CODEX-aligned dietary fiber definitions help to bridge the ‘fiber gap’
Nutrition Journal volume 13, Article number: 34 (2014)
A comprehensive dietary fiber (DF) definition was adopted by the CODEX Alimentarius Commission (CAC) (1) to reflect the current state of knowledge about DF, (2) to recognize that all substances that behave like fiber regardless of how they are produced can be named as DF if they show physiological benefits, and (3) to promote international harmonization for food labeling and food composition tables. This review gives the history and evolution of the state of DF knowledge as looked at by refinements in DF methods and definitions subsequent to the launch of the DF hypothesis. The refinements parallel both interventional and epidemiological research leading to better understanding of the role of DF in contributing to the numerous physiological benefits imparted by all the various digestion resistant carbohydrates. A comparison of the CODEX definition (including its footnote that authorizes the inclusion of polymers with DP 3–9) and approved CODEX Type 1 methods with other existing definitions and methods will point out differences and emphasize the importance of adoption of CODEX-aligned definitions by all jurisdictions. Such harmonization enables comparison of nutrition research, recommendations, food composition tables and nutrition labels the world over. A case will be made that fibers are analogous to vitamins, in that they vary in structure, function and amount needed, but each when present in the right amount contributes to optimal health. Since the intake of DF is significantly below recommended levels throughout the world, the recognition that ‘all fibers fit’ is an important strategy in bridging the ‘fiber gap’ by enfranchising and encouraging greater intake of foods with inherent and added DF. Fortifying foods with added DF makes it easier to increase intakes while maintaining calories at recommended levels.
Dietary fiber’s (DF) introduction as a concept in the latter half of the last century sparked the need to define DF and to develop a method that emulates the fate of these digestion-resistant materials and that characterizes its health-promoting roles. Defining DF has been both challenging and controversial for several reasons. First, DF can neither be defined as a single chemical entity nor group of related compounds. Second, different fiber types may have one or more physiological functions or health benefits. These may be similar or overlapping and, in some cases, may be unique for a particular fiber entity. Not all fibers perform all functions. So it is difficult to define it by health outcomes. Third, controversy swirls around whether DF has positive benefits only within the food matrix or whether it functions when isolated. Thus, numerous definitions have been proposed in order to address some of these various issues.
In 2009 CODEX published its DF definition, which resulted from nearly two decades of discussion among scientists and delegates from member nations. CODEX’s mission is to promote international harmonization, therefore it strives for a definition with worldwide acceptance [1, 2]. Since the publishing of the CODEX definition, many countries have adopted aligned definitions [3–5]. The newly adopted definitions will increase the need for revisions to food composition tables and nutrition labels. Since the format and content of nutrition labels are under discussion and in some countries have been formally proposed, it is useful to consider labeled nutrients such as DF and to evaluate how differences amongst the various definitions affect labeled values.
DF intake in most countries around the world is far below recommended levels [11–13]. The gap between DF recommendations and intakes is so extreme that the U.S. Dietary Guidelines Advisory Committee (DGAC) listed DF as one of five ‘nutrients of concern’ .
All DF definitions, including the one not using the term DF, but rather uses ‘non-starch polysaccharides’ (NSP) , identify DF as carbohydrate (CHO) polymers and oligomers materials that escape digestion in the small intestine and pass into the large intestine, where they are slightly or nearly completely fermented. DFs per se and their fermentation products contribute to the many physiological benefits associated with their consumption. DF can directly influence the colon and microbiome, and its fermentation products can be absorbed from the large bowel to exert systemic influence in various parts of the body.
This review will give a brief history of the DF research, definitions and methods; compare and contrast the various DF definitions to the CODEX definition; provide justification for inclusion of DF materials that meet the definition including those with a degree of polymerization (DP) 3–9; underline the need for international harmonization in DF research, food composition tables and food labeling; outline the alarming gap between recommended and actual intakes; suggest that a balance of fiber types is important- making DF analogous to vitamins; and give rationale for including all three CODEX categories of DF - intrinsic, added and synthesized or modified for addressing the “fiber gap” and improving human health.
Evolution of the DF definition
In 130 A.D. the physician Galen unknowingly referred to DF when he wrote about foods that “excite the bowels to evacuate and those that prevent them” . He noted that white bread is “the stickiest and slowest to pass and that brown bread is good for the bowels”. From this moment on, the undigested material that ‘excites the bowels’ has been associated with gut health.
In the first part of the last century, studies of non-digestible materials in animal studies assessed their impact on utilization of macronutrients , but the term ‘dietary fiber’ was not used until the 1940s . In human nutrition, the term ‘DF’ was first used in a study of pregnant women where it was observed that those eating diets high in DF had a lower incidence of toxemia .
Until the 1970s, nutrition textbooks covered DF in a single paragraph that noted it was a CHO that resisted digestion and improved laxation. Measurement at that time was part of the proximate composition analysis and was reported as crude fiber (CF). This changed with observations in the late 1960s and early 1970s by British physicians working in rural Africa. They observed that diseases common in the West were rare, and proposed that the observed differences were due to the unrefined nature of African diets. Thus, the DF hypothesis, suggesting that undigested CHO could reduce chronic disease, was launched [19–21].
The search for a DF definition, methods and role
The DF hypothesis spurred a quest for methods and a definition that would adequately characterize this material in food and emulate conditions in the digestive tract. It also launched many research projects looking at its health benefits. The only existing DF method, the CF method, was found wanting because its strong solvents and harsh conditions failed to approximate DF’s fate in the digestive tract [22–25].
