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Providing evidence to support the development of whole grain dietary recommendations in the United Kingdom

Published online by Cambridge University Press:  21 October 2016

Kay D. Mann*
Affiliation:
Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, UK Institute of Health & Society, Newcastle University, Newcastle upon Tyne, UK
Mark S. Pearce
Affiliation:
Institute of Health & Society, Newcastle University, Newcastle upon Tyne, UK
Chris J. Seal
Affiliation:
Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, UK School of Agriculture Food and Rural Development, Newcastle University, Newcastle upon Tyne, UK
*
*Corresponding author: Miss K. D. Mann, fax +44 (0) 191 282 4724, email kay.mann@ncl.ac.uk
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Abstract

Observational evidence suggests that increased whole grain (WG) intake reduces the risks of many non-communicable diseases, such as CVD, type 2 diabetes, obesity and certain cancers. More recently, studies have shown that WG intake lowers all-cause and cause-specific mortality. Much of the reported evidence on risk reduction is from US and Scandinavian populations, where there are tangible WG dietary recommendations. At present there is no quantity-specific WG dietary recommendation in the UK, instead we are advised to choose WG or higher fibre versions. Despite recognition of WG as an important component of a healthy diet, monitoring of WG intake in the UK has been poor, with the latest intake assessment from data collected in 2000–2001 for adults and in 1997 for children. To update this information we examined WG intake in the National Diet and Nutrition Survey rolling programme 2008–2011 after developing our database of WG food composition, a key resource in determining WG intake accurately. The results showed median WG intakes remain low in both adults and children and below that of countries with quantity-specific guidance. We also found a reduction in C-reactive protein concentrations and leucocyte counts with increased WG intake, although no association with other markers of cardio-metabolic health. The recent recommendations by the UK Scientific Advisory Committee on Nutrition to increase dietary fibre intake will require a greater emphasis on consuming more WG. Specific recommendations on WG intake in the UK are warranted as is the development of public health policy to promote consumption of these important foods.

Type
Conference on ‘New technology in nutrition research and practice’
Copyright
Copyright © The Authors 2016 

What are whole grains and whole-grain foods?

Cereal grains, such as barley, corn, oats, rice, rye and wheat, are a staple food in the human diet and are important sources of dietary carbohydrate and protein. Whole-grain (W-G) foods are foods made from cereals and starch, which contain all three anatomical components of the grain: the outer bran, endosperm and germ. Although there is not one single definition of whole grain (WG), similar definitions from the American Association of Cereal Chemists International and the Healthgrain forum, a European consortium of scientists and industrial partners, are widely used. These definitions state that  WG must contain the three component parts of the grain in the same relative proportions found in the intact kernel( 1 ). Additionally, the Healthgrain forum definition allows for small component losses due to processing of the grain( Reference Van Der Kamp, Poutanen and Seal 2 ). Other definitions found in country-specific reports are very similar to these( Reference Mejborn, Biltoft-Jensen and Trolle 3 5 ) giving a general consensus on what constitutes a WG. As such, products that state ‘WG’, ‘wholegrain’ or ‘whole’ followed by the type of cereal or pseudo-cereal (named so because their composition is similar to that of cereal grains) in the ingredients list should comply with the consensus WG definitions and can be recognised as W-G foods. Similarly the term wholemeal, a regulated term for breads and flours in the UK( 6 ), has requirements that align with WG definitions. Some cereal and pseudo-cereal ingredients, such as oats, oatmeal, brown rice, buckwheat and quinoa, often do not carry the whole/WG prefix. However, in the case of oats the largest majority is consumed as a WG since oats are rarely refined to separate the bran and endosperm. Brown rice is so called because the bran is retained. The small seeds of most pseudo-cereals precludes refining( Reference Seal, Jones and Whitney 7 , 8 ). At present there is no legal definition of a W-G food except for some specific in-country recommendations. For example, in the US foods must contain at least 51 % WG by weight per reference amount customarily consumed to comply with a WG health claim. In Denmark flours, grains and rice must contain 100 % WG, breakfast cereals 60 % and bread 50 % WG and in Germany pasta must contain 100 % WG, whereas wheat and rye breads must contain 90 % WG.

Health benefits of whole grains: observational evidence

CVD, type 2 diabetes, obesity and cancer are the most prevalent non-communicable diseases across the world( 9 ). CVD (diseases of the heart or blood vessels such as CHD) are the number one cause of death globally (31 % in 2012( 9 )) and are currently the second biggest killer in the UK, after cancer( 10 ).

