Next Article in Journal
The Assessment of Bone Regulatory Pathways, Bone Turnover, and Bone Mineral Density in Vegetarian and Omnivorous Children
Previous Article in Journal
Vitamin B12 Status of Various Ethnic Groups Living in New Zealand: An Analysis of the Adult Nutrition Survey 2008/2009

Lower Dietary Inflammatory Index Scores Are Associated with Lower Glycemic Index Scores among College Students

Department of Human Environmental Studies, Central Michigan University, Mount Pleasant, MI 48858, USA
School of Human Ecology, Louisiana Tech University, Ruston, LA 71270, USA
South Carolina Statewide Cancer Prevention and Control Program, University of South Carolina, Columbia, SC 29208, USA
Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC 29208, USA
Connecting Health Innovations LLC, Columbia, SC 29201, USA
College of Nursing, University of South Carolina, Columbia, SC 29208, USA
Author to whom correspondence should be addressed.
Nutrients 2018, 10(2), 182;
Received: 16 October 2017 / Revised: 31 January 2018 / Accepted: 2 February 2018 / Published: 7 February 2018


The association between the Dietary Inflammatory Index (DII®), the glycemic index (GI), and the glycemic load (GL) is not known, although it is known that carbohydrates are pro-inflammatory. We aimed to measure the association between the DII and both GI and GL among college students. In this cross-sectional study, 110 college students completed a 3-day food diary, which was used to calculate the DII, the GI, the GL, and the healthy eating index (HEI)-2010. Least square means and 95% confidence intervals of the GI, the GL, and the HEI-2010 were presented per DII tertile using generalized linear mixed models. Participants in tertile 1 of DII scores had lower GI and GL scores, but higher HEI-2010 scores than those in tertile 3. Pearson correlations showed that DII score was positively correlated with the GI score (r = 0.30, p < 0.01), but negatively correlated with the HEI-2010 (r = −0.56, p < 0.001). DII score was not correlated with GL score. Results from this study suggest that increased inflammatory potential of diet, as represented by higher DII scores, was associated with increased GI scores and lower quality of diet on the HEI-2010. Use of the DII suggests new directions for dietary approaches for preventing chronic diseases that moves beyond convention by decreasing systemic inflammation.
Keywords: dietary inflammatory index; glycemic index; glycemic load; healthy eating index-2010; college students dietary inflammatory index; glycemic index; glycemic load; healthy eating index-2010; college students

1. Introduction

Chronic low-grade inflammation is a major contributor to chronic diseases, including diseases such as diabetes and cardiovascular disease [1]. Although inflammation is a normal biological process needed for competent immune, vascular, and endothelial response, chronic inflammation can be caused by chronic infections that do not resolve and are associated with unhealthy lifestyle patterns, such as an unhealthy diet and tobacco use [2]. Given the significant effect of diet on developing inflammation and dietary modulation of the inflammatory cascade [3], diet has received special attention with respect to inflammation. The Dietary Inflammatory Index (DII®) was developed by researchers at the University of South Carolina specifically to measure the inflammatory potential of diet based on the overall inflammatory properties of dietary components, such as macronutrients, vitamins and minerals, flavonoids, and other bioactive compounds. The index classifies an individual’s diet on a continuum from maximally anti-inflammatory to maximally pro-inflammatory. The current DII is based on inflammation-focused, peer-reviewed literature and is standardized to the distribution of dietary intake from representative populations around the world [4].
In previous cross-sectional studies conducted in middle-aged adults and the elderly, the DII was validated against inflammatory biomarkers, such as C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor (TNF)-α [5,6,7,8,9,10,11]. Furthermore, the DII has been shown to be positively related to lower cognitive functioning [12] and higher risk of insulin resistance [13], cardiovascular disease (CVD) [11,14,15,16,17,18], and metabolic syndrome [15,19].
The glycemic index (GI) is a physiological carbohydrate-classification system based on glycemic response after consuming a carbohydrate-containing food compared to the response to a reference food, such as glucose solution or white bread containing the same amount of available carbohydrate [20]. The glycemic load (GL) is determined by multiplying a food’s GI by the amount of available carbohydrates in each serving size and dividing that number by 100 [21]. High GI foods, which are characteristically highly refined carbohydrates and/or carbohydrates with little fiber, are one of the major dietary factors affecting inflammation [22]. For example, cross-sectional studies reported a strong positive relationship between dietary GI [23] and GL [24] and plasma CRP in healthy, middle-aged women. Moreover, intervention studies showed that a low GI diet [25,26] and a low GL diet [27] lowered plasma CRP in short-term and long-term studies in overweight and obese adults.
Most DII studies have focused on middle-aged and elderly populations. To date, no DII study has compared DII scores with GI, GL and healthy eating index (HEI) scores among college students. A large body of research reports that most college students develop unhealthy eating habits, including excess consumption of calories, fat, refined grains, and processed foods [28,29,30,31,32,33]. In light of probable increased chronic disease risk resulting from college students’ unhealthy behaviors [34] and the crucial role of inflammation in developing chronic disease [16], it would be important to measure their DII scores and compare to GI, GL and HEI scores. It was hypothesized that college students will have pro-inflammatory diets (indicated by higher DII scores), and that higher DII scores will be associated with higher GI and GL scores, but lower HEI scores.

2. Materials and Methods

2.1. Subjects

Undergraduate students attending Louisiana Tech University (Ruston, LA, USA), which is located in the rural Southern USA, participated in this cross-sectional study from January 2013 to May 2013. Participants were recruited through advertising on campus. Potential participants were excluded if they were >29 years old, were on a diet, were pregnant, or had any chronic disease, such as diabetes mellitus, heart disease, or hypertension. This study was conducted according to the guidelines laid down in the Declaration of Helsinki. The study was approved by the Louisiana Tech University Human Subjects Review Committee. A signed consent form was obtained from each participant prior to the start of the study.

