Skip to main content

The combined association of dietary inflammatory index and resting metabolic rate on cardiorespiratory fitness in adults

Abstract

Background

No study has examined the combined association of dietary inflammatory index (DII) of the diet and resting metabolic rate (RMR) on cardiorespiratory fitness (CRF). Therefore, we investigated the combined association between DII and RMR on CRF.

Methods

This cross-sectional study was conducted on 270 adult subjects. The DII was calculated using a validated semi-quantified food frequency questionnaire. RMR was measured using an indirect calorimetric method. Socioeconomic status, anthropometric measures, body composition and blood pressure were documented by a trained interviewer. CRF was assessed by using Bruce protocol. Binary logistic regression was performed to find the association of CRF with DII/RMR categories in various models.

Results

The participants categorized into four groups including: (1) low DII/high RMR, (2) low DII/low RMR, (3) high DII/low RMR, (4) high DII/high RMR. The mean of VO2Max (mL/kg/min), VO2max (L/min) and VO2max relative to lean body mass (LBM) was lower in participants that were classified as high DII/low RMR compared to those in low DII/high RMR. After controlling for age, sex, education status, smoking status, and physical activity those who were in the high DII/low RMR group, compared to the low DII/high RMR group were 28% less likely to have higher VO2max (ml/kg/min) (OR 0.72; 95% CI 0.18, 0.82, p = 0.04). Moreover, had 25% lower odds of VO2max (L/min) which was significant (OR 0.75, 95% CI 0.11, 0.89, p = 0.03). In addition, were 21% less likely to have higher VO2max (LBM) (OR 0.79; 95% CI 0.30, 0.92, p = 0.02).

Conclusions

Overall, consumption of a pro-inflammatory diet in combination with low RMR status is associated with lower odds of CRF compared to those who had anti-inflammatory diet in combination with high RMR status among Iranian healthy adults. This study suggests that researchers should focus on combined relationships rather than single pair-wise associations for having a better judgment.

Introduction

Resting metabolic rate (RMR) is the least energy needed to keep up essential body function during a stable resting state and fasting status [1]. It is estimated that lean body mass is accounts for 60–85% of RMR [2]. Previous studies have shown significant inverse association between RMR and body fat mass and body weight, such that decreasing in RMR may resulted in increasing body fat mass and body weight [3, 4]. Additionally, inflammation may play a role in weight gain through leptin and insulin resistance leading to increased FM and a balance between energy intake and expenditure [5, 6]. Indeed, increased body fat mass in obese individuals results in increasing C-reactive protein (CRP) and inflammatory cytokines [7]. Therefore, obesity is considered a low-grade inflammatory condition [8]. Besides, this chronic inflammation in adipose tissue accelerates the complications and diseases caused by obesity [9]. The study results showed that there was a positive relationship between C-reactive protein synthesis index (CRP) and the risk of coronary heart disease and mortality from cardiovascular disease [10, 11]. Accumulating evidence also suggests that obesity reduces cardiorespiratory fitness (CRF) [12]. CRF is a modifiable and independent risk factor for mortality from cardiovascular disease (CVD) [13]. Previous studies have shown that high CRF, which is evaluated by the peak of oxygen uptake (VO2Max), is associated with a reduced risk of cardiovascular disease and related mortality [14]. Therefore, inflammation and VO2Max are significantly associated with other major cardiovascular risk factors [14]. One of the key and modifiable factors effective in reducing or causing inflammation is diet which led to the development of the dietary inflammatory index (DII) [15]. In fact, DII is a scoring algorithm that ranks individuals' diets based on their inflammatory potential [16]. The purpose of making this index is to classify people’s diet from maximally anti-inflammatory to maximally pro-inflammatory [15,16,17,18]. The DII authors evaluated the association of dietary components with six markers of inflammation:

IL-1β, IL-4, IL-6, IL-10, TNF-α and CRP [16]. Accumulating evidence illustrate that a high DII diet is associated with an increased risk of metabolic syndrome, diabetes, hypertension, and cancer [7, 12, 13, 19]. In addition, a recent umbrella review showed that anti-inflammatory dietary patterns play a significant role in the prevention of chronic diseases [20].

Given that Iran has an increasing rate of obesity and several inflammatory diseases, we designed this cross-sectional study to investigate whether the combined association of dietary inflammatory index and resting metabolic rate is related to cardiorespiratory fitness in adults. We hypothesized that the higher inflammatory index of the diet in our participants is associated with low RMR and CRF in Iranian adults.