Observational epidemiology studies suggest there is an inverse association between increased habitual WG intake and reduced risk of non-communicable disease. Results of systematic reviews and meta-analyses suggest that there is a 20–30 % risk reduction of CVD and type 2 diabetes, comparing low or non-consumers with WG intakes of 48–80 g/d( Reference Ferruzzi, Jonnalagadda and Liu 11 , Reference Ye, Chacko and Chou 12 ). These reported associations may also be dose-respondent with meta-analyses suggesting 22 % CVD risk reduction by increasing W-G food intake to 90 g/d (i.e. three daily servings of foods containing WG) and an absolute risk reduction of 0·3 % in the type 2 diabetes rate for each 10 g/d of WG consumed( Reference Aune, Keum and Giovannucci 13 , Reference Chanson-Rolle, Meynier and Aubin 14 ). Increased WG intakes have also been associated with reduced risks of cancer, particularly colorectal cancers where a 10 % relative risk reduction was estimated for an increment of three daily W-G food servings( Reference Aune, Chan and Lau 15 ). Furthermore, high v. low WG intakes have been associated with reduced risks of digestive tract cancers as well as breast, prostate and pancreatic cancers( Reference Jacobs, Marquart and Slavin 16 Reference Mourouti, Kontogianni and Papavagelis 18 ). One of the major risk factors for CVD, type 2 diabetes and cancer is obesity, which has become a global health concern as the rate has more than doubled since the 1980s( 19 ). Intake of WG  may have a beneficial role in weight management or maintenance( Reference Thielecke and Jonnalagadda 20 ). A meta-analysis of three prospective cohort studies with a total of 119 054 participants, concluded that three to five daily servings of WG was associated with consistently less weight gained during 8–13 years of follow-up, compared with never/rare consumers( Reference Ye, Chacko and Chou 12 ). These three cohort studies were conducted in US populations and the data are supported by a recent examination of trends in national data over 12 years, which confirmed that W-G foods may contribute to weight management( Reference Albertson, Reicks and Joshi 21 ). Most recently, meta-analyses have focused on investigating WG consumption in relation to mortality from non-communicable diseases, with similar results to the non-communicable disease risks( Reference Huang, Xu and Lee 22 ). All-cause mortality and disease-specific (CVD or events, diabetes, cancers and respiratory disease) mortality risks are shown to be reduced by 5–30 % for a doubling of W-G food intake as well as per 16 g/d and three daily servings of WG ( Reference Johnsen, Frederiksen and Christensen 23 Reference Wei, Gao and Liang 26 ).

Many of the observational studies included in the systematic reviews and meta-analyses adjust their risk estimations for confounding factors, which may also explain the suggested associations. Age, sex, smoking, physical activity, body mass, history of disease, health markers and other dietary intakes such as energy intake, have all been considered and included in multivariable analyses. Varying effects of confounding are seen, for example, an age- and sex-adjusted hazard ratio of 0·61 (95 % CI 0·59, 0·62) was attenuated to 0·77 (95 % CI 0·75, 0·79) after adjustment for smoking and further attenuated to 0·83 (95 % CI 0·81, 0·86) after additional adjustments for race/ethnicity, alcohol intake, education, marital status, health status, obesity, physical activity, red meat, fruit, vegetables and total energy intakes and hormone use( Reference Huang, Xu and Lee 22 ). These results show that there is evidence of confounding, but the reported significant 17 % reduction in all-cause mortality hazard ratio, for the highest WG consumers compared with the lowest, appears be independent of the confounders tested. Although this study, and the majority of the observational studies, consistently report independent inverse associations even after adjustment for relevant confounding factors, it is important to note that the potential for residual confounding may still remain. In addition, the majority of the studies included in the meta-analyses come from US and Scandinavian populations with a small number of studies from European cohorts and a very few from middle or far-Eastern populations. Therefore, the applicability of the findings to populations with differing dietary patterns and cultural habits should be further investigated.

Heath benefits of whole grains: intervention evidence

The results of intervention studies do not consistently corroborate the findings from observational studies. Some interventions show beneficial effects of consuming WG on health markers, whereas others fail to find significant results. For example, obese participants with metabolic syndrome who were given a 12-week dietary advice intervention to obtain all grain servings from  WG, showed a reduction in plasma C-reactive protein concentrations and percentage body fat in the abdominal region compared with a WG avoidance group (refined grain group). In another randomised controlled trial, markers of inflammation were reduced in overweight and obese but otherwise healthy participants, with suboptimal diets, following a W-G wheat intervention v. a refined grain control group for 8 weeks. However, no significant variations in body composition, plasma lipids or glycaemia were found in these participants or between intervention and the refined grain control( Reference Vitaglione, Mennella and Ferracane 27 ). Similarly, in a 16-week WG intervention, no changes in CVD markers between intervention groups and controls were seen( Reference Brownlee, Moore and Chatfield 28 ). A meta-analysis of randomised controlled WG intervention studies on body weight and body composition concluded that the trials did not support the role of WG in body weight management. However, beneficial effects of WG on body weight may be more apparent for body fat percentage or abdominal adiposity, which may be mediated through decreased inflammatory responses( Reference Pol, Christensen and Bartels 29 ).

Explanation for the differing findings of intervention studies to those of observation studies are thought to be due mainly to the differences in study design. Intervention studies are time-restricted with no reported trial lasting longer than 4 months, which may not be long enough for sustained health benefits to be seen. Sample sizes are often small, although usually authors claim that they are powered to be able to detect any significant meaningful changes in disease markers resulting from the intervention. The type, variety and quantity of  WG used in intervention studies differ and this may be another reason for inconsistent results. Some  WG, such as oats, rye and barley, contain higher fibre, particularly soluble fibre, than wheat and rice. Therefore, the physiological effects on the body may differ between grain types and if one grain type or a mix of grains are included in the diet.

The outcomes of intervention studies are reported as the outcome on risk markers for disease, not the occurrence of a disease as this would not be possible within the time frame of an intervention study. Therefore, comparison with observational studies where a particular disease or event has occurred may not be appropriate. Interestingly observational studies that report on markers for disease risk also have varying results( Reference Seal and Brownlee 30 ). For example, in our recent analysis of UK WG intakes, no significant differences or trends in blood pressure, blood lipids or anthropometric measures between non-consumers and increasing tertile of WG intake were observed. However, a reduction in leucocyte counts by increasing tertile of WG intake, and a difference in adults with a small intake of WG compared with non-consumers was seen in C-reactive protein concentrations( Reference Mann, Pearce and McKevith 31 ). This suggests that intervention studies and observational studies, which report biomarkers of disease risk, are more aligned in the inconsistency of their results compared with those that only report disease outcomes. Finally, intervention studies that report no changes in disease markers are most often carried out in healthy or overweight but otherwise ‘healthy’ volunteers. This raises the question, whether improvement in disease risk markers should be expected, if the participants are otherwise healthy. Some of the largest effects are seen in intervention studies with ‘at risk’ participants with dyslipidaemia or obesity. Furthermore, it is known that as we age our health and health markers in general decline. We should re-consider the pharmacological paradigm, which suggests that short-term dietary intervention with  WG should improve or reduce disease risk in favour of a longer-term model, which suggests that increased WG intake in the longer-term reduces age-related declines in health.

