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Nut consumption is associated with better nutrient intakes: results from the 2008/09 New Zealand Adult Nutrition Survey

Published online by Cambridge University Press:  20 October 2015

Rachel C. Brown*
Affiliation:
Department of Human Nutrition, University of Otago, PO Box 56, Dunedin 9054, New Zealand
Siew Ling Tey
Affiliation:
Clinical Nutrition Research Centre, Singapore Institute for Clinical Sciences, A*STAR, 14 Medical Drive, #07-02, Singapore 117599, Singapore
Andrew R. Gray
Affiliation:
Department of Preventive and Social Medicine, University of Otago, PO Box 56, Dunedin 9054, New Zealand
Alex Chisholm
Affiliation:
Department of Human Nutrition, University of Otago, PO Box 56, Dunedin 9054, New Zealand
Claire Smith
Affiliation:
Department of Human Nutrition, University of Otago, PO Box 56, Dunedin 9054, New Zealand
Elizabeth Fleming
Affiliation:
Department of Human Nutrition, University of Otago, PO Box 56, Dunedin 9054, New Zealand
Winsome Parnell
Affiliation:
Department of Human Nutrition, University of Otago, PO Box 56, Dunedin 9054, New Zealand
*
*Corresponding author: R. C. Brown, fax +64 3 479 7958, email [email protected]
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Abstract

A limited number of studies have examined associations between nut consumption and nutrient intakes or diet quality. None has investigated these associations in the Southern Hemisphere. The purpose of this study was to examine associations between nut consumption and nutrient intakes among adult New Zealanders. Data from the 24-h recalls of 4721 participants from the cross-sectional 2008/09 New Zealand Adult Nutrition Survey (2008/09 NZANS) were used to determine whole nut intake and total nut intake from all sources as well as nutrient intakes. Regression models, both unadjusted and adjusted for potential confounders, were used to estimate differences in nutrient intakes between those consuming and those not consuming nuts. From adjusted models, compared with non-whole nut consumers, whole nut consumers had higher intakes of energy and percentage of energy from total fat, MUFA and PUFA, whereas percentage of energy from SFA and carbohydrate was lower (all P≤0·025). After the additional adjustment for energy intake, whole nut consumers had higher intakes of dietary fibre, vitamin E, folate, Cu, Mg, K, P and Zn (all P≤0·044), whereas cholesterol and vitamin B12 intakes were significantly lower (both P≤0·013). Total nut consumption was associated with similar nutrient profiles as observed in whole nut consumers, albeit less pronounced. Nut consumption was associated with better nutrient profiles, especially a lower intake of SFA and higher intakes of unsaturated fats and a number of vitamins and minerals that could collectively reduce the risk for chronic disease, in particular for CVD.

Type
Full Papers
Copyright
Copyright © The Authors 2015 

Nuts are rich in unsaturated fatty acids, vitamins, minerals and bioactive compounds, which collectively are likely to contribute to their well-recognised health properties, in particular to reduce CVD risk( Reference Kris-Etherton, Yu-Poth and Sabate 1 Reference Ros 3 ). If consumed in sufficient amounts, the nutrients present in nuts are likely to improve diet quality, which should translate into overall improved health outcomes for nut consumers compared with non-nut consumers.

Although individual nuts differ in types and amounts of nutrients, all nuts are considered to be nutrient dense( Reference Ros 3 , Reference Alasalvar and Bolling 4 ). Nuts are generally rich sources of cis-unsaturated fatty acids, fibre and plant protein including arginine( Reference Ros 3 , Reference Brufau, Boatella and Rafecas 5 ). In addition, individual nuts can contribute important amounts of folate, vitamin E, Ca, Mg, Cu, Zn, Se and K. Nuts also contain bioactive substances such as phytosterols, antioxidants and phenolic compounds, which are further likely to contribute positively to health outcomes( Reference Bolling, Chen and McKay 6 ). Thus, frequent nut consumption is likely to make important contributions towards a healthy diet. Indeed O’Neil et al.( Reference O’Neil, Keast and Fulgoni 7 ) showed that tree nut consumption improved nutrient intake and diet quality in the National Health and Nutrition Examination Survey (NHANES) 1999–2004 cohort. In particular, the diets of tree nut consumers contained greater amounts of dietary fibre, vitamin E, Ca, Mg and K and lower amounts of Na compared with non-consumers. Using the Healthy Eating Index-2005, diet quality was found to be higher in nut consumers. This was also seen in their analysis of the NHANES 2005–2010 cohort( Reference O’Neil, Nicklas and Fulgoni 8 ). In addition, this group found similar improvements in diet quality when assessing ‘out-of-hand’ tree nut consumers( Reference O’Neil, Keast and Nicklas 9 ). ‘Out-of-hand’ consumers, defined as those who ate at least 7 g/d of nuts solely as nuts and not as part of other products, were studied because they were thought to make a more conscious decision to eat nuts. These consumers had higher intakes of energy, MUFA, PUFA, dietary fibre, Cu and Mg and lower intakes of carbohydrate, cholesterol and Na when compared with non-consumers. Similarly, King et al.( Reference King, Blumberg and Ingwersen 10 ) reported that nuts made an important contribution to the diets of both nut consumers and nut snackers (individuals who consume nuts as snacks).