Methods

Study design

This study consisted of 270 apparently healthy adults (118 men and 152 women). The social network was used to recruit participants through a recruitment message. Convenience sampling was used to select the subjects. Based on previously calculated correlation coefficient between diet and cardiorespiratory fitness [21], our target number of participants was 256 \(\left( {\left( {{{Z_{{1 - \frac{\alpha }{2}}} + Z_{1 - \beta } \times \sqrt {1 - r^{2} } } \mathord{\left/ {\vphantom {{Z_{{1 - \frac{\alpha }{2}}} + Z_{1 - \beta } \times \sqrt {1 - r^{2} } } r}} \right. \kern-0pt} r}} \right) = 256} \right)\). However, in order to replace patients who were excluded due to under- or over-reported food intakes, we continued sampling until enrolling 273 individuals. Research criteria included apparently healthy adults living in Tehran, aged 18–70, who were interested in participating in the study, and were willing to participate in study. Individuals with extreme values of dietary intake (less than 800 kcal per day or more than 4200 kcal per day, respectively), those with kidney, liver, digestive, hormonal and lung disease, infectious and active inflammatory diseases, pregnancy, lactation, routine supplement and drug use, such as weight loss, hormonal, sedative drugs, thermogenic supplements such as caffeine and green tea and conjugated linoleic acid (CLA), were excluded. After removing three subjects due to above-mentioned reasons, only 270 participants remained for statistical analysis (Fig. 1).

Fig. 1
figure 1

Participants flow diagram

Anthropometric measures

A wall stadiometer was used to determine the height of participants without shoes (Seca, Germany). Waist circumference (WC) was measured at narrowest point between lower rib and iliac crest by non-elastic tape. Body mass index (BMI), weight, fat mass (FM), fat free mass (FFM), and lean body mass (LBM) were measured by InBody (InBody720, Biospace, Tokyo, Japan). The established protocol entailed abstaining from food consumption for a minimum of 4 h, consuming at least 2 L of water the day prior, and refraining from consuming coffee or alcoholic beverages for a minimum of 12 h. Prior to the test, participants were instructed to void their bladder [22].

Assessment of other variables

The participants filled out a self-administered questionnaire to assess their demographics, including their age, sex, smoking status (smokers, non-smokers or quitters), as well as their education status (under diploma/diploma/educated). To assess blood pressure, first, we demanded individuals to rest for at least ten minutes. Blood pressure was then measured using a standard mercury sphygmomanometer, twice with a 5-min interval, while participants were sitting. The mean of the two measurements was recorded as the participant’s blood pressure. The levels of physical activity were measured using the international physical activity questionnaire (IPAQ) [23]. Three categories were developed to categorize the subjects, including very low (< 600 METs/week), low (600–3000 METs/week), moderate, and high (> 3000 METs/week) based on metabolic equivalents (METs) [24].

Dietary intakes

In order to evaluate habitual food consumption, a validated semi-quantitative food frequency questionnaire were used [25]. The questionnaire included 168 food items, with standard serving sizes as commonly consumed by Iranians. A team of experienced nutritionists interviewed each participant in detail to collect nutritional information. Participants were queried on their consumption of various food items, with two questions posed for each item: Firstly, the frequency of food group consumption, measured in annual, monthly, weekly, and daily intervals over the past year, and secondly, the approximate amount of each item consumed per occasion. Subsequently, all food items' frequency and quantity of consumption were converted into grams per day, utilizing “household measures” [26]. The authors added Iranian foods and recipes to the software and the macronutrient and micronutrient content of the diets were then determined using modified Nutritionist IV software developed specifically for Iranian foods (version 7.0; N-Squared Computing, Salem, OR, USA).

Resting metabolic rate

The resting metabolic rate (RMR) was estimated through indirect calorimetry (Cortex Metalyser 3B, Leipzig, Germany). As per established procedures, two calibrations were undertaken: (1) The gas analyzer was calibrated prior to each measurement using ambient air and a standard gas mixture (16% O2, 4.96% CO2), and (2) the flow calibration was executed via a 3-L syringe (Hans Rudolph, UK). Upon completion of the calibration process, data pertaining to the patient's date of birth, sex, height, weight, and mask size were entered. Patients were instructed to abstain from food and non-water fluids for 12 h and refrain from smoking for a minimum of 4 h prior to the test. Participants were provided with guidelines to remain alert and relaxed while positioned supine on a bench, and refrain from talking or moving during the examination. The measurement was conducted within a serene environment with controlled temperature and humidity, lasting for 45 min after donning a gas collection mask. Readings were taken without interruption, and the first 10 min were excluded from the data analysis [27].

Cardiorespiratory fitness testing

To estimate cardiorespiratory fitness (CRF), study participants commenced their exercise regimen at a velocity of 5 miles per hour (mph) for a duration of 5 min, employing a standard treadmill model (h/p/cosmos). VO2max was evaluated through the implementation of the Bruce Protocol [28], which is systematically structured into incremental 3-min stages that initiate at a pace of 1.7 mph and an incline of 10% gradient for 3 min, subsequently advancing in stages (Fig. 2) until a stop-test indicator is attained. This protocol consisted of seven stages that each stage last 3 min. The test is halted if the patient experiences chest pain, shortness of breath or fatigue. The test is also terminated if more than 90% of maximum heart rate predicted for age is reached, respiratory exchange ratio is ≥ 1.10, and a plateau (< 150 mL/min increase) in oxygen consumption is detected in contrast with an increase in speed. At least two of the three criteria must be met. Finally, participants engage in a cool-down process consisting of a 3-min walk at 4 mph and stretching exercises. Following the Bruce protocol, the treadmill and respiration gas analyzer (Cortex Metabolizer 3B) were used to measure the three type of maximum oxygen consumption including relative to body mass [VO2max(ml/kg/min)], absolute [VO2max(L/min)], and relative to LBM [VO2max(LBM)].