Interest in DF’s physiological role stimulated both a re-examination of older intervention studies and new research, especially epidemiological research, which tried to characterize the relationship of DF to various health conditions. Existing studies, most with isolated fibers, indicated DF’s beneficial effects on laxation, gut health, nutrient availability, enzyme activity, and cholesterol or atherosclerosis reduction [26–28].
Current DF definitions and methods
Table 1 gives some DF definitions from around the world including those from CODEX, the U.S. Institute of Medicine (IOM), Health Canada, European Food Safety Authority (EFSA), Food Standards Australia and New Zealand (FSANZ), and American Association of Cereal Chemists International (AACCI) and fiber as described as NSP [1, 3–6, 14, 29].
The 2009 Codex definition resulted from a nearly two-decade process undertaken by CODEX Alimentarius Commission (CAC), whose mission it is to provide global guidance and harmonization about matters regarding food and international trade [1, 2]. (Table 2 gives a brief overview of the CAC.) The definition and its two footnotes read as follows:
Dietary fibre means carbohydrate polymers 1 with 10 or more monomeric units 2 , which are not hydrolysed by the endogenous enzymes in the small intestine of humans and belong to the following categories:
Edible carbohydrate polymers naturally occurring in the food as consumed.
Carbohydrate polymers, which have been obtained from food raw material by physical, enzymatic or chemical means and which have been shown to have a physiological effect of benefit to health as demonstrated by generally accepted scientific evidence to competent authorities,
Synthetic carbohydrate polymers, which have been shown to have a physiological effect of benefit to health as demonstrated by generally accepted scientific evidence to competent authorities.
Footnote 1 states, “when derived from a plant origin, dietary fibre may include fractions of lignin and/or other compounds associated with polysaccharides in the plant cell walls. These compounds also may be measured by certain analytical method(s) for dietary fibre.
Footnote 2 states that, “Decision on whether to include carbohydrates of 3 to 9 monomeric units should be left up to national authorities.”
The two footnotes require comment. Footnote 1 aligns with most definitions and recognizes ‘associated substances’ and lignin when part of, but not isolated from, the DF complex.
The CODEX definition and footnote 2
Footnote 2 allows national authorities the option of including digestion-resistant oligomers with DP 3–9, thus enabling different operative definitions of DF. This is counter to CODEX’s mission, which is to facilitate international harmonization for food labeling, food composition tables, and interpretation of research. For example, results of studies including DP 3–9 could differ from those excluding them. DF values for foods such as wheat and onions that contain digestion-resistant oligomers with DP 3–9 or resistant starch (RS) could differ on food labels and in food composition tables. Thus, epidemiological research using food composition tables might also differ if some countries include these materials and others do not.
The exclusion of resistant CHOs with DP < 10 is an artifact of early DF methods and is not helpful for two reasons. First, an initial alcohol wash elutes short-chained fibrous materials. The loss of this short-chain, non-digestible material is not based on differences in physiological impact or data showing different health outcomes, but merely differences in solubility. Second, the alcohol separation has been shown to lack a precise cutoff at DP = 10, and may elute materials with DP > 10 . Thus, the arbitrary cut-off at DP 10 does NOT have a sound basis either analytically or physiologically.
Resistant short-chain oligomers (DP 3–9) should be DF because they fit the definition in the following ways: 1) they are neither digested nor absorbed by the enzymes in the small intestine, 2) they are fermentable in the large intestine, 3) they aid laxation in the large bowel, and 4) they may increase mineral absorption [30–32]. If these materials are not included as DF, they would be cast into a ‘no-man’s land’ of being neither a digestible CHO nor DF . DF experts from around the world attending the 2010 International Vahouny Dietary Fiber conference voted overwhelmingly for the inclusion of all indigestible CHO oligomers and polymers with DPs of 3 or higher .
In the spirit of international harmonization, many experts recommend the acceptance of the entire CODEX definition including footnote 2, which accepts all digestion-resistant polymers with a DP > 3 . To that end many jurisdictions have adopted the CODEX-aligned definitions in its entirety. Table 3 contains a list of regions that have definitions aligned with the entire CODEX definition.
‘All fibers fit’
All DF definitions recognize non-digested fibrous materials inherent in food as part of the fiber complex. Most definitions also enfranchise these non-digested CHO materials, when they are extracted from edible material, synthesized, or modified, IF they have at least one proven health benefit.
Determination of health benefits requires consideration of both epidemiological and intervention studies because each study type has limitations. Intervention studies are conducted with a specific DF (or DF blend) are usually limited in duration, have few subjects and require a measurable disease biomarker. Subjects in the small pool may not be at risk for the endpoint being measured. Further, the study’s short duration or design may fail to document the impact of DF on disease because of the inability to assess the effects of habitual intakes or to show synergies with other dietary components [36, 37]. Epidemiological studies, on the other hand, have the advantage of huge numbers of subjects with a wide range of disease susceptibility. However, they may be subject to confounding as those with high DF intakes frequently have a number of healthy lifestyle and dietary patterns . Further, dietary intake instruments often fail to accurately characterize habitual diets or food preparation effects. The analysis of epidemiological data relies on food composition databases, which have not been updated to include short-chained oligomers and RS or to have accurate data on DF added to food [39, 40].
The various definitions: similarities and differences
While the various DF definitions show many similarities, some important differences exist (Table 1). All definitions enfranchise CHO polymers that resist digestion and absorption in the human small intestine. However, the NSP definition only recognizes plant cell wall fibers, and does not include synthetic, resistant CHO polymers or polymers extracted from raw food material by physical, enzymatic or chemical means.
