Key Messages
Since strong food cravings and emotional overeating can impair adherence to dietary recommendations, increasing awareness of patients with T2DM about managing physiological and cognitive processes related to eating may provide additional contribution to the management of T2DM.
It should not be forgotten that the idea that glycemic control can only be achieved with IE and ME in T2DM patients may lead to poor glycemic control.
Introduction
About 422 million individuals worldwide suffer from diabetes, and 1.5 million deaths are attributed to diabetes each year1. A healthy diet is one of the cornerstones of diabetes management. However, deciding what to eat is the most challenging part of the treatment plan for these individuals2.
Intuitive eating (IE) is a dietary behavior associated with psychological well-being, characterized by eating in response to physiological hunger and satiety cues rather than external conditions and emotional factors3,4. The Intuitive Eating Scale 2 (IES-2) is a validated tool which measures the degree of adherence to IE behaviors and attitudes5. It was originally developed against the failures of classical diets or energy-restricted diets in weight control of individuals and their negative effects on the body. The basic principles are to respond to innate hunger and satiety signals without restriction in the types of food consumed6. No restrictions on the types of food an individual can eat are set, unless there are no certain health problems such as diabetes or food allergies, as it is thought that the body can instinctively choose a variety of foods that provide nutritional balance6. In some studies, on intuitive eating in individuals with type 2 diabetes, it has been reported that intuitive eating may reduce the risk of inadequate glycemic control, while in some studies it is reported that it will have a positive effect on glycemic control by reducing body weight7-9.
Mindful eating (ME) is the state of being aware of the effect of eating on thoughts, feelings, bodily sensations, and behaviors. Given the various physiological and cognitive processes associated with eating such as memory, attention, and metabolic state, a wide variety of different practices can be defined as ME10. Most diets follow eating guidelines (i.e., what to eat, how much to eat, and what not to eat) aiming at specific outcomes such as weight loss, good glycemic control, and improved glycated hemoglobin (HbA1c). All diets have the potential for success or failure based on body weight results. Individuals may be aware of that their body weight results depend on their calorie intake and energy expenditure, and they may understand that it is related to their behavior; however, it is difficult to maintain behavior change without seeing results on body weight11. In a study evaluating the eating awareness of individuals with type 2 diabetes, 81% of individuals with T2DM were found to be slightly overweight and obese, while the incidence of eating disorders in these individuals was changed to be between 7.5% and 9%12. Kes et al. In a study conducted by 2021 using the MEQ scale, it was found that higher scale scores were associated with decreased BMI values and a lower risk of developing T2DM13.
Mindful eating seems to be an effective approach for body weight control and glycemic control in individuals with type 2 diabetes mellitus (T2DM) with promising outcomes. In the present study, we aimed to evaluate the effect of IE and ME on the dietary treatment of T2DM and to investigate their relationship with glycemic control and obesity.
Methodology
This single-center, analytical cross-sectional study was conducted at the Department of Nutrition and Dietetics of a tertiary care center between March 2022 and April 2022. A total of 153 adult patients aged between 19 and 64 years with T2DM who were referred from the Mersin City Training and Research Hospital, Department of Endocrinology and Metabolic Disorders of our center and were diagnosed with T2DM within at least one year were included. Exclusion criteria were as follows: having type 1 diabetes, pregnancy and lactation, malignancies, previous history of bariatric surgery, hypothyroidism, Stage 4-5 chronic renal failure, receiving dialysis, having an eating disorder, psychological disorders, and non-communicable neurological disease.
The study power analysis and sample size calculation were performed using the G*Power 3.1 software (Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany). With an alpha (α)=0.05, power (1-β)=0.95, and medium effect size (d)=0.50, the study power was calculated as 100% with a sample size of 150. A written informed consent was obtained from each participant. The study was approved by the institutional Toros University Scientific Research and Publication Ethics Committee with Approval No: 113 and Date: 10/12/2021 and Ministry of Health of the Republic of Turkey Approval No: 2 and Date: 09/03/2022. The study was conducted following the principles of the Declaration of Helsinki.
Descriptive characteristics of the patients were questioned using face-to-face interviews including age, sex, marital status, education status, age at the time of diagnosis, treatment duration, and medications used. Anthropometric measurements including body weight, height, body mass index (BMI) waist circumference (WC), and hip circumference (HC) were done. The Intuitive Eating Scale 2 (IES-2) was used to evaluate IE behaviors14 and the Mindful Eating Questionnaire (MEQ) was used to assess ME behaviors15. Data including biochemical parameters such as fasting blood glucose (FBG), HbA1c, fasting insulin, total cholesterol (TC), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and very low-density lipoprotein cholesterol (VLDL-C) were retrieved from the patient files.
