Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-17T19:51:25.480Z Has data issue: false hasContentIssue false

Evaluating energy intake measurement in free-living subjects: when to record and for how long?

Published online by Cambridge University Press:  22 September 2009

Claire L Fyfe
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
Joanne Stewart
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
Sandra D Murison
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
Diane M Jackson
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
Kellie Rance
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
John R Speakman
Affiliation:
School of Biological Sciences, University of Aberdeen, Aberdeen, UK
Graham W Horgan
Affiliation:
Biomathematics and Statistics Scotland, Aberdeen, UK
Alexandra M Johnstone*
Affiliation:
Division of Obesity and Metabolic Health, Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen AB21 9SB, UK
*
*Corresponding author: Email Alex.Johnstone@abdn.ac.uk
Rights & Permissions [Opens in a new window]

Abstract

Objective

To nutritionally analyse mean energy intake (EI) from different 3 d intervals within a 7 d recording period and to evaluate the seasonal effect on energy and nutrient intake.

Design

Cross-sectional study of dietary intake collected with 7 d food diaries.

Setting

Aberdeen, north-east Scotland, UK, between 2002 and 2004.

Subjects

Participants from two long-term trials were pooled. These trials, investigating genetic and environmental influences on body weight, were the Genotyping And Phenotyping (GAP) study and a cohort observational study, Rowett Assessment of Childhood Appetite and metaboLism (RASCAL). There were 260 Caucasian adults, BMI range 16·7–49·3 kg/m2, age range 21–64 years.

Results

Mean EI for Wednesday, Friday and Saturday had the closest approximation to the 7 d mean (0·1 % overestimate). A gender × season interaction (P = 0·019) with a different intake pattern for females and males was observed. For females, lower mean (se) EI was recorded in summer (8117 (610) kJ) and autumn (7941 (699) kJ) compared with spring (8929 (979) kJ) and winter (8132 (1041) kJ). For males, higher mean (se) EI was recorded in summer (10 420 (736) kJ) and autumn (10 490 (1041) kJ) compared with spring (9319 (1441) kJ) and winter (9103 (1505) kJ).

Conclusions

The study results indicate that 3 d weighed intakes recorded from Wednesday, Friday and Saturday are most representative of 7 d habitual intake in free-living subjects. They also indicate that seasonality has a limited effect on EI and no effect on macronutrient intake.

Type
Research Paper
Copyright
Copyright © The Authors 2009

Weighed diet records are considered the ‘gold standard’ when examining free-living energy and nutrient intake, with seven days of recording regarded as the best compromise between accuracy, investigator workload and subject compliance(Reference Black, Goldberg, Jebb, Livingstone, Cole and Prentice1). In practice however, 3 d weighed dietary records are often the assessment tool chosen by investigators for intervention studies, as they are deemed to be less intrusive for subjects(Reference Tomoyasu, Toth and Poehlman2) and can therefore improve subject recruitment. With the shorter recording period comes the concern whether the three recording days are representative of habitual intake(Reference Trabulsi and Schoeller3). Therefore, much research has focused on identifying feasible intakes and attempting to correct intake data. Specifically, the effects of ‘misreporting’ or ‘under-reporting’ of food intake(Reference Whybrow, Horgan and Stubbs4) has been a main focus of attention, following better energy expenditure (and thus energy balance) methodology(Reference de Castro5). Within the literature, there has been less emphasis on the practical issues such as when to ask subjects to record, i.e. which day(s) or the effect of season, which may have an effect on achieving an assessment of habitual intake. Hartman et al.(Reference Hartman, Brown, Palmgren, Pietinen, Verkasalo, Myer and Virtamo6) reported that non-consecutive days were preferable due to a correlation between eating behaviour on consecutive days and Bingham(Reference Bingham7) recommended a 3 d diary to include one weekend day and two weekdays, since weekend days are known to indicate higher reported energy intakes(Reference Taggart8, Reference de Castro9). Food intake patterns have changed since these recommendations were made over 20 years ago(10), with the potential that intake towards the end of the working week may reflect similar patterns to weekend intake. It is also anecdotally thought that season can affect food patterns, e.g. increased salad intake in summer and soup intake in winter, but it is not clear whether this actually influences habitual nutrient intake.

Thus, the aims of the present study were: (i) to compare different 3 d periods with the 7 d mean to identify if a shorter recording period is representative of habitual intake; and (ii) to compare energy and nutrient results from different seasons to assess if seasonality has an effect on energy and nutrient intake. The weekday and weekend energy and nutrient intakes were also analysed to assess whether our results agree with previous findings(Reference Taggart8, Reference de Castro9). All of these issues could have practical implications for large nutritional assessment studies where baseline data are collected over a prolonged time.

Materials and methods

Subject characteristics

Data from two nutritional studies based at the Human Nutrition Unit, Rowett Institute of Nutrition and Health, Aberdeen, UK, were pooled for the present analysis, totalling 260 adult subjects.

Subjects were recruited for Study 1 by newspaper advertisement to participate in a study investigating genetic and environmental influences on body weight, why do some people gain weight more easily than others? The aim of the Genotyping And Phenotyping (GAP) study was to explore the hypothesis that the susceptibility of people to be obese results from an interaction between environment and genotype. Measurements of metabolism, food intake, physical activity and health status (e.g. blood pressure, cholesterol) were carried out over a period of 8 d to phenotype and genotype obese individuals to determine if there was an interaction present. More details on this study population are given elsewhere(Reference Johnstone, Murison, Duncan, Rance and Speakman11, Reference Johnstone, Rance, Murison, Duncan and Speakman12).

