- Open Access
- Open Peer Review
A randomized, controlled, crossover trial to assess the acute appetitive and metabolic effects of sausage and egg-based convenience breakfast meals in overweight premenopausal women
© Rains et al.; licensee Biomed Central. 2015
- Received: 29 August 2014
- Accepted: 20 January 2015
- Published: 10 February 2015
Dietary protein at breakfast has been shown to enhance satiety and reduce subsequent energy intake more so than carbohydrate or fat. However, relatively few studies have assessed substitution of protein for carbohydrate on indicators of appetite and glucose homeostasis simultaneously.
The acute appetitive and metabolic effects of commercially-prepared sausage and egg-based breakfast meals at two different protein levels (30 g and 39 g/serving), vs. a low-protein pancake breakfast (3 g protein) and no breakfast (water), were examined in premenopausal women (N = 35; age 32.5 ± 1.6 yr; BMI 24.8 ± 0.5 kg/m2). Test products provided ~280 kcal/serving and similar fat (12–14 g) and fiber contents (0–1 g). Visual Analog Scale ratings for appetite (hunger, fullness, prospective consumption, desire to eat) and repeated blood sampling for plasma glucose and insulin concentrations were assessed throughout each test day. Energy intake was recorded at an ad libitum lunch meal at 240 min.
Results showed increased satiety ratings for both the 30 and 39 g protein meals vs. the low-protein and no breakfast conditions (p < 0.001 for all). Postprandial glucose and insulin excursions were lower following the 30 g and 39 g protein conditions vs. the low-protein condition, with smaller responses following the 39 g vs. 30 g protein condition (p < 0.05 for all). Energy intake at lunch was significantly less (p < 0.001) following the 39 g protein meal (692 kcal) vs. the low-protein and no breakfast conditions (789 and 810 kcal, respectively). Total energy intake from the test condition + lunch was higher (p < 0.01) for the 30 and 39 g meals (982 and 983 kcal, respectively) vs. no breakfast (810 kcal), and less than the low protein breakfast (1064 kcal; p < 0.01 vs. 39 g condition only).
Results suggest that convenience meals providing 30 or 39 g protein/serving produce greater appetite control, lower postprandial glycemia and insulinemia, and reduced subsequent intake at lunch relative to a low-protein control, or no breakfast.
- Glycemic control
Protein is generally regarded to be more satiating than an equivalent amount of digestible carbohydrate or fat [1-4]. This may be particularly true when protein is consumed at breakfast versus later in the day, as studies that have fed protein at lunch or dinner have shown more variable results . Acute intervention studies have shown that protein-rich breakfast meals reduce appetite and increase satiety throughout the morning relative to moderate or low-protein breakfast meals [6-8]. Protein-rich breakfast meals have also been shown to reduce energy intake at a subsequent ad libitum lunch meal [6,7,9-11]. Such effects have been demonstrated at protein intakes ≥20 g, and most consistently at intakes ≥30 g of protein per meal [6,7,9-12].
The effects of a protein-rich breakfast may extend beyond the immediate postprandial period. Several investigators have reported reduced energy intakes over the 24 hour period following egg-based breakfast meals rich in protein [7,10], although not all studies have produced similar results . Leidy et al.  found that higher protein intake at breakfast (35 vs. 13 g) was associated not only with greater satiety and less hunger throughout the morning, but also with reduced energy intake from snacks in the evening hours, particularly high-fat snacks.
Limited data exist regarding postprandial glucose and insulin excursions and their relationships to appetitive responses following high vs. lower protein meals. In addition to the satiety properties of dietary protein, the consumption of higher protein meals has been proposed to improve glucose homeostasis. Several meta-analyses from long-term, higher protein, weight loss and/or weight maintenance diets report reductions in glycated hemoglobin and/or fasting insulin concentrations with higher vs. normal protein diets [14,15]. Since larger postprandial glucose elevations have been shown to be associated with an increased risk for the development of type 2 diabetes mellitus  and cardiovascular disease , it is of interest to identify dietary strategies, such as higher protein intake at breakfast, that might improve glucose homeostasis through the reductions in these responses.