The IOM definition  bears similarity to CODEX-aligned definitions in that it accepts that all resistant carbohydrate materials whether intrinsic or extracted or synthesized. However, it reserves the term ‘dietary fiber’ only for materials that are intrinsic and intact within food. Extracted, modified or synthesized fibers are defined as ‘functional fiber’. The sum functional and intrinsic DF is ‘total fiber’, rather than DF as in all other definitions except the NSP definition [6, 14].
While difference between the IOM and the CODEX definition is small, it may create analytical challenges and cause confusion for several reasons. First, the term ’DF’ is used in labeling and nutrient databases and nutrition research, where fibers from foods and fibers added to the diet are usually considered collectively and not separately. Second, the two IOM categories cannot be differentiated analytically when the food inherently contains the fiber that is being added (e.g. an oatmeal muffin with added β-glucan) [24, 25]. Third, not referring to both types as DF is inconsistent with the reporting of other nutrients in food composition tables, food labels and nutrient intake surveys. For other nutrients, reported values are the sum of that nutrient irrespective of whether it was added or inherent. Thus, the small nuance of difference between the IOM definition and other CODEX-aligned definitions could cause unintended points of difference.
Most definitions require that at least one physiological benefit be shown for fibers added back to food, e.g. those fibers in CODEX categories 2 or 3. Some definitions list specific physiological effects, as did all iterations of the CODEX definition except the final one [1, 3–5, 24]. These were: 1) improved intestinal transit time and increased stool bulk; 2) fermentation by colonic microflora; 3) reduction in blood total and/or LDL cholesterol levels; and 4) reduction in post-prandial blood glucose and/or insulin levels. Other definitions may include other physiological effects [3–5, 24].
Most DF definitions accept Codex Footnote 1 and agree with the inclusion of lignin and associated substances as DF, but only when part of the native fiber complex. Some definitions allow only CHO from plants, while others recognize DF from animals (e.g. chitin). (Whether included or not, such fibers are captured by current analytical methods.)
Like the CODEX DF definition, many definitions include RS and resistant oligomers [1, 3–5, 24]. The AOAC 2009.01 (AACCI 32–45), a CODEX Type 1 method, best matches the CODEX definition and captures these digestion-resistant entities [2, 39–43]. However, many food databases report values obtained using older methods. The NSP definition and method (not a Type 1 method) fail to capture resistant oligomers or RS [14, 44]. (Note: The CAC strives to have a single Type 1 method with the imprimatur of AOAC International and the AACCI because of the rigorous collaborative testing in labs around the world prove them to be both rugged and reproducible. The NSP method is defined by CODEX as an empirical method, rather than a rationale method, and does not get full CODEX imprimatur as the method of choice).
DF intake recommendations for adults range from 18–38 g/d [3–6, 45–48] (Table 4). WHO/FAO and EFSA recommend 25 g/d with their recommendations based on amounts needed for healthy laxation [5, 46]. Some countries such as Singapore, the U.S. and Canada tie DF requirements to caloric intake, so recommended amounts for men, women and elderly vary. Thus, recommended levels are 25 g/d for women and 38 g/d for men in the U.S. and Canada. These are among the highest recommended levels not only because they are tied to calories, but also because they are based on the median intake associated with the lowest risk of coronary disease in prospective cohort studies . The 18 g/d recommended by the UK Food Standards Agency is lower than most other recommendations and reflects the use of NSP definition and methods rather than the CODEX definition and method . This is an example where confusion is caused by different jurisdictions using non- CODEX aligned definitions and methods .
There is a concerning gap between recommendations and intake worldwide [11–13, 49]. For example in North America, the average daily consumption of adults is 15 g/d, which means that those in the lowest quintiles of intake ingest below half the recommended levels [50–52]. Evaluation of NHANES 2003–2006 data show that under 5% of the US population ingests the recommended intake [11, 12].
A few initiatives have been successful in reducing the DF gap, such as programs from the Grains & Legumes Nutrition Council (formerly GoGrains) in Australia and New Zealand . However, in most countries intake has not increased, despite a consistent body of evidence associating DF with reduced health risks [54–64] and messages from health promotion organizations to increase DF intake for both prevention and management of disease [13, 65–67]. Food intake surveys in the U.S. show that intake has remained roughly the same for over nearly two decades [11, 12, 50]. The DF gap even occurs in children in many countries and manifests itself as chronic constipation [68, 69]. Inadequate intake of DF in childhood is thought to be associated with health risks including obesity in later life .
“All fibers fit” to address the fiber gap
Adoption of CODEX-aligned definitions provides a strategy to help address the fiber gap by acknowledging the role of both intrinsic and added fibers. The ‘all fibers fit’ mantra means that healthy diets include the various fiber types . Constructing a diet with a balance of DF types is analogous to constructing a diet with the correct amount and balance of the vitamins needed for optimal health. The similarities are outlined as follows. First, vitamin requirements are fulfilled only when all vitamins are present both in quantity and type. In like manner for DF, the optimal diet would have both right quantity of total DF and balance of fiber types. Second, vitamins inherently in food and those added through fortification and enrichment can work together to fulfill the requirements [71, 72]. The same can apply to DF in that added fibers can interact with intrinsic fibers to meet the requirement act synergistically actually to reap health benefits.
Variety is one of the important concepts of healthy diets. Just as a balanced diet incorporates adequate amounts of each vitamin and avoids excesses of any one kind, an optimal diet should incorporate the right amount and balance of fiber different types needed to perform DFs’ many functions. Thus a varied diet that uses fiber-fortified foods together with fiber-rich foods has multiple benefits. It ensures inclusion of associated substances that are trapped in the DF matrix of natural foods, allows health benefits from the synergy of DF types and functions, and the fiber gap while staying within a day’s calorie allotment.
