Maintenance of optimal nutritional status in women of reproductive age can help to ensure normal fetal development( Reference Ramakrishnan, Grant and Goldenberg 1 ). It has been shown that vitamin D has important benefits during fetal and neonatal development( Reference Basit 2 ). Vitamin D, a fat-soluble vitamin, can be attained through diet, supplements or exposure to sunlight. The primary function of vitamin D is to control Ca homeostasis and in doing so aid absorption of Ca from the intestine and ensure adequate bone metabolism( Reference Basit 2 ). Vitamin D status before and during pregnancy is implicated in fetal growth( Reference Kaludjerovic and Vieth 3 ). In addition, vitamin D is important for the prevention of adverse pregnancy outcomes including pre-eclampsia and gestational diabetes mellitus( Reference Grober, Spitz and Reichrath 4 – Reference Hypponen, Cavadino and Williams 6 ).
The RDA for vitamin D set by the US Institute of Medicine (IOM) is 15 µg/d for ages 1–70 years with no additional amount during pregnancy or lactation( Reference Ross, Manson and Abrams 7 ). As many as 41 % of all pregnancies worldwide are unplanned( Reference Secura 8 ). To ensure that the general population and women of childbearing age consume enough vitamin D prior to becoming pregnant, many countries have introduced mandatory vitamin D fortification of food, which is not the case in Serbia. To date voluntary fortification in Serbia is limited to one milk product and imported products.
Mapping low intakes of vitamin D and other micronutrients across Europe with a focus on Central Eastern European (CEE) countries showed no differences in micronutrient intake/status compared with other European regions and highlighted the lack of comparable studies on micronutrient intake/status across all age ranges in the CEE region( Reference Novakovic, Cavelaars and Bekkering 9 ). Available evidence for Serbia indicated that intake of vitamin D is below 15 µg/d suggested by the authorities( Reference Mensink, Fletcher and Gurinovic 10 ).
In order to identify possible vitamin D nutritional inadequacies in women of reproductive age in CEE countries, there is a need for standardized dietary assessment tools. To address this concern we developed an FFQ and undertook the present study to determine whether the FFQ is valid for assessing the dietary intake of vitamin D in women of reproductive age in a Balkan region. This validation study was conducted at the end of winter, when subcutaneous production of vitamin D is negligible because UVB exposure is minimal and therefore it would make a minor contribution to vitamin D status.
Materials and methods
FFQ are a widely used dietary assessment tool for estimating the usual dietary intake( Reference Willett, Sampson and Stampfer 11 ). In terms of validation of an FFQ, it has been suggested that two reference methods should be used, such as repeated 24 h dietary recalls, weighed food records, food diaries or biomarkers( Reference Willett, Sampson and Stampfer 11 – Reference Willett 13 ). Biomarkers as a reference method have the advantage of having errors uncorrelated with those that may be shared by methods relying on self-report( Reference Potischman 14 ). Therefore, in the present study, the FFQ was validated against 24 h recalls and a biomarker, plasma 25-hydroxyvitamin D (25(OH)D), using the lower bound of the true questionnaire validity approach( Reference Willett 13 ). We used the method of triads, a triangular approach to validation that uses the correlations between each of the three methods to calculate a validity coefficient. The validity coefficient is the correlation between the dietary intake reported by the FFQ and the unknown ‘true’ dietary intake( Reference Kaaks 15 ).
Participants
As a part of national integrated project, a cross-sectional study was conducted between November 2010 and April 2011 in order to investigate dietary intake and status of vitamin D in Serbian women of reproductive age.
Females, aged 18 to 35 years, were recruited using flyers and verbal referral from three universities in Serbia that spread across three provinces (University of Belgrade, University of Novi Sad and University of Nis) to represent 0·1 % of the total number of women aged 18–35 years in Serbia( 16 ). Inclusion criteria comprised healthy women without chronic diseases. Professional athletes, pregnant or breast-feeding women were excluded from the study.