In support of these findings, intervention studies have reported improvements to nutrient profiles resulting from the addition of nuts to participants’ diets without any other dietary advice. Increases in cis-unsaturated fat, vegetable protein, dietary fibre, vitamin E, Cu and Mg have been observed( Reference Griel, Eissenstat and Juturu 11 Reference Tey, Brown and Gray 13 ).

To date, no research has examined the nutrient contribution of nuts to the New Zealand diet, where dietary patterns may differ from countries where nut intake patterns have been previously described( Reference O’Neil, Keast and Fulgoni 7 , Reference O’Neil, Keast and Nicklas 9 , Reference King, Blumberg and Ingwersen 10 ). Traditionally, New Zealand diets have contained more meat and butter than that of other countries that are part of the Organisation for Economic Co-operation and Development, and, although declining over the last few decades, bread, potatoes and beef remain major sources of energy and nutrients( Reference Smith, Gray and Mainvil 14 ). This differs substantially from a Mediterranean eating pattern common to a number of European countries( Reference Willett, Sacks and Trichopoulou 15 ). Compared with the USA, a greater percentage of energy is consumed from foods prepared at home in New Zealand, as opposed to fast food and restaurant food( Reference Smith, Gray and Fleming 16 ). Also, unlike in the USA, fortification of flour with folic acid is not mandatory, and fortification of foods with vitamin D is uncommon( Reference Crider, Bailey and Berry 17 , Reference Nowson, McGrath and Ebeling 18 ). In addition, New Zealand soils are low in Se and I, meaning intakes of these micronutrients are relatively low( Reference Thomson 19 ). Therefore, the aim of this study was to compare the nutrient profiles of nut consumers with that of non-nut consumers in a cross-section of the New Zealand population.

Methods

Study population

The 2008/09 New Zealand Adult Nutrition Survey (2008/09 NZANS) was a cross-sectional survey of New Zealanders aged 15 years and over, carried out from October 2008 to October 2009. A full description of the study design and methods is available elsewhere( 20 ), and only a summary is presented here. Participants were recruited using a three-stage process where 607 meshblocks were selected using a probability-proportional-to-size design. A meshblock is defined as a small geographical area within New Zealand defined by Statistics New Zealand. Each meshblock contains about 110 people in urban areas and sixty in rural areas. After random selection of a household, random selection of a participant within the household occurred. Oversampling of Māori and Pacific people and age groups 15–18 and 71 years was used in order to achieve adequate numbers for subgroup analyses by ethnicity and age.

Informed, written consent was obtained from each participant, or from the guardian of participants aged <18 years, before interviews. Ethical approval was gained from the New Zealand Health and Disability Multi-Region Ethics Committee (MEC/08/04/049). This study was conducted according to the guidelines laid down in the Declaration of Helsinki.

Dietary assessment

Survey data were collected at participants’ homes by trained interviewers using computer-assisted personal interview software. An interviewer-administered multiple-pass 24-h diet recall method was used to collect quantitative information on all foods and drinks the participant consumed the previous day (from midnight to midnight). It included all foods and drinks consumed, both at and away from home.

In the first stage of the recall, a ‘quick list’ of all foods, beverages and dietary supplements consumed during the preceding day was obtained. In the second stage, detailed descriptions of all the foods and beverages consumed were collected. Information on any additions made to food before eating was also collected. In the third stage, estimates of the amounts of all foods and beverages consumed were obtained. The amount eaten was described by volume wherever possible (e.g. cups or tablespoons). In addition, food photographs, shape dimensions, food portion assessment aids (e.g. dried beans) and packaging information were used. Finally, in the fourth stage, the foods were reviewed and the information collected was checked. Any additions and changes were made at this point. Repeat interviews were conducted on 1180 participants, but these were not used here.

