Abstract
Background
Psychological disorders including depression, anxiety, and stress comprise a huge public health problem. The aim of this cross-sectional study is to assess the relationship between dietary glycemic index (DGI) and glycemic load (DGL) and mental disorders.
Method
Participants (n = 10,000) aged 20–69 were randomly selected from 200 clusters in Yazd from the recruitment phase of Yazd Health Study. The dietary intake of study participants was collected by a reliable and validated food frequency questionnaire consisting of 178 food items. DGI and DGL were calculated from the FFQ data using previously published reference values. To assess psychological disorders an Iranian validated short version of a self-reported questionnaire Depression Anxiety Stress Scales 21 was used.
Results
There were no significant associations between DGI and DGL with odds of depression or anxiety in crude and adjusted models. However, individuals in the highest quartiles of DGL had the lowest odds of stress (OR: 0.69; 95% CI 0.47–1, P-trend = 0.023). This association remained significant after adjustment for potential confounding variables in model I (OR: 0.45; 95% CI 0.22–0.9, P-trend = 0.023), model II (OR: 0.46; 95% CI 0.22–0.96, P-trend = 0.039) and model III (OR: 0.46; 95% CI 0.22–0.96, P-trend = 0.042).
Conclusion
In conclusion, consumption of foods with higher GL was associated with lower odds of stress; however, no significant association was found between DGI or DGL and risk of depression and anxiety. Performing further studies with longitudinal design is suggested to confirm these results.
Keywords: Anxiety, Depression, Dietary glycemic index, Dietary glycemic load, Stress
Introduction
Psychological disorders including depression, anxiety, and stress comprise a huge public health problem, affecting about 31% to 41% of the world population in 2020 [1]. The pathophysiology of mental disorders is complex, with genetic, biological, and environmental factors involved in its onset and progression [2]. The underlying mechanisms are not fully understood, which may explain the poor response (50%) of current pharmacotherapies [3].
Among the environmental factors, dietary intakes have long been demonstrated to be associated with mental disorders. For example, diets rich in fruits and vegetables have a general positive impact on mental health [4] whereas a western diet (characterized by high intake of fried food, processed meat, refined carbohydrate and confectionary) is associated with mental disorders [5]. The impact of dietary carbohydrate intake on health outcomes and disease has increasingly been in focus in recent years [6]. However, the link between the various aspects of carbohydrate and psychological health remains unclear. The effects of foods to increase blood glucose are different and this property is considered the glycemic index (GI), a quality rating of how individual foods raise blood sugar levels. In fact, GI is the increase in postprandial blood glucose after consumption of a specific carbohydrate portion of a food compared with glucose or white bread [7]. When we consume high-GI foods, blood glucose and subsequently insulin concentrations are rapidly increased, while smaller and slower elevation of postprandial blood glucose and insulin levels are observed following intake of low-GI foods. Refined grains such as white bread, rice, potatoes and sugary products are considered high-GI foods, whereas vegetables, whole grain and legumes are included in low-GI groups [8]. Dietary glycemic load (GL) is the product of a food’s GI and total available carbohydrate content, and provides both the quality and quantity the of carbohydrates [9]. Thus, GL represents a more accurate view of a food’s real-life effects on postprandial glucose and insulin response.
The prevalence of psychological disorders is much higher in patients with diabetes [10] and some studies show a link between DGI and DGL with psychological disorders [11–13], suggesting glucose metabolism might play a mechanistic role. Indeed, high GI and GL foods provoke insulin secretion leading to subsequent hypoglycemia which impact on the nervous system and result in psychological disorders [14]. However, increased insulin levels from high GI/GL diets may facilitate delivery of tryptophan in the brain and increase the synthesis of serotonin, a neurotransmitter associated with mood improvement [15]. On the other hand, most of fruits and vegetables which are the good source of dietary fiber and several antioxidant compound such as phytochemical are classified in the medium and low GI foods [16]. These nutrients had positive effects on mental disorders in previous studies [17, 18].
Totally, the literature in this field is equivocal, probably due to study design, sample size, duration, and other components of the diet that may explain this inconsistency [19–23]. Therefore, due to the necessity of conducting more high-quality research, we investigated the association of DGI and DGL with depression, anxiety, and stress in a large Iranian population.