A total of 500 women were recruited on a voluntary basis to participate in the study with 422 females completing the FFQ on one occasion, a response rate 84·4 %.
A subgroup of randomly selected participants (n 50) was studied for additional measures in March 2011 which included three repeated 24 h recalls, anthropometric measurements and a blood sample. The response rate for the anthropometry and 24 h recalls was 88·0 % (n 44) and for blood sampling was 46·0 % (n 23). However, three women were excluded due to UVB exposure.
Anthropometry
Anthropometry was performed without shoes and jacket, including height to the nearest 0·1 cm (Perspective Enterprises, Kalamazoo, MI, USA) and weight to the nearest 0·5 kg using a body composition analyser (TBF-300; Tanita Corp., Tokyo, Japan).
FFQ
The Women and Reproductive Health FFQ (WRH-FFQ) was developed by combining the NCI/Block Health Habits and History Questionnaire( Reference Block and Subar 17 ) with a validated FFQ for folate in the Balkan region( Reference Colic Baric, Satalic and Keser 18 ). The combined FFQ was further adapted by inclusion of a wider section of foods containing vitamin D as well as traditional foods consumed in Serbia. A translation was conducted from English to Serbian by three bilingual experts in nutrition and dietetics and back-translated to ensure content validity.
The WRH-FFQ reflected the previous 30 d and was self-administered in the presence of trained dietitians. Instructions related to frequencies of consumption and portion sizes (small, medium, large) were presented on photographs included in the WRH-FFQ. For the food items, the frequency intervals were ‘never’, ‘once per month’, ‘2–3 times per month’, ‘once a week’, ‘2–3 times per week’, ‘4–6 times per week’ and ‘every day’. All reported frequencies were converted to frequencies per day. The questionnaire contained ninety food items and twelve additional questions regarding the frequency of use of multivitamin/mineral and other supplements as well as voluntary and imported vitamin D-fortified products available in Serbia. Foods consumed sometimes, but not captured in the food list, were recorded at the end of the FFQ. The WRH-FFQ also contained a general questionnaire on age, education level, previous medical conditions, detailed vitamin supplements and medication use, lifestyle habits (smoking, physical activity/exercise, alcohol and coffee/tee consumption), as well as tanning from a solarium or natural sunlight (on vacation) during the last 3 months.
Twenty-four hour dietary recall
Three 24 h dietary recalls were performed by multiple pass in March 2011. The first one was conducted by trained professionals in our clinic on the day of blood sampling, during the last week of the month covered by the FFQ. The second and third recalls were conducted after the FFQ by telephone within 2 weeks( Reference Subar, Dodd and Guenther 19 ), with two of the recalls being on weekdays and one on a weekend day. Women reported the dietary intake for each day from breakfast until the next morning. Pictures of household measures were used for specific information on portion sizes.
Calculation of nutrient intakes
Nutrient intakes resulting from the FFQ and 24 h recalls were estimated using the Serbian Food Composition Database( Reference Gurinovic, Milesevic and Kadvan 20 ). Manufacturer specifications were used to estimate the nutrient content of supplements. The total daily intake of vitamin D (μg/d) was calculated using the dietary assessment software tool DIET ASSESS used in national and regional consumption studies and evaluated in a European Food Safety Authority (EFSA) project( Reference Gurinovic, Milesevic and Novakovic 21 ). Energy-adjusted dietary vitamin D intake was calculated using the nutrient density method proposed by Willett( Reference Willett, Howe and Kushi 22 ). Intake of vitamin D from supplements is not related to energy intake and thus the raw value of vitamin D intake from supplements was added to the crude or energy-adjusted dietary vitamin D intake to obtain a single value for total vitamin D intake( Reference Flood, Peters and Chatterjee 23 ). Finally, the total vitamin D intake of participants was related to both the RDA (15 µg/d) and the Estimated Average Requirement (EAR; 10 µg/d) for vitamin D for adults (19–50 years) according to the IOM recommendations( Reference Ross, Taylor and Yaktine 24 ). The proportions of women above and below the RDA and the EAR were calculated since these recommendations are set based on dietary intake data( Reference Barr 25 ) and are meant to represent healthy levels of intake in accordance with good vitamin D status in the absence of UVB exposure( 26 ).
