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A case–control study on dietary quality indices and glioma

Published online by Cambridge University Press:  24 June 2019

Omid Sadeghi
Affiliation:
Students’ Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Mehdi Shayanfar
Affiliation:
Department of Clinical Nutrition and Dietetics, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Minoo Mohammad-Shirazi
Affiliation:
Department of Clinical Nutrition and Dietetics, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Giuve Sharifi
Affiliation:
Department of Neurosurgery, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Ahmad Esmaillzadeh*
Affiliation:
Obesity and Eating Habits Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran Food Security Research Center, Department of Community Nutrition, Isfahan University of Medical Sciences, Isfahan, Iran
*
*Corresponding author: Ahmad Esmaillzadeh, email [email protected]
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Abstract

No study is available that has assessed the association of dietary diversity score (DDS) and alternative healthy eating index (AHEI) with glioma. The present study aimed to assess this association in Iranian adults. Overall, 128 pathologically confirmed cases of glioma were enrolled from hospitals and 256 age- and sex-matched controls were recruited from other wards of the hospital between 2009 and 2011. Dietary assessment was done using a validated block-format 123-item semi-quantitative FFQ. Dietary indices including DDS and AHEI-2010 were constructed according to standard methods. After controlling for potential confounders, a significant inverse association was found between DDS and risk of glioma (OR 0·42, 95 % CI 0·19, 0·94). Such finding was also seen when further adjustment was made for BMI; such that participants in the highest quartile of DDS were 56 % less likely to have glioma compared with those in the lowest quartile (OR 0·44, 95 % CI, 0·20, 0·97). In addition, a significant inverse association was found between adherence to AHEI and glioma; such that in the fully adjusted model, participants in the fourth quartile of AHEI had 74 % lower risk of glioma compared with those in the first quartile (OR 0·26, 95 % CI 0·12, 0·56). In conclusion, we found that greater adherence to the healthy, as measured by AHEI, and diverse, as measured by DDS, diets was associated with decreased odds of glioma.

Type
Full Papers
Copyright
© The Authors 2019 

Gliomas are the most common primary brain tumour that occurs most frequently in adults and are associated with a high mortality rate(Reference Morgan1, Reference Dolecek, Propp and Stroup2). It accounts for 81 % of brain tumours among adults(Reference Morgan1). Although the prevalence of glioma is low around the world, its morbidity and mortality are high(Reference Williams3). National estimates in Iran have shown a mortality rate of 2·92/100 000 in men and 2·46 per 100 000 in women(Reference Alimohamadi, Ghodsi and Ketabchi4). Therefore, it is required to find contributing factors in the occurrence and development of glioma.

Dietary intakes are greatly contributing to cancers, including glioma(Reference Chen, Ward and Tucker5). Earlier studies have shown that dietary intake of red meat, salt and alcohol is associated with greater risk of glioma, while intake of fruits, nuts, legumes, vitamin A and antioxidants is associated with decreased odds of brain tumour(Reference Chen, Ward and Tucker5Reference Wei, Zou and Cao11). Along with the assessment of link between foods and nutrients with several diseases, assessment of the association with the whole dietary patterns is suggested. Only one case–control study considered dietary patterns in relation to glioma and showed interesting findings(Reference Benisi-Kohansal, Shayanfar and Mohammad-Shirazi12). Based on this study, high adherence to Dietary Approaches to Stop Hypertension (DASH)-style diet was associated with decreased risk of glioma(Reference Benisi-Kohansal, Shayanfar and Mohammad-Shirazi12). However, other types of dietary pattern or diet quality indices including alternative healthy eating index (AHEI), dietary diversity score (DDS), mean adequacy ratio of nutrients, and dietary energy density have not assessed in relation to glioma until now. These indices consider the whole diet rather than its individual components. DDS along with AHEI have been shown as a measure of healthy diet rich in fruits, vegetables and photochemicals(Reference Hashemi Kani, Alavian and Esmaillzadeh13Reference Shiao, Grayson and Lie15). Although different measures of diet have been linked with cancers, no study examined these indicators in relation to glioma.

Assessing the association between priori defined dietary patterns and glioma is particularly relevant for Middle Eastern countries, because the dietary diversity is low in this region due to low socio-economic status(Reference Talaei, Rabiei and Talaei16). In addition, besides diet other environmental factors are contributing to this condition in the region. Therefore, finding the association of dietary indices such as DDS and AHEI with glioma might present interesting results. The present study aimed to assess these associations among Iranian adults.