Materials and methods
Study population
We used data from the enrollment phase of Yazd Health Study (YaHS) conducted from September 2014 to December 2015. YaHS is a prospective cohort study which has been conducted on 10,000 participants aged 20–70 years since 2014. The participants were randomly selected from 200 clusters in Yazd Greater Area. The profile and details of this study were published elsewhere [24]. Written informed consent was taken from all participants. The research was approved by the Ethics Committee of Shahid Sadoughi University of Medical Sciences, Yazd, Iran (Ethic code: 931188). Data regarding current and history of chronic diseases, smoking status, socio-demographic characteristics including age, gender, marital status and education level were obtained by interview and standard questionnaires. Participants were excluded on the following: under or over estimation of energy intake (total daily energy intake less than 800 or higher than 6500 kcal/day), pregnancy, following a special diet and taking antidepressants. After exclusion, 7384 participants (3673 men and 3711women) participated in the study.
Dietary assessment
Dietary intake of study participants was collected by a reliable and validated food frequency questionnaire (FFQ) consisting of 178 food items designed for an Iranian population [25]. FFQs were completed during face-to-face interviews and reported dietary intakes in household measures were converted to grams and entered to the Nutritionist IV software (First Databank Inc., Hearst Corp., San Bruno, CA, USA). To calculate daily nutrient intake values for each participant, the US Department of Agriculture’s (USDA) national nutrient databank was used [26].
Dietary glycemic index and load calculation
The total DGI was calculated based on the following formula: The available carbohydrate content of foods was calculated as total carbohydrate minus fiber [27]. The total carbohydrate and fiber contents of foods were adapted from the US Department of Agriculture food-composition table [28]. Food items with low carbohydrate content (less than 3.5 g available carbohydrate per serving) like tomatoes, pickles, cabbage, cucumbers, lettuce, cheese, sausages, eggs, mayonnaise were excluded because GI values of these foods could not be tested [29]. Of the 178 and 121 food and beverage items in the FFQs of YaHS-TAMYS study, 43 (24.1%) and 32 (24.4%) items contained less than 3.5 g available carbohydrate/serving, respectively. Eventually, the calculation of GI was carried out based on the remaining 135 items in the YaHS-TAMYS. GI values for 108 food items in the YaHS-TAMYS study were adapted from the international references [16, 30]. for Iranian specific foods not covered in the international tables (6 items), the Iranian GI tables were used [31], because the GI of all food items was not covered. GI values for the remaining food items which were not available, neither in Iranian nor on the international tables, such as some traditional sweets and desserts, were gained based on physically and chemically similar foods. For example, the GI value for gaz, a traditional food item highly consumed in Yazd city and mainly made of flour, almonds, and sugar, was considered to be the same as sugar. When more than one GI value from a different brand was available, the mean GI value was applied (e.g. rice and dates). The GIs of mixed meals were obtained based on GI values of each of the meal’s components [28]. For all derived GI values, glucose was used as the reference food. Finally, DGL was calculated by multiplying the dietary GI by the total daily available carbohydrate intake and dividing the result by 100 [28].
Anthropometric measurements
Body weight was measured using a portable digital scale analyzer with an accuracy of 0.1 kg. The participants stood in the middle of the scale, wearing the minimum possible clothing. Height was also measured in a standing position, while barefoot with the head placed in the Frankfurt position. Body Mass Index (BMI) was calculated, body weight (kg)/height (m2).
Psychological health assessment
An Iranian validated short version of the self-report questionnaire for depression, anxiety and stress (DASS 21) consisting of seven items per subscale was used [32]. The individuals read each statement and recorded their reply according to a 4-point Likert scale ranging from 0 (does not apply to me at all) to 3 (applies to me very much or most of the time). The scores were summed for items of each scale. As the long form of DASS has 42 items, we multiplied the final score of each scale by two. The individuals were considered to have depression, anxiety, and stress if they obtain total scores of ≥ 10, ≥ 8 and ≥ 15, respectively.
Statistical analysis
The normality of data was assessed using the Kolmogorov–Smirnov test. Continuous and categorical variables were compared across quartiles of DGI and DGL using analysis of variance (ANOVA) and chi-square tests respectively. The differences between nutrients and dietary intake of each quartile were assessed using a Bonferroni post-hoc analysis. Logistic regression was applied to evaluate the relationship between DGI and DGL with psychological disorders in crude and adjusted models. Model I was adjusted for age, gender, and total energy intake. In model II, marital status, smoking, education level, employment status, salt intake, multi-vitamins use, diabetes, and hypertension were additionally adjusted. Further adjustment was for BMI in the final model. P-values < 0.05 were considered statistically significant. To analyze the data, the statistical Package for Social Sciences (SPSS) (version 23.0, SPSS Inc., Chicago, Illinois, USA) was used.