Average dietary protein intake in the US is adequate based on current recommendations . However, data from the National Health and Nutrition Examination Survey (NHANES) survey suggest that the majority of dietary protein is consumed at dinner, with protein intakes at breakfast averaging ~10 g in women and 15 g in men, well below levels shown to favorably affect appetite and metabolism . In addition, approximately 20% of US men and women do not consume breakfast . In an analysis of NHANES data, our group found that higher protein intake at breakfast was inversely associated with energy intake at lunch, and higher non-protein intake at breakfast was positively associated with energy intake at lunch .
Given ready-to-eat cereals and other foods requiring little preparation are frequently consumed at breakfast, convenient breakfast options high in protein would be potentially beneficial for individuals interested in reducing morning hunger and energy intake later in the day as well as glycemic excursions. The present study was undertaken to evaluate the effects of consuming two higher-protein sausage and egg-based frozen convenience breakfast meals, providing 30 or 39 g of protein, compared with a lower-protein, higher carbohydrate frozen convenience breakfast meal (pancakes and syrup, 3 g protein), and breakfast skipping, on appetite ratings, postprandial glycemic and insulinemic responses, and ad libitum energy intake at a lunch meal in normal weight to overweight, premenopausal women.
This was a randomized, controlled, crossover study conducted at Biofortis Clinical Research (Addison, IL) according to Good Clinical Practice Guidelines, the Declaration of Helsinki (2000), and the United States 21 Code of Federal Regulations. An institutional review board (Quorum Review IRB, Seattle, WA) approved the protocol before initiation of the study and subjects provided written informed consent before any study procedures were performed. The study included 1 screening visit and 4 test visits, each separated by at least 5 days.
Healthy premenopausal women aged 18 to 55 y, each with a body mass index (BMI) 18.5 to 29.9 kg/m2 and who were regular consumers of breakfast and lunch (≥5 days/week), were recruited to participate. Subjects were excluded if they were self-defined smokers; reported a recent weight change of ±2.7 kg; had history of surgical intervention for the treatment of obesity; used weight loss medications, supplements, programs, or meal replacement products; used medications or dietary supplements likely to markedly affect taste, smell, or appetite; or scored >11 on a dietary restraint scale . Subjects with a history of cardiac, renal, hepatic, endocrine, pulmonary, biliary, pancreatic, gastrointestinal or neurologic disorders, or cancer (in the last 2 years); known sensitivity, allergy, or taste aversion to any of the ingredients in the study products; a history of eating disorders or alcohol abuse; and use of medications known to influence carbohydrate metabolism were also excluded from the study. Subjects who developed symptoms of active infection during the study period (e.g., upper respiratory infection) or reported antibiotic use were allowed to continue only after symptoms had been resolved and antibiotic use had been discontinued at least 5 days prior to testing.
Efficacy evaluable population
Body mass index (kg/m2)
Restraint score (Arbitrary units)
Validated Visual Analog Scale (VAS) ratings  for appetite sensations (hunger, fullness, desire to eat, and prospective food consumption) were completed prior to study product intake (t = −25 and −15 min) and at 30 min intervals until 240 min. VAS ratings were recorded on a 100-mm horizontal line anchored by “not at all” to “extremely” in response to questions worded as “How strong is your feeling of”. Palatability was assessed by a 9-point scale with the anchors “dislike extremely” and “like extremely” immediately following the last bite of study product.
Blood draws were performed at specific times (Figure 1). Seven blood samples (4 ml/sample; 28 ml/testing day) were collected throughout each testing day. The samples were collected in test tubes containing ethylenediaminetetraacetic acid. Within 10 min of collection, the samples were centrifuged at −4 °C for 10 min. The plasma was separated and stored in microcentrifuge tubes at −80 °C for future analysis. Plasma glucose was measured through an in-house glucose oxidase assay (Thermo Fisher Scientific, USA). Plasma insulin was measured using the Milliplex MAP magnetic bead-based multi-analyte, metabolic panel (Millipore, St. Charles, MO) and Magpix Luminex technologies (Luminex Corporation, Austin, TX).
An ad libitum lunch consisting of tortellini and sauce was provided to participants following the last blood collection. Subjects were allowed 25 min for lunch and instructed to eat until “comfortably full”. Food was weighed to the nearest gram prior to and following consumption. Subjects were provided with a standard amount of water during lunch and the quantity of water consumed was recorded. A final VAS rating was recorded following lunch at t = 270 min.
