JACN
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saltzman, E.
Right arrow Articles by Roberts, S. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saltzman, E.
Right arrow Articles by Roberts, S. B.
Journal of the American College of Nutrition, Vol. 20, No. 1, 50-57 (2001)
Published by the American College of Nutrition


Original Research

Effects of a Cereal Rich in Soluble Fiber on Body Composition and Dietary Compliance during Consumption of a Hypocaloric Diet

Edward Saltzman, MD, Julio C. Moriguti, MD, Sai Krupa Das, MS, Alberto Corrales, Paul Fuss, Andrew S. Greenberg, MD and Susan B. Roberts, PhD

Energy Metabolism Lab, The Jean Mayer U.S.D.A. Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts

Address reprint requests to: S.B. Roberts, Ph.D., Jean Mayer U.S.D.A. Human Nutrition Research Center on Aging at Tufts University, 711 Washington St., Boston, MA 02111. E-mail: sroberts{at}hnrc.tufts.edu


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Objectives: To investigate the effects of oats, a cereal rich in soluble fiber, on body composition changes and dietary compliance during consumption of a weight loss diet.

Methods: Subjects were 41 healthy men and women aged 18 to 78 years. Weight maintenance energy requirements were established over two weeks during consumption of a control diet with low soluble fiber content. Subjects then consumed a hypocaloric diet for six weeks, either consuming a low soluble fiber control diet or a diet containing 45 g/1000 kcal rolled oats, a whole grain cereal rich in soluble fiber (mean energy deficit -895 ± 18 kcal/day relative to weight maintenance energy requirements). Changes in body fat and fat-free mass were determined by underwater weighing, and dietary compliance was assessed using the urinary osmolar excretion rate technique. In a final phase of the study, subjects ate ad libitum for six months, and changes in body weight and composition were monitored.

Results: There was no significant effect of the oat-containing diet on body weight or composition changes during the hypocaloric regimen or in the subsequent ad libitum period. In addition, fecal energy excretion was not significantly different between groups. However, there were non-significant trends indicating reduced hunger in the oat group compared to controls (frequency of hunger 2.5±0.5 vs. 3.6±0.4, P=0.1). In addition, fewer oat subjects were non-compliant (four versus seven subjects dropped out or had urinary osmolar excretions greater than 130% of values predicted from dietary intake), but again the difference was not significant.

Conclusions: These results suggest that use of a cereal rich in soluble fiber in a closely monitored hypocaloric feeding regimen does not improve weight loss or dietary compliance. Further studies are needed to examine the possibility that cereals containing soluble fiber may have effects on hunger and dietary compliance that could be important in less tightly controlled protocols than the one described here.

Key words: energy intake, obesity, oats, soluble fiber, weight loss, body fat, compliance


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The prevalence of obesity is increasing nationally and worldwide. Recent longitudinal data from the National Health and Nutrition Examination Survey [1] showed that the mean body mass index of adult men and women in the United States increased from 25.3 to 26.3 kg/m2 between the periods of 1960 to 1962 and 1988 to 1991, corresponding to a body weight gain of 3.6 kg. In parallel with this trend, an increasing number of the adult population are using weight-loss diets, and up to 40% of women and 24% of men may be attempting to reduce weight at any given time [2]. However, there is no scientific consensus over what (if any) dietary macronutrient composition is optimal for promoting successful weight loss in the short-term and preventing weight gain over the long-term. Currently popular weight-loss diets span the range from high-carbohydrate/low fat to high-fat/high protein, emphasizing the lack of adequate information in this area.

Several factors may potentially influence the effectiveness and acceptability of weight-loss diets, including the digestibility of food energy as well as hunger and satiety for a given level of energy intake. In particular, diets promoting some degree of energy malabsorption could theoretically enhance negative energy balance if they did not also promote increased hunger. Similarly, if dietary regimens could be identified that minimize hunger or promote satiety, they could potentially improve weight loss success by improving compliance. From these perspectives, diets high in soluble fiber might be expected to promote weight loss success, since soluble fiber reduces rate of macronutrient digestion and absorption from the small intestine and enhances short-term satiety [3, 4]. Soluble fiber also lowers the glycemic index of foods, a factor recently associated with suppression of hunger in a one-day study [5].

There is currently controversy over whether soluble fiber can aid weight loss [6], with some studies showing a positive effect of fiber on weight loss [3, 4, 712] and others showing no effect [4, 9, 1316]. It is possible that these inconsistent results may be due to differences in study protocols, as well as the type, amount and physical form of fiber utilized. It is also possible that these inconsistencies may be due to differences in subject compliance, but this possibility has not been examined.

