Background
Mental disorders can contribute to the higher risk of chronic diseases, years lost due to disability, and mortality among people [
1,
2]. Depression and anxiety are two common mental disorders worldwide and are also more common among females than males [
3]. According to an Iranian report, females are more likely than males to express mental disorders (28.2% compared to 19.28%) [
4]. Iranian studies that examined depression, anxiety, and stress based on the Depression Anxiety Stress Scales-21 item (DASS-21) have shown a consistent result; they reported a higher mean score for all three parameters in females than males [
5,
6]. Additionally, it is noted that 10 to 20% of adolescents (aged 10–19 years) are affected by mental disorders, which makes them vulnerable to poor mental health and related physical problems, including infection, respiratory conditions, and weight problems [
7,
8]. Overall, mental disorders have been indicated to correspond to 13% of the global burden of disease and injury in adolescents [
9]. Considering the high burden of this condition that adversely affects the quality of this critical period of life and its high prevalence among female adolescents, it is crucial to assess the practical approaches that attenuate this disorder.
Social support, socioeconomic status (SES), and health behaviors are affecting factors that concern nutritional status and could influence mental health [
10,
11]. Therefore, along with various factors, diet is a critical modifiable factor that appears to have a vital role in psychological status [
12]. Studies concerning healthy dietary patterns, nutritional factors, and dietary habits indicate the diets which are high in vegetables, fruits, whole grains, fish, lean meats, and nuts, including the Mediterranean diet, Norwegian diet, and the Prudent diet, are associated with a lower risk of mental disorders [
13‐
16]. While, unhealthy dietary patterns such as a western diet high in red meat, processed products, saturated fat, alcohol, and sugar are linked to a higher risk of mental disorders. These unhealthy dietary patterns are known as pro-inflammatory factors that trigger the induction of inflammation [
13‐
15,
17]. Oxidative stress is induced by inflammation, which lowers cellular antioxidant capacity [
18]. Investigations indicate that diets with high antioxidant content may play a key role in modulating inflammation [
19]. In the context of the indicated investigations, it seems that some nutritional assessment tools such as dietary inflammatory index (DII) and dietary antioxidant index (DAI) [
20,
21] can be used as a practical strategy for assessing the nutritional status and related mental health [
22].
The DII has been developed to determine the pro- and anti-inflammatory potential of the whole diet [
23] and has been demonstrated to be related to inflammatory biomarkers [
24‐
26]. Several studies have conducted investigations into the relationship of DII and conditions, including metabolic syndrome in American and French adults [
27,
28], cardiovascular disease in French and Spanish adults [
28,
29], cancer in postmenopausal American women, French, Italian, and American adults [
30‐
36], and mortalities in British adults [
37,
38]. Additionally, this index has been validated in Iran [
39,
40]. To date, limited studies have examined the relationship between DII and mental health. We are aware of studies concentrating on DII and depression and anxiety [
13,
41‐
45], but little attention has been devoted to DII and other mental health parameters.
The DAI is used to estimate antioxidant content in the whole diet [
46,
47]. The relationship between the DAI and the risk of several diseases such as metabolic syndrome [
48], cancer [
49], cardiovascular disease [
50], and although mortality [
51,
52] has been shown recently. Studies regarding dietary total antioxidant capacity (DTAC) and mental health parameters, including stress, depression, and anxiety, also indicated that DTAC was inversely associated with these mental health parameters [
20,
21,
53‐
55]. Therefore, due to the association between DTAC and mental health problems, it seems that DAI may be used as a key tool for reducing mental health problems. In the current study, the DAI was used as a comprehensive tool that can evaluate the whole diet, while other related tools like dietary antioxidant quality score can assess only limited micronutrients [
56]. In previous studies, the effect of single micronutrients affecting the antioxidant system was mainly investigated [
57,
58], but in the DAI, the impact of six major micronutrients with an antioxidant role is examined as an index [
59]. Using this index allows researchers to analyze the effects of antioxidants more comprehensively.