Glycemic Control. The glycemic control status of individuals with type 2 diabetes participating in the study was evaluated using the HbA1c levels obtained from the individuals’ medical records. It was categorized as adequate glycemic control when HbA1c levels ≤7% and insufficient glycemic control when HbA1c >7%2.
Anthropometric measurements. The body weight, height, WC, and HC were measured by a researcher during face-to-face interviews16. The BMI values (body weight (kg) / height (m2)) were calculated from body weight and height measurements and classified according to the World Health Organization (WHO) as follows: BMI <18.5 kg/m2 underweight, 18.5-24.9 kg/m2 normal, 25.0-29.9 kg/m2 overweight, and ≥30.0 kg/m2 obese17. The WC measurements were classified according to the WHO classification as follows: men, <94 cm low risk, 94-101 cm high risk, and ≥102 cm very high risk; women, <80 cm low risk, 80-87 cm high risk, and ≥88 cm very high risk18. The HC and waist-to-hip ratio (WHR) were also measured and classified according to the WHO classification (>0.90 for men and >0.85 for women)18. The waist-to-height ratio (WHtR) was calculated as waist measurement divided by height measurement as described by Ashwell et al.19 as follows: <0.5 low risk, 0.5-0.6 high risk, and ≥0.6 very high risk).
IES-2. The IES-2 is a 21-item scale which is used to evaluate IE behaviors. It was developed by Tylka and Kroon Van Diest in 20135 and its validity and reliability studies were carried out by Baş et al.14 in the Turkish population. It uses a 5-point Likert-type scale from 1=strongly disagree to 5=strongly agree. It consists of four domains of IE: unconditional permission to eat (UPE), eating for physical rather than emotional reasons (EPR), reliance on hunger and satiety cues (RHSC), and body-food choice congruence (B-FCC). The total scores are calculated by dividing the four domains and total score by the total number of items in the relevant area. Higher scores indicate a higher tendency to IE behavior14.
MEQ. The MEQ is a reliable tool for the assessment of ME behavior of individuals. It was developed by Framson et al.20 and its validity and reliability studies were carried out by Köse et al.15 in the Turkish population. It consists of 30 items and seven subscales (i.e., disinhibition-mindless eating, emotional eating, eating control, mindfulness, eating discipline, conscious nutrition, and interference). It uses a 5-point Likert-type scale from 1=None to 5=Always. The total scores are calculated by dividing the seven subscales and total score by the total number of items in the relevant area. Higher scores indicate more mindful attitudes toward eating15.
Statistical Analysis. Statistical analysis was performed using the SPSS version 26.0 software (IBM Corp., Armonk, NY, USA). Descriptive data were presented in mean ± standard deviation (SD), median (min-max) or interquartile range (IQR) or number and frequency, where applicable. The normality of distribution of variables was checked using the Shapiro-Wilk test. The Levene test was used to determine the homogeneity of variance. Independent samples T-test was used to compare normally distributed variables between the two groups, while the Pearson correlation analysis was used to determine the relationship between variables. The Mann-Whitney U test was used to compare non-normally distributed variables and the Spearman correlation analysis was performed to analyze the relationship between variables. The Chi-square test was used to compare continuous variables with the Yates and Fisher correction tests. Binary logistic regression analysis was used to identify the factors affecting the HbA1c groups. First, FBG, diabetes management plan, treatment duration, age at the time of diagnosis, and IES-2 total score were included in the regression model. Next, a final logistic regression model (reduced model) was created using the log-likelihood-based backward elimination (backward-LR) method, eliminating non-significant factors. The alpha (α) values of IES-2 and MEQ were calculated as 0.767 and 0.715, respectively. A p value of <0.05 was considered statistically significant.
Results
Sociodemographic characteristics and biochemical test results of the patients according to the HbA1c groups are shown in Table 1. The majority of the patients with inadequate glycemic control were male (n=77, 59.2%) and were on oral antidiabetic medications alone (n=64, 49.2%). In these patients, age at the time of diagnosis, treatment duration, and FBG levels were significantly higher than those with adequate glycemic control (p<0.05). In addition, a statistically significant correlation was observed between inadequate glycemic control and WC of women and WHR of both men and women (p<0.05).
