvements in insulin sensitivity with successful weight maintenance at 12 and 18 month follow-up, other studies have shown either continued improvement or a reversal with weight regain.27, 28, 29 It is however unclear whether weight reduced or weight loss relapsed individuals eventually return to a level of insulin sensitivity that is in line with phenotypically similar individuals with no history of weight gain and loss or whether over the long term they are metabolically worse off as a result of this weight history. The aim of this study is therefore firstly to compare the metabolic profile of the following: (1) weight-reduced individuals; (2) overweight/obese, weight-relapsed individuals; and (3) BMI-matched controls with no history of weight loss or regain and secondly to identify any factors that might explain variations in insulin sensitivity within this sample.


Subject selection and screening

Recruitment advertisements were placed at local institutions and on the Sport Science Institute of South Africa website. Subjects were screened and subsequently placed into four groups. Successful weight reduction has been defined as weight loss of 10%, maintained for over 12 months with weight fluctuations of 3% considered acceptable.30, 31 During recruitment it was stipulated that previous weight loss had to be intentional/deliberate, without the use of unregulated products, a lifestyle-related approach (diet and exercise or a combination of the two), unrelated to stress and/or anxiety and free of eating pathology. Based on these criteria, successfully reduced (RED) individuals were recruited, having previously lost 15% of their body weight (BW) from a BMI27 kg m−2 and maintained this for over 12 months with 5% fluctuation from goal BW over the previous 12 months. Age-matched, stable low-weight (LSW) controls were recruited with a BMI 27 kg m−2, but with no prior weight loss history. Weight-relapsed (REL) individuals were recruited with a BMI27 kg m−2, having previously lost15% of their BW, but subsequently regained all of this weight. Age-matched, overweight and obese stable weight (OSW) controls were then recruited with a BMI 27 kg m−2 but no weight-loss history. Sample size was determined from a study that compared lean participants with weight-reduced and obese individuals, indicating a sample size of nine participants per group would be required to detect significant differences in fasting insulin at a significance of 0.05 and power (1−β) of 0.80.32

Participants were female, aged between 20 and 45 years. Exclusion criteria covered being pregnant or lactating, irregular menstrual cycles (defined as <7 cycles per year or cycle intervals >35days), diagnosis of a chronic medical condition and/or a condition requiring chronic medication known to affect metabolic rate (B2 agonists, β-blockers, corticosteroids and so on), finger-prick fasting blood glucose exceeding 7.0 mmol l−1 at screening, medication or Supplementary Appendix for weight loss, diagnosis of thyroid dysfunction or diagnosis of an eating condition. The study protocol was approved by the University of Cape Town Faculty of Health Science and Human Research Ethics Committee (HREC 214/2012). Before testing, all participants were given full information of test procedures, signed informed consent forms and were at liberty to withdraw at any time.

Laboratory visit

Participants attended the laboratory between 6am to 9am in a fasted state. Resting metabolic rate (RMR) and respiratory quotient (RQ) were measured, along with body composition, heart rate (HR) and blood pressure. A 75 g oral glucose tolerance test was performed and thereafter participants performed an 8–10 min, single-stage submaximal fitness test and completed a number of questionnaires covering medical history, general health, reproductive history, basic socio-demographic, as well as weight history. Accelerometers were fitted and instructions given on how to wear these and were subsequently collected 7 days later. A registered dietitian guided participants through an online 24 h food recall and requested that two further 24 h food recalls were completed (covering one weekend day and two weekdays).

Metabolic rate measurements and calculations

Subjects attended the laboratory in the morning after a 10–12 h overnight fast. RMR and RQ were measured for 20 min using the ventilated hood technique (Cosmed Quark CPET, Rome, Italy), whereas subjects rested in the supine position, in a quiet, isolated temperature-controlled (21–24 °C) room. Before each trial the metabolic cart was calibrated with a Hans Rudolph 3L syringe and analysers calibrated using normal room air (21% O2, 4% CO2 with the balance nitrogen) and standard gas mixtures (5% CO2, 16% O2 and the balance nitrogen) (BOC Special Gas, Afrox Cape Town, South Africa). RMR and total rates of fat and carbohydrate oxidation were calculated using the equations of Weir32 and Frayn,33 respectively.


Weight (BW-150, NAGATA, Tainan, Taiwan) and height were measured (3PHTROD-WM, Detecto, Missouri, USA) along with waist and hip circumference using a standard, non-elastic tape measure. Body composition was measured using Bioelectrical Impedance Analysis ((Quantum II, RJL Systems, Clinton Township, MI, USA).