Vitamin D status assessment
A single measurement of 25(OH)D, with a known half-life to up to 1 month, was selected to reflect vitamin D status consistent with the time period reflected in the FFQ( Reference Zerwekh 27 ). After an overnight fast, venous blood samples were collected from twenty-three randomly selected participants into lithium heparin tubes by clinical staff at the Centre of Research Excellence in Nutrition and Metabolism, University of Belgrade, March 2011. Blood was immediately processed and plasma frozen at −80°C. Plasma samples were shipped to Canada (McGill University) on dry ice and stored at −80°C until analysis. Vitamin D concentration was measured using the LIAISON total 25(OH)D assay (DiaSorin Inc., Stillwater, MN, USA). The intra-assay CV of 3·18 % (range 0·55–7·17 %) was calculated from repeated measurement of a pooled plasma sample used as a laboratory reference range for healthy adults and from DiaSorin high and low controls. The accuracy using the mid-range of manufacturer specifications was 104 % for DiaSorin low control and 103 % for DiaSorin high control; and 97·00 % for NIST SRM 972a level 1 and 90·44 % for NIST SRM 972a level 2 (Standard Reference Material from the National Institute of Standards and Technology, Gaithersburg, MD, USA). This laboratory participates in the DEQAS (Vitamin D External Quality Assessment Scheme) programme and obtained a Certificate of Proficiency for 2013–2014, which reflects that 75 % or more of the reported results fell within 25 % of the ALTM (all-laboratory trimmed mean).
Ethical approval
The study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures were approved by the Ethics Review Board in Serbia and the McGill Institutional Review Board of the Faculty of Agricultural and Environmental Science for analyses in Canada. Written informed consent was obtained from all participants.
Statistical analysis
Several methods were used to assess the validity of the WRH-FFQ. Data were not normally distributed and crude as well as energy-adjusted Spearman rank-correlation coefficients were calculated between daily vitamin D intake and the biomarker of vitamin D status. Bland–Altman plots were used to compare the FFQ and 24 h recall for quantifying vitamin D intake. As variability of the difference between measurements was not uniform along the range of the measurement values, the Bland–Altman analysis was performed on the log scale (log-transformed difference)( Reference Bland and Altman 28 ). The ability of the WRH-FFQ to correctly classify participants into quartiles of the referent method (24 h recall) and biomarker was also determined. Percentages of those correctly classified (participants classified within the same quartiles), closely classified (participants classified within the same or adjacent quartiles) and grossly misclassified (participants classified in the opposite quartiles) were calculated. The triangular approach to validation, known as the method of triads, was applied as well. The following equation was used to calculate the validity coefficient (VC) for the FFQ:
where ρ QI represents the validity coefficient for the FFQ, r QB the correlation between the FFQ and the biomarker, r BR the correlation between the 24 h recall and the biomarker, and r QR the correlation between the FFQ and the 24 h recall. This method has been described in detail by Ocke and Kaaks( Reference Ocke and Kaaks 29 ). Calculated validity coefficient was used as the upper limit of the validity coefficient, whereas the correlation between the biomarker and the FFQ was interpreted as the lower limit of the validity coefficient. The 95 % confidence intervals for the validity coefficients were estimated using bootstrap sampling where 1000 samples of equal size (n 20) were obtained with replacement from the study subjects( Reference Ocke and Kaaks 29 , Reference Kabagambe, Baylin and Allan 30 ).