2.2. Data Collection

Dietary information was collected through a 3-day food diary. Participants were instructed to record their food intake for three days, including two non-consecutive weekdays and one weekend day. Food Processor Nutrition Analysis Software (ESHA Research, Salem, OR, USA) was used to analyze total calorie and nutrient intakes from the 3-day food diaries. Dietary data obtained after analyzing a 3-day food diary were used to calculate DII, GI, GL, and HEI-2010 scores.
To calculate DII scores, the method previously reported by Shivappa et al. [4] was used. In short, a literature review focusing on the association between food parameters and inflammatory markers was conducted to derive inflammatory effect scores for the food parameters. These scores were standardized to a world database, which includes a mean and standard deviation for each food parameter from 11 countries around the world. The mean value for each food parameter in the world database was subtracted from the actual reported intake of the food parameter, and then divided by the standard deviation to calculate a Z-score, which then was converted to a proportion (i.e., with values from 0 to 1) to minimize the effect of outliers. The proportion was then centered by doubling the proportion and subtracting 1. This value was multiplied by the inflammatory effect score for each food parameter. These were then summed across all food parameters to calculate the overall DII score. A higher DII score means greater pro-inflammatory potential of the diet. In this study the DII scores were calculated per 1000 calories consumed to account for inter-individual differences in energy intake [4]. The following 30 parameters were available to calculate the DII in the present study: carbohydrates, protein, total fat, alcohol, fiber, cholesterol, saturated fatty acids, trans fatty acids, monounsaturated fatty acids, polyunsaturated fatty acids, omega-3 fatty acids, omega-6 fatty acids, niacin, thiamine, riboflavin, vitamin B6, vitamin B12, vitamin A, vitamin C, vitamin D, vitamin E, folic acid, beta carotene, iron, magnesium, selenium, calcium, zinc, and caffeine. Energy (total caloric intake) was used as the divisor of the DII score to derive the energy-adjusted-DII (E-DII) score.
The GI values for carbohydrate-containing foods were extracted from the International Tables of GI and GL values for 2002 and 2008. The GI values in which glucose was employed as the reference food were used [35,36]. Each food had a number of GI values, and the selection of GI was made hierarchically in this order: (1) the same brand of food and method of preference; (2) a food produced in the USA; (3) average GI value of the same type of foods; or (4) otherwise closest match. The formula in which a meal GI was calculated from the individual food GI is as follows: Meal GI = {(GIfoodA × g available carbohydratefoodA) + (GIfoodB × g available carbohydratefoodB) + ∙∙∙}/total g available carbohydrate [37]. The GL values were calculated by multiplying the available carbohydrate amount in a serving size by its GI value, divided by 100 [37].
The HEI-2010, developed by the United States Department of Agriculture, was used to assess diet quality among the U.S. population. The HEI-2010 consists of 12 components, including nine adequacy components and three moderation components. The nine adequacy components, for which increased intake is recommended, are total fruit, whole fruit, total vegetables, greens and beans, whole grains, dairy, total protein foods, seafood and plant proteins, and fatty acids. In contrast, the three moderation components, for which decreased intake is recommended, include refined grains, sodium, and empty calories. Each component is proportionally scored from 0 to 10 based on minimum and maximum standards. The total score of the HEI-2010 ranges from 0 to 100 [38].
Weight and height of each participant were measured using a portable mechanical scale and stadiometer (SECA®, Road Rod 214, Hamburg, Germany), respectively. Weight was measured in light clothing and without shoes. Height was measured without shoes. Body mass index (BMI) was calculated by weight in kilograms divided by height in meters square (CDC). Waist circumference was measured at the midpoint between the lower ribs and the iliac crest using a non-stretchable measuring tape. Percent body fat was measured using the Tanita® digital scale (TBF-300A, Tanita, Arlington Heights, IL, USA).

2.3. Statistical Analysis

Statistical Package for the Social Sciences (SPSS)® software (Version 23.0, SPSS, Inc., Chicago, IL, USA) was used to perform the data analysis. Descriptive statistics included sex, race, smoking and drinking status, BMI classification, exercise status, age, BMI, percent body fat, and waist circumference. Descriptive statistics were conducted with chi-square tests for categorical variables and analysis of variance (ANOVA) tests for continuous variables. DII scores were converted into tertiles, and analyses were conducted using generalized linear mixed models, adjusting for age, sex, BMI, smoking status, drinking status, and physical activity level. The least squares means and 95% confidence intervals of the GI, the GL, and the HEI-2010 scores were presented per DII tertile using generalized linear mixed models. Pearson correlation coefficients were calculated to evaluate the association between the DII, the GI, the GL, and the HEI-2010 using the scores as continuous variables. Results were considered significant if the p-value of the analysis was <0.05.

3. Results

Participants’ demographic information is shown in Table 1. Fifty males (45%) and sixty females (55%) completed the study. The majority of the participants were European American (61.8%), non-smokers (88.2%), and non-drinkers (62.7%). Slightly more than half of the participants (52.7%) were normal weight, with an average BMI of 25.4 kg/m2. There were no significant differences on sex; race; smoking, drinking, and physical activity status; BMI; body-fat percentage; and waist circumference based on DII tertiles.
Participants’ intakes of nutrients and dietary components based on DII tertiles are provided in Table 2. Participants in the lowest DII tertile, indicating more anti-inflammatory diets, had higher consumption of total calories, monounsaturated fats, and all vitamins and minerals than individuals in the highest DII tertile, whose diets were more pro-inflammatory. In contrast, college students in the lowest DII tertile consumed lower amounts of total fat and saturated fat than participants in the highest DII tertile (p = 0.05 and <0.001, respectively).
College students in the lowest DII tertile had higher scores for the HEI-2010 than those in the highest DII tertile (50.7 vs. 35.4, p < 0.001). However, participants in the DII tertile 1 had lower scores for the GI than those in DII tertile 3 (50.1 vs. 54.8, p = 0.02). Only females in the lowest DII tertile had lower scores for the GI than those in the DII tertile 3 (47.5 vs. 53.8, p = 0.02) (Table 3). DII score was positively correlated with GI score (r = 0.30, p < 0.01), but negatively correlated with the HEI-2010 score (r = −0.56, p < 0.001). DII score was not related to the GL (r = −0.03, p = 0.76) (Table 4).
In this present study, among college students residing in the rural Southern US, the ten most popular food items, based on frequency of consumption, included French fries, wheat bread, lemonade, pepperoni pizza, chicken sandwich, sweet tea, chicken nugget, apple, banana, and Cajun style rice, in descending order (Table 5).