Efforts to increase the intake of fiber-rich foods - whole grain breads and cereals or pseudocereals (wheat, maize, oats, rye, barley, triticale, millet, sorghum, buckwheat, etc.), legumes and soy, fruits, vegetables, nuts, and seeds - must continue. While diets constructed using USDA MyPlate and DGAC recommendations can attain DF levels as high as 50 g/d with the selection of high-fiber options within and among the food groups (Table 5), analysis of food consumption data show that most consumers chose low-fiber foods frequently. Since a serving of many common foods provides 1–3 g of DF, individuals eating according to the MyPlate guidelines could ingest on average 20–24 g/d, but might ingest as little as 12–15 g/d. However, only 3-8% of the US population eats according to USDA MyPlate, and the fiber-containing food groups are most frequently omitted [13, 50–52, 73–81].
NHANES data from 2001–2004 document that under 5% of consumers in most age and gender categories meet the adequate intake (AI) for fiber . Less than 10% of the population meets the whole grain recommendation [80, 81]. Fruit and vegetable intakes are about half that recommended, and again the higher-fiber choices within each groups are selected less frequently . Per capita consumption of legumes is extremely low at 25 g/d (0.1 cup/d or 20 calories/day) .
Addressing the ‘fiber gap’ not only requires a continuing push towards greater intake of fiber-rich foods and the use of more foods with added fibers, but also needs to include consumer education about fiber sources. Surveys show that consumers are looking for more DF, but also reveal that they have difficulty choosing foods or groups of foods that are DF sources, identifying isolated fibers on the ingredient statement, or estimating the DF content of foods and diets [82–84].
Statements by some health professionals and in corporate advertising campaigns suggest that added fibers are ‘fake’, and that only foods with natural fiber can fulfill DF requirements. While it is true that added fibers may not carry all the ‘co-passengers’ found in the food fiber matrix, isolated fibers do show documented health benefits . In fact these benefits are so well documented that many countries allow health claims for isolated fibers such as wheat bran and β-glucan and its derivatives. In some cases isolated fibers and their derivatives are more concentrated both in terms of DF and trapped co-passengers enabling intake of a smaller amount of food for an equivalent physiological dose than would required from the whole food. For example, the addition of oat bran and β-glucan to a serving of oatmeal yields a cholesterol-lowering dose of DF with half the calories of an equivalent dose of oatmeal without added DF .
The synergy of fiber inherent in foods and that added to foods has been documented and needs to be emphasized [87–89]. For example, a meta-analysis of intervention studies suggests that type 2 diabetes risk reduction is reached either with isolated fiber or with DF from whole foods . Improved blood lipids and weight management was shown to occur with isolated fiber added to a diet with a baseline of 20 g of DF. Discounting of the contribution of added fibers because of their lack of epidemiological evidence fails to consider studies such as this cited meta-analysis .
Teasing out the effects of isolated DFs from epidemiological studies is methodologically challenging because food databases used in the analysis of food frequency only report total DF and do not attribute DF source. Thus health impacts of added fibers may be not be captured. Further, food composition data may not reflect added fibers especially those that are short-chain oligomers and resistant starch, so their presence may be underestimated . Thus, epidemiological studies attribute all health benefits to DF that are inherent in foods and fail to recognize the contribution of added fiber or its synergy in impacting health and disease. However, data from intervention studies clearly show that increases in total DF intake through fibers added to a baseline of diet rich in whole grains, fruits and vegetables, legumes and other fiber-rich foods synergistically improves health outcomes over those observed with lower fiber intakes [87–89].
Worldwide there is a ‘fiber gap’ because intake is far below the recommendations. The gap is so extreme that the 2010 U.S. DGAC followed previous committees in naming DF as one of five ‘nutrients of concern’. Less than one in ten Americans meets the fiber requirement.
The new CODEX definition enfranchising added fibers along with fibers traditionally found in food underscores the need for all types of fibers – those which naturally occur in vegetables, fruits, whole grains, nuts, seeds and legumes and those that are isolated or synthesized and added to foods - as part of a strategy to address the inadequate intake of DF. The new definition reflects advances in the knowledge of dietary fiber types and roles and shows that all CHOs with DP > 3 that resist digestion and that have a beneficial physiological effect are included and include them even though certain earlier methods did not necessarily capture these materials. Acceptance as a DF is based on proof of a physiological benefit.
With CODEX-aligned definitions across jurisdictions, the development of great-tasting, high-fiber foods by the food industry is facilitated. Consumer education programs can heighten awareness of the ‘fiber gap’ and suggest workable dietary strategies to address the problem. This can include programs that help consumers identify isolated DFs, choose foods naturally rich in fiber, and model diets which achieve fiber recommendations with a combination of foods naturally high in fiber and those with added fiber. Such models can show consumers how to increase fiber intake while helping consumers to stay within their calorie budget and encourage them to act on the principle laid out in the CODEX definition that ‘all fibers fit’.
In summary, adoption of CODEX-aligned definitions and approved methods, which include resistant oligomers DP 3–9 (included in Footnote 2) and resistant starches, is needed in all jurisdictions because such an action recognizes the current state of fiber research and methodology, facilitates the conduct of nutrition research that is comparable, harmonizes nutrition labeling and food composition tables, and provides a platform to educate consumers about the benefits of dietary fiber and risks of not choosing it. A single voice with consistent messaging about the benefits of DF can help consumers build diets that will meet intake goals to address the ‘fiber gap’ and reap the benefits of diets that have increased DF.