Results
Overall, 7384 participants were included (3673 men and 3711 women). The prevalence of psychological disorders did not significantly differ among quartiles of DGI and DGL. BMI, marital status, education level, multi-vitamin supplement use, and hypertension were significantly different among quartiles of DGI. Furthermore, significant differences were seen for age, physical activity, marital status, gender, employment status, education level, multi-vitamin supplement use, hypertension, and diabetes across quartiles of DGL (Table 1).
Table 1.
Variable | GI | GL | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Total | Q1 | Q2 | Q3 | Q4 | P-valuea | Q1 | Q2 | Q3 | Q4 | P-value | |
Depression, yes (%) | 578 (8.1)a | 148 (8.3) | 142 (7.9) | 130 (7.2) | 158 (8.9) | 0.326 | 158 (8.8) | 153 (8.6) | 132 (7.3) | 135 (7.6) | 0.252 |
Anxiety, yes (%) | 754 (10.5) | 186 (10.4) | 186 (10.3) | 170 (9.5) | 212 (11.9) | 0.113 | 200 (11.1) | 190 (10.7) | 183 (10.1) | 181 (10.2) | 0.710 |
Stress, yes (%) | 238 (3.3) | 58 (3.2) | 65 (3.6) | 54 (3) | 61 (3.4) | 0.776 | 68 (3.8) | 69 (3.9) | 54 (3) | 47 (2.7) | 0.106 |
BMI (kg/m2) | |||||||||||
< 18.5 | 247 (3.3) | 61 (3.2) | 63 (3.3) | 75 (4) | 48 (2.5) | 0.018 | 57 (3) | 55 (2.9) | 73 (3.9) | 62 (3.3) | 0.112 |
18.5–24.9 | 2339 (30.9) | 595 (31.4) | 618 (32.6) | 586 (30.9) | 540 (28.5) | 577 (30.5) | 630 (33.3) | 577 (30.5) | 555 (29.3) | ||
> 25 | 4988 (65.9) | 1237 (65.3) | 1213 (64) | 1233 (65.1) | 1305 (68.9) | 1259 (66.5) | 1209 (63.8) | 1244 (65.7) | 1276 (67.4) | ||
Age (%) | |||||||||||
20–29 years | 1586 (21.5) | 419 (22.7) | 404 (21.8) | 404 (217) | 359 (19.6) | 0.052 | 322 (17.4) | 404 (22) | 433 (23.4) | 427 (23.2) | < 0.01 |
30–39 years | 1598 (20.8) | 383 (20.8) | 395 (21.4) | 380 (20.4) | 440 (24) | 324 (17.5) | 405 (22) | 429 (23.1) | 440 (23.9) | ||
40–49 years | 1586 (21.5) | 387 (21) | 413 (22.3) | 393 (21.1) | 393 (21.4) | 404 (21.8) | 397 (21.6) | 399 (21.5) | 386 (21) | ||
50–59 years | 1402 (19) | 377 (20.4) | 347 (18.8) | 348 (18.7) | 330 (18) | 392 (21.2) | 341 (18.5) | 323 (17.4) | 346 (18.8) | ||
60–69 years | 1215 (16.4) | 279 (15.1) | 290 (15.7) | 334 (18) | 312 (17) | 409 (22.1) | 293 (15.9) | 270 (14.6) | 243 (13.2) | ||
Physical activity (Met_min/week) | 901.1b ± 905.1 | 890.8 ± 883.1 | 894.5 ± 910.5 | 877.5 ± 875 | 942.4 ± 950.3 | 0.156 | 826.6 ± 876.7 | 896.8 ± 896.4 | 932.8 ± 903 | 949 ± 939.7 | < 0.01 |
Marriage (%) | |||||||||||
Single | 856 (11.6) | 232 (12.6) | 225 (12.2) | 206 (11.1) | 193 (10.6) | 0.019 | 178 (9.6) | 224 (12.2) | 220 (11.9) | 234 (12.8) | 0.001 |
Married | 6264 (85.1) | 1575 (85.6) | 1567 (84.8) | 1570 (85.9) | 1570 (85.9) | 1587 (86) | 1541 (84.2) | 1585 (85.6) | 1551 (84.6) | ||
Widowed or divorced | 240 (3.3) | 61 (3.3) | 40 (2.2) | 75 (4.1) | 64 (3.5) | 80 (4.3) | 65 (3.6) | 46 (2.5) | 49 (2.7) | ||
Smoking status (%) | |||||||||||
Never smoker | 6328 (87.8) | 1582 (87.6) | 1576 (87) | 1617 (89) | 1553 (87.5) | 0.496 | 1609 (88.4) | 1567 (86.9) | 1587 (87.7) | 1565 (88.3) | 0.520 |
Current smoker | 766 (10.6) | 194 (10.7) | 207 (11.4) | 177 (9.7) | 188 (10.6) | 190 (10.4) | 200 (11.1) | 192 (10.6) | 184 (10.4) | ||