As far as we are aware, no previous study has evaluated the association of DII and DAI with depression, anxiety, and stress in female adolescents. Given the limited data, we aimed to assess DII and DAI's association with depression, anxiety, and stress in Iranian adolescent girls.
Results
The study flowchart was depicted in Fig.
1. The demographic findings of the participants are presented in Table
1 based on DII and DAI tertiles. The mean (SD) of age for all participants was 15.4 (1.1). The frequency of normal weight and overweight based on BMI z-score for all participants was 69.8%, 19.4%, respectively. Depression, anxiety, and stress were present in 21.4%, 26.6%, and 25.7% of the subjects, respectively. Demographic variables including mother and father education and father job were significantly different between DII tertiles (
p < 0.05). However, there was no statistically significant difference considering other demographic variables including weight, height, BMI z-scores, mother job and family income. In different tertiles of DAI, the mean (SD) of age was significantly different (
p = 0.009). Other demographic variables were not statistically different.
Table 1
Demographic characteristics of the study subjects (n = 350)
Age (years) | 15.4 (1.1) | 15.5 (1.1) | 15.4 (1.2) | 15.4 (1.1) | 0.894 | 15.7 (1.2) | 15.4 (1.1) | 15.2 (1.1) | 0.009 |
Weight (kg) | 57.2 (11.9) | 55.7 (11.0) | 57.9 (12.4) | 58.1 (12.2) | 0.207 | 58.6 (13.0) | 57.1 (11.6) | 56.0 (10.9) | 0.228 |
Height (cm) | 161.1 (5.58) | 160.7 (5.7) | 161.7 (5.6) | 160.9 (5.4) | 0.362 | 160.8 (5.3) | 161.6 (5.8) | 161.1 (5.6) | 0.621 |
BMI z-score |
Severe Thin | 7 (2.1) | 4 (3.5) | 1 (0.9) | 2 (1.8) | 0.249 | 2 (1.7) | 1 (0.9) | 4 (3.4) | 0.518 |
Thin | 30 (8.8) | 13 (11.3) | 13 (11.6) | 4 (3.5) | 6 (5.2) | 11 (10.1) | 13 (11.2) |
Normal | 238 (69.8) | 76 (66.1) | 76 (67.9) | 86 (75.4) | 82 (70.7) | 77 (70.6) | 79 (68.1) |
Overweight | 66 (19.4) | 22 (19.1) | 22(19.7) | 22 (19.3) | 26 (22.5) | 20 (18.3) | 20 (17.2) |
Mother education |
Illiterate | 11 (3.17) | 4 (3.4) | 4 (3.6) | 3 (2.6) | 0.012 | 5 (4.3) | 3 (2.6) | 3 (2.6) | 0.365 |
Under Diploma | 149 (43.0) | 34 (28.8) | 53 (47.3) | 62 (53.0) | 48 (41.0) | 51 (45.1) | 50 (42.7) |
Diploma | 130 (37.5) | 56 (47.5) | 36 (32.1) | 38 (32.5) | 39 (33.3) | 40 (35.4) | 51 (43.6) |
Academic | 57 (16.4) | 24 (20.3) | 19 (17.0) | 14 (12.0) | 25 (21.4) | 19 (16.8) | 13 (11.1) |
Father Education |
Illiterate | 8 (2.33) | 3 (2.6) | 3 (2.7) | 2 (1.7) | 0.001 | 5 (4.3) | 2 (1.7) | 1 (0.88) | 0.367 |
Under Diploma | 138 (40.1) | 29 (24.8) | 51 (45.9) | 58 (50.0) | 45 (38.8) | 53 (46.1) | 40 (35.4) |
Diploma | 104 (30.2) | 51 (43.6) | 26 (23.4) | 27 (23.3) | 34 (29.3) | 30 (26.1) | 40 (35.4) |
Academic | 94 (27.3) | 34 (29.1) | 31 (27.9) | 29 (25.0) | 32 (27.6) | 30 (26.1) | 32 (28.3) |
Mother Job |
Housewife | 305 (89.2) | 99 (85.3) | 101 (89.4) | 105 (92.9) | 0.332 | 102 (88.7) | 100 (88.5) | 103 (90.3) | 0.973 |
Retired | 7 (2.1) | 2 (1.7) | 3 (2.6) | 2 (1.8) | 3 (2.6) | 2 (1.8) | 2 (1.7) |