Participants’ vitamin D status was classified as deficiency or into categories generally considered inadequate or adequate for bone and overall health in healthy individuals, based on 25(OH)D level( Reference Ross, Taylor and Yaktine 24 ). The report from the IOM in 2011 proposed definitions for deficient (25(OH)D level <30 nmol/l), inadequate (25(OH)D level between 30 and 50 nmol/l), sufficient (25(OH)D level between 50 and 125 nmol/l) and potentially toxic (25(OH)D level >125 nmol/l) levels of 25(OH)D( Reference Ross, Manson and Abrams 7 , Reference Ross 31 , Reference Ross, Manson and Abrams 32 ).
Statistical analysis was performed using the software MedCalc version 10·2·0·0 and the statistical software package IBM SPSS Statistics 20·0. A P value <0·05 was considered statistically significant.
Results
The WRH-FFQ was completed by 422 participants. A subgroup of forty-four women completed both the FFQ and three 24 h dietary recalls, while twenty-three of them were enrolled in the validation study with assessed vitamin D status. Mean age (23·3 (sd 2·4) years v. 25·5 (sd 2·2) years v. 25·6 (sd 2·4) years), height (166·2 (sd 26·2) cm v. 170·6 (sd 5·5) cm v. 171·6 (sd 5·2) cm), weight (58·3 (sd 12·8) kg v. 61·5 (sd 6·4) kg v. 61·9 (sd 5·7) kg) and BMI (20·7 (sd 2·2) kg/m2 v. 21·2 (sd 2·2) kg/m2 v. 21·0 (sd 2·1) kg/m2) did not differ between the main sample, the subgroup and the validation group, respectively. Self-reported BMI in the FFQ (21·5 (sd 2·1) kg/m2) was very similar to measured BMI (21·2 (sd 2·2) kg/m2) in the subgroup. All participants were highly educated or enrolled in a university when the study was conducted, 15·0 % were smokers and 68·3 % consumed alcohol on a weekly basis, 47·3 % consumed 2–3 cups coffee/d and 47·7 % consumed 4–5 cups/d. No physical activity was reported by 30 % of all participants, while up to 70 % stated some physical activity. In the subgroup, 22·7 % were not active while 77·3 % were physically active typically between 30 min and 3·5 h weekly.
Plasma 25(OH)D was 29·5 (sd 13·8) nmol/l (n 20). Ninety per cent had 25(OH)D level below 50 nmol/l, while 70 % had 25(OH)D level below 30 nmol/l. Vitamin D intake was below the EAR for 96 % of all participants as assessed by the WRH-FFQ (n 422). None of the 422 participants in the main sample consumed vitamin D-fortified food and only 4·7 % used vitamin D in multivitamin supplements. No participants of the subgroup reported vitamin supplement use.
Regardless of methodology, all women were below the RDA. Estimated daily energy and nutrient intakes assessed by the WRH-FFQ and the average of the three 24 h dietary recalls are presented in Table 1. The top six food sources of vitamin D in Serbia identified by the WRH-FFQ and 24 h recalls were fatty fish (Table 2), with all varieties being imported with the exception of trout (freshwater fish).
WRH-FFQ, Women and Reproductive Health FFQ; %TEI, percentage of total energy intake.
* 1 µg vitamin D=40 IU vitamin D; 4184 kJ=1000 kcal.
WRH-FFQ, Women and Reproductive Health FFQ.
Freshwater fish includes trout, catfish and carp; meat includes pork, beef, lamb, veal, chicken, turkey, liver, weiners, cold cuts, dried sausage and other dried meats.
Correlations between the WRH-FFQ, 24 h recalls and biomarker of vitamin D status are presented in Fig. 1. The crude and energy-adjusted Spearman rank-correlation coefficients between total vitamin D intakes assessed by the FFQ, 24 h recalls and biomarker of vitamin D status have similar patterns. Although the energy-adjusted Spearman rank-correlation coefficient between total vitamin D intake assessed by the FFQ and the vitamin D biomarker was 0·415 (P=0·001, data not shown), the relationship was similar using the crude data (r=0·422, P=0·032). The Spearman rank-correlation coefficient between energy-adjusted vitamin D intake assessed by the 24 h recalls and biomarker was not statistically significant (r=0·346, P=0·067; data not shown), whereas it was significant using the crude data (r=0·404, P=0·039).
