Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-27T20:58:53.599Z Has data issue: false hasContentIssue false

Using an FFQ to assess intakes of dietary flavonols and flavones among female adolescents in the Suihua area of northern China

Published online by Cambridge University Press:  06 May 2014

Caihong Sun
Affiliation:
Department of Children Health and Hygiene, School of Public Health, Harbin Medical University, 157 Baojian Road, 150081 Harbin, People’s Republic of China
Hui Wang
Affiliation:
Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Harbin, People’s Republic of China
Dong Wang
Affiliation:
Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Harbin, People’s Republic of China
Yanping Chen
Affiliation:
Department of Children’s Health Care, Harbin Children’s Hospital, Harbin, People’s Republic of China
Yan Zhao
Affiliation:
Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Harbin, People’s Republic of China
Wei Xia*
Affiliation:
Department of Children Health and Hygiene, School of Public Health, Harbin Medical University, 157 Baojian Road, 150081 Harbin, People’s Republic of China
*
* Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective

The present study aimed to (i) evaluate the reproducibility and validity of a designed FFQ, (ii) apply the FFQ for estimating the dietary intakes of four flavonols and two flavones in female adolescents and (iii) explain their major dietary sources.

Design

The reproducibility between the first and second FFQ administrations (1 year interval) was estimated using the intra-class correlation coefficient. The validity of the first FFQ relative to the average of four three-day 24 h dietary recalls (24-HR) from four seasons was assessed using the Spearman correlation coefficient. Using a flavonoid content database, the individual flavonol and flavone intakes were calculated and the major food sources were estimated.

Setting

Middle school in Suihua area of Heilongjiang Province, northern China.

Subjects

Female adolescents (n 887) aged 12–18 years.

Results

Better reproducibility and validity were obtained in the present study. The flavonol and flavone intakes were 16·29 and 4·31 mg/d, respectively. Quercetin and kaempferol were the major contributors (26·8 % and 23·7 %, respectively) to the total intake of flavonols and flavones. The main food sources of flavonols and flavones were apples (14·1 %), followed by potatoes (7·5 %), lettuce (7·3 %) and oranges (7·3 %).

Conclusions

The dietary flavonol and flavone intakes among female adolescents in northern China were similar to those reported in several countries, but significant differences were observed in the food sources ascribed to the geographical location and dietary characteristics.

Type
Research Papers
Copyright
Copyright © The Authors 2014 

Foods have many components other than the commonly known nutrients such as proteins, fats, carbohydrates, vitamins and minerals, many of which are associated with biological activities related to the reduced risk of several chronic diseases and cancer( Reference Craig 1 Reference Hung 3 ). Flavonoids possess a wide range of biochemical and pharmacological effects, including anti-inflammatory and antioxidant effects( Reference Beecher 4 Reference Prior and Cao 7 ). In addition, recent studies have suggested that flavonoid intake may contribute to body weight maintenance in the general female population( Reference Hughes, Arts and Ambergen 8 ). Flavonol and flavone contents are the highest in plant-based foods, and are concentrated mainly in leafy vegetables and some fruits.

Although flavonoids have various biological activities, their biological function depends mainly on their intakes and bioavailabilities. Databases of flavonoids in Chinese plant foods are currently limited and few data on the estimated flavonoid intake of the Chinese population have been published. Cao et al.( Reference Cao, Chen and Zhang 9 ) reported the major flavonols (quercetin, kaempferol, myricetin and isorhamntin) and flavones (apigenin and luteolin) found in 100 types of vegetables and fruits consumed by the Chinese population. Based on their findings, a preliminary database of flavonols and flavones was built.

Several international studies have reported flavonoid intakes of adults and a few studies have focused on the intake of minor populations, e.g. among the elderly and women( Reference Chun, Chung and Song 10 Reference Otaki, Kimira and Katsumata 12 ), but few have focused on adolescent girls. Adolescence is an important period of growth and development. Given the special physiological and psychological factors that define adolescence among girls, as well as the phenomenon of blind weight loss, their health has received increasing attention among researchers in recent years( Reference Johnson, Wardle and Griffith 13 ). Suihua is located in northern China, where the economic condition is not as prosperous as in the southern parts of the country. Seasonal vegetables and fruits are still much less eaten, especially during winter. The flavonol and flavone intakes of female adolescents in this area remain unclear. Based on available data on flavonol and flavone contents, the present study was performed to estimate the intakes of two subgroups of flavonoids (flavonols and flavones) and to explain their major dietary sources among female adolescents in the Suihua area in northern China using an FFQ. To demonstrate the feasibility of the FFQ on the target population, the reproducibility and validity of the FFQ were also evaluated. This study would facilitate further investigation on the relationship between flavonoids and chronic diseases.