Ex_smoker | 113 (1.6) | 29 (1.6) | 29 (1.6) | 22 (1.2) | 33 (1.9) | 22 (1.2) | 36 (2) | 31 (1.7) | 24 (1.4) | ||
Gender, male (%) | 3673 (49.7) | 909 (49.1) | 927 (50.2) | 917 (49.5) | 920 (50.2) | 0.877 | 831 (44.8) | 923 (50.3) | 967 (52) | 952 (51.9) | < 0.01 |
Job (%) | |||||||||||
Unemployed | 1415 (19.5) | 353 (19.6) | 325 (17.9) | 357 (19.6) | 380 (21.1) | 0.336 | 358 (19.8) | 359 (19.9) | 306 (16.8) | 392 (21.7) | < 0.01 |
Government employee | 3537 (48.8) | 898 (49.8) | 898 (49.5) | 904 (49.6) | 837 (46.5) | 960 (53.1) | 898 (49.7) | 876 (48.1) | 803 (44.4) | ||
Manual worker | 247 (3.4) | 60 (3.3) | 66 (3.6) | 56 (3.1) | 65 (3.6) | 61 (3.4) | 53 (2.9) | 67 (3.7) | 66 (3.6) | ||
Freelance job | 2046 (28.2) | 492 (27.3) | 530 (29.1) | 505 (27.7) | 519 (28.8) | 428 (23.7) | 497 (27.5) | 572 (31.4) | 549 (30.3) | ||
Education (%) | |||||||||||
Illiterate | 1776 (24.1) | 438 (23.7) | 418 (22.7) | 500 (27) | 420 (23.1) | 0.004 | 562 (30.5) | 401 (21.8) | 406 (22) | 407 (22.3) | < 0.01 |
Middle school | 2095 (28.5) | 501 (27.2) | 508 (27.6) | 514 (27.7) | 527 (31.4) | 527 (28.6) | 549 (29.9) | 494 (26.7) | 525 (28.7) | ||
Diploma | 2289 (31.1) | 611 (33.1) | 590 (32) | 553 (29.8) | 535 (29.4) | 520 (28.2) | 557 (30.3) | 629 (34) | 583 (31.9) | ||
Bachelors degree | 995 (13.5) | 253 (13.7) | 261 (14.2) | 204 (12.9) | 241 (13.2) | 201 (10.9) | 270 (14.7) | 260 (14.1) | 264 (14.4) | ||
Master and doctor | 205 (2.8) | 42 (2.3) | 65 (3.5) | 47 (2.5) | 51 (2.8) | 35 (1.9) | 62 (3.4) | 59 (3.2) | 49 (2.7) | ||
Multi-vitamins supplement (%) | |||||||||||
Never | 6407 (86.1) | 1727 (94.3) | 1715 (91.9) | 1619 (86.4) | 1346 (72.1) | > 0.01 | 1741 (94.2) | 1727 (93.7) | 1691 (90) | 1248 (66.8) | < 0.01 |
1–3/month | 482 (6.5) | 44 (2.4) | 67 (3.6) | 95 (5.1) | 276 (14.8) | 34 (1.8) | 37 (2) | 64 (3.4) | 347 (18.6) | ||
Minimal once a week | 549 (7.4) | 60 (3.3) | 85 (4.6) | 159 (8.5) | 245 (13.1) | 73 (4) | 79 (4.3) | 124 (6.6) | 273 (14.6) | ||
Diabetes, yes (%) | 912 (12) | 233 (12.3) | 209 (11) | 244 (12.9) | 226 (11.9) | 0.358 | 313 (16.5) | 229 (12.1) | 194 (10.2) | 176 (9.3) | < 0.01 |
Hypertension, yes (%) | 1135 (15) | 280 (14.8) | 280 (14.8) | 321 (16.9) | 254 (13.4) | 0.023 | 350 (18.5) | 286 (14.1) | 277 (14.6) | 240 (12.7) | < 0.01 |
GI glycemic index, GL glycemic load
aObtained from χ2 test and one-way anova for categorical and continuous variables, respectively
bData are presented as mean ± standard deviation (SD)
Dietary nutrients and energy adjusted food groups are presented in Table 2. The one-way ANOVA test followed by Bonferroni post-hoc analysis revealed significant differences between all dietary nutrients and food groups including, energy intake; percentage energy from protein, carbohydrate, and fat intake; cholesterol; saturated fatty acid; vitamin E; vitamin C; folic acid; magnesium; fruits; vegetables; red meat; fish, dairy; whole grains; refined grains; sugars; salt; legumes and nuts. Significant differences among the quartiles of DGI and DGL are shown with different letters “a” or “b”.