Study 2 was a cohort observational study recruiting whole families; more details of this study population are given elsewhere(Reference Jackson, Djafarian, Stewart and Speakman13, Reference Speakman, Djafarian, Stewart and Jackson14). The aim of the Rowett ASsessment of Childhood Appetite and metaboLism (RASCAL) study was to investigate how much influence genetic and environmental factors have on a child’s susceptibility or resistance to becoming overweight. The same measurements of metabolism, food intake, physical activity and health status recorded in the GAP study were carried out on the RASCAL families. The data from the children participating in the RASCAL study are not analysed in the current paper.

For both studies, subjects were only included if they were not eating any special diet; had stable weight (weight change of no more than 2 kg in the previous 3 months); and were otherwise healthy, based on a medical examination and by contacting their general practitioner for recent medical and medication status. They took no regular prescribed medication, vitamin or mineral supplements, with the exception of the contraceptive pill or hormone replacement therapy for women. The North of Scotland Research Ethics Service approved both studies. Written informed consent was obtained.

Measurement of baseline anthropometry and BMR

Subjects attended for measurements of body composition and metabolic rate (BMRmeas) under standardised fasted conditions. Subjects were instructed not to consume caffeinated products or to smoke prior to attending the unit, and arrived between 07.00 and 08.30 hours. They were allowed to relax for about 30 min prior to measurements being conducted. Height was measured to the nearest 0·1 cm using a stadiometer (Holtain Ltd, Crymych, UK). Subjects were weighed after voiding, wearing light clothing, to the nearest 100 g on a digital scale (DIGI DS-410; CMS Weighing Equipment Ltd, London, UK). BMR was measured by indirect calorimetry over 30–40 min using a ventilated hood system (Deltatrac II, MBM-200; Datex-Ohmeda Instrumentarium Corporation, Helsinki, Finland). During the measurement, subjects lay on a bed in a thermoneutral room and were instructed to lie still but not to fall asleep. BMR was calculated from minute-by-minute data, using the equations of Livesey and Elia(Reference Livesey and Elia15). This method analyses the mean of 15 min of stable measurements, with the first and last 5 min excluded. Details of calibration burns and repeatability testing have been described previously(Reference Johnstone, Murison, Duncan, Rance and Speakman11).

Early on in the analysis process we removed data from apparent ‘under-reporters’. The EI:BMRmeas ratio was calculated for each subject and compared with the two cut-off points defined by Goldberg et al.(Reference Goldberg, Black, Jebb, Cole, Murgatroyd, Coward and Prentice16) and Black et al.(Reference Black, Goldberg, Jebb, Livingstone, Cole and Prentice1). Where BMRmeas data were missing for twenty-four subjects, estimated BMR (BMRest), as defined by Schofield(Reference Schofield17), was used instead. There were eighty-nine subjects (35 %) below cut-off 1 and thirty-four subjects (13 %) below cut-off 2, with the remaining 132 subjects (52 %) above cut-off 1. The same significant trends were observed between the results from the original data set and that of the data set minus the under-reporters. There was no discernible bias observed for gender. The mean EI:BMRmeas for all subjects was 1·39 (se 0·02; range 0·60–2·40). We therefore present the results from the full data set in the current paper.

Food intake recording

For measurement of food and macronutrient intake, subjects in Study 1 (GAP) were asked to record all foods and drinks consumed for a consecutive 7 d period, using weighed dietary record methodology. They were provided with digital electronic scales (Soehnle model 820; Soehnle-Waagen GmbH & Co. KG, Murrhardt, Germany), which have a tare facility and weigh up to 1 kg with a resolution of 1 g. The scales were calibrated before each measurement period at four points over the scale’s range using reference weights (Thomson Scientific, Cults, Aberdeen, UK). Subjects were also provided with a food diary notebook for recording a description of the food or drink, time of consumption, weight of food, cooking method and leftovers. They were encouraged to record all recipe formulations and to keep all packaging for ready-to-eat food products, as described by Bingham(Reference Bingham7). When the use of the scales was difficult, e.g. when eating out, the subjects were instructed to record as much information as possible about the quantity of the food they ate by using household measures (tablespoon, cup, slice, etc.). It has been previously reported that to be effective, the dietary record must provide adequate detail not only of the types of foods consumed but also details of the way in which they were prepared for consumption(Reference Rutishauser18). The subjects were therefore asked to indicate where applicable how their food was cooked (boiled, fried, baked, etc.) to assist analysis. A similar technique was used in the RASCAL study; subjects recorded their food intake for 7 d in a food diary but, due to measurement constraints, the foods were not weighed. Instead food portion sizes were estimated using images from the food portion atlas(Reference Nelson, Atkinson and Meyer19). Both of these methods of food intake recording have different strengths(Reference Willett20). Weighed intakes rely less on memory as portion size is recorded directly at the time of measurement. Un-weighed intakes place lower burden on subjects, who are therefore less likely to alter eating behaviour. From issues raised by Friedenreich(Reference Friedenreich21) regarding pooled data, statistical analysis was carried out to compare the results from both studies. This was to ensure that there was no significant difference in results due to recording methodology (weighed v. un-weighed intakes). The difference in results was not significant; therefore the data were pooled.

