Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-19T06:53:27.889Z Has data issue: false hasContentIssue false

The introduction of simple cardiorespiratory fitness testing in overweight/obese type 2 diabetics: a pilot study

Published online by Cambridge University Press:  14 January 2018

Ľubica Cibičková
Affiliation:
Department of Internal Medicine III – Nephrology, Rheumatology and Endocrinology, University Hospital, Olomouc, Czech Republic
David Karásek
Affiliation:
Department of Internal Medicine III – Nephrology, Rheumatology and Endocrinology, University Hospital, Olomouc, Czech Republic
Jiří Lukeš
Affiliation:
Department of Clinical Biochemistry, University Hospital, Olomouc, Czech Republic
Norbert Cibiček*
Affiliation:
Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic Department of Exercise Medicine and Cardiovascular Rehabilitation, University Hospital, Olomouc, Czech Republic
*
Correspondence to: Norbert Cibiček, Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Hněvotínská 3, 775 15 Olomouc, Czech Republic. Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Background

Low level of cardiorespiratory fitness has been recognized as an important independent and modifiable risk factor of increased morbidity and mortality. However, in standard outpatient settings, patients are not routinely screened for fitness and advantages of such testing for the management of type 2 diabetes have not been defined.

Aim

To describe the toleration of a fast, simple and practicable fitness test (2-min step-in-place test) by overweight/obese type 2 diabetics and their performance indicated by 2-min step-in-place test score (STS). To study short-term anthropometric, functional and metabolic changes following the implementation of the test in the selected population.

Methods

A total of 33 overweight/obese type 2 diabetics underwent, besides routine examination at the outpatient clinic, the fitness test (group A). Patients were asked to increase their regular physical activity with focus on walking without change in diet and chronic medication. Three to four months later, the subjects were tested again. An identical number of age- and sex-matched obese diabetics followed in our outpatient clinic (without fitness testing), was randomly selected from the Hospital Information System (control group B).

Findings

All patients subjected to fitness testing completed the protocol successfully. STS score was found to have a considerable range with differences between males and females at the borderline of statistical significance. The data are compliant with lower aerobic endurance of obese diabetics compared with healthy population. Within study period, the tested group presented with improvements in STS (referring especially to the males) as well as in several laboratory parameters of glucose and lipid homeostasis, glomerular function and subclinical inflammation with no reflection in anthropometry. Group B demonstrated no significant change. In conclusion, 2-min step-in-place test is fast, undemanding and well-tolerated by patients and personnel. Following its validation based on cardiopulmonary exercise testing, the test may prove recommendable for screening or self-monitoring purposes.

Type
Research
Copyright
© Cambridge University Press 2018 

Introduction

Low level of physical activity and cardiorespiratory fitness has recently been recognized and widely accepted as an independent modifiable risk factor of increased morbidity and premature cardiovascular and all-cause mortality (Blair et al.,Reference Blair, Kohl, Paffenbarger, Clark, Cooper and Gobbons1989; Lee et al., Reference Lee, Jackson and Blair1998; Kodama et al., Reference Kodama, Saito, Tanaka, Maki, Yachi, Asumi, Sugawara, Totsuka, Shimano, Ohashi, Yamada and Sone2009; Barry et al., Reference Barry, Baruth, Beets, Durstine, Liu and Blair2014; McAuley and Beavers, Reference McAuley and Beavers2014; Bouchard et al., Reference Bouchard, Blair and Katzmarzyk2015) in healthy (Blair et al., Reference Blair, Kohl, Paffenbarger, Clark, Cooper and Gobbons1989), obese (Wei et al., Reference Wei, Kampert, Barlow, Nichaman, Gibbons, Paffenbarger and Blair1999; Church et al., Reference Church, LaMonte, Barlow and Blair2005) and/or diabetic patients (Wei et al., Reference Wei, Gibbons, Kampert, Nichman and Blair2000). It is notable that the significance of the contribution of cardiorespiratory fitness to morbidity and mortality prediction exceeds that of ‘classical’ cardiovascular disease risk factors such as smoking, cholesterol, hypertension, obesity or diabetes (Church et al., Reference Church, LaMonte, Barlow and Blair2005; Després, Reference Després2016). Therefore, the level of individual fitness was recommended for incorporation into cardiovascular disease risk factor evaluation and management (Israel et al., Reference Israel, Kivity, Sidi, Segev, Berkovitch, Klempfner, Lavi, Goldenberg and Maor2016; Ross et al., Reference Ross, Blair, Arena, Church, Després, Franklin, Haskell, Kaminsky, Levine, Lavie, Myers, Niebauer, Sallis, Sawada, Sui and Wisløff2016). In spite of impressive body of evidence corroborating the need for large-scale fitness testing, patients’ aerobic endurance is not routinely screened as advantages of such testing for the management of type 2 diabetes have not been clearly defined.