Fig. 2
figure 2

Bruce protocol for maximal and sub maximal efforts

DII development

Dietary inflammatory index scores were calculated by multiplying 29-item nutrients or foods based on the inflammatory weights they carry according to Shivappa et al. method [16]. Firstly, in order to reduce the variation in dietary intake between people, macronutrients and micronutrients (carbohydrate, protein, total fat, cholesterol, saturated fatty acids, monounsaturated fatty acids (MUFA), polyunsaturated fatty acids (PUFA), n-3 fatty acids, n-6 fatty acids, β-carotene, vitamin A, vitamin C, vitamin D, vitamin E, vitaminB6, vitaminB12, fiber, folic acid, niacin, riboflavin, thiamin, iron, zinc, selenium, magnesium, onion, caffeine) were computed on a daily basis [29]; our documents lacked some nutrients (trans FAs, flavan-3-ol, flavones, flavonols, flavanones, anthocyanidins, isoflavones, pepper, thyme/oregano, rosemary, garlic, ginger, saffron, and turmeric and tea), so we excluded them. Food parameters were adjusted to their corresponding global mean and standard deviation for each individual [16]. To normalize the scoring system and avoid skewness, the Z score values were converted to percentiles and centered by doubling them and subtracting one. DII scores for food parameters are derived by multiplying the centered percentile value of each food parameter by the overall food parameter score [16]. Lastly, all food parameter-specific DII scores were summed to determine the DII score. Diets with higher DII scores tend to be pro-inflammatory, while diets with lower DII scores tend to be anti-inflammatory. We set median value of DII score as threshold level (DII median = 7.70) such that upper median values of DII considered as high inflammatory diet and vice versa.

Statistical analysis

Statistical tests such as Kolmogorov–Smirnov and Shapiro–Wilk were used to determine the normality of distributions. There was a normal distribution for all variables. After that, subjects were categorized according to their DII and RMR median values. We computed four independent groups by combining DII and RMR dichotomized groups (low DII/low RMR, low DII/high RMR, high DII/low RMR and high DII/high RMR). To compare general characteristics across the four groups, we used one-way analysis of variance (ANOVA) and chi-square tests for quantitative and qualitative variables, respectively. To compare participants’ dietary intakes within four groups, analysis of covariance (ANCOVA) to adjust for energy intake. We used ANOVA to examine significant differences across the four above-mentioned groups. Post hoc Tukey test was used to compare pair-wise mean differences. CRF values were then transformed into binary variables according to the upper and lower median values. The median values were VO2max(ml/kg/min) = 30.0, VO2max(L/min) = 2.04, and VO2max(LBM) = 47.94. ANCOVA test was performed to compare the mean of CRF among DII/RMR groups after adjusting for potential confounders such as age, sex, smoking status, energy intake, physical activity and BMI. Binary logistic regression was performed to find the association of CRF with DII/RMR categories in various models. First, we adjusted age and sex. Then, we additionally controlled for smoking and physical activity status. To obtain the overall trend of odds ratios across the combined effect of DII and RMR, we considered these classifications as an ordinal variable in the logistic regression models and the first tertiles regarded as the reference group. All statistical analysis was performed with the SPSS (Statistical Package for Social Sciences) for Windows 25.0 software package (SPSS, Chicago, IL). The level of statistical significance was pre-set at p < 0.05.

Results

The general characteristics of participants are shown in Table 1. This research included a total of 270 participants (118 men and 152 women) with an age range of 18–70 years old. The mean of age, height, weight, BMI, WC, FFM and systolic blood pressure (SBP) had significant differences across study groups. For other variables, we did not see any significant difference. The distribution of sex among the four groups was significantly different.

Table 1 General characteristics of the participants in the study

Table 2 indicates the dietary intake of study participants by DII/RMR categories. There were significant differences in intake of protein, fiber, energy, vitamins (B12, B6, C) and total cholesterol between DII/RMR groups. Other dietary intakes had no significant differences.

Table 2 Dietary intake of study participants

The mean of VO2Max (mL/kg/min) was lower in participants that were classified as high DII/low RMR compared to those in low DII/high RMR (p value = 0.02), this significant association was remained significant after controlling for confounders (p value = 0.04). Post hoc Tukey test revealed no significant differences between other categories in comparison with low DII/high RMR group. Participants with a high DII score and low RMR had lower VO2Max (L/min) and VO2Max (LBM) compared with those with low DII score and high RMR. However, the mean of VO2max (L/min) and VO2max (LBM) after adjustment for confounders, had no significant differences in any classification (Table 3).