Analysis of food intake data

All diets from both studies were analysed by trained staff using the WinDiets Nutritional Analysis Software Suite version 1·0 (The Robert Gordon University, Aberdeen, UK), a computerized version of McCance and Widdowson’s The Composition of Foods (22). To input foods recorded with household measures, or with missing weights or portion sizes, standard portions sizes were used(Reference Crawley23). Thus, total food energy and nutrient intake for every meal could be quantified. To reduce investigator bias and inputting errors, all diets were cross-checked by at least one other trained member of staff. The database of nutritional information was updated for unusual food products (from food packaging provided by subjects).

In order to examine seasonal effects of when intake was recorded, we designated the following classifications: spring was defined as March to May, summer was June to August, autumn was September to November and winter was December to February.

Weekdays were considered to be Monday to Friday inclusively, weekend as Saturday and Sunday. The 3 d diary periods examined were Tuesday–Thursday–Saturday, Wednesday–Friday–Sunday and Thursday–Saturday–Monday, following the suggestions of Hartman et al.(Reference Hartman, Brown, Palmgren, Pietinen, Verkasalo, Myer and Virtamo6) to use non-consecutive days of recording and of Bingham(Reference Bingham7) to include one weekend day and two weekdays.

Statistical analysis

Bland and Altman plots(Reference Bland and Altman24) were examined to compare the results for 3 d and 7 d EI (kJ/d). The differences were calculated as the 3 d average minus the 7 d average. Intakes were analysed by hierarchical (split-plot) ANOVA with terms for study, gender, season and their interaction in the subject stratum, and weekday and its interaction with study and gender in the within-subject stratum. Subject age and BMI were included as covariates. All data were analysed using the GenStat for Windows statistical software package 9th edition (GenStat Committee; VSN International, Hemel Hempstead, UK). Results are expressed as mean and standard error of the mean, with P values below 0·05 considered indicative of a statistically significant effect.

For purposes of presentation of trends, the data were split first by study (GAP, n 150; RASCAL, n 110), then by gender (females, n 169; males, n 91), BMI (normal weight, BMI ≤ 24·9 kg/m2, n 123; overweight and obese, BMI ≥ 25·0 kg/m2, n 127) and age (21–44 years, n 177; 45–64 years, n 83).

Results

Subject characteristics

There were 260 subjects in total (169 females, ninety-one males), with a mean age of 40·1 (se 0·6) years (range 21–64 years) and a mean BMI of 26·0 (se 0·4) kg/m2 (range 16·7–49·3 kg/m2). There were 150 subjects in Study 1 (GAP; 107 females, forty-three males). The GAP subjects were, on average, 43·7 (se 0·9) years of age (range 21–64 years) with a mean BMI of 26·5 (se 0·5) kg/m2 (range 16·7–49·3 kg/m2). There were 110 adults in Study 2 (RASCAL; sixty-two females, forty-eight males), with a mean age of 35·5 (se 0·5) years (range 23–50 years) and a mean BMI of 25·8 (se 0·5) kg/m2 (range 20·3–46·3 kg/m2).

Energy intake: 7 d results

The mean 7 d EI results (range 3878–16 688 kJ) are shown in Table 1. The difference in mean EI between the GAP and RASCAL studies (GAP mean was −202 kJ, 2·3 % lower) was not significant and, on this basis, we pooled the data. Males reported a 1909 kJ (19 %, P < 0·001) higher EI than females and younger subjects ate slightly more (590 kJ, 6·5 %, P < 0·001) than the older subjects; however, obese and lean subjects reportedly ate a similar amount (97 kJ, 0·97 %, P = 0·351). The UK Department of Health Estimated Average Requirements(25) for EI is 10 676 kJ for males and 8122 kJ for females. Our results are 5 % lower (559 kJ) and 1 % higher (76 kJ), for males and females, respectively. The EI:BMR ratio was calculated by dividing average 7 d EI by measured or estimated BMR. There was a significant difference in EI:BMR between BMI groups (13 % greater in overweight compared with normal weight, P < 0·001) but not between age groups (4 % difference, P = 0·244).

Table 1 7 d energy intake among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004

GAP, Genotyping And Phenotyping study; RASCAL, Rowett Assessment of Childhood Appetite and metaboLism.

a,bMean values within a column with unlike superscript letters were significantly different (P < 0·05).

Weekday (Monday–Friday) v. weekend (Saturday–Sunday) energy intakes

Figure 1 shows mean (se) EI by day of the week and indicates that weekend intakes were significantly greater than weekdays (P < 0·001), with average intakes of 9830 (219) kJ and 9126 (183) kJ on Saturday and Sunday, respectively, in comparison to an average of 8634 (82) kJ for weekdays. This represents a 10 % increase on these days.

Fig. 1 Mean energy intake by day of the week among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. Values are means with their standard errors represented by vertical bars. Energy intake was significantly different on Saturday and Sunday compared with the average of the weekday values (P < 0·001)

Weekday v. weekend macronutrient intakes

Mean macronutrient intakes were examined to explore the variance observed in EI between weekdays and weekend days. The results (mean (se)) were 12 % higher (2896 (40) kJ v. 3248 (64) kJ, P < 0·001) for fat intake, 6 % higher (1329 (15) kJ v. 1416 (26) kJ, P = 0·003) for protein intake and 78 % higher (356 (20) kJ v. 627 (46) kJ, P < 0·001) for alcohol intake on weekend days v. weekdays, respectively. The difference in carbohydrate intake, a 3 % increase, was not significant (4023 (41) kJ v. 4148 (67) kJ, P = 0·110) between weekdays and weekend days, respectively.