Table 1. Sociodemographic characteristics and biochemical test results of the patients according to the HbA1c levels.
HbA1c | Test statistics | p | ||
---|---|---|---|---|
≤7 % (n=23) | >7 % (n=130) | |||
Age, year (median) | 69.6 | 78.3 | U=1323 | 0.381 |
Sex, n (%) | ||||
Male | 15(65.2) | 77(59.2) | Fisher X2=0.292 | 0.650 |
Female | 8(34.8) | 53(40.8) | ||
Age at the time of diagnosis, month (median) | 57.1 | 80.5 | U=1036 | 0.019 |
Treatment duration, month (median) | 58.7 | 80.3 | U=1072 | 0.030 |
Treatment plan, n (%) | ||||
Insulin | 2(8.7) | 21(16.2) | Fisher X2=8.962 | 0.009 |
OAD | 19(82.6) | 64(49.2) | ||
Insulin + OAD | 2(8.7) | 45(34.6) | ||
BMI (kg/m2) (mean±SD) | 33.9±8.9 | 31.3±6.1 | T=1.714 | 0.089 |
Classification (kg/m2), n (%) | ||||
Underweight (<18.5) | 1(4.3) | 2(1.5) | Fisher X2=4.084 | 0.230 |
Normal (18.5-24.9) | 4(17.4) | 18(13.8) | ||
Overweight (25.0-29.9) | 3(13.0) | 39(30.0) | ||
Obese (≥30.0) | 15(65.2) | 71(54.6) | ||
Waist circumference (cm) (male) (mean±SD) | 108.3±12.9 | 106.8±13.5 | T=0.429 | 0.673 |
Classification (cm), n (%) | ||||
Low risk (<94) | 2(13.3) | 12(15.6) | Fisher X2=0.368 | 0.902 |
High risk (94-101) | 1(6.7) | 10(13.0) | ||
Very high risk (≥102) | 12(80.0) | 55(71.4) | ||
Waist circumference (cm) (female) (mean±SD) | 98.3±12.3 | 108.3±12.3 | T=-1.536 | 0.163 |
Classification (cm), n (%) | ||||
Low risk (<80) | 1(12.5) | - | Fisher X2=10.552 | 0.006 |
High risk (80-87) | 2(25.0) | 1(1.9) | ||
Very high risk (≥88) | 5(62.5) | 52(98.1) | ||
WHR (male) (mean±SD) | 0.8±0.1 | 0.9±0.1 | T=-3.784 | <0.001 |
Classification (cm), n (%) | ||||
Low risk (0.90) | 11(73.3) | 20(26.0) | Fisher X2=10.573 | <0.001 |
High risk (≥0.90) | 4(26.7) | 57(74.0) | ||
WHR (female) (mean±SD) | 0.9±0.0 | 1.0±0.0 | T=-1.607 | 0.146 |
Classification, n (%) | ||||
Low risk (0.85) | 2(25.0) | - | 0.015 | |
High risk (≥0.85) | 6(75.0) | 53(100) | ||
WHtR (mean±SD) | 0.7±0.1 | 0.7±0.0 | T=-0.432 | 0.626 |
Classification, n (%) | ||||
Low risk (<0.5) | 16(69.6) | 96(85.7) | Fisher X2=3.506 | 0.181 |
High risk (0-5-0.6) | 5(21.7) | 32(24.6) | ||
Very high risk (≥0.6) | 2(8.7) | 2(1.5) | ||
Biochemical test results (median) | ||||
FBG (mg/dL) | 18.9 | 87.3 | U=157 | <0.001 |
TG (mg/dL) | 64.7 | 79.2 | U=1213 | 0.150 |
TC (mg/dL) | 78.9 | 76.7 | U=1451 | 0.824 |
LDL-C (mg/dL) | 79.2 | 69.4 | U=1168 | 0.292 |
HDL-C (mg/dL) | 92.4 | 74.3 | U=1140 | 0.070 |
VLDL-C (mg/dL) | 67.6 | 78.7 | U=1278 | 0.269 |
*T-test; Mann-Whitney U; Fisher Chi-square.