Determination of nut consumption

For the purpose of this analysis, the term ‘nuts’ included tree nuts, mixed nuts and peanuts. Chestnuts, coconut and coconut products were not included in this analysis as their nutrient profiles differ from the aforementioned ‘nuts’. Tree nuts include almonds, Brazil nuts, cashews, hazelnuts, macadamias, mixed nuts, pecans, pine nuts, pistachios and walnuts. Nut intake was assessed using the 24-h recall data from the 2008/09 NZANS, and nut consumption was subsequently divided into three categories: (i) whole nuts including tree nuts, mixed nuts and peanuts eaten whole as part of a snack (e.g. mixed-nut snacks) or as an addition to a food/meal (e.g. almonds sprinkled on a salad); (ii) nut butters including those made from peanuts and tree nuts (e.g. peanut butter, hazelnut spread); and (iii) other sources including tree nuts, peanuts and mixed nuts eaten as ingredients in recipes or as part of commercial products (e.g. breakfast cereals, snack bars, satay). ‘Total nuts’ encompass whole nuts, nut butters and nuts from hidden sources. Participants who reported consuming zero quantity of any nuts in their 24-h recall were classified as ‘non-nut consumers’. ‘Whole nut consumers’ were participants who reported consuming any amount of whole nuts, and ‘total nut consumers’ were participants who reported consuming any of whole nuts, nut butters and/or hidden sources of nuts.

Demographic variables

Demographic variables were selected a priori after reviewing the literature. Variables included sex, age category (15–18, 19–30, 31–50, 51–70, 71+ years), prioritised ethnicity, New Zealand Index of Deprivation (NZDep06), education, BMI and smoking status.

Ethnicity

Self-reported ethnicity was categorised into one of three ethnic groups based on a priority classification system using the coding prioritisation order (from highest to lowest) of Māori, Pacific and New Zealand European and Other.

New Zealand Index of Deprivation

NZDep06 is an area-based measure of deprivation, which uses nine variables from the New Zealand Census reflecting specified dimensions of both material and social deprivation. Each meshblock in New Zealand is given a score between 1 and 10, with a score of 1 reflecting the least deprived areas and 10 the most deprived. For the purpose of the 2008/09 NZANS, these scores were divided into quintiles where quintile 1 represents the 20 % least deprived and quintile 5 the 20 % most deprived areas.

Education

Participants were asked to report their highest school-level qualification and where appropriate their highest post-school qualification. Three groups comprising no formal school qualification, secondary school qualification only or post-school qualification (including trade certificates and university degrees) were used for these analyses.

Smoking status

Information was collected on smoking status during the interview, and participants were classified as a never smoker, ex-smoker or current smoker.

Anthropometric measurements

Trained interviewers carried out height and weight measurements in duplicate. Standing height was measured using a stadiometer (Seca 214) and weight using electronic scales (Tanita HD-351). BMI was calculated as weight (kg)/height squared (m2). The WHO BMI cut-offs were used to categorise BMI status in participants aged 19 years and over (underweight: <18·5 kg/m2; normal range: 18·5–24·99 kg/m2; overweight: ≥25–29·99 kg/m2; obese: ≥30 kg/m2). Relatively few individuals were classified as underweight (n 58), and this category was combined with the normal weight category. The Cole age- and sex-specific BMI cut-offs were used to categorise BMI status in those aged 15–18 years( Reference Cole, Bellizzi and Flegal 21 , Reference Cole, Flegal and Nicholls 22 ).

Statistical analysis

The complex survey design described above was accounted for in all analyses presented here. This includes incorporating both weights and clustering. The weights used were post-stratification weights for the questionnaire component of the 2008/09 NZANS and are intended to reflect the New Zealand population aged 15 years and above.

Log transformations were made where this improved residual normality and/or homoscedasticity. Variables that were log transformed are presented as geometric means with differences reported as the percentage of difference between the geometric means. Unadjusted and adjusted differences for nutrient intakes between nut consumers and non-nut consumers are presented. Adjusted regression models included sex, age group, prioritised ethnicity, BMI category, NZDep06 quintile, education and smoking status. We also adjusted for energy intake in a third model for each intake outcome to determine the effects of nuts on nutrient intake, independent of energy. This is both to adjust for any potential confounding between micronutrient intakes and health by physical activity and metabolic efficiency (not measured in this study) not accounted for through including BMI in the models and to acknowledge that some nutrients are required in absolute amounts irrespective of energy, and others are required in relative amounts.

Stata Statistical Software 12.1 (StataCorp LP) was used for all statistical analyses. All statistical tests were two-sided and P<0·05 was considered statistically significant.

Results

Characteristics of the sample

Table 1 describes the characteristics of the 2008/09 NZANS sample and that of total and whole nut consumers. A total of 4721 participants were recruited and completed a 24-h diet recall.