Despite the inconsistent results from WG interventions, to our knowledge, no study has shown or reported negative effects or outcomes of increasing WG intake on health markers. Therefore, advice to consume more  WG could be a low-risk public health strategy. Of course it is important to note that for a small proportion of the population with gluten intolerance, caution must be made when consuming WG containing gluten. However, gluten-free WG alternatives such as amaranth, brown rice, buckwheat and quinoa are available and their consumption by those with gluten intolerance can be encouraged. WG oats do not contain gluten, but are sometimes cross-contaminated with wheat during harvesting or factory processing. Thus, consumers should always check product labels for gluten-free oat ingredients for clarification.

Health benefits of whole grains: mechanisms of action

There is no one clear mechanism identified for which WG benefit the body, instead there are a combination of several processes suggested, which may also interact with one another. Essentially the accepted pathways in which WG have an effect on chronic diseases can be split into two: dietary fibre and bioactive components (Fig. 1).

Fig. 1. Accepted mechanisms for effects of whole grain (WG) on chronic disease, from Fardet( Reference Fardet 43 ): Current accepted mechanisms for how WG protects against major chronic diseases. GI, glycaemic index; II, insulinaemic index.

WG contain cereal fibre and have increased amounts compared with refined grain counterparts. For example, the Association of Official Analytical Chemists dietary fibre content of wholemeal bread is more than twice as high at 7 g/100 g, whereas for white bread it is 2·9 g/100 g( 32 ). Insoluble and soluble dietary fibres improve digestive health through a range of effects such as stool bulking, altered intestinal transit time as well as increased colonic fermentation, which induces the production of SCFA( Reference Slavin 33 ). Beta-glucan, a soluble fibre found in higher concentrations in oats and barley, has been shown to lower blood cholesterol concentrations and improve postprandial insulin and glucose responses( Reference Lattimer and Haub 34 , Reference Tiwari and Cummins 35 ). In addition, these physiological effects of both soluble and insoluble fibres may also have satiating effects on appetite, which may have a role in weight management( Reference Jonnalagadda, Harnack and Liu 36 ). Cereal fibre, in particular, has been highlighted as one fibre source that may reduce the CHD risk( Reference Wu, Qian and Pan 37 ), and the need for trials investigating the effects of cereal fibre on type 2 diabetes risk has been emphasised( Reference Whincup and Donin 38 ). It is also important to consider that the associated benefits of WG are above and beyond those of just the cereal fibre. WG also contain a large amount of bioactive components such as phenolic acids, lignans, plant sterols, totcols, benzoxazinoids and alkylresorcinols as well as a variety of vitamins and minerals( Reference Andersson, Dimberg and Åman 39 , Reference Borneo and Leon 40 ). Many of these have anti-oxidant and anti-inflammatory properties as well as providing essential nutrients into the diet of WG consumers, which could lead to protection from later disease( Reference Kris-Etherton, Hecker and Bonanome 41 Reference Fardet 43 ). New and emerging research into the gut microbiome suggests that  WG may influence the type of bacteria that make up the gut microbiota, which has beneficial effects on the host gut health( Reference Zhou, Hergert and Rompato 44 Reference Rose 46 ). In a human trial, it was shown that a mixture of WG types, a combination of WG barley and brown rice, increased gut microbial diversity, which induced some beneficial changes on the profile of bacterial populations in the host; evidence that in the short term, increased intake from a mixture of  WG alters the gut environment and results in improvements in systematic inflammation( Reference Walter, Martínez and Rose 47 ).

Whole grain intake recommendations

There are currently some recommendations to consume  WG across the globe. These vary by country with some offering generic advice and others, which give merit to the observational evidence, providing quantity-specific daily target intakes( Reference Seal, Nugent and Tee 48 ). For example, in the USA and Canada advice to ‘make one-half of your grains whole grains’ is followed by a quantity recommendation of a minimum 3–5 ounce-equivalents (servings)/d (48–80 g/d)( 49 ). Similarly quantity-specific dietary guidance is given in Denmark, however, with a higher target to consume 75 g/d WG per 10 MJ diet (four daily portions). Semi-quantity-specific intake targets are advised in Singapore where advice for adults is to consume sufficient amount of grains, especially  WG with at least one serving of rice and alternatives from W-G foods( 5 ). In the UK, generic advice in the Eatwell Guide, is to ‘choose wholegrain or higher fibre versions with less added fat, salt and sugar’. In the majority of other countries with food-based dietary public guidance (including Australia, China, France, Germany and Ireland) generic advice to choose or include WG and consume more WG is given( Reference Ferruzzi, Jonnalagadda and Liu 11 , Reference Seal, Nugent and Tee 48 ). The variety of WG recommendations across many countries could be confusing, particularly where quantity-specifics do not match. Target intakes are largely based on dietary fibre and endorsing  WG as a source of fibre. Clearly targets need to reflect country-specific cultural and traditional diets; however, some consistency between countries based on scientific evidence would be useful.