Current approach to the screening and identification of inactive individuals with poor fitness level in outpatient clinics may involve the use of an appropriate standardized physical activity questionnaire. Nonetheless, self-report questionnaires, albeit fast, inexpensive and convenient, are not employed routinely, perhaps due to bias with subjective perception leading to possible physical activity overestimation (Prince et al., Reference Prince, Adamo, Hamel, Hardt, Connor Gorber and Tremblay2008; Garriguet and Colley, Reference Garriguet and Colley2014; Brett et al., Reference Brett, Wilson, Ferraro and Adamo2015) or for being less strongly associated with cardio-metabolic risk variables and risk prediction scores than cardiorespiratory fitness assessed using an exercise test (Gray et al., Reference Gray, Stephens, Williams, Davies, Turner and Bracken2015). Objective measures of physical activity include the use of an accelerometer. Using this tool, however, physical activity is usually monitored for seven consecutive days (Brett et al., Reference Brett, Wilson, Ferraro and Adamo2015; Olsson et al., Reference Olsson, Borjesson, Ekblom-Bak, Hemmingsson, Hellenius and Kallings2015), making the examination long and impractical for routine screening purposes. Direct evaluation of cardiorespiratory fitness is based on cardiopulmonary exercise testing or spiroergometry (Herdy et al., Reference Herdy, Ritt, Stein, Araújo, Milani, Meneghelo, Ferraz, Hossri, Almeida, Fernandes-Silva and Serra2016). Owing to technical reasons such as sophisticated equipment (with expensive gas analyser) requiring trained personnel, the univocal indications for this ‘golden standard’ are limited.

With increasing frequency of obesity and type 2 diabetes in paediatric as well as adult population of the developed world (Cruz et al., Reference Cruz, Shaibi, Weigensberg, Spruijt-Metz, Ball and Goran2005; Stevens et al., Reference Stevens, Singh, Lu, Dannaei, Lin, Finucane, Bahalim, McIntire, Gutierrez, Cowan, Paciorek, Farzadfar, Riley and Ezzati2012) it becomes imperative to effectively stratify high-risk (ie, obese, diabetic and unfit) individuals by introducing fitness screening tests. These tests have to be economical, convenient for everyday outpatient routine and should be widely applicable for most patients, especially for obese diabetics. If such testing is established, the awareness of an integer reflecting the subject’s level of fitness may, presumably, act also psychologically – as an aid to put additional emphasis on regular physical activity and encourage the patients for increased involvement in self-management, thus reinforcing the current pharmacological treatment of the disease (Kokkinos et al., Reference Kokkinos, Faselis, Myers, Panagiotakos and Doumas2013). To address the aforementioned issues, a number of simple tests of functional fitness or aerobic endurance have been developed and standardized, for example 6-min walk test (Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006) or Chester Step Test (Sykes and Roberts, Reference Sykes and Roberts2004).

The present pilot study was designed with the intention to introduce a 2-min step-in-place test into the routine outpatient management of overweight/obese type 2 diabetics in stabilized condition. This test was opted for due to its fast and simple protocol practicable for temporally and spatially restricted outpatient settings (Jones and Rikli, Reference Jones and Rikli2002; Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006). As the test was originally proposed for seniors and it has not been validated for the population in question thus far, we aimed at describing the toleration of the test by our overweight/obese type 2 diabetics and their performance indicated by 2-min step-in-place test score (STS). We were also interested to know if the introduction of the new mode of examination could be accompanied by any beneficial effect on anthropometric [eg, body mass index (BMI)], functional (resting systolic blood pressure and STS) or laboratory parameters (eg, blood glucose) in the short term. Therefore, the measurements were taken two times in three- to four-month period and the results were compared with randomly selected age- and sex-matched obese diabetic controls followed at our workplace in a standard regimen without fitness testing.

Methods

Study population

During the year 2016, in total 66 overweight or obese diabetic patients (50 males and 16 females, aged 36–77 and 30–66, respectively) followed up at the outpatient’s surgery of the Department of Internal Medicine III – Nephrology, Rheumatology and Endocrinology, University Hospital, Olomouc, were enrolled in the study. The selection of the patients was based on fulfilling the inclusion criteria that were as follows: age between 30 and 80 years, presence of type 2 diabetes mellitus and overweight/obesity (ie, BMI>25 kg/m2 and/or waist circumference >102 cm for males or >88 cm for females). The diagnosis of diabetes had to be established for at least three months with no documented indication of coronary heart disease. The patients had to be clinically stabilized on standard antidiabetic therapy with no concomitant use of β-blockers. For group A, the criteria also included the willingness of the subjects to participate in the study declared by signing the informed consent. Due to markedly lower frequency of female entries the enrolment (applicable for group A only) has finished as soon as the accepted statistical minimum of eight women were recruited. The exclusion criteria for group A comprised the incidence of any event or condition requiring hospitalization during the three to four-month follow-up, acute change in chronic medication (owing to deteriorated compensation of diabetes, hypertensive crisis, severe infection, etc.) and indispositions decreasing the validity of the endurance test or participant´s ability/readiness to undergo it (eg, musculoskeletal trauma associated with pain perception, escalated psychological stress or loss of interest). Volunteers in group A (25 males and eight females aged 36–77 and 30–66, respectively, see Table 1) underwent, besides standard procedures, fitness testing. Group B was composed of an identical number of age- and sex-matched peers followed at our outpatient clinic without fitness testing. The group was formed post hoc by a professional blinded to the results of group A. Its database was created with the aid of hospital information system by random selection of patients fulfilling the aforementioned criteria with the exception of the time taken between two consecutive visits (for technical reasons this was increased to three to six months). No informed consent was required from group B.