Employed | 30 (8.8) | 15 (12.9) | 9 (8.0) | 6 (5.3) | 10 (8.7) | 11 (9.7) | 9 (7.9) |
Father Job |
Retired | 39 (12.0) | 16 (14.2) | 15 (14.4) | 8 (7.4) | 0.029 | 15 (14.0) | 10 (9.1) | 14 (13.0) | 0.732 |
Unemployed | 187 (57.5) | 55 (48.7) | 57 (54.8) | 75 (69.4) | 63 (58.9) | 64 (58.2) | 60 (55.6) |
Employed | 99 (30.5) | 42 (37.2) | 32 (30.8) | 25 (23.1) | 29 (27.1) | 36 (32.7) | 34 (31.5) |
Family Income |
Low | 41 (12.3) | 15 (13.2) | 17 (15.6) | 9 (8.2) | 0.169 | 18 (16.2) | 12 (10.7) | 11 (10.0) | 0.632 |
Moderate | 260 (78.1) | 84 (73.7) | 82 (75.2) | 94 (85.4) | 84 (75.7) | 88 (78.6) | 88 (80.0) |
High | 32 (9.6) | 15 (13.2) | 10 (9.2) | 7 (6.4) | 9 (8.1) | 12 (10.7) | 11 (10.0) |
Distribution of energy and nutrient intake according to the DII and DAI tertiles is shown in Table
2. Significant differences in energy and nutrients were observed in the DAI tertiles but did not differ among the DII tertiles. Linear regression analysis of the association between DII and score of depression, anxiety, and stress showed that this association was not statistically significant after adjusting for confounding variables including: age, energy intake, BMI, family income and mother and father education (Table
3).
Table 2
Dietary intakes of subjects across tertiles of dietary inflammatory index (DII) and dietary antioxidant index (DAI) a
Energy (kcal/day) b | 1889.07 (899.67) | 1819.95 (885.31) | 1940.72 (999.66) | 0.613 | 1327.49 (460.70) | 1709.97 (527.44) | 2612.52 (1107.91) | < 0.001 |
Carbohydrate (g/day) b | 286.53 (118.01) | 278.48 (110.08) | 283.05 (123.21) | 0.871 | 217.90 (82.49) | 263.29 (76.35) | 366.88 (129.76) | < 0.001 |
Protein (g/day) b | 66.44 (27.80) | 63.32 (26.61) | 64.29 (29.75) | 0.625 | 49.07 (14.63) | 56.70 (16.46) | 87.05 (36.95) | < 0.001 |
Fat (g/day) | 46.66 (30.88–75.00) | 48.09 (29.00–64.12) | 49.00 (33.95–73.14) | 0.341 | 30.08 (21.72–40.97) | 48.09 (34.00–70.00) | 71.32 (55.04–98.33) | < 0.001 |
SFA (g/day) | 16.30 (10.99–23.67) | 15.80 (10.90–21.95) | 16.36 (12.42–25.50) | 0.223 | 11.30 (8.39–14.33) | 16.15 (12.24–21.95) | 23.00 (18.55–34.45) | < 0.001 |
MUFA (g/day) | 13.00 (8.94–21.98) | 14.32 (7.58–19.47) | 15.00 (9.31–21.36) | 0.303 | 8.73 (5.32–12.14) | 14.03 (9.57–20.42) | 21.66 (16.65–28.80) | < 0.001 |
PUFA (g/day) | 10.58 (5.22–16.70) | 10.67 (4.33–17.49) | 9.54 (5.94–16.45) | 0.968 | 5.70 (2.84–8.99) | 10.04 (5.45–16.50) | 16.66 (11.90–26.90) | < 0.001 |
Linoleic Acids (g/day) | 9.03 (4.49–15.30) | 9.45 (3.68–16.06) | 8.68 (4.60–15.30) | 0.970 | 4.29 (1.94–7.55) | 9.03 (4.37–15.67) | 15.00 (10.38–23.94) | < 0.001 |
Linolenic Acids (g/day) | 0.19 (0.06–0.38) | 0.13 (0.05–0.40) | 0.11 (0.45–0.34) | 0.650 | 0.06 (0.01–0.12) | 0.18 (0.05–0.37) | 0.30 (0.13–0.57) | < 0.001 |
Dietary Fiber (g/day) b | 13.31 (7.07) | 11.82 (5.03) | 13.44 (7.35) | 0.117 | 8.25 (4.04) | 12.80 (5.46) | 17.54 (6.45) | < 0.001 |
Vitamin A (RE/day) | 658.90 (394.00–1081.00) | 671.45 (342.25–1014.25) | 593.10 (343.55–1033.50) | 0.850 | 378.50 (228.70–555.35) | 659.45 (388.52–933.25) | 1038.00 (672.00–1888.00) | < 0.001 |