4. Discussion

The present study found that DII score was positively associated with GI score, but negatively associated with the HEI-2010 among rural, Southern US college students. Previous studies that measured the association between the DII and the HEI-2010 among participants 21 to 35 years of age, also reported an inverse relationship between the DII and the HEI-2010 [39,40,41].
Studies have reported the mechanism by which high GI diets induce inflammation. High GI diets induce hyperglycemia, which in turn induces oxidative stress [42] and increases pro-inflammatory cytokines, including IL-6 and TNF-α, among both healthy subjects and those with impaired glucose tolerance [43]. The increased level of pro-inflammatory cytokines, in turn, causes disruptions in insulin signaling, subsequently leading to insulin resistance [44]. Furthermore, insulin-resistance-related hyperglycemia causes accumulation of advanced glycation end products, which increase production of pro-inflammatory cytokines in vascular endothelial cells [45]. Altered endothelial permeability and reduced blood flow may augment insulin resistance, resulting in exacerbating hyperglycemia, leading to a vicious cycle of reduced blood flow and insulin resistance [46].
Given the impact of hyperglycemia on inflammatory pathways, achieving normoglycemia has been recognized as key to improving outcomes and minimizing pro-inflammatory mechanisms. Studies have shown a positive association between dietary GI and GL and inflammation biomarkers [22,23] because a low GI diet reduces the rate of glucose absorption by the body, subsequently diminishing hyperglycemia and hyperinsulinemia, which then induce a reduction in systemic inflammation. For example, a low GI [47,48] or low GL diet [27,49,50] resulted in weight loss in overweight and obese subjects, along with improvements in insulin sensitivity. The weight loss also caused reduction in pro-inflammatory cytokines. Considering the recognized benefits of a low-GI diet, it has been recommended by various health organizations to prevent or manage diabetes and coronary heart disease, and a likely weapon against obesity [51,52].
GI scores have been reported to be associated inversely with HEI-2010 scores [53,54]. The HEI-2010 is a measure of diet quality to assess adherence to the 2010 Dietary Guidelines for Americans and to describe Americans’ [38] eating patterns. Moreover, the HEI-2010 assesses the healthfulness of the overall diet, as the index captures all dietary components, rather than only selected nutrients or food groups [38]. According to the results of the National Health and Nutrition Examination Survey (NHANES) 2007–2010, the average HEI-2010 score among U.S. adults ages 20 to 29 was 48.8 (95% confidence interval (CI) 47.2, 50.5), while the average score among all U.S. adults was 55.9 (95% CI 54.5, 57.3) [55]. In the present study, the average HEI-2010 score was 43.6, which is slightly lower than the national average of young adults in their 20s. Given that a diet with a score of less than 51 is considered poor [38], the overall diet quality of the college students participating in the present study seems poor. It is well known that college students’ eating habits fall far short of general dietary recommendations. For example, they tend to skip meals frequently, eat few servings of fruits and vegetables, and consume too many calories and too much total fat [33]. Furthermore, the ten most popular foods among college students fit typical Western dietary patterns, with sweetened beverages, candies, instant noodles, refined grains, and pizza among the top ten [33,45]. The Western pattern had a positive association with CRP after adjustment for all confounding factors, including BMI [45].
Although values for U.S. college students could not be separated from those of others, the mean dietary GI and GL of adults in the NHANES 2003–2006 were 56.2 and 138.1, respectively [56]. In the current study, the average dietary GI and GL were 52.3 and 158.0, respectively. Based on the definition of low-GI foods (GI value 55 or less) [57], 5 out of top ten popular food items were classified as low GI foods. Wheat bread and pepperoni pizza were the 2nd and the 4th most popular-foods, respectively, in the present study and their GI values were a little higher than 55, which is the cut-off point for low GI foods. Including fruits and wheat bread in the list of their popular foods consumed by the participants would explain the relatively low GI value in this group. Due to the Southern culture, sweet tea and Cajun-style rice were ranked as 6th and 10th, respectively, in this population. Although some of the popular items listed are high-fat foods, such as French fries, their GI scores are not high. The GI scores are affected by the amount of fat and protein [58]. A study showed that consuming a low GI diet for 30 days reduced body fat and TNF-α in patients with type 2 diabetes when both high GI and low GI diets had similar energy density, dietary fiber, and macronutrient contents [59].
In middle-aged American women, cooked potato, cold breakfast cereal, and white bread were, the major contributors to dietary GL [58]. In older Australian women, white bread, potatoes, breakfast cereals, and fruit, specifically banana, contributed to dietary carbohydrate and GL significantly [24]. In the present study conducted in Southern US college students, French fries and wheat bread were major contributor to GL. The GL can be reduced by consumption of a diet high in low-GI carbohydrates or a diet low in carbohydrates and high in protein and fat. In trying to achieve acceptable macronutrient distribution range and a high-quality diet, it would be reasonable to recommend smaller portions of less healthy high-GI foods and larger portions of low-GI foods [60].
In this study the correlation coefficient of 0.30 between DII score and GI score is much lower than the absolute values of correlation coefficients that we have observed between the DII score and other indices in other studies [39,40,41]. This is revealing in that less than 10% of the variability in the DII score is explained by the GI score. This is reasonable on its face because simple carbohydrates are just one of the contributors to the DII score. The implication that factors that are associated with high glycemic load account for only a small fraction of the total inflammatory capacity of diet, is important.
Because there has been increased research interest in inflammation’s effect on health, a diet plan emphasizing a selection of foods that reduce inflammatory pathways while discouraging consumption of foods that promote inflammation is ideal [26]. Specifically, an anti-inflammatory diet contains fruits and vegetables with high concentrations of fiber, vitamins, minerals, and polyphenols, as well as herbs and spices. Moreover, most fruits and vegetables have low glycemic indexes because of high amounts of fiber [27]. Considering the characteristics of an anti-inflammatory diet plan, the DII was developed specifically to measure the inflammatory potential of any diet [4]. Numerous studies showed that the DII predicts concentrations of inflammatory biomarkers, including CRP, IL-6, TNF-α, etc., in cross-sectional and longitudinal studies [7,8,10,13,61].
Considering the positive association between the DII and inflammation biomarkers, the DII appears to be an excellent tool to determine dietary inflammatory potential [8]. The DII also suggests new directions for nutrition education and dietary approaches for preventing chronic diseases by decreasing systemic inflammation. Several factors affect the development of systemic inflammation, including age, genetic makeup, obesity, and diet. Among contributing factors, diet is critical because it can be changed [12].
One strength of the present study is that it is the first study in which DII, GI, and GL were measured among college students. In light of the importance of developing good eating habits in early adulthood, the present study’s results showed the current status of dietary inflammatory potential and the need for college students to improve their diets. Furthermore, a 3-day food diary was used to assess dietary intake to minimize day-to-day variations. Another strength is the relative sex balance in participants, at 45% male and 55% female, which enabled data analysis stratified by sex.
Despite the strengths of the study, several limitations must be considered. First, because of the current study design, the temporality criterion of the Criteria for Judging Causality is not met [62]. Hence, direct causal inference could not be made. Second, college students attending a rural, public, Southern U.S. University participated in the present study; so, caution is needed when extrapolating study results to other populations. Third, because participants recorded their 3-day food diary, there might have been reporting errors. However, to minimize any errors, participants were interviewed by the principal investigator upon completion of their food diaries to confirm their food consumption.
The DII was developed to assess dietary inflammatory potential. Of several studies that have examined these relationships, virtually all have observed a positive association between DII score and inflammation biomarkers (though, admittedly, there is variability across studies and across markers) [7,8,41,61,63,64,65]. Although the DII can be used successfully in nutritional studies, it might be challenge for laypersons to use to measure their dietary inflammatory potential on their own, without technical assistance (i.e., providing web or other technology-based tools for dietary assessment). Given that a low-GI diet reduces inflammatory responses and the present study reported an association between DII and GI scores, the GI may be used as very crude tool to provide a rough estimate of dietary inflammatory response.