Table 1 Characteristics of groups A and B with between-group and within-group comparisons

All data are presented, for clarity, as mean±SD (indexn indicates that Kolmogorov–Smirnov normality test was not passed). P-values for within-group comparisons are given. Student’s t-test or Wilcoxon matched-pairs signed-ranks test (where indicated by indexa) was utilized. Differences between respective changes in group A versus changes in group B were tested using unpaired t-test or Mann–Whitney Test (where indicated by indexb). Symbols * and *** denote P<0.05 and P<0.001, respectively. Some variables in group B (eg, hsCRP) were considered unnecessary for routine follow-up of the patients. Hence, these data were missing in the Hospital Information System. (The analyses in group A were made possible due to grant support.) Lower number of measurements were largely due to the character of the calculation employed (eGFR>1.5 ml/s/1.73 m2). In case of other parameters (especially ACR, Apo B and insulin) the reasons were mainly technical (such as analytical interference).

FPG=fasting plasma glucose; TC=total cholesterol; Apo B=Apolipoprotein B; TG=triglycerides; AIP=atherogenic index of plasma; hsCRP=high-sensitivity C-reactive protein; eGFR=estimated GFR; ACR=albumin–creatinine ratio; STS=step-in-place test score.

Study design

Standard services provided by the outpatient’s surgery clinic (applicable for group B) included the following. First, harvesting of overnight fasting blood (sometimes accompanied also by the first morning urine) samples for routine laboratory markers of diabetes compensation and kidney function (for details refer to Tab., group B). Second, taking patients’ history – concisely, focused on subjective complaints and possible pharmacological or lifestyle changes in the last several months. Third, simple physical examination involving the measurement of resting blood pressure and basic anthropometric parameters used to calculate BMI (body weight in kilograms/height in meters2). Finally, complex evaluation of the data and the patient’s condition followed by necessary lifestyle recommendations (usually involving provision of educative brochures) and prescription of medication. Under normal circumstances the next visit took place three to four (up to six) months later.

The study protocol for group A encompassed additional examinations and laboratory tests. Markers of insulin resistance and cardiovascular risk factors included, besides routine parameters, also fasting plasma insulin, C-peptide, apolipoprotein B, high-sensitivity C-reactive protein and urinary albumin–creatinine ratio (for detailed list of parameters refer to Tab., group A). Waist and hip circumference were measured to calculate waist-to-hip ratio (WHR). Lifestyle was enquired in a more detailed manner, however, no standardized questionnaire was used. Following 2-min step-in-place test, the patients were individually educated about the relevance of cardiorespiratory fitness (as well as about the consequences of the opposite) and encouraged to increase their regular physical activity with focus on walking. The instructor’s approach was strictly personalized, depending on the motivation or ability of the individual to cooperate in the long-term by introducing a small, yet realistic and tolerable change (typically an addition of two 30-min walks per week) in lifestyle without urgent modification of dietary habits (ie, collaborative goal setting, Peyrot and Rubin, Reference Peyrot and Rubin2007). The next visit took place three to four months later.

Fitness testing protocol

2-min step-in-place test was performed as described previously (Jones and Rikli, Reference Jones and Rikli2002; Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006). Briefly, patients were calmed down for at least 5 min in a sitting position. Following instruction, the subjects stood up and started stepping on a place, alternately raising both knees, with maximum tolerated frequency, to a point midway between the patella and the iliac crest. The patients could stabilize themselves by holding tight to a chair, a piece of furniture or leaning against the wall. 2-min step-in-place test score (STS) was defined as the number of times right knee reached the required height within 2 min.

Clinical chemistry and calculations

Biochemical analyses of glycated haemoglobin (HbA1c), fasting plasma glucose (FPG), human insulin, C-peptide, total cholesterol (TC), triglycerides (TG), high density lipoprotein-cholesterol (HDL), apolipoprotein B (Apo B), high-sensitivity C-reactive protein (hsCRP), albumin and creatinine were performed at the Department of Clinical Biochemistry, University Hospital, Olomouc in accordance with standard protocols subjected to valid directives. No sample required a freezing-thawing cycle.