Table 1 Characteristics of survey participants in the 2008/09 New Zealand Adult Nutrition Survey (Numbers and percentages)

NZEO, New Zealand European and Other; NZDep06, New Zealand Index of Deprivation; Q, quintile.

* P value for difference between all survey participants and total nut consumers.

P value for difference between all survey participants and whole nut consumers.

Nut intake

We had previously described the nut intakes of New Zealanders( Reference Brown, Tey and Gray 23 ). In brief, the percentage of the population consuming whole nuts and total nuts on the day of the 24-h recall was 6·9 % (n 240) and 28·9 % (n 1167), respectively. Among whole nut consumers, the mean portion size was 40 (95 % CI 33, 47) g/d for whole nuts, and, among consumers of any nut, the mean portion size was 18 (95 % CI 16, 20) g/d for total nuts.

Nutrient intakes among whole nut consumers compared with non-whole nut consumers

When adjusted for potential confounders (not including energy intake), reported energy intakes and total fat expressed both in absolute terms and as a percentage of total energy (%TE) were significantly higher among whole nut consumers compared with non-whole nut consumers (all P<0·001) (Table 2). When examining the different types of fat, SFA as %TE was significantly lower among whole nut consumers compared with non-whole nut consumers (P=0·025). Conversely, both MUFA and PUFA when expressed in absolute amounts and as %TE were significantly higher in whole nut consumers (all P<0·001). Carbohydrate intakes expressed as %TE (P<0·001) were significantly lower among whole nut consumers, whereas protein intakes did not differ (P=0·165). Dietary fibre intake was significantly higher in whole nut consumers (P<0·001).

Table 2 Mean daily nutrient intake by consumption of whole nuts in the 2008/09 New Zealand Adult Nutrition SurveyFootnote * (Mean values and 95 % confidence intervals)

%TE, percentage of total energy.

* All variables were log transformed and geometric means are presented, with differences reported as the percentage difference between geometric means.

Adjustment for age, sex, ethnicity, BMI, New Zealand Index of Deprivation, education and smoking status.

In terms of micronutrients, overall intakes were higher among whole nut consumers. When adjusted for potential confounders (not including energy intake), intakes of thiamin, riboflavin, niacin, vitamin B6, total folate, vitamin C, vitamin E, Ca, Cu, Fe, Mg, P, K, Se and Zn were all significantly higher among whole nut consumers compared with non-whole nut consumers (all P<0·011).

When intakes were further adjusted for energy intake, dietary cholesterol was significantly lower among whole nut consumers (P<0·001), although dietary fibre remained significantly higher (P<0·001). Of the micronutrients, folate, vitamin E, Cu, Mg, P, K and Zn remained higher among whole nut consumers compared with non-whole nut consumers (all P≤0·044). Conversely, vitamin B12 intake was significantly lower among whole nut consumers (P=0·013).

Nutrient intakes among total nut consumers compared with non-total nut consumers

After adjustment for potential confounders (not including energy intake), mean reported energy intakes were significantly higher among total nut consumers compared with non-total nut consumers (P<0·001) (Table 3). When expressed in absolute terms and as %TE, total fat, MUFA and PUFA were all significantly higher among total nut consumers (all P<0·001). Intakes of SFA and carbohydrate were significantly higher in total nut consumers when expressed in absolute terms (all P<0·001) but not when expressed as %TE (all P≥0·082). Intakes of dietary fibre were 27 % higher in nut consumers compared with non-nut consumers (P<0·001).

Table 3 Mean daily nutrient intake by consumption of total nuts in the 2008/09 New Zealand Adult Nutrition SurveyFootnote * (Mean values and 95 % confidence intervals)

%TE, percentage of total energy.

* All variables were log transformed and geometric means are presented, with differences reported as the percentage difference between geometric means.

Adjustment for age, sex, ethnicity, BMI, New Zealand Index of Deprivation, education and smoking status.

For micronutrients, following adjustment for potential confounders (not including energy intake), the intakes of vitamin A, thiamin, riboflavin, niacin, vitamin B6, folate, vitamin C, vitamin E, Ca, Cu, Fe, Mg, P, K, Se and Zn were significantly higher among total nut consumers (all P≤0·009).

When intakes were further adjusted for energy intake, dietary fibre remained significantly higher (P<0·001) and dietary cholesterol significantly lower (P<0·001) in total nut consumers compared with non-total nut consumers. Of the micronutrients, vitamin E, Ca, Cu, Fe, Mg and P remained statistically significantly higher among total nut consumers (all P≤0·007).