5. Conclusions

In conclusion, the results of the present study suggest an inverse association between the DII and dietary GI among college students. The results of the present study also are in line with epidemiological findings on the association between dietary GI and HEI, a widely used dietary index. Given deepening understanding of the role of inflammation in a wide variety of health conditions [11,14,15,16,17,19,65], aging [63] and cognitive decline [12], the DII represents a potential tool for clinical or even individual use. However, this will require that individuals are provided with the necessary technical tools to compute scores from their dietary self-reports.


N.S., M.D.W. and J.R.H. were supported by the United States National Institute for Diabetes, Digestive and Kidney Diseases (grant no. R44DK103377). Sponsor’s Role: The sponsors had no role in the design, methods, subject recruitment, data collection, analysis or preparation of this paper.

Author Contributions

Y.K. conceptualized the study question, conducted data collection and data analysis, interpreted the results, and wrote the first draft of the manuscript. J.C. conducted data collection and data analysis and contributed to the manuscript editing. N.S., M.D.W. and J.R.H. calculated the DII and critically revised the manuscript. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declare no conflict of interest. However, we wish to disclose that James R. Hébert owns a controlling interest in Connecting Health Innovations LLC (CHI), a company planning to license the right to his invention of the dietary inflammatory index (DII) from the University of South Carolina to develop computer and smart phone applications for patient counseling and dietary intervention in clinical settings. Nitin and Shivappa and Michael D. Wirth are employees of CHI.