Index of insulin resistance – homeostasis model assessment (HOMA-IR) was calculated as glucose×insulin/22.5 (Matthews et al., Reference Matthews, Hosker, Rudenski, Naylor, Treacher and Turner1985). Non-HDL was calculated as TC−HDL. Low-density lipoprotein cholesterol (LDL) was calculated, where applicable (TG of <4.5 mmol/L), using Friedewald formula (Friedewald et al., Reference Friedewald, Levy and Fredrickson1972). Atherogenic index of plasma (AIP) was calculated as log (TG/HDL) (Frohlich and Dobiasova, Reference Frohlich and Dobiasova2003). Estimated glomerular filtration rate (eGFR) was calculated, where applicable, using the 2009 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine equation with plasma creatinine, age, ethnicity and sex (Levey et al., Reference Levey, Stevens, Schmid, Zhang, Castro, Feldman, Kusek, Eggers, Van Lente, Greene and Coresh2009).

Statistical analyses

Statistical analyses were performed using GraphPad InStat software version 3.06 (GraphPad Software, San Diego, CA, USA). Data distribution was tested for normality by Kolmogorov–Smirnov test. Unless otherwise noted, data are expressed as means±standard deviation (SD). For paired data (ie, within-group comparisons) Student’s t-test or, where appropriate, (nonparametric) Wilcoxon matched-pairs signed-ranks test were utilized. For comparisons between males and females or between-group comparisons of changes recorded over time in group A versus group B, unpaired t-test or (nonparametric) Mann–Whitney Test were applied. In each case, two-tailed P-value was selected. Selected level of significance was P<0.05.

Results

Regarding group A, all patients completed the fitness test successfully with no clinical complication. Differences between absolute values of STS in males versus females (85±16 in males versus 82±19 in females at entry, and 96±19 in males versus 86±18 in females three to four months later) were statistically insignificant, although significant increment (P<0.001) could be observed in males in contrast to females (P=0.13). There were five males and two females aged above 60 in our cohort. Compared with heathy seniors of adequate age (Jones and Rikli, Reference Jones and Rikli2002; Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006), the performance of the seniors in our cohort was as follows. At entry, two males and one female were below average and three males and one female were at average. Three to four months later, one male and one female remained below average, two males and one female remained at average, one male advanced to average and one male progressed above average. At entry, 10 (out of 20) males and two (out of six) females of <60 years of age did not reach average fitness level of healthy 60–64-year-old seniors. In total, group A presented with a significant increment in STS (P<0.0001). The results are summarized (in combination with other parameters) in Table 1.

Group A also presented with significantly improved markers of glucose and lipid homeostasis (decreased FPG and HbA1c, lowered Apo B and AIP and elevated HDL), mitigated inflammation (hsCRP) and augmented glomerular function (rise in eGFR with fall in ACR). In addition, these changes were accompanied by statistically insignificant trends for reduction in a number of other parameters, such as waist circumference, TG, non-HDL or C-peptide. Decreases in WHR and BMI were unsubstantial. There were no statistically significant trends documented in Group B. When compared with those noted in group A, however, the directions had deleterious clinical connotations: HbA1c decreased significantly less than in group A, FPG, TG and AIP increased producing significant differences from the changes distinguished in group A. The changes in HDL and eGFR were also significantly lower than those recognized in group A. In general, the data indicate positive development in group A, whereas group B remained globally unchanged (Table 1).

Discussion

Poor cardiorespiratory fitness is an independent risk factor for cardiovascular morbidity and cardiac or all-cause mortality. Long-term weight loss, decreased blood pressure and lipids as well as enhanced cardiorespiratory fitness are regarded as the most powerful steps to prevent macrovascular diabetic complications in type 2 diabetics (Boulé et al., Reference Boulé, Kenny, Haddad, Wells and Sigal2003; Tanasescu et al., Reference Tanasescu, Leitzmann, Rimm and Hu2003). Therefore, regular physical activity is a fundamental part of the complex therapeutic approach to diabetics with influence on insulin resistance (Svačinová, Reference Svačinová2007). In order to assess the level of physical activity, estimate individual fitness and predict the associated mortality risk in daily praxis, either standardized questionnaires or exercise testing can be used. In our study, we have decided to apply the simple 2-min step-in-place test without a standardized questionnaire. This decision was motivated by reports showing that poor fitness, rather than reported physical inactivity, is independently associated with increased mortality risk (Lee et al., Reference Lee, Sui, Ortega, Kim, Church, Winett, Ekelund, Katzmarzyk and Blair2011). Other data suggest that the level of physical activity determined by the General Practice Physical Activity Questionnaire tool reveals less associations with markers of cardiovascular disease or type 2 diabetes mellitus compared with cardiorespiratory fitness evaluated by a simple test (Gray et al., Reference Gray, Stephens, Williams, Davies, Turner and Bracken2015). Therefore, it seems reasonable to propose that a simple physiological metric should be incorporated as a vital sign in cardiovascular disease risk factor evaluation and management (Després, Reference Després2016). For this purpose we have opted for a simple and convenient 2-min step-in-place test enabling us to put, as immediate feedback, additional emphasis on the relevance of being physically fit for life’s quality and longevity.