Methods

Ethics statement

The study was approved by the Research Ethics Committee of Harbin Medical University. Written informed consent was obtained from either the participants or their parents (for participants below 18 years old) before the participants were enrolled in the study.

Study population

Female adolescents aged 12–18 years were enrolled in the study using a stratified multistage cluster sampling method. The participants were randomly recruited from three middle schools in the Suihua area of Heilongjiang Province, China. Each school had six grades. A total of twenty-five resident (living in the countryside) and twenty-five non-resident (living in the city) female students were selected from each grade. A total of 887 adolescents from the 900 potential participants joined in the study, excluding those who did not satisfactorily complete the FFQ (n 13). Among the qualified participants, 120 girls were expected to participate in the 24 h dietary recalls (24-HR) and answer the FFQ again after one year.

Study design

The study began in March 2011 and continued into the following year. Four three-day 24-HR were quarterly collected from 120 participants, who also completed the second FFQ (FFQ2). The first FFQ (FFQ1, n 887) was administered during the first three-day 24-HR, whereas the FFQ2 (n 120) was administered in February 2012. The reproducibility of the FFQ was estimated using intra-class correlation coefficient (ICC) analysis between FFQ1 and FFQ2, whereas its validity was assessed by comparing FFQ1 with the average of the four three-day 24-HR using Spearman’s correlation coefficient.

FFQ and 24 h dietary recalls

The FFQ was developed according to the methodology proposed by Willett( Reference Willett 14 ). Revisions were made to ensure that the list of foods reflected the Chinese diet, according to the 2002 National Health and Dietary Survey( Reference Li, Rao and Kong 15 ). Further revisions were made to improve the estimates of flavonoid-rich food intakes. The FFQ collected consumption information across eight food groups and eighty-six food items (Table 1). Respondents were requested to recall the average consumption of a given amount of each food item during the previous 1-year period using a graded scale with seven levels, ranging from never to ≥3 times per day. The portion size was also considered for the survey. For the 24-HR, each participant was asked to choose from a set of colour photographs showing different-sized portions of twenty-three specific food items, whereas photographs of dishes, bowls and cups were used to represent the average portion size for the other sixty-three food items. Participants had to describe qualitatively and quantitatively all food consumed during the previous day using the correct pictures to allow the dietitian to estimate their food intakes. All FFQ data were double entered into a computer and any discrepancies were resolved by referring to the original forms. Two dietitians visited each participant four times to complete the three-day 24-HR and these data were used as a standard to measure the relative validity of the FFQ. The dietitians were instructed to ask the participants key questions for a better qualitative description of food items (e.g. green leafy vegetables and fruits).

Table 1 Food grouping used in the present study

* Assigned portion sizes for all eighty-six food items used in the FFQ.

Intakes of dietary nutrients, flavonols and flavones

The nutrient calculator software Fei Hua V2·3 (Institute for Nutrition and Food Security, Chinese Center for Disease Control and Prevention, Beijing, China) was used to calculate the daily intakes of energy and nutrients. The database of flavonols and flavones established by our laboratory was used to calculate the daily flavonol and flavone intakes in our study.

Statistical analysis

Means and standard deviations of daily energy, flavonol and flavone intakes were calculated for the two FFQ and the average of the four three-day 24-HR, and analysed using the Wilcoxon signed-rank test. The residual method was used to help exclude the possibility of variations caused by energy intake( Reference Willett 14 ). Reproducibility between the two FFQ administrations was estimated using ICC( Reference Willett 14 ). The validity of the FFQ relative to the 24-HR was assessed using Spearman’s correlation coefficient. Considering within-person variations caused by day-to-day fluctuations and seasonal variations, Spearman’s correlation coefficients were ‘de-attenuated’ using the within- and between-person components of variation from the 24-HR( Reference Rosner and Willett 16 ). All statistical analyses were performed using the SPSS statistical software package version 13·0 and Microsoft® Excel 2003. Unless stated otherwise, P<0·05 was considered significant.