The Bland–Altman plots showed high agreement between vitamin D intakes calculated by the WRH-FFQ and 24 h dietary recalls (Fig. 2).
Nutrient intakes were divided into quartiles in order to evaluate the ability of the WRH-FFQ to rank women into the same quartiles as the 24 h dietary recalls and 25(OH)D concentration (Table 3). Classification into quartiles showed that, on average, 80 % of the women were classified into the same or adjacent quartile when ranked by the FFQ and 24 h recalls as well as according to their vitamin D status (biomarker) and less than 20 % were misclassified into opposite quartiles by both methods (Table 3).
WRH-FFQ, Women and Reproductive Health FFQ.
The correlations between each of the three methods were used to calculate the validity coefficients (VC: ρ QI, ρ BI, ρ RI) for the WRH-FFQ using the method of triads approach. The validity coefficients for the FFQ and 24 h dietary recalls were higher than those for the serum biomarker (Fig. 3). However, the validity coefficients for the FFQ tended to be higher than those for both the 24 h recalls and the biomarker.
Discussion
The aim of the present study was to validate the WRH-FFQ for the assessment of vitamin D intake in young women of reproductive age in a country without mandatory vitamin D food fortification. Therefore, we collected dietary intake data by two dietary assessment methods (FFQ and three 24 h dietary recalls), determined concentrations of a nutritional biomarker (plasma 25(OH)D) and applied the method of triads for validation analyses.
In the present study, validity coefficients were high between the ‘true’ intake (I) and the FFQ (0·847) as well as the 24 h recalls (0·810) and moderate for the biomarker (0·499). Our results for validity coefficients are similar to those in studies that used the method of triads model for validation of FFQ for different nutrients such as erythrocyte folate (0·750), vitamin B12 (0·850), α-carotene (0·850) and total carotenoids (0·550)( Reference McNaughton, Marks and Gaffney 33 – Reference Verkleij-Hagoort, de Vries and Stegers 35 ). The 95 % confidence intervals for the validity coefficients in our study are narrow and the upper limit for the intervals is lower than 1. This is a strength which reflects an absence of random sampling variations between dietary methods or violations in the underlying assumptions of the model( Reference Ocke and Kaaks 29 , Reference Daures, Gerber and Scali 36 ).
In our study of 422 healthy young women who completed the WRH-FFQ, the estimated vitamin D intake was 4 µg/d. This is comparable with published data from Serbia for adult women (5 µg/d assessed by 7 d food record)( Reference Gurinovic, Kadvan and Vukotic 37 ), but the age range for women was wider in that study and the relative difference could be explained by nutrient intake calculations using an older version of food composition data that relied on calculated vitamin D content rather than analytical assessment. Our vitamin D intake assessed by WRH-FFQ and 24 h recall is similar to findings from other studies in the region that assessed vitamin D intake by an alternative FFQ (Portugal: 4 µg/d)( Reference Elmadfa and Freisling 38 ) as well as by 24 h recall using calculated values (Poland: 4 µg/d; Hungary: 2 µg/d)( Reference Novakovic, Cavelaars and Bekkering 9 , Reference Rodler, Biro and Greiner 39 ). Vitamin D-containing supplements were used by less than 5 % of all 422 participants and no one reported consumption of the voluntarily vitamin D-fortified food product on the market (i.e. long-lasting pasteurised milk with added vitamin A and vitamin D).