As all participants comprehended and successfully completed the protocol with no documented clinical complication attributable to the test, we can see a few obstacles for its wide implementation within the scope of preventive diabetology. In agreement with previous findings (Hansen et al., Reference Hansen, Landstad, Gundersen and Svebak2012), STS indicated a somewhat lower level of cardiorespiratory fitness of obese type 2 diabetics compared with healthy subjects of comparable or higher age categories (Jones and Rikli, Reference Jones and Rikli2002; Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006). Contrary to healthy seniors (Jones and Rikli, Reference Jones and Rikli2002; Różańska-Kirschke et al., Reference Różańska-Kirschke, Kocur, Wilk and Dylewicz2006), no significant gender-dependent differences in the absolute values of STS were found as far as the whole cohort was concerned. This may be, at least in part, explained by the low number of female entries. As to females, a rather reluctant attitude towards being physically stressed was experienced. The reasons were mostly subjective and psychological (such as embarrassment).

One of the most interesting findings of this study was the statistically significant enhancement of the volunteers’ performance over time. However, statistical significance was lost when females were considered separately. Another noteworthy observation was the favourable development in several biochemical markers confined to group A (Table 1). Although accompanied by (but not necessarily related to) increased aerobic endurance, the complex laboratory improvement was not reflected in anthropometric parameters. If augmented physical activity was the cause, lower FPG and HbA1c might have resulted from more effective action of insulin at the adipocytes without concomitant reduction in body weight and fat stores (Hughes et al., Reference Hughes, Fiatrone, Fielding, Kahn, Ferrara, Shepherd, Fisher, Wolfe, Elahi and Evans1993; Kelley and Goodpaster, Reference Kelley and Goodpaster1999). The enhancement of insulin action is an important (and often overlooked) salutary effect suggesting that physical activity may be as efficacious in preventing insulin resistance as is losing body weight. Low level of cardiorespiratory fitness associated with physical inactivity is typical for patients with insulin resistance and results in higher risk of cardiovascular disease than obesity itself – a phenomenon that may shortly be put as ‘fit and fat is better than unfit and unfat’ (Lee et al., Reference Lee, Blair and Jackson1999). Concerning dyslipidaemia, the studied population presented with a typical diabetic profile involving high TG and low HDL with almost normal total and LDL cholesterol. Following the introduction of fitness testing, the levels of apoB and AIP decreased and the level of HDL rose in group A patients as opposed to their counterparts in group B (Table 1). It would be speculative to account for these differences using the limited data obtained. hsCRP, as a sensitive marker of subclinical inflammation, belongs among established predictors of cardiovascular risk associated with insulin resistance, metabolic syndrome, hyperglycaemia and type 2 diabetes (Rivero et al., Reference Rivero, Mora, Muros, Garcia, Herrera and Navarro-González2009). In parallel to the elevation of STS, the level of subclinical inflammation subsided three to four months following the first fitness examination in group A. Even though physical activity and exercise training have been associated with reductions in hsCRP, we cannot ascertain as to how far these activities in the tested group had changed and, moreover, even if they did change, the mechanism whereby such interventions could lead to a reduction in hsCRP remains unclear (Hammonds et al., Reference Hammonds, Gathright, Goldstein, Penn and Hughes2016). Exercise training was found to possess a potential to increase kidney function (Baria et al., Reference Baria, Kamimura, Aoike, Ammirati, Rocha, De Mello and Cuppari2014). Despite a lower number of measurements mainly due to eGFR exceeding 1.5 ml/s/1.73 m2 the data (eGFR and ACR) suggest an improvement in glomerular function in the tested population. Although no significant difference was observed in group B, it is notable that the trends in creatinine and eGFR were clinically unfavourable and in the case of the latter parameter, they were significantly different from the tested group A (Table 1).

Although a direct causal relationship may exist between aerobic endurance and several metabolic markers (Schwingshackl et al., Reference Schwingshackl, Dias, Strasser and Hoffmann2013), the laboratory progress observed in group A can be, as for this study, exclusively attributed neither to physical fitness, nor to the introduction of fitness testing per se, for a number of reasons. Individuals in group A were all ready to undergo the fitness test – a fact that would probably not be true for all group B counterparts. Some evidence indicates that patient trust in physician and desire for involvement and collaborating care may be associated with better self-care behaviours, adherence and positive diabetes outcomes including biochemical markers such as FPG or HbA1c (Lee and Lin, Reference Lee and Lin2009; Charles, Reference Charles2015). Furthermore, a lack of employment of a standardized cardiorespiratory fitness method opened a possibility of patient dissimulation, especially during the final examination. Based on marked discrepancies repeatedly found between subjective and objective measures of physical activity (questionnaires versus accelerometers, Brett et al., Reference Brett, Wilson, Ferraro and Adamo2015), reported glycaemia (self-report diaries versus glucometer memory, Armstrong, Reference Armstrong1991) and food intake (reported energy intake in dietary history questionnaires versus resting metabolic rate, Fricker et al., Reference Fricker, Baelde, Igoin-Apfelbaum, Huet and Apfelbaum1992), self-enhancement may be expected to be abundant in obese diabetics. Therefore, the reasons behind improvements in group A are likely to be multifactorial, involving, besides the introduction of fitness testing, a number of lifestyle factors (unmonitored in this study) and psychological influences such as self-motivation, willingness to compete or to please the researchers. Some of these elements (eg, competitiveness) may have played more important roles in males than in females. The investigation of the extent to which the respective factors might have participated on the favourable outcomes would require a different study design employing a multivariate analysis.