Current whole grain intake

As with WG recommendations, WG intake varies across countries. Assessing intake of  WG is challenging. Along with the universal issues of dietary intake reporting from either FFQ or diet records, further difficulties arise for  WG since the identification of these partly rely on participant knowledge, manufacturer information and standardised databases on the content of  W-G in foods. Such databases are publically available in the USA through the United States Department of Agriculture Patterns Equivalents Database( 50 ) and recently updated data have been published for W-G foods consumed in Australia( Reference Galea, Dalton and Beck 51 ). We have recently published our database of W-G foods consumed in the UK covering the period 1986–2016( Reference Jones, Mann and Kuznesof 52 ). Despite the difficulties in assessing and measuring WG intake, the available data show that consumption and intake of  WG in the majority of countries is low (Table 1). Average WG intakes for adults range from as little as 4 g/d in Italy, measured in 2005–2006, and 5 g/d in France measured in 2009–2010, to as high as 58 g/d (63 g/d/10 MJ) in Denmark measured in 2011–2013( Reference Sette, D'Addezio and Piccinelli 53 Reference Mejborn, Ygil and Fagt 55 ). The higher reported WG intakes in the Danish population are attributed to a combination of traditional diets that include WG foods, such as rye bread, and the recent success of the Danish WG campaign( 56 ). The campaign, a public and private company partnership, aiming to increase accessibility and awareness of  WG and the associated health benefits, has seen an increase in average Danish intakes of 75 % from 2004 to 2013. In the UK, WG intake from foods with at least 10 % WG content was reported to be 7 g/d for children and 14 g/d for adults from the 2000–2001 and 1997 national dietary survey, respectively( Reference Thane, Jones and Stephen 57 , Reference Thane, Jones and Stephen 58 ). We (the authors) have worked to update these data using the UK National Diet and Nutrition Survey data from 2008 to 2011, covering the first 3 years that the survey has been run on a rolling programme basis. We reported average WG intakes of 20 and 13 g/d in adults and children, a slight increase on the previous survey( Reference Mann, Pearce and McKevith 59 ). Although our assessment included food with any WG content we found very minimal differences when assessing intakes only from foods with at least 10 % WG content. As such we concluded that WG intakes in the UK remain low, particularly in teenagers and younger adults as well as for those with lower socioeconomic status. To investigate any potential health benefit of higher WG consumption, we split the WG consumers into tertiles of intake and compared health marker levels between the three groups and non-consumers. As previously mentioned, no significant association was found between higher WG intakes and measures of body composition or blood pressure, which may have been due to the small variability in the population and overall low level of WG intake. Only 17 % of adults consumed at least 48 g/d or more WG, the current US intake recommendation and the amount suggested to be associated with reduced disease risks. We found that WG intake came mainly from breads and ready-to-eat breakfast cereals, but we noted very small intakes from pasta. However, ‘white bread’ and ‘pasta, rice, pizza and other miscellaneous cereals’ were the two most commonly consumed cereals and cereal products, eaten by more than 70 % of the total population( Reference Bates, Lennox and Prentice 60 ). This gives opportunity for replacement of refined grain breads and pastas with WG varieties and the potential to increase population WG intakes. In particular, increased consumption of WG provides opportunity to increase dietary fibre intakes since our analysis showed that dietary fibre intakes were 5 and 3 g/d significantly higher in adult and child WG consumers compared with non-consumers.

Table 1. Whole grain (WG) intakes of adults in national surveys

se, standard error; sd, standard deviation; TP, total population; M, male; F, female.

* Median and 97·5th percentile.

Median and 95th percentile.

Ounce-equivalents (1 oz-eq can be either 16 or 28·35 g depending on the food source hence is not converted in grams( Reference Albertson, Reicks and Joshi 21 )).

Barriers to new whole grain intake recommendations

Although the new Eatwell Guide and advice from Public Health England has raised the profile of W-G foods( 61 ), we believe that a more explicit recommendation is required. We also suggest that a global recommendation would be useful to improve clarity and encourage industry to develop more W-G products. However, before any new recommendation can be made consideration is needed of potential difficulties that may arise. Consumer desirability of  WG, particularly in the taste, texture, price and availability will be key factors in aiding an increase in WG intakes. The availability of W-G food products has increased as has the popularity of foods perceived as being more healthy( 62 ). However, as a consequence in some cases these foods can be more expensive( Reference Jones, Conklin and Suhrcke 63 ). Food manufacturers should seek opportunities to develop new W-G foods, which are appealing and affordable for the consumer. Manufacturers must be allowed to label their foods effectively and in a way which is regulated for the consumer. This is linked to a second potential barrier to a quantity-specific WG recommendation, which is to have a clear definition of a W-G food. As part of the present work on updating national intake data in the UK we have developed a database of the WG contents of foods consumed from several UK surveys( Reference Jones, Mann and Kuznesof 52 ). Following the guidelines by Ross et al. ( Reference Ross, Kristensen and Seal 64 ) we report on a dry weight basis from which intakes can be calculated in g/d given the portion size consumed. The database also contains W-G foods as single raw ingredients as well as on an as consumed basis so that intake can be calculated either from recipe ingredients with weights or as the food as eaten. For example, the WG content of dry wholemeal pasta is estimated to be 89·5 % DM, whereas wholemeal pasta boiled is estimated to be 30·9 % WG DM as eaten. This database, as with other databases, highlights the differing amounts of WG contained in food products. In the USA, the health claim ‘Diets rich in wholegrain foods and other plant foods, and low in saturated fat and cholesterol may help reduce the risk of heart disease’ is allowed for use only on foods that contain at least 51 % WG( 65 , 66 ). Previously in 2002 the UK also had a health claim that was allowed for the use on foods containing at least 51 % WG: ‘People with a healthy heart tend to eat more whole-grain foods as part of a healthy lifestyle’( 67 ). However, this claim is no longer permitted for use, since in 2010, the European Foods Standard Agency rejected the use of all WG health claims in Europe on the basis that WG was ‘insufficiently characterised’( 68 ). More recently the US American Association of Cereal Chemists International and a multidisciplinary expert roundtable have proposed a characterisation that W-G foods must deliver at least 8 g WG per 30 g serving (about 27 % WG content)( Reference Ferruzzi, Jonnalagadda and Liu 11 , 69 ). The Healthgrain forum have recently proposed that a W-G food should contain at least 30 % WG content on a DM basis with more W-G ingredients than refined grain ingredients in the final product. This is in addition to compliance with country-specific fat, salt and sugar limitations( Reference Ross, van Der Kamp and King 70 ). A scientific consensus and subsequent studies using one definition of a W-G food would add to the evidence concerning health benefits of  WG and aid public bodies in recommending food-based WG guidance.