The study described here was designed to test the hypothesis that a hypocaloric diet high in oats, a whole-grain cereal rich in soluble fiber, would enhance weight loss by reducing both energy digestibility and hunger, thereby increasing both negative energy balance and subject compliance. This study was also designed to assess the influence of hypocaloric diets on energy regulation and subsequent weight regain in young and older persons. Compliance was assessed using the Osmol Excretion Rate Technique (OER) [17], a method developed previously by our group specifically for the assessment of dietary compliance in metabolic balance studies.


    METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Subjects
Fifty-two adult men and women aged 19 to 78 years were recruited for a study of diet and weight loss at the Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University. Forty-one of the subjects successfully completed the protocol and their characteristics are summarized in Table 1. All subjects were weight-stable, free of disease, not taking any medications that influence energy regulation and judged healthy according to normal results on physical examination, electrocardiogram and routine blood and urine tests. Although the study included a hypocaloric diet for weight loss, the trial was also designed to investigate aspects of energy regulation in normal as well as overweight persons; thus subjects with a BMI 18 to 38 kg/m2 were included. Usual fiber intake was <=16 g/day (assessed at screening) for all subjects, as a habitually high intake of fiber was thought to potentially preclude further additional benefit of the study diet. Exclusion criteria also included vegetarian diet, self-reported strenuous physical activity of more than one hour a day, a dietary restraint score greater than 10 [18] and self-reported consumption of more than two alcoholic drinks a day. The protocol was approved by the Human Investigation Review Committee at New England Medical Center, and all subjects gave written informed consent before participating.


View this table:
[in this window]
[in a new window]
 
Table 1. Baseline Characteristics of the Subjects1,2

 
Protocol
The protocol was an eight-month study divided into three phases, and all food and energy-containing beverages were provided during the first 10 weeks (which encompassed all of Phases 1 and 2 and the first two weeks of Phase 3). Residency was required on nights before metabolic testing, but otherwise subjects could sleep at home or at the center as they preferred. If subjects chose to live at home, they came to the center at least five times per week during the first week of the study, and then three to four times per week during the next nine weeks, to collect their food for the following days and return containers. Physical activity was not restricted, but subjects were requested to maintain their usual level and types of strenuous activities.

During weeks 1 and 2 (Phase 1) all subjects consumed a provided control diet low in soluble fiber. Maintenance energy requirements were established for each subject during the first week of the phase and were generally maintained at that fixed level during the second week. The amount of dietary energy provided to the subjects on study day 1 was based on a dietitian’s estimate of energy requirements, taking into account age, gender, fasting body weight on day 1 and the self-reported level of physical activity. Body weight was monitored at least five times during the first week, and energy intake was adjusted as necessary to maintain weight within 500g of the value on day 1; diets were adjusted by the addition of muffins (each 250 kcal, with a macronutrient content similar to the control diet) or reduction of portions. Subjects were allowed to leave partial portions of food, which were re-weighed to estimate their energy content. During the second week of Phase 1, subjects were given the calculated average of energy consumed during the first week and were required to completely consume all portions of food and rinse and scrape food containers unless a noticeable trend in body weight occurred (in which case an adjustment to intake was again made). In the second week of Phase 1, a series of tests were performed including a three-day fecal collection for determination of fecal energy content. To obtain baseline information relative to Phase 2 (described below), fasting body weight was assessed at the end of the phase to ±100g (Toledo Weight Plate, Toledo Scale, Worthington, OH), and body fat and fat-free mass were determined by underwater weighing as described below.

During the following six weeks (weeks 3 to 8, Phase 2) subjects were randomly assigned within gender and age-group categories (ages 20 to 40 or 60 to 80 years) to receive either the control diet (Control group or Group 1) or an oat-containing diet (Oat group or Group 2). Both diets had the same amounts of fat, protein, carbohydrate and insoluble fiber, but had 45g/1000 kcal of rolled oats per day substituted for an equivalent amount of wheat products. Energy intake in Phase 2 was decreased by 1000 kcal/day relative to Phase 1 in all but seven subjects, who had initial energy intakes that were low and a 1000 kcal reduction was considered too severe (in these cases, subjects were typically older and had a lower BMI than the group average, and a 800–900 kcal/day deficit was generally employed). The energy and macronutrient composition of diets in Phases 1 and 2 are shown in Table 2. Subjects were not told that two different diets were being tested, rather that metabolic parameters were being examined over the course of weight loss. A three-day fecal collection was again obtained in Phase 2 to assess fecal energy losses, and in addition two three-day complete urine collections were obtained for measurement of osmolar excretion rate and assessment of dietary compliance [17]. Fasting body weight and body composition by underwater weighing were measured at the end of the phase in duplicate.