BMI: Body mass index; DM: Diabetes mellitus; FBG: Fasting blood glucose; HbA1c: Glycohemoglobin; HDL-C: High-density lipoprotein cholesterol; LDL-C: Low-density lipoprotein cholesterol; OAD: Oral antidiabetic; TC: Total cholesterol; TG: Triglyceride; VLDL-C: Very low-density lipoprotein cholesterol; WHR: Waist-to-hip ratio; WHtR: Waist-to-height ratio.
The IES-2 and total MEQ scores and subscale scores according to the HbA1c groups revealed that only IES-2 total scores were significantly higher in the patients with inadequate glycemic control (p<0.05) (Table 2).
Table 2. Intuitive eating and mindful eating of patients according to HbA1c levels.
HbA1c | Test statistics | p | ||
---|---|---|---|---|
≤7% | >7% | |||
IES-2 | ||||
UPE | 3.3±1.1 | 3.7±1.0 | T=-1.660 | 0.107 |
EPR | 3.4±1.0 | 3.7±1.1 | T=-1.884 | 0.070 |
RHSC | 3.4±1.5 | 3.4±1.3 | T=-1.251 | 0.220 |
B-FCC | 3.2±0.7 | 3.5±0.6 | T=-0.054 | 0.957 |
Total score | 2.8±0.9 | 3.2±0.9 | T=-2.329 | 0.027 |
MEQ | ||||
Disinhibition | 3.3±1.0 | 3.6±0.9 | T=-1.235 | 0.227 |
Emotional eating | 4.0±1.1 | 4.2±0.8 | T=-1.094 | 0.276 |
Eating control | 3.9±1.0 | 3.7±1.0 | T=0.763 | 0.451 |
Mindfulness | 3.5±0.5 | 3.5±0.5 | T=-0.185 | 0.855 |
Eating discipline | 3.1±0.9 | 2.8±0.9 | T=1.731 | 0.094 |
Conscious nutrition | 2.9±0.6 | 3.0±0.6 | T=-1.059 | 0.297 |
Interference | 4.0±0.9 | 3.9±0.9 | T=0.237 | 0.814 |
Total score | 3.5±0.6 | 3.5±0.4 | T=-0.324 | 0.746 |
*T-test;
HbA1c: Glycohemoglobin; IES-2: Intuitive eating scale 2; MEQ: Mindful eating questionnaire; UPE: Unconditional permission to eat; EPR: Eating for physical rather than emotional reasons; RHSC: Reliance on hunger and satiety cues; B-FCC: Body-food choice congruence.
The correlations between anthropometric and biochemical test results of the patients according to the HbA1c groups and IE and ME behavior are shown in Table 3. There was a moderate negative correlation between the total MEQ score and body weight, BMI, WC, and WHtR in the patients with adequate glycemic control (r=-0.526, r=-0.537, r=-0.506, r=-0.510, respectively; p<0.05). There was a weak negative correlation between the total IES-2 score and BMI and between the total MEQ score and WHtR, TG, and VLDL-C in the patients with inadequate glycemic control (r=-0.225, r=-0.224, r=-0.114, r=-0.178, respectively; p<0.05).
Table 3. Correlation of intuitive eating and mindful eating with anthropometric and biochemical measurements.
HbA1c | ||||||||
---|---|---|---|---|---|---|---|---|
≤7 % | >7 % | |||||||
IES-2 | MEQ | IES-2 | MEQ | |||||
r | p | r | p | r | p | r | p | |
Body weight (kg) | -0.328 | 0.127* | -0.526 | 0.010* | 0.117 | 0.184* | -0.120 | 0.173* |
BMI (kg/m2) | -0.391 | 0.065* | -0.537 | 0.008* | -0.225 | 0.010* | -0.099 | 0.260* |
WC (cm) | -0.257 | 0.236* | -0.506 | 0.014* | -0.163 | 0.064* | -0.170 | 0.053* |
WHR | 0.275 | 0.203* | 0.055 | 0.805* | 0.156 | 0.076** | -0.061 | 0.493** |
WHtR | -0.300 | 0.164* | -0.510 | 0.013* | -0.130 | 0.141* | -0.224 | 0.010* |
FBG (mg/dL) | -0.149 | 0.498* | 0.222 | 0.309* | 0.021 | 0.810** | -0.058 | 0.513** |
TG (mg/dL) | -0.266 | 0.219* | 0.116 | 0.599* | 0.089 | 0.313** | -0.114 | 0.027** |
TC (mg/dL) | -0.075 | 0.735* | 0.112 | 0.610* | 0.005 | 0.953** | -0.091 | 0.305** |
LDL-C (mg/dL) | 0.113 | 0.608* | 0.112 | 0.332* | -0.086 | 0.357** | -0.006 | 0.951** |
HDL-C (mg/dL) | -0.316 | 0.634** | 0.360 | 0.092** | 0.042 | 0.637** | 0.085 | 0.335** |
VLDL-C (mg/dL) | -0.265 | 0.221* | 0.117 | 0.594* | 0.061 | 0.493** | -0.178 | 0.043** |
*Pearson;