7 d v. 3 d energy intakes

Mean (se) EI for the 3 d periods Tuesday–Thursday–Saturday (9018 (115) kJ), Wednesday–Friday–Saturday (8885 (106) kJ) and Thursday–Saturday–Monday (9015 (116) kJ) were not significantly different (2·6 % higher, 0·1 % and 1·6 %, lower respectively) from the 7 d mean (8874 (72) kJ). Bland–Altman plots of the 3 d v. 7 d energy intakes with 95 % confidence limits (±2sd) can be seen in Fig. 2. In all 3 d periods v. 7 d there is an upward trend, the difference becomes more positive at greater intakes. The bias, or average of the differences, should be close to zero if the two methods being compared are similar. Our results for bias were 160, −25 and 129 kJ for Tuesday–Thursday–Saturday, Wednesday–Friday–Sunday and Thursday–Saturday–Monday, respectively. This indicates that intake recorded on Wednesday–Friday–Sunday is the most comparable of the 3 d periods to the 7 d intake and Tuesday–Thursday–Saturday is the least comparable.

Fig. 2 Bland–Altman plots of 3 d v. 7 d energy intake, with 95 % confidence limits (±2sd), among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. (a) Tuesday–Thursday–Saturday v. Monday–Sunday (y = 0·1663x–1328·8, R 2 = 0·127, P = 0·29); (b) Wednesday–Friday–Sunday v. Monday–Sunday (y = 0·0749x–689·45, R 2 = 0·0172, P = 0·94); (c) Thursday–Saturday–Monday v. Monday–Sunday (y = 0·1658x–1352·1, R 2 = 0·1137, P = 0·30)

There was no significant difference between these 3 d periods and the 7 d mean for macronutrient intake (results not shown).

Micronutrient intake: 7 d results

Day-to-day variation in nutrient intake in free-living subjects is large, creating practical study design issues for researchers if more days of recording are required to evaluate habitual intake(Reference Hartman, Brown, Palmgren, Pietinen, Verkasalo, Myer and Virtamo6, Reference Wassertheil-Smoller, Davis, Breuer, Chang, Oberman and Blaufox26, Reference Thompson and Byers27). Willett(Reference Willett20) reported that shorter recording periods may provide a reasonable estimation of mean intake but with overestimated standard deviations.

The UK Food Standards Agency Recommended Daily Allowance(28) (RDA) for vitamin A is 700 μg and 600 μg for men and women, respectively. The mean (se) intake from our weighed intakes was 533 (62) μg for men (24 % below the RDA) and 501 (71) μg for women (16 % below the RDA). The mean was 513 (51) μg for all subjects. The UK RDA for vitamin C is 40 mg. The mean (se) intake from our weighed intakes was 95 (9) mg for men (137 % above the RDA) and 96 (7) mg for women (140 % above the RDA). The mean was 96 (5) mg for all subjects, 140 % above the RDA. The UK RDA for vitamin D is 2·50 μg. The mean (se) intake from the weighed intakes was 2·98 (0·48) μg for men (19 % above the RDA) and 2·45 (0·29) μg for women (2 % below the RDA). The mean for all subjects was 2·64 (0·25) μg, 6 % above the RDA. The UK RDA for vitamin E is 4·0 mg and 3·0 mg for men and women, respectively. The mean (se) intake from the weighed intakes was 6·1 (0·4) mg for men (52 % above the RDA) and 5·2 (0·3) mg for women (73 % above the RDA). The mean for all subjects was 5·5 (0·2) mg, well above the RDA.

Micronutrient intake: 7 d v. 3 d

Mean (se) vitamin A intake on Tuesday–Thursday–Saturday was 17 % lower than on Wednesday–Friday–Sunday (467 (16) μg v. 562 (40) μg, P = 0·03). However, none of the 3 d periods were significantly different (all within 12 %) from the 7 d mean (513 (51) μg). No significance was found for vitamin C (all within 4 %), D (all within 7 %) or E (all within 3 %) when comparing the 3 d periods with the 7 d mean or with each other.

Seasonal variation: energy and macronutrient intake

In comparing seasons, no significant difference was found in average EI (P = 0·543). However, there was a gender × season interaction (P = 0·019) with a different intake pattern for females than for males. This can be seen in Fig. 3. For females only, lower mean (se) EI was recorded in summer (8117 (610) kJ) and autumn (7941 (699) kJ) compared with that recorded in spring (8929 (979) kJ) and winter (8132 (1041) kJ). Conversely for males, higher mean (se) EI was recorded in summer (10 420 (736) kJ) and autumn (10 490 (1041) kJ) compared with spring (9319 (1441) kJ) and winter (9103 (1505) kJ).

Fig. 3 Energy intake by gender (, females; , males) and season among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. Values are means with their standard errors represented by vertical bars. There was a significant gender × season interaction (P = 0·02); females recorded lower energy intakes in summer and autumn compared with spring and winter, while males recorded higher mean energy intakes in summer and autumn compared with spring and winter

There was no seasonal difference found for fat, protein or carbohydrate intake (results not shown).