Methods

Sample

This hospital-based case–control study was carried out on 128 newly diagnosed patients (maximum 1 month elapsed since the detection) and 256 controls without glioma in Tehran, Iran, between 2009 and 2011. Cases were individuals with pathologically confirmed glioma (International Classification of Diseases for Oncology second edition (ICD-O-2) morphology codes 938--9481) during the previous month that had been referred to the Neurosurgery department of the hospitals. Controls were apparently healthy individuals who were relatives of patients or those who attended to the outpatients’ clinics of the hospital. As we did not examine them in terms of health conditions, they could not be called as absolutely healthy individuals.

Procedure

Patients with glioma and controls were selected by using convenience-sampling method from the hospitals affiliated to Shahid Beheshti University of Medical Sciences. Cases and controls were matched in terms of age (±5 years) and sex. Individuals with a history of any type of pathologically confirmed cancer (except glioma), chemotherapy and radiotherapy (due to cancer) were not included in this study. After selection of cases and controls, data on demographic variables, dietary intakes, physical activity and anthropometric measures were collected. Missing information about any variable were completed through contacting subjects. However, in terms of dietary data, we considered unanswered items as null. All cases and controls provided written informed consent. The study was ethically approved by the Medical Ethics Committee of the Tehran University of Medical Sciences, Tehran, Iran.

Assessment of glioma

Glioma was diagnosed based on pathological test by using ICD-O-2 morphology codes 9380–9481(Reference Merve, Millner and Marino17). Only patients with a maximally 1 month of the confirmation of glioma were included in the study.

Variables

Dietary assessment

Usual dietary intakes of participants during a year before the diagnosis of glioma in cases and during a year before the interview in controls were examined by a validated Block-format 123-item semi-quantitative FFQ(Reference Talaei, Rabiei and Talaei16). The FFQ was consisted of 123 food items with standard portion sizes commonly consumed by Iranian people. Trained interviewers administered the FFQ through face-to-face interviews in the presence of individuals who were involved in the preparation and cooking of foods. All reported consumption frequencies were converted to g/d using household measures. Daily intakes of energy and nutrients were computed for each person by using the modified US Department of Agriculture (USDA) food consumption database which was modified for Iranian foods.

Validation study of this FFQ revealed good correlations between dietary intakes assessed by FFQ and those obtained from 24 dietary recalls (two 24-h recalls per month). The reliability of the FFQ was assessed by comparing nutrient intakes obtained from two questionnaires that filled 1 year apart. The correlation coefficients for the reliability of the FFQ for dietary vitamin E, β-carotene and vitamin C were 0·78, 0·84 and 0·83(Reference Esfahani, Asghari and Mirmiran18). The energy-adjusted correlation coefficients between the dietary intakes obtained from the FFQ and those from the multiple 24-h dietary recalls were 0·65, 0·68 and 0·65 for vitamin E, β-carotene and vitamin C(Reference Talaei, Rabiei and Talaei16). Overall these data indicated that the FFQ provides reasonably valid measures of the average long-time dietary intakes.

Dietary diversity score

A method described by Kant et al. was used for scoring dietary diversity(Reference Kant, Block and Schatzkin19, Reference Kant, Schatzkin and Ziegler20). This method was based on five groups including grains, vegetables, fruits, meats and dairy products, all food groups in the USDA food guide pyramid. The grains group was composed of five components: refined bread, macaroni, whole grain bread, corn flakes and rice. However, in the method of Kant et al., there are seven components in the grains group. As we had no data about intake of biscuits and refined flour, we decided to consider five components. Fruit was defined by summing up fruit and fruit juice, berries and citrus fruits. The story about vegetables was summing up of mixed vegetables, potato, tomato, other starchy vegetables, legumes, yellow vegetables and green vegetables. The group of meat was composed of red meat, poultry, fish and eggs) and the group of dairy products was composed of milk, yoghurt and cheese.

Participants were considered as a ‘consumer’, and scored as 1, for each components of food groups if they had intakes higher than median levels; otherwise they were given the score of 0. Then the scores for components in each food group were summed up to have total score of that food group. Then, we divided total scores obtained in each group to the number of components in that group. This value was then multiplied by 2. Total DDS for each participant was then computed by summing up the figures for food groups. For example, in the grains group, if a person had dietary intakes of whole grain bread, macaroni and rice higher than the median values, his or her score was calculated as (3/5)×2=1·2. Therefore, the diversity score for the grains group would be 1·2 for that person. After computing the diversity score for the other four groups in that person, total DDS would be computed. Therefore, minimum and maximum scores of total dietary diversity for each participant were between 0 and 10.