Vitamin D (µg/day) | 0.90 (0.12–1.97) | 0.81 (0.06–2.09) | 0.52 (0.04–1.81) | 0.787 | 0.18 (0.02–1.27) | 0.82 (0.10–2.09) | 1.16 (0.35–2.40) | < 0.001 |
Vitamin K (µg/day) | 43.20 (22.37–90.54) | 39.65 (19.60–67.70) | 37.00 (17.94–62.68) | 0.157 | 22.21 (13.95–39.24) | 42.68 (20.62–75.95) | 61.80 (35.67–144.90) | < 0.001 |
α-Tocopherol (mg/day) | 4.43 (2.07–8.41) | 4.11 (2.45–7.18) | 3.70 (2.53–6.22) | 0.965 | 2.51 (1.68–3.71) | 4.00 (2.47–6.33) | 7.38 (4.30–12.42) | < 0.001 |
Vitamin C (mg/day) | 68.27 (39.50–115.00) | 61.77 (39.32–105.20) | 64.86 (41.62–104.95) | 0.775 | 36.30 (18.41–49.08) | 73.30 (49.34–96.22) | 118.20 (84.62–156.00) | < 0.001 |
Calcium (mg/day) b | 580.51 (278.05) | 573.04 (321.58) | 533.38 (287.90) | 0.425 | 436.67 (182.51) | 523.37 (230.91) | 726.60 (364.32) | < 0.001 |
Iron (mg/day) b | 13.80 (6.46) | 12.76 (5.22) | 13.86 (7.38) | 0.342 | 9.31 (2.70) | 12.57 (3.88) | 18.56 (7.59) | < 0.001 |
Zinc (mg/day) | 6.14 (4.91–8.71) | 6.05 (4.64–7.31) | 6.00 (4.96–7.93) | 0.495 | 4.60 (3.71–5.38) | 5.93 (5.06–6.91) | 8.90 (7.12–11.24) | < 0.001 |
Copper (mg/day) | 0.91 (0.65–1.30) | 0.88 (0.62–1.25) | 0.93 (0.63–1.23) | 0.679 | 0.62 (0.46–0.79) | 0.90 (0.70–1.19) | 1.25 (0.99–1.87) | < 0.001 |
Selenium (mg/day) | 0.05 (0.03–0.09) | 0.05 (0.02–0.08) | 0.05 (0.03–0.07) | 0.728 | 0.03 (0.01–0.05) | 0.05 (0.03–0.07) | 0.08 (0.05–0.12) | < 0.001 |
Table 3
Association of dietary inflammatory index and mental health disorders profile’s scores
Depression |
Model 1 | Ref | -0.002 (-0.96 to -0.96) | 0.58 (-0.37 to 1.54) | 0.230 |
Model 2 | Ref | -0.15 (-1.12 to 0.83) | 0.45 (-0.52 to 1.43) | 0.359 |
Model 3 | Ref | -0.27 (-1.29 to 0.75) | 0.32 (-0.69 to 1.34) | 0.536 |
Anxiety |
Model 1 | Ref | -1.05 (-2.31 to 0.20) | 0.37 (-0.87 to 1.62) | 0.566 |
Model 2 | Ref | -1.25 (-2.51 to 0.004) | 0.29 (-0.95 to 1.55) | 0.645 |
Model 3 | Ref | -1.20 (-2.50 to -0.09) | 0.46 (-0.84 to 1.76) | 0.488 |
Stress |
Model 1 | Ref | -0.35 (-1.46 to 0.74) | 0.11 (-0.97 to 1.21) | 0.836 |
Model 2 | Ref | -0.54 (-1.66 to 0.57) | -0.0001 (-1.11 to 1.11) | 0.999 |
Model 3 | Ref | -0.57 (-1.73 to 0.59) | 0.14 (-1.02 to 1.31) | 0.806 |
Table
4 represents the data of association between DAI and score of mental health profile. After adjusting for confounders, there was a significant inverse association of DAI with depression and anxiety. However, there was not a statistically significant association between DAI and stress.
Table 4
Association of dietary antioxidant index and mental health disorders profile’s scores
Depression |
Model 1 | Ref | -1.17 (-2.13 to -0.21) | -1.25 (-2.21 to -0.30) | 0.010 |
Model 2 | Ref | -0.96 (-1.94 to 0.02) | -1.20 (-2.17 to -0.22) | 0.016 |
Model 3 | Ref | -1.006 (-2.04 to 0.02) | -1.29 (-2.53 to -0.04) | 0.034 |
Anxiety |
Model 1 | Ref | -1.65 (-2.90 to -0.40) | -1.79 (-3.03 to -0.54) | 0.005 |
Model 2 | Ref | -1.30 (-2.57 to -0.03) | -1.51 (-2.78 to -0.25) | 0.019 |