  1. Stojkovic, V.; Simpson, C.A.; Sullivan, R.R.; Cusano, A.M.; Kerstetter, J.E.; Kenny, A.M.; Insogna, K.L.; Bihuniak, J.D. The effect of dietary glycemic properties on markers of inflammation, insulin resistance, and body composition in postmenopausal American women: An ancillary study from a multicenter protein supplementation trial. Nutrients 2017, 9, 484. [Google Scholar] [CrossRef] [PubMed]
  2. Libby, P. Inflammatory mechanisms: The molecular basis of inflammation and disease. Nutr. Rev. 2007, 65, S140–S146. [Google Scholar] [CrossRef] [PubMed]
  3. Dawson, D.R., III; Branch-Mays, G.; Gonzalez, O.A.; Ebersole, J.L. Dietary modulation of the inflammatory cascade. Periodontology 2000, 64, 161–197. [Google Scholar] [CrossRef] [PubMed]
  4. Shivappa, N.; Steck, S.E.; Hurley, T.G.; Hussey, J.R.; Hebert, J.R. Designing and developing a literature-derived, population-based dietary inflammatory index. Public Health Nutr. 2014, 17, 1689–1696. [Google Scholar] [CrossRef] [PubMed]
  5. Cho, Y.A.; Lee, J.; Oh, J.H.; Shin, A.; Kim, J. Dietary inflammatory index and risk of colorectal cancer: A case-control study in Korea. Nutrients 2016, 8, 469. [Google Scholar] [CrossRef] [PubMed]
  6. Kizil, M.; Tengilimoglu-Metin, M.; Gumus, D.; Sevim, S.; Turkoglu, I.; Mandiroglu, F. Dietary inflammatory index is associated with serum C-reactive protein and protein energy wasting in hemodialysis patients: A cross-sectional study. Nutr. Res. Pract. 2016, 10, 404–410. [Google Scholar] [CrossRef] [PubMed]
  7. Shivappa, N.; Steck, S.E.; Hurley, T.G.; Hussey, J.R.; Ma, Y.; Ockene, I.S.; Tabung, F.; Hébert, J.R. A Population-based dietary inflammatory index predicts levels of C-reactive protein in the Seasonal Variation of Blood Cholesterol Study (SEASONS). Public Health Nutr. 2013, 17, 1825–1833. [Google Scholar] [CrossRef] [PubMed]
  8. Shivappa, N.; Hebert, J.R.; Rietzschel, E.R.; De Buyzere, M.L.; Langlois, M.; Debruyne, E.; Marcos, A.; Huybrechts, I. Associations between dietary inflammatory index and inflammatory markers in the Asklepios study. Br. J. Nutr. 2015, 113, 665–671. [Google Scholar] [CrossRef] [PubMed]
  9. Tabung, F.K.; Smith-Warner, S.A.; Chavarro, J.E.; Wu, K.; Fuchs, C.; Hu, F.B.; Chan, A.T.; Willett, W.C.; Giovannucci, E.L. Development and validation of an empirical dietary inflammatory index. J. Nutr. 2016, 146, 1560–1570. [Google Scholar] [CrossRef] [PubMed]
  10. Tabung, F.K.; Steck, S.E.; Zhang, J.; Ma, Y.; Liese, A.D.; Agalliu, I.; Hingle, M.; Hou, L.; Hurley, T.G.; Jiao, L.; et al. Construct validation of the dietary inflammatory index among postmenopausal women. Ann. Epidemiol. 2015, 25, 398–405. [Google Scholar] [CrossRef] [PubMed]
  11. Vissers, L.E.T.; Waller, M.A.; van der Schouw, Y.T.; Herbert, J.R.; Shivappa, N.; Schoenaker, D.A.J.M.; Mishra, G.D. The relationship between the dietary inflammatory index and risk of total cardiovascular disease, ischemic heart disease and cerebrovascular disease: Findings from an Australian population-based prospective cohort study of women. Atherosclerosis 2016, 253, 164–170. [Google Scholar] [CrossRef] [PubMed]
  12. Kesse-Guyot, E.; Assmann, K.E.; Andreeva, V.A.; Touvier, M.; Neufcourt, L.; Shivappa, N.; Hébert, J.R.; Wirth, M.D.; Hercberg, S.; Galan, P.; et al. Long-term association between the dietary inflammatory index and cognitive functioning: Findings from the SU.VI.MAX study. Eur. J. Nutr. 2017, 56, 1647–1655. [Google Scholar] [CrossRef] [PubMed]
  13. Van Woudembergh, G.J.; Theofylaktopoulou, D.; Kuijsten, A.; Ferreira, I.; van Greevenbroek, M.M.; van der Kallen, C.J.; Schalkwijk, C.G.; Stehouwer, C.D.; Ocké, M.C.; Nijpels, G.; et al. Adapted dietary inflammatory index and its association with a summary score for low-grade inflammation and markers of glucose metabolism: The Cohort study on Diabetes and Atherosclerosis Maastricht (CODAM) and the Hoorn study. Am. J. Clin. Nutr. 2013, 98, 1533–1542. [Google Scholar] [CrossRef] [PubMed]
  14. O’Neil, A.; Shivappa, N.; Jacka, F.N.; Kotowicz, M.A.; Kibbey, K.; Hebert, J.R.; Pasco, J.A. Pro-inflammatory dietary intake as a risk factor for CVD in men: A 5-year longitudinal study. Br. J. Nutr. 2015, 114, 2074–2082. [Google Scholar] [CrossRef] [PubMed]
  15. Ruiz-Canela, M.; Bes-Rastrollo, M.; Martinez-Gonzalez, M.A. The role of dietary inflammatory index in cardiovascular disease, metabolic syndrome and mortality. Int. J. Mol. Sci. 2016, 17, 1265. [Google Scholar] [CrossRef] [PubMed]
  16. Ramallal, R.; Toledo, E.; Martinez-Gonzalez, M.A.; Hernandez-Hernandez, A.; Garcia-Arellano, A.; Shivappa, N.; Hébert, J.R.; Ruiz-Canela, M. Dietary inflammatory index and incidence of cardiovascular disease in the SUN cohort. PLoS ONE 2015, 10, e0135221. [Google Scholar] [CrossRef] [PubMed]
  17. Garcia-Arellano, A.; Ramallal, R.; Ruiz-Canela, M.; Salas-Salvado, J.; Corella, D.; Shivappa, N.; Schröder, H.; Hébert, J.R.; Ros, E.; Gómez-Garcia, E.; et al. Dietary inflammatory index and incidence of cardiovascular disease in the PREDIMED Study. Nutrients 2015, 7, 4124–4138. [Google Scholar] [CrossRef] [PubMed]
  18. Gambardella, J.; Santulli, G. Integrating diet and inflammation to calculate cardiovascular risk. Atherosclerosis 2016, 253, 258–261. [Google Scholar] [CrossRef] [PubMed]
  19. Neufcourt, L.; Assmann, K.E.; Fezeu, L.K.; Touvier, M.; Graffouillere, L.; Shivappa, N.; Hebert, J.R.; Wirth, M.D.; Hercberg, S.; Galan, P.; et al. Prospective association between the dietary inflammatory index and metabolic syndrome: Findings from the SU.VI.MAX study. Nutr. Metab. Cardiovasc. Dis. 2015, 25, 988–996. [Google Scholar] [CrossRef] [PubMed]
  20. Jenkins, D.J.; Wolever, T.M.; Taylor, R.H.; Barker, H.; Fielden, H.; Baldwin, J.M.; Bowling, A.C.; Newman, H.C.; Jenkins, A.L.; Goff, D.V. Glycemic index of foods: A physiological basis for carbohydrate exchange. Am. J. Clin. Nutr. 1981, 34, 362–366. [Google Scholar] [CrossRef] [PubMed]