Table 2.
Quartiles of GI | Quartiles of GL | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Total | Q1 | Q2 | Q3 | Q4 | P-value I | Q1 | Q2 | Q3 | Q4 | P-value | |
Nutrients | |||||||||||
Energy intake (kcal) | 2897 ± 1378 | 2438 ± 1061a | 2864 ± 1351b | 3634 ± 1351b | 2897 ± 1378b | < 0.001 | 1646 ± 419.3a | 2199 ± 494.1b | 3019 ± 744.9b | 4721 ± 1111b | < 0.001 |
Protein (% of total daily energy) | 16.16 ± 0.04 | 16.82 ± 0.04a | 16.73 ± 0.03 | 16.24 ± 0.04b | 14.86 ± 0.04b | < 0.001 | 17.84 ± 0.04a | 16.59 ± 0.03b | 16.11 ± 0.03b | 14.10 ± 0.04b | < 0.001 |
Carbohydrate (% of total daily energy) | 56.12 ± 0.09 | 53.81 ± 0.08a | 54.58 ± 0.08 | 56.00 ± 0.08b | 60.09 ± 11.21b | < 0.001 | 52.55 ± 0.07a | 55.40 ± 0.07b | 55.87 ± 0.09b | 60.67 ± 0.10b | < 0.001 |
Fat (% of total daily energy) | 33.61 ± 0.09 | 32.90 ± 0.07a | 32.67 ± 0.07 | 32.85 ± 0.07 | 0.36 ± 0.12b | < 0.001 | 33.24 ± 0.06a | 31.53 ± 0.06b | 33.38 ± 0.09 | 36.28 ± 0.11b | < 0.001 |
Cholesterol (mg) | 394.8 ± 391.3 | 363.5 ± 396.1a | 394.1 ± 326.6 | 391.1 ± 336.4 | 430.6 ± 483.4b | < 0.001 | 286.3 ± 322.9a | 318.4 ± 206.4 | 432.7 ± 390.9b | 542 ± 521.8b | < 0.001 |
SFA (g) | 31.04 ± 18.36 | 27.13 ± 15.36a | 29.58 ± 17.43b | 30.48 ± 17.28b | 36.98 ± 21.39b | < 0.001 | 19.56 ± 9.62a | 24.3 ± 11.47b | 32.47 ± 15.22b | 47.8 ± 20.82b | < 0.001 |
Vitamin E (mg/day) | 11.36 ± 11.66 | 11.92 ± 11.85 | 11.52 ± 11.80 | 10.98 ± 12.02 | 11.01 ± 10.92 | 0.038 | 7.70 ± 7.16a | 9.55 ± 8.93b | 12.72 ± 13.28b | 15.45 ± 14.19b | < 0.001 |
Vitamin C (mg) | 210.5 ± 188.7 | 196.2 ± 169a | 218.3 ± 214.3b | 219.2 ± 169.6b | 208.5 ± 197.1 | < 0.001 | 115.1 ± 54.12a | 166.8 ± 92b | 243.2 ± 148.4b | 317.1 ± 292.6b | < 0.001 |
Folic acid (µg) | 379.8 ± 228 | 354.6 ± 215.5a | 361.9 ± 217.7 | 370.8 ± 216.6 | 432.1 ± 251.8b | < 0.001 | 230.7 ± 93.18a | 300 ± 127.6b | 410.8 ± 193.8b | 577.8 ± 276.8b | < 0.001 |
Magnesium (mg) | 339.3 ± 179.6 | 309.6 ± 155.2a | 322.9 ± 166.2 | 336.2 ± 180.7b | 339.3 ± 179.6b | < 0.001 | 199.7 ± 58.38a | 262.8 ± 79.31b | 359 ± 125.2b | 535.7 ± 198.7b | < 0.001 |
Food groups (g/1000 kcal) | |||||||||||
Fruits | 184.3 ± 138.4 | 205.6 ± 145.1a | 202.3 ± 141.8 | 192.3 ± 130.3b | 136.9 ± 124.1b | < 0.001 | 187.8 ± 109.9a | 204.8 ± 128.1b | 202.8 ± 151.3b | 184.3 ± 138.4b | < 0.001 |
Vegetables | 96.6 ± 77.29 | 112 ± 82.82a | 104.1 ± 78.03b | 97.77 ± 75.50b | 72.76 ± 66.25b | < 0.001 | 119.6 ± 81.3a | 104.7 ± 69.75b | 96.78 ± 81.41b | 65.57 ± 65.10b | < 0.001 |