To be fit-for-purpose, 2-min step-in-place test requires better characterization and validation for obese diabetics using a widely accepted indicator of cardiorespiratory fitness, namely peak oxygen consumption, VO2peak, as determined by cardiopulmonary exercise testing (Herdy et al., Reference Herdy, Ritt, Stein, Araújo, Milani, Meneghelo, Ferraz, Hossri, Almeida, Fernandes-Silva and Serra2016). Subsequent effort should also address the question of objective measurement of physical activity (eg, using an accelerometer) and the need for study population enlargement.

Conclusion

2-min step-in-place test is temporally and spatially undemanding and well-tolerated by patients and personnel. STS score of overweight/obese type 2 diabetics was found to have a considerable range with differences between males and females at the borderline of statistical significance for the cohort studied. In general, the data are compliant with lower cardiorespiratory fitness of obese type 2 diabetics compared with healthy population. Within three to four-month period, the tested group presented with improvements in STS (referring especially to the males) as well as in several laboratory parameters of glucose and lipid homeostasis, glomerular function and subclinical inflammation with no reflection in anthropometry. Further effort is warranted to better characterize and validate the fitness test for obese diabetics so that it could become recommendable for future implementation into screening strategies or for self-monitoring purposes. Subsequent studies should also investigate the possibility of an existence of a causal relationship between the implementation of aerobic endurance testing into routine services provided by outpatient surgery clinics and the benefits observed.

Acknowledgements

The authors acknowledge skilful technical assistance of our pre-graduate students (E.R. and D.H.) during data processing and valuable correspondence with doctor M.B. in the phase of manuscript preparation.

Financial Support

This study was supported by grants MH CZ – DRO (FNOL, 00098892) – 87-62 from the Czech Ministry of Health and IGA-LF-2016-014 from the Palacky University, Olomouc, Czech Republic.

Conflicts of Interest

None.

Ethical Standards

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional guidelines on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. The study was approved by the Local Ethics Committee of the University Hospital, Olomouc, Czech Republic (Ref. No.: 147/16). Before inclusion into the study, all active participants provided their informed consent.

