Skip to main content

Adherence to the nordic diet is associated with anxiety, stress, and depression in recovered COVID-19 patients, a case-control study

Abstract

Background

Follow-up of COVID-19 recovered patients to discover important adverse effects on other organs is required. The psychological health of COVID-19 patients may be affected after recovery.

Aim

We aimed to evaluate the association between adherence to the Nordic diet (ND) and psychological symptoms caused by COVID-19 after recovery.

Method

Dietary data on 246 qualified adults (123 cases and 123 controls). The dietary intake in this case-control study was calculated by a reliable and valid food frequency questionnaire (FFQ). Depression Anxiety Stress Scale (DASS), Pittsburgh Sleep Quality Index (PSQI), Insomnia Severity Index (ISI), and Short-Form Health Survey (SF-36) were used to analyze participant’s anxiety, stress, depression, sleep quality, insomnia, and quality of life of participants.

Results

There was a significant inverse relationship between total anxiety, stress, and depression scores and the intake of whole grains (P < 0.05). Furthermore, there was a significant inverse association between depression and fruit intake (P < 0.05). A significant negative correlation was found between insomnia and sleep quality and the intake of root vegetables (P < 0.05). In the multinomial-regression model, a significant association between the Nordic diet and anxiety, stress, and depression was found only in the case group (OR = 0.719, 95% CI 0.563–0.918, p-value = 0.008; OR = 0.755, 95% CI 0.609–0.934, P-value = 0.010, and, OR = 0.759, 95% CI 0.602–0.956, P-value = 0.019 respectively).

Conclusion

Adherence to the Nordic diet might reduce anxiety, stress, and depression in recovered COVID-19 patients.

Peer Review reports

Introduction

Coronavirus disease 2019 (COVID-19) is an infectious disease that caused patients a wide range of physical and psychological problems [1]. Some studies noticed COVID-19 patients experience psychological and psychiatric problems after infection such as insomnia, anxiety, depression, delirium, memory loss, and loss of concentration [2, 3]. These psychological symptoms may continue after convalescence from COVID-19 and harm the mental health of recovered patients. Impaired mental health reduces the quality of life [4], so it should be considered during hospitalization and recovery. These patients suffer from psychological sequelae after COVID-19, so it is essential to follow up patients that recovered from COVID-19 [5]. Li et al. reported that 35% of COVID-19 patients have severe to moderate psychological symptoms [6]. A systematic review found anxiety and insomnia to occurred in 35.7% and 41.9% of patients with acute SARS, falling to 12.3% and 12.1% at follow-up [4].

Dietary interventions with relatively moderate effect sizes can significantly reduce the mental and neurological disease burden through food and nutrient-based approaches [7, 8]. ND is a “plant-based” dietary pattern that recommends protein intake from plant sources. It also recommends consumption of fruits and vegetables, whole grains, seeds, and nuts [9]. To increase protein intake, ND recommends increased the consumption of legumes and fish [9]. Along with all these recommendations, there is a limit on the use of red meat and processed foods [10]. Some studies have shown that ND has beneficial effects on psychological symptoms [10, 11]. Therefore, it is essential to assess the diet of COVID − 19 recovered patients based on their symptoms. Nutraceutical interventions are increasingly being used in psychiatric practice [5]. Jacka et al. demonstrated impressive effects of a 3-month dietary intervention on moderate-to-severe depression with a 32% remission in the intervention group [12]. Another study of the Nordic diet reported better improvement in depression in the ND group compared to the control group [13].

Recovered COVID-19 patients faced a severely stressful experience that challenged their psychological health. It is necessary to follow up these people and control their diet to improve their impaired mental health. Considering a healthy diet can improve psychological symptoms after COVID-19. Few studies have been performed to analyse the Nordic diet on psychological disorders. In this case-control study, we attempted to investigate the association between adherence to the ND and psychological responsibility in both recovered COVID-19 patients and healthy people.

Method

Study design

The present case-control study was performed between November 2020 to January 2021 at the clinic of Qaem Hospital, Mashhad, Iran. Adult subjects aged ≥ 30 years old who were affected by COVID-19 within the last 1 month. Participants had a negative CT scan or PCR test for COVID-19 when the interview was started. Also, we randomly selected the control group from adults > 30 years who did not have a COVID-19 history. These participants were referred to the nutrition clinic of the Qaem Hospital. Subjects who had a history of depression treatment in the last 6 months, autoimmune diseases, cancer, renal or hepatic failure, and metabolic bone disease were excluded. Adherence to a special dietary pattern such as a vegetarian diet was another exclusion criteria.

In the control group, subjects with a history of COVID-19 according to CT scan or PCR test, renal or hepatic failure, autoimmune diseases, having a history of depression treatment in the last 6 months, cancer, and adherence to a special diet were excluded. We enrolled one matched control subject for every case. Also, the case and control groups corresponded according to age and gender (± 5 years). In the present study, 246 subjects who had the eligibility criteria were recruited, of which a total of 240 subjects (120 cases and 120 controls) were encompassed in the last analysis. The mean energy of two cases and four controls were outside ± 3 standard deviation (SD), so they were excluded. All cases and control filled out noticed written agreement, and all methods were performed based on related guidelines and regulations or the Helsinki affirmation.

General and anthropometric characteristics

Demographic and anthropometric features, such as age, gender, height, weight, and education level were carried out by an expert nurse. Weight was measured by a calibrated personal scale. the fixed measuring tape was used to find out the height. Body weight (kg)/ (body height (m))2 was applied for calculating body mass index (BMI).

Dietary intake assessment

The food intake of patients was determined by a reliable and valid 68-item semi-quantitative food frequency questionnaire (FFQ) [14, 15]. The FFQ was completed through face-to-face interviews. Food analysis was undertaken using Nutritionist IV software (N-Squared Computing, Cincinnati, OH, USA). Healthy Nordic Food Index (HNFI) scores were assessed based on the method of Olsen et al. [16]. To calculate the HNFI, we consider six groups with the same micronutrient amount. Daneshzad et al. [17] validated the modified ND score for the Iranian population, including (a) fish (fish conserved in oil and salt and other fish), (b) legumes (soybeans, beans, and lentils), (c) whole grains, (d) fruit (fresh and dried fruits, fruit juice) (e) root vegetables (onion, garlic, and potato) and (f) cabbages and vegetables (lettuce, tomato, cucumber, spinach, and leafy vegetables), We calculated below- and above-average intake for every item. Each group was classified based on the score obtained (scoring 0–1 points shows “low adherence”, scoring 2–3 points “medium adherence”, and scoring 4–6 points “high adherence”). ND was not given to any individuals and agreement to ND was assessed.

Depression anxiety stress scales (DASS)

Depression anxiety stress scales (DASS) are among the most valid and exact tools to analyze mental conditions [18]. It is a questionnaire that generally includes three subscales, seven questions, and 21 items. Each question score ranges from 0 to 3 on a four-point scale to recognize the severity of mental disorders, consisting of depression, anxiety, and stress. In DASS, a lower score reveals a lower degree of negative mood, and a higher score indicates a more severe degree of negative emotion. In the Iranian population, the validity and reliability of the used version of DASS in this study, have been reported formerly [19]. The anxiety, stress, and depression scores were separated into two categories: No or minimal scores and some degree of mental disorder. According to the scores obtained from each item decided as follows: (≤ 7, No), (> 7, some degree of anxiety), (≤ 14, No), (> 14 some degree of stress), (≤ 9, No), (> 9, some degree of depression)

Pittsburgh sleep quality index (PSQI)

The sleep quality of the patients was analyzed using a 19-item self-reported PSQI questionnaire that evaluates sleep quality during the last 30 days [20]. It consists of 19 objects combined for 7 component scores, containing sleep duration, sleep latency, subjective sleep quality, sleep disturbances, use of sleep medication, daytime dysfunction, and habitual sleep competence. The responses are scored on a 3-point scale, ranging from 0 to 3. The total score for sleep quality is measured by combining the 7 component scores, which range from 0 to 21. Subjects were categorized into two groups according to their PSQI score: the good-sleeper group (PSQI ≤ 5) and the poor-sleeper group (PSQI > 5). Also, the validity of the PSQI Persian version has been confirmed in 2012 [21].

Insomnia severity index (ISI)

The Insomnia Severity Index (ISI) is a seven-item self-report tool for determining patients’ insomnia symptoms and their outcomes. The aspects measured included severeness of sleep onset, interference of sleep difficulties with daytime functioning, sleep dissatisfaction, early morning awakening problems, sleep preservation, distress caused by sleep difficulties, and noticeability of sleep problems by others [22]. According to severeness, each item scored on a 0–4 scale with a full scale ranging from 0 to 28. The scoring system reports as follows: severe insomnia [22,23,24,25,26,27,28], mild insomnia [15,16,17,18,19,20,21], sub-threshold insomnia [8,9,10,11,12,13,14], and no insomnia (0–7). In the Iranian population the reliability and validity of the Persian version of this questionnaire have been confirmed (Cronbach’s a > 0.8 and intra-class correlation coefficient > 0.7) [23].

Quality of life questionnaire

We used the Short-Form Health Survey (SF-36) validated questionnaire to analyze the general quality of life. SF-36 calculated the overall healthy quality of life based on Mental Health, General Health, Vitality, Role Emotional, Social Functioning, Body Pain, Role Physical, and Physical Functioning. Scores of this questionnaire range from 0 to 100 and the higher score shows a higher quality of life. The SF-36 was assessed in the Iranian population in a prior study and revealed construct validity and good reliability [24].

Statistical analysis

The Kolmogorov-Smirnov test was used to analyze the normality of variables. Descriptive statistics, such as SD and mean, were determined for all variables and expressed as mean ± SD for normally distributed variables and median and interquartile range (IQR) for non-normally distributed variables. Also, categorical indices were indicated by percent. We used Chi-square test and independent sample t-test to compare variables between case and control groups. For food intake comparison among two groups besides tertiles of HNFI score, a Multivariate Analysis of Variance (MANOVA) test was performed. Pearson correlation test was used to show an association between components of the Nordic diet and psychological scores. Eventually, we used multinomial logistic regression to evaluate the correlation between the classification of the adherence ND and psychological scores. Statistical package for social sciences (SPSS) version 18 (IBM Inc. Chicago, IL, USA) was used to perform statistical analyses, and rpart package in R version 4.1.2 (R Core Team. 2020). Statistical significance was considered as p-value < 0.05.

Results

Demographic and anthropometric characteristics of the participants in case and control groups are shown in Fig. 1. The case and control group mean age was 60.38 ± 13.61 and 57.43 ± 7.71 years, respectively (Fig. 1c). The case group had 45% females and the control group had 45.6% females (Fig. 1a). There were no significant differences in gender, age, weight, and BMI between case and control groups (p > 0.05). Nevertheless, there was a significant difference in educational level and height between the two groups (p < 0.05) (Fig. 1b).

Fig. 1
figure 1

Demographic and clinical characteristics of the participants between groups. (a) Gender, (b) Education, (c) Age, (d) Anthropometric measurements

Table 1. demonstrates the comparison of the mean energy, macronutrients, and components of the HNFI score in classification of adherence ND between both groups. There was a significant difference in energy consumption between the case and control groups (p = 0.036). Regarding components of the HNFI score, there were significant differences between fruits, legumes, cabbage and vegetables, fish intakes, and classification of HNFI score in both groups (p < 0.05). There was a significant difference in carbohydrate and whole grain intakes between classification of adherence HNFI score in case subjects (p < 0.05).

Table 1 Comparison of energy-adjusted dietary intakes in Nordic diet adherence between groups

Heat map (Fig. 2) demonstrates that there was a significant opposite association between total anxiety, stress, and depression scores and the consumption of whole grains (r = − 0.35; P < 0.05, r = − 0.36; P < 0.05, r = − 0.33; P < 0.05 respectively). Furthermore, there was a significant opposite relation between depression and fruit intake (r = -0.29; P < 0.05). A significant negative association was observed between insomnia and sleep quality and the consumption of root vegetables (r = − 0.26; P < 0.05, r = − 0.28; P < 0.05, respectively).

Fig. 2
figure 2

Correlation between components of Nordic diet and psychological tests in case and control groups

Multinomial logistic regression analyses were applied to evaluate the relationship between psychological function and the Nordic diet in crude and adjusted models. As observed in Table 2, the odds ratio was adjusted for gender, age, educational levels, and energy intake in the adjusted model. High adherence to the ND was significantly related to anxiety, stress, and depression in the adjusted model (OR = 0.759, 95% CI 0.602–0.956, P-value = 0.019; OR = 0.719, 95% CI 0.563–0.918, p-value = 0.008; OR = 0.755, 95% CI 0.609–0.934, P-value = 0.010, respectively) only in the case group.

Table 2 Multiple-adjusted odds ratio (OR) and 95% confidence intervals (CI) for OR between classification of adherence the Nordic diet

Discussion

This case-control study evaluated the relationship between adherence to the ND and psychological role in 240 adults aged ≥ 30 years old who were healthy and recovered from COVID-19. In this study, we found that more adherence to ND was related to lower odds of anxiety, stress, and depression in recovered COVID-19 patients. Regarding components of the Nordic style, only in the case group, we found a significant opposite correlation between total anxiety, stress, and depression scores and the consumption of whole grains. Also, there was a significant opposite relation between depression and fruit consumption in this group.

The relationship between dietary patterns and psychological health has been considered an important issue [25]. Multiple studies recommended consuming food sources of vitamins and fibre during COVID-19, that are rich in the Nordic diet [26,27,28]. Choosing food like fruits, vegetables, and whole grains which are rich in fibre, antioxidant, and anti-inflammatory constituents might be important in COVID-19 [29]. Brown et al. found that a diet containing mostly whole grains, vegetables, and fruits with low amounts of foods with animal sources decreased the severity of COVID-19 [30]. Another study showed that increasing the intake of fruits, vegetables, and whole grains and decreasing the consumption of red meat, processed meat, sweets, refined cereals, fried food, and sugary drinks have antidepressant effects [31]. In line with our study, a randomized controlled trial performed in 2021 showed that a healthy Nordic diet improves depressive symptoms [13]. Also, a cross-sectional study with 181 subjects, aged between 18 and 25 years old, showed that adherence to a Nordic diet with a high intake of fruits and vegetables reduces stress and anxiety scores [11]. A plant-based diet rich in fibre, resistant starch, and carbohydrates appears to be advantageous because it fills the host’s intestinal with beneficial microbes that have health benefits for COVID-19 patients [29]. Enhancing diet quality improved mood. Dietary patterns rich in omega-3 and fibre may be related to decreased symptoms of anxiety, stress, and depression [32].

People suffer from mental problems after contracting COVID-19 due to the fear of losing people and social rejection. A dietary pattern rich in vegetables and fruits plays a role in improving mental distress [33]. In this study, we revealed that more adherence to ND was associated with less odds of anxiety, stress, and depression score through recovered COVID-19 patients. Our results were in line with the findings of prior studies [11, 13]. We concluded that depression scores were inversely associated with the consumption of fruit. Also, root vegetable consumption was correlated with insomnia and sleep quality among recovered COVID-19 patients. Root vegetable and Fruit intake improve life satisfaction and mental health. A meta-analysis consisting of 446,551 subjects, revealed that vegetable and fruit intake may play an essential function in reducing the depression risk [34]. Some studies estimated that the consumption of fruits can negatively affect mental health [35, 36]. Liu et al. in their meta-analysis indicated that fruit intake lowered depression and anxiety symptoms [37]. Various possible mechanisms could link fruit and vegetable intake with psychological symptoms. Oxidative stress has negative effects on mental health. A large number of antioxidants in vegetables and fruits, such as beta-carotene, folic acid, vitamin E, and vitamin C reduce the harmful oxidative stress effects on mental well-being and improve depression [38]. Fruits and vegetables are rich in different minerals and vitamins like folate. Folate and vitamin B12 deficiency increase the levels of homocysteine and the risk of depression [39]. Also, magnesium deficiency may increase inflammatory factors like C-reactive protein which helps the development of depression [40].

A healthy diet and lifestyle could affect symptoms of mood disorder in recovered COVID-19 patients [5, 41]. Inflammation caused by COVID-19 can affect neurological mechanisms, so having a healthy diet should be prioritized to prevent long-term neurological symptoms from COVID-19 [11]. Therefore, consumption of fibre and whole grains is recommended [42]. Our results revealed a significant relationship between whole grains anxiety, stress, and depression which confirms previous studies [43,44,45]. A cohort study found that regular consumption of whole grains, fruits, and vegetables is inversely related to anxiety and depression risk in elderly persons [6]. Mohammadi et al. in their randomized clinical trial study recognized a positive association between stress and anxiety and whole grains [44]. A previous study revealed that a greater intake of non-refined grains concluded to decrease depression and anxiety severeness [45]. A dietary pattern identified by high whole grain consumption was significantly connected with decreased depression risk [46]. In contrast, high consumption of refined grains was related to more depression risk [47]. Nutritional factors also have a direct and potent effect on neurophysiology [48, 49]. Berk et al. recognized inflammation as a mediating pathway for the development of depression [50]. Evidence suggests that frequent consumption of magnesium-rich foods may improve COVID-induced inflammation. A healthy diet provides sources of magnesium. For example, whole grains are identified as one of the best sources of food due to their magnesium content [51,52,53]. Also, a previous study revealed that a dietary pattern with higher intake of whole grains, fruits, and vegetables reduces inflammation by decreasing IL-6 and CRP in plasma [3]. Whole grains are a rich source of B vitamins like Thiamine, nicotinic acid, pyridoxine, and pantothenic acid but they are not rich in folates unless fortified with folic acid. These vitamins can positively affect mental health [54]. For instance, folate and pyridoxine deficiency are effective in mental health due to their function in the synthesis of neurotransmitters for example serotonin, as well as their coenzyme role in one-carbon metabolism pathways [55].

Conclusion

Our study suggests that adherence to the ND may reduce anxiety, stress, and depression in patients recovered from COVID-19. A dietary pattern rich in fruit and whole grains might be beneficial in treating depressive symptoms in patients who have recovered from COVID-19. Additional large-scale longitudinal studies are essential to substantiate.

Tables.

Data availability

The datasets collected and/or analyzed during the present study are not publicly accessible due to ethical concerns but the corresponding author may provide datasets upon request.

Abbreviations

ND:

Nordic diet

FFQ:

food frequency questionnaire

DASS:

Depression anxiety stress scales

PSQI:

Pittsburgh Sleep Quality Index

ISI:

Insomnia Severity Index

SF-36:

Short-Form Health Survey

COVID-19:

Coronavirus disease 2019

SD:

standard deviation

BMI:

body mass index

HNFI:

Healthy Nordic Food Index

IQR:

interquartile range

MANOVA:

Multivariate Analysis of Variance

SPSS:

Statistical package for social sciences

References

  1. World Health Organization. WHO coronavirus (covid-19) Dashbord [2022-12-23]. Available from: https://covid19.who.int/.

  2. Balachandar V, Mahalaxmi I, Subramaniam M, Kaavya J, Senthil Kumar N, Laldinmawii G, et al. Follow-up studies in COVID-19 recovered patients - is it mandatory? Sci Total Environ. 2020;729:139021.

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  3. Barthorpe A, Rogers JP. Coronavirus infections from 2002 to 2021: neuropsychiatric manifestations. Sleep Med. 2022;91:282–8.

    Article  PubMed  Google Scholar 

  4. Rogers JP, Chesney E, Oliver D, Pollak TA, McGuire P, Fusar-Poli P, et al. Psychiatric and neuropsychiatric presentations associated with severe coronavirus infections: a systematic review and meta-analysis with comparison to the COVID-19 pandemic. Lancet Psychiatry. 2020;7(7):611–27.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Khorasanchi Z, Ahmadihoseini A, Hajhoseini O, Zare-Feyzabadi R, Haghighi M, Heidari M, et al. Adherence to dietary approaches to stop hypertension (DASH) diet in relation to psychological function in recovered COVID-19 patients: a case–control study. BMC Nutr. 2022;8(1):130.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Li H, Xue Q, Xu X. Involvement of the nervous system in SARS-CoV-2 infection. Neurotox Res. 2020;38:1–7.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Owen L, Corfe B. The role of diet and nutrition on mental health and wellbeing. Proc Nutr Soc. 2017;76(4):425–6.

    Article  PubMed  Google Scholar 

  8. Khorasanchi Z, Vahedifard M, Mohammadhasani K, Sharifan Y, Dehnavi Z, Naderian R, et al. Psychological function and serum vitamin D concentration in COVID-19 patients: a cross-sectional study. Reviews Clin Med. 2023;10(3):6–12.

    Google Scholar 

  9. Mithril C, Dragsted LO, Meyer C, Tetens I, Biltoft-Jensen A, Astrup A. Dietary composition and nutrient content of the New Nordic Diet. Public Health Nutr. 2013;16(5):777–85.

    Article  PubMed  Google Scholar 

  10. Hemler EC, Hu FB. Plant-based diets for Personal, Population, and Planetary Health. Adv Nutr. 2019;10(Suppl4):275–s83.

    Article  Google Scholar 

  11. Abbaszadeh A, Saharkhiz M, Khorasanchi Z, Karbasi S, Askari M, Hoseini ZS, et al. Impact of a nordic diet on psychological function in young students. Nutr Health. 2021;27(1):97–104.

    Article  CAS  PubMed  Google Scholar 

  12. Jacka FN, O’Neil A, Opie R, Itsiopoulos C, Cotton S, Mohebbi M, et al. A randomised controlled trial of dietary improvement for adults with major depression (the ‘SMILES’ trial). BMC Med. 2017;15(1):23.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Sabet JA, Ekman MS, Lundvall AS, Risérus U, Johansson U, Öström Å et al. Feasibility and acceptability of a healthy nordic Diet intervention for the treatment of Depression: a Randomized Controlled Pilot Trial. Nutrients. 2021;13(3).

  14. Ahmadnezhad M, Asadi Z, Miri HH, Ebrahimi-Mamaghani M, Ghayour-Mobarhan M, Ferns GA. Validation of a short semi-quantitative food frequency questionnaire for adults: a pilot study. J Nutritional Sci Dietetics. 2017:49–55.

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

    Article  CAS  PubMed  Google Scholar 

  16. Olsen A, Egeberg R, Halkjær J, Christensen J, Overvad K, Tjønneland A. Healthy aspects of the Nordic diet are related to lower total mortality. J Nutr. 2011;141(4):639–44.

    Article  CAS  PubMed  Google Scholar 

  17. Daneshzad E, Emami S, Mofrad MD, Saraf-Bank S, Surkan PJ, Azadbakht L. Association of modified nordic diet with cardiovascular risk factors among type 2 diabetes patients: a cross-sectional study. J Cardiovasc Thorac Res. 2018;10(3):153.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Henry JD, Crawford JR. The short-form version of the Depression anxiety stress scales (DASS‐21): construct validity and normative data in a large non‐clinical sample. Br J Clin Psychol. 2005;44(2):227–39.

    Article  PubMed  Google Scholar 

  19. Sahebi A, Asghari MJ, Salari RS. Validation of depression anxiety and stress scale (DASS-21) for an Iranian population. 2005.

  20. Buysse D, Reynolds C, Monk T, Berman SR, CF DJ III. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice. Res Psychiatry Res. 1989;28(2):193–213.

    Article  CAS  PubMed  Google Scholar 

  21. Moghaddam JF, Nakhaee N, Sheibani V, Garrusi B, Amirkafi A. Reliability and validity of the Persian version of the Pittsburgh Sleep Quality Index (PSQI-P). Sleep Breath. 2012;16(1):79–82.

    Article  Google Scholar 

  22. Morin CM, Belleville G, Bélanger L, Ivers H. The Insomnia Severity Index: psychometric indicators to detect insomnia cases and evaluate treatment response. Sleep. 2011;34(5):601–8.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Yazdi Z, Sadeghniiat-Haghighi K, Zohal MA, Elmizadeh K. Validity and reliability of the Iranian version of the insomnia severity index. Malaysian J Med Sciences: MJMS. 2012;19(4):31.

    Google Scholar 

  24. Montazeri A, Goshtasebi A, Vahdaninia M, Gandek B. The short Form Health Survey (SF-36): translation and validation study of the Iranian version. Qual Life Res. 2005;14(3):875–82.

    Article  PubMed  Google Scholar 

  25. Saharkhiz M, Khorasanchi Z, Karbasi S, Jafari-Nozad AM, Naseri M, Mohammadifard M, et al. The association between adherence to a dietary approaches to stop hypertension (DASH) diet and neuro-psychological function in young women. BMC Nutr. 2021;7(1):21.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Pal J, Sethi D, Taywade M, Pal R. Role of Nutrition and Diet during COVID-19 pandemic: a narrative review. J Family Med Prim Care. 2022;11(9):4942–8.

    Article  PubMed  PubMed Central  Google Scholar 

  27. de Faria Coelho-Ravagnani C, Corgosinho FC, Sanches FFZ, Prado CMM, Laviano A, Mota JF. Dietary recommendations during the COVID-19 pandemic. Nutr Rev. 2021;79(4):382–93.

    Article  PubMed  Google Scholar 

  28. Kiely K, Mase WA, Hansen AR, Schwind J. Association between the Health Belief Model, Exercise, and Nutrition behaviors during the COVID-19 pandemic. Int J Environ Res Public Health. 2022;19(23).

  29. Rishi P, Thakur K, Vij S, Rishi L, Singh A, Kaur IP, et al. Diet, Gut Microbiota and COVID-19. Indian J Microbiol. 2020;60(4):420–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Brown RB. Low dietary sodium potentially mediates COVID-19 prevention associated with whole-food plant-based diets. Br J Nutr. 2022:1–6.

  31. Jacka FN, O’Neil A, Opie R, Itsiopoulos C, Cotton S, Mohebbi M, et al. Correction to: a randomised controlled trial of dietary improvement for adults with major depression (the ‘SMILES’ trial). BMC Med. 2018;16(1):236.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Taylor AM, Holscher HD. A review of dietary and microbial connections to depression, anxiety, and stress. Nutr Neurosci. 2020;23(3):237–50.

    Article  CAS  PubMed  Google Scholar 

  33. Shabbir MA, Mehak F, Khan ZM, Ahmed W, Haq S, Khan MR, et al. Delving the role of nutritional psychiatry to mitigate the COVID-19 pandemic induced stress, anxiety and depression. Trends Food Sci Technol. 2022;120:25–35.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Liu X, Yan Y, Li F, Zhang D. Fruit and vegetable consumption and the risk of depression: a meta-analysis. Nutrition. 2016;32(3):296–302.

    Article  CAS  PubMed  Google Scholar 

  35. Adams TB, Colner W. The association of multiple risk factors with fruit and vegetable intake among a nationwide sample of college students. J Am Coll Health. 2008;56(4):455–61.

    Article  PubMed  Google Scholar 

  36. Allgöwer A, Wardle J, Steptoe A. Depressive symptoms, social support, and personal health behaviors in young men and women. Health Psychol. 2001;20(3):223–7.

    Article  PubMed  Google Scholar 

  37. Liu MW, Chen QT, Towne SD Jr., Zhang J, Yu HJ, Tang R, et al. Fruit and vegetable intake in relation to depressive and anxiety symptoms among adolescents in 25 low- and middle-income countries. J Affect Disord. 2020;261:172–80.

    Article  PubMed  Google Scholar 

  38. Kaur C, Kapoor HC. Antioxidants in fruits and vegetables–the millennium’s health. Int J Food Sci Technol. 2001;36(7):703–25.

    CAS  Google Scholar 

  39. Kim JM, Stewart R, Kim SW, Yang SJ, Shin IS, Yoon JS. Predictive value of folate, vitamin B12 and homocysteine levels in late-life depression. Br J Psychiatry. 2008;192(4):268–74.

    Article  PubMed  Google Scholar 

  40. King DE, Mainous AG III, Geesey ME, Woolson RF. Dietary magnesium and C-reactive protein levels. J Am Coll Nutr. 2005;24(3):166–71.

    Article  CAS  PubMed  Google Scholar 

  41. Khorasanchi Z, Jafazadeh Esfehani A, Sharifan P, Hasanzadeh E, Shadmand Foumani Moghadam MR, Ahmadi O, et al. The effects of high dose vitamin D supplementation as a nutritional intervention strategy on biochemical and inflammatory factors in adults with COVID-19: study protocol for a randomized controlled trial. Nutr Health. 2022;28(3):311–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Mazloom Z, Ekramzadeh M, Hejazi N. Efficacy of supplementary vitamins C and E on anxiety, depression and stress in type 2 diabetic patients: a randomized, single-blind, placebo-controlled trial. Pak J Biol Sci. 2013;16(22):1597–600.

    Article  CAS  PubMed  Google Scholar 

  43. Tsai AC, Chang TL, Chi SH. Frequent consumption of vegetables predicts lower risk of depression in older Taiwanese - results of a prospective population-based study. Public Health Nutr. 2012;15(6):1087–92.

    Article  PubMed  Google Scholar 

  44. Mohammadi MR, Mostafavi S-A, Khalkhali A. Nutrition Bio Shield (NBS) supplement effects on depression, anxiety, stress and food craving in women with depression and obesity: a double-blind randomized controlled trial. Nutrition & Food Science. 2022(ahead-of-print).

  45. Gibson-Smith D, Bot M, Brouwer IA, Visser M, Giltay EJ, Penninx B. Association of food groups with depression and anxiety disorders. Eur J Nutr. 2020;59(2):767–78.

    Article  PubMed  Google Scholar 

  46. Li Y, Lv MR, Wei YJ, Sun L, Zhang JX, Zhang HG, et al. Dietary patterns and depression risk: a meta-analysis. Psychiatry Res. 2017;253:373–82.

    Article  PubMed  Google Scholar 

  47. Moludi J, Moradinazar M, Hamzeh B, Najafi F, Soleimani D, Pasdar Y. Depression relationship with dietary patterns and dietary inflammatory index in women: result from Ravansar Cohort Study. Neuropsychiatr Dis Treat. 2020;16:1595–603.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Gómez-Pinilla F. Brain foods: the effects of nutrients on brain function. Nat Rev Neurosci. 2008;9(7):568–78.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Lyles E, Banks S, Ramaswamy M, Ismail S, Leidman E, Doocy S. Acute malnutrition recovery rates improve with COVID-19 adapted nutrition treatment protocols in South Sudan: a mixed methods study. BMC Nutr. 2023;9(1):1–9.

    Article  Google Scholar 

  50. Berk M, Williams LJ, Jacka FN, O’Neil A, Pasco JA, Moylan S, et al. So depression is an inflammatory disease, but where does the inflammation come from? BMC Med. 2013;11:200.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Al Alawi AM, Majoni SW, Falhammar H. Magnesium and Human Health: perspectives and research directions. Int J Endocrinol. 2018;2018:9041694.

    Article  PubMed  PubMed Central  Google Scholar 

  52. McCarty MF. Magnesium may mediate the favorable impact of whole grains on insulin sensitivity by acting as a mild calcium antagonist. Med Hypotheses. 2005;64(3):619–27.

    Article  CAS  PubMed  Google Scholar 

  53. Fung TT, Hu FB, Pereira MA, Liu S, Stampfer MJ, Colditz GA, et al. Whole-grain intake and the risk of type 2 diabetes: a prospective study in men. Am J Clin Nutr. 2002;76(3):535–40.

    Article  CAS  PubMed  Google Scholar 

  54. Fardet A. New hypotheses for the health-protective mechanisms of whole-grain cereals: what is beyond fibre? Nutr Res Rev. 2010;23(1):65–134.

    Article  CAS  PubMed  Google Scholar 

  55. Hindmarch I. Beyond the monoamine hypothesis: mechanisms, molecules and methods. Eur Psychiatry. 2002;17(Suppl 3):294–9.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

We sincerely thank all patients participating in this study.

Funding

This study is supported by Mashhad University of Medical Sciences (grant nu: 981873).

Author information

Authors and Affiliations

Authors

Contributions

MGH, and ZKH initially conceptualized and designed the study. MGH contributed to obtaining the initial funding. The manuscript was written by AA, ZKH, KMH, and MVF and was reviewed by all members. PSH, NT and RAD were responsible for the design optimization and statistical analysis. EH, ML, PAS, MKHB, MSHFM, and AGH contribute sampling. GF performed English editing. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Zahra Khorasanchi or Majid Ghayour-Mobarhan.

Ethics declarations

Ethics approval and consent to participants

was obtained from the ethics committee of Mashhad University of Medical Sciences (code: IR.MUMS.REC.1399.237). Informed consent was obtained from all study participants. All methods were performed based on related guidelines and regulations or the Helsinki Affirmation.

Consent for publication

Not applicable as no personal data was used in this article.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

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

Rights and permissions

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

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Araste, A., Moghadam, M.R.S.F., Mohammadhasani, K. et al. Adherence to the nordic diet is associated with anxiety, stress, and depression in recovered COVID-19 patients, a case-control study. BMC Nutr 10, 38 (2024). https://doi.org/10.1186/s40795-024-00845-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40795-024-00845-x

Keywords