Alternative healthy eating index

We calculated AHEI-2010 using information obtained from FFQ. The AHEI incorporates several aspects of the original HEI designed by Kennedy et al. (Reference Kennedy21Reference Akbaraly, Ferrie and Berr23). This method considered eleven components including fruit, vegetables, whole grains, nuts and legumes, long-chain n-3 fats (DHA and EPA), PUFA, wine consumption, sugar-sweetened drinks and fruit juice, red and processed meats, trans-fat and Na intake. Due to lack of data on wine consumption and trans-fat in our database, we considered nine components to compute AHEI in the present study. Individuals in the highest decile of whole grains, vegetables, fruits, nuts and legumes, PUFA and long-chain n-3 fats were given the score of 10 and those in the lowest decile received the score of 1. Individuals in other deciles received the corresponding scores. In contrast, individuals with the highest intake of sugar-sweetened drinks and fruit juice, red and processed meats, and Na were given the score of 1 and those with the lowest consumption of these components received the score of 10. Total AHEI score for each participant was then computed by summing up the scores for these ten components. It was varied from 9 to 81.

Assessment of other variables

A pretested questionnaire was used to collect data on age, sex, marital status, place of residence, education, occupation, smoking status, use of supplements, family history of cancers and glioma, history of allergy and trauma, history of hypertension, exposure to chemicals in the past 10 years, cooking methods (barbecue/microwave/canned foods/fried foods), drug use, personal hair dye use, duration of cell phone use and history of exposure to radiographic X-rays. International Physical Activity Questionnaire (IPAQ) was used for measuring physical activity of participants through face to face interview. All results of the IPAQ were expressed as metabolic equivalents per week (MET/week). Body weight was quantified by digital scale to the nearest 500 g with the subjects wearing the light clothing and no shoes. Height was measured by a tape measure to the nearest 0·5 cm in standing status while the subjects shoulders were in normal position. BMI was calculated by dividing weight in kg by height in m squared. All measurements were completed by a trained dietitian.

On the basis of previous studies, we considered farmers as those having a high-risk occupation for glioma(Reference Ruder, Carreon and Butler24). Individuals who lived in places near the electromagnetic fields and cell phone and broadcast antennas in the last 10 years were defined as living in high-risk areas(Reference Morgan, Miller and Sasco25). Individuals who consumed fried foods at least twice per week were considered as frequent fried food users. This definition was also used for barbecue use, microwave use as well as for consumption of canned foods.

Analysis plan

Cases and controls were compared in terms of general characteristics and dietary intakes using independent-samples t test and χ 2, where appropriate. After construction of DDS and AHEI, as mentioned above, we obtained energy-adjusted scores of DDS and AHEI using residual method(Reference Willett, Howe and Kushi26). Then, participants were categorised based on quartile cut-off points of DDS and AHEI that were obtained from the control group. We used one-way ANOVA and χ 2 tests to assess continuous and categorical variables across quartiles of DDS and AHEI. Binary logistic regression in different models was applied to evaluate the association of DDS and AHEI with glioma. First, we included all confounders into models and then, we retained those variables that had a significant contribution to glioma. In the first model, we controlled for energy intake (continues). Further adjustments were made for family history of glioma (yes/no), marital status (married/single/divorced), high-risk occupation (farmer/non-farmer), high-risk residential area (yes/no), supplement use (yes/no), history of exposure to radiographic X-rays (yes/no), history of head trauma (yes/no), smoking (smoker/non-smoker), drug use (yes/no), personal hair dye use (yes/no), frequent fried food intake (yes/no) and frequent use of microwave (yes/no) in the second model. Additional controlling was performed for BMI (continues) in the last model. All confounders were chosen based on earlier publications(Reference Foerster, Thielens and Joseph27Reference Malmir, Shayanfar and Mohammad-Shirazi30). In these analyses, the first quartile of DDS and AHEI was considered as the reference category. To obtain the overall trend of OR across increasing quartiles of DDS and AHEI, we considered these quartiles as an ordinal variable in the logistic regression models. All statistical analyses were conducted using SPSS software (version 19.0; SPSS Inc). P values less than 0·05 was considered as significant level.

Results

General characteristics and dietary intakes of cases and controls are presented in Table 1. Cases were more likely to have high-risk jobs, history of exposure to radiographic X-rays, history of head trauma, family history of glioma and history of exposure to chemicals and live in high-risk residential areas than controls. Cases were also more likely to be frequent fried food users and had higher intakes of red meat, Na, and refined and whole grains than controls. Controls were more likely to be current smokers, hair dye users, supplement users, microwave users and have a long duration of cell phone use than cases. Controls had higher intakes of Ca, PUFA, fruits, dairy products, salt, legumes and nuts, and higher scores of AHEI compared with cases.