Test meal characteristics 1
30 g Pro
39 g Pro
Total fat (g)
7 (7, 8)
7 (6, 8)
6 (4, 7)
Statistical analyses – VAS responses and subsequent food intake
Statistical analyses were conducted using SAS version 9.1.3 (SAS Institute, Cary, NC). An evaluable sample size of 33 subjects was expected to provide 85% power to detect a difference of 2400 mm * min in the net incremental area under the curve (niAUC) for postprandial VAS scores between treatment conditions, assuming a standard deviation of 3816 mm * min (based on prior work by our group), for an effect size of 62%. A nominal alpha of 0.017 was used for sample size calculations to account for three primary comparisons between the three energy-containing meal conditions .
VAS rating niAUCs were calculated by applying the trapezoidal rule for both positive and negative increments from pre-meal (average of timepoints, nominal time 0 min was calculated as the average of the values at −25 and −15 min) to 240 min, whereas total AUC was calculated for the plasma glucose and insulin concentrations throughout the 240 min . Repeated measures analysis of variance (ANOVA) was used to assess differences between test conditions for continuous outcome variables. Initial models contained terms for treatment condition, sequence, period, age and baseline BMI, with subject included as a random effect. Models were reduced in a stepwise manner until only significant terms or treatment condition remained in the model. The Shapiro-Wilk test was used to assess normality of the distribution of residuals in the analysis models. The normality assumption was rejected for palatability, energy intake at lunch, and preload plus energy intake, therefore rank transformations were employed and the models were rerun using the transformed data. When treatment condition main effects were detected, pairwise comparisons between conditions were conducted using Tukey’s adjustment for multiple comparisons. Sensitivity analyses were conducted using the overall liking palatability score as a covariate in models for appetite ratings and energy intake at lunch with the no breakfast condition excluded.
For the appetite and food intake outcomes, the primary efficacy analysis was completed on an efficacy evaluable (EE) sample that included all subjects who consumed the 39 g protein breakfast and at least one other condition. A secondary analysis was completed on a per protocol (PP) sample, a subset of the EE population excluding those subjects who had significant protocol deviations (e.g., use of an excluded medication, illness that caused rescheduling of visits) during the treatment period. Subjects in the PP population completed all test visits. All decisions were made prior to breaking the treatment code or locking the database by people unaware of the order of treatments. Results were similar for the EE and PP analyses; therefore, outcomes are presented only for the EE sample. However, for the glucose and insulin measures, only those completing all test conditions were included and thus a PP analysis was performed.
Ratings for appearance, texture, flavor, and overall liking were higher (more palatable) for the LP and 30 g protein conditions versus the 39 g protein conditions (p < 0.02 for all). There were no differences between the 30 g and LP conditions. Despite the fact that there were differences, there were no statistically significant associations between overall liking and any of the appetitive ratings or energy intake at lunch. Similarly, when palatability rating was included as a covariate in a subset analysis that excluded the no breakfast condition, palatability rating was did not significantly reduce the unexplained variance.
Appetite sensation ratings
Appetite sensation ratings at 240 min by breakfast meal condition 1
30 g Pro
39 g Pro
Median (interquartile limits)
91 (79, 96)a
81 (70, 91)b
71 (50, 84)c
69 (49, 80)c
3 (1, 12)a
15 (9, 24)b
26 (10, 54)c
33 (14, 59)c
Desire to eat (mm)
89 (81, 95)a
76 (69, 92)b
69 (47, 83)c
69 (39, 80)c
Prospective food consumption (mm)
85 (77, 93)a
77 (64, 84)b
67 (50, 82)b,c
69 (40, 79)c
Main effects of treatment condition were detected for the insulin AUC response, peak insulin, and postprandial changes (p < 0.001 for all). Pairwise comparisons showed that the NB condition led to lower insulin AUC (p < 0.001 for all) compared to all other breakfast conditions. The 30 g and 39 g protein conditions led to lower insulin AUC (p < 0.05 for both) vs. the LP breakfast with no differences between the 30 g and 39 g protein conditions. The NB condition led to a lower insulin peak (7 ± 1 pg/mL; p < 0.001 for all) compared to all breakfast conditions (i.e., low-protein (pancakes): 37 ± 3 pg/ml; 30 g protein: 20 ± 2 pg/mL; and 39 g protein: 16 ± 2 pg/mL). The 39 g protein condition led to a lower insulin peak (p < 0.05 for both) compared to the LP and the 30 g protein conditions. The 30 g protein condition led to a lower insulin peak (p < 0.001) vs. LP condition. Lastly, the NB condition led to the smallest postprandial change from pre-breakfast in insulin (−4 ± 1 pg/mL; p < 0.001 for all) compared to all breakfast meals (i.e. LP: −34 ± 3 pg/ml; 30 g protein: −17 ± 2 pg/mL; and 39 g protein: −11 ± 2 pg/mL. The 39 g protein condition led to a smaller postprandial change in insulin (p < 0.01 for both) compared to the LP and the 30 g protein conditions. The 30 g protein condition led to a smaller postprandial change in insulin (p < 0.001) vs. the LP condition.