Results

The mean age and BMI of the participants (n 887) were 16·1 (sd 1·3) years and 23·9 (sd 3·5) kg/m2, respectively. The mean intakes of energy, protein, fat, carbohydrate, eight food groups, four flavonols and two flavones of 120 adolescent girls, who completed FFQ1 and four three-day 24-HR from four seasons and FFQ2 for over 1 year, were calculated using the questionnaires as bases, with the aid of the nutrient calculator software and flavonoid database. The aforementioned data are shown in Table 2. The intake of beans from FFQ2 and the intake of drinks from FFQ1 were significantly higher than those from the 24-HR (P<0·05), and the intake of drinks from FFQ2 was lower than that from FFQ1 (P<0·05). No differences were observed for the intakes of energy, protein, fat, carbohydrate and other food groups derived from the 24-HR, FFQ1 and FFQ2. The mean daily flavonoid intake derived from the 24-HR, FFQ1 and FFQ2 was 18·51 (sd 9·98) mg/d, 20·21 (sd 10·12) mg/d and 20·24 (sd 11·18) mg/d, respectively. No significant differences were detected for the mean total flavonoid intake (flavonols+flavones) and the individual flavonol and flavone intakes.

Table 2 Daily mean intakes of energy, macronutrients, food groups, flavonols and flavones of female adolescents aged 12–18 years from the Suihua area of northern China (n 120), estimated using two FFQ and the average of four three-day 24 h dietary recalls (24-HR), March 2011–February 2012

* Significantly different from 24-HR, Wilcoxon signed-rank test, P<0·05.

Significantly different from FFQ1, Wilcoxon signed-rank test, P<0·05.

Reproducibility and relative validity of FFQ

The crude- and energy-adjusted ICC for FFQ1 v. FFQ2 were calculated to assess the reproducibility of the FFQ (Table 3). All flavonols and flavones were moderately correlated (ICC=0·4–0·7). After adjusting for energy, all ICC decreased. The mean crude ICC was 0·52 from a range of 0·45 (isorhamntin) to 0·65 (quercetin), whereas the mean energy-adjusted ICC was 0·42 from a range of 0·35 (isorhamntin) to 0·50 (quercetin).

Table 3 Reproducibility and validity of the FFQ designed for evaluation of the daily flavonol and flavone intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

* Intra-class correlation coefficient (ICC) was used to assess the reproducibility between FFQ1 and FFQ2 administrations (n 120).

Spearman’s correlation analysis was used to assess the validity of FFQ1 relative to the average of four three-day 24 h dietary recalls (24-HR; n 120).

All ICC values were significant (P<0·05).

§ All Spearman’s correlation coefficients were significant (P<0·05).

The crude, energy-adjusted and de-attenuated Spearman’s correlation coefficients for FFQ1 v. the average resulting from the four three-day 24-HR are also presented in Table 3. These values were used to assess the relative validity of the FFQ. The crude Spearman’s correlation coefficient between FFQ1 and 24-HR ranged from 0·53 (apigenin) to 0·77 (quercetin), with a mean value of 0·62. The energy-adjusted coefficient ranged from 0·40 (apigenin) to 0·59 (luteolin), with a mean of 0·48. The de-attenuated coefficients ranged from 0·55 (apigenin) to 0·78 (quercetin), with a mean of 0·64. All energy-adjusted Spearman’s correlation coefficients were lower than the crude ICC in terms of FFQ1 and FFQ2. However, de-attenuation to correct for intra-individual variability improved the Spearman’s correlation coefficients and led to an increase in the mean Spearman’s correlation coefficient for FFQ1 v. 24-HR (from 0·62 to 0·64).

Estimated flavonol and flavone intakes and major food sources

The mean daily dietary flavonol and flavone intakes were estimated from the FFQ (FFQ1, n 887) completed by female adolescents in the Suihua area of northern China. The total flavonoid intake (flavonols+flavones) was 20·60 (sd 14·12) mg/d, mainly from quercetin and kaempferol (26·8 % and 23·7 %, respectively), followed by luteolin (15·9 %), isorhamntin (14·6 %) and myricetin (11·1 %). The contribution of apigenin was relatively minimal (5·0 %). The flavonol intake was 16·29 (sd 11·91) mg/d (79·1 %) and the flavone intake was 4·31 (sd 2·21) mg/d (20·9 %; Table 4).

Table 4 Daily flavone and flavonol intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

* Data from FFQ1 (n 887).

The primary food items contributing to the individual flavonol and flavone intakes are shown in Table 5. After colligating the daily dietary intakes, the results show that apple was the primary food item contributing to the total flavonol and flavone intakes (11·7 %), followed by potatoes (9·9 %) and lettuce (7·3 %). Other main contributors included oranges (7·0 %), Chinese cabbage (4·7 %), tomatoes (4·2 %), celery (4·2 %), soyabean sprouts (4·2 %), leeks (3·9 %) and aubergine (3·9 %). The sources of the total flavonoid intakes (flavonols+flavones) were vegetables (55·6 %), fruits (26·6 %) and others (17·8 %; e.g. cereals, tea, fruit juice and coffee).

Table 5 Main food sources and their contribution (%) to the flavone and flavonol intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

* Percentage of individual flavonols or flavones.

Percentage of total flavonols and flavones.

Discussion

Given that the FFQ method is inexpensive and reflects the long-term dietary conditions of participants, it is generally considered to be a good tool for conducting dietary nutritional epidemiological studies. The results from FFQ differ depending on cultural background, eating habits, food sources, season, climate, age, economy and other factors, even in the same country. Thus, a special FFQ should be designed for the target population while considering the differences in food items that contribute to the daily supply of nutrients or phytochemicals with biological activities( Reference Zhang and Ho 17 ). Suihua is located in north-east China, where winter lasts for more than five months and the economic condition is not as prosperous as that of the southern part of the country. In the current study, a new FFQ was designed for adolescent girls from Suihua, with the specific aim of selecting food groups that contribute significantly to flavonol and flavone intakes.

The reproducibility and relative validity of the FFQ were evaluated. The crude and energy-adjusted ICC for the mean daily flavonol and flavone intakes from FFQ1 v. FFQ2 were 0·52 and 0·42, respectively, for reproducibility. The crude, energy-adjusted and de-attenuated Spearman’s correlation coefficients for the mean daily flavonol and flavone intakes from FFQ1 v. 24-HR were 0·62, 0·48 and 0·64, respectively, for validity, indicating that better correlations were obtained. Our study population consisted of a group of female adolescents with similar lifestyles (i.e. students in three middle schools who frequently dine in the school canteen), which possibly contributed to the moderate correlations. The ability of an individual to deal with abstract concepts and form mental images of her dietary regimen that are as close as possible to the truth( Reference Yaroch and Resnicow 18 ), was another crucial factor in producing reliable estimates of habitual intake using the FFQ. Thus, colour photographs of foods taken in classrooms were used to make the task less tedious and encourage the interviewees to provide more accurate dietary information( Reference Tooze, Midthune and Dodd 19 ). When the 24-HR were used to estimate the individual dietary intakes, we used a method that provided better estimates of the intake of even episodically consumed foods by accounting for the correlation between the probability of consumption and the amount consumed, and incorporating covariate information( Reference Souverein, Dekkers and Geelen 20 , Reference Goodwin, Brule and Junkins 21 ). Adjusting for energy decreased the correlation in almost all subclasses of flavonoids, as high-energy foods may contain little to no amounts of flavonols and flavones( Reference Mullie, Clarys and Deriemaeker 22 ).

Despite numerous reports on the health-improving effects of flavonoids, a limited number of studies on flavonoid intake are available worldwide. The flavonol and flavone intakes from several countries are listed in Table 6, showing that the estimates varied widely among studies. In the current study, the mean flavonoid (four flavonols and two flavones) intake of 887 female adolescents was 20·6 mg/d. The total flavonol intake was 16·3 mg/d and the total flavone intake was 4·3 mg/d. These results are similar to those in studies conducted in Australia( Reference Johannot and Somerset 23 ), the Netherlands( Reference Hertog, Hollman and Katan 24 ), China( Reference Zhang, Li and Cao 25 ) and the USA( Reference Sampson, Rimm and Hollman 26 ), and are even higher than those in other studies reported from the USA( Reference Hertog, Kromhout and Aravanis 27 , Reference Chun, Floegel and Chung 28 ), Finland( Reference Ovaskainen, Torronen and Koponen 11 , Reference Knekt, Kumpulainen and Jarvinen 29 ) and Japan( Reference Kimira, Arai and Shimoi 30 , Reference Arai, Watanabe and Kimira 31 ). However, our results are lower than those found in studies conducted in Belgium( Reference Mullie, Clarys and Deriemaeker 22 ) and Spain( Reference Zamora-Ros, Andres-Lacueva and Lamuela-Raventos 32 ).

Table 6 Estimated flavonol and flavone intakes in several countries

*M, males; F, females.

The major dietary sources of flavonol and flavone intakes reported in some of the aforementioned countries are onions and tea, followed by apples, broccoli and lettuce( Reference Hertog, Hollman and Katan 24 , Reference Sampson, Rimm and Hollman 26 , Reference Hertog, Feskens and Hollman 33 ). In the present study, apples, potatoes, lettuce, oranges, soyabean sprouts and leeks were the main food sources of flavonols, whereas tomatoes, aubergine, white radishes, celery and sweet potatoes were the main sources of flavones, similar to the results of a study on the Australian population with a sample population aged 16–18 years( Reference Johannot and Somerset 23 ). The participants in our study were adolescent girls with special dietary characteristics and much lower intakes of tea and onions compared with the respective populations of Western countries, leading to differences in both intake amounts and major sources. The contributions of cereals and cereal-containing foods, which the girls consumed in large amounts, to the flavonol and flavone intakes were minimal (7·2 %) in the present study. The differences in results could also be explained by the potato consumption. Our participants living in the Suihua area partly ate potatoes instead of the staple food, e.g. rice, making potato the primary food item that subsequently contributed to the total flavonol and flavone intake.

The current study had several limitations. First, only two subgroups of flavonoids were studied. However, other subclasses of flavonoids, such as isoflavones and isoflavanones, are also consumed in high amounts in China. This limitation could be ascribed to the flavonoid database, which has a limited number of food items, although the database is constantly being updated. Therefore, broader evaluations on other subclasses of flavonoids must be conducted. The second limitation was the time for the FFQ to be completed. The flavonoid contents of foods are influenced by region, season, sunlight and other factors( Reference Hertog, Hollman and Katan 24 ). For instance, the quercetin content of onions measured in our laboratory was 1·23 mg/100 g (fresh weight), which was much lower than that in the US flavonoid database (7·29–33·43 mg/100 g, fresh weight) and the contents reported by Arabbi et al. (38·3–93·6 mg/100 g, fresh weight)( Reference Arabbi, Genovese and Lajolo 34 ). Third, the content changes in the storage and processing of the foods were not considered. As previously mentioned, food storage temperature, processing and peeling can influence flavonoid content( Reference Srivastava, Akoh and Yi 35 ). Thus, more in-depth studies must be performed.

Conclusion

In conclusion, based on the proven reproducibility and validity of the FFQ, the present study estimated the dietary intakes and sources of flavonols and flavones among female adolescents. The dietary flavonoid intakes among female adolescents in the Suihua area were similar to those reported in previous studies, even though winter is longer and the economy is relatively poor in this area. The food sources showed significant differences because of the geographical position and dietary characteristics. This work provides data for epidemiological studies on the proposed relationship between these flavonoids and human health.

Acknowledgements

Financial support: This study was supported by a grant from the Science and Technology Agency of Heilongjiang Province, China (Youth Fund to W.X., QC06C059). The funder, W.X., contributed to the study design, conduct of the study, analysis of samples or data, interpretation of findings or the preparation of the manuscript. Conflict of interest: None. Authorship: W.X. conceived and designed the study, and is responsible for final editing and approval of the manuscript. C.S., H.W., D.Z. and Y.C. performed the investigations. C.S. and Y.Z. analysed the data and wrote the manuscript. All authors approved the final version of the paper for publication. Ethics of human subject participation: This study was approved by the Research Ethics Committee of Harbin Medical University. Written informed consent was obtained from either the participants or their parents before they were enrolled in the study.