Seasonal variation: micronutrient intake

Table 2 indicates the average seasonal intake for each gender of vitamins A, C, D and E over 7 d. Vitamin A is represented as a total of retinol and carotenoids, as retinol equivalents (1 μg RE = 12 μg carotenoids). A significant difference was found between genders for vitamins D and E across all seasons but not for vitamins A or C. The intake for males was 18 % higher (P < 0·01) and 14 % higher (P < 0·001) than that for females for vitamins D and E, respectively. When the data for both genders were combined, no significant difference was found with respect to season for vitamin C, D or E (results not shown) and, despite a difference of 28 % between the intake of vitamin A in spring and summer, there was no statistical significance.

Table 2 Micronutrient intake among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004

a,bMean values within a column with unlike superscript letters were significantly different (P < 0·05).

Discussion

Energy and nutrient intake results from 7 d and 3 d records

The 3 d weighed intake is a common assessment tool in nutrition research. It has been recommended that the three days should consist of one weekend day and two weekdays(Reference Bingham7) – but which three days are most representative of habitual intake? There are limited data on the variability of energy and nutrient intake with respect to either the effect of day(s) of recording or seasonal effect, but both of these issues may have practical implications for researchers conducting nutritional assessment studies. Therefore, the first aim of the current study was to compare EI results from 7 d food intakes with different 3 d periods within the same week. Average intakes for each of the seven days of the week were also examined. In accordance with previous work(Reference Taggart8, Reference de Castro9, Reference Jula, Seppanen and Alanen29) we found that there was a significant difference between EI collected on Monday–Friday compared with Saturday and Sunday, with the weekend EI recorded to be higher. This could have implications in the selection of which days should be collected during a 3 d weighed record. Most importantly, the definition of what is a ‘weekend day’ may be an issue of interest. We found that there was a significant difference for EI between Monday–Thursday and Friday, but not between Friday and Sunday. Does this indicate that Friday could be classified as a ‘weekend day’ rather than a ‘weekday’? Our results for EI from all the 3 d periods we examined, most noticeably Wednesday–Friday–Sunday, were found to be comparable to the 7 d mean (within 3 %). Similar findings have been noted previously when comparing 3 d and 7 d EI results(Reference Burnett, O’Connor, Koltyn, Raglin and Morgan30). Our results suggest that Wednesday–Friday–Sunday should be used in future comparisons with 7 d intakes.

The fat, protein and alcohol intakes were also significantly higher at the weekend (Saturday and Sunday) compared with weekdays (Monday–Friday), explaining the elevated EI results. This supports work carried out by Haines et al.(Reference Haines, Hama, Guilkey and Popkin31) and de Castro(Reference de Castro9), who also found that weekend intakes were higher for energy, fat and alcohol. Our results showed no significant differences for macro- or micronutrient intake when comparing the 3 d results with the 7 d mean. This suggests that, for the evaluation of nutrient intake, a 3 d record is sufficient to be representative of habitual intake.

Seasonal variation in energy and nutrient intake

The second aim of the present study was to compare the energy and nutrient results for seasonal variation. Ideally, to examine seasonal variation each volunteer would have recorded four 7 d intakes, one in each of our designated seasons. However, this was not possible owing to practical limitations. There have been largely differing results published previously for the effect of seasonality on EI, showing no significance(Reference Van Staveren, Deurenberg, Burema, De Groot and Hautvast32), higher values observed in autumn/winter compared with spring/summer(Reference Tokudome, Imaeda, Nagaya, Fujiwara, Sato, Kuriki, Kikuchi, Maki and Tokudome33Reference Ma, Olendzki, Li, Hafner, Chiriboga, Hebert, Campbell, Sarnie and Ockene35) or higher values observed in winter/spring compared with summer/autumn(Reference Subar, Frey, Harlan and Kahle36, Reference Fowke, Schlundt, Gong, Jin, Shu, Wen, Liu, Gao and Zheng37). Some studies compared winter and summer intakes only, and reported winter intakes to be significantly higher(Reference Lee, Lawler, Panemangalore and Street38Reference Shahar, Yerushalmi, Lubin, Froom, Shahar and Kristal-Boneh40). It should be noted that the methodology for all of these studies varied, either in terms of subjects studied (females only(Reference Van Staveren, Deurenberg, Burema, De Groot and Hautvast32Reference de Castro34, Reference Fowke, Schlundt, Gong, Jin, Shu, Wen, Liu, Gao and Zheng37, Reference Lee, Lawler, Panemangalore and Street38), males only(Reference Shahar, Yerushalmi, Lubin, Froom, Shahar and Kristal-Boneh40) or both(Reference Ma, Olendzki, Li, Hafner, Chiriboga, Hebert, Campbell, Sarnie and Ockene35, Reference Subar, Frey, Harlan and Kahle36, Reference Capita and Alonso-Calleja39)) or recording techniques for EI (7 d recorded intakes(Reference Tokudome, Imaeda, Nagaya, Fujiwara, Sato, Kuriki, Kikuchi, Maki and Tokudome33, Reference de Castro34, Reference Lee, Lawler, Panemangalore and Street38, Reference Capita and Alonso-Calleja39), FFQ(Reference Subar, Frey, Harlan and Kahle36, Reference Fowke, Schlundt, Gong, Jin, Shu, Wen, Liu, Gao and Zheng37, Reference Shahar, Yerushalmi, Lubin, Froom, Shahar and Kristal-Boneh40) or 24 h recalls(Reference Van Staveren, Deurenberg, Burema, De Groot and Hautvast32, Reference Ma, Olendzki, Li, Hafner, Chiriboga, Hebert, Campbell, Sarnie and Ockene35)), with no obvious pattern between methodology and results.