Contribution of whole nuts to daily energy and nutrient intakes

When the study population was considered collectively, whole nuts contributed relatively minor amounts of energy and nutrients (Table 4). For example, whole nuts contributed only 0·7 %TE, 1·4 % total fat (0·54 %TE), 0·76 % SFA (0·08 %TE), 1·84 % MUFA (0·28 %TE), 2·04 % PUFA (0·15 %TE) and 0·68 % of protein (0·23 %TE). When broken down by sex, these did not differ to a meaningful extent between men and women.

Table 4 Contribution of whole nuts to daily energy and nutrients overall and for whole nut consumers in the 2008/09 New Zealand Adult Nutrition Survey (Mean values and 95 % confidence intervals)

However, among whole nut consumers, whole nuts made a substantial contribution to energy and nutrient intakes. Whole nuts provided about 10 %TE intake for whole nut consumers. Whole nuts also provided about 20 % of total fat intake for nut consumers, contributing about 8 %TE. When examining the different types of fat, it can be seen that whole nuts supplied about 11 % of SFA (contributing 3 %TE), with higher contributions of 27 % (4 %TE) to MUFA and 30 % (2·2 %TE) to PUFA. Whole nuts comprised approximately 10 % of the protein intake of nut consumers, providing 3·4 %TE. When broken down by sex, these did not differ to a meaningful extent between men and women, especially when looked at as percentages of total intake.

Discussion

This was the first study to assess dietary intake in relation to nut consumption, in a cross-sectional survey of a population from the Southern Hemisphere, more specifically New Zealand. This study confirms the results from dietary surveys undertaken in the USA, which show nut consumption is associated with an improvement in nutrient intakes and overall diet quality. Among nut consumers in New Zealand, nuts made a substantial contribution to TE, fat, MUFA, PUFA and dietary fibre. Nut consumers also had a more nutrient-dense diet in terms of micronutrients than did non-nut consumers.

We analysed the data both for whole nut consumers and total nut consumers. It has been previously postulated that ‘out-of-hand’ nut consumers may differ from total nut consumers, in that they make a conscious decision to consume nuts, which may be associated with a desire for a healthier lifestyle( Reference O’Neil, Keast and Nicklas 9 ). This group is similar to the whole nut consumers in the present study. Given total nut consumption included nuts from other sources, which include confectionery and snacks that contain added sugar, fat and salt, consuming whole nuts might be expected to be associated with improved diet quality compared with other total nut consumers. We found that SFA and carbohydrate when expressed as %TE were significantly lower for whole nut consumers compared with non-whole nut consumers, whereas this difference was not evident when comparing total nut consumers with non-nut consumers. Micronutrient intakes differed between nut consumers and non-nut consumers for both whole nut and total nut intakes, although the differences were more pronounced for most nutrients among whole nut consumers.

Tree nuts and peanuts are rich sources of MUFA and PUFA, although low in SFA. This is reflected in the intakes of whole and total nut consumers, where the intake of unsaturated fats was significantly higher among nut consumers both in absolute terms and when expressed as %TE intake. Conversely, when SFA was expressed as %TE, intake was significantly lower in whole nut consumers. Intakes of dietary fibre were also higher among nut consumers compared with non-nut consumers. It is plausible that these intakes may account for much of the beneficial effects of nuts on cardiovascular health observed among nut consumers in both epidemiological( Reference Bao, Han and Hu 24 Reference Zhou, Yu and He 27 ) and clinical studies( Reference Blanco Mejia, Kendall and Viguiliouk 28 Reference Viguiliouk, Kendall and Blanco Mejia 30 ).

The 2008/09 NZANS reported that the mean contribution of SFA to daily energy intake among the New Zealand population was 13·1 % for both males and females, which is above the acceptable macronutrient distribution range of <10 %( 31 ). Conversely, the contribution to daily energy from both MUFA (12·4 and 13·3 % for males and females, respectively) and PUFA (4·8 and 4·9 % for males and females, respectively) was lower than that was reported for SFA. A heart-healthy dietary fatty acid profile promotes predominantly unsaturated fats, with low intakes of SFA. Given the fatty acid composition of nuts, and our data indicating a more favourable dietary fatty acid intake among nut consumers, increasing the nut intake of the general population is likely to result in positive effects on risk factors for chronic disease, in particular CVD.