Table 3 Mean of cardiorespiratory fitness by combined effect of dietary inflammatory index and resting metabolic rate

Multivariate adjusted odds ratios and 95% confidence intervals for CRF by the combined effect of DII and RMR are given in Table 4. In the crude model, those who were in the high DII/low RMR group, compared to the low DII/high RMR group, were less likely to have higher VO2max (ml/kg/min) (OR 0.75; 95% CI 0.10, 0.85, p = 0.02); this association remained significant after adjusting for confounding variables (OR 0.72; 95% CI 0.18, 0.82, p = 0.04). Moreover, we found that participants in high DII/low RMR group, had lower odds of VO2max (L/min) which was significant (OR 0.84, 95% CI 0.18, 0.89, p = 0.03). When potential confounders were taken into account, such association remained significant (OR 0.75, 95% CI 0.11, 0.89, p = 0.03). In the crude model, those who were in the high DII/low RMR group, compared to the low DII/high RMR group, were less likely to have higher VO2max (LBM) (OR 0.85; 95% CI 0.05, 0.90, p = 0.01); this association remained significant after adjusting for confounding variables (OR 0.79; 95% CI 0.30, 0.92, p = 0.02). There was also no significant combined association of dietary inflammatory index and resting metabolic rate on cardiorespiratory fitness even after controlling for covariates.

Table 4 Odd ratios and 95% CIs for cardiorespiratory fitness by combined effect of dietary inflammatory index and resting metabolic rate

Discussion

According to our cross-sectional study, the mean of VO2Max (mL/kg/min), VO2max (L/min) and VO2max (LBM) was lower in participants that were classified as high DII/low RMR compared to those in low DII/high RMR. After controlling for covariates, those who were in the high DII/low RMR group, compared to the low DII/high RMR group were 28% less likely to have higher VO2max (ml/kg/min). Moreover, we found that participants in high DII/low RMR group had 25% lower odds of VO2max (L/min) which was significant. In the final model, those who were in the high DII/low RMR group, compared to the low DII/high RMR group were 21% less likely to have higher VO2max (LBM).

In line with our results, a study by Potteiqer et al. [30] showed that participants lost 5 kg of body weight and about 4% of their adipose tissue during a 16-month exercise program. Also, after nine months, it was associated with a significant increase in VO2max and a significant increase in RMR in both sexes. Eventually, the results showed that following a moderate-intensity aerobic exercise program along with reduced caloric intake from foods lead to an increased RMR and weight loss and body fat in obese people [30]. A cross-sectional study on apparently healthy adults with mean BMI equal to 25.6 kg/m2 showed that VO2max is positively associated with RMR [31]. Moreover, this study revealed that those with VO2max and lower RMR, had better body composition profiles including lower visceral fat, trunk fat, and body fat mass [31]. Moreover, a study conducted by Broeder and colleges on normal-to-overweight men failed to show any relationship between RMR and CRF [32]. On the other hand, positive stepwise gradient in RMR according to tertiles of CRF in a cross-sectional study by shook et al. indicate the key role of aerobic capacity on resting metabolic rate. In this study, participants with moderate to high CRF had higher RMR than those with low CRF [33]. Previous results by Kim and colleges have also shown that a difference in measured RMR and predicted RMR in obese men and also shown that there is a significant difference between measured RMR and predicted RMR in Korean obese men. This study also reported a positive association between their aerobic capacity and RMR [34]. Another study by Smith et al. showed there is no significant relationship between aerobic capacity and RMR in healthy women in the age range of 19 to 30 years [35]. In addition, Ormsbee et al. [36] showed that a period of 35–42 days of swim detraining such as light-moderate physical exercise after a competitive swim in healthy men and women leads to the following results: (a) 1.3%, 12.2% increase in weight and body fat, respectively. (b) 7.7% decrease in VO2Max, and (c) 7% decrease in RMR, without any change in blood lipids. It should be noted that increasing in body weight and specially body fat may cause the drop in CRF and RMR.

The highest quantity of oxygen that an individual may utilize when participating in intense or strenuous activity is known as VO2 max or maximal oxygen consumption. This measurement is generally considered the best indicator of cardiovascular fitness and aerobic endurance [37]. Payandeh et al. [37] show that higher adherence to a higher pro-inflammatory potential diet may be associated with less VO2Max (ml/kg/min). In contrast, previous results from a case–control study by Scott et al. showed the DII score was associated with systemic inflammation increase and less lung function. They also reported that an increase by one unit of DII score can elevate the risk of asthma by 70% [38].

Contrarily, in Asia, Ren et al. found only a slight association between the DII and the prevalence of the metabolic syndrome components (with the exception of blood pressure) among adults in eight Chinese cities [39]. Similarly, in a study conducted among the Lebanese population [40] and in the Fasa Cohort Study (FACS) [41] conducted in Iran, no significant association was reported between the DII and the prevalence of Metabolic syndrome. Furthermore, Asadi et al.'s study of a middle-aged Iranian population revealed no association between the DII and total cardiovascular disease, myocardial infarction, stable angina, or unstable angina [42]. Result of an umbrella review of meta-analyses of observational studies indicated that adherence to a diet with high inflammatory index might be associated with a higher risk of colorectal cancer, cardiovascular disease, and all-cause mortality [20]. The reasons for these conflicting findings may be related to the various sample sizes of studies or also various studies design, even though lack of adjustment for different confounders such as individuals medical and family history.