References

Armstrong, D. 1991: The social context of technology in diabetes care: “compliance“ and “control”. Introduction. In Bradley, C., Christie, M. and Home, P., editors. Technology of diabetes care: converging medical and psychosocial perspectives. Chur, Switzerland: Harwood Academic Publishers, 1724.Google Scholar
Baria, F., Kamimura, M.A., Aoike, D.T., Ammirati, A., Rocha, M.L., De Mello, M.T. and Cuppari, L. 2014: Randomized controlled trial to evaluate the impact of aerobic exercise on visceral fat in overweight chronic kidney disease patients. Nephrology, Dialysis, Transplantation 29, 857864.Google Scholar
Barry, V.W., Baruth, M., Beets, M.W., Durstine, J.L., Liu, J. and Blair, S.N. 2014: Fitness vs. fatness on all-cause mortality: a meta-analysis. Progress in Cardiovascular Diseases 56, 382390.Google Scholar
Blair, S.N., Kohl, H.W., Paffenbarger, R.S. Jr., Clark, D.G., Cooper, K.H. and Gobbons, L.W. 1989: Physical fitness and all-cause mortality: a prospective study of healthy men and women. Journal of the American Medical Association 262, 23952401.Google Scholar
Bouchard, C., Blair, S.N. and Katzmarzyk, P.T. 2015: Less sitting, more physical activity, or higher fitness? Mayo Clinic Proceedings 90, 15331540.Google Scholar
Boulé, N.G., Kenny, G.P., Haddad, D., Wells, G.A. and Sigal, R.J. 2003: Meta-analysis of the effect of structured exercise training on cardiorespiratory fitness in type 2 diabetes mellitus. Diabetologia 46, 10711081.Google Scholar
Brett, K.E., Wilson, S., Ferraro, Z.M. and Adamo, K.B. 2015: Self-report pregnancy physical activity questionnaire overestimates physical activity. Canadian Journal of Public Health 106, e297e302.Google Scholar
Charles, S. 2015: Implications of the patient-physician relationship for people with diabetes, thesis. Dietrich College of Humanities and Social Sciences.Google Scholar
Church, T.S., LaMonte, M.J., Barlow, C.E. and Blair, S.N. 2005: Cardiorespiratory fitness and body mass index as predictors of cardiovascular disease mortality among men with diabetes. Archives of Internal Medicine 165, 2114–20.Google Scholar
Cruz, M.L., Shaibi, G.Q., Weigensberg, M.J., Spruijt-Metz, D., Ball, G.D. and Goran, M.I. 2005: Pediatric obesity and insulin resistance: chronic disease risk and implications for treatment and prevention beyond body weight modification. Annual Review of Nutrition 25, 435468.Google Scholar
Després, J.P. 2016: Physical activity, sedentary behaviours, and cardiovascular health: when will cardiorespiratory fitness become a vital sign? Canadian Journal of Cardiology 32, 505513.Google Scholar
Fricker, J., Baelde, D., Igoin-Apfelbaum, L., Huet, J.M. and Apfelbaum, M. 1992: Underreporting of food intake in obese “small eaters”. Appetite 19, 273283.Google Scholar
Friedewald, W.T., Levy, R.I. and Fredrickson, D.S. 1972: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clinical Chemistry 18, 499502.Google Scholar
Frohlich, J. and Dobiasova, M. 2003: Fractional esterification rate of cholesterol and ratio of triglycerides to HDL-cholesterol are powerful predictors of positive findings on coronary angiography. Clinical Chemistry 49, 18731880.Google Scholar
Garriguet, D. and Colley, R.C. 2014: A comparison of self-reported leisure-time physical activity and measured moderate-to-vigorous physical activity in adolescents and adults. Health Reports 25, 311.Google Scholar
Gray, B.J., Stephens, J.W., Williams, S.P., Davies, C.A., Turner, D. and Bracken, R.M., Prosiect Sir Gâr Group 2015: Cardiorespiratory fitness is a stronger indicator of cardiometabolic risk factors and risk prediction than self-reported physical activity levels. Diabetes and Vascular Disease Research 12, 428435.Google Scholar
Hammonds, T.L., Gathright, E.C., Goldstein, C.M., Penn, M.S. and Hughes, J.W. 2016: Effects of exercise on c-reactive protein in healthy patients and in patients with heart disease: a meta-analysis. Heart and Lung: the Journal of Critical Care 45, 273282.Google Scholar
Hansen, E., Landstad, B.J., Gundersen, K.T. and Svebak, S. 2012: The relative importance of aerobic capacity, physical activity and body mass index in impaired glucose tolerance and Type 2 diabetes. Vulnerable Groups & Inclusion 3, http://dx.doi.org/10.3402/vgi.v3i0.10232.Google Scholar
Herdy, A.H., Ritt, L.E., Stein, R., Araújo, C.G., Milani, M., Meneghelo, R.S., Ferraz, A.S., Hossri, C., Almeida, A.E., Fernandes-Silva, M.M. and Serra, S.M. 2016: Cardiopulmonary exercise test: background, applicability and interpretation. Arquivos Brasileiros de Cardiologia 107, 467481.Google Scholar
Hughes, V.A., Fiatrone, M.A., Fielding, R.A., Kahn, B.B., Ferrara, C.M., Shepherd, P., Fisher, E.C., Wolfe, R.R., Elahi, D. and Evans, W.J. 1993: Exercise increases muscle GLUT-4 levels and insulin action in subjects with impaired glucose tolerance. American Journal of Physiology 264, E85562.Google Scholar
Israel, A., Kivity, S., Sidi, Y., Segev, S., Berkovitch, A., Klempfner, R., Lavi, B., Goldenberg, I. and Maor, E. 2016: Use of exercise capacity to improve SCORE risk prediction model in asymptomatic adults. European Heart Journal 37, 23002306.Google Scholar
Jones, C.J. and Rikli, R.E. 2002: Measuring functional fitness of older adults. The Journal on Active Aging 1, 2430.Google Scholar
Kelley, D.E. and Goodpaster, B.H. 1999: Effects of physical activity on insulin action and glucose tolerance in obesity. Medicine and Science in Sports and Exercise 31, 619623.Google Scholar