Table 1. General characteristics and dietary intakes of cases and controls (n 384)

(Mean values and standard deviations; percentages)

MET, metabolic equivalents; SSB, sugar-sweetened beverages; DDS, dietary diversity score; AHEI, alternative healthy eating index.

* Obtained from independent-samples t test or χ 2 test, where appropriate.

Farmers were considered as having a high-risk occupation.

Individuals who lived in places near electromagnetic fields and cell phone and broadcast antennas in the last 10 years were defined as living in high-risk areas.

§ Individuals who consumed fried food at least twice per week considered as frequent fried food users.

Individuals who used barbecue, microwave and canned foods at least twice per week were considered as frequent users.

To convert kcal to kJ, multiply by 4·184.

General characteristics of participants across quartiles of DDS and AHEI scores are shown in Table 2. Individuals in the top quartile of DDS were less likely to be a current smokers and have a high-risk job compared with those in the bottom quartile. No other significant difference was found in terms of general characteristics across quartiles of DDS. In addition, compared with participants in the lowest quartile of AHEI, those in the highest quartile were more likely to be female, older, married, have a high-risk job and history of allergy, use hair colour, and less likely to be a current smoker, frequently exposed to microwave, use cell phone, frequently use fried foods and barbecue. We found no other significant difference in terms of general characteristics across quartiles of AHEI.

Table 2. General characteristics of study participants cross quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)

(Mean values and standard deviations; percentages)

MET, metabolic equivalents.

* Obtained from ANOVA or χ 2 test, where appropriate.

Farmers were considered as having a high-risk occupation.

Individuals who lived in places near electromagnetic fields and cell phone and broadcast antennas in the last 10 years were defined as living in high-risk areas.

§ Individuals who consumed fried food at least twice per week considered as frequent fried food users.

Individuals who used barbecue, microwave and canned foods at least twice per week were considered as frequent users.

Dietary intakes of cases and controls across quartiles of DDS and AHEI scores are presented in Table 3. Those in the top quartile of DDS had higher intakes of fruit, vegetables, fish, legumes and nuts, dairy products, protein, fat, SFA and Ca compared with individuals in the bottom quartile. In addition, compared with participants in the first quartile of AHEI, those in the fourth quartile had higher intakes of fruit, vegetables, dairy products, legumes and nuts, whole grains, fat, protein, PUFA and Ca and lower intakes of red meat, refined grains, salt, sugar-sweetened beverages and Na. No other significant difference was found in terms of dietary intakes across quartiles of DDS and AHEI scores.

Table 3. Dietary and nutrient intakes of study participants across quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)†

(Mean values with their standard errors; percentages)

SSB, sugar-sweetened beverages; LC-FA, long-chain fatty acids.

* Obtained from ANOVA.

All values, except energy intake, are energy-adjusted.

To convert kcal to kJ, multiply by 4·184.

Multivariable-adjusted OR and 95 % CI for glioma across quartiles of DDS and AHEI are shown in Table 4. After controlling for energy intake and other potential confounders, a significant inverse association was found between DDS and risk of glioma (OR 0·42, 95 % CI 0·19, 0·94). Such finding was also seen when further adjustment was made for BMI; such that participants in the highest quartile of DDS were 56 % less likely to have glioma compared with those in the lowest quartile (OR 0·44, 95 % CI 0·20, 0·97). We also found a significant inverse association between AHEI and odds of glioma; such that in the fully adjusted model, participants in the top quartile of AHEI had 74 % lower risk of glioma compared with those in the bottom quartile after taking all potential confounders, including BMI, into account (OR 0·26, 95 % CI 0·12, 0·56).

Table 4. Risk for glioma according to quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)

(Odds ratios and 95 % confidence intervals)

* Model 1: adjusted for energy intake.

Model 2: additionally adjusted for family history of glioma, marital status, high-risk occupation, high-risk residential area, supplement use, history of exposure to radiographic X-rays, history of head trauma, smoking, drug use, personal hair dye use, frequent fried food intake and frequent use of a microwave.

Model 3: further adjustment for BMI.

Discussion

We found an inverse association between DDS and risk of glioma. This association was obtained after adjusting for potential confounders including socioeconomic characteristic and BMI. Such inverse association was also seen for AHEI either before or after controlling for potential confounders. To the best of our knowledge, this study is the first to examine the association of DDS and AHEI with glioma.