Conclusion

The observational evidence on the long-term health benefits of higher WG consumption is clear and consistent. As a result some public health groups advise quantity-specific daily WG intake recommendations. Since grains are important dietary sources of energy and other nutrients including dietary fibre, and WG varieties contain higher amounts of fibre compared with refined grain varieties, recommendation to consume them should be emphasised. The current UK advice from the Eatwell Guide, now includes images of W-G foods and the emphasis on choosing ‘wholegrain and higher fibre versions with small amounts of salt fat and sugar’( 61 ). The inclusion of W-G food images within the ‘carbohydrates’ section of the plate is a step in the right direction. The recent Scientific Advisory Committee on Nutrition Report on Carbohydrates and Health, has advised that dietary fibre intakes should be raised to a minimum of 30 g/d for adults and 15–25 g/d for children with no more than 5 % of dietary energy coming from free sugars( 71 ). We believe that a quantity-specific recommendation for WG intake would be more helpful to the general public than the general statement in the Eatwell Guide, since 30 g/d fibre will be impossible to achieve without the inclusion of  WG. For example, the British Nutrition Foundation have developed a 7-d meal plan, which is designed to indicate the amount of different foods needed to achieve the fibre and free sugars targets( 72 ). Within this meal plan more than half of the carbohydrate-rich foods are W-G foods. To achieve 30 g/d of dietary fibre an adult would need to consume almost six daily servings of WG, in addition to over eight daily portions of fruits and vegetables (Table 2). This gives a very clear indication of the need to consume substantial quantities of WG, in addition to fruit, vegetables together with high-fibre beans and pulses, which are also included in the meal plan.

Increasing WG intakes may be difficult. Studies in the USA have shown that despite having a quantity-specific recommendation of 3 oz-eq/d, this target has not been achieved. Assessing trends across 12 years of the National Health and Nutrition Examination Survey showed that, although recommended intakes of total grains are being met, only small increases in WG intake were observed and <10 % of Americans currently meet the recommendation for WG intakes. This suggests that despite the increasing consumer interest and availability of W-G foods, little progress in replacing intake of refined grains with  WG has occurred in the past 12 years( Reference Albertson, Reicks and Joshi 21 ). In contrast, as previously mentioned, the Danish population has shown considerable success in improving WG intakes, demonstrating that with public and private partnership campaigns population dietary habits can change.

It is important that any new dietary recommendations focus on replacement of refined grain foods with W-G foods, so that overall energy intake does not increase. Finally, there may be potential for co-ordinating a WG recommendation with the current UK fruits and vegetables guidance. For example, the current ‘5-a-d’ campaign for portions of fruits and vegetables could be mirrored by a ‘3-a-d’ campaign for WG. This would require clarity in definitions of WG, W-G foods and mechanisms to enable consumers to identify portions of W-G foods.

Table 2. Estimated whole grain (WG) servings based on a sample meal plan to achieve the new fibre and free sugars recommendations

* Portion sizes from Food Standards Agency( 77 ).

16 g WG per serve.

Acknowledgements

The authors would like to thank NatCen Social Research, MRC Human Nutrition Research and University College London Medical School for conducting and co-ordinating the National Diet and Nutrition Survey (NDNS) rolling programme, the UK data service for supply of the data and all participants of the NDNS rolling programme. The authors would also like to thank the British Nutrition Foundation for allowing the use of their meal planner and Rebecca Williams of the Grains & Legumes Nutrition Council, for supply of data from the Australian Grain and Legumes Consumption and Attitudinal Study 2014.

Financial Support

No specific grant from any funding agency, commercial or not-for-profit, has been received for the writing of this article. The authors have received unrestricted research funding from Cereal Partners Worldwide for whole-grain-related research including some of the results presented in this article.

Conflict of Interest

None.

Authorship

K. D. M. collated the evidence, analysed UK data, gave the presentation at the Nutrition Society's Summer Meeting and drafted the article. C. J. S. supervised the research, contributed to writing and critical review of the manuscript. M. S. P. supervised the research and critically revised the manuscript for intellectual content.