Kodama, S., Saito, K., Tanaka, S., Maki, M., Yachi, Y., Asumi, M., Sugawara, A., Totsuka, K., Shimano, H., Ohashi, Y., Yamada, N. and Sone, H. 2009: Cardiorespiratory fitness as a quantitative predictor of all-cause mortality and cardiovascular events in healthy men and women: a meta-analysis. Journal of the American Medical Association 301, 20242035.Google Scholar
Kokkinos, P.F., Faselis, C., Myers, J., Panagiotakos, D. and Doumas, M. 2013: Interactive effects of fitness and statin treatment on mortality risk in veterans with dyslipidemia: a cohort study. Lancet 381, 394399.Google Scholar
Lee, C.D., Jackson, A.S. and Blair, S.N. 1998: US weight guidelines: is it also important to consider cardiorespiratory fitness? International Journal of Obesity and Related Metabolic Disorders 22, S27.Google Scholar
Lee, D.C., Sui, X., Ortega, F.B., Kim, Y.S., Church, T.S., Winett, R.A., Ekelund, U., Katzmarzyk, P.T. and Blair, S.N. 2011: Comparisons of leisure-time physical activity and cardiorespiratory fitness as predictors of all-cause mortality in men and women. British Journal of Sports Medicine 45, 504510.Google Scholar
Lee, D.D., Blair, S.N. and Jackson, A.S. 1999: Cardiorespiratory fitness, body composition, and all cause cardiovascular disease mortality in men. American Journal of Clinical Nutrition 69, 373380.Google Scholar
Lee, Y.Y. and Lin, J.L. 2009: The effects of trust in physician on self-efficacy, adherence and diabetes outcomes. Social Science & Medicine (1982) 68, 10601068.Google Scholar
Levey, A.S., Stevens, L.A., Schmid, C.H., Zhang, Y.L., Castro, A.F. 3rd, Feldman, H.I., Kusek, J.W., Eggers, P., Van Lente, F., Greene, T. and Coresh, J., CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) 2009: A new equation to estimate glomerular filtration rate. Annals of Internal Medicine 150, 604612.Google Scholar
Matthews, D.R., Hosker, J.P., Rudenski, A.S., Naylor, B.A., Treacher, D.F. and Turner, R.C. 1985: Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 28, 412419.Google Scholar
McAuley, P.A. and Beavers, K.M. 2014: Contribution of cardiorespiratory fitness to the obesity paradox. Progress in Cardiovascular Diseases 56, 434440.Google Scholar
Olsson, S.J., Borjesson, M., Ekblom-Bak, E., Hemmingsson, E., Hellenius, M.L. and Kallings, L.V. 2015: Effects of the Swedish physical activity on prescription model on health related quality of life in overweight older adults: a randomized controlled trial. BioMed Central Public Health 15, 687696.Google Scholar
Peyrot, M. and Rubin, R.R. 2007: Behavioral and psychosocial interventions in diabetes: a conceptual review. Diabetes Care 30, 24332440.Google Scholar
Prince, S.A., Adamo, K.B., Hamel, M.E., Hardt, J., Connor Gorber, S. and Tremblay, M. 2008: A comparison of direct versus self-report measures for assessing physical activity in adults: a systematic review. The International Journal of Behavioral Nutrition and Physical Activity 5, 5679.Google Scholar
Rivero, A., Mora, C., Muros, M., Garcia, J., Herrera, H. and Navarro-González, J.F. 2009: Pathogenic perspectives for the role of inflammation in diabetic nephropathy. Clinical Science (London) 116, 479492.Google Scholar
Ross, R., Blair, S.N., Arena, R., Church, T.S., Després, J.P., Franklin, B.A., Haskell, W.L., Kaminsky, L.A., Levine, B.D., Lavie, C.J., Myers, J., Niebauer, J., Sallis, R., Sawada, S.S., Sui, X. and Wisløff, U. 2016: Importance of assessing cardiorespiratory fitness in clinical practice: a case for fitness as a clinical vital sign: a scientific statement from the American Heart Association. Circulation 134, e653e699.Google Scholar
Różańska-Kirschke, A., Kocur, P., Wilk, M. and Dylewicz, P. 2006: The Fullerton Fitness Test as an index of fitness in the elderly. Medical Rehabilitation 10, 916.Google Scholar
Schwingshackl, L., Dias, S., Strasser, B. and Hoffmann, G. 2013: Impact of different training modalities on anthropometric and metabolic characteristics in overweight/obese subjects: a systematic review and network meta-analysis. Public Library of Science one 8, e82853.Google Scholar
Stevens, G.A., Singh, G.M., Lu, Y., Dannaei, G., Lin, J.K., Finucane, M.M., Bahalim, A.N., McIntire, R.K., Gutierrez, H.R., Cowan, M., Paciorek, C.J., Farzadfar, F., Riley, L. and Ezzati, M., Global Burden of Metabolic Risk Factors of Chronic Diseases Collaborating Group (Body Mass Index) 2012: National, regional, and global trends in adult overweight and obesity prevalences. Population Health Metrics 10, 2237.Google Scholar
Svačinová, H. 2007: Exercise therapy for patients with metabolic syndrome. Vnitr̆ní lékar̆ství 53, 540544.Google Scholar
Sykes, K. and Roberts, A. 2004: The Chester step test – a simple yet effective tool for the prediction of aerobic capacity. Physiotherapy 90, 183188.Google Scholar
Tanasescu, M., Leitzmann, M.F., Rimm, E.G. and Hu, F.B. 2003: Physical activity in relation to cardiovascular disease and total mortality among men with type 2 diabetes. Circulation 107, 24352439.Google Scholar
Wei, M., Gibbons, L.W., Kampert, J.B., Nichman, M.Z. and Blair, S.N. 2000: Low cardiorespiratory fitness and physical inactivity as predictors of mortality in men with type 2 diabetes. Annals of Internal Medicine 132, 605611.Google Scholar
Wei, M., Kampert, J.B., Barlow, C.E., Nichaman, M.Z., Gibbons, L.W., Paffenbarger, R.S. Jr. and Blair, S.N. 1999: Relationship between low cardiorespiratory fitness and mortality in normal-weight, overweight, and obese men. Journal of the American Medical Association 282, 15471553.Google Scholar
Figure 0

Table 1 Characteristics of groups A and B with between-group and within-group comparisons