Model 3 | Ref | -1.22 (-2.55 to 0.10) | -1.60 (-3.21 to -0.003) | 0.041 |
Stress |
Model 1 | Ref | -0.69 (-1.78 to -0.40) | -1.11 (-2.20 to -0.01) | 0.046 |
Model 2 | Ref | -0.56 (-1.69 to 0.56) | -0.98 (-2.10 to 0.14) | 0.087 |
Model 3 | Ref | -0.52 (-1.71 to 0.66) | -0.98 (-2.42 to 0.45) | 0.175 |
Discussion
The present analytical study examining the association of DII and DAI with depression, anxiety, and stress in Iranian females of 14 to 16 years old, revealed a significant negative association between DAI and depression, anxiety, and stress. Besides, the results demonstrate a non-significant positive association between DII and mental health profile score. To date, this study is the first which simultaneously investigates the association of DAI and DII with depression, anxiety, and stress in female adolescents.
We found that there is a non-significant positive association between DII and depression, anxiety, and stress. This finding agrees with a recent study conducted on 3523 participants from France, aged 35–60 years, who were initially free of depressive symptoms. The current prospective study reported no remarkable relationship between DII and depressive symptoms among women. However, a marginally significant link was seen among men [
68]. Moreover, another study regarding DII and anxiety among 11,592 United States adults > 20 years indicated no association between the mentioned parameters [
69]. Our results were in line with another cross-sectional study carried out on 7083 adults aged 35 to 65 years in Iran. The mentioned study did not report a significant association between DII and depression among men. However, a remarkable association was reported among women [
43]. Our findings contrast with other studies conducted on Iranian adolescent girls, which indicated that a higher DII was significantly associated with higher odds of depression and stress levels in adolescent girls of Tehran [
70,
71]; Therefore, due to the different study regions, factors such as residence, ethnicity, local eating habits, would explain these differences. Also, Sánchez-Villegas et al
. assessed 15,093 Spanish participants in a cohort study and found that a higher DII was associated with a higher risk of depression. Furthermore, they reported that this correlation was stronger among older individuals and others with cardiometabolic comorbidities [
45]. The result’s inconsistency may be due to differences in sample size, study populations, geographic areas, study design, eating behavior questionnaires, cooking methods, and applied indices. Regarding statistical procedures, it should be mentioned that Villegas et al
. conducted a cohort study and calculated adjusted hazard ratio using the Cox method, while in our study, due to the cross-sectional design of it, linear regression method was used for analysis and adjusted regression coefficient has been reported in the current study. Therefore, the different statistical procedures could be a reason for the discrepancy between the findings.