It has been suggested that any seasonal effect may be less pronounced in an industrialised society(Reference Bingham7), as more foods are available throughout the year due to improved food preservation techniques and increased importation(Reference Van Staveren, Deurenberg, Burema, De Groot and Hautvast32). Despite fewer volunteers in winter/spring compared with summer/autumn (seventy-one v. 187), our results are in line with this suggestion; with no difference on average between seasons for the 7 d data from all subjects. However, there was found to be a gender × season interaction. The EI for females was lower in summer and autumn compared with spring and winter, with the converse observed for males. These results support work published previously from studies in the USA(Reference Subar, Frey, Harlan and Kahle36, Reference Lee, Lawler, Panemangalore and Street38), China(Reference Fowke, Schlundt, Gong, Jin, Shu, Wen, Liu, Gao and Zheng37) and Spain(Reference Capita and Alonso-Calleja39) for females’ EI and in Finland(Reference Hartman, Brown, Palmgren, Pietinen, Verkasalo, Myer and Virtamo6) for males’ EI. This may be in part explained by females being more selective with food choices e.g. low-fat foods during the warmer months of the year, perhaps as an attempt at ‘healthy eating’, or by being more prone to ‘comfort eat’ in the winter.

Our results for micronutrient intake were above recommended UK values for all the vitamins we analysed for except vitamin A, supporting results published from the National Diet and Nutrition Survey(Reference Swann41). This is a positive finding for the Scottish population, which is reported to have the lowest vitamin levels in Great Britain(Reference Gillie42Reference Mishra, Malik, Paul, Wadsworth and Bolton-Smith44) and is often referred to as the ‘sick man of Europe’ with respect to mortality and morbidity risk. When examining the variation in vitamin intakes, significance was found only for vitamins D (P < 0·01) and E (P < 0·001) between genders. No significance was found between seasons for males, females or all subjects. Previous studies(Reference Hartman, Brown, Palmgren, Pietinen, Verkasalo, Myer and Virtamo6, Reference Subar, Frey, Harlan and Kahle36, Reference Fowke, Schlundt, Gong, Jin, Shu, Wen, Liu, Gao and Zheng37, Reference Shahar, Yerushalmi, Lubin, Froom, Shahar and Kristal-Boneh40, Reference Hill, O’Brien, Cashman, Flynn and Kiely45) have looked at the actual food groups eaten, e.g. fruit and vegetables, with respect to vitamin intakes and seasonality. This could be a further area of research for this data set to examine the vitamin intakes more closely.

Implications

To collect data on habitual EI in free-living subjects, the ‘gold standard’ 7 d weighed record should ideally be used. However, our results support the use of a 3 d record as a suitable tool to obtain data in large nutritional studies if use of a 7 d record is not feasible, despite 3 d records being more affected by variability. Errors in self-reported dietary intakes have long been an issue under research. At least nine possible sources of errors in food intake assessment have been identified(Reference Bingham7, Reference Stubbs, Johnstone, O’Reilly and Poppitt46). These errors can be attributed to subject compliance (reporting errors, wrong weights of foods, variation with time, wrong frequency of consumption, change in diet and response bias) or to the study investigators (errors from food tables, coding errors and sampling bias). In conclusion, the most representative 3 d period of the 7 d mean and therefore the best compromise in addressing the issues above is Wednesday–Friday–Sunday.

Acknowledgements

Sources of funding: The authors gratefully acknowledge funding from the Scottish Executive. Conflict of interest declaration: None of the authors had a conflict of interest. Author contributions: A.M.J., J.R.S., D.M.J. and K.R. were responsible for the study concept and design. A.M.J., D.M.J., C.L.F., S.D.M. and J.S. were responsible for the data collection. C.L.F., A.M.J., S.D.M. and J.S. were responsible for the data analysis. G.W.H. was responsible for the statistical analysis. C.L.F. and A.M.J. were responsible for the first draft and all authors for critical revision of the manuscript for important intellectual content. Acknowledgments: We would like to thank all of the volunteers who participated in the studies as well as Sylvia Hay, Marion Scott and Jean Bryce for assistance in the Human Nutrition Unit.