Two possible mechanisms mentioned in studies regarding the effect of physical activity on RMR are as follows: physical activity can affect RMR by accelerating muscle growth and affecting physiological processes. Cardiorespiratory fitness also appears to be a key predictor of RMR, although it operates independently of skeletal muscle mass [43]. This difference in RMR according to CRF groups is probably due to physiological processes [33]. Other mechanisms for explaining how CRF and physical activity affect RMR levels may be related to sympathetic nervous system regulations [44,45,46], the function of neuroendocrine system [47, 48], structure changing of myocytes [49], and various immune responses [50].

Several limitations are better to be considered in the explanation of our findings. The main limitation of our study is its cross-sectional design which does not accurately state the cause-and-effect relationship. Another limitation is the low sample size of our study. Also, we calculated DII based on 29 dietary items and data regarding 16 dietary items were not available in this study. However, some strengths of our study should be noted that the present study is the first study from Iran to examine the combined association of dietary inflammatory index and RMR on cardiorespiratory fitness. As well, we have used the standardized 168 items FFQ that has been collected for the Iranian eating habits assessment. Moreover, we adjusted several important confounders which could affect our main results. Therefore, the results of the present study can be a positive step in the direction of anti-inflammatory diet recommendations by physicians.

Conclusion

In conclusion, consumption of a pro-inflammatory diet in combination with low RMR status is associated with 28% lesser odds of having better CRF compared with those with anti-inflammatory diet with high RMR among Iranian healthy men and women. In other words, we have observed the importance of physical activity and how the inflammatory index can influence it. However, more studies on this area are needed to confirm the veracity of our results. This study suggests that researchers should focus on dietary indexes rather than single antioxidant nutrients for having a better judgment.

Availability of data and materials

The datasets generated or analyzed during the current study are not publicly available due to restrictions, e.g., their containing information that could compromise the privacy of research participants but are available from the corresponding author on reasonable request.

Abbreviations

DII:

Dietary inflammatory index

BMI:

Body mass index

FFQ:

Food frequency questionnaire

RMR:

Resting metabolic rate

ANOVA:

Analysis of variance

ANCOVA:

Analysis of covariance

MUFA:

Monounsaturated fatty acids

PUFA:

Polyunsaturated fatty acids

WHtR:

Waist-to-height ratio

CRF:

Cardiorespiratory fitness

WC:

Waist circumference

FM:

Fat mass

FFM:

Fat free mass

LBM:

Lean body mass

CRP:

C-reactive protein

CVD:

Cardiovascular disease

VO2Max :

Maximum (max) rate (V) of oxygen (O2) consumption

CLA:

Conjugated linoleic acid

References

  1. Lutsey PL, Steffen LM, Stevens J. Dietary intake and the development of the metabolic syndrome: the atherosclerosis risk in communities study. Circulation. 2008;117(6):754–61. https://doi.org/10.1161/circulationaha.107.716159.

    Article  PubMed  Google Scholar 

  2. Aghamohammadi V, Sajjadi SF, Jarrahi F, Abdollahi A, Mirzaei K. The association between total antioxidant capacity and resting metabolic rate (RMR)/respiratory quotient (RQ) in overweight and obese woman. Diabetes Metab Syndr. 2019;13(4):2763–7. https://doi.org/10.1016/j.dsx.2019.07.030.

    Article  PubMed  Google Scholar 

  3. Saleh V, Afroundeh R, Siahkouhian M, Asadi A. Relationship between resting metabolic rate and body composition factors in obese and normal weight gymnast children. Int J Pediatr. 2021;9(9):14331–40. https://doi.org/10.22038/ijp.2020.50908.4042.

    Article  Google Scholar 

  4. Miller WM, Spring TJ, Zalesin KC, Kaeding KR, Nori Janosz KE, McCullough PA, et al. Lower than predicted resting metabolic rate is associated with severely impaired cardiorespiratory fitness in obese individuals. Obesity. 2012;20(3):505–11. https://doi.org/10.1038/oby.2011.262.

    Article  CAS  PubMed  Google Scholar 

  5. Shahinfar H, Payandeh N, Ebaditabar M, Babaei N, Davarzani S, Djafarian K, et al. Association of major dietary patterns with resting metabolic rate and body fatness in middle-aged men and women: results from a cross-sectional study. Nutr Health. 2021;29(1):139–47. https://doi.org/10.1177/02601060211063070.

    Article  CAS  PubMed  Google Scholar 

  6. Ellulu MS, Patimah I, Khaza’ai H, Rahmat A, Abed Y. Obesity and inflammation: the linking mechanism and the complications. Arch Med Sci. 2017;13(4):851–63. https://doi.org/10.5114/aoms.2016.58928.PMC5507106.