The IOM suggests the plasma 25(OH)D threshold for vitamin D deficiency is 30 nmol/l and between 30 and 50 nmol/l is generally considered inadequate for bone and overall health in the general population( Reference Ross, Taylor and Yaktine 24 ). According to IOM criteria 90 % (n 18) of participants in the validation group had 25(OH)D plasma below 50 nmol/l and 70 % (n 16) had status <30 nmol/l. Part of the reason for low vitamin D status is ascribed to the late winter collection of blood samples (March 2011). According to studies from other European countries, the prevalence of hypovitaminosis D is highest during the winter and early spring (January–March). For example, in a study conducted between February and March in Finland, serum 25(OH)D concentration of healthy women was 47 nmol/l on average( Reference Lamberg-Allardt, Outila and Karkkainen 40 ). Similarly, when serum 25(OH)D concentrations were measured in a population of healthy adults from Ireland prevalence rates for serum 25(OH)D concentrations <30 nmol/l and <50 nmol/l were 11 % and 55 % in winter, respectively( Reference Cashman, Muldowney and McNulty 41 ). Overall in Serbia expenditure on seafood and fish, as a main natural source of vitamin D, is extremely low (3·1 % of total expenditure on food) due to dietary habits and traditional cuisine based mostly on meat( 42 ).
According to other studies, for most nutrients, correlation coefficients with biomarkers are in the range of 0·3 to 0·5( Reference Hu 43 ) and these correlations provide useful and objective evidence for the validity of nutrient intake assessed by a dietary instrument. In our study, the Spearman rank-correlation coefficient between total vitamin D intake assessed by the FFQ and biomarker showed moderate agreement, with a correlation coefficient for energy-adjusted vitamin D intake (r=0·415, P=0·001) similar to the crude value (r=0·422, P=0·032). One possible reason for the moderate agreement between total vitamin D intake assessed by the FFQ and biomarker might be the time of the year when samples are collected, at the end of the winter. During winter months, when vitamin D production is minimal, the human body can rely on tissue stores of vitamin D for between 30 and 60 d assuming levels are adequate prior to winter( Reference Mawer, Backhouse and Holman 44 ). However, after more than 2 months with inadequate vitamin D intake, stores are depleted, consistent with the end of winter. In addition, our study participants are young healthy women with percentage of fat and fat mass in the normal range (see online supplementary material, Supplemental Table 1); thus low vitamin D status is not caused by sequestration of vitamin D in adipose tissue as is observed in those who are obese( Reference Vimaleswaran, Berry and Lu 45 ).
In our validation work we chose to assess vitamin D status during a time when UVB sources would be minimal. Our winter-time assessment, combined with the healthy weights of the participants, make this an ideal study framework to look at dietary assessment tools. Results of our study show that no women met the IOM RDA recommendations according to either dietary assessment tool and 96 % did not meet the EAR. Vitamin D intake for 100 % of participants was below the RDA (15 µg/d) and plasma 25(OH)D concentration was below 50 nmol/l for 90 % of participants. In the subgroup, all of the vitamin D was from food with no use of dietary supplements. However, the main study group did consume supplements at 4·7 % and intakes from the FFQ and 24 h recalls were related, suggesting the WRH-FFQ suitably captures this information. As the Serbian market introduces affordable vitamin D-containing supplements as well as single vitamin D supplements for all age ranges, the FFQ should be further adapted to ensure capture of new sources and higher intakes of vitamin D.
It is not mandatory to fortify food with vitamin D in Serbia and therefore milk is not in the top six food sources of vitamin D. Milk consumption assessed by 24 h recall in our study is 116·5 (sd 90·1) ml/d and yoghurt intake is 109·2 (sd 93·6) ml/d. If just milk was fortified with vitamin D as is common in North America( Reference Calvo, Whiting and Barton 46 ) (0·87–1 µg/100 ml), vitamin D intake would be higher by 1·5 (sd 1·1) µg/d, which would improve total intake in people but likely not sufficiently enough to improve vitamin D status during the winter months. As vitamin D is now recognized as one of the ‘big two’ in vitamin fortification in Europe( Reference de Lourdes Samaniego-Vaesken, Alonso-Aperte and Varela-Moreiras 47 ), it might be wise to consider mandatory fortification in Serbia as well.
Strengths of the present validation study include: the nature of data collection (i.e. interviewer-administered FFQ, collection during the winter months); inclusion of overall healthy, non-obese or non-overweight young women; inclusion of detailed food lists with food photographs; questions on intake of supplements; and the vitamin D analyses in a laboratory in Canada.