Nut consumers also had significantly higher intakes of many micronutrients including thiamin, niacin, riboflavin, vitamin B6, folate, vitamin C, vitamin E, Ca, Cu, Fe, Mg, P, K, Se and Zn. Of these folate, vitamin E, Cu, Mg, P, K and Zn remained significantly higher when additionally adjusted for energy intake. The nutrient compositions of different nuts vary, but particular nuts can be good sources of vitamin E, folate, Mg, Ca, Zn, Cu and Se. Therefore, the inclusion of nuts into the regular diet may improve the adequacy of intake of many of these essential micronutrients. It is important to note that for some of these nutrients the risk of inadequate intake among the New Zealand population was relatively high( 31 ). For example, the risk of inadequate intake of Ca, Se and Zn was 59, 45 and 25 %, respectively. In addition, it was noted in the USA that tree nut consumers had higher intakes of ‘shortfall’ nutrients in the USA, including fibre, vitamin E, Ca and Mg( Reference O’Neil, Keast and Fulgoni 7 ). In addition, a recent analysis of the NHANES 2005–2010 cohort using usual intake data found that tree nut consumers were less likely to have inadequate intakes of vitamins A, E and C, folate, Ca, Fe, Mg and Zn compared with non-consumers( Reference O’Neil, Nicklas and Fulgoni 8 ).

Our findings are in general agreement with that of other national nutrition surveys from the USA, which have reported greater intakes of unsaturated fat and a number of micronutrients among nut consumers in comparison with non-consumers( Reference O’Neil, Keast and Fulgoni 7 , Reference O’Neil, Keast and Nicklas 9 , Reference King, Blumberg and Ingwersen 10 ). Using NHANES 1999–2004 data, O’Neil et al. ( Reference O’Neil, Keast and Fulgoni 7 ) reported that intakes of fibre, vitamins A, B6, C, E and K, thiamin, riboflavin, folate, Ca, Mg, P, Fe, Zn, Cu and Mg were higher, whereas the intake of Na was lower among tree nut consumers compared with non-consumers. Similarly, using data from the What We Eat in America/NHANES 2001–2004, King et al. ( Reference King, Blumberg and Ingwersen 10 ) reported that, among individuals reporting consumption of nuts as snacks, nuts contributed between 25 and 35 % of selected nutrients including fat, PUFA, MUFA, linoleic acid, Mg, Cu and vitamin E. This is similar to our study where whole nuts contributed 27 % (4 %TE) to MUFA and 30 % (2·2 %TE) to PUFA intake. King et al. ( Reference King, Blumberg and Ingwersen 10 ) also identified nutrients and food components that were consumed in significantly higher quantities by nut consumers compared with non-nut consumers, namely vitamins E and K, folate, β-carotene, lutein, zeaxanthin, Mg, P, Cu, Se, K and Zn. Conversely, vitamin B12, retinol, lycopene and Na were consumed in significantly lower amounts by nut consumers( Reference King, Blumberg and Ingwersen 10 ). In our study, vitamin B12 was the only nutrient consumed in significantly lower quantities among nut consumers. It is possible that this may reflect the higher rates of nut consumption among vegetarians and vegans.

The results of the present study should be interpreted with several limitations in mind. First, the cross-sectional design of the study means that we cannot draw causal inferences. Although a better diet quality was observed among nut consumers compared with non-nut consumers in our study and others due to the addition of nutrient-dense nuts to the diet, an alternative explanation is that nut consumption may be a marker of a better diet overall or an indicator of particular dietary patterns (such as vegetarianism). Thus, residual confounding where a healthier lifestyle may mediate the association of nuts with diet quality and health outcomes cannot be excluded. Although BMI and smoking status were collected as part of the 2008/09 NZANS, measures of physical activity were not. Nut consumers may simply be more health conscious than non-nut consumers. In addition, dietary intake included only one 24-h diet recall for the majority of participants and therefore may not represent usual nut intake. Under (and potentially over)-reporting can also be an issue given that diet was self-reported. We were unable to discriminate between under-reporters and under-consumers; thus, all participants were included in the analysis. However, rigorous coding of food items collected through a multi-stage process and the use of New Zealand-specific food composition data allow confidence in the collected estimates of intake for both nuts and nutrients. In addition, 24-h recalls yield reasonably accurate group estimates of nutrient intake( Reference Thompson and Byers 32 ). Even if there are biases leading to under- or over-reporting of total dietary intakes, there are no reasons to suspect these would affect the associations reported here. Other strengths of the study include its large sample size, permitting precise estimation of effects, and the use of a representative, after weighting, population-based sample.

Conclusions

This is the first study using national data from a population in the Southern Hemisphere, more specifically New Zealand, to examine the effects of nut consumption on dietary intake. In agreement with the results of other studies conducted in the USA, nut consumption was associated with improved nutrient profiles, especially an increase in unsaturated fats and a number of essential vitamins and minerals, which could collectively reduce the risk for chronic disease, in particular for CVD.

Acknowledgements

The authors thank the 4721 New Zealanders who participated in the 2008/09 New Zealand Adult Nutrition Survey.

The New Zealand Ministry of Health funded the 2008/09 New Zealand Adult Nutrition Survey. The New Zealand Crown is the owner of the copyright for the survey data. The results presented in this paper are the work of the authors.

The authors’ contributions were as follows: R. C. B., W. P., A. R. G. and E. F. designed and/or conducted the research; R. C. B. performed the statistical analyses with assistance from A. R. G.; C. S., E. F. and R. C. B. managed the dietary analysis; W. P. was the principal investigator of the 2008/09 New Zealand Adult Nutrition Survey; R. C. B., S. L. T., A. R. G. and A. C. wrote the manuscript; all authors reviewed and approved the final manuscript.

There are no conflicts of interest.

References

1. Kris-Etherton, PM, Yu-Poth, S, Sabate, J, et al. (1999) Nuts and their bioactive constituents: effects on serum lipids and other factors that affect disease risk. Am J Clin Nutr 70, 504S511S.CrossRefGoogle ScholarPubMed
2. Nash, SD & Nash, DT (2008) Nuts as part of a healthy cardiovascular diet. Curr Atheroscler Rep 10, 529535.CrossRefGoogle ScholarPubMed
3. Ros, E (2010) Health benefits of nut consumption. Nutrients 2, 652682.CrossRefGoogle ScholarPubMed
4. Alasalvar, C & Bolling, BW (2015) Review of nut phytochemicals, fat-soluble bioactives, antioxidant components and health effects. Br J Nutr 113, S68S78.CrossRefGoogle ScholarPubMed
5. Brufau, G, Boatella, J & Rafecas, M (2006) Nuts: source of energy and macronutrients. Br J Nutr 96, S24S28.CrossRefGoogle ScholarPubMed
6. Bolling, BW, Chen, CY, McKay, DL, et al. (2011) Tree nut phytochemicals: composition, antioxidant capacity, bioactivity, impact factors. A systematic review of almonds, Brazils, cashews, hazelnuts, macadamias, pecans, pine nuts, pistachios and walnuts. Nutr Res Rev 24, 244275.CrossRefGoogle ScholarPubMed
7. O’Neil, CE, Keast, DR, Fulgoni, VL, et al. (2010) Tree nut consumption improves nutrient intake and diet quality in US adults: an analysis of National Health and Nutrition Examination Survey (NHANES) 1999–2004. Asia Pac J Clin Nutr 19, 142150.Google ScholarPubMed
8. O’Neil, CE, Nicklas, TA & Fulgoni, VL 3rd (2015) Tree nut consumption is associated with better nutrient adequacy and diet quality in adults: National Health and Nutrition Examination Survey 2005–2010. Nutrients 7, 595607.CrossRefGoogle ScholarPubMed
9. O’Neil, CE, Keast, DR, Nicklas, TA, et al. (2012) Out-of-hand nut consumption is associated with improved nutrient intake and health risk markers in US children and adults: National Health and Nutrition Examination Survey 1999–2004. Nutr Res 32, 185194.CrossRefGoogle ScholarPubMed
10. King, JC, Blumberg, J, Ingwersen, L, et al. (2008) Tree nuts and peanuts as components of a healthy diet. J Nutr 138, 1736S1740S.CrossRefGoogle ScholarPubMed
11. Griel, AE, Eissenstat, B, Juturu, V, et al. (2004) Improved diet quality with peanut consumption. J Am Coll Nutr 23, 660668.CrossRefGoogle ScholarPubMed
12. Jaceldo-Siegl, K, Joan, S, Rajaram, S, et al. (2004) Long-term almond supplementation without advice on food replacement induces favourable nutrient modifications to the habitual diets of free-living individuals. Br J Nutr 92, 533540.CrossRefGoogle Scholar
13. Tey, SL, Brown, R, Gray, A, et al. (2011) Nuts improve diet quality compared to other energy-dense snacks while maintaining body weight. J Nutr Metab 2011, 357350.CrossRefGoogle ScholarPubMed
14. Smith, C, Gray, AR, Mainvil, LA, et al. (2015) Secular changes in intakes of foods among New Zealand adults from 1997 to 2008/09. Public Health Nutr, 111.Google ScholarPubMed
15. Willett, WC, Sacks, F, Trichopoulou, A, et al. (1995) Mediterranean diet pyramid: a cultural model for healthy eating. Am J Clin Nutr 61, 1402S1406S.CrossRefGoogle ScholarPubMed