View this table:
[in this window]
[in a new window]
 
Table 2. Dietary Intake and Energy Excretion1,2

 
Phase 3 (weeks 9 to 32) was a six-month follow-up period during which time subjects were free to consume as much or as little food as they wished. The purpose of Phase 3 was to observe weight regain and parameters of energy regulation after weight loss. Food was provided during the initial 14-day period (data not shown), and subsequently subjects prepared their own food at home. They returned to the center at approximately six-week intervals for measurements of fasting body weight and body composition. During this time, subjects were not given instructions on prevention of weight regain.

Diets
All food and caloric beverages consumed by the subjects during Phases 1 and 2 and during the first 14 days of Phase 3 were provided by the research center. Except during the first week of Phase 1 and during Phase 3, subjects were required to consume all items and rinse and scrape containers. Meals consisted of normal food and beverage items divided between three meals and a snack each day, and three daily menus were provided on a rotating basis. Coffee and tea were included in the menus in fixed daily amounts if they formed part of the subject’s normal diet. Sodium intake was fixed in Phase 1, remained constant throughout Phases 1 and 2, and subjects were advised to add no additional salt.

The nutrient content of the diets provided during Phase 1 mimicked a typical American diet, providing 35% of energy from fat, 12% of energy from protein and 53% from carbohydrate. Total fiber intake was approximately 6 g/1000 kcal dietary energy, distributed as 1/3 soluble and 2/3 insoluble fiber as summarized in Table 2; this level of fiber intake was provided to minimize differences between average pre-study fiber intake and the control diet. During Phase 2, the Oat group was provided with a diet consisting of food items incorporating 45 g/1000 kcal of rolled oats ("quick cooking" Quaker® rolled oats, divided between all meals and snacks), and the Control group was provided with the control diet that all subjects received in Phase 1, which contained nearly identical macronutrient and insoluble fiber content to that of the Oat group.

Nutrient composition of the diets was calculated using standard dietary composition software (NDS 93 Version 2.4, Minnesota Nutrition Data System, Nutrition Coordination Center, University of Minnesota, Minneapolis, MN). Use of this software resulted in minor discrepancies between calculated total fiber and the sum of soluble and insoluble fiber (Table 2).

Assessment of Dietary Compliance
Dietary compliance was assessed by comparison of the calculated urinary osmolar load, based on dietary intakes of sodium, potassium and nitrogen, with measured urinary osmolar loads in six 24-hour urine collections obtained in Phase 2; three consecutive 24-hour collections of urine were conducted in study week 5 and repeated in study week 7 or 8. The basis of this method is described by Roberts et al. [17]. Briefly, the urinary osmol load consists primarily of compounds derived from consumed foods and, in particular, nitrogen-containing compounds and sodium and potassium salts. Thus, the urinary osmol load can be predicted from dietary protein, sodium and potassium, taking into account obligatory non-urinary losses of these nutrients and correcting for other nutrients contributing to urine osmolality. A measured osmol load significantly greater than predicted indicates the consumption of additional or non-study foods, while a measured osmol load significantly less than predicted suggests either that provided foods are not being consumed or than the 24-hour urine collection is incomplete. The theoretical urinary osmolar load for the Phase 2 diet was calculated as:

where tOER is the theoretical osmolar excretion rate in mosmol/day, N, Na and K are nitrogen, sodium and potassium intakes in mmol/day and 43 is the contribution of other dietary constituents to tOER in mmol/day.

The measured urinary osmolar rate (mOER) in Phase 2 was calculated as the product of urine volume and urine osmolality (model 3MO Micro-osmometer, Advanced Instruments Inc., Needham, MA) for each of the six 24-hour periods when urine was collected. These values were then expressed as a percent of tOER, and values were then averaged over the six-day measurement period.

Weight and Body Composition
Body weight and height were measured to the nearest ±100 g and 0.1 cm, respectively. Body density was measured by hydrostatic weighing after an overnight fast as described elsewhere [19], and conducted twice during Phase 1 and twice at the end of Phase 2 and averaged for each phase. Body density was corrected for predicted residual lung volume [20]. Fat mass and fat-free mass were calculated using the equation of Siri [21] and the average of three tests within ±1% body fat was used for analysis.

Fecal Energy
Three-day stool collections were obtained during Phases 1 (study week 2) and 2 (study week 6 or 7) to determine energy excretion. The collections were weighed, freeze dried to constant weight (Virtis Model #6203-3006-OG freeze drier, The Virtis Co., Gardiner, NY), homogenized and analyzed in duplicate for fecal energy by isoperibol bomb calorimetry (Parr Instrument Co., Model 1261, Moline, IL).

Hunger and Satiety Ratings
A sub-group of subjects (n=19) completed a questionnaire at the end of Phases 1 and 2 to help quantify changes in hunger, satiety, thirst (a control variable) and constipation. Subjects were asked to quantify the frequency of satiety, hunger, constipation and thirst using a 5-point scale where 0=never or no change, 1=rarely once or twice only, 2=occasionally or 3 to 6 times in the phase, 4=frequently or 2 to 3 times per week, 5=very frequently or more than once a day.