I have worked on the AACCI committee looking at the dietary fiber definition. I was part of an ILSI team presenting at the Vahouny Dietary Fiber conference. I have done much work in the area of carbohydrate nutrition, resistant starch, sugars, whole grains and dietary fiber. I presented at a symposium prior to a CODEX meeting on definitions and methods for dietary fiber.
American Association of Cereal Chemists International
Association of Analytical Chemists
- CAC CODEX:
Dietary Guidelines Advisory Committee
Degree of polymerization
European Food Safety Authority
Food and Agriculture Organization
Food Standards Australia and New Zealand
US Food and Drug Administration
International Life Sciences Institute
Institute of Medicine
World Health Organization.
Joint FAO/WHO Food Standards Programme, Secretariat of the CODEX Alimentarius Commission: CODEX Alimentarius (CODEX) Guidelines on Nutrition Labeling CAC/GL 2–1985 as Last Amended 2010. 2010, Rome: FAO
Zielinski G, DeVries JW, Craig SA, Bridges AR: Dietary fiber methods in Codex Alimentarius: Current status and ongoing discussions. Cereal Food World. 2013, 58: 148-153. 10.1094/CFW-58-3-0401.
Bureau of Nutritional Sciences Food Directorate, Health Products and Food Branch, Health Canada: Policy for labelling and advertising of dietary fibre-containing food. 2013, http://www.hc-sc.gc.ca,
Food Standards Australia New Zealand (FSANZ): Food standards Australia New Zealand code issue 115, standard 1.2.8. nutrition information requirements. http://www.nrv.gov.au/nutrients/dietary-fibre,
European Food Safety Authority: Outcome of the Public consultation on the Draft Opinion of the Scientific Panel on Dietetic Products, Nutrition, and Allergies (NDA) on Dietary Reference Values for carbohydrates and dietary fibre. EFSA Journal. 2010, 8: 1508-1569. http://www.efsa.europa.eu/en/search/doc/1462.pdf,
Institute of Medicine (IOM), U.S. National Academy of Sciences: Dietary Reference Intakes: Proposed Definition of Dietary Fiber. 2001, Washington, D.C: National Academy Press
Food Labeling Modernization Act of 2013 (H.R. 3147). Fed Regist. 2013, 78 (104): [https://www.govtrack.us/congress/bills/113/hr3147]
Ginter K: Are nutrition labels going to change?. [http://www.fda.gov/food/guidanceregulation/guidancedocumentsregulatoryinformation/labelingnutrition/ucm385663.htm November 29, 2011]
Carvajal R: Time for food labeling reform? Introducing the Food Labeling Modernization Act of 2013. http://www.fdalawblog.net/fda_law_blog_hyman_phelps/2013/09/time-for-food-labeling-reform-introducing-the-food-labeling-modernization-act-of-2013. Accessed August 2013
Vyth EL, Steenhuis IH, Roodenburg AJ, Brug J, Seidell JC: Front-of-pack nutrition label stimulates healthier product development: a quantitative analysis. Int J Behav Nutr Phys Act. 2010, 8: 65-72.
Jones JM: Dietary fiber intake, disease prevention, and health promotion: an overview with emphasis on evidence from epidemiology. Bioactive Carbohydrates for Food and Feed. Edited by: van der Kamp JW, Asp N-G, Miller-Jones J, Schaafsma G. 2004, Wageningen, Netherlands: Academic Publishers, 143-164.
Marriott BP, Olsho L, Hadden L, Connor P: Intake of added sugars and selected nutrients in the United States, National Health and Nutrition Examination Survey (NHANES) 2003—2006. Crit Rev Food Sci Ntr. 2010, 50: 228-258. 10.1080/10408391003626223.
US Department of Agriculture and US Department of Health and Human Services: Dietary Guidelines for Americans. 2010, Washington, D.C: , 40-46. [http://www.cnpp.usda.gov/dgas2010-dgacreport.htm], 7
Englyst KN, Liu S, Englyst HN: Nutritional characterization and measurement of dietary carbohydrates. Eur J Clin Nutr. 2007, 61 (Suppl 1): 19-39.
Galen: On the Properties of Foodstuffs. 2003, Cambridge, UK: Cambridge University Press, Translated by O. Powell
Mendel LB, Fine MS: Studies in nutrition. IV. The utilization of the proteins of the legumes. J Biochem. 1912, 10: 433-460.
Duckworth J, Godden WJ: The influence of dietary fibre on secretory activities of the alimentary tract: Observations on faecal phosphatase excretion and calcium and nitrogen balances of rats. Biochem J. 1941, 35: 16-23.
Hipsley EH: Dietary "fibre" and pregnancy toxaemia. Br Med J. 1953, 2 (4833): 420-422. 10.1136/bmj.2.4833.420.
Burkitt DP, Trowell HC: Refined Carbohydrate Foods and Disease: Some Implications of Dietary Fibre. 1975, London: Academic. Press
Burkitt DP, Walker AR, Painter NS: Effect of dietary fibre on stools and the transit-times, and its role in the causation of disease. Lancet. 1972, 2 (7792): 1408-1412.
Trowell H: Why a new term for dietary fiber?. Amer J Clin Nutr. 1977, 30: 1003-1004.
Lee SC, Prosky L: International survey on dietary fiber: definition, analysis and reference materials. J AOAC Int. 1995, 78: 22-36.
Cho S, DeVries JW, Prosky L: AOAC Dietary Fiber Analysis and Applications. 1997, Gaithersburg, VA: AOAC International
AACC Dietary Fiber Definition Committee: Definition of dietary fiber: Report of the Dietary Fiber Definition Committee to the Board of Directors of the American Association of Cereal Chemists. Cereal Foods World. 2001, 46: 112-126.