Oral glucose tolerance test blood sampling and analysis

Following fasting RMR measurements, a cannula attached to a three-way stopcock was inserted into the antecubital vein for blood sampling. A fasting blood sample (~18 ml) was drawn for the determination of fasting plasma glucose and insulin. Thereafter, the participants consumed a 75 g glucose solution and blood samples were collected at 2 h. Samples were kept on ice until centrifuged at 3,000 r.p.m. at 4 °C for 10 min and subsequently stored at −80 °C for later analysis. Plasma glucose concentrations were determined using the glucose oxidase method (Glucose Analyzer 2, Beckman Instruments, Fullerton, CA, USA). Commercial radio immunoassays were used to measure plasma insulin (Axsym Insulin Assay, Abbott Laboratories, Lake Bluff, IL, USA). Insulin sensitivity was estimated using the Homeostasic Model Assessment (HOMA-IR, using fasting glucose and insulin measures) and the insulin sensitivity index (ISI(0,120), using fasting and 120 min glucose and insulin values) reflecting hepatic and peripheral insulin sensitivity, respectively.34 HOMA-IR and ISI(0,120) were determined using the following formulae: HOMA-IR=(fasting glucose (mmol l−1) × fasting insulin (mU l−1))/22.5 and ISI(0, 120)=mean clearance rate/log mean serum insulin; where mean clearance rate=(75 000 mg+(0 min glucose−120 min glucose) × 0.19 × BW (kg)/120 min)/mean plasma glucose) as validated by Gutt et al.35

Dietary intake—automated self-administered 24 h recall

Dietary intake data were recorded and subsequently analysed using the validated, automated online self-administered 24 h dietary recall (ASA24, Applied Research Programme, National Cancer Institute, Bethesda, MD, USA) based on the automated, multiple pass method.36 A dietitian guided participants through the first 24 h recall entry and then requested that two further days were entered. To control for variation in food consumption during the week compared with at weekends, two weekdays and one weekend day were recorded. The online ASA24 software is shown to perform well against interviewer administrated 24 h recall and in comparisons with actual energy and macronutrient intake.37

Predicted maximal volume of oxygen consumption

Previously validated Ebbeling single-stage submaximal treadmill walking test was used to predict maximal volume of oxygen consumption.38, 39 This protocol is a low-risk test for non-athletic adults. Treadmill walking speed is determined for each participant based on their age and fitness level. Following a 4 min warm-up on a flat gradient at a speed that induced 50–70% of age-predicted maximal HR, participants continued to walk at the same speed but at 5% gradient. Steady-state HR was then determined in the final 30 s of this segment, provided HR did not fluctuate more than 5 b.p.m. in the final 2 min and maximal volume of oxygen consumption was then determined using the Ebbeling equation(38). If HR fluctuations exceeded 5 b.p.m. the participant continued on this segment for a further minute until a steady state was achieved.

Objectively measured physical activity

ActiGraph GT3X (ActiGraph, Shalimar, FL, USA) tri-axial accelerometers were used to objectively measure physical activity. Participants wore the device on their right hip for seven consecutive days of usual activity, only removing the belt during night-time sleep, bathing, showering and swimming. A minimum of 4 days with at least 600 min per day was required for data analysis, as this is shown to provide 80% reliability.40, 41 Accelerometer data was downloaded, exported to Excel data tables using the ActiLife Software Version 5 (ActiLife 5, Pensacola, FL, USA) and analysed for light, moderate and vigorous activity taking place in 1 min count intervals (unbouted) using cutoff points according to Matthews and colleagues.42, 43, 44 These cut points were determined from studies which calibrated accelerometer counts against energy expenditure (metabolic equivalent of task), determined using a portable metabolic unit that measured the volume of oxygen consumption during a variety of tasks including lifestyle activities such as household chores. The Matthews equation stipulates that counts between 101 and 759 (inclusive, equivalent to 2–2.9 metabolic equivalent of tasks) represent light intensity physical activity, counts between 760 and 5998 (inclusive, equivalent to 3–6 metabolic equivalent of tasks) represent moderate intensity physical activity, and counts above 5999 (equivalent to over 6 metabolic equivalent of tasks) are indicative of vigorous activity.44

Statistical analysis

Data were assessed for normality using histogram plots and the Shapiro–Wilks test, where P<0.05 indicated that data was not normally distributed. For normally distributed data mean and standard deviation were reported, a two sample t-test for independent groups with equal variance or a Satterthwaite’s independent sample t-test for unequal variance was used for two-group comparisons and a one-way analysis of variance was used for comparisons across all four groups with a Bonferroni post-hoc test to identify significant differences between individual groups. For non-parametric data median and interquartile ranges were reported, a Wilcoxon rank-sum test was used for two group comparisons, a Kruskal–Wallis (non-parametric) analysis of variance was used for multiple comparisons and differences between groups were assessed using a Wilcoxon rank-sum test using a Bonferroni adjustment of P-value for multiple comparisons (significance at 0.008, α=0.05/6 tests). Both HOMA-IR and ISI0,120 were log transformed to give a normal distribution. Pearson’s correlation coefficient and simple linear regression models were used to test for associations between variables and log HOMA-IR and log ISI0,120, respectively. Multiple linear regression was used to model predictors of variability in HOMA-IR and ISI(0,120). The multiple linear regression models were tested for normality of residuals, linearity and homoscedasticity. Outliers were checked for influence and leverage and multicollinearity of predictors was assessed using the variance inflation factor>5. For all tests, a P-value<0.05 was considered statistically significant.


Participant characteristics are presented in Table 1.