  21. Salmerón, J.; Manson, J.E.; Stampfer, M.J.; Colditz, G.A.; Wing, A.L.; Willett, W.C. Dietary fiber, glycemic load, and risk of non-insulin-dependent diabetes mellitus in women. JAMA 1997, 277, 472–477. [Google Scholar] [CrossRef] [PubMed]
  22. Ricker, M.A.; Haas, W.C. Anti-inflammatory diet in clinical practice: A review. Nutr. Clin. Pract. 2017, 32, 318–325. [Google Scholar] [CrossRef] [PubMed]
  23. Levitan, E.B.; Cook, N.R.; Stampfer, M.J.; Ridker, P.M.; Rexrode, K.M.; Buring, J.E.; Manson, J.E.; Liu, S. Dietary glycemic index, dietary glycemic load, blood lipids, and C-reactive protein. Metab. Clin. Exp. 2008, 57, 437–443. [Google Scholar] [CrossRef] [PubMed]
  24. Liu, S.; Manson, J.E.; Buring, J.E.; Stampfer, M.J.; Willett, W.C.; Ridker, P.M. Relation between a diet with a high glycemic load and plasma concentrations of high-sensitivity C-reactive protein in middle-aged women. Am. J. Clin. Nutr. 2002, 75, 492–498. [Google Scholar] [CrossRef] [PubMed]
  25. Gogebakan, O.; Kohl, A.; Osterhoff, M.A.; van Baak, M.A.; Jebb, S.A.; Papadaki, A.; Martinez, J.A.; Handjieva-Darlenska, T.; Hlavaty, P.; Weickert, M.O.; et al. Effects of weight loss and long-term weight maintenance with diets varying in protein and glycemic index on cardiovascular risk factors: The diet, obesity, and genes (DiOGenes) study: A randomized, controlled trial. Circulation 2011, 124, 2829–2838. [Google Scholar] [CrossRef] [PubMed]
  26. Wolever, T.M.; Gibbs, A.L.; Mehling, C.; Chiasson, J.L.; Connelly, P.W.; Josse, R.G.; Leiter, L.A.; Maheux, P.; Rabasa-Lhoret, R.; Rodger, N.W.; et al. The Canadian trial of Carbohydrates in Diabetes (CCD), a 1-y controlled trial of low-glycemic index dietary carbohydrate in type 2 diabetes: No effect on glycated hemoglobin but reduction in C-reactive protein. Am. J. Clin. Nutr. 2008, 87, 114–125. [Google Scholar] [PubMed]
  27. Neuhouser, M.L.; Schwarz, Y.; Wang, C.; Breymeyer, K.; Coronado, G.; Wang, C.Y.; Noar, K.; Song, X.; Lampe, J.W. A low-glycemic load diet reduces serum C-reactive protein and modestly increases adiponectin in overweight and obese adults. J. Nutr. 2012, 142, 369–374. [Google Scholar] [CrossRef] [PubMed]
  28. Brunt, A.R.; Rhee, Y.S. Obesity and lifestyle in U.S. College students related to living arrangements. Appetite 2008, 51, 615–621. [Google Scholar] [CrossRef] [PubMed]
  29. Driskell, J.A.; Meckna, B.R.; Scales, N.E. Differences exist in the eating habits of university men and women at fast-food restaurants. Nutr. Res. 2006, 26, 524–530. [Google Scholar] [CrossRef]
  30. Dumanovsky, T.; Nonas, C.A.; Huang, C.Y.; Silver, L.D.; Bassett, M.T. What people buy from fast-food restaurants: Caloric content and menu item selection, New York City 2007. Obesity 2009, 17, 1369–1374. [Google Scholar] [CrossRef] [PubMed]
  31. Larson, N.; Neumark-Sztainer, D.; Laska, M.N.; Story, M. Young adults and eating away from home: Associations with dietary intake patterns and weight status differ by choice of restaurant. J. Am. Diet. Assoc. 2011, 111, 1696–1703. [Google Scholar] [CrossRef] [PubMed]
  32. Taveras, E.M.; Rifas-Shiman, S.L.; Berkey, C.S.; Rockett, H.R.H.; Field, A.E.; Frazier, A.L.; Colditz, G.A.; Gillman, M.W. Family dinner and adolescent overweight. Obesity 2005, 13, 900–906. [Google Scholar] [CrossRef] [PubMed]
  33. Li, K.-K.; Concepcion, R.Y.; Lee, H.; Cardinal, B.J.; Ebbeck, V.; Woekel, E.; Readdy, R.T. An examination of sex differences in relation to the eating habits and nutrient intakes of University students. J. Nutr. Educ. Behav. 2012, 44, 246–250. [Google Scholar] [CrossRef] [PubMed]
  34. Winkleby, M.A.; Cubbin, C. Changing patterns in health behaviors and risk factors related to chronic diseases, 1990–2000. Am. J. Health Prompt. 2004, 19, 19–27. [Google Scholar] [CrossRef]
  35. Foster-Powell, K.; Holt, S.H.A.; Brand-Miller, J.C. International Tables of Glycemic Index and Glycemic Load values: 2002. Am. J. Clin. Nutr. 2002, 76, 5–56. [Google Scholar] [CrossRef] [PubMed]
  36. Atkinson, F.S.; Foster-Powell, K.; Brand-Miller, J.C. International Tables of Glycemic Index and Glycemic Load values: 2008. Diabetes Care 2008, 31, 2281–2283. [Google Scholar] [CrossRef] [PubMed]
  37. Dodd, H.; Williams, S.; Brown, R.; Venn, B. Calculating glycemic index by using measured and published food values compared with directly measured meal glycemic index. Am. J. Clin. Nutr. 2011, 94, 992–996. [Google Scholar] [CrossRef] [PubMed]
  38. Guenther, P.M.; Casavale, K.O.; Reedy, J.; Kirkpatrick, S.I.; Hiza, H.A.B.; Kuczynski, K.J.; Kahle, L.L.; Krebs-Smith, S.M. Update of the Healthy Eating Index: HEI-2010. J. Acad. Nutr. Diet. 2013, 113, 569–580. [Google Scholar] [CrossRef] [PubMed]
  39. Wirth, M.D.; Hébert, J.R.; Shivappa, N.; Hand, G.A.; Hurley, T.G.; Drenowatz, C.; McMahon, D.; Shook, R.P.; Blair, S.N. Anti-inflammatory Dietary Inflammatory Index scores are associated, with healthier scores on other dietary indices. Nutr. Res. 2016, 36, 214–219. [Google Scholar] [CrossRef] [PubMed]
  40. Alkerwi, A.; Vernier, C.; Crichton, G.E.; Sauvageot, N.; Shivappa, N.; Hebert, J.R. Cross-comparison of diet quality indices for predicting chronic disease risk: Findings from the Observation of Cardiovascular Risk Factors in Luxembourg (ORISCAV-LUX) study. Br. J. Nutr. 2015, 28, 259–269. [Google Scholar] [CrossRef] [PubMed]
  41. Wirth, M.D.; Burch, J.; Shivappa, N.; Violanti, J.M.; Burchfiel, C.M.; Fekedulegn, D.; Andrew, M.E.; Hartley, T.A.; Miller, D.B.; Mnatsakanova, A.; et al. Association of a dietary inflammatory index with inflammatory indices and metabolic syndrome among police officers. J. Occup. Environ. Med. 2014, 56, 986–989. [Google Scholar] [CrossRef] [PubMed]