Data Analysis
Values are expressed as means ± SEM except where stated. Statistical analysis was performed using SPSS® software, Version 7.5 (SPSS, Inc., Chicago, IL). Differences between groups in Phase 1 were assessed by using Student’s t test for unpaired data. Within-subject changes over time were calculated as Phase 2—Phase 1, and changes in weight were expressed as absolute changes or as a percentage of initial weight. Analysis of covariance was used to compare differences between groups over time, while controlling for values in Phase 1, and to assess interactions of diet with initial BMI, age and gender. All tests were considered significant at p <0.05.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Table 1 shows general characteristics of the subjects. There was no significant difference in any of the characteristics between the groups.

Table 2 shows the dietary intake and fecal energy excretion of the subjects who completed the study. As shown, the primary difference between the groups was the increase in soluble (and therefore total) fiber in the Oat group during Phase 2. Although there was a statistically significant difference in soluble fiber between the groups in Phase 1, the difference was extremely small and of no practical importance. Fecal energy excretion tended to be greater in the Oat group, but the difference was not significant.

Oat group subjects tended to have both a lower dropout rate (Oats five subjects vs. Control three subjects) and better compliance as measured by fewer subjects providing urine collections with osmolality greater than 130% (Oats 2 vs. Control 1) and less than 70% of expected (Oats 2 vs. Control 1), but the numbers were small and were not significantly different between groups. Note that data from subjects with urinary osmolar excretions of >130% expected were not included in the primary study analyses, but those with expected excretions <70% were included because of the possibility that low excretion rates were due to incomplete urine collection rather than dietary noncompliance.

Table 3 shows differences between the groups in weight and body composition changes over the course of the study. Weight loss in Phase 2 was very similar in the two groups, as was weight regain during Phase 3 and weight change over the entire study, and differences were not significant. There were no significant major effects of BMI, age or gender on weight loss in kg or as a percent of initial, nor were there any significant interactions between diet and these variables on weight loss. Trends in body weight over the course of the study are shown in more detail in Fig. 1 and again emphasize the similarity between the groups.


View this table:
[in this window]
[in a new window]
 
Table 3. Weight and Body Composition Changes during the Study1,2

 


View larger version (13K):
[in this window]
[in a new window]
 
Fig. 1. Body weight change over Phases 2 and 3. Group 1 subjects (control diet throughout) are represented by solid circles, and Group 2 subjects (Oat diet in Phase 2) are open circles.

 
Table 4 shows data on the reported frequency of diet-related symptom. As seen, there were no significant changes between Phases 1 and 2 for any symptom. However, reported frequency of hunger tended to be lower for subjects consuming the Oat diet in Phase 2 (p=0.1). There were also no significant interactions between diet and BMI, age, or gender.


View this table:
[in this window]
[in a new window]
 
Table 4. Frequency of Symptoms Related by Subjects during the Study (Scores out of 5)1,2

 

    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Soluble fiber has multiple effects throughout the gastrointestinal tract that have the potential to exert favorable effects on energy regulation. Soluble fiber and soluble fiber-containing foods encourage gel formation in the stomach, which can increase gastric distention and reduce the rate of gastric emptying. Gastric distention, while difficult to characterize experimentally, has been proposed to increase fullness and decrease hunger [3, 4, 22, 23]. A reduced rate of gastric emptying delays access of macronutrients to digestive processes and to absorptive surfaces of the small intestine, which will blunt glycemic and insulinemic responses; these changes, in turn, may be associated with a delayed return of hunger, based on a recent study by our group [5]. Delayed digestion and absorption of macronutrients may also lead to diminished food intake at a subsequent meal, the so-called "second meal effect" [24, 25] originally described for glycemic responses at subsequent meals.

Despite fermentation of some soluble fiber to metabolizable forms of energy, fecal energy loss due to reduced fat (and possibly other macronutrient) absorption is thought to persist following consumption of soluble fiber [26, 27], sometimes exceeding the energy value of the fiber itself.

Based on these effects of soluble fiber, we tested the hypothesis that soluble fiber as a component of food would enhance compliance with hypocaloric diets by reducing both digestible energy intake and hunger and, through these mechanisms, would enhance compliance and total weight loss. There are no known published trials investigating these issues in which soluble fiber has been provided as an intrinsic component of food during a hypocaloric diet. As summarized elsewhere [6], previous studies on soluble fiber and weight loss [3, 4, 716] have yielded inconsistent results, possibly due to the effect of uncontrolled differences between studies such as study duration, protocol, compliance with study diets, amount and type of fiber and how incorporated into the diet, and dietary macronutrient content. There are insufficient numbers of trials to establish if soluble fiber as a food component benefits body weight, and the trials of soluble supplements do not support a clear dose-response relationship. In trials where soluble fiber was provided as a supplement (often as a preload prior to meals), beneficial effects on weight have been noted with ad libitum feeding with soluble fiber between 3 and 20 g/day [11, 12, 28] and with fixed energy deficits with at 18 g/day [10]. However, other investigators report no weight-loss benefit of supplemental soluble fiber, such as in recently diagnosed diabetics, who were provided 15 g/day of cereal fiber or guar vs. no supplement over 20 weeks while consuming a 1200 kcal/day diet [29] or in children supplemented with glucomannan 2 g/day vs. placebo for two months [30].