Lunch energy intake
The results of this study showed that consumption of protein-rich convenience breakfast meals led to reductions in perceived hunger, increased satiety, and reductions in postprandial glucose and insulin excursions compared to a low-protein meal in normal to overweight, premenopausal women. The protein-rich breakfast meals also resulted in reduced energy intake at the ad libitum lunch meal, although results only reached significance for the 39 g protein meal. Thus, consumption of a high protein, sausage and egg-based, ready-to-heat meal may be an option for facilitating satiety throughout the morning, reducing postprandial glycemic and insulinemic excursions, and moderating energy intake at lunch.
The satiety and food intake findings are similar to results reported by other investigators in acute intervention trials using breakfasts based on solid food sources of protein. Eggs and meat as sources of protein, in particular, have been associated with greater perceived satiety and/or improved glycemic control in several studies [1,6,7,10,12,25,26]. For example, Ratliff et al.  compared the effects of an egg-based breakfast to a bagel-based breakfast in a group of healthy men. Similar to the results of the present study, perceived hunger, glucose, insulin, and energy intake at the lunch meal were all reduced following the higher protein breakfast. However, to the best of our knowledge, very few prior studies have evaluated the appetitive effects of protein-based, frozen convenience meals. Such meals serve as an easy to prepare option, compared to other high-protein foods traditionally consumed at breakfast in the U.S. (e.g., fresh breakfast meats, fresh eggs), which require a greater degree of preparation. This is further supported by data indicating that a primary barrier associated with breakfast is the lack of availability and convenience .
The present work included two levels of protein served as part of a commonly consumed breakfast meal. There were minimal differences in responses between the protein-containing meals, suggesting that both protein levels were sufficient to elicit a greater satiety response and to reduce postprandial glycemic and insulinemic excursions compared with the low-protein meal. The differences in glucose and insulin responses elicited by the test meals were expected because a substitution of protein for carbohydrate was employed, thus reducing the available carbohydrate load. Nevertheless, chronic reduction of dietary carbohydrate has been demonstrated to produce notable metabolic effects, including lowering the circulating concentration of triglycerides, reducing blood pressure, and lessening the demand for insulin production by the pancreatic beta-cells . Moreover, ingestion of protein at a meal tends to increase insulin secretion without significantly increasing the plasma glucose concentration (compared to water ingestion) in the postprandial period . Lastly, elevations in plasma insulin and glucose have been shown to reduce appetitive sensations [30,31]. Thus, it is notable that the appetitive effects observed with higher protein and lower carbohydrate were present despite lower insulin and glucose concentrations.
Other investigations utilizing beverages or semi-liquid applications (e.g., yogurt or custard) to evaluate the satiating properties of protein have shown similar effects to those observed in the present study [32-36]. However, such vehicles are not among the top breakfast choices in the U.S. . Further, the present work included overweight and normal weight women, a group more likely to engage in strategies to reduce body weight than their male counterparts . Results from several long-term intervention trials have provided evidence that higher protein, reduced carbohydrate diets may help to enhance weight loss and/or maintain lean body mass during weight loss [14,15,38-40]. Increased satiation, and therefore better adherence to caloric restriction, is one potential mechanism by which high protein diets may facilitate weight loss. High protein, easy to prepare breakfast options with greater satiating potential would likely facilitate the consumption of calorically-restricted, protein-rich diets.