Although the relationship between DII and assessed parameters was insignificant, the positive reported association could be considered clinically noteworthy. The mechanisms through which the higher DII scores might induce mental disorders are not entirely elucidated. However, the presented mechanisms propose that higher DII increases the level of inflammatory biomarkers, which may interact with neural function. The released cytokines such as interleukin
(IL)-6, IL-1Ɓ, and tumour necrosis factor alpha develop depression by changing the metabolism of the neurotransmitters [
72‐
74]. Another proposed route is concentrating on the inflammation, stress, and hypothalamic–pituitary–adrenal axis. The related research has shown that the higher DII of diet increases the susceptibility to stress which its mechanisms are not entirely clarified [
75]. Stress affects the hypothalamic–pituitary–adrenal axis and alters the balance of related neurochemicals, leading to depression [
76,
77]. Our results’ non-significant p-value could be due to our sample size, which probably reflects significant results in larger sample sizes.
The DAI significant inverse association with depression and anxiety was noted in the adjusted and unadjusted models. However, the significant relationship between DAI and stress was only observed in the unadjusted model. Our study was in line with the previous findings, which indicated that dietary patterns, which are higher in vegetables, fruits, and fish, demonstrate an inverse relationship with depression [
78‐
80], dysthymia, and anxiety [
80]. In addition, other studies reported that lower antioxidant intake in the diet is associated with depression, which does not always appear with a meaningful difference in the antioxidant status of normal and depressed cases [
81]. In contrast with present findings, several studies did not report a remarkable relationship between dietary antioxidant capacity and depression [
53], anxiety [
82], and stress [
20].
Based on the existing research, the oxidant-antioxidant imbalance has a crucial role in developing mental disorders. It has been indicated that the high levels of reactive oxygen and nitrogen species may result in the dysfunction of biomolecules such as DNA and mitochondria, which is the underlying cause of the psychiatric disorder [
83]. Oxidative stress and DNA damages are explained in light of telomeres. Telomeres are structures that consist of repetitive DNA sequences and are aimed to protect the chromosome ends. The process of telomere shortening leads to DNA damage. High levels of oxidative stress accelerate the telomere shortening, contributing to mental health problems [
84,
85]. On the other hand, alternations in the oxidation rate of synaptic molecules and increased oxygen levels result in the decline of neurotransmitters, which play an essential role in increasing the odds of mental health conditions [
86,
87].
As the strengths of the current study, we should mention that the use of dietary record in this study reduced the likelihood of recall bias. In addition, the information was collected by a trained expert, which minimized the measurement error. Moreover, the validated questionnaires were used, and a broad range of confounders was controlled. Also, it is noteworthy that DAI and DII have been validated in Iran [
40,
59,
67]. Finally, the data were finalized by a nutrition epidemiologist, and its quality was confirmed. However, our findings should be noted in light of potential limitations. The cross-sectional design of the present study cannot determine causality. Also, a validated 3-day food record was used to estimate dietary intake; thus, some measurement errors should be considered. It is also worth noting that there are not any measurements of inflammatory biomarkers in this study. In addition, no data is presented regarding the age of menarche. The present study was carried out on female cases that indicate that future prospective studies should be conducted on both sexes and different study populations with various dietary patterns. Additionally, it is recommended that future studies measure inflammatory biomarkers and provide data regarding the age of menarche to shed light on these points.
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