DeVries JW, Rader JI: Historical perspective as a guide for identifying and developing applicable methods for dietary fiber. J AOAC Int. 2005, 88: 1349-1366.
Schmitt R, Kleibel F: Modern therapy of constipation with cellulose derivatives. Arztl Wochensch. 1952, 7: 1133-1135.
Vignec AJ, Mitty VC: Treatment of chronic constipation in childhood. J Pediatr. 1952, 40: 576-578. 10.1016/S0022-3476(52)80148-9.
Keys A, Grande F, Anderson JT: Fiber and pectin in the diet and serum cholesterol concentration in man. Proc Soc Exp Biol Med. 1961, 106: 555-558.
Englyst HN, Quigley ME, Hudson GJ: Definition and measurement of dietary fibre. Eur J Clin Nutr. 1995, 49 (Suppl 3): 48-62.
de Menezes EW, Giuntini EB, Dan MC, Sardá FA, Lajolo FM, Lanza E, Jones DY: Codex dietary fibre definition - Justification for inclusion of carbohydrates from 3 to 9 degrees of polymerisation. Food Chem. 2013, 140: 581-5. 10.1016/j.foodchem.2013.02.075.
Raninen K, Lappi J, Mykkanen H, Poutanen K: Dietary fiber type reflects physiological functionality: comparison of grain fiber, inulin, and polydextrose. Nutr Rev. 2011, 69: 9-21. 10.1111/j.1753-4887.2010.00358.x.
Gray J: Dietary Fibre: Definition, Analysis, Physiology & Health. 2006, ILSI Europe: Brussels
Caers W: Dietary Fibre and Prebiotics: Science and Regulatory Update. Oligosaccharides: Its Commercial Application as Dietary Fibres and Prebiotics. 2011, Bangkok: ILSI SE Asia and Nutrition Society of Thailand
Howlett JF, Betteridge VA, Champ M, Craig SA, Meheust A, Jones JM: The definition of dietary fiber – discussions at the ninth Vahouny fiber symposium: building scientific agreement. Food Nutr Res. 2010, 54: 1-5.
Lupton JR, Betteridge VA, Pijls LTJ: Codex final definition of dietary fibre: Issues of implementation. Qual Assur Saf Crops Food. 2009, 1: 206-212. 10.1111/j.1757-837X.2009.00043.x.
Potischman N: Biologic and methodologic issues for nutritional biomarkers. J Nutr. 2003, 133 (Suppl 3): 875S-880.
Pal S, Radavelli-Bagatini S: Effects of psyllium on metabolic syndrome risk factors. Obes Rev. 2012, 13: 1034-1047. 10.1111/j.1467-789X.2012.01020.x.
Aune D, Chan DS, Lau R, Vieira R, Greenwood DC, Kampman E, Norat T: Dietary fibre, whole grains, and risk of colorectal cancer: systematic review and dose–response meta-analysis of prospective studies. BMJ. 2011, 343: d6617-10.1136/bmj.d6617.
Westenbrink S, Brunt K, van der Kamp JW: Dietary fibre: challenges in production and use of food composition data. Food Chem. 2013, 140: 562-567. 10.1016/j.foodchem.2012.09.029.
Hollmann J, Themeier H, Neese U, Lindhauer MG: Dietary fibre fractions in cereal foods measured by a new integrated AOAC method. Food Chem. 2013, 140: 586-589. 10.1016/j.foodchem.2012.12.005.
McCleary BV: Dietary fibre analysis. Proc Nutr Soc. 2003, 62: 3-9. 10.1079/PNS2002204.
McCleary BV, DeVries JW, Rader JI, Cohen G, Prosky L, Mugford DC, Okuma K: Determination of insoluble, soluble, and total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study. J AOAC Int. 2012, 95: 824-44. 10.5740/jaoacint.CS2011_25.
McCleary BV, DeVries JW, Rader JI, Cohen G, Prosky L, Mugford DC, Champ M, Okuma K: Determination of total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study. J AOAC Int. 2010, 93: 221-33.
Englyst KN, Liu S, Englyst HN: Nutritional characterization and measurement of dietary carbohydrates. Eur J Clin Nutr. 2007, 61 (Suppl 1): S19-S39.
Institute of Medicine (IOM),The National Academies of Science: Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids. 2002, Washington, DC: National Academies Press, 339-61.
Nishida C, Uauy R, Kumanyika S, Shetty P: Joint FAO/WHO Expert Consultation. Carbohydrates in human nutrition. Food and Agriculture Organization. World Health Organization. FAO Food and Nutrition. Publ Health Nutr. 2004, 7: 245-250.
UK Food Standards Agency: FSA Nutrient and Food Based Guidelines for UK Institutions. 2006, http://www.food.gov.uk. 2006
Cheong T: Why Is Dietary Fibre So Important?. Singapore Health Promotion Board http://www.healthxchange.com.sg/healthyliving/DietandNutrition/Pages/Why-Is-Dietary-Fibre-So-Important.aspx
Jonsdottir SE, Brader L, Gunnarsdottir I, Kally Magnusdottir O, Schwab U, Kolehmainen M, Risérus U, Herzig KH, Cloetens L, Helgegren H, Johansson-Persson A, Hukkanen J, Poutanen K, Uusitupa M, Hermansen K, Thorsdottir I: Adherence to the Nordic Nutrition Recommendations in a Nordic population with metabolic syndrome: high salt consumption and low dietary fibre intake (The SYSDIET study). Nutr Res: Food. 2013, 57:
King DE, Mainous AG, Lambourne CA: Trends in dietary fiber intake in the United States, 1999–2008. J Acad Nutr Diet. 2012, 112: 642-8. 10.1016/j.jand.2012.01.019.