Red meat | 20.46 ± 18.37 | 22.60 ± 17.77a | 24.60 ± 21.13b | 20.12 ± 16.43b | 14.51 ± 16.16b | < 0.001 | 25.29 ± 20.43a | 23.65 ± 16.75b | 20.90 ± 19.34b | 11.99 ± 13.15b | < 0.001 |
Fish | 7 ± 13.56 | 5.90 ± 11.50a | 6.70 ± 12.80 | 7.48 ± 14.42b | 7.91 ± 15.14b | < 0.001 | 5.85 ± 9.99a | 5.65 ± 10.98 | 7.65 ± 14.93b | 8.85 ± 16.90b | < 0.001 |
Dairy | 89.84 ± 60.16 | 106.99 ± 76.74a | 94.95 ± 53.32b | 89.96 ± 53.41b | 67.47 ± 45.57b | < 0.001 | 104.2 ± 53.30a | 95.85 ± 52.83b | 86.20 ± 59.35b | 73.09 ± 69.35b | < 0.001 |
Legumes and nuts | 25.20 ± 19.14 | 29.78 ± 25.53a | 25.64 ± 18.63b | 24.07 ± 14.99b | 21.31 ± 14.35b | < 0.001 | 27.80 ± 18.12a | 25.24 ± 18.01b | 25.30 ± 20.19b | 22.46 ± 19.80b | < 0.001 |
Whole grains | 29.95 ± 27.33 | 26.68 ± 20.58a | 32.32 ± 24.55b | 33.81 ± 27.92b | 27.01 ± 33.82 | < 0.001 | 34.97 ± 24.53a | 37.83 ± 28.35b | 29.25 ± 28.89b | 17.77 ± 22.65b | < 0.001 |
Refined grains | 85.67 ± 58.18 | 126.70 ± 66.74a | 93.05 ± 47.27b | 67.95 ± 41.92b | 55 ± 45.87b | < 0.001 | 100.5 ± 54a | 102 ± 49.75 | 82.02 ± 59.34b | 58.11 ± 58.05b | < 0.001 |
Sugars | 12.63 ± 11.64 | 10.21 ± 7.58a | 11.88 ± 9.05b | 13.36 ± 11.61b | 15.07 ± 15.98b | < 0.001 | 12.14 ± 9.27 | 12.74 ± 9.42 | 12.80 ± 12.58 | 12.84 ± 14.47 | 0.210 |
Salt | 2.94 ± 3.68 | 3.21 ± 2.94a | 3.22 ± 3.45 | 3.14 ± 3.89 | 2.21 ± 4.21b | < 0.001 | 4.24 ± 3.83a | 3.61 ± 3.11b | 2.41 ± 3.37b | 1.52 ± 3.73b | < 0.001 |
GI glycemic index, GL glycemic load
IObtained from one-way ANOVA followed by Bonferroni post-hoc test
aFirst quartile is considered as reference quartile
bSignificant difference between quartile with reference quartile (P value < 0.05)
The association between DGI and DGL with the respective prevalence of depression, anxiety and stress in crude and adjusted models are presented in Table 3. There were no significant associations between DGI and DGL with odds of depression or anxiety in crude and adjusted models. However, individuals in the highest quartiles of DGL had the lowest odds of stress (OR: 0.69; 95% CI 0.47–1, P-trend = 0.023). This association remained significant after adjustment for potential confounding variables in model I (OR: 0.45; 95% CI 0.22–0.9, P-trend = 0.023), model II (OR: 0.46; 95% CI 0.22–0.96, P-trend = 0.039) and model III (OR: 0.46; 95% CI 0.22–0.96, P-trend = 0.042).