References

1. Craig, WJ (2010) Nutrition concerns and health effects of vegetarian diets. Nutr Clin Pract 25, 613620.Google Scholar
2. Alvarez-Parrilla, E, De La Rosa, LA, Legarreta, P et al. (2010) Daily consumption of apple, pear and orange juice differently affects plasma lipids and antioxidant capacity of smoking and non-smoking adults. Int J Food Sci Nutr 61, 369380.CrossRefGoogle ScholarPubMed
3. Hung, H (2007) Dietary quercetin inhibits proliferation of lung carcinoma cells. Forum Nutr 60, 146157.Google Scholar
4. Beecher, GR (2003) Overview of dietary flavonoids: nomenclature, occurrence and intake. J Nutr 133, issue 10, 3248S3254S.Google Scholar
5. Blumberg, J (2003) Introduction to the proceedings of the Third International Scientific Symposium on Tea and Human Health: Role of Flavonoids in the Diet. J Nutr 133, issue 10, 3244S3246S.Google Scholar
6. Hollman, PC & Katan, MB (1999) Dietary flavonoids: intake, health effects and bioavailability. Food Chem Toxicol 37, 937942.CrossRefGoogle ScholarPubMed
7. Prior, RL & Cao, G (1999) Antioxidant capacity and polyphenolic components of teas: implications for altering in vivo antioxidant status. Proc Soc Exp Biol Med 220, 255261.Google Scholar
8. Hughes, LA, Arts, IC, Ambergen, T et al. (2008) Higher dietary flavone, flavonol, and catechin intakes are associated with less of an increase in BMI over time in women: a longitudinal analysis from the Netherlands Cohort Study. Am J Clin Nutr 88, 13411352.Google Scholar
9. Cao, J, Chen, W, Zhang, Y et al. (2010) Content of selected flavonoids in 100 edible vegetables and fruits. Food Sci Technol Res 16, 395402.CrossRefGoogle Scholar
10. Chun, OK, Chung, SJ & Song, WO (2007) Estimated dietary flavonoid intake and major food sources of US adults. J Nutr 137, 12441252.Google Scholar
11. Ovaskainen, ML, Torronen, R, Koponen, JM et al. (2008) Dietary intake and major food sources of polyphenols in Finnish adults. J Nutr 138, 562566.Google Scholar
12. Otaki, N, Kimira, M, Katsumata, S et al. (2009) Distribution and major sources of flavonoid intakes in the middle-aged Japanese women. J Clin Biochem Nutr 44, 231238.CrossRefGoogle ScholarPubMed
13. Johnson, F, Wardle, J & Griffith, J (2002) The adolescent food habits checklist: reliability and validity of a measure of healthy eating behaviour in adolescents. Eur J Clin Nutr 56, 644649.CrossRefGoogle ScholarPubMed
14. Willett, W (1987) Nutritional epidemiology: issues and challenges. Int J Epidemiol 16, 312317.Google Scholar
15. Li, LM, Rao, KQ, Kong, LZ et al. (2005) A description on the Chinese national nutrition and health survey in 2002. Zhonghua Liu Xing Bing Xue Za Zhi 26, 478484.Google Scholar
16. Rosner, B & Willett, WC (1988) Interval estimates for correlation coefficients corrected for within-person variation: implications for study design and hypothesis testing. Am J Epidemiol 127, 377386.Google Scholar
17. Zhang, CX & Ho, SC (2009) Validity and reproducibility of a food frequency questionnaire among Chinese women in Guangdong province. Asia Pac J Clin Nutr 18, 240250.Google Scholar
18. Yaroch, AL & Resnicow, K (2000) Development of a modified picture-sort food frequency questionnaire administered to low-income, overweight, African-American adolescent girls. J Am Diet Assoc 100, 10501056.Google Scholar
19. Tooze, JA, Midthune, D, Dodd, KW et al. (2006) A new statistical method for estimating the usual intake of episodically consumed foods with application to their distribution. J Am Diet Assoc 106, 15751587.Google Scholar
20. Souverein, OW, Dekkers, AL, Geelen, A et al. (2011) Comparing four methods to estimate usual intake distributions. Eur J Clin Nutr 65, Suppl. 1, S92S101.Google Scholar