References

1.Black, AE, Goldberg, GR, Jebb, SA, Livingstone, MB, Cole, TJ & Prentice, AM (1991) Critical evaluation of energy intake data using fundamental principles of energy physiology: 2. Evaluating the results of published surveys. Eur J Clin Nutr 45, 583599.Google ScholarPubMed
2.Tomoyasu, NJ, Toth, MJ & Poehlman, ET (2000) Misreporting of total energy intake in older African Americans. Int J Obes Relat Metab Disord 24, 2026.CrossRefGoogle ScholarPubMed
3.Trabulsi, J & Schoeller, DA (2001) Evaluation of dietary assessment instruments against doubly labeled water, a biomarker of habitual energy intake. Am J Physiol Endocrinol Metab 281, E891E899.CrossRefGoogle Scholar
4.Whybrow, S, Horgan, G & Stubbs, RJ (2008) Low-energy reporting and duration of recording period. Eur J Clin Nutr 62, 11481150.CrossRefGoogle ScholarPubMed
5.de Castro, JM (2006) Varying levels of food energy self-reporting are associated with between-group, but not within-subject, differences in food intake. J Nutr 136, 13821388.CrossRefGoogle Scholar
6.Hartman, AM, Brown, CC, Palmgren, J, Pietinen, P, Verkasalo, M, Myer, D & Virtamo, J (1990) Variability in nutrient and food intakes among older middle-aged men. Am J Epidemiol 132, 9991012.CrossRefGoogle ScholarPubMed
7.Bingham, SA (1987) The dietary assessment of individuals; methods, accuracy, new techniques and recommendations. Nutr Abstr Rev 57, 705742.Google Scholar
8.Taggart, N (1962) Diet, activity and body-weight. A study of variations in a woman. Br J Nutr 16, 223235.CrossRefGoogle ScholarPubMed
9.de Castro, JM (1991) Weekly rhythms of spontaneous nutrient intake and meal pattern of humans. Physiol Behav 50, 729738.CrossRefGoogle ScholarPubMed
10.DEFRA Economics & Statistics (undated) National Food Survey 2000: annual report on food expenditure, consumption and nutrient intakes. https://statistics.defra.gov.uk/esg/publications/nfs/2000/default.asp (accessed January 2009).Google Scholar
11.Johnstone, AM, Murison, SD, Duncan, JS, Rance, KA & Speakman, JR (2005) Factors influencing variation in basal metabolic rate include fat-free mass, fat mass, age, and circulating thyroxine but not sex, circulating leptin, or triiodothyronine. Am J Clin Nutr 82, 941948.CrossRefGoogle ScholarPubMed
12.Johnstone, AM, Rance, KA, Murison, SD, Duncan, JS & Speakman, JR (2006) Additional anthropometric measures may improve the predictability of basal metabolic rate in adult subjects. Eur J Clin Nutr 60, 14371444.CrossRefGoogle ScholarPubMed
13.Jackson, DM, Djafarian, K, Stewart, J & Speakman, JR (2009) Increased television viewing is associated with elevated body fatness but not with lower total energy expenditure in children. Am J Clin Nutr 89, 10311036.CrossRefGoogle Scholar
14.Speakman, JR, Djafarian, K, Stewart, J & Jackson, DM (2007) Assortative mating for obesity. Am J Clin Nutr 86, 316323.CrossRefGoogle ScholarPubMed
15.Livesey, G & Elia, M (1988) Estimation of energy expenditure, net carbohydrate utilization, and net fat oxidation and synthesis by indirect calorimetry: evaluation of errors with special reference to the detailed composition of fuels. Am J Clin Nutr 47, 608628.CrossRefGoogle Scholar
16.Goldberg, GR, Black, AE, Jebb, SA, Cole, TJ, Murgatroyd, PR, Coward, WA & Prentice, AM (1991) Critical evaluation of energy intake data using fundamental principles of energy physiology: 1. Derivation of cut-off limits to identify under-recording. Eur J Clin Nutr 45, 569581.Google ScholarPubMed
17.Schofield, WN (1985) Predicting basal metabolic rate, new standards and review of previous work. Hum Nutr Clin Nutr 39, Suppl. 1, 541.Google ScholarPubMed
18.Rutishauser, IH (2005) Dietary intake measurements. Public Health Nutr 8, 11001107.CrossRefGoogle ScholarPubMed
19.Nelson, M, Atkinson, M & Meyer, J (1997) A Photographic Atlas of Food Portion Sizes. London: MAFF Publications.Google Scholar
20.Willett, W (1990) Nutritional Epidemiology. Oxford: Oxford University Press.Google Scholar
21.Friedenreich, CM (1994) Methodologic issues for pooling dietary data. Am J Clin Nutr 59, 1 Suppl., 251S252S.CrossRefGoogle ScholarPubMed
22.Food Standards Agency (2002) McCance and Widdowson’s The Composition of Foods, 6th summary ed. Cambridge: Royal Society of Chemistry.Google Scholar
23.Crawley, H (1988) Food Portion Sizes. London: Food Standards Agency.Google Scholar
24.Bland, JM & Altman, DG (1986) Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1, 307310.CrossRefGoogle ScholarPubMed
25.Department of Health (1991) Dietary Reference Values for Food Energy and Nutrients in the United Kingdom. London: HMSO.Google Scholar
26.Wassertheil-Smoller, S, Davis, BR, Breuer, B, Chang, CJ, Oberman, A & Blaufox, MD (1993) Differences in precision of dietary estimates among different population subgroups. Ann Epidemiol 3, 619628.CrossRefGoogle ScholarPubMed
27.Thompson, FE & Byers, T (1994) Dietary Assessment Resource Manual. J Nutr 124, 2245s2317s.Google ScholarPubMed
28. Food Standards Agency (undated) Nutrition, Vitamins and Minerals. http://www.eatwell.gov.uk/healthydiet/nutritionessentials/vitaminsandminerals (accessed March 2008).Google Scholar
29.Jula, A, Seppanen, R & Alanen, E (1999) Influence of days of the week on reported food, macronutrient and alcohol intake among an adult population in south western Finland. Eur J Clin Nutr 53, 808812.CrossRefGoogle ScholarPubMed
30.Burnett, KF, O’Connor, PJ, Koltyn, KF, Raglin, JS & Morgan, WP (1994) Use of three-day food records as estimates of seven-day calorie intake during physical training. Med Exerc Nutr Health 3, 185193.Google Scholar
31.Haines, PS, Hama, MY, Guilkey, DK & Popkin, BM (2003) Weekend eating in the United States is linked with greater energy, fat, and alcohol intake. Obes Res 11, 945949.CrossRefGoogle ScholarPubMed
32.Van Staveren, WA, Deurenberg, P, Burema, J, De Groot, LC & Hautvast, JG (1986) Seasonal variation in food intake, pattern of physical activity and change in body weight in a group of young adult Dutch women consuming self-selected diets. Int J Obes 10, 133145.Google Scholar
33.Tokudome, Y, Imaeda, N, Nagaya, T, Fujiwara, N, Sato, J, Kuriki, K, Kikuchi, S, Maki, S & Tokudome, S (2002) Daily, weekly, seasonal, within- and between-individual variation in nutrient intake according to four season consecutive 7 day weighed diet records in Japanese female dieticians. J Epidemiol 12, 8592.CrossRefGoogle Scholar
34.de Castro, JM (1991) Seasonal rhythms of human nutrient intake and meal patterns. Physiol Behav 50, 243248.CrossRefGoogle Scholar
35.Ma, Y, Olendzki, BC, Li, W, Hafner, AR, Chiriboga, D, Hebert, JR, Campbell, M, Sarnie, M & Ockene, IS (2006) Seasonal variation in food intake, physical activity, and body weight in a predominantly overweight population. Eur J Clin Nutr 60, 519528.CrossRefGoogle Scholar
36.Subar, AF, Frey, CM, Harlan, LC & Kahle, L (1994) Differences in reported food frequency by season of questionnaire administration: the 1987 National Health Interview Survey. Epidemiology 5, 226233.CrossRefGoogle ScholarPubMed
37.Fowke, JH, Schlundt, D, Gong, Y, Jin, F, Shu, XO, Wen, W, Liu, DK, Gao, YT & Zheng, W (2004) Impact of season of food frequency questionnaire administration on dietary reporting. Ann Epidemiol 14, 778785.CrossRefGoogle ScholarPubMed
38.Lee, CJ, Lawler, GS, Panemangalore, M & Street, D (1987) Nutritional status of middle-aged and elderly females in Kentucky in two seasons: Part 1. Body weight and related factors. J Am Coll Nutr 6, 209215.CrossRefGoogle ScholarPubMed
39.Capita, R & Alonso-Calleja, C (2005) Differences in reported winter and summer dietary intakes in young adults in Spain. Int J Food Sci Nutr 56, 431443.CrossRefGoogle Scholar
40.Shahar, DR, Yerushalmi, N, Lubin, F, Froom, P, Shahar, A & Kristal-Boneh, E (2001) Seasonal variations in dietary intake affect the consistency of dietary assessment. Eur J Epidemiol 17, 129133.CrossRefGoogle ScholarPubMed
41.Swann, G (2004) Findings from the latest National Diet and Nutrition Survey. Proc Nutr Soc 63, 505512.CrossRefGoogle Scholar
42.Gillie, O (2008) Scotland’s Health Deficit: An Explanation and a Plan. London: Health Research Forum.Google Scholar
43.Davies, PSW, Bates, CJ, Cole, TJ, Prentice, A & Clarke, PC (1999) Vitamin D: seasonal and regional differences in preschool children in Great Britain. Eur J Clin Nutr 53, 195198.CrossRefGoogle ScholarPubMed
44.Mishra, GD, Malik, NS, Paul, AA, Wadsworth, MEJ & Bolton-Smith, C (2003) Childhood and adult dietary vitamin E intake and cardiovascular risk factors in mid-life in the 1946 British Birth Cohort. Eur J Clin Nutr 57, 14181425.CrossRefGoogle ScholarPubMed
45.Hill, TR, O’Brien, MM, Cashman, KD, Flynn, A & Kiely, M (2004) Vitamin D intakes in 18–64-y-old Irish adults. Eur J Clin Nutr 58, 15091517.CrossRefGoogle ScholarPubMed
46.Stubbs, RJ, Johnstone, AM, O’Reilly, LM & Poppitt, SD (1998) Methodological issues relating to the measurement of food, energy and nutrient intake in human laboratory-based studies. Proc Nutr Soc 57, 357372.CrossRefGoogle Scholar
Figure 0