The mechanisms whereby dietary protein promotes satiety are not completely understood. It has been hypothesized that a high-protein meal may modulate the post-absorptive release of hormones and neurochemicals in the gastrointestinal tract that down-regulate appetite . In particular, consumption of high-protein meals has been shown to decrease levels of the hunger-stimulating hormone ghrelin and/or promote the increase in the satiety-stimulating hormones peptide YY (PYY) and glucagon-like peptide-1 (GLP-1), resulting in increased perceptions of satiety [8,9,26,42,43]. Unfortunately, data for ghrelin, PYY, and GLP-1 for the present study are not available. A majority of studies that have assessed the relationship between postprandial insulin levels and appetite sensations have suggested that insulin has an acute effect to suppress appetite [30,44], although conflicting results have been reported [45,46]. Intracerebroventricular or systemic injections of insulin suppress food intake in a dose-dependent manner in animal models, suggesting a direct involvement in satiety . It is therefore notable that appetite ratings were reduced with the high protein conditions compared to the low protein (higher carbohydrate) breakfast, despite lower insulin (and glucose) responses. Some investigators have suggested that increased thermogenesis following consumption of high-protein meals, as well as changes in substrate oxidation may influence appetitive signals that affect food intake [48,49]. Additional studies will be needed to more fully define the mechanisms responsible for the effects of substituting protein for carbohydrate observed in the present study. It is also suggested that additional research is needed to assess the substitution of protein for dietary fat. Future research of interest would also include studies in which protein is substituted for fat, since the current study cannot separate the effects of increasing the protein content of the study breakfast meals from those of reducing the carbohydrate content.
Both buffet lunch and uniform food models, such as the tortellini and sauce lunch used in the present study, have been used extensively in appetite research . A uniform food model was used in the present investigation because the main objective was related to energy intake rather than food selection. Thus, a limitation of the study is that possible differences in food or macronutrient preferences at lunch could not be assessed.
Another limitation is the short-term nature of the measurement period. It is possible that appetitive sensations or energy intake would increase later in the day to compensate, or even overcompensate, for reductions in energy intake observed at the lunch meal. However, results from Leidy et al. suggest that this may not be the case, as total daily energy intake was reduced when a high-protein breakfast was consumed, compared with a lower protein breakfast meal. Notably, in that trial, a 7-day period of acclimation was employed for both breakfast conditions, suggesting that the effects of higher protein breakfasts on appetite do not dissipate, at least after several days of consumption.
The possibility cannot be ruled out that expectations surrounding each breakfast condition and differences in the sensory characteristics influenced the results. The present trial evaluated commercially-available breakfast options, therefore matching the sensory properties of the test conditions was not possible. However, all products were considered to be relatively well-liked and there were only measurable differences in the palatability of the highest protein condition relative to the low protein and 30 g protein conditions. Inclusion of the overall palatability rating as a covariate in sensitivity analyses for appetite ratings and energy intake at lunch did not significantly reduce the unexplained variance, suggesting that differences in palatability were unlikely to have materially influenced the results.
Differences in the physical characteristics of the study products may have also influenced orogastric transit time. In an effort to control this to the degree possible, subjects were instructed to eat a portion of each condition at specific intervals over a 12-minute period (approximately one-third during each of three 4-min periods). However, we cannot rule out the possibility that differences in consumption patterns (e.g., chewing) or orogastric transit time influenced our findings. Further, the weight and volume of the products differed. Such characteristics have been previously shown to affect perceived satiety, however our objective was to evaluate conventional breakfast options at an equivalent caloric level, and as such, differences in weight and volume were unavoidable due to the nature of the breakfast meals .
In conclusion, the results of the present investigation suggest that sausage/egg convenience meals providing 30 g or 39 g protein per serving produce greater appetite control, reduce postprandial glycemic and insulinemic responses, and lower energy intake at lunch relative to a lower-protein, higher carbohydrate, breakfast meal.
The authors thank the study participants for their dedication and compliance during the testing days. This trial was funded by Hillshire Brands, Chicago, IL. Financial supporters had no role in the design, implementation, analysis or interpretation of data or preparation of the manuscript.