**Spearman.
BMI: Body mass index; FBG: Fasting blood glucose; HbA1c: Glycohemoglobin; HDL-C: High-density lipoprotein cholesterol; IES-2: Intuitive eating scale 2; LDL-C: Low-density lipoprotein cholesterol; VLDL-C: Very low-density lipoprotein cholesterol; MEQ: Mindful eating questionnaire; TG: Triglyceride; TC: Total cholesterol; WC: Waist circumference; WHR: Waist-to-hip ratio; WHtR: Waist-to-height ratio.
The coefficients of independent variables included in the full and reduced logistic regression analysis are shown in Table 4. In the full model, only FBG was a significant independent variable (p<0.05). In the reduced model, treatment duration was excluded and FBG, age at the time of diagnosis, and IES-2 scores were found to have a statistically significant effect on HbA1c (p<0.05). In the reduced model using odds ratios, a one-unit increase in FBG, a one-year increase in the age at the time of diagnosis, and a one-point increase in the IES-2 score increased the probability of HbA1c levels above 7% by 9.9%, 13.2%, and 25.2%, respectively.
Table 4. Coefficient statistics for regression models.
Model | Coefficient | OR | 95%CI | p | |
---|---|---|---|---|---|
Lower | Upper | ||||
Full model | FBG | 1.105 | 1.048 | 1.164 | <0.001 |
Treatment plan (Ref=Insulin+OAD) | |||||
Treatment plan (OAD) | 6.401 | 0.211 | 193.997 | 0.286 | |
Treatment plan (Insulin) | 0.420 | 0.059 | 2.998 | 0.387 | |
Treatment duration | 0.827 | 0.512 | 1.336 | 0.438 | |
Age at the time of diagnosis | 1.350 | 0.840 | 2.170 | 0.215 | |
IES-2 total | 3.052 | 0.996 | 9.353 | 0.051 | |
Constant | 0.000 | <0.001 | |||
Reduced model | FBG | 1.099 | 1.047 | 1.153 | <0.001 |
Treatment plan (Ref=Insulin+OAD) | |||||
Treatment plan (OAD) | 5.518 | 0.202 | 150.376 | 0.311 | |
Treatment plan (Insulin) | 0.351 | 0.048 | 2.564 | 0.302 | |
Age at the time of diagnosis | 1.132 | 1.005 | 1.275 | 0.041 | |
IES-2 total | 3.252 | 1.063 | 9.946 | 0.039 | |
Constant | 0.000 | <0.001 |
OR: Odds ratio; CI: Confidence interval; FBG: Fasting blood glucose; OAD: Oral antidiabetic; IES-2: Intuitive eating scale 2.
Discussion
In the present study, we investigated the effect of IE and ME on the dietary treatment of T2DM and examined their relationship with glycemic control and obesity. Our study results showed that IE adversely affected glycemic control in patients with T2DM, while ME did not have a direct effect on HbA1c, although it was positively correlated with body weight control.
The American Diabetes Association (ADA) recommends an HbA1c of ≤7% for the treatment of adults with T2DM2. To achieve this goal, it is recommended to support body weight loss and reduce energy intake in T2DM adults who are mildly overweight or have obesity. In addition, the ADA recommends that a variety of eating patterns (i.e., combinations of different foods or food groups) can be applied for the management of T2DM, considering individual preferences such as tradition, culture, religion, health beliefs and goals, economics and metabolic goals while choosing an eating pattern over the other2.