16. Smith, C, Gray, AR, Fleming, EA, et al. (2014) Characteristics of fast-food/takeaway-food and restaurant/cafe-food consumers among New Zealand adults. Public Health Nutr 17, 23682377.CrossRefGoogle ScholarPubMed
17. Crider, KS, Bailey, LB & Berry, RJ (2011) Folic acid food fortification – its history, effect, concerns, and future directions. Nutrients 3, 370384.CrossRefGoogle ScholarPubMed
18. Nowson, CA, McGrath, JJ, Ebeling, PR, et al. (2012) Vitamin D and health in adults in Australia and New Zealand: a position statement. Med J Aust 196, 686687.CrossRefGoogle ScholarPubMed
19. Thomson, CD (2004) Selenium and iodine intakes and status in New Zealand and Australia. Br J Nutr 91, 661672.CrossRefGoogle Scholar
20. University of Otago and Ministry of Health (2011) Methodology Report for the 2008/09 New Zealand Adult Nutrition Survey. Wellington: Ministry of Health.Google Scholar
21. Cole, TJ, Bellizzi, MC, Flegal, KM, et al. (2000) Establishing a standard definition for child overweight and obesity worldwide: international survey. BMJ 320, 12401243.CrossRefGoogle ScholarPubMed
22. Cole, TJ, Flegal, KM, Nicholls, D, et al. (2007) Body mass index cut offs to define thinness in children and adolescents: international survey. BMJ 335, 194197.CrossRefGoogle ScholarPubMed
23. Brown, RC, Tey, SL, Gray, AR, et al. (2014) Patterns and predictors of nut consumption: results from the 2008/09 New Zealand Adult Nutrition Survey. Br J Nutr 112, 20282040.CrossRefGoogle Scholar
24. Bao, Y, Han, J, Hu, FB, et al. (2013) Association of nut consumption with total and cause-specific mortality. N Engl J Med 369, 20012011.CrossRefGoogle ScholarPubMed
25. Hshieh, TT, Petrone, AB, Gaziano, JM, et al. (2015) Nut consumption and risk of mortality in the Physicians’ Health Study. Am J Clin Nutr 101, 407412.CrossRefGoogle ScholarPubMed
26. Luo, C, Zhang, Y, Ding, YS, et al. (2014) Nut consumption and risk of type 2 diabetes, cardiovascular disease, and all-cause mortality: a systematic review and meta-analysis. Am J Clin Nutr 100, 256269.CrossRefGoogle ScholarPubMed
27. Zhou, DH, Yu, HB, He, F, et al. (2014) Nut consumption in relation to cardiovascular disease risk and type 2 diabetes: a systematic review and meta-analysis of prospective studies. Am J Clin Nutr 100, 270277.CrossRefGoogle ScholarPubMed
28. Blanco Mejia, S, Kendall, CW, Viguiliouk, E, et al. (2014) Effect of tree nuts on metabolic syndrome criteria: a systematic review and meta-analysis of randomised controlled trials. BMJ Open 4, e004660.CrossRefGoogle ScholarPubMed
29. Sabate, J, Oda, K & Ros, E (2010) Nut consumption and blood lipid levels: a pooled analysis of 25 intervention trials. Arch Intern Med 170, 821827.CrossRefGoogle Scholar
30. Viguiliouk, E, Kendall, CW, Blanco Mejia, S, et al. (2014) Effect of tree nuts on glycemic control in diabetes: a systematic review and meta-analysis of randomized controlled dietary trials. PLOS ONE 9, e103376.CrossRefGoogle ScholarPubMed
31. University of Otago and Ministry of Health (2011) A Focus on Nutrition: Key Findings of the 2008/09 New Zealand Adult Nutrition Survey. Wellington: Ministry of Health.Google Scholar
32. Thompson, FE & Byers, T (1994) Dietary assessment resource manual. J Nutr 124, 2245S2317S.Google ScholarPubMed
Figure 0

Table 1 Characteristics of survey participants in the 2008/09 New Zealand Adult Nutrition Survey (Numbers and percentages)

Figure 1

Table 2 Mean daily nutrient intake by consumption of whole nuts in the 2008/09 New Zealand Adult Nutrition Survey* (Mean values and 95 % confidence intervals)

Figure 2

Table 3 Mean daily nutrient intake by consumption of total nuts in the 2008/09 New Zealand Adult Nutrition Survey* (Mean values and 95 % confidence intervals)

Figure 3

Table 4 Contribution of whole nuts to daily energy and nutrients overall and for whole nut consumers in the 2008/09 New Zealand Adult Nutrition Survey (Mean values and 95 % confidence intervals)