Table 1 7 d energy intake among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004

Figure 1

Fig. 1 Mean energy intake by day of the week among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. Values are means with their standard errors represented by vertical bars. Energy intake was significantly different on Saturday and Sunday compared with the average of the weekday values (P < 0·001)

Figure 2

Fig. 2 Bland–Altman plots of 3 d v. 7 d energy intake, with 95 % confidence limits (±2sd), among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. (a) Tuesday–Thursday–Saturday v. Monday–Sunday (y = 0·1663x–1328·8, R2 = 0·127, P = 0·29); (b) Wednesday–Friday–Sunday v. Monday–Sunday (y = 0·0749x–689·45, R2 = 0·0172, P = 0·94); (c) Thursday–Saturday–Monday v. Monday–Sunday (y = 0·1658x–1352·1, R2 = 0·1137, P = 0·30)

Figure 3

Fig. 3 Energy intake by gender (, females; , males) and season among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004. Values are means with their standard errors represented by vertical bars. There was a significant gender × season interaction (P = 0·02); females recorded lower energy intakes in summer and autumn compared with spring and winter, while males recorded higher mean energy intakes in summer and autumn compared with spring and winter

Figure 4

Table 2 Micronutrient intake among Caucasian adults (n 260), Aberdeen, north-east Scotland, UK, 2002–2004