21. Goodwin, RA, Brule, D, Junkins, EA et al. (2001) Development of a food and activity record and a portion-size model booklet for use by 6- to 17-year olds: a review of focus-group testing. J Am Diet Assoc 101, 926928.Google Scholar
22. Mullie, P, Clarys, P, Deriemaeker, P et al. (2008) Estimation of daily human intake of food flavonoids. Int J Food Sci Nutr 59, 291298.Google Scholar
23. Johannot, L & Somerset, SM (2006) Age-related variations in flavonoid intake and sources in the Australian population. Public Health Nutr 9, 10451054.Google Scholar
24. Hertog, MG, Hollman, PC, Katan, MB et al. (1993) Intake of potentially anticarcinogenic flavonoids and their determinants in adults in The Netherlands. Nutr Cancer 20, 2129.CrossRefGoogle ScholarPubMed
25. Zhang, Y, Li, Y, Cao, C et al. (2010) Dietary flavonol and flavone intakes and their major food sources in Chinese adults. Nutr Cancer 62, 11201127.Google Scholar
26. Sampson, L, Rimm, E, Hollman, PC et al. (2002) Flavonol and flavone intakes in US health professionals. J Am Diet Assoc 102, 14141420.CrossRefGoogle ScholarPubMed
27. Hertog, MG, Kromhout, D, Aravanis, C et al. (1995) Flavonoid intake and long-term risk of coronary heart disease and cancer in the seven countries study. Arch Intern Med 155, 381386.Google Scholar
28. Chun, OK, Floegel, A, Chung, SJ et al. (2010) Estimation of antioxidant intakes from diet and supplements in US adults. J Nutr 140, 317324.Google Scholar
29. Knekt, P, Kumpulainen, J, Jarvinen, R et al. (2002) Flavonoid intake and risk of chronic diseases. Am J Clin Nutr 76, 560568.Google Scholar
30. Kimira, M, Arai, Y, Shimoi, K et al. (1998) Japanese intake of flavonoids and isoflavonoids from foods. J Epidemiol 8, 168175.Google Scholar
31. Arai, Y, Watanabe, S, Kimira, M et al. (2000) Dietary intakes of flavonols, flavones and isoflavones by Japanese women and the inverse correlation between quercetin intake and plasma LDL cholesterol concentration. J Nutr 130, 22432250.Google Scholar
32. Zamora-Ros, R, Andres-Lacueva, C, Lamuela-Raventos, RM et al. (2010) Estimation of dietary sources and flavonoid intake in a Spanish adult population (EPIC-Spain). J Am Diet Assoc 110, 390398.Google Scholar
33. Hertog, MG, Feskens, EJ, Hollman, PC et al. (1994) Dietary flavonoids and cancer risk in the Zutphen Elderly Study. Nutr Cancer 22, 175184.Google Scholar
34. Arabbi, PR, Genovese, MI & Lajolo, FM (2004) Flavonoids in vegetable foods commonly consumed in Brazil and estimated ingestion by the Brazilian population. J Agric Food Chem 52, 11241131.CrossRefGoogle ScholarPubMed
35. Srivastava, A, Akoh, CC, Yi, W et al. (2007) Effect of storage conditions on the biological activity of phenolic compounds of blueberry extract packed in glass bottles. J Agric Food Chem 55, 27052713.Google Scholar
Figure 0

Table 1 Food grouping used in the present study

Figure 1

Table 2 Daily mean intakes of energy, macronutrients, food groups, flavonols and flavones of female adolescents aged 12–18 years from the Suihua area of northern China (n 120), estimated using two FFQ and the average of four three-day 24 h dietary recalls (24-HR), March 2011–February 2012

Figure 2

Table 3 Reproducibility and validity of the FFQ designed for evaluation of the daily flavonol and flavone intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

Figure 3

Table 4 Daily flavone and flavonol intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

Figure 4

Table 5 Main food sources and their contribution (%) to the flavone and flavonol intakes of female adolescents aged 12–18 years from the Suihua area of northern China, March 2011–February 2012

Figure 5

Table 6 Estimated flavonol and flavone intakes in several countries