In some trials investigating effects of mixed fibers on body weight when subjects consume ad libitum diets, significant effects have been observed when 14 to 35 g/day are provided [31, 32], while no benefit was observed in other trials with 10 to 20 g/day [3335]. When mixed fibers are provided with hypocaloric diets of fixed energy deficit, weight loss benefits have been noted with 6 g/day [36], 15 g/day [37] and 30 g/day [38], while no effect on weight loss was observed with 5 g/day [39]. Addition of approximately 20 g/day of bran or ispaghula before meals was not associated with weight benefits in dieting subjects over two weeks [14]. Astrup [40] also found no weight loss benefit of adding predominantly insoluble fiber 30 g/day to a very low energy diet. Thus, there appear to be factors beyond fiber type or dose that influence effects on weight.

In this study of adult men and women spanning a wide range of adult ages and body composition, there was no significant difference between the groups in weight loss or body composition change during the hypocaloric phase of the study (Phase 2). Using standard factors of 9.25 kcal/g and 1 kcal/g for the energy content of fat and fat-free mass, respectively [41], body composition data indicated that there was a mean body energy loss of 621 kcal/day during Phase 2 in both groups combined. The mean decrease in energy intake during Phase 2 was 896 kcal/day, indicating that body energy mobilization was equivalent to 69% of the deficit in energy intake. Previous work from our group has suggested that energy expenditure decreases during underfeeding by approximately 1/3 of the energy deficit and that body energy mobilization is equivalent to 2/3 of the decrease in energy intake [42]. Thus, our finding in this study of body energy mobilization equal to 69% of the decrease in energy intake is completely consistent with previous research and is also consistent with our removal of non-compliant subjects, as determined by higher-than-expected urinary osmolar excretion.

The hypothesis that inclusion of oats would improve weight loss and satiety was based on several factors. The additional fiber provided in the Oat diet was within, but in the lower end, of ranges employed in other trials. Provision of a whole food that contains fiber, as opposed to an isolated supplement, has the potential benefit of ease and may result in phenomena such as delayed digestion and absorption of macronutrients on the basis of physical form as well as fiber content. The oat dose of 45 g/1000 kcal was chosen as this represents a readily achievable goal for most persons and is also consistent with doses demonstrated to benefit blood lipids [43]. It should be noted that while the energy deficit in our study was fixed, the addition of oats was based on energy intake and encompassed a wide range; however, no dose response relationship was observed for weight loss, satiety or compliance measures (data not shown). It is possible that the dose of oats in this study was too low to bring about a beneficial effect on weight loss or that the energy deficit achieved by subjects may have been too low to be influenced by the addition of oats in this amount. Further trials are needed to establish if a higher dose would be effective at this or other dietary energy levels.

The additional finding that there was no significant difference in the frequency of reported symptoms of hunger, satiety or constipation between the groups suggests that the oat-containing diet used in this study was ineffective in minimizing adverse symptoms associated with consuming a hypocaloric diet. This may be because the amount of oats was insufficient to modify symptoms, because the provision of soluble fiber as a component of food is less effective than provision as a separate supplement, because the degree of energy restriction was too great to be influenced by a singular dietary factor such as inclusion of oats or because oats were an ineffective modulator of these symptoms. Other investigators have reported salutary effects of fiber on hunger in studies lasting hours or days or during weight loss efforts. The provision of soluble fiber supplements ranging from five to twenty grams prior to meals has been associated with decreased hunger or increased satiety [3, 4446]. In two trials examining effects of different doses of guar or pectin as preloads, no dose-response relationship was observed in effects on hunger or satiety [44, 46]. It should be noted, however, that the mean frequency of hunger reported by the Oat group tended to be lower than reported ratings of subjects consuming the control diet (p=0.1), suggesting the possibility of an effect that might have been detected with a bigger supplement and/or a larger number of subjects and suggesting in turn that further research in this area is needed. On the other hand, the fact that the control diet was used in both Phase 1 and Phase 2 for the Control group, while the Oat group had different diets in Phase 1 and Phase 2, may have influenced the results inasmuch as continued consumption of the control diet may have predisposed to a sense of monotony regarding the diet. The fact that there was no significant difference in measured compliance or drop-out between the groups is consistent with the finding of no significant difference between the groups in hunger and satiety, though again non-compliance tended to be worse in the Control group, whose members also tended to report more frequent hunger. Further studies are needed to resolve the question of whether there may be an effect of an oat-enriched diet on the frequency of hunger and subject dropout in studies involving the use of hypocaloric diets and whether diets containing more oats or soluble fiber may be more effective. In a less tightly controlled study, or in the free-living situation, the effect of an oat or soluble fiber enriched diet may be more evident since subjective factors (such as hunger or satiety) would have substantially greater importance.