References

1. American Association of Cereal Chemists International (1999) Whole grains definition. http://www.aaccnet.org/initiatives/definitions/Pages/WholeGrain.aspx (accessed October 2013).Google Scholar
2. Van Der Kamp, JW, Poutanen, K, Seal, CJ et al. (2014) The HEALTHGRAIN definition of ‘whole grain’. Food Nutr Res, 58, 22100.Google Scholar
3. Mejborn, H, Biltoft-Jensen, A, Trolle, E et al. (2008) Wholegrain: Definition and Scientific Background for Recommendations of Wholegrain Intake in Denmark. DTU Fødevareinstituttet. Available at: www.food.dtu.dk.Google Scholar
4. Food Standards Australia New Zealand (2015) Australia New Zealand Food Standards Code – Standard 2.1.1-Cereal and cereal products. Commonwealth of Australia Gazette No. FSC 96.Google Scholar
5. Health Promotion Board Singapore (2012) Food-based dietary guidelines for adults. http://www.hpb.gov.sg/HOPPortal/health-article/2758 (accessed March 2016).Google Scholar
6.(1998) The Bread and Flour Regulations 1998, No. 141. UK Statutory Instruments. Available at: http://www.legislation.gov.uk/uksi/1998/141/contents/made (accessed May 2016).Google Scholar
7. Seal, CJ, Jones, AR & Whitney, AD (2006) Whole grains uncovered. Nutr Bull 31, 129137.CrossRefGoogle Scholar
8. Oldways Whole Grains Council (2003–2013) Whole grains A to Z. http://wholegrainscouncil.org/whole-grains-101/whole-grains-a-to-z (accessed May 2016).Google Scholar
9. World Health Organization (2014) Global status report on noncommunicable diseases 2014. http://www.who.int/nmh/publications/ncd-status-report-2014/en/ (accessed July 2016).Google Scholar
10. Office for National Statistics (2016) Deaths registered in England and Wales: 2015. Statistical Bulletin. https://www.ons.gov.uk/peoplepopulationandcommunity/birthsdeathsandmarriages/deaths/bulletins/deathsregistrationsummarytables/2015 (accessed July 2016).Google Scholar
11. Ferruzzi, MG, Jonnalagadda, SS, Liu, S et al. (2014) Developing a standard definition of whole-grain foods for dietary recommendations: summary report of a multidisciplinary expert roundtable discussion. Adv Nutr 5, 164176.Google Scholar
12. Ye, EQ, Chacko, SA, Chou, EL et al. (2012) Greater whole-grain intake is associated with lower risk of type 2 diabetes, cardiovascular disease, and weight gain. J Nutr 142, 13041313.Google Scholar
13. Aune, D, Keum, N, Giovannucci, E et al. (2016) Whole grain consumption and risk of cardiovascular disease, cancer, and all cause and cause specific mortality: systematic review and dose-response meta-analysis of prospective studies. BMJ 353, i2716.Google Scholar
14. Chanson-Rolle, A, Meynier, A, Aubin, F et al. (2015) Systematic review and meta-analysis of human studies to support a quantitative recommendation for whole grain intake in relation to type 2 diabetes. PLoS ONE 10, e0131377.Google Scholar
15. Aune, D, Chan, DS, Lau, R et al. (2011) Dietary fibre, whole grains, and risk of colorectal cancer: systematic review and dose-response meta-analysis of prospective studies. BMJ 343, d6617.CrossRefGoogle ScholarPubMed
16. Jacobs, DR Jr, Marquart, L, Slavin, J et al. (1998) Whole-grain intake and cancer: an expanded review and meta-analysis. Nutr Cancer 30, 8596.Google Scholar
17. Lei, Q, Zheng, H, Bi, J et al. (2016) Whole grain intake reduces pancreatic cancer risk: a meta-analysis of observational studies. Medicine 95, e2747.Google Scholar
18. Mourouti, N, Kontogianni, MD, Papavagelis, C et al. (2015) Whole grain consumption and breast cancer: a case-control study in women. J Am Coll Nutr 35, 143149.CrossRefGoogle ScholarPubMed
19. World Health Organization (2016) Obesity and overweight – Fact sheet. http://www.who.int/mediacentre/factsheets/fs311/en/ (accessed April 2016).Google Scholar
20. Thielecke, F & Jonnalagadda, SS (2014) Can whole grain help in weight management? J Clin Gastroenterol 48, S70S77.Google Scholar
21. Albertson, AM, Reicks, M, Joshi, N et al. (2016) Whole grain consumption trends and associations with body weight measures in the United States: results from the cross sectional National Health and Nutrition Examination Survey 2001–2012. Nutr J 15, 114.Google ScholarPubMed
22. Huang, T, Xu, M, Lee, A et al. (2015) Consumption of whole grains and cereal fiber and total and cause-specific mortality: prospective analysis of 367,442 individuals. BMC Med 13, 59.Google Scholar
23. Johnsen, NF, Frederiksen, K, Christensen, J et al. (2015) Whole-grain products and whole-grain types are associated with lower all-cause and cause-specific mortality in the Scandinavian HELGA cohort. Br J Nutr 114, 608623.Google ScholarPubMed
24. Chen, G-C, Tong, X, Xu, J-Y et al. (2016) Whole-grain intake and total, cardiovascular, and cancer mortality: a systematic review and meta-analysis of prospective studies. Am J Clin Nutr 104, 164172.Google Scholar
25. Zong, G, Gao, A, Hu, FB et al. (2016) Whole grain intake and mortality from all causes, cardiovascular disease, and cancer: a meta-analysis of prospective cohort studies. Circulation 133, 23702380.CrossRefGoogle Scholar
26. Wei, H, Gao, Z, Liang, R et al. (2016) Whole-grain consumption and the risk of all-cause, CVD and cancer mortality: a meta-analysis of prospective cohort studies. Br J Nutr 116, 514525.CrossRefGoogle ScholarPubMed