    Article  CAS  PubMed  Google Scholar 

  7. Varkaneh K, Varkaneh HK, Rahmani J, Tajik S, Zarezadeh M, Nazari A, et al. Association between dietary inflammatory index with obesity in Women who referred to health centers affiliated to Tehran University of Medical Sciences. Razi J Med Sci. 2017;24(161):21–30.

    Google Scholar 

  8. Mirmajidi S. Association of dietary inflammatory index and food pattern with insulin resistance and serum levels of chemerin and omentin-1 in people with abdominal obesity. Tabriz University of Medical Sciences, Faculty of Nutrition and Food Sciences; 2019.

    Google Scholar 

  9. Choi MS, Kim YJ, Kwon EY, Ryoo JY, Kim SR, Jung UJ. High-fat diet decreases energy expenditure and expression of genes controlling lipid metabolism, mitochondrial function and skeletal system development in the adipose tissue, along with increased expression of extracellular matrix remodelling- and inflammation-related genes. Br J Nutr. 2015;113(6):867–77. https://doi.org/10.1017/s0007114515000100.

    Article  CAS  PubMed  Google Scholar 

  10. Libby P, Ridker PM, Hansson GK. Inflammation in atherosclerosis: from pathophysiology to practice. J Am Coll Cardiol. 2009;54(23):2129–38. https://doi.org/10.1016/j.jacc.2009.09.009.PMC2834169.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Sarwar N, Gao P, Seshasai SR, Gobin R, Kaptoge S, Di Angelantonio E, et al. Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies. Lancet. 2010;375(9733):2215–22. https://doi.org/10.1016/s0140-6736(10)60484-9.PMC2904878.

    Article  CAS  PubMed  Google Scholar 

  12. Schjerve IE, Tyldum GA, Tjonna AE, Stolen T, Loennechen JP, Hansen HE, et al. Both aerobic endurance and strength training programmes improve cardiovascular health in obese adults. Clin Sci. 2008;115(9):283–93. https://doi.org/10.1042/cs20070332.

    Article  Google Scholar 

  13. Prabhu S, Padmanabha B, Doddamani B. Correlation between obesity and cardiorespiratory fitness. Int J Med Sci Public Health. 2013;2(2):300–4.

    Article  Google Scholar 

  14. Madssen E, Skaug EA, Wisloff U, Ellingsen O, Videm V. Inflammation Is strongly associated with cardiorespiratory fitness, sex, bmi, and the metabolic syndrome in a self-reported healthy population: HUNT3 fitness study. Mayo Clin Proc. 2019;94(5):803–10. https://doi.org/10.1016/j.mayocp.2018.08.040.

    Article  PubMed  Google Scholar 

  15. Shivappa N, Wirth MD, Hurley TG, Hébert JR. Association between the dietary inflammatory index (DII) and telomere length and C-reactive protein from the National Health and Nutrition Examination Survey-1999–2002. Mol Nutr Food Res. 2017. https://doi.org/10.1002/mnfr.201600630.PMC5380547.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Shivappa N, Steck SE, Hurley TG, Hussey JR, Hébert JR. Designing and developing a literature-derived, population-based dietary inflammatory index. Public Health Nutr. 2014;17(8):1689–96. https://doi.org/10.1017/s1368980013002115.Pmc3925198.

    Article  PubMed  Google Scholar 

  17. Shivappa N, Bonaccio M, Hebert JR, Di Castelnuovo A, Costanzo S, Ruggiero E, et al. Association of proinflammatory diet with low-grade inflammation: results from the Moli-sani study. Nutrition. 2018;54:182–8. https://doi.org/10.1016/j.nut.2018.04.004.PMC6138548.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Yang Y, Hozawa A, Kogure M, Narita A, Hirata T, Nakamura T, et al. Dietary inflammatory index positively associated with high-sensitivity C-reactive protein level in Japanese from NIPPON DATA2010. J Epidemiol. 2020;30(2):98–107. https://doi.org/10.2188/jea.JE20180156.PMC6949183.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Church TS, Barlow CE, Earnest CP, Kampert JB, Priest EL, Blair SN. Associations between cardiorespiratory fitness and C-reactive protein in men. Arterioscler Thromb Vasc Biol. 2002;22(11):1869–76.

    Article  CAS  PubMed  Google Scholar 

  20. Farazi M, Jayedi A. Dietary inflammatory index and the risk of non-communicable chronic disease and mortality: an umbrella review of meta-analyses of observational studies. Crit Rev Food Sci Nutr. 2023;63(1):57–66. https://doi.org/10.1080/10408398.2021.1943646.

    Article  PubMed  Google Scholar 

  21. Floegel A, Wientzek A, Bachlechner U, Jacobs S, Drogan D, Prehn C, et al. Linking diet, physical activity, cardiorespiratory fitness and obesity to serum metabolite networks: findings from a population-based study. Int J Obes. 2014;38(11):1388–96. https://doi.org/10.1038/ijo.2014.39.Pmc4229626.