Concerning the ad libitum phase of the study (Phase 3) subjects tended to gain back some but not all of the weight lost in Phase 2, with the result of a mean weight loss in both groups over the entire study period. However, there was no difference in weight regain and body composition change between the groups. Thus, at the end of the eight-month study period, both groups had very similar body composition changes relative to Phase 1.

In summary, a weight-loss diet enriched with whole grain oats did not measurably improve weight loss relative to a control diet without oats in this study of highly compliant, carefully monitored subjects. These results suggest that cereals containing soluble fiber may be of limited utility in promoting weight loss in highly controlled programs. However, further studies are needed to examine the possibility that soluble-fiber-containing foods or supplements may reduce hunger and thereby enhance compliance during less intensively supervised weight loss programs, which represent the majority of weight loss efforts.


    ACKNOWLEDGMENTS
 
We thank the volunteers who made this study possible and the staff of the Metabolic Research Unit and Nutrition Evaluation Laboratory for their assistance in completing the study. Funding for this study was provided in part by an unrestricted grant from the Quaker Oats Company (Barrington, IL) and by NIH grant AG12829. J.C.M. was supported by a grant from the Fundação do Amparo a Pesquisa do Estado de São Paulo, FAPESP, Sao Paulo, Brazil.

Received June 16, 2000. Accepted November 5, 2000.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Kuczmarski RJ, Flegal KM, Campbell SM, Johnson CL: Increasing prevalence of overweight among US adults. The national health and nutrition examination surveys, 1960 to 1990. JAMA 272: 205–211, 1994.[Abstract/Free Full Text]
  2. Summary of the second report on the National Cholesterol Education Program (NCEP) Expert Panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel II). JAMA 269: 3015–3023, 1993.[Abstract/Free Full Text]
  3. Krotkiewski M: Effect of guar gum on body-weight, hunger ratings and metabolism in obese subjects. Br J Nutr 52: 97–105, 1984.[Medline]
  4. Krotkiewski M: Use of fibres in different weight reduction programs. In Bjoerntorp, P, Vahoung GV, Kritchevsky, D (eds): "Current Topics in Nutrition and Disease: Dietary Fiber and Obesity." New York: AR Liss, pp 85–109, 1985.
  5. Ludwig DS, Majzoub JA, Al-Zahrani A, Dallal GE, Blanco I, Roberts SB: High glycemic index foods, overeating, and obesity. Pediatrics 103: E26, 1999.
  6. Saltzman E, Roberts SB: Soluble fiber and energy regulation: current knowledge and future directions. In Kritchevsky D, Bonfield C (eds): "Dietary Fiber in Health and Disease." New York: Plenum Press, pp 89–97, 1997.
  7. Yudkin J: The causes and cure of obesity. Lancet 2: 1135, 1959.[Medline]
  8. Evans E, Miller DS: Bulking agents in the treatment of obesity. Nutr Metab 18: 199–203, 1975.[Medline]
  9. Jenkins DJ, Leeds AR, Slavin LB, Mann J, Jepson EM: Dietary fiber and blood lipids: reduction of serum cholesterol in type II hyperlipidemia by guar gum. Am J Clin Nutr 32: 16–18, 1979.[Abstract/Free Full Text]
  10. Valle-Jones JC: The evaluation of a new appetite-reducing agent (Prefil) in the management of obesity. Br J Clin Prac 34: 72–74, 1980.[Medline]
  11. Tuomilehto J, Voutilainen E, Huttunen J, Vinni S, Shoman K: Effect of guar gum on body weight and serum lipids in hypercholesterolemic females. Acta Med Scand 208: 45–48, 1980.[Medline]
  12. Walsh DF, Yaghoubian L, Behforooz A: Effect of glucomannan on obese patients: a clinical study. Int J Obes 8: 289–293, 1984.[Medline]
  13. Duncan LJP, Rose K, Meiklejohn AP: Phenmetrazine hydrochloride and methylcellulose in the treatment of refractory obesity. Lancet 1: 1262, 1960.[Medline]
  14. Hylander B, Rossner S: Effects of dietary fiber intake before meals on weight loss and hunger in a weight-reducing club. Acta Med Scand 13: 217–220, 1983.
  15. Stevens J, Levitsky DA, Van Soest PJ, Robertson JB, Kalkwarf HJ, Roe DA: The effect of psyllium gum and wheat bran on spontaneous energy intake. Am J Clin Nutr 46: 812, 1987.[Abstract/Free Full Text]
  16. Dodson PM, Stocks J, Holdsworth G, Galton DJ: High-fibre and low-fat diets in diabetes mellitus. Br J Nutr 46: 289–294, 1981.[Medline]
  17. Roberts SB, Ferland G, Young VR, Morrow FM, Heyman MB, Melanson K, Dallal GE: Objective verification of dietary intake by measurement of urine osmolality. Am J Clin Nutr 54: 774–782, 1991.[Abstract/Free Full Text]
  18. Stunkard A, Messick S: The three-factor eating questionnaire to measure dietary restraint, disinhibition, and hunger. J Psychosom Res 29: 71–83, 1985.[Medline]
  19. Roberts SB, Young VR, Fuss P, Fiatarone MA, Richard B, Rasmussen H, Wagner D, Joseph L, Holehouse E, Evans WJ: Energy expenditure and subsequent nutrient intakes in overfed young men. Am J Physiol 259: R461–R469, 1990.[Abstract/Free Full Text]
  20. Quanjer PH, Tammeling GJ, Cotes JE, Pederson OF, Peslin R, Yernault JC: Lung volumes and forced ventilatory flow. Eur Respir J 6(Suppl): 5–40, 1993.[Medline]