27. Vitaglione, P, Mennella, I, Ferracane, R et al. (2015) Whole-grain wheat consumption reduces inflammation in a randomized controlled trial on overweight and obese subjects with unhealthy dietary and lifestyle behaviors: role of polyphenols bound to cereal dietary fiber. Am J Clin Nutr 101, 251261.Google Scholar
28. Brownlee, IA, Moore, C, Chatfield, M et al. (2010) Markers of cardiovascular risk are not changed by increased whole-grain intake: the WHOLEheart study, a randomised, controlled dietary intervention. Br J Nutr 104, 125134.CrossRefGoogle Scholar
29. Pol, K, Christensen, R, Bartels, EM et al. (2013) Whole grain and body weight changes in apparently healthy adults: a systematic review and meta-analysis of randomized controlled studies. Am J Clin Nutr 98, 872884.Google Scholar
30. Seal, CJ & Brownlee, IA (2010) Whole grains and health, evidence from observational and intervention studies. Cereal Chem 87, 167174.CrossRefGoogle Scholar
31. Mann, KD, Pearce, MS, McKevith, B et al. (2015) Whole grain intake and its association with intakes of other foods, nutrients and markers of health in the National Diet and Nutrition Survey rolling programme 2008–11. Br J Nutr 113, 15951602.Google Scholar
32. Public Health England (2015) McCance and Widdowson's composition of foods integrated dataset. https://www.gov.uk/government/publications/composition-of-foods-integrated-dataset-cofid (accessed July 2016).Google Scholar
33. Slavin, J (2010) Whole grains and digestive health. Cereal Chem 87, 292296.Google Scholar
34. Lattimer, JM & Haub, MD (2010) Effects of dietary fiber and its components on metabolic health. Nutrients 2, 12661289.Google Scholar
35. Tiwari, U & Cummins, E (2011) Meta-analysis of the effect of β-glucan intake on blood cholesterol and glucose levels. Nutrition 27, 10081016.Google Scholar
36. Jonnalagadda, SS, Harnack, L, Liu, RH et al. (2011) Putting the whole grain puzzle together: health benefits associated with whole grains–summary of American Society for Nutrition 2010 Satellite Symposium. J Nutr 141, 1011S1022S.Google Scholar
37. Wu, Y, Qian, Y, Pan, Y et al. (2015) Association between dietary fiber intake and risk of coronary heart disease: a meta-analysis. Clin Nutr 34, 603611.Google Scholar
38. Whincup, P & Donin, A (2015) Cereal fibre and type 2 diabetes: time now for randomised controlled trials? Diabetologia 58, 13831385.Google Scholar
39. Andersson, AAM, Dimberg, L, Åman, P et al. (2014) Recent findings on certain bioactive components in whole grain wheat and rye. J Cereal Sci 59, 294311.Google Scholar
40. Borneo, R & Leon, AE (2012) Whole grain cereals: functional components and health benefits. Food Funct 3, 110119.Google Scholar
41. Kris-Etherton, PM, Hecker, KD, Bonanome, A et al. (2002) Bioactive compounds in foods: their role in the prevention of cardiovascular disease and cancer. Am J Med 113, 7188.Google Scholar
42. Slavin, J (2003) Why whole grains are protective: biological mechanisms. Proc Nutr Soc 62, 129134.Google Scholar
43. Fardet, A (2010) New hypotheses for the health-protective mechanisms of whole-grain cereals: what is beyond fibre? Nutr Res Rev 23, 65134.Google Scholar
44. Zhou, AL, Hergert, N, Rompato, G et al. (2015) Whole grain oats improve insulin sensitivity and plasma cholesterol profile and modify gut microbiota composition in C57BL/6J mice. J Nutr 145, 222230.CrossRefGoogle ScholarPubMed
45. Zhong, Y, Nyman, M & Fåk, F (2015) Modulation of gut microbiota in rats fed high-fat diets by processing whole-grain barley to barley malt. Mol Nutr Food Res 59, 20662076.Google Scholar
46. Rose, DJ (2014) Impact of whole grains on the gut microbiota: the next frontier for oats? Br J Nutr 112, S44S49.Google ScholarPubMed
47. Walter, J, Martínez, I & Rose, DJ (2013) Holobiont nutrition: considering the role of the gastrointestinal microbiota in the health benefits of whole grains. Gut Microbes 4, 340346.Google Scholar
48. Seal, CJ, Nugent, AP, Tee, ES et al. (2016) Whole-grain dietary recommendations: the need for a unified global approach. Br J Nutr 115, 20312038.Google Scholar
49. U.S. Department of Health and Human Services, U.S. Department of Agriculture (2015–2020) Dietary guidelines for Americans. https://health.gov/dietaryguidelines/2015/guidelines/ (accessed January 2016).Google Scholar
50. U.S. Department of Agriculture (2014) Food patterns equivalents database. http://www.ars.usda.gov/Services/docs.htm?docid=23871 (accessed July 2016).Google Scholar
51. Galea, LM, Dalton, SMC, Beck, EJ et al. (2016) Update of a database for estimation of whole grain content of foods in Australia. J Food Compost Anal 50, 2329.Google Scholar
52. Jones, AR, Mann, KD, Kuznesof, SA et al. (2017) The whole grain content of foods consumed in the UK. Food Chem 214, 453459.Google Scholar
53. Sette, S, D'Addezio, L, Piccinelli, R et al. (2015) Intakes of whole grain in an Italian sample of children, adolescents and adults. Eur J Nutr (Epublication ahead of print version).Google Scholar
54. Bellisle, F, Hebel, P, Colin, J et al. (2014) Consumption of whole grains in French children, adolescents and adults. Br J Nutr 112, 16741684.Google Scholar