    Article  CAS  Google Scholar 

  22. Schiavo L, Scalera G, Pilone V, De Sena G, Iannelli A, Barbarisi A. Fat mass, fat-free mass, and resting metabolic rate in weight-stable sleeve gastrectomy patients compared with weight-stable nonoperated patients. Surg Obes Relat Dis. 2017;13(10):1692–9. https://doi.org/10.1016/j.soard.2017.06.007.

    Article  PubMed  Google Scholar 

  23. Vasheghani-Farahani A, Tahmasbi M, Asheri H, Ashraf H, Nedjat S, Kordi R. The Persian, last 7-day, long form of the international physical activity questionnaire: translation and validation study. Asian J Sports Med. 2011;2(2):106–16. https://doi.org/10.5812/asjsm.34781.Pmc3289200.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Wareham NJ, Jakes RW, Rennie KL, Schuit J, Mitchell J, Hennings S, et al. Validity and repeatability of a simple index derived from the short physical activity questionnaire used in the European prospective investigation into cancer and nutrition (EPIC) study. Public Health Nutr. 2003;6(4):407–13. https://doi.org/10.1079/phn2002439.

    Article  PubMed  Google Scholar 

  25. Mirmiran P, Hosseini Esfahani F, Mehrabi Y, Hedayati M, Azizi F. Reliability and relative validity of an FFQ for nutrients in the Tehran Lipid and Glucose Study. Public Health Nutr. 2009;13(5):654–62. https://doi.org/10.1017/S1368980009991698.

    Article  PubMed  Google Scholar 

  26. Ghafarpour M, Houshiar-Rad A, Kianfar H, Ghaffarpour M. The manual for household measures, cooking yields factors and edible portion of food. Tehran: Keshavarzi Press; 1999.

    Google Scholar 

  27. Korth O, Bosy-Westphal A, Zschoche P, Glüer C, Heller M, Müller M. Influence of methods used in body composition analysis on the prediction of resting energy expenditure. Eur J Clin Nutr. 2007;61(5):582.

    Article  CAS  PubMed  Google Scholar 

  28. Bruce R, Blackmon J, Jones J, Strait GJP. Exercising testing in adult normal subjects and cardiac patients. Pediatrics. 1963;32(4):742–56.

    Article  Google Scholar 

  29. Shahinfar H, Shahavandi M, Tijani AJ, Jafari A, Davarzani S, Djafarian K, et al. The association between dietary inflammatory index, muscle strength, muscle endurance, and body composition in Iranian adults. Eat Weight Disord Stud Anorex Bulim Obes. 2022;27(2):463–72.

    Article  Google Scholar 

  30. Potteiger JA, Kirk EP, Jacobsen DJ, Donnelly JE. Changes in resting metabolic rate and substrate oxidation after 16 months of exercise training in overweight adults. Int J Sport Nutr Exerc Metab. 2008;18(1):79–95. https://doi.org/10.1123/ijsnem.18.1.79.

    Article  CAS  PubMed  Google Scholar 

  31. Ebaditabar M, Imani H, Babaei N, Davarzani S, Shab-Bidar S. Maximal oxygen consumption is positively associated with resting metabolic rate and better body composition profile. Obes Med. 2021;21:100309.

    Article  Google Scholar 

  32. Broeder CE, Burrhus KA, Svanevik LS, Wilmore JH. The effects of aerobic fitness on resting metabolic rate. Am J Clin Nutr. 1992;55(4):795–801. https://doi.org/10.1093/ajcn/55.4.795.

    Article  CAS  PubMed  Google Scholar 

  33. Shook RP, Hand GA, Paluch AE, Wang X, Moran R, Hébert JR, et al. Moderate cardiorespiratory fitness is positively associated with resting metabolic rate in young adults. Mayo Clin Proc. 2014;89(6):763–71. https://doi.org/10.1016/j.mayocp.2013.12.017.

    Article  PubMed  Google Scholar 

  34. Kim DK. Accuracy of predicted resting metabolic rate and relationship between resting metabolic rate and cardiorespiratory fitness in obese men. J Exerc Nutr Biochem. 2014;18(1):25–30. https://doi.org/10.5717/jenb.2014.18.1.25.PMC4241941.

    Article  Google Scholar 

  35. Smith SR. The endocrinology of obesity. Endocrinol Metab Clin North Am. 1996;25(4):921–42. https://doi.org/10.1016/s0889-8529(05)70362-5.

    Article  CAS  PubMed  Google Scholar 

  36. Ormsbee MJ, Arciero PJ. Detraining increases body fat and weight and decreases VO2peak and metabolic rate. J Strength Cond Res. 2012;26(8):2087–95. https://doi.org/10.1519/JSC.0b013e31823b874c.