Table 1 Participant Characteristics

Table 2 shows that OSW consumed significantly more energy than LSW (P<0.001) and RED (P=0.003), but when adjusted for BW this was not significantly different. The LSW consumed more carbohydrates and less fat than the other three groups, although only significant between the LSW and OSW. There were no significant differences in sedentary, light and moderate activity. The RED engaged in more vigorous activity compared with the other three groups (P=0.050), but this was only significant between the RED and OSW. In terms of overall fitness, the LSW had higher maximal oxygen consumption compared with OSW (P<0.05) and the RED was higher than both OSW and REL (P<0.05), whereas the two lean groups (RED vs LSW) were not different. There were no differences in RMR or substrate utilization between the groups.

Table 2 Dietary intake, physical activity and metabolic measurements

Results of the 75 g oral glucose tolerance test (Table 3) shows that although blood glucose levels are largely comparable across all groups, the RED have significantly lower fasting and 2 h insulin levels compared with all other groups (P<0.005). Eight individuals recorded fasting PG7.0 mmol l−1, a diagnostic criteria for T2DM, despite having previously had fasting blood glucose levels <7.0 mmol l−1 at screening. Of these, two subsequently recorded 2hr PG levels 11.1 mmol l−1, which is a diagnostic criterion for T2DM. Removing these individuals from the analysis did not alter the results significantly.

Table 3 Results of the 75g OGTT

RED were significantly more insulin sensitive than all other groups (Figure 1). This was shown (Figure 1a) using fasting values and determining insulin sensitivity as measured by HOMA-IR (RED 0.85 (0.64–1.25), LSW 1.86 (1.01–2.43), REL 2.36 (1.91–3.73) and OSW 3.10 (2.34–4.45); P<0.001 for all comparisons with RED). REL were not different to either the LSW (P=0.138) or OSW (P=0.324). LSW-CTL had lower HOMA-IR values compared with OSW (P=0.015), whereas both the OSW and REL were not different. The same result was shown in Figure 1b using both fasting and two hour values as determined by ISI(0,120) (RED 115.1 (89.8–134.7), LSW 80.0 (66.1–96.4), REL 58.7 (56.2–69.7) and OSW 55.7 (43.7–59.9); P<0.001 for all comparisons with RED). LSW were more insulin sensitive compared with both overweight groups (P<0.05), whereas the REL and OSW were not different on either measure.

Figure 1

Comparison of insulin sensitivity as measured by HOMA-IR (A) and ISI(0,120) (a) HOMA-IR (b) ISI(0,120): *RED significantly more insulin sensitive compared with all other groups (P<0.001).

The total sample was analysed to identify significant associations of variables against both log HOMA and ISI(0,120) (Table 4).

Table 4 Associations with log HOMA-IR and ISI(0,120)

The regression models (Table 5 below) were able to predict 61.4% (P<0.001) and 59.7% (P<0.001) of the variability in log HOMA-IR (Model 1) and log ISI(0,120) (Model 2), respectively, in this sample. Using β-coefficients, the strongest predictors in Model 1 were % BW lost (β −0.508) followed by % BW regained (β 0.314) and RQ ratio (β 0.298), whereas for Model 2% BW lost (β 0.612), %BW regained (β −0.600) and RQ ratio (−0.231), respectively. Light activity contributed to Model 1 but was not a strong predictor in Model 2 and for Model 2 waist-to-hip ratio was a stronger predictor than % body fat. Removing the two individuals who exceeded diagnostic criteria for T2DM from the analysis did not significantly alter these results (see Supplementary Appendix).

Table 5 Regression Models predicting variability in log HOMA-IR and log ISI(0,120)

Applying reported mean or median values for these predictors into the fitted model equation, a reduction in predicted HOMA-IR of 15% could be achieved for this sample through a 4.5% reduction in BW, a 55 min per day increase in light activity or a 5 min per day increase in vigorous activity, holding all other variables constant. For insulin sensitivity, 5 min of extra vigorous activity per day improved predicted insulin sensitivity by just 7%. However, 5% BW loss would yield predicted improvements in insulin sensitivity of 15 and 5% BW regain would reduce predicted insulin sensitivity by around 17% in this sample, holding all other variables equal.


This study compared metabolic, physiological and lifestyle variables across four groups of women classified exclusively according to weight status and weight loss history. The main finding from this study showed that successfully maintained, weight-reduced individuals were significantly more insulin sensitive compared with all other groups investigated. What is remarkable is that women in the RED had maintained substantial weight loss of around 15% for a lengthy period (median 30 months (12–60 months)) and yet were found to be more insulin sensitive relative to phenotypically similar, age- and BMI-matched controls with no weight-loss history. There were no significant differences in metabolic rate, substrate utilization or dietary intake that might explain the lower insulin resistance in this group, besides a modest engagement in vigorous activity. Multiple linear regression models were able to explain 61.4% of the variability in log HOMA-IR (P<0.001) and 59.7% in log ISI(0,120) (P<0.001) in the total sample. In these models, previous percentage BW lost was a significant predictor of improved insulin sensitivity, independent of the current physical activity level and metabolic measures, whereas previous percentage BW regained predicted reduced insulin sensitivity. Increased fasting fat oxidation and physical activity, particularly vigorous activity, were also associated with greater insulin sensitivity (light activity was a significant predictor only in Model 1 predicting variability in log HOMA), whereas none of the dietary intake variables were found to be significant predictors.

Weight loss intervention studies have shown sustained improvements in glucose regulation at 6 month follow-up, but longer term, with weight regain these improvements were reversed.28 However, other groups have demonstrated that improved insulin sensitivity following weight loss was retained and even enhanced despite weight regain, and here the continued increase in adiponectin and insulin-like growth factor 1, along with no change in visceral fat, were highlighted as possible explanations for this.29 Our results show that individuals, who have undergone meaningful weight loss in excess of 15% of BW and subsequently maintained this well beyond 1 year and up to 5 years, are more insulin sensitive than BMI-matched controls. However, compared with RED, the REL group demonstrated lower levels of insulin sensitivity, as well as greater 2 h insulin levels in the 75 g oral glucose tolerance test, supporting existing evidence that metabolic benefits that accompany weight loss are not present in subjects who have regained weight. It is interesting to note that individuals who had always been lean and had not gone through the process of weight loss were not significantly more insulin sensitive than the REL, despite having significantly lower BMI. Undoubtedly, physiological and metabolic parameters, along with lifestyle choices, have an important role in improving metabolic health.22, 45 However, it is also important to recognise that individuals who have a history of substantial weight loss are evidently more insulin sensitive than those who have no weight loss history.

The RED displayed very low HOMA-IR values, with a tight clustering of individuals falling in the bottom half and even below suggested 95% reference cut points.46 It is therefore pertinent to consider the implications of this, particularly whether very high levels of insulin sensitivity could potentially predispose individuals to subsequent weight regain. In obese, insulin resistant populations lower relative insulin resistance is associated with increased prospective weight gain.47, 48 Greater weight regain following weight loss has also been shown in individuals who subsequently consumed a high glycaemic load diet.49 Changes in adipose tissue histology may also have a role as weight regain after sustained weight loss is accompanied by adipocyte hyperplasia.50 The greater number of smaller, newly reduced adipocytes are potentially more insulin sensitive, with lower rates of lipolysis and increased rates of fat storage following weight loss.51 This would suggest that weight cycling increases the number of adipocytes, thereby reducing the inflammatory profile of adipose tissue and improving insulin sensitivity, but also increases the efficiency and capacity for fat storage, thus raising the risk for future weight regain.51 This emphasises the importance of dietary recommendations and support in the weight maintenance phase following substantial weight loss in order to retain metabolic improvements.

Exercise has beneficial effects on body composition and improves insulin sensitivity through enhanced oxidative capacity and reduced intramuscular triglycerides that impair insulin signalling within the cell.10, 12, 13 Weight loss incorporating diet and aerobic exercise confers further beneficial effects on insulin sensitivity at 1 year follow-up that is independently associated with improved cardiovascular fitness.52 Both light and vigorous activity were significant predictors of insulin sensitivity as measured by HOMA-IR. There was also a strong negative correlation between sedentary time and light activity and together this demonstrates that increasing light activity at the expense of sedentary time improved fasting measures of insulin sensitivity (HOMA-IR), which is also indicative of hepatic insulin sensitivity. It is possible that with sedentary behaviour the reduced number of muscle contractions reduces skeletal muscle glucose clearance as well as lipoprotein lipase activity, resulting in reduced triglyceride clearance, thus potentially increasing ectopic fat deposition.53 Small amounts of vigorous activity predicted improved insulin sensitivity, which is supported by interventions showing improvements in insulin sensitivity after just 2 weeks of short duration sprint interval training.54 Exercise improves fasting fat oxidation which in turn improves insulin sensitivity and is confirmed in our model whereby fasting RQ significantly predicted insulin sensitivity.55 All groups met the ACSM Guidelines of 150 min per week of moderate to vigorous activity and this remains an important component of daily physical activity, while explicitly incorporating small amounts of vigorous activity may further improve the effect of exercise on insulin sensitivity. All participants undertook large amounts of moderate activity per day, but this did not contribute to insulin sensitivity, possibly indicating that it was lower intensity, intermittent activity rather than more structured activity over a continuous period of time. Using the regression equation generated by the model, predicted insulin sensitivity could be improved by 15% through an additional 55 min of light activity or just 5 min of vigorous activity per day.

Dietary intake variables were not found to be predictors of insulin resistance. Other studies, considering dietary glycaemic load and macronutrient composition, have also found no association with insulin sensitivity.56, 57, 58, 59 Other components of food intake and diet quality may be more predictive of insulin resistance than macronutrient composition per se.60 Obtaining accurate dietary intake information is inherently problematic, with day-to-day variability making it difficult to determine habitual dietary intake from three 24-h recalls.61 There is also some evidence of inter- and intra-individual variability in glycaemic response to the same food thereby potentially eliciting a variable insulin response.62, 63

One of the strengths of this study was the ability to identify individuals who had undergone substantial weight loss and either successfully maintained this weight loss for periods in excess of a year or regained all of the weight previously lost. This enabled an investigation into the longer term effects of weight loss and regain in comparison to individuals with no weight loss history. Actual measurements of physical activity also avoided issues around over or under reporting. However, limitations of the study included it being cross sectional and therefore only able to point to associations rather than cause and effect. Our research question also related to identifying differences in the metabolic profile of individuals with a weight loss and regain history compared with phenotypically similar controls and as such weight loss history was used to assign participants to experimental groups. Weight loss is accomplished through energy deficit, by increasing energy expenditure and/or decreasing energy intake. Data on how weight loss was achieved in this sample was not collected and so it is not possible to determine to what extent the weight loss associated improvements in insulin sensitivity were attributable to dietary restriction, increased physical activity or a combination of both. Finally, there were relatively fewer participants in the REL and OSW groups which may have underpowered the effects shown. Future studies should analyse the dietary data in more detail, perhaps using indices and their components to assess associations with dietary intake and insulin resistance. It would also be of interest to consider mechanisms that might contribute to explaining the improved insulin sensitivity that accompanies weight loss, to identify to what extent these might be associated with either dietary restriction or physical activity modalities and how this develops over the longer term during weight maintenance.

In conclusion, successfully weight-reduced individuals, maintaining reduced weight for extended periods of time, are more insulin sensitive than their BMI-matched controls with no weight-loss history, independent of dietary intake and physical activity. With weight-loss relapse, these metabolic benefits are no longer evidenced. Being physically active, engaging in light activity rather than being sedentary and in particular including small amounts of vigorous physical activity predicted improved insulin sensitivity. Weight-loss maintenance programs should therefore be emphasised in the period following substantial weight loss in order to retain these benefits. Research is needed to consider dietary strategies that can facilitate weight loss maintenance in light of the enhanced insulin sensitivity, not just in the immediate period following weight loss, but over the long term.


  1. 1

    Wang YC, McPherson K, Marsh T, Gortmaker SL, Brown M . Health and economic burden of the projected obesity trends in the USA and the UK. Lancet 2011; 378: 815–825.

    Article  Google Scholar 

  2. 2

    Dietz WH . Reversing the tide of obesity. Lancet 2011; 378: 744–746.

    Article  Google Scholar 

  3. 3

    Kruger HS, Puoane T, Senekal M, van der Merwe M-T . Obesity in South Africa: challenges for government and health professionals. Public Health Nutr 2005; 8: 491–500.

    Article  Google Scholar 

  4. 4

    Despres JP, Moorjani S, Lupien PJ, Tremblay A, Nadeau A, Bouchard C . Regional distribution of body fat, plasma lipoproteins, and cardiovascular disease. Arteriosclerosis 1990; 10: 497–511.

    CAS  Article  Google Scholar 

  5. 5

    Brancati FL, Wang N-Y, Mead LA, Liang K-Y, Klag MJ . Body weight patterns from 20 to 49 years of age and subsequent risk for diabetes mellitus: the Johns Hopkins Precursors Study. Arch Intern Med 1999; 159: 957–963.

    CAS  Article  Google Scholar 

  6. 6

    Kaneto C, Toyokawa S, Miyoshi Y, Suyama Y, Kobayashi Y . Long-term weight change in adulthood and incident diabetes mellitus: MY Health Up Study. Diabetes Res Clin Pract 2013; 102: 138–146.

    Article  Google Scholar 

  7. 7

    Tremblay A, Boulé N, Doucet E, Woods SC . Is the insulin resistance syndrome the price to be paid to achieve body weight stability? Int J Obes (Lond) 2005; 29: 1295–1298.

    CAS  Article  Google Scholar 

  8. 8

    Koves TR, Li P, An J, Akimoto T, Slentz D, Ilkayeva O et al. Peroxisome proliferator-activated receptor-gamma co-activator 1alpha-mediated metabolic remodeling of skeletal myocytes mimics exercise training and reverses lipid-induced mitochondrial inefficiency. J Biol Chem 2005; 280: 33588–33598.

    CAS  Article  Google Scholar 

  9. 9

    Koves TR, Ussher JR, Noland RC, Slentz D, Mosedale M, Ilkayeva O et al. Mitochondrial overload and incomplete fatty acid oxidation contribute to skeletal muscle insulin resistance. Cell Metab 2008; 7: 45–56.

    CAS  Article  Google Scholar 

  10. 10

    Muoio DM, Neufer PD . Lipid-induced mitochondrial stress and insulin action in muscle. Cell Metab 2012; 15: 595–605.

    CAS  Article  Google Scholar 

  11. 11

    Yu C, Chen Y, Cline GW, Zhang D, Zong H, Wang Y et al. Mechanism by which fatty acids inhibit insulin activation of insulin receptor substrate-1 (IRS-1)-associated phosphatidylinositol 3-kinase activity in muscle. J Biol Chem 2002; 277: 50230–50236.

    CAS  Article  Google Scholar 

  12. 12

    Samuel VT, Petersen KF, Shulman GI . Lipid-induced insulin resistance: unravelling the mechanism. Lancet 2010; 375: 2267–2277.

    CAS  Article  Google Scholar 

  13. 13

    Dubé JJ, Amati F, Toledo FGS, Stefanovic-Racic M, Rossi A, Coen P et al. Effects of weight loss and exercise on insulin resistance, and intramyocellular triacylglycerol, diacylglycerol and ceramide. Diabetologia 2011; 54: 1147–1156.

    Article  Google Scholar 

  14. 14

    Coen PM, Menshikova EV, Distefano G, Zheng D, Tanner CJ, Standley RA et al. Exercise and weight loss improve muscle mitochondrial respiration, lipid partitioning, and insulin sensitivity after gastric bypass surgery. Diabetes 2015; 64: 3737–3750.

    CAS  Article  Google Scholar 

  15. 15

    Nordby P, Auerbach PL, Rosenkilde M, Kristiansen L, Thomasen JR, Rygaard L et al. Endurance training per se increases metabolic health in young, moderately overweight men. Obesity (Silver Spring) 2012; 20: 2202–2212.

    CAS  Article  Google Scholar 

  16. 16

    van der Heijden G-J, Wang ZJ, Chu ZD, Sauer PJJ, Haymond MW, Rodriguez LM et al. A 12-week aerobic exercise program reduces hepatic fat accumulation and insulin resistance in obese, Hispanic adolescents. Obesity (Silver Spring) 2010; 18: 384–390.

    Article  Google Scholar 

  17. 17

    Sullivan S, Kirk EP, Mittendorfer B, Patterson BW, Klein S . Randomized trial of exercise effect on intrahepatic triglyceride content and lipid kinetics in nonalcoholic fatty liver disease. Hepatology 2012; 55: 1738–1745.

    CAS  Article  Google Scholar 

  18. 18

    Johnson NA, Sachinwalla T, Walton DW, Smith K, Armstrong A, Thompson MW et al. Aerobic exercise training reduces hepatic and visceral lipids in obese individuals without weight loss. Hepatology 2009; 50: 1105–1112.

    CAS  Article  Google Scholar 

  19. 19

    Hallsworth K, Fattakhova G, Hollingsworth KG, Thoma C, Moore S, Taylor R et al. Resistance exercise reduces liver fat and its mediators in non-alcoholic fatty liver disease independent of weight loss. Gut 2011; 60: 1278–1283.

    Article  Google Scholar 

  20. 20

    Brouwers B, Hesselink MKC, Schrauwen P, Schrauwen-Hinderling VB . Effects of exercise training on intrahepatic lipid content in humans. Diabetologia 2016; 59: 2068–2079.

    CAS  Article  Google Scholar 

  21. 21

    Weickert MO . Nutritional modulation of insulin resistance. Scientifica (Cairo) 2012; 2012: 424780.

    Google Scholar 

  22. 22

    Petersen KF, Dufour S, Morino K, Yoo PS, Cline GW, Shulman GI . Reversal of muscle insulin resistance by weight reduction in young, lean, insulin-resistant offspring of parents with type 2 diabetes. Proc Natl Acad Sci USA 2012; 109: 8236–8240.

    CAS  Article  Google Scholar 

  23. 23

    Straznicky NE, Lambert EA, Grima MT, Eikelis N, Richards K, Nestel PJ et al. The effects of dietary weight loss on indices of norepinephrine turnover: modulatory influence of hyperinsulinemia. Obesity (Silver Spring) 2014; 22: 652–662.

    CAS  Article  Google Scholar 

  24. 24

    Leufkens AM, Van Duijnhoven FJB, Siersema PD, Boshuizen HC, Vrieling A, Agudo A et al. Cigarette smoking and colorectal cancer risk in the European Prospective Investigation into Cancer and Nutrition study. Clin Gastroenterol Hepatol 2011; 9: 137–144.

    Article  Google Scholar 

  25. 25

    Franz MJ, Boucher JL, Rutten-Ramos S, VanWormer JJ . Lifestyle weight-loss intervention outcomes in overweight and obese adults with type 2 diabetes: a systematic review and meta-analysis of randomized clinical trials. J Acad Nutr Diet 2015; 115: 1447–1463.

    Article  Google Scholar 

  26. 26

    Weiss EP, Albert SG, Reeds DN, Kress KS, Ezekiel UR, McDaniel JL et al. Calorie restriction and matched weight loss from exercise: independent and additive effects on glucoregulation and the incretin system in overweight women and men. Diabetes Care 2015; 38: 1253–1262.

    CAS  Article  Google Scholar 

  27. 27

    Beavers DP, Beavers KM, Lyles MF, Nicklas BJ . Cardiometabolic risk after weight loss and subsequent weight regain in overweight and obese postmenopausal women. J Gerontol A Biol Sci Med Sci 2013; 68: 691–698.

    Article  Google Scholar 

  28. 28

    Beavers KM, Case LD, Blackwell CS, Katula JA, Goff DC, Vitolins MZ . Effects of weight regain following intentional weight loss on glucoregulatory function in overweight and obese adults with pre-diabetes. Obes Res Clin Pract 2015; 9: 266–273.

    Article  Google Scholar 

  29. 29

    Lien LF, Haqq AM, Arlotto M, Slentz Ca, Muehlbauer MJ, McMahon RL et al. The STEDMAN project: biophysical, biochemical and metabolic effects of a behavioral weight loss intervention during weight loss, maintenance, and regain. OMICS 2009; 13: 21–35.

    CAS  Article  Google Scholar 

  30. 30

    Raynor HA, Jeffery RW, Phelan S, Hill JO, Wing RR . Amount of food group variety consumed in the diet and long-term weight loss maintenance. Obes Res 2005; 13: 883–890.

    Article  Google Scholar 

  31. 31

    Weinsier RL, Hunter GR, Desmond Ra, Byrne NM, Zuckerman Pa, Darnell BE . Free-living activity energy expenditure in women successful and unsuccessful at maintaining a normal body weight. Am J Clin Nutr 2002; 75: 499–504.

    CAS  Article  Google Scholar 

  32. 32

    De Weir JB . New methods for calculating metabolic rate with special reference to protein metabolism. J Physiol 1949; 109: 1–9.

    Article  Google Scholar 

  33. 33

    Frayn KN . Calculation of substrate oxidation rates in vivo from gaseous exchange rates. J Appl Physiol 1983; 55: 628–634.

    CAS  Article  Google Scholar 

  34. 34

    Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC . Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985; 28: 412–419.

    CAS  Article  Google Scholar 

  35. 35

    Gutt M, Davis CL, Spitzer SB, Llabre MM, Kumar M, Czarnecki EM et al. Validation of the insulin sensitivity index (ISI0,120): comparison with other measures. Diabetes Res Clin Pract 2000; 47: 177–184.

    CAS  Article  Google Scholar 

  36. 36

    Subar AF, Kirkpatrick SI, Mittl B, Zimmerman TP, Thompson FE, Bingley C et al. The Automated Self-Administered 24-hour dietary recall (ASA24): a resource for researchers, clinicians, and educators from the National Cancer Institute. J Acad Nutr Diet 2012; 112: 1134–1137.

    Article  Google Scholar 

  37. 37

    Kirkpatrick SI, Subar AF, Douglass D, Zimmerman TP, Thompson FE, Kahle LL et al. Performance of the Automated Self-Administered 24-hour Recall relative to a measure of true intakes and to an interviewer-administered 24-h recall. Am J Clin Nutr 2014; 100: 233–240.

    CAS  Article  Google Scholar 

  38. 38

    Ebbeling CB, Ward A, Puleo EM, Widrick J, Rippe JM . Development of a single-stage submaximal treadmill walking test. Med Sci Sports Exerc 1991; 23: 966–973.

    CAS  Article  Google Scholar 

  39. 39

    Mitros M, Gabriel KP, Ainsworth B, Lee C, Herrmann S, Campbell K et al. Comprehensive evaluation of a single-stage submaximal treadmill walking protocol in healthy, middle-aged women. Eur J Appl Physiol 2011; 111: 47–56.

    CAS  Article  Google Scholar 

  40. 40

    Matthews CE, Ainsworth BE, Thompson RW, Bassett DR . Sources of variance in daily physical activity levels as measured by an accelerometer. Med Sci Sport Exerc 2002; 34: 1376–1381.

    Article  Google Scholar 

  41. 41

    Trost SG, Mciver KL, Pate RR . Conducting accelerometer-based activity assessments in field-based research. Med Sci Sport Exerc 2005; 37 (Supplement): S531–S543.

    Article  Google Scholar 

  42. 42

    Mâsse LC, Fuemmeler BF, Anderson CB, Matthews CE, Trost SG, Catellier DJ et al. Accelerometer data reduction: a comparison of four reduction algorithms on select outcome variables. Med Sci Sport Exerc 2005; 37 (Supplement): S544–S554.

    Article  Google Scholar 

  43. 43

    Ward DS, Evenson KR, Vaughn A, Rodgers AB, Troiano RP . Accelerometer use in physical activity: best practices and research recommendations. Med Sci Sport Exerc 2005; 37 (Supplement): S582–S588.

    Article  Google Scholar 

  44. 44

    Matthews C . Calibration of accelerometer output for adults. Med Sci Sport Exerc 2005; S512 (Supplement): S512–S522.

    Article  Google Scholar 

  45. 45

    Moscavitch SD, Kang HC, Filho RAC, Mesquita ET, Neto HCCF, Rosa MLG . Comparison of adipokines in a cross-sectional study with healthy overweight, insulin-sensitive and healthy lean, insulin-resistant subjects, assisted by a family doctor primary care program. Diabetol Metab Syndr 2016; 8: 9.

    Article  Google Scholar 

  46. 46

    Tohidi M, Ghasemi A, Hadaegh F, Derakhshan A, Chary A, Azizi F . Age- and sex-specific reference values for fasting serum insulin levels and insulin resistance/sensitivity indices in healthy Iranian adults: Tehran Lipid and Glucose Study. Clin Biochem 2014; 47: 432–438.

    CAS  Article  Google Scholar 

  47. 47

    Swinburn BA, Nyomba BL, Saad MF, Zurlo F, Raz I, Knowler WC et al. Insulin resistance associated with lower rates of weight gain in Pima Indians. J Clin Invest 1991; 88: 168–173.

    CAS  Article  Google Scholar 

  48. 48

    Wong MHT, Holst C, Astrup A, Handjieva-Darlenska T, Jebb SA, Kafatos A et al. Caloric restriction induces changes in insulin and body weight measurements that are inversely associated with subsequent weight regain. PLoS One 2012; 7: e42858.

    CAS  Article  Google Scholar 

  49. 49

    Gower BA, Hunter GR, Chandler-Laney PC, Alvarez JA, Bush NC . Glucose metabolism and diet predict changes in adiposity and fat distribution in weight-reduced women. Obesity (Silver Spring) 2010; 18: 1532–1537.

    CAS  Article  Google Scholar 

  50. 50

    Jackman MR, Steig A, Higgins Ja, Johnson GC, Fleming-Elder BK, Bessesen DH et al. Weight regain after sustained weight reduction is accompanied by suppressed oxidation of dietary fat and adipocyte hyperplasia. Am J Physiol Regul Integr Comp Physiol 2008; 294: R1117–R1129.

    CAS  Article  Google Scholar 

  51. 51

    Ochner CN, Barrios DM, Lee CD, Pi-Sunyer FX . Biological mechanisms that promote weight regain following weight loss in obese humans. Physiol Behav 2013; 120: 106–113.

    CAS  Article  Google Scholar 

  52. 52

    Fisher G, Hunter GR, Gower BA . Aerobic exercise training conserves insulin sensitivity for 1 yr following weight loss in overweight women. J Appl Physiol 1985; 112: 688–693.

    Article  Google Scholar 

  53. 53

    Strasser B . Physical activity in obesity and metabolic syndrome. Ann N Y Acad Sci 2013; 1281: 141–159.

    Article  Google Scholar 

  54. 54

    Richards JC, Johnson TK, Kuzma JN, Lonac MC, Schweder MM, Voyles WF et al. Short-term sprint interval training increases insulin sensitivity in healthy adults but does not affect the thermogenic response to beta-adrenergic stimulation. J Physiol 2010; 588 (Pt 15): 2961–2972.

    CAS  Article  Google Scholar 

  55. 55

    Goodpaster BH, Katsiaras A, Kelley DE . Enhanced fat oxidation through physical activity is associated with improvements in insulin sensitivity in obesity. Diabetes 2003; 52: 2191–2197.

    CAS  Article  Google Scholar 

  56. 56

    Joslowski G, Halim J, Goletzke J, Gow M, Ho M, Louie JC-Y et al. Dietary glycemic load, insulin load, and weight loss in obese, insulin resistant adolescents: RESIST study. Clin Nutr 2015; 34: 89–94.

    CAS  Article  Google Scholar 

  57. 57

    Sjaarda LA, Schisterman EF, Schliep KC, Plowden T, Zarek SM, Yeung E et al. Dietary carbohydrate intake does not impact insulin resistance or androgens in healthy, eumenorrheic women. J Clin Endocrinol Metab 2015; 100: 2979–2986 jc20151957.

    CAS  Article  Google Scholar 

  58. 58

    McCullough ML, Feskanich D, Rimm EB, Giovannucci EL, Ascherio A, Variyam JN et al. Adherence to the Dietary Guidelines for Americans and risk of major chronic disease in men. Am J Clin Nutr 2000; 72: 1223–1231.

    CAS  Article  Google Scholar 

  59. 59

    Willett W, Stampfer MJ . Total energy intake: implications for epidemiologic analyses. Am J Epidemiol 1986; 124: 17–27.

    CAS  Article  Google Scholar 

  60. 60

    Akbaraly TN, Ferrie JE, Berr C, Brunner EJ, Head J, Marmot MG et al. Alternative Healthy Eating Index and mortality over 18 y of follow-up: results from the Whitehall II cohort. Am J Clin Nutr 2011; 94: 247–253.

    CAS  Article  Google Scholar 

  61. 61

    Bingham SA . Limitations of the various methods for collecting dietary intake data. Ann Nutr Metab 1991; 35: 117–127.

    CAS  Article  Google Scholar 

  62. 62

    Vega-López S, Ausman LM, Griffith JL, Lichtenstein AH . Interindividual variability and intra-individual reproducibility of glycemic index values for commercial white bread. Diabetes Care 2007; 30: 1412–1417.

    Article  Google Scholar 

  63. 63

    Vrolix R, Mensink RP . Variability of the glycemic response to single food products in healthy subjects. Contemp Clin Trials 2010; 31: 5–11.

    CAS  Article  Google Scholar 

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We thank the participants who gave of their time to participate in this trial. We also thank Professor Julia Goedecke for editorial input. This study received no specific grant from any funding agency, commercial or not-for-profit sectors.

Author contributions

EVL, JK, DJH and LDC designed the study. DJH and LDC conducted the study and were responsible for data collection. Analysis, interpretation of results and writing of the manuscript was carried out by LC.

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Correspondence to J Kroff.

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Supplementary Information accompanies this paper on the Nutrition & Diabetes website

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Clamp, L., Hume, D., Lambert, E. et al. Enhanced insulin sensitivity in successful, long-term weight loss maintainers compared with matched controls with no weight loss history. Nutr. Diabetes 7, e282 (2017). https://doi.org/10.1038/nutd.2017.31

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