55. Mejborn, H, Ygil, KH, Fagt, S et al. (2014) Danskernes fuldkornsindtag 2011–2013. E-artikel fra DTU Fødevareinstitutet 2014, 17.Google Scholar
56. Danish Whole Grain Partnership (2014) Press release: whole grain intake sets new record. http://www.fuldkorn.dk/english (accessed November 2015).Google Scholar
57. Thane, CW, Jones, AR, Stephen, AM et al. (2005) Whole-grain intake of British young people aged 4–18 years. Br J Nutr 94, 825831.Google Scholar
58. Thane, CW, Jones, AR, Stephen, AM et al. (2007) Comparative whole-grain intake of British adults in 1986–7 and 2000–1. Br J Nutr 97, 987992.Google Scholar
59. Mann, KD, Pearce, MS, McKevith, B et al. (2015) Low whole grain intake in the UK: results from the National Diet and Nutrition Survey rolling programme 2008–11. Br J Nutr 113, 16431651.Google Scholar
60. Bates, B, Lennox, A, Prentice, A et al. (2014) National Diet and Nutrition Survey Results from Years 1, 2, 3 and 4 (Combined) of the Rolling Programme (2008/9–2011/12). Public Health England Publications. Available at: https://www.gov.uk/government/statistics/national-diet-and-nutrition-survey-results-from-years-1-to-4-combined-of-the-rolling-programme-for-2008-and-2009-to-2011-and-2012.Google Scholar
61. Public Health England (2016) The eatwell guide. http://www.nhs.uk/Livewell/goodfood/Pages/the-eatwell-guide.aspx (accessed February 2016).Google Scholar
62. Oldways Whole Grains Council (2003–2013) Whole grain statistics. http://wholegrainscouncil.org/newsroom/whole-grain-statistics (accessed May 2016).Google Scholar
63. Jones, NRV, Conklin, AI, Suhrcke, M et al. (2014) The growing price gap between more and less healthy foods: analysis of a novel longitudinal UK dataset. PLoS ONE 9, e109343.Google Scholar
64. Ross, AB, Kristensen, M, Seal, CJ et al. (2015) Recommendations for reporting whole-grain intake in observational and intervention studies. Am J Clin Nutr 101, 903907.CrossRefGoogle ScholarPubMed
65. U.S. Food and Drug Administration (1999) Health claim notification for whole grain foods. http://www.fda.gov/Food/IngredientsPackagingLabeling/LabelingNutrition/ucm073639.htm (accessed April 2016).Google Scholar
66. U.S. Food and Drug Administration (2003) Health claim notification for whole grain foods with moderate fat content. http://www.fda.gov/Food/IngredientsPackagingLabeling/LabelingNutrition/ucm073634.htm (accessed April 2016).Google Scholar
67. Joint Health Claims Initiative (2002) Generic health claim for wholegrain foods and heart health. http://webarchive.nationalarchives.gov.uk/nobanner/20130404135254/ http://www.jhci.org.uk/approv/wgrainh.htm (accessed October 2013).Google Scholar
68. EFSA Panel on Dietetic Products and Nutrition Allergies (2010) Scientific opinion on the substantiation of health claims related to whole grain (ID 831, 832, 833, 1126, 1268, 1269, 1270, 1271, 1431) pursuant to Article 13(1) of Regulation (EC) No 1924/2006. Available at: www.efsa.europa.eu/efsajournal.htm.CrossRefGoogle Scholar
69. American Association of Cereal Chemists International (2013) AACCI's whole grains working group unveils new whole grain products characterization. http://www.aaccnet.org/about/newsreleases/Pages/WholeGrainProductCharacterization.aspx (accessed May 2016).Google Scholar
70. Ross, A, van Der Kamp, JW, King, R et al. (2016) A definition for whole-grain food – recommendations from the Healthgrain Forum (In the Press).Google Scholar
71. Scientific Advisory Committee on Nutrition (SACN) (2015) Carbohydrates and Health. London: The Stationery Office.Google Scholar
72. British Nutrition Foundation (2015) Adult weekly meal plan: what does 5% free sugars and 30 g fibre look like? https://www.nutrition.org.uk/attachments/article/872/FINALCOPY%20free%20sugars%20meal%20planner_updated%20December%202015.pdf (accessed June 2016).Google Scholar
73. Health Promotion Board Singapore (2010) Report of the National Nutritional Survey 2010. Research and Strategic Planning Division.Google Scholar
74. Grain & Legumes Nutrition Council (2014) Australians at Risk, 2014 Australian Grains and Legumes Consumption and Attitudinal Study. http://www.glnc.org.au/wp-content/uploads/2015/04/Australians-at-Risk-2014-Grains-Legumes-Consumption-Attitudinal-Study.pdf (accessed July 2016).Google Scholar
75. Burns, AM, Devlin, NFC, McNulty, BA et al. (2013) Dietary intake of whole grain in Irish adults. Proc Nutr Soc 72, E135.Google Scholar
76. Kyro, C, Skeie, G, Dragsted, LO et al. (2012) Intake of whole grain in Scandinavia: intake, sources and compliance with new national recommendations. Scand J Public Health 40, 7684.Google Scholar
77. Food Standards Agency (2002) Food Portion Sizes. London: Stationery Office.Google Scholar
Figure 0

Fig. 1. Accepted mechanisms for effects of whole grain (WG) on chronic disease, from Fardet(43): Current accepted mechanisms for how WG protects against major chronic diseases. GI, glycaemic index; II, insulinaemic index.

Figure 1

Table 1. Whole grain (WG) intakes of adults in national surveys

Figure 2

Table 2. Estimated whole grain (WG) servings based on a sample meal plan to achieve the new fibre and free sugars recommendations