  42. Dandona, P.; Chaudhuri, A.; Ghanim, H.; Mohanty, P. Pro-inflammatory effects of glucose and anti-inflammatory effect of insulin: Relevance to cardiovascular disease. Am. J. Cardiol. 2007, 99, 15–26. [Google Scholar] [CrossRef] [PubMed]
  43. Esposito, K.; Nappo, F.; Marfella, R.; Giugliano, G.; Giugliano, F.; Ciotola, M.; Quagliaro, L.; Ceriello, A.; Giugliano, D. Inflammation cytokine concentrations are acutely increased by hyperglycemia in humans: Role of oxidative stress. Circulation 2002, 106, 2067–2072. [Google Scholar] [CrossRef] [PubMed]
  44. Piya, M.K.; McTernan, P.G.; Kumar, S. Adipokine inflammation and insulin resistance: The role of glucose, lipids and endotoxin. J. Endocrinol. 2013, 216, T1–T15. [Google Scholar] [CrossRef] [PubMed]
  45. Lopez-Garcia, E.; Schulze, M.B.; Fung, T.T.; Meigs, J.B.; Rifai, N.; Manson, J.E.; Hu, F.B. Major dietary patterns are related to plasma concentrations of markers of inflammation and endothelial dysfunction. Am. J. Clin. Nutr. 2004, 80, 1029–1035. [Google Scholar] [PubMed]
  46. Pinkney, J.H.; Stehouwer, C.D.; Coppack, S.W.; Yudkin, J.S. Endothelial dysfunction: Cause of the insulin resistance syndrome. Diabetes 1997, 46 (Suppl. 2), S9–S13. [Google Scholar] [CrossRef] [PubMed]
  47. Bouche, C.; Rizkalla, S.W.; Luo, J.; Vidal, H.; Veronese, A.; Pacher, N.; Fouquet, C.; Lang, V.; Slama, G. Five week, long glycemic index diet decreases total fat mass and improves plasma lipid profile in moderately overweight nondiabetic men. Diabetes Care 2002, 25, 822–828. [Google Scholar] [CrossRef] [PubMed]
  48. Qi, L.; van Dam, R.M.; Liu, S.; Franz, M.; Mantzoros, C.; Hu, F.B. Whole grain, bran, and cereal fiber intakes and markers of systematic inflammation in diabetic women. Diabetes Care 2006, 29, 207–211. [Google Scholar] [CrossRef] [PubMed]
  49. Heggen, E.; Klemsdal, T.O.; Haugen, F.; Holme, I.; Tonstad, S. Effect of a low fat versus a low glycemic load diet on inflammatory biomarker and adipokine concentrations. Metab. Syndr. Relat. Disord. 2012, 10, 437–442. [Google Scholar] [CrossRef] [PubMed]
  50. Joslowski, G.; Halim, J.; Goletzke, J.; Gow, M.; Ho, M.; Louie, J.C.-Y.; Buyken, A.E.; Cowell, C.T.; Garnett, S.P. Dietary glycemic load, insulin load, and weight loss in obese, insulin resistant adolescents: RESIST study. Clin. Nutr. 2015, 34, 89–94. [Google Scholar] [CrossRef] [PubMed]
  51. Augustin, L.S.; Kendall, C.W.; Jenkins, D.J.; Willett, W.C.; Astrup, A.; Barclay, A.W.; Björck, I.; Brand-Miller, J.C.; Brighenti, F.; Buyken, A.E.; et al. Glycemic index, glycemic load and glycemic response: An International Scientific Consensus Summit from the International Carbohydrate Quality Consortium (ICQC). Nutr. Metab. Cardiovasc. Dis. 2015, 25, 795–815. [Google Scholar] [CrossRef] [PubMed]
  52. American Diabetes Association. Standards of medical care in diabetes-2011. Diabetes Care 2011, 34 (Suppl. 1), S11–S61. [Google Scholar]
  53. Gangwisch, J.E.; Hale, L.; Garcia, L.; Malaspina, D.; Opler, M.G.; Payne, M.E.; Rossom, R.C.; Lane, D. High glycemic index diet as a risk factor for depression: Analyses from the Women’s Health Initiative. Am. J. Clin. Nutr. 2015, 102, 454–463. [Google Scholar] [CrossRef] [PubMed]
  54. Azadbakht, L.; Mohammadifard, N.; Akhavanzanjani, M.; Taheri, M.; Golshahi, J.; Haghighatdoost, F. The association between dietary glycemic index, glycemic load and diet quality indices in Iranian adults: Results from Isfahan Healthy Heart Program. Int. J. Food Sci. Nutr. 2016, 67, 161–169. [Google Scholar] [CrossRef] [PubMed]
  55. Rehm, C.D.; Monsivais, P.; Drewnowski, A. Relation between diet cost and Healthy Eating Index 2010 scores among adults in the United States 2007–2010. Prev. Med. 2015, 73, 70–75. [Google Scholar] [CrossRef] [PubMed]
  56. Lin, C.-S.; Kimokoti, P.W.; Brown, L.S.; Kaye, E.A.; Nunn, M.E.; Millen, B.E. Methodology for adding glycemic index to the National Health and Nutrition Examination Survey Nutrient Database. J. Acad. Nutr. Diet. 2012, 112, 1843–1851. [Google Scholar] [CrossRef] [PubMed]
  57. Standards Australia. Glycemic Index of Foods. Available online: (accessed on 25 November 2017).
  58. Wolever, T.M.S.; Jenkins, D.; Jenkins, A.; Josse, R. The glycemic index: Methodology and clinical implications. Am. J. Clin. Nutr. 1991, 54, 846–854. [Google Scholar] [CrossRef] [PubMed]
  59. Gomes, J.M.G.; Fabrini, S.P.; Alfenas, R. Low glycemic index diet reduces body fat and attenuates inflammatory and metabolic responses in patients with type 2 diabetes. Arch. Endocrinol. Metab. 2017, 61, 137–144. [Google Scholar] [CrossRef] [PubMed]
  60. O’Sullivan, T.A.; Bremner, A.P.; Cedaro, P.C.; O’Neill, S.; Lyons-Wall, P. Glycemic index and glycemic load intake patterns in older Australian women. Nutr. Diet. 2009, 66, 138–144. [Google Scholar] [CrossRef][Green Version]
  61. Shivappa, N.; Hébert, J.R.; Rietzschel, E.R.; De Buyzere, M.L.; Langlois, M.; Debruyne, E.; Marcos, A.; Huybrechts, I. Association between dietary inflammatory index and inflammatory markers in the HELENA study. Mol. Nutr. Food Res. 2017, 61. [Google Scholar] [CrossRef] [PubMed]
  62. Hill, A.B. Observation and experiment. N. Engl. J. Med. 1953, 248, 995–1001. [Google Scholar] [CrossRef] [PubMed]
  63. Shivappa, N.; Wirth, M.D.; Hurley, T.G.; Hebert, J.R. 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, 61. [Google Scholar] [CrossRef] [PubMed]
  64. Julia, C.; Assmann, K.E.; Shivappa, N.; Hebert, J.R.; Wirth, M.D.; Hercberg, S.; Touvier, M.; Kesse-Guyot, E. Long-term associations between inflammatory dietary scores in relation to long-term C-reactive protein status measured 12 years later: Findings from the Supplémentation en Vitamines et Minéraux Antioxydants (SU.VI.MAX) cohort. Br. J. Nutr. 2017, 117, 306–314. [Google Scholar] [CrossRef] [PubMed]
  65. Deng, F.E.; Shivappa, N.; Tang, Y.; Mann, J.R.; Hebert, J.R. Association between diet-related inflammation, all-cause, all-cancer, and cardiovascular disease mortality, with special focus on prediabetics: Findings from NHANES III. Eur. J. Nutr. 2016, 56, 1085–1093. [Google Scholar] [CrossRef] [PubMed]
Table 1. Participants’ characteristics by Dietary Inflammatory Index (DII) tertiles.
Table 1. Participants’ characteristics by Dietary Inflammatory Index (DII) tertiles.
Total (n = 110)DII Tertile 1
(n = 37)
DII Tertile 2
(n = 37)
DII Tertile 3
(n = 36)
Sex 0.25
Male50 (45.5%)20 (54.1%)13 (35.1%)17 (47.2%)
Female60 (54.5%)17 (45.9%)24 (64.9%)19 (52.8%)
Race 0.21
European American68 (61.8%)28 (75.7%)22 (59.5%)18 (50.0%)
African American36 (32.7%)8 (21.6%)12 (32.4%)16 (44.4%)
Asian6 (5.5%)1 (2.7%)3 (8.1%)2 (5.6%)
Smoker 0.26
No97 (88.2%)34 (91.9%)30 (81.1%)33 (91.7%)
Yes13 (11.8%)3 (8.1%)7 (18.9%)3 (8.3%)
Drinker 0.81
No69 (62.7%)23 (62.2%)22 (59.5%)24 (66.7%)
Yes41 (37.3%)14 (37.8%)15 (40.5%)12 (33.3%)
BMI classification 1 0.38
Normal58 (53.2%)17 (47.2%)21 (56.8%)20 (55.6%)
Overweight32 (29.4%)11 (30.6%)13 (35.1%)8 (22.2%)
Obese19 (17.4%)8 (22.2%)3 (8.1%)8 (22.2%)
Exercise 0.42
No18 (16.4%)4 (10.8%)6 (16.2%)8 (22.2%)
Yes92 (83.6%)33 (89.2%)31 (83.8%)28 (77.8%)
Age (years)21.0 ± 2.521.3 ± 2.721.4 ± 3.020.0 ± 1.40.09
BMI (kg/m2)25.4 ± 4.625.9 ± 4.724.8 ± 3.525.3 ± 5.60.61
Body fat (%)21.3 ± 9.420.6 ± 10.022.7 ± 8.920.7 ± 9.40.57
Waist circumference (cm)81.2 ± 11.882.5 ± 10.980.0 ± 9.081.0 ± 15.00.67
Values are expressed as mean ± standard deviation (SD). 1 n = 109. BMI: body mass index.
Table 2. Nutrient intake of participants by DII tertiles.
Table 2. Nutrient intake of participants by DII tertiles.
DII Tertile 1
(n = 37)
DII Tertile 2
(n = 37)
DII Tertile 3
(n = 36)
Calories (cal)2674.2 ± 778.92227.1 ± 778.92499.3 ± 778.90.05
Carbohydrates (g)300.3 ± 67.9296.1 ± 68.2292.3 ± 31.10.88
Protein (g)105.4 ± 31.598.4 ± 31.787.4 ± 67.10.05
Total fat (g)92.8 ± 21.097.8 ± 21.6105.2 ± 21.30.05
Saturated fat (g)27.2 ± 8.4229.3 ± 8.435.7 ± 8.3<0.001
Monounsaturated fatty acid (g)17.8 ± 9.716.5 ± 9.712.0 ± 9.50.03
Polyunsaturated fatty acid (g)9.2 ± 7.49.9 ± 7.46.2 ± 7.30.08
Cholesterol (mg)362.7 ± 306.2394.5 ± 307.5408.1 ± 302.30.81
Trans fat (g)1.5 ± 2.51.9 ± 2.52.8 ± 2.50.09
Vitamin A (RE)664.9 ± 474.8305.8 ± 476.9189.5 ± 468.8<0.001
Vitamin B1 (mg)1.3 ± 0.50.9 ± 0.50.6 ± 0.5<0.001
Vitamin B2 (mg)2.2 ± 1.11.4 ± 1.10.8 ± 1.1<0.001
Niacin (mg)28.1 ± 9.821.2 ± 9.811.2 ± 9.7<0.001
Vitamin B6 (mg)1.9 ± 0.91.2 ± 0.90.7 ± 0.8<0.001
Vitamin B12 (μg)6.0 ± 3.34.0 ± 3.31.6 ± 3.3<0.001
Vitamin C (mg)101.8 ± 62.875.5 ± 63.145.7 ± 62.00.001
Vitamin D (IU)3.8 ± 3.12.2 ± 3.11.3 ± 3.10.004
Vitamin E
-α-tocopherol (mg)
6.6 ± 4.53.3 ± 4.51.4 ± 4.4<0.001
Folate (μg)337.1 ± 118.8218.7 ± 119.4123.1 ± 117.3<0.001
Vitamin K (μg)99.9 ± 91.720.3 ± 92.315.9 ± 91.9<0.001
Calcium (mg)1064.3 ± 381.9738.8 ± 383.6685.9 ± 377.1<0.001
Iron (mg)18.3 ± 6.917.1 ± 6.910.9 ± 6.8<0.001
Magnesium (mg)218.3 ± 64.3120.1 ± 64.673.3 ± 63.5<0.001
Phosphorus (mg)963.8 ± 361.9715.9 ± 363.5500.5 ± 357.3<0.001
Potassium (mg)1942.4 ± 591.61346.1 ± 594.3890.2 ± 584.2<0.001
Selenium (μg)77.2 ± 45.562.3 ± 45.625.7 ± 44.9<0.001
Sodium (mg)4100.3 ± 1154.54493.8 ± 1159.94746.9 ± 1140.0<0.057
Zinc (mg)8.0 ± 3.26.0 ± 3.23.4 ± 3.2<0.001
Caffeine66.7 ± 79.653.7 ± 79.945.0 ± 79.70.50
Values are expressed as mean ± standard deviation (SD). Values are adjusted for energy, age, and sex.
Table 3. Healthy eating index (HEI)-2010, Glycemic index, and Glycemic load by DII tertiles.
Table 3. Healthy eating index (HEI)-2010, Glycemic index, and Glycemic load by DII tertiles.
Dietary IndicesDII Tertile 1
(n = 37)
DII Tertile 2
(n = 37)
DII Tertile 3
(n = 36)
Glycemic Index (GI)50.1 (47.9–52.3)51.9 (49.7–54.0)54.8 (52.5–57.0)0.02
Glycemic Load (GL)170.7 (149.4–192.0)145.8 (125.0–166.6)157.6 (136.0–179.3)0.27
Healthy Eating Index (HEI)-201050.7 (47.3–54.0)44.6 (41.3–47.9)35.4 (32.0–38.8)<0.001
GI52.5 (49.1–55.9)53.9 (49.4–58.3)56.7 (52.7–60.8)0.30
GL167.5 (135.8–199.2)174.7 (135.2–214.2)185.0 (148.8–221.2)0.79
HEI-201048.1 (43.2–53.0)39.9 (33.4–46.4)29.5 (24.1–35.0)<0.001
GI47.5 (44.3–50.6)50.0 (47.5–52.4)53.8 (51.0–56.7)0.02
GL149.8 (130.3–169.2)137.4 (121.9–152.9)146.4 (128.0–164.8)0.56
HEI-201055.6 (50.5–60.7)46.8 (42.8–50.8)39.1 (34.3–43.9)<0.001
Values are expressed as means and 95% confidence intervals of the HEI-2010, GI, and GL. Values are adjusted for age, race, sex, BMI, percent body fat, smoker, drinker, and physical activity level.
Table 4. Correlation between DII and HEI, Glycemic index (GI), and Glycemic load (GL).
Table 4. Correlation between DII and HEI, Glycemic index (GI), and Glycemic load (GL).
Values are adjusted for age, race, sex, BMI, percent body fat, smoker, drinker, and physical activity level.
Table 5. Ten most popular food items.
Table 5. Ten most popular food items.
Food ItemGI ValueReference
1French fries64#1658 from International Table of GI and GL values, 2008 [36]
2Wheat bread58#96 from International Table of GI and GL values, 2002 [35]
3Lemonade54#50 from International Table of GI and GL values, 2008 [36]
4Pepperoni pizza60#488, cheese pizza from International Table of GI and GL values, 2002 [35]
5Chicken sandwich66#1178, McChickenTM burger from International Table of GI and GL values, 2008 [36]
6Sweet tea65#589 from International Table of GI and GL values, 2002 [35]
7Chicken nuggets46#482 from International Table of GI and GL values, 2002 [35]
8Apple40#388, apple (USA) from International Table of GI and GL values, 2002 [35]
9Banana42#397, Banana, slightly underripe, yellow with green sections (USA) from International Table of GI and GL values, 2002 [35]
10Cajun-style rice51#281 from International Table of GI and GL values, 2002 [35]
Back to TopTop