Even though our study is adequately powered with 422 participants( Reference Osowski, Beare and Specker 48 , Reference Pritchard, Seechurn and Atkinson 49 ), only twenty participants were available for the biomarker validation analyses, which is a low sample size. However, other validation studies where the method of triads is applied used a similar number of participants (n 29). Narrow 95 % confidence intervals for the validity coefficients indicate adequate sample size for the study and it might extend beyond the range of the validity coefficient which was the case in some studies that used a triangular approach( Reference McNaughton, Marks and Gaffney 33 ). A potential limitation of the applied method of triads is the impact of using a single measure of 25(OH)D which does not account for random measurement error in the biomarker( Reference Preis, Spiegelman and Zhao 50 ). An additional limitation that might have a potential impact on the study results is correlated person-specific bias between self-report instruments, which may inflate the observed validity of the self-report instruments( Reference Kipnis, Midthune and Freedman 51 , Reference Kipnis, Midthune and Freedman 52 ). The main reason why some of the participants were classified in the opposite quartile during cross-classification (20 %) was due to fish consumption (tuna steak or fish pate) reported in our 30 d WRH-FFQ but not in any of the three 24 h recalls (see online supplementary material, Supplemental Table 2). Agreement between the FFQ and three 24 h recalls as assessed in the Bland–Altman plots using the log values clarifies that the relationship is not different across the group among participants, which accounts for well-known fact that as the intake increases the variation will also increase. Although the 24 h recall method tends to rely on memory of the participants and the ability to evaluate portion sizes, in our study it is not a weakness since our participants were young healthy women and we used a food photograph album( Reference Cade, Thompson and Burley 53 ). The main strengths of our FFQ are the inclusion of traditional foods used in the CEE region and its ease of administration, enhanced by inclusion of food photographs that emphasized portion sizes, which reduced time needed for administration to less than 30 min( Reference Cade, Thompson and Burley 53 ). Additional advantages of our FFQ are the potential use as a dietary assessment tool in health and some clinical research due to the low cost of administration and processing.
However, all of our participants were highly educated and thus further studies among women from other segments of the population are required to ensure that the WRH-FFQ is valid.
Conclusion
To our knowledge, the present study is among the first to assess the validity of intake of vitamin D using the method of triads. The upper limits of the validity coefficients were less than one and validity coefficients were high between the true intake and the FFQ (0·847) and 24 h recall (0·810), which reflects a strong relationship, although this is not the case for the biomarker (0·499). This suggests that the applied WRH-FFQ is a valid tool for assessing dietary vitamin D intake in women living in Serbia, a region without mandatory vitamin D food fortification. Furthermore, the study provided novel data regarding vitamin D intake and status of young Serbian women with important ramifications for public health nutrition policy.
Acknowledgements
Financial support: This work was supported by the Ministry of Education, Science and Technological Development of the Republic of Serbia (grant numbers III 41030, 46013 and 41028). The Ministry of Education, Science and Technological Development of the Republic of Serbia had no role in the design, analysis or writing of this article. Conflict of interest: The authors declare that there are no conflicts of interest. Authorship: M. Glibetic formulated the research questions; M. Gurinovic and L.M.M. designed the research; M.D.-I. and A.K. conducted research; H.A.W. and M.D.-I. conducted biochemical analyses; M.D.-I., H.A.W. and M.N. analysed data; M.D.-I. and H.A.W. drafted and revised the paper; M.D.-I. had primary responsibility for the final content. All authors read and approved the final manuscript. Ethics of human subject participation: The study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures were approved by the Ethics Review Board in Serbia and the McGill Institutional Review Board of the Faculty of Agricultural and Environmental Science for analyses in Canada. Written informed consent was obtained from all participants.
Supplementary material
To view supplementary material for this article, please visit http://dx.doi.org/10.1017/S136898001500138X