- Holt SH, Miller JC, Petocz P, Farmakalidis E. A satiety index of common foods. Eur J Clin Nutr. 1995;49:675–90.PubMedGoogle Scholar
- Stubbs J, Ferres S, Horgan G. Energy density of foods: effects on energy intake. Crit Rev Food Sci Nutr. 2000;40:481–515.View ArticlePubMedGoogle Scholar
- Porrini M, Santangelo A, Crovetti R, Riso P, Testolin G, Blundell JE. Weight, protein, fat, and timing of preloads affect food intake. Physiol Behav. 1997;62:563–70.View ArticlePubMedGoogle Scholar
- Johnstone AM, Stubbs RJ, Harbron CG. Effect of overfeeding macronutrients on day-to-day food intake in man. Eur J Clin Nutr. 1996;50:418–30.PubMedGoogle Scholar
- Leidy HJ, Bossingham MJ, Mattes RD, Campbell WW. Increased dietary protein consumed at breakfast leads to an initial and sustained feeling of fullness during energy restriction compared to other meal times. Br J Nutr. 2009;101:798–803.View ArticlePubMedGoogle Scholar
- Fallaize R, Wilson L, Gray J, Morgan LM, Griffin BA. Variation in the effects of three different breakfast meals on subjective satiety and subsequent intake of energy at lunch and evening meal. Eur J Nutr. 2013;52:1353–9.View ArticlePubMedGoogle Scholar
- Vander Wal JS, Marth JM, Khosla P, Jen KL, Dhurandhar NV. Short-term effect of eggs on satiety in overweight and obese subjects. J Am Coll Nutr. 2005;24:510–5.View ArticlePubMedGoogle Scholar
- Leidy HJ, Carnell NS, Mattes RD, Campbell WW. Higher protein intake preserves lean mass and satiety with weight loss in pre-obese and obese women. Obesity. 2007;15:421–9.View ArticlePubMedGoogle Scholar
- Leidy HJ, Racki EM. The addition of a protein-rich breakfast and its effects on acute appetite control and food intake in ‘breakfast-skipping’ adolescents. Int J Obes (Lond). 2010;34:1125–33.View ArticleGoogle Scholar
- Ratliff J, Leite JO, de Ogburn R, Puglisi MJ, VanHeest J, Fernandez ML. Consuming eggs for breakfast influences plasma glucose and ghrelin, while reducing energy intake during the next 24 hours in adult men. Nutr Res. 2010;30:96–103.View ArticlePubMedGoogle Scholar
- Clegg M, Shafat A. Energy and macronutrient composition of breakfast affect gastric emptying of lunch and subsequent food intake, satiety and satiation. Appetite. 2010;54:517–23.View ArticlePubMedGoogle Scholar
- Leidy HJ, Ortinau LC, Douglas SM, Hoertel HA. Beneficial effects of a higher-protein breakfast on the appetitive, hormonal, and neural signals controlling energy intake regulation in overweight/obese, “breakfast-skipping”, late-adolescent girls. Am J Clin Nutr. 2013;97:677–88.View ArticlePubMedPubMed CentralGoogle Scholar
- Alfenas Rde C, Bressan J, Paiva AC. Effects of protein quality on appetite and energy metabolism in normal weight subjects. Arq Bras Endocrinol Metabol. 2010;54:45–51.View ArticlePubMedGoogle Scholar
- Dong JY, Zhang ZL, Wang PY, Qin LQ. Effects of high-protein diets on body weight, glycaemic control, blood lipids and blood pressure in type 2 diabetes: meta-analysis of randomised controlled trials. Br J Nutr. 2013;110:781–9.View ArticlePubMedGoogle Scholar
- Clifton PM, Condo D, Keogh JB. Long term weight maintenance after advice to consume low carbohydrate, higher protein diets–a systematic review and meta analysis. Nutr Metab Cardiovasc Dis. 2014;24:224–35.View ArticlePubMedGoogle Scholar
- Lorenzo C, Okoloise M, Williams K, Stern MP, Haffner SM. The metabolic syndrome as predictor of type 2 diabetes: the San Antonio heart study. Diabetes Care. 2003;26:3153.View ArticlePubMedGoogle Scholar
- Brunner EJ, Shipley MJ, Witte DR, Fuller JH, Marmot MG. Relation between blood glucose and coronary mortality over 33 years in the Whitehall Study. Diabetes Care. 2006;29:26–31.View ArticlePubMedGoogle Scholar
- Fulgoni 3rd VL. Current protein intake in America: analysis of the National Health and Nutrition Examination Survey, 2003–2004. Am J Clin Nutr. 2008;87:1554S–7.PubMedGoogle Scholar
- Rains TM, Maki KC, Fulgoni 3rd VL, Auestad N. Protein intake at breakfast is associated with reduced energy intake at lunch: an analysis of NHANES 2003–2006. FASEB J. 2013;27:349.7.Google Scholar
- Kant AK, Graubard BI. Secular trends in patterns of self-reported food consumption of adult Americans: NHANES 1971–1975 to NHANES 1999–2002. Am J Clin Nutr. 2006;84:1215–23.PubMedPubMed CentralGoogle Scholar
- Stunkard AJ, Messick S. The three-factor eating questionnaire to measure dietary restraint, disinhibition and hunger. J Psychosom Res. 1985;29:71–83.View ArticlePubMedGoogle Scholar
- Flint A, Raben A, Blundell JE, Astrup A. Reproducibility, power and validity of visual analogue scales in assessment of appetite sensations in single test meal studies. Int J Obes Relat Metab Disord. 2000;24:38–48.View ArticlePubMedGoogle Scholar
- Šidák Z. On probabilities of rectangles in multivariate normal Student distributions: their dependence on correlations. Ann Math Statist. 1971;41:169–75.Google Scholar
- Brouns F, Bjorck I, Frayn KN, Gibbs AL, Lang V, Slama G, et al. Glycaemic index methodology. Nutr Res Rev. 2005;18:145–71.View ArticlePubMedGoogle Scholar
- Meinert L, Kehlet U, Aaslyng MD. Consuming pork proteins at breakfast reduces the feeling of hunger before lunch. Appetite. 2012;59:201–3.View ArticlePubMedGoogle Scholar
- Belza A, Ritz C, Sorensen MQ, Holst JJ, Rehfeld JF, Astrup A. Contribution of gastroenteropancreatic appetite hormones to protein-induced satiety. Am J Clin Nutr. 2013;97:980–9.View ArticlePubMedGoogle Scholar
- International Food Information Council, IFIC. (2008, December 19). IFIC Review: Breakfast and Health. Retreived from http://www.foodinsight.org/Content/6/IFIC%20Brkfast%20Review%20FINAL.pdf. Accessed November 6, 2012.
- Sacks FM, Carey VJ, Anderson CAM, Miller III ER, Copeland T, Charleston J, et al. Effects of high vs low glycemic index of dietary carbohydrate on cardiovascular disease risk factors and insulin sensitivity. JAMA. 2014;312:2531–41.View ArticlePubMedPubMed CentralGoogle Scholar
- Gannon MC, Nuttall JA, Damberg G, Gupta V, Nuttall FG. Effect of protein ingestion on the glucose appearance rate in people with type 2 diabetes. J Clin Endocrinol Metab. 2001;86:1040–7.PubMedGoogle Scholar
- Anderson HG, Catherine NLA, Woodend DM, Wolever TMS. Inverse association between the effect of carbohydrates on blood glucose and subsequent short-term food intake in young men. Am J Clin Nutr. 2002;76:1023–30.PubMedGoogle Scholar
- Karatsoreos IN, Thaler JP, Borgland SL, Champagne FA, Hurd YL, Hill MN. Food for thought: hormonal, experiential, and neural influences on feeding and obesity. J Neurosci. 2013;33:17610–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Probst A, Humpeler S, Heinzl H, Blasche G, Ekmekcioglu C. Short-term effect of macronutrient composition and glycemic index of a yoghurt breakfast on satiety and mood in healthy young men. Forsch Komplementmed. 2012;19:247–51.View ArticlePubMedGoogle Scholar
- Bertenshaw EJ, Lluch A, Yeomans MR. Satiating effects of protein but not carbohydrate consumed in a between-meal beverage context. Physiol Behav. 2008;93:427–36.View ArticlePubMedGoogle Scholar
- Dove ER, Hodgson JM, Puddey IB, Beilin LJ, Lee YP, Mori TA. Skim milk compared with a fruit drink acutely reduces appetite and energy intake in overweight men and women. Am J Clin Nutr. 2009;90:70–5.View ArticlePubMedGoogle Scholar