  21. Siri WE: Body composition from fluid spaces and density: Analysis of methods. In Brozek J, Henschel A (ed): "Techniques for Measuring Body Composition." Washington, DC: National Academy of Sciences-National Research Council, 1961.
  22. Delargy HJ, Burley VJ, O’Sullivan KR, Fletcher RJ, Blundell JE: The effects of fiber in the breakfast upon short-term appetite control: a comparison of soluble and insoluble fiber. Proc Nutr Soc 52: 318A, 1993.
  23. Raben A, Christensen NJ, Madsen J, Holst JJ, Astrup A: Decreased postprandial thermogenesis and fat oxidation but increased fullness after a high-fiber meal compared with a low-fiber meal. Am J Clin Nutr 59: 1386–1394, 1994.[Abstract/Free Full Text]
  24. Wolever TM, Jenkins DJ, Ocana AM, Rao VA, Collier GR: Second-meal effect: low glycemic index foods eaten at dinner improve subsequent breakfast glycemic response. Am J Clin Nutr 48: 1041–1047, 1988.[Abstract/Free Full Text]
  25. Holl JO, Lin D, Yakubu F, Peters JC: Development of dietary obesity in rats: influence of amount and composition of dietary fat. Int J Obes 16: 321–333, 1992.
  26. Wisker E, Maltz A, Feldheim W: Metabolizable energy of diets low or high in dietary fiber from cereals when eaten by humans. J Nutr 118: 945–952, 1988.
  27. Livesey G: Energy values of unavailable carbohydrates and diet: an inquiry and analysis. Am J Clin Nutr 51: 617–637, 1990.[Abstract/Free Full Text]
  28. Pasman WJ, Saris WHM, Wauters MAJ, Westerterp-Plantegna MS: Effect of one week of fibre supplementation on hunger and satiety ratings and energy intake. Appetite 29: 77–87, 1997.[Medline]
  29. Beattie VA, Edwards CA, Hosker JP, Cullen DR, Ward JD, Read NW: Does adding fibre to a low energy, high carbohydrate, low fat diet confer any benefit to the management of newly diagnosed overweight type II diabetics? Br Med J 296: 1147–1149, 1988.
  30. Vido L, Facchin P, Antonello I, Gobber D, Rogon F: Childhood obesity treatment: double blinded trial on dietary fibres (glucomannan) versus placebo. Paediatr Paedol 28: 133–136, 1993.
  31. Raben A, Jensen ND, Marckmann P, Sandstrom B, Astrup A: Spontaneous weight loss during 11 weeks’ ad libitum intake of a low fat/high fiber diet in young, normal weight subjects. Int J Obes 19: 916–923, 1995.
  32. Mickelsen O, Makdani DD, Cotton RH, Titcomb ST, Colmey JC, Gatty R: Effects of a high fiber bread on weight loss in college-age males. Am J Clin Nutr 32: 1703–1709, 1979.[Free Full Text]
  33. Walker KZ, O’Dea K, Nicholson GC, Muir JG: Dietary composition, body weight, and NIDDM. Comparison of high-fiber, high-carbohydrate, and modified-fat diets. Diabetes Care 18: 401–403, 1995.[Abstract]
  34. Walker KZ, O’Dea K, Johnson L, Sinclair AJ, Piers LS, Nicholson GC, Muir JG: Body fat and non-insulin-dependent diabetes: comparison of a fiber-rich, high-carbohydrate, low-fat (23%) diet and a 35% fat diet high in monosaturated fat. Am J Clin Nutr 63: 254–260, 1996.[Abstract/Free Full Text]
  35. Henry RW, Stout RW, Love AHG: Lack of effect of bran enriched bread on plasma lipids, calcium, glucose and body weight. Ir J Med Sci 147: 249–251, 1978.[Medline]
  36. Solum TT, Ryttig KR, Solum E, Larsen S: The influence of a high-fibre diet on body weight, serum lipids, and blood pressure in slightly overweight persons. Int J Obes 11 Suppl 1: 67–71, 1987.
  37. Pena M, Bacallao J, Barta L, Amador M, Johnston FE: Fiber and exercise in the treatment of obese adolescents. J Adol Health Care 10: 30–34, 1989.[Medline]
  38. Kaul L, Brown MR, Wilson ME, Ulep DE, Nidiry JN: High fibre diet in the treatment of obesity. Intl Clin Nutr Rev 7: 174–179, 1987.
  39. Baron JA, Schori A, Crow B, Carter R, Mann JI: A randomized controlled trial of low carbohydrate and low fat/high fiber diets for weight loss. Am J Pub Health 76: 1293–1296, 1986.[Abstract/Free Full Text]
  40. Astrup A, Vrist E, Flemming Q: Dietary fibre added to a very low calorie diet reduces hunger and alleviates constipation. Int J Obes 14: 105–112, 1990.
  41. Roberts SB, Young VR: Energy costs of fat and protein deposition in the human infant. Am J Clin Nutr 48: 951–955, 1988.[Abstract/Free Full Text]
  42. Saltzman E, Roberts SB: Effects of energy imbalance on energy expenditure and respiratory quotient in young and older men: A summary of data from two metabolic studies. Aging Clin Exp Res 8: 370–378, 1996.
  43. Ripsin CM, Keenan JM, Jacobs DR Elmer PJ, Welch RR, Van Horn L, Liu K, Turnbull WH, Thye FW, Kestin M et al.: Oat products and lipid lowering. JAMA 267: 3317–3325, 1992.[Abstract/Free Full Text]
  44. Van de Ven MLHM, Westerterp-Plantegna MS, Wouters L, Saris WHM: Effects of liquid preloads with different fructose/fibre concentrations on subsequent food intake and ratings of hunger in women. Appetite 23: 139–146, 1994.[Medline]
  45. French SJ, Read NW: Effect of guar gum on hunger and satiety after meals of differing fat content: relationship with gastric emptying. Am J Clin Nutr 59: 87–91, 1994.[Abstract/Free Full Text]
  46. Tiwary CM, Ward JA, Jackson BA: Effect of pectin on satiety in healthy US army adults. J Am Coll Nutr 16: 423–428, 1997.[Abstract]