It is well studied that whole diet rather than individual foods or nutrients can better represent overall diet quality and help predicting the association between diet and diseases(Reference Newby and Tucker31). DDS and AHEI, as indicators of diet quality, were assessed in relation to non-communicable diseases including CVD and some cancers(Reference Arem, Reedy and Sampson32Reference Lim, Cho and Kim34). Despite this, no observational study has evaluated the association of these dietary indices with brain cancers such as glioma. In the present study, we found that high dietary diversity was associated with decreased odds of glioma. In line with our findings, some studies had shown an inverse association between DDS and risk of cancers. In a case–control study, adherence to a diet with a high diversity, in particular fruit diversity, was associated with a lower risk of bladder cancer(Reference Isa, Xie and Hu35). In a prospective study, after a mean follow-up of 8·4 years, variety in the consumption of vegetables and fruit combined and of fruit consumption alone were inversely associated with the risk of oesophageal squamous cell carcinoma(Reference Jeurnink, Buchner and Bueno-de-Mesquita36). In contrast, another study failed to find any significant association between diversity in each food group and risk of breast cancer(Reference Ko, Kim and Ma37). However, in that study dietary diversity was assessed in a single food group and several confounders were not adjusted for to determine the independent association between dietary diversity and breast cancer. The different nature of breast cancer compared with other cancers might also be another reason for different findings on the association between DDS and cancer. Therefore, further studies are needed to shed light on this issue.

The protective association of DDS against glioma might be explained by the high nutrient content of diverse diet. Antioxidants are one of these nutrients. A large number of studies have shown an inverse association between dietary intake of antioxidants and risk of cancer(Reference Lucas, Bosetti and Boffetta38Reference Vance, Wang and Su40). This association was also reported for glioma(Reference Mazzio and Soliman41). Another feature of diet with a high DDS is its high content of fruits and vegetables which have been shown to be protective against glioma(Reference Li8). Diets with a high diversity score are usually rich in fibre which helps the body to reduce carcinogens(Reference Zeng, Lazarova and Bordonaro42).

In the present study, we found that greater adherence to AHEI was associated with decreased odds of glioma. In our earlier study, adherence to DASH diet, known as a high-quality dietary pattern, was associated with 72 % lower risk of glioma(Reference Benisi-Kohansal, Shayanfar and Mohammad-Shirazi12). Findings of previous studies on the association between AHEI and risk of other cancers were also in line with our findings. In a large population-based study in Germany, after controlling for potential confounders, individuals in the highest category of AHEI were less likely to have colorectal cancer compared with those in the lowest category(Reference Erben, Carr and Holleczek43). Another study revealed an inverse association for ovarian cancer(Reference Qin, Moorman and Kelemen44). In addition, a systematic review and meta-analysis of observational studies showed that high adherence to AHEI was associated with reduced risk of mortality from cancer(Reference Onvani, Haghighatdoost and Surkan45). The inverse association between AHEI and glioma might be explained by high content of fruits and vegetables. As reported in prior studies, fruit consumption and vegetable consumption have a preventive role for incidence of glioma(Reference Holick, Giovannucci and Rosner6, Reference Li8). In addition, dietary intake of antioxidants, as anti-carcinogenic nutrients, is high among people with greater adherence to AHEI(Reference Vitale, Jirillo and Magrone46, Reference Weinstein, Vogt and Gerrior47). High AHEI score is also associated with a lower intake of red and processed meats which is a known risk factor for glioma(Reference Saneei, Willett and Esmaillzadeh9).

This study has several strengths. This was the first study to examine the association of DDS and AHEI with glioma. We controlled for a wide range of confounders in the present study to reach an independent association between the dietary scores and risk of glioma. In addition, patients enrolled in the study were new cases of glioma who had been diagnosed with this malignancy in the past 1 month. This reduces the possibility of changing usual dietary intakes in these patients. It must also be kept in mind that the study comes from the under-studied region of the Middle East where available information on diet–disease relations is very limited.

Some limitations should also be considered when interpreting our findings. The first is the case–control design of the study that is subject to several biases including selection and recall bias. In addition, due to study design we cannot confer causality. Although case–control studies are efficient in terms of time and cost, they are highly susceptible to both selection and recall biases. Recall bias, in which cases may recall their past diet differently in the context of their cancer diagnosis, is problematic because dietary assessment occurs after diagnosis. An additional concern for case–control studies is that cases might have altered their diet before diagnosis due to early symptoms of the disease. However, glioma-related symptoms may lead patients to consume healthy foods rather than unhealthy ones. This would result in attenuated estimates. In addition, cases in the present study were selected from hospitals; therefore, identified risk factors may be unique to these hospitals. However, case–control studies are suitable for studying the association of diet with rare disease with long latency period including cancers. In addition, some controls were selected from those who attended to the outpatients’ clinics of the hospital. Although controls had no history of any cancer, they might have a disease with high level of oxidative stress which is known risk factor for several chronic diseases, particularly different cancers(Reference Saha, Lee and Won48). Nevertheless, this factor cannot affect dietary intakes and consequently dietary data obtained for controls in the present study. To account for recall bias in this study design, we enrolled hospital-based controls to report exposures in a year before enrolment. As with all epidemiological studies that apply FFQ, misclassification of study participants is unavoidable. Although we controlled for several confounders, one cannot exclude the possibility of residual confounding. In addition, as the dietary intakes of Middle Eastern population are different from Western nations, the generalisability of the findings to other populations should be made cautiously.

In conclusion, greater adherence to a diet with a high diversity was associated with decreased odds of glioma. Such finding was also observed for AHEI; such that participants with a greater adherence to the AHEI diet were less likely to have glioma compared with those with the lowest adherence.

Research and policy implications

Policies to promote adherence to healthy and diverse dietary patterns in general people might help preventing the incidence of glioma. The beneficial effects of such policies on other chronic conditions have earlier been reported.

Acknowledgements

This research was supported by the Students’ Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran (code: 97-02-61-38468).

M. S., M. M.-S., G. S. and A. E. contributed in conception, design, statistical analyses, data interpretation and manuscript drafting. O. S. and A. E. contributed in data analysis, data interpretation and manuscript drafting. A. E. finalised the manuscript. All authors approved the final manuscript for submission.

The authors declare that there are no conflicts of interest.

Footnotes

Co-first author: Mehdi Shayanfar

References

Morgan, LL (2015) The epidemiology of glioma in adults: a “state of the science” review. Neuro Oncol 17, 623624.CrossRefGoogle ScholarPubMed
Dolecek, TA, Propp, JM, Stroup, NE, et al. (2012) CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005-2009. Neuro Oncol 14, Suppl. 5, v1v49.CrossRefGoogle ScholarPubMed
Williams, PT (2014) Reduced risk of brain cancer mortality from walking and running. Med Sci Sports Exerc 46, 927932.CrossRefGoogle ScholarPubMed
Alimohamadi, SM, Ghodsi, SM & Ketabchi, SE (2008) Epidemiologic patterns of primary brain tumors in Iran. Asian Pac J Cancer Prev 9, 361362.Google ScholarPubMed
Chen, H, Ward, MH, Tucker, KL, et al. (2002) Diet and risk of adult glioma in eastern Nebraska, United States. Cancer Causes Control 13, 647655.CrossRefGoogle ScholarPubMed
Holick, CN, Giovannucci, EL, Rosner, B, et al. (2007) Prospective study of intake of fruit, vegetables, and carotenoids and the risk of adult glioma. Am J Clin Nutr 85, 877886.CrossRefGoogle ScholarPubMed
Zhou, S, Wang, X, Tan, Y, et al. (2015) Association between vitamin C intake and glioma risk: evidence from a meta-analysis. Neuroepidemiology 44, 3944.CrossRefGoogle ScholarPubMed
Li, Y (2014) Association between fruit and vegetable intake and risk for glioma: a meta-analysis. Nutrition 30, 12721278.CrossRefGoogle ScholarPubMed
Saneei, P, Willett, W & Esmaillzadeh, A (2015) Red and processed meat consumption and risk of glioma in adults: a systematic review and meta-analysis of observational studies. J Res Med Sci 20, 602612.Google ScholarPubMed
Michaud, DS, Holick, CN, Batchelor, TT, et al. (2009) Prospective study of meat intake and dietary nitrates, nitrites, and nitrosamines and risk of adult glioma. Am J Clin Nutr 90, 570577.CrossRefGoogle ScholarPubMed
Wei, Y, Zou, D, Cao, D, et al. (2015) Association between processed meat and red meat consumption and risk for glioma: a meta-analysis from 14 articles. Nutrition 31, 4550.CrossRefGoogle ScholarPubMed
Benisi-Kohansal, S, Shayanfar, M, Mohammad-Shirazi, M, et al. (2016) Adherence to the Dietary Approaches to Stop Hypertension-style diet in relation to glioma: a case–control study. Br J Nutr 115, 11081116.CrossRefGoogle ScholarPubMed
Hashemi Kani, A, Alavian, SM, Esmaillzadeh, A, et al. (2013) Dietary quality indices and biochemical parameters among patients with non alcoholic fatty liver disease (NAFLD). Hepat Mon 13, e10943.CrossRefGoogle Scholar
Caswell, BL, Talegawkar, SA, Siamusantu, W, et al. (2018) A 10-food group dietary diversity score outperforms a 7-food group score in characterizing seasonal variability and micronutrient adequacy in rural Zambian children. J Nutr 148, 131139.CrossRefGoogle ScholarPubMed
Shiao, SPK, Grayson, J, Lie, A, et al. (2018) Predictors of the Healthy Eating Index and glycemic index in multi-ethnic colorectal cancer families. Nutrients 10, E674.CrossRefGoogle ScholarPubMed
Talaei, M, Rabiei, K, Talaei, Z, et al. (2013) Physical activity, sex, and socioeconomic status: a population based study. ARYA Atheroscler 9, 5160.Google ScholarPubMed
Merve, A, Millner, TO & Marino, S (2019) Integrated phenotype-genotype approach in diagnosis and classification of common CNS tumours. Histopathology (In the Press).CrossRefGoogle Scholar
Esfahani, FH, Asghari, G, Mirmiran, P, et al. (2010) Reproducibility and relative validity of food group intake in a food frequency questionnaire developed for the Tehran Lipid and Glucose Study. J Epidemiol 20, 150158.CrossRefGoogle Scholar
Kant, AK, Block, G, Schatzkin, A, et al. (1991) Dietary diversity in the US population, NHANES II, 1976–1980. J Am Diet Assoc 91, 15261531.Google ScholarPubMed
Kant, AK, Schatzkin, A & Ziegler, RG (1995) Dietary diversity and subsequent cause-specific mortality in the NHANES I epidemiologic follow-up study. J Am Coll Nutr 14, 233238.CrossRefGoogle ScholarPubMed
Kennedy, E (2008) Putting the pyramid into action: the healthy eating index and food quality score. Asia Pac J Clin Nutr 17, Suppl. 1, 7074.Google ScholarPubMed
Kennedy, ET, Ohls, J, Carlson, S, et al. (1995) The healthy eating index: design and applications. J Am Diet Assoc 95, 11031108.CrossRefGoogle ScholarPubMed
Akbaraly, TN, Ferrie, JE, Berr, C, et al. (2011) Alternative Healthy Eating Index and mortality over 18 y of follow-up: results from the Whitehall II cohort. Am J Clin Nutr 94, 247253.CrossRefGoogle Scholar
Ruder, AM, Carreon, T, Butler, MA, et al. (2009) Exposure to farm crops, livestock, and farm tasks and risk of glioma: the Upper Midwest Health Study. Am J Epidemiol 169, 14791491.CrossRefGoogle ScholarPubMed
Morgan, LL, Miller, AB, Sasco, A, et al. (2015) Mobile phone radiation causes brain tumors and should be classified as a probable human carcinogen (2A) (review). Int J Oncol 46, 18651871.CrossRefGoogle Scholar
Willett, WC, Howe, GR & Kushi, LH (1997) Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr 65, 1220S1228S.CrossRefGoogle ScholarPubMed
Foerster, M, Thielens, A, Joseph, W, et al. (2018) A prospective cohort study of adolescents’ memory performance and individual brain dose of microwave radiation from wireless communication. Environ Health Perspect 126, 077007.CrossRefGoogle ScholarPubMed
Brandes, AA & Paris, MK (2004) Review of the prognostic factors in medulloblastoma of children and adults. Crit Rev Oncol Hematol 50, 121128.CrossRefGoogle ScholarPubMed
Barnholtz-Sloan, JS, Ostrom, QT & Cote, D (2018) Epidemiology of brain tumors. Neurol Clin 36, 395419.CrossRefGoogle ScholarPubMed
Malmir, H, Shayanfar, M, Mohammad-Shirazi, M, et al. (2018) Patterns of nutrients intakes in relation to glioma: a case–control study. Clin Nutr 21, 3118031184.Google Scholar
Newby, PK & Tucker, KL (2004) Empirically derived eating patterns using factor or cluster analysis: a review. Nutr Rev 62, 177203.CrossRefGoogle ScholarPubMed
Arem, H, Reedy, J, Sampson, J, et al. (2013) The Healthy Eating Index 2005 and risk for pancreatic cancer in the NIH-AARP study. J Natl Cancer Inst 105, 12981305.CrossRefGoogle ScholarPubMed
Aigner, A, Becher, H, Jacobs, S, et al. (2018) Low diet quality and the risk of stroke mortality: the Multiethnic Cohort study. Eur J Clin Nutr 72, 10351045.CrossRefGoogle ScholarPubMed
Lim, H, Cho, G & Kim, S (2012) Evaluation of nutrient intake and diet quality of gastric cancer patients in Korea. Nutr Res Pract 6, 213220.CrossRefGoogle ScholarPubMed
Isa, F, Xie, LP, Hu, Z, et al. (2013) Dietary consumption and diet diversity and risk of developing bladder cancer: results from the South and East China case–control study. Cancer Causes Control 24, 885895.CrossRefGoogle Scholar
Jeurnink, SM, Buchner, FL, Bueno-de-Mesquita, HB, et al. (2012) Variety in vegetable and fruit consumption and the risk of gastric and esophageal cancer in the European Prospective Investigation into Cancer and Nutrition. Int J Cancer 131, E963E973.CrossRefGoogle ScholarPubMed
Ko, KP, Kim, SW, Ma, SH, et al. (2013) Dietary intake and breast cancer among carriers and noncarriers of BRCA mutations in the Korean Hereditary Breast Cancer Study. Am J Clin Nutr 98, 14931501.CrossRefGoogle ScholarPubMed
Lucas, AL, Bosetti, C, Boffetta, P, et al. (2016) Dietary total antioxidant capacity and pancreatic cancer risk: an Italian case–control study. Br J Cancer 115, 102107.CrossRefGoogle Scholar
Rossi, M, Tavani, A, Ciociola, V, et al. (2016) Dietary total antioxidant capacity in relation to endometrial cancer risk: a case–control study in Italy. Cancer Causes Control 27, 425431.CrossRefGoogle ScholarPubMed
Vance, TM, Wang, Y, Su, LJ, et al. (2016) Dietary total antioxidant capacity is inversely associated with prostate cancer aggressiveness in a population-based study. Nutr Cancer 68, 214224.CrossRefGoogle ScholarPubMed
Mazzio, EA & Soliman, KF (2004) Glioma cell antioxidant capacity relative to reactive oxygen species produced by dopamine. J Appl Toxicol 24, 99106.CrossRefGoogle ScholarPubMed
Zeng, H, Lazarova, DL & Bordonaro, M (2014) Mechanisms linking dietary fiber, gut microbiota and colon cancer prevention. World J Gastrointest Oncol 6, 4151.CrossRefGoogle ScholarPubMed
Erben, V, Carr, PR, Holleczek, B, et al. (2018) Dietary patterns and risk of advanced colorectal neoplasms: a large population based screening study in Germany. Prev Med 111, 101109.CrossRefGoogle ScholarPubMed
Qin, B, Moorman, PG, Kelemen, LE, et al. (2017) Dietary quality and ovarian cancer risk in African-American women. Am J Epidemiol 185, 12811289.CrossRefGoogle ScholarPubMed
Onvani, S, Haghighatdoost, F, Surkan, PJ, et al. (2017) Adherence to the Healthy Eating Index and Alternative Healthy Eating Index dietary patterns and mortality from all causes, cardiovascular disease and cancer: a meta-analysis of observational studies. J Hum Nutr Diet 30, 216226.CrossRefGoogle ScholarPubMed
Vitale, E, Jirillo, E & Magrone, T (2014) Correlations between the Youth Healthy Eating Index, body mass index and the salivary nitric oxide concentration in overweight/obese children. Endocr Metab Immune Disord Drug Targets 14, 93101.CrossRefGoogle ScholarPubMed
Weinstein, SJ, Vogt, TM & Gerrior, SA (2004) Healthy Eating Index scores are associated with blood nutrient concentrations in the third National Health and Nutrition Examination Survey. J Am Diet Assoc 104, 576584.CrossRefGoogle ScholarPubMed
Saha, SK, Lee, SB, Won, J, et al. (2017) Correlation between oxidative stress, nutrition, and cancer initiation. Int J Mol Sci 18, E1544.CrossRefGoogle Scholar
Figure 0

Table 1. General characteristics and dietary intakes of cases and controls (n 384)(Mean values and standard deviations; percentages)

Figure 1

Table 2. General characteristics of study participants cross quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)(Mean values and standard deviations; percentages)

Figure 2

Table 3. Dietary and nutrient intakes of study participants across quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)†(Mean values with their standard errors; percentages)

Figure 3

Table 4. Risk for glioma according to quartiles (Q) of dietary diversity score (DDS) and alternative healthy eating index (AHEI) scores (n 384)(Odds ratios and 95 % confidence intervals)