- Hursel R, van der Zee L, Westerterp-Plantenga MS. Effects of a breakfast yoghurt, with additional total whey protein or caseinomacropeptide-depleted alpha-lactalbumin-enriched whey protein, on diet-induced thermogenesis and appetite suppression. Br J Nutr. 2010;103:775–80.View ArticlePubMedGoogle Scholar
- Tsuchiya A, Almiron-Roig E, Lluch A, Guyonnet D, Drewnowski A. Higher satiety ratings following yogurt consumption relative to fruit drink or dairy fruit drink. J Am Diet Assoc. 2006;106:550–7.View ArticlePubMedGoogle Scholar
- Bish CL, Blanck HM, Serdula MK, Marcus M, Kohl 3rd HW, Khan LK. Diet and physical activity behaviors among Americans trying to lose weight: 2000 behavioral risk factor surveillance system. Obesity Res. 2005;13:596–607.View ArticleGoogle Scholar
- Maki KC, Rains TM, Kaden VN, Raneri KR, Davidson MH. Effects of a reduced-glycemic-load diet on body weight, body composition, and cardiovascular disease risk markers in overweight and obese adults. Am J Clin Nutr. 2007;85:724–34.PubMedGoogle Scholar
- Vander Wal JS, Gupta A, Khosla P, Dhurhandar NV. Egg breakfast enhances weight loss. Int J Obes (Lond). 2008;32:1545–51.View ArticleGoogle Scholar
- Weigle DS, Breen PA, Matthys CC, Callahan HS, Meeuws KE, Burden VR, et al. A high-protein diet induces sustained reductions in appetite, ad libitum caloric intake, and body weight despite compensatory changes in diurnal plasma leptin and ghrelin concentrations. Am J Clin Nutr. 2005;82:41–8.PubMedGoogle Scholar
- Bowen J, Noakes M, Trenerry C, Clifton PM. Energy intake, ghrelin, and cholecystokinin after different carbohydrate and protein preloads in overweight men. J Clin Endocrinol Metab. 2006;91:1477–83.View ArticlePubMedGoogle Scholar
- Batterham RL, Heffron H, Kapoor S, Chivers JE, Chandarana K, Herzog H, et al. Critical role for peptide YY in protein-mediated satiation and body-weight regulation. Cell Metab. 2006;4:223–33.View ArticlePubMedGoogle Scholar
- Blom WA, Lluch A, Stafleu A, Vinoy S, Holst JJ, Schaafsma G, et al. Effect of a high-protein breakfast on the postprandial ghrelin response. Am J Clin Nutr. 2006;83:211–20.PubMedGoogle Scholar
- Schloegl H, Percik R, Horstmann A, Villringer A, Stumvoll M. Peptide hormones regulating appetite–focus on neuroimaging studies in humans. Diabetes Metab Res Rev. 2011;27:104–12.View ArticlePubMedGoogle Scholar
- Holt SH, Miller JB. Increased insulin responses to ingested foods are associated with lessened satiety. Appetite. 1995;24:43–54.View ArticlePubMedGoogle Scholar
- Leidy HJ, Apolzan JW, Mattes RD, Campbell WW. Food form and portion size affect postprandial appetite sensations and hormonal responses in healthy, nonobese, older adults. Obesity. 2010;18:293–9.View ArticlePubMedGoogle Scholar
- Sobrino Crespo C, Perianes Cachero A, Puebla Jimenez L, Barrios V, Arilla Ferreiro E. Peptides and food intake. Front Endocrinol. 2014;5:58.View ArticleGoogle Scholar
- Crovetti R, Porrini M, Santangelo A, Testolin G. The influence of thermic effect of food on satiety. Eur J Clin Nutr. 1998;52:482–8.View ArticlePubMedGoogle Scholar
- Veldhorst M, Smeets A, Soenen S, Hochstenbach-Waelen A, Hursel R, Diepvens K, et al. Protein-induced satiety: effects and mechanisms of different proteins. Physiol Behav. 2008;94:300–7.View ArticlePubMedGoogle Scholar
- Blundell J, de Graaf C, Hulshof T, Jebb S, Livingstone B, Lluch A, et al. Appetite control: methodological aspects of the evaluation of foods. Obes Rev. 2010;11:251–70.View ArticlePubMedPubMed CentralGoogle Scholar
- Williams RA, Roe LS, Rolls BJ. Assessment of satiety depends on the energy density and portion size of the test meal. Obesity. 2014;22:318–24.View ArticlePubMedGoogle Scholar
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