    Article  PubMed  Google Scholar 

  37. Payandeh N, Shahinfar H, Babaei N, Davarzani S, Ebaditabar M, Djafarian K, et al. Association between the empirical dietary inflammatory index and cardiorespiratory fitness in Tehranian adults in 2017–2018. Front Nutr. 2022;9:928308.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Scott HA, Jensen ME, Wood LG. Dietary interventions in asthma. Curr Pharm Des. 2014;20(6):1003–10. https://doi.org/10.2174/13816128113190990421.

    Article  CAS  PubMed  Google Scholar 

  39. Ren Z, Zhao A, Wang Y, Meng L, Szeto IM, Li T, et al. Association between dietary inflammatory index, C-reactive protein and metabolic syndrome: a cross-sectional study. Nutrients. 2018. https://doi.org/10.3390/nu10070831.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Naja F, Shivappa N, Nasreddine L, Kharroubi S, Itani L, Hwalla N, et al. Role of inflammation in the association between the western dietary pattern and metabolic syndrome among Lebanese adults. Int J Food Sci Nutr. 2017;68(8):997–1004. https://doi.org/10.1080/09637486.2017.1312297.

    Article  PubMed  Google Scholar 

  41. Ariya M, Shahraki HR. Dietary inflammatory index and metabolic syndrome in Iranian population (Fasa Persian Cohort Study). Sci Rep. 2020;10(1):16762. https://doi.org/10.1038/s41598-020-73844-0.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Asadi Z, Yaghooti-Khorasani M, Ghazizadeh H, Sadabadi F, Mosa-Farkhany E, Darroudi S, et al. Association between dietary inflammatory index and risk of cardiovascular disease in the Mashhad stroke and heart atherosclerotic disorder study population. IUBMB Life. 2020;72(4):706–15. https://doi.org/10.1002/iub.2172.

    Article  CAS  PubMed  Google Scholar 

  43. Speakman JR, Selman C. Physical activity and resting metabolic rate. Proc Nutr Soc. 2003;62(3):621–34. https://doi.org/10.1079/pns2003282.

    Article  PubMed  Google Scholar 

  44. Bullough RC, Gillette CA, Harris MA, Melby CL. Interaction of acute changes in exercise energy expenditure and energy intake on resting metabolic rate. Am J Clin Nutr. 1995;61(3):473–81. https://doi.org/10.1093/ajcn/61.3.473.

    Article  CAS  PubMed  Google Scholar 

  45. Hunter GR, Moellering DR, Carter SJ, Gower BA, Bamman MM, Hornbuckle LM, et al. Potential causes of elevated REE after high-intensity exercise. Med Sci Sports Exerc. 2017;49(12):2414–21. https://doi.org/10.1249/mss.0000000000001386.PMC5688014.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Ravussin E. Low resting metabolic rate as a risk factor for weight gain: role of the sympathetic nervous system. Int J Obes Relat Metab Disord. 1995;19(Suppl 7):S8-s9.

    PubMed  Google Scholar 

  47. Herring JL, Molé PA, Meredith CN, Stern JS. Effect of suspending exercise training on resting metabolic rate in women. Med Sci Sports Exerc. 1992;24(1):59–65.

    Article  CAS  PubMed  Google Scholar 

  48. Menozzi R, Bondi M, Baldini A, Venneri MG, Velardo A, Del Rio G. Resting metabolic rate, fat-free mass and catecholamine excretion during weight loss in female obese patients. Br J Nutr. 2000;84(4):515–20.

    Article  CAS  PubMed  Google Scholar 

  49. Hather BM, Tesch PA, Buchanan P, Dudley GA. Influence of eccentric actions on skeletal muscle adaptations to resistance training. Acta Physiol Scand. 1991;143(2):177–85. https://doi.org/10.1111/j.1748-1716.1991.tb09219.x.

    Article  CAS  PubMed  Google Scholar 

  50. Cannon JG, Meydani SN, Fielding RA, Fiatarone MA, Meydani M, Farhangmehr M, et al. Acute phase response in exercise. II. Associations between vitamin E, cytokines, and muscle proteolysis. Am J Physiol. 1991;260(6 Pt 2):R1235–40. https://doi.org/10.1152/ajpregu.1991.260.6.R1235.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank all those who participated in this study.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

HSH and SS-b contributed to conception/design of the research; KT, NP, SM, NB and ME contributed to acquisition, analysis, or interpretation of the data; HSH and NP drafted the manuscript; KD and SS-b critically revised the manuscript; and SS-b agrees to be fully accountable for ensuring the integrity and accuracy of the work. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sakineh Shab-Bidar.

Ethics declarations

Ethics approval and consent to participate

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the ethics committee of Tehran University of Medical Sciences (Ethics Number: IR.TUMS.VCR.REC.1396.4058). Written informed consent was obtained from all subjects/patients.

Consent for publication

Participants were provided a study overview, and verbal consent was attained.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Shahinfar, H., Payandeh, N., Torabynasab, K. et al. The combined association of dietary inflammatory index and resting metabolic rate on cardiorespiratory fitness in adults. J Health Popul Nutr 42, 68 (2023). https://doi.org/10.1186/s41043-023-00413-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s41043-023-00413-2

Keywords