Table 3.
GI quartile | GL quartiles | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Variables | Q1 | Q2 | Q3 | Q4 | P-trend‡ | Q1 | Q2 | Q3 | Q4 | P-trend |
Depression [n (%)] | ||||||||||
Crude | 1.00 | 0.94 (0.74–1.20)† | 0.86 (0.67–1.10) | 1.08 (0.85–1.36) | 0.672 | 1.00 | 0.96 (0.75–1.22) | 0.78 (0.61–1.01) | 1.10 (0.87–1.39) | 0.717 |
Adjusted model1a | 1.00 | 0.96 (0.75–1.22) | 0.87 (0.68–1.12) | 1.16 (0.90–1.48) | 0.403 | 1.00 | 1.01 (0.79–1.29) | 0.86 (0.64–1.15) | 0.97 (0.63–1.50) | 0.546 |
Adjusted model2b | 1.00 | 0.096 (0.74–1.24) | 0.84 (0.64–1.10) | 1.11 (0.85–1.46) | 0.679 | 1.00 | 1.00 (0.77–1.30) | 0.86 (0.63–1.18) | 0.97 (0.61–1.56) | 0.579 |
Adjusted model3c | 1.00 | 0.096 (0.74–1.24) | 0.84 (0.64–1.10) | 1.12 (0.85–1.46) | 0.653 | 1.00 | 1.00 (0.77–1.30) | 0.86 (0.63–1.18) | 0.97 (0.61–1.55) | 0.604 |
Anxiety [n (%)] | ||||||||||
Crude | 1.00 | 0.99 (0.80–1.22) | 0.90 (0.72–1.12) | 1.16 (0.94–1.43) | 0.248 | 1.00 | 0.95 (0.77–1.17) | 0.89 (0.72–1.10) | 0.90 (0.73–1.12) | 0.292 |
Adjusted model1a | 1.00 | 1.00 (0.80–1.24) | 0.91 (0.73–1.13) | 1.22 (0.98–1.52) | 0.157 | 1.00 | 0.96 (0.77–1.20) | 0.90 (0.70–1.17) | 0.94 (0.64–1.38) | 0.568 |
Adjusted model2b | 1.00 | 0.99 (0.78–1.25) | 0.89 (0.70–1.13) | 1.17 (0.92–1.49) | 0.343 | 1.00 | 0.94 (0.74–1.20) | 0.90 (0.68–1.19) | 0.91 (0.60–1.38) | 0.542 |
Adjusted model3c | 1.00 | 0.99 (0.78–1.25) | 0.89 (0.70–1.13) | 0.94 (0.87–1.02) | 0.323 | 1.00 | 0.94 (0.74–1.20) | 0.90 (0.68–1.18) | 0.91 (0.60–1.38) | 0.573 |
Stress [n (%)] | ||||||||||
Crude | 1.00 | 1.11 (0.77–1.60) | 0.92 (0.63–1.35) | 1.06 (0.73–1.53) | 0.990 | 1.00 | 1.02 (0.72–1.44) | 0.77 (0.54–1.11) | 0.69 (0.47–1.00) | 0.023 |
Adjusted model1a | 1.00 | 1.13 (0.79–1.63) | 0.93 (0.63–1.36) | 1.12 (0.76–1.65) | 0.839 | 1.00 | 0.97 (0.67–1.38) | 0.64 (0.41–1.00) | 0.45 (0.22–0.90) | 0.023 |
Adjusted model2b | 1.00 | 1.02 (0.69–1.51) | 0.87 (0.57–1.31) | 1.09 (0.072–1.65) | 0.881 | 1.00 | 1.07 (0.68–1.50) | 0.65 (0.40–1.05) | 0.46 (0.22–0.96) | 0.039 |
Adjusted model3c | 1.00 | 1.02 (0.69–1.51) | 0.87 (0.57–1.31) | 1.10 (0.72–1.66) | 0.888 | 1.00 | 0.98 (0.68–1.42) | 0.72 (0.40–1.05) | 0.46 (0.22–0.96) | 0.042 |
GI glycemic index, GL glycemic load
†These values are odds ratios (95% CIs)
‡Obtained from logistic regression by considering quartiles of GI & GL as ordinal variable
aAdjusted for age, gender and total energy intake
bAdditionally adjusted for physical activity, marital status, smoking, education, job status, multi-vitamins use, diabetes, hypertension
cFurther adjustment BMI
Discussion
This cross-sectional study assessed the association of dietary DGI and DGL with psychological disorders in an Iranian population. No significant association was observed between DGI and odds of depression, anxiety, and stress in crude and adjusted models. There was also no significant relationship between DGL and odds of depression or anxiety in crude and adjusted models; however, higher DGL was associated with lower odds of stress in all models.