Marlett JA, McBurney MI, Slavin JL, American Dietetic Association: Position of the American Dietetic Association: health implications of dietary fiber. J Am Diet Assoc. 2002, 102: 993-1000.
Slavin JL: Position of the American Dietetic Association: Health implications of dietary fiber. J Am Diet Assoc. 2008, 108: 1716-1731.
Anderson JW, Randles KM, Kendall CW, Jenkins DJ: Carbohydrate and fiber recommendations for individuals with diabetes: A quantitative assessment and meta-analysis of the evidence. J Am Coll Nutr. 2004, 2004 (23): 5-17.
Park Y, Subar AF, Hollenbeck A, Schatzkin A: Dietary fiber intake and mortality in the NIH-AARP diet and health study. Arch Intern Med. 2011, 171: 1061-1068.
Papathanasopoulos A, Camilleri M: Dietary fiber supplements: effects in obesity and metabolic syndrome and relationship to gastrointestinal functions. Gastroenterology. 2010, 138: 65-72. 10.1053/j.gastro.2009.11.045.
El Khoury D, Cuda C, Luhovyy BL, Anderson GH: Beta glucan: health benefits in obesity and metabolic syndrome. J Nutr Metab. 2012, 2012: 851362-
Bajorek SA, Morello CM: Effects of dietary fiber and low glycemic index diet on glucose control in subjects with type 2 diabetes mellitus. Ann Pharmacother. 2010, 44: 1786-1792. 10.1345/aph.1P347.
Shamliyan TA, Jacobs DR, Raatz SK, Nordstrom DL, Keenan JM: Are your patients with risk of CVD getting the viscous soluble fiber they need?. J Fam Pract. 2006, 55: 761-769.
Jones JM, Lineback DR, Levine MJ: Dietary reference intakes: implications for fiber labeling and consumption: a summary of the international life sciences institute North America fiber workshop. June 1–2, 2004; Washington, DC. Nutrition Rev. 2006, 64: 31-38.
Wolfram T, Ismail-Beigi F: Efficacy of high -fiber diets in the management of type 2 diabetes mellitus. Endocr Pract. 2011, 17: 132-142. 10.4158/EP10204.RA.
Brennan CS: Dietary fibre, glycaemic response, and diabetes. Mol Nutr Food Res. 2005, 49: 560-570. 10.1002/mnfr.200500025.
Wallace TC, Guarner F, Madsen K, Cabana MD, Gibson G, Hentges E, Sanders ME: Human gut microbiota and its relationship to health and disease. Nutr Rev. 2011, 69: 392-403. 10.1111/j.1753-4887.2011.00402.x.
Roberfroid M, Gibson GR, Hoyles L, McCartney AL, Rastall R, Rowland I, Wolvers D, Watzl B, Szajewska H, Stahl B, Guarner F, Respondek F, Whelan K, Coxam V, Davicco MJ, Léotoing L, Wittrant Y, Delzenne NM, Cani PD, Neyrinck AM, Meheust A: Prebiotic effects: metabolic and health benefits. Br J Nutr. 2010, 104 (Suppl 2): 1-63.
American Heart Association: Whole grains and fiber. http://www.heart.org/HEARTORG/GettingHealthy/NutritionCenter/HealthyDietGoals/Whole-Grains-and-Fiber_UCM_303249_Article.jsp#.T0J8oMx1F4s,
Bantle JP, Wylie-Rosett J, Albright AL, Apovian CM, Clark NG, Franz MJ, Hoogwerf BJ, Lichtenstein AH, Mayer-Davis E, Mooradian AD, Wheeler ML, American Diabetes Association: Nutrition recommendations and interventions for diabetes: a position statement of the American Diabetes Association. Diabetes Care. 2008, 31 (Suppl 1): 61-78.
Rock CL, Doyle C, Demark-Wahnefried W, Meyerhardt J, Courneya KS, Schwartz AL, Bandera EV, Hamilton KK, Grant B, McCullough M, Byers T, Gansler T: Nutrition and physical activity guidelines for cancer survivors. CA Cancer J Clin. 2012, 62: 243-274.
Mugie SM, Di Lorenzo C, Benninga MA: Constipation in childhood. Nat Rev Gastroenterol Hepatol. 2011, 8: 502-511. 10.1038/nrgastro.2011.130.
Tabbers MM, Boluyt N, Berger MY, Benninga MA: Nonpharmacologic treatments for childhood constipation: systematic review. Pediatrics. 2011, 128: 753-761. 10.1542/peds.2011-0179.
Kranz S, Brauchla M, Slavin JL, Miller KB: What do we know about dietary fiber intake in children and health? The effects of fiber intake on constipation, obesity, and diabetes in children. Adv Nutr. 2012, 3: 47-53. 10.3945/an.111.001362.
Flynn A, Hirvonen T, Mensink GB, Ocké MC, Serra-Majem L, Stos K, Szponar L, Tetens I, Turrini A, Fletcher R, Wildemann T: Intake of selected nutrients from foods, from fortification and from supplements in various European countries. Food Nutr Res. 2009, 12: 53-
Fulgoni VL, Keast DR, Bailey RL, Dwyer J: Foods, fortificants, and supplements: Where do Americans get their nutrients?. J Nutr. 2011, 141: 1847-1854. 10.3945/jn.111.142257.