Eating behavior models such as IE and ME have recently gained importance in body weight control and have been proposed to play a role in providing glycemic control21; therefore, these models have begun to be studied in patients with diabetes7,22,23. Previous studies have shown that the IES-2 total score and B-FCC subscale score are effective in providing better glycemic control in patients with T2DM7. A study including children and adolescents with type 1 diabetes reported that higher IES-2 total score and EPR subscale scores were associated with lower HbA1c23. In another study, the IES-2 total score and EPR subscale score positively affected HbA1c and FBG in gestational diabetes22. Unlike the aforementioned studies, we obtained controversial results in our study. The IES-2 total scores were significantly higher in the patients with inadequate glycemic control. In addition, a one-point increase in the IES-2 increased the probability of HbA1c level above 7% by 25.2%. Consistent with our findings, a study of African-American women with T2DM showed poor agreement of self-reported dietary practices with IE concepts24. Therefore, the difference in portion perception in some T2DM patients results in confusion in portion control. In the aforementioned study, patients with T2DM believed that larger-sized individuals needed much more energy and, therefore, they did not respect to the advice to eat less after being diagnosed with diabetes. It is thought that, in T2DM, the changes in brain responses to food stimuli are different from healthy individuals and the IE method may be misleading due to their strong cravings for food stimuli and changes in brain responses to emotional overeating25. We think that these results, which contradict the positive effect of the intuitive eating model on T2DM according to the literature, may be due to the fact that the number of individuals with poor glycemic control in the study was higher than those with good glycemic control.
Overeating can be overcome by improving attention, improving awareness of current events, and focusing on the food itself26. Mindful eating can facilitate body weight management by promoting healthier eating27. It is helpful for individuals to develop awareness of both internal and external stimuli for eating, stop eating automatically, and eat in response to natural physiological cues of hunger and satiety. It can also improve irregular eating and dietary habits28. However, in a systematic review, a limited number of evidence showed that IE and ME interventions affected energy intake or diet quality29. Furthermore, some studies on ME and T2DM have demonstrated that ME reduces HbA1c levels30,31, while some others have not observed significant changes in HbA1c levels32,33. Our study results do not support the presence of an association between ME and HbA1c. We think that this may be due to the difference in the amount of food consumption of individuals with type 2 diabetes who participated in the study.
It has been well established that there is a strong relationship between T2DM development and abdominal obesity34. Obesity markers such as WHR and WHtR are better predictors than BMI for poor glycemic control35. In a study, Miller et al.30 reported that ME and diabetes self-management education improved body weight loss and glycemic control. In addition, changes in body composition that develop with weight loss provide improvements in glycemic control markers and metabolic improvements. Therefore, blood glucose regulation control with individual nutrition programs and body composition monitoring in consultation with a dietician is recommended for individuals with diabetes36-38. In our study, the number of male and female patients with high WHR was significantly higher among those with inadequate glycemic control. On the other hand, there was a negative and significant correlation between ME and body weight, BMI, WC, and WHtR in patients with adequate glycemic control. These findings suggest that ME has positive effects on body weight control with improved glucose control. However, short-term appetite regulation with insulin, not blood glucose level in healthy individuals, has been shown to be impaired in overweight and obese individuals39. Therefore, it may be risky to conclude that only ME can be used reliably to reduce energy intake for patients with diabetes.
Dietary habits and diet therapy are one of the mainstays to achieve blood glucose targets in diabetes2. While IE is the main determinant for eating habits in response to physiological hunger and satiety cues, ME consists of making conscious food choices, being aware of physical and psychological hunger and satiety cues, and eating health3,4,10. In the present study, we investigated the effects of IE and ME on the glycemic control of patients with T2DM. The main limitation to this study is the relatively small sample size with good glycemic control, as the vast majority of the patients who were admitted to the Department of Nutrition and Dietetics had impaired glycemic control. Another limitation is the lack of food consumption records of individuals with type 2 diabetes who participated in the study.
Conclusions
In conclusion, T2DM is a preventable disease, and its associated complications can be prevented with healthy and regular dietary habits. Several aspects should be considered while evaluating HbA1c levels in these patients. Of note, living with diabetes for long years may result in fatigue or non-adherence to diet therapy. A strong craving for food, particularly emotional overeating, may impair adherence to dietary recommendations. Therefore, improving the awareness of patients with T2DM to manage the physiological and cognitive processes related to eating in diet therapy may provide additional contribution to the T2DM management. However, it should be kept in mind that the idea that glycemic control of T2DM patients can be achieved with only IE and ME may yield poor glycemic control. Although dietary habits are the leading factors affecting glucose control in T2DM, age at the time of diagnosis is also a prognostic factor. Further large-scale, prospective studies including age matched T2DM patients with good glycemic control are needed to elucidate the direct effects of IE and ME on T2DM.