A systematic review and meta-analysis by Salari-moghaddam et al. [33] was performed on studies with different designs to investigate the possible relation between DGI or DGL and depression. In line with our results, no significant association between DGI or DGL and odds of depression was found in cross-sectional studies. Although a positive association was observed between DGI and risk of depression in cohort studies, the number of studies was limited (n = 2) with significant heterogeneity between them [33].
Our results showed no significant association between DGI or DGL and odds of anxiety. In agreement with the current study, Haghighatdoost et al., after adjusting for confounders (marital status, education, physical activity, smoking, dietary intakes, and BMI) showed similar findings [19]. Another study with a cross-over clinical trial design examined the effects of a high GL diet on mental health. Consuming 28 days of a high GL diet did not alter tension-anxiety compared to the diet with a low GL [34].
There was also no association between DGI and stress. However, in line with a previous study [19], being in the highest quartiles of DGL in our study was associated with lower odds of stress. This inverse association can be attributed to the effects of sugar-rich foods on the hypothalamic–pituitary–adrenal (HPA) axis. Under stressful conditions, the HPA releases stress hormones (corticosteroids) that increase the desire for sugar rich foods that provide inhibitory feedback on the hypothalamus. Therefore, participants of the higher quartiles of DGL consumed more sugar-rich foods, which can lower stress by decreasing HPA axis activity [35, 36]. Furthermore, serotonin is a neurotransmitter that has an essential role in mood regulation. Foods with high GL induce insulin secretion which facilitates tryptophan uptake and serotonin production in the brain and thereby lowers stress [15]. However, it must be kept in mind that long-term consumption of food with high GL leads to blood glucose fluctuations and increase the risk of diabetes [37]. Thus, caution should be taken to account when interpreting these results since several studies reported that patients with diabetes have a higher risk of mental disorders compared to healthy people [38–40].
Besides the potential strengths of our study such as a large sample size covering both urban and rural areas, recruitment of well-trained interviewers, using a comprehensive and validated FFQ for evaluating dietary intake, and controlling for possible confounders, there are some limitations. First, the cross-sectional data of this study prevents any inference of causality between DGL and stress. Second, no biochemical measures were assessed in our study, which might limit the detection of patients with chronic disease. Furthermore, although the FFQ used in this study was validated for carbohydrate and intake of other nutrients, the validation for DGI or DGL was not performed. Thus, the observed association may be real or related to the quality of the questionnaire. Also, due to the absence of a reliable Iranian food composition table the USDA food-nutrient database was used, which is another limitation of this study. Finally, residual confounding from unknown or unmeasured variables could affect our results.
Conclusion
In summary, an inverse association was found between DGL and likelihood of stress among Iranian adults. However, considering this point that long-term consumption of food with high GL may increase the risk of chronic diseases especially obesity and diabetes, we can not recommend high glycemic load dietary sources to the general population. Therefore, to clarify the effects of DGL or DGI on psychological profiles, further longitudinal studies such as randomized controlled trials are needed in at-risk populations.
Acknowledgements
We thank Yazd people who participated in YaHS.
Author contributions
SK, MaM, AN and AA: designed and conducted the study; MD and MoM: analyzed the data; MD and AA: wrote the manuscript SK, ID, and MoM: critically revised the manuscript; SK, AN and MaM: supervised the study. All authors read and approved the final manuscript.
Funding
This study is supported by Shahid Sadoughi University of Medical Sciences.
Availability of data and materials
The data and materials of the current study are available from the corresponding author on reasonable request.
Declarations
Ethics approval and consent to participate
We confirm that all methods were carried out in accordance with Shahid Sadoughi University of Medical Sciences guidelines and regulations. Written informed consent was taken from all participants. The research was approved by the Ethics Committee of Shahid Sadoughi University of Medical Sciences, Yazd, Iran (Ethic code: 931188).
Consent for publication
Not applicable.
Competing interests
Not applicable.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Ali Amirinejad and Mina Darand are both in the first name position
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Associated Data
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Data Availability Statement
The data and materials of the current study are available from the corresponding author on reasonable request.