U.S. Department of Agriculture and U.S. Department of Health and Human Services: Dietary guidelines for Americans. http://www.dietaryguidelines.gov,
Juan WY, Guenther PM, Kott PS: Nutrition Insight 41. Diet quality of older Americans in 1994–96 and 2001–02 as measured by the Healthy Eating Index-2005. 2008, Alexandria (VA): USDA, Center for Nutrition Policy and Promotion
Guenther PM, Juan WY, Lino M, Hiza HA, Fungwe T, Lucas R: Nutrition Insight 42. Diet Quality of Low-Income and Higher Income Americans in 2003–04 as measured by the Healthy Eating Index-2005. 2008, Alexandria (VA): USDA, Center for Nutrition Policy and Promotion
Fungwe T, Guenther PM, Juan WY, Hiza HA, Lino M: Nutrition Insight 43. The Quality of Children's Diets in 2003–04 as measured by the Healthy Eating Index-2005. 2009, Alexandria (VA): USDA, Center for Nutrition Policy and Promotion
Krebs-Smith SM, Reedy J, Bosire C: Healthfulness of the U.S. food supply: little improvement despite decades of dietary guidance. Am J Prev Med. 2010, 38: 472-477. 10.1016/j.amepre.2010.01.016.
Bachman JL, Reedy J, Subar AF, Krebs-Smith SM: Sources of food group intakes among the US population, 2001–2002. J Am Diet Assoc. 2008, 108: 804-814.
Krebs-Smith SM, Guenther PM, Subar AF, Kirkpatrick SI, Dodd KW: Americans do not meet federal dietary recommendations. J Nutr. 2010, 140: 1832-1838. 10.3945/jn.110.124826.
Hornick B, Liska D, Dolven C, Wrick K: The fiber deficit, part 1: Whole grain contributions to health and fiber intakes. Nutr Today. 2011, 46: 293-298. 10.1097/NT.0b013e318239635f.
Busby JC, Wells HF: Dietary assessment of major trends in U.S. food consumption, 1970-2005. Econ Inform Bull. March 2008, 27-http://www.ers.usda.gov/publications/eib33/eib33.pdf, EIB-33,
Food & health survey: consumer attitudes toward food safety, nutrition and health. Food and Health Survey IFIC. 2013, http://www.foodinsight.org/LinkClick.aspx?fileticket=rH%2bcRQoWh2s%3d&tabid=65,
Kessler K, Wunderlich SM: Relationship between use of food labels and nutrition knowledge of people with diabetes. Diabetes Educ. 1999, 25: 549-559. 10.1177/014572179902500407.
Kellogg C: Americans may be looking to the wrong foods to boost their fiber intake, research reveals. Kellogg Company's Whole Grains & Fiber Omnibus Survey. http://newsroom.kelloggcompany.com/index.php?s=27529&item=76360,
Eshak ES, Iso H, Date C, Kikuchi S, Watanabe Y, Wada Y, Wakai K, Tamakoshi A, JACC Study Group: : Dietary fiber intake is associated with reduced risk of mortality from cardiovascular disease among Japanese men and women. J Nutr. 2010, 140: 1445-1453. 10.3945/jn.110.122358.
Davidson MH, Dugan LD, Burns JH, Bova J, Story K, Drennan KB: The hypercholesterolemic effects of beta-glucan in oatmeal and oat bran. A dose-controlled study. JAMA. 1991, 265: 1833-1839. 10.1001/jama.1991.03460140061027.
Pal S, Khossousi A, Binns C, Dhaliwal S, Ellis V: The effect of a fibre supplement compared to a healthy diet on body composition, lipids, glucose, insulin and other metabolic syndrome risk factors in overweight and obese individuals. Br J Nutr. 2011, 105: 90-100. 10.1017/S0007114510003132.
Jenkins AL, Kacinik V, Lyon M, Wolever TM: Effect of adding the novel fiber, PGX®, to commonly consumed foods on glycemic response, glycemic index and GRIP: a simple and effective strategy for reducing post prandial blood glucose levels–a randomized, controlled trial. Nutr J. 2010, 9: 58-10.1186/1475-2891-9-58.
Al-Tamimi EK, Seib PA, Snyder BS, Haub MD: Consumption of Cross-Linked Resistant Starch (RS4(XL)) on glucose and insulin responses in humans. J Nutr Metab. 2010, 2010: 651063
Post RE, Mainous AG, King DE, Simpson KN: Dietary fiber for the treatment of type 2 diabetes mellitus: a meta-analysis. J Am Board Fam Med. 2012, 25: 16-23. 10.3122/jabfm.2012.01.110148.
Dilzer A, Jones JM, Latulippe M: The family of dietary fibers: dietary variety for maximum health benefit. Nutr Today. 2013, 48: 108-118. 10.1097/NT.0b013e3182941d82.
The work was sponsored by the Calorie Control Council.
Funds to help with the preparation of this manuscript were given by the Calorie Control Council. In the past 5 years, I have given speeches and written articles where travel grants and honoraria are received from the food industry some of which produce or use whole grains and fibers such as ADM, Beneo, Campbell Soup Company, Ingredion, Kraft Foods, Proctor & Gamble, Tate & Lyle and Uncle Ben’s. I am a scientific advisor to the carbohydrate committee of the International Life Sciences Institute – North America, the WK Kellogg Corporation, the Quaker Oats Company, the Joint Institute of Food Safety and Applied Nutrition of the University of Maryland and the US Food and Drug Administration.
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Jones, J.M. CODEX-aligned dietary fiber definitions help to bridge the ‘fiber gap’. Nutr J 13, 34 (2014). https://doi.org/10.1186/1475-2891-13-34