This article has been cited by other articles:


Home page
Am. J. Clin. Nutr.Home page
H. P. Peters, H. M Boers, E. Haddeman, S. M Melnikov, and F. Qvyjt
No effect of added {beta}-glucan or of fructooligosaccharide on appetite or energy intake
Am. J. Clinical Nutrition, January 1, 2009; 89(1): 58 - 63.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
J. W. Apolzan, N. S. Carnell, R. D. Mattes, and W. W. Campbell
Inadequate Dietary Protein Increases Hunger and Desire to Eat in Younger and Older Men
J. Nutr., June 1, 2007; 137(6): 1478 - 1482.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
J. W Krieger, H. S Sitren, M. J Daniels, and B. Langkamp-Henken
Effects of variation in protein and carbohydrate intake on body mass and composition during energy restriction: a meta-regression 1
Am. J. Clinical Nutrition, February 1, 2006; 83(2): 260 - 274.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
R. J. Norman, M. Noakes, R. Wu, M. J. Davies, L. Moran, and J. X. Wang
Improving reproductive performance in overweight/obese women with effective weight management
Hum. Reprod. Update, May 1, 2004; 10(3): 267 - 280.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
L. J. Kruskall, W. W. Campbell, and W. J. Evans
The Atwater Energy Equivalents Overestimate Metabolizable Energy Intake in Older Humans: Results from a 96-Day Strictly Controlled Feeding Study
J. Nutr., August 1, 2003; 133(8): 2581 - 2584.
[Abstract] [Full Text] [PDF]


Home page
JAMAHome page
D. M. Bravata, L. Sanders, J. Huang, H. M. Krumholz, I. Olkin, C. D. Gardner, and D. M. Bravata
Efficacy and Safety of Low-Carbohydrate Diets: A Systematic Review
JAMA, April 9, 2003; 289(14): 1837 - 1850.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saltzman, E.
Right arrow Articles by Roberts, S. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saltzman, E.
Right arrow Articles by Roberts, S. B.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS