Next Article in Journal
Effect on Insulin, Glucose and Lipids in Overweight/Obese Australian Adults of 12 Months Consumption of Two Different Fibre Supplements in a Randomised Trial
Previous Article in Journal
A2 Milk Enhances Dynamic Muscle Function Following Repeated Sprint Exercise, a Possible Ergogenic Aid for A1-Protein Intolerant Athletes?
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Nutrients
Volume 9
Issue 2
10.3390/nu9020089
nutrients-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Consuming Two Eggs per Day, as Compared to an Oatmeal Breakfast, Decreases Plasma Ghrelin while Maintaining the LDL/HDL Ratio

by
Amanda Missimer
1,
Diana M. DiMarco
1,
Catherine J. Andersen
2,
Ana Gabriela Murillo
1,
Marcela Vergara-Jimenez
3 and
Maria Luz Fernandez
1,*
1
Department of Nutritional Sciences, University of Connecticut, Storrs, CT 06269, USA
2
Department of Biology, Fairfield University, Fairfield, CT 06824, USA
3
Department of Nutrition, Universidad Autonoma de Sinaloa, Culiacán 80040, Mexico
*
Author to whom correspondence should be addressed.
Nutrients 2017, 9(2), 89; https://doi.org/10.3390/nu9020089
Submission received: 1 December 2016 / Revised: 24 December 2016 / Accepted: 13 January 2017 / Published: 29 January 2017
Browse Figures
Versions Notes

Abstract

:
Eggs contain high quality protein, vitamins, minerals and antioxidants, yet regular consumption is still met with uncertainty. Therefore, the purpose of this study was to compare the effects of consuming two eggs per day or a heart-healthy oatmeal breakfast on biomarkers of cardiovascular disease (CVD) risk and satiety measures in a young, healthy population. Fifty subjects participated in a randomized crossover clinical intervention; subjects were randomly allocated to consume either two eggs or one packet of oatmeal per day for breakfast for four weeks. After a three-week washout period, participants were allocated to the alternative breakfast. Fasting blood samples were collected at the end of each intervention period to assess plasma lipids and plasma ghrelin. Subjects completed visual analog scales (VAS) concurrent to dietary records to assess satiety and hunger. Along with an increase in cholesterol intake, there were significant increases in both low-density lipoprotein (LDL) and high-density lipoprotein (HDL) cholesterol following the egg consumption period (p < 0.01). However, there was no difference in the LDL/HDL ratio, a recognized biomarker of CVD risk, nor in the plasma glucose, triglycerides or liver enzymes, between diet periods. Several self-reported satiety measures were increased following the consumption of eggs, which were associated with lower plasma ghrelin concentrations (p < 0.05). These results demonstrate that compared to an oatmeal breakfast, two eggs per day do not adversely affect the biomarkers associated with CVD risk, but increase satiety throughout the day in a young healthy population.

1. Introduction

Cardiovascular disease (CVD) is currently the leading cause of death among adult men and women in the United States [1]. In order to prevent its development, beneficial diet and lifestyle habits should be implemented while young and healthy. Habitual breakfast consumption has been associated with a healthy lifestyle and good nutritional status, while studies have reported it to be predictive of lower body mass index (BMI), and inversely related to obesity later in life [2,3]. Whole eggs, which are typically consumed as a breakfast food, are inexpensive, readily available, and contain high quality proteins, essential vitamins and minerals, as well as the antioxidant carotenoids lutein and zeaxanthin, lecithin, choline and cholesterol [4]. In the past, whole egg consumption has been controversial, due to the cholesterol content of eggs (~185–200 mg/egg), although this amount of dietary cholesterol has been long since identified as a non-significant independent risk factor for CVD [5]. Currently, the American Heart Association is recommending egg whites without the yolks as a heart-healthy source of protein [6], despite the removal of the 300 mg/day limit of dietary cholesterol in the 2015–2020 Dietary Guidelines for Americans [7]. The negative connotation associated with dietary cholesterol has been challenged by numerous studies demonstrating the lack of increased biomarkers associated with risk of CVD and the beneficial effects of daily egg consumption [8,9,10]. Whole egg consumption studies have not only resulted in the absence of increases in factors associated with CVD risk but also in improved markers of chronic inflammation, glucose intolerance, and insulin resistance in several distinct populations: children, individuals with metabolic syndrome and people with diabetes [11,12,13,14]. A previous study showed that the consumption of one egg per day reduces insulin resistance and contributes to higher weight loss associated with increased satiety [15]. In several studies, when compared to an isoenergetic, equal-weight breakfast, an egg-based breakfast has been shown to increase satiety and decrease energy intake [13,16,17]. Satiety, or the feeling of satisfaction, can be measured objectively, by biochemical measures, or subjectively by self-report. Increased satiety can lead to changes in nutrient intake patterns, which can have favorable roles in the reduction of CVD risk [18,19,20]. Specifically, ghrelin, a growth hormone—releasing peptide secreted by the stomach in a fasted state, promotes food intake and has roles in energy balance and weight maintenance, as well as proposed roles in various body systems [21]. The regulation of this hormone is effected by both chronic energy balance and acute feeding. It is a marker for increased appetite, and is associated with a counter hormone, leptin, which has been implicated in the regulation of adipocyte homeostasis [18,22,23]. Decreased levels of ghrelin have been related to decreased appetite and can increase weight loss [24,25].
For the purpose of this study, whole egg consumption was compared to oatmeal consumption. Oatmeal is also a good source of fiber, B vitamins, iron, magnesium, and selenium, and an American Heart Association “certified heart healthy food” [26]. The main benefit of oatmeal for CVD protection is the ability to lower low-density lipoprotein cholesterol (LDL-C), which can be attributed to its soluble fiber content [27]. The main objective of this study was to investigate the effects of two different breakfasts on anthropometrics, dietary patterns, lipid profile, and satiety in a healthy population in order to evaluate the biomarkers of CVD risk and effect on appetite. We hypothesized that compared to daily consumption of oatmeal, the intake of two eggs per day would not result in changes of CVD risk biomarkers, but would increase satiety in a young, healthy population.

2. Materials and Methods

2.1. Experimental Design

Fifty healthy individuals (26 females and 24 males) between the ages of 18–30 years were recruited to participate in an 11-week, randomized, crossover, intervention study. Participants were mainly college students recruited from the University of Connecticut, Storrs, CT and young professionals from local surrounding communities. Based on the standard deviation from our previous studies and using a Z value of 1.96 (95% confidence interval) we estimated that 40 subjects would be sufficient to observe differences in plasma high-density lipoprotein cholesterol (HDL-C) between groups [11,12,15]. We recruited 50 subjects to allow for attrition. The study took place between August–December 2014.
Participants signed a written, informed consent form prior to any measures or experimental procedures. Inclusion criteria included age (18–30 years), body mass index (BMI) (18.5–29.9 kg/m2) and willingness to consume the intervention foods daily.
Exclusion criteria included plasma triglycerides (TG) > 500 mg/dL, total cholesterol (TC) > 240 mg/dL or glucose (GLU) > 126 mg/dL. Current or previous history of liver disease, renal disease, diabetes, cancer, endocrine disorders, metabolic disorders, stroke or heart disease, taking glucose lowering drugs or supplements, current pregnancy or lactation, BMI ≥ 30 kg/m2, blood pressure > 140/90, egg or gluten allergy/sensitivity or celiac disease. All analysis was performed blinded to breakfast allocation. All visits took place in the Nutritional Sciences Department at the University of Connecticut, Storrs, CT. This study was approved by the Institutional Review Board at the University of Connecticut (protocol #H14-032). This trial is registered at ClinicalTrials.gov as NCT02181244.

2.2. Dietary Intervention

Enrolled participants were randomly allocated to consume either two eggs per day (EGGS) or one packet of oatmeal per day (OATS) for four weeks (Big Y Foods, Inc., Springfield, MA, USA). Following a three-week washout, participants crossed over to the alternate intervention food for four weeks. Each daily serving of two eggs contained 370 mg cholesterol, 0 g carbohydrate, 12 g protein, 10 g fat, 0 g fiber and 140 calories. Each daily serving of one packet of oatmeal had 0 mg cholesterol, 0–14 g carbohydrate, 3–4 g protein, 1.5–2 g fat, 3 g fiber and 100–160 calories depending on the flavor choice, of which there were five. Participants were instructed to consume the intervention foods as the first meal of the day, and were allowed to add vegetables, meat, cheese, syrup, yogurt, etc. to their breakfast intervention food, if desired. Participant compliance was monitored daily by self-report and bi-weekly visits to our laboratory for product pickup. During the intervention and washout periods, participants were asked to avoid consuming whole eggs or foods containing predominately eggs or oats. Aside from treatment, habitual dietary intake, exercise, medication usage, and supplement intake was maintained throughout the study.

2.3. Blood Collection and Processing

After a 12 h overnight fast, blood was drawn at baseline, and at the end of each dietary period. Whole blood was collected from participants in EDTA and SST blood collection tubes and was centrifuged at 2000× g for 20 min at 4 °C. Plasma and serum were collected and aliquots were placed at −80 °C for storage.

2.4. Anthropometrics, Blood Pressure, Waist Circumference, and Dietary Intake

Anthropometric measures of weight, height, BMI, and waist circumference (WC), and dietary intake were collected from participants at the end of each dietary period. Weight was measured to the nearest 0.1 kg, height to the nearest centimeter, and BMI was calculated. Blood pressure (BP) was measured with an automated blood pressure monitor (Omron, Healthcare Inc., Bannockburn, IL, USA) after a 5 min rest. The average of three separate recordings is reported. WC was measured on bare skin, at the top of the iliac crest to the nearest 0.1 cm. The average of 3 separate recordings is reported. Subjects were responsible for recording all food and beverages consumed, for two non-consecutive weekdays and one weekend day. Dietary intake was analyzed using Nutrition Data System for Research (NDSR) 2014 (Nutrition Coordinating Center, University of Minnesota) to quantify macronutrient, micronutrient and carotenoid intake, glycemic index, and glycemic load.

2.5. Plasma Lipids, Glucose, and Liver Enzymes

Fasting plasma samples from the end of each intervention period were analyzed for TC, HDL-C, TG, GLU, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) levels. Samples were measured using an automated clinical chemistry analyzer (Cobas c111, Roche Diagnostics, Indianapolis, IN, USA), LDL-C was estimated using the Friedewald equation [28].

2.6. Measures of Satiety

Satiety was analyzed by subjective (satiety visual analog (VAS) scales) and objective (plasma ghrelin) measurements. Participants completed corresponding VAS on the same days as the three-day dietary intake records [15]. Satiety scales were completed prior to breakfast, lunch and dinner. Each VAS questionnaire was composed of eight open-ended questions regarding hunger, satisfaction, fullness, satiety and taste preference for savory, salty, sweet, or fatty foods. The VAS was a 10 cm line, ranging from “not at all” to “yes very much”. Participants marked along the line indicating their feelings, which was then assigned a quantifiable value by measuring from the beginning of the line to where the participant had marked. Values were recorded to the tenth position for analysis. To measure ghrelin, fasting plasma from the end of each intervention period was acidified with 1 M hydrochloric acid to retain stability at −80 °C. Total ghrelin was quantified using a sandwich ELISA kit, (Mercodia AB, Uppsala, Sweden).

2.7. Statistical Analysis

All statistical analyses were performed using SPSS version 22. Paired t-tests were used to assess differences between dietary treatments and baseline values were used as a covariate. Data are reported as mean ± SD unless noted otherwise. p < 0.05 was considered significant.

3. Results

3.1. Study Flow Chart

Of the 55 potential participants screened, five were excluded due to a personal decision not to participate. During the first phase of the study, two participants dropped out due to failed compliance while consuming oatmeal; 48 participants completed the study (Figure 1).

3.2. Baseline Characteristics

Characteristics of participants at baseline are shown in Table 1. The average age of participants was 23.3 years with a distribution of 26 females and 24 males. Baseline anthropometrics were within healthy ranges, with an average BMI of 23.2, a WC of 81.3 and an average BP of 112/72 mmHg. Participants had a healthy lipid profile, with average TC < 3.9 mmol/L, LDL-C < 1.9 mmol/L, TG < 0.8 mmol/L, and HDL > 1.7 mmol/L. The average fasting GLU < 5.1 mmol/L and C-reactive protein (CRP) of 0.2 mg/L indicated no significant glucose sensitivity or inflammation, respectively, at baseline.

3.3. Dietary Intake

While there was no significant difference in energy intake between treatment periods, following the EGGS period, the percentage of calories from protein and fat increased (p < 0.001), while the percentage of calories from carbohydrates decreased (p < 0.001), (Table 2). The intake of both saturated fatty acids (SFA) and monounsaturated fatty acids (MUFA) was increased with egg consumption (p < 0.001), while there was no difference in the intake of polyunsaturated fatty acids (PUFA) between treatment groups. As expected, the dietary cholesterol intake was increased during the EGGS period (p < 0.001). Comparatively, the total and soluble fiber intake was significantly increased during the OATS period (p < 0.05). Despite egg yolks serving as a bioavailable source of lutein and zeaxanthin [29], there was no difference in the dietary intake of the carotenoids lutein and zeaxanthin between the EGGS and OATS periods. Similarly, no changes in the glycemic index were observed between treatments, whereas the glycemic load was decreased during the EGGS period (p < 0.05) (Table 2).

3.4. Anthropometrics, Blood Pressure, Plasma Lipids, Glucose, and Liver Enzymes

There were no differences in the anthropometric measures of WC, BMI, and systolic or diastolic BP between the two breakfasts. Following egg intake there was an increase in TC, LDL-C, and HDL-C (p < 0.05), with no change in the LDL-C/HDL-C ratio. There were no significant differences in TG, GLU, ALT or AST when participants were consuming eggs or oatmeal for breakfast (Table 3).

3.5. Measurements of Satiety: VAS and Plasma Ghrelin

The analysis of VAS revealed that participants consuming eggs for breakfast felt more satisfied prior to consuming dinner than participants consuming oatmeal, suggesting a prolonged effect of egg intake on satiety throughout the day (Figure 2a). Participants consuming eggs felt more of a desire to consume something sweet for breakfast, then less of a desire for something sweet prior to lunch and dinner (Figure 2b). Finally, participants consuming eggs felt less of a desire to consume something salty or savory for breakfast, as compared to participants consuming oatmeal for breakfast (Figure 2c,d).
We further aimed to examine an objective measure of satiety. Following four weeks of eggs consumption for breakfast, fasting plasma ghrelin was significantly decreased as compared to an oatmeal breakfast, indicating less feelings of hunger upon waking as compared to an oatmeal breakfast (Figure 3). A negative correlation was identified between ghrelin and BMI, indicating an association between the biological indication of hunger and body weight (Figure 4).

4. Discussion

Despite the recent removal of the dietary cholesterol intake limit [30], habitual egg consumption remains controversial and misunderstood by the general public. Therefore, the purpose of this study was to determine whether an egg-based breakfast as compared to a certified heart-healthy breakfast of oatmeal would increase the biomarkers associated with CVD risk and affect appetite in a young, healthy population. Although there was an increase in both LDL-C and HDL-C, we found the consumption of two eggs per day as compared to an oatmeal breakfast did not increase the LDL-C/HDL-C ratio, while increasing satiety as measured by fasting plasma ghrelin and VAS.
The impact of dietary cholesterol on plasma lipids varies among individuals, potentially due to variations in the negative feedback regulation of endogenous cholesterol production in response to cholesterol intake [31]. In this study, the consumption of two eggs per day did raise TC levels, corresponding to the increased intake of dietary cholesterol as compared to oatmeal. Notably, egg-induced increases in TC are related to concurrent increases in both LDL-C and HDL-C, which has been observed in previous egg studies [12,32,33]. The maintenance of the LDL-C/HDL-C ratio, an accepted CVD prediction model, does not impact CVD risk, which, in contrast to previous epidemiological studies that associated egg consumption with increased LDL-C only, then extrapolated that data to an increased risk of CVD with egg intake [34].
This concurrent increase in HDL-C may be suggestive of improved reverse cholesterol transport (RCT) because it is indicative of greater amounts of cholesterol being removed from the tissues [35]. It is hypothesized that the phospholipids from eggs are involved in this modulation of RCT by impacting the HDL size and function, as well as the expression of hepatic HDL uptake receptors [36]. In a human clinical trial, ex vivo cholesterol efflux, the critical first step of RCT, was found to be increased following egg consumption [37]. Two large meta-analyses have reported no association between regular egg consumption and the risk of CVD, myocardial infarction or stroke in the general population [38,39]. Thus, although TC, LDL-C and HDL-C levels were increased following egg consumption, regulatory mechanisms may have compensated for the added dietary cholesterol and biomarkers of CVD risk remained unchanged in this population.
Our results reported the increased consumption of protein and fat throughout the day, with no impact on the total energy intake or change in body weight following the consumption of two eggs at breakfast. High-protein diets have been found to increase energy expenditure, and promote a negative energy balance [17]. In a study in healthy individuals who consumed low- or high-protein diets, with sustained carbohydrate consumption (50%), researchers found a decrease in appetite and caloric intake with high-protein intake. In our study, a decrease in hunger and an increase in fullness were seen between weeks 3 and 4 of the isocaloric high-protein diet; however, a decrease in caloric intake was sustained for the ad libitum high-protein leg of the study. This correlated with increased plasma ghrelin over time. Although this study did not reduce the amount of carbohydrates in the diet, we found similar results to a high-protein diet with a decreased carbohydrate intake as well [18]. The glycemic load is an accurate measure of the degree to which carbohydrate-containing foods will affect plasma glucose levels [40]. Reductions in glycemic load have previously been associated with carbohydrate-restricted diets and egg consumption [41]. The reduction in carbohydrates following the consumption of eggs is the likely cause of the reduction in the glycemic load, which has been implicated in the control of glucose and lipid metabolism [42].
Protein increases satiety and thus may explain the decrease in ghrelin levels. In a study investigating the effect of protein intake on the plasma ghrelin concentration, there was a significant reduction in ghrelin over time when consuming higher-protein diets compared to carbohydrate diets [18]. A study in children and adolescents evaluated satiety at lunchtime following either an egg or bagel breakfast [43]. There were no significant differences in dietary intake at lunchtime in either group, according to dietary intake analysis and VAS. However, the peptide YY (PYY) was increased following egg consumption, which is also suggestive of increased satiety. This increase was observed often after consuming foods higher in protein and fat. The authors attributed the lack of correlation between dietary consumption and ghrelin levels to the children’s ability to self-regulate food intake better than adolescents and adults [44]. Conversely, a study investigating the impact of macronutrient intake on levels of cortisol, which stimulates food intake, found decreased levels throughout the day following the intake of protein and fat as compared to carbohydrates [45]. Equally, the intake of carbohydrates for breakfast caused an increase in the cortisol concentration, which may be related to increased feelings of hunger throughout the day. Eating comfort food, high in sugar, is proposed to cause stress that further increases cortisol concentrations throughout the day [45]. Ghrelin is down-regulated in positive energy balance, and up-regulated in negative energy balance, in healthy-weight individuals [46]. Tschop et al. [43,47] also reported a negative correlation between fasting ghrelin and percent body fat. In our study, we found similar results, with those individuals with higher BMIs having the lowest plasma ghrelin. This can be attributed to a negative feedback mechanism, in which the body is attempting to maintain energy balance homeostasis and the regulation of feeding [48].
Following egg consumption, we likewise observed decreased circulating ghrelin. This may be related to the increased protein intake as a result of egg intake. Egg protein has the highest biological value of any other protein at an 88–95/100 rating, indicating the presence of all amino acids, both dispensable and indispensable. High-biological-value proteins have been suggested to delay gastric emptying and to have a stronger effect on decreasing post-prandial ghrelin concentrations [24]. Ghrelin also follows a diurnal pattern, dipping around 2 p.m. and steadily increasing as the night continues, which can be implicated in hunger upon waking [47]. From comparing our results, in which we observed decreased plasma ghrelin and increased satisfaction at dinnertime with egg consumption, we can hypothesize that eggs play a long-term role in satiety. In a study investigating the effect of protein intake on plasma ghrelin concentrations, there was a significant reduction in ghrelin over time when consuming higher-protein diets as compared to carbohydrate diets [49]. This may be due to the satiating effects of protein and the impact of easy digestion. In the case of egg consumption, the high biological value helps with the digestibility and improved satisfaction at dinnertime compared to the oatmeal breakfast [50].
There are several limitations to this study including the use of whole foods for the intervention, which does not allow the participants to be blinded to the specific breakfast. However, any bias over the foods consumed was removed since no expectations of the data were shared with the participants. Another limitation would be ghrelin measurement, which was assessed prior to consuming breakfast only. The post-prandial assessment of ghrelin would have strengthened the results found by VAS analysis. While appetite was affected following the consumption of eggs, there were no observed differences in energy intake. This could be considered a limitation, because though satiety was improved, this may not be considered an effective treatment for weight loss. There were also some strengths to this study including the use of whole foods, as the results can be easily extrapolated to the general population, because these foods are normally consumed for breakfast. The assessment of satiety via VAS and the plasma measurement of ghrelin were also strengths of this study in evaluating and correlating hunger and the desire to eat throughout the day.
The intake of two eggs per day as compared to an oatmeal breakfast promoted a shift in dietary intake patterns, did not lead to an increase in biomarkers associated with CVD, and resulted in both subjective and objective measures of satiety in a healthy population. The results of the study are important to confirming eggs as a healthy habitual breakfast food with additional benefits of increased satiety throughout the day.

Acknowledgments

Supported by funds provided by the Esperance Family Foundation.

Author Contributions

A.M. was in charge of recruiting and acquiring consent from participants, conducting the intervention, measuring plasma lipids and plasma ghrelin, participating in data analysis and the writing of the manuscript; D.M. participated in recruitment and acquiring consent of subjects, conducting the intervention, analyzed the dietary records, and provided input in data analysis. C.J.A. participated in the design of the experiment and the recruitment and acquiring consent of participants and provided input for data analysis and the writing of the manuscript; A.G.M. participated in recruitment and acquiring consent of subjects, conducting the intervention and provided input on the writing of the manuscript. M.V.-J. participated in the laboratory analysis and the writing of the manuscript; M.L.F. had a major responsibility in the design of the study, data analysis and interpretation, supervising the experiments, and the writing of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kupper, W.; Hamm, C.W.; Bleifeld, W. Distribution of ApoA-I-Containing HDL Subpopulations in Patients With Coronary Heart Disease. Arterioscler. Thromb. Vasc. Biol. 2000, 20, 2670–2676. [Google Scholar]
  2. Tolfrey, K.; Zakrzewski, J.K. Breakfast, glycaemic index and health in young people. J. Sport Heal. Sci. 2012, 1, 149–159. [Google Scholar] [CrossRef]
  3. Nicklas, T.A.; Reger, C.; Myers, L.; O’Neil, C. Breakfast consumption with and without vitamin-mineral supplement use favorably impacts daily nutrient intake of ninth-grade students. J. Adolesc. Health 2000, 27, 314–321. [Google Scholar] [CrossRef]
  4. Kovacs-Nolan, J.; Phillips, M.; Mine, Y. Advances in the value of eggs and egg components for human health. J. Agric. Food Chem. 2005, 53, 8421–8431. [Google Scholar] [CrossRef] [PubMed]
  5. McNamara, D.J. The fifty year rehabilitation of the egg. Nutrients 2015, 7, 8716–8722. [Google Scholar] [CrossRef] [PubMed]
  6. American Heart Association. Heart and Stroke Encyclopedia: Eggs. Available online: http://www.heart.org/HEARTORG/ (accessed on 11 January 2016).
  7. U.S. Department of Health and Human Services; U.S. Department of Agriculture. Available online: http://health.gov/dietaryguidelines/2015/ (accessed on 15 January 2016).
  8. Mutungi, G.; Waters, D.; Ratliff, J.; Puglisi, M.; Clark, R.M.; Volek, J.S.; Fernandez, M.L. Eggs distinctly modulate plasma carotenoid and lipoprotein subclasses in adult men following a carbohydrate-restricted diet. J. Nutr. Biochem. 2010, 21, 261–267. [Google Scholar] [CrossRef] [PubMed]
  9. Herron, K.L.; Vega-Lopez, S.; Conde, K.; Ramjiganesh, T.; Shachter, N.S.; Fernandez, M.L. Men classified as hypo- or hyperresponders to dietary cholesterol feeding exhibit differences in lipoprotein metabolism. J. Nutr. 2003, 133, 1036–1042. [Google Scholar] [PubMed]
  10. Barona, J.; Fernandez, M.L. Dietary cholesterol affects plasma lipid levels, the intravascular processing of lipoproteins and reverse cholesterol transport without increasing the risk for heart disease. Nutrients 2012, 4, 1015–1025. [Google Scholar] [CrossRef] [PubMed]
  11. Blesso, C.N.; Andersen, C.J.; Barona, J.; Volek, J.S.; Fernandez, M.L. Whole egg consumption improves lipoprotein profiles and insulin sensitivity to a greater extent than yolk-free egg substitute in individuals with metabolic syndrome. Metabolism 2013, 62, 400–410. [Google Scholar] [CrossRef] [PubMed]
  12. Ballesteros, M.N.; Valenzuela, F.; Robles, A.E.; Artalejo, E.; Aguilar, D.; Andersen, C.J.; Valdez, H.; Fernandez, M.L. One egg per day improves inflammation when compared to an oatmeal-based breakfast without increasing other cardiometabolic risk factors in diabetic patients. Nutrients 2015, 7, 3449–3463. [Google Scholar] [CrossRef] [PubMed]
  13. Vander Wal, J.S.; Marth, J.M.; Khosla, P.; Jen, K.-L.C.; Dhurandhar, N.V. Short-term effect of eggs on satiety in overweight and obese subjects. J. Am. Coll. Nutr. 2005, 24, 510–515. [Google Scholar] [CrossRef] [PubMed]
  14. Iannotti, L.L.; Lutter, C.K.; Bunn, D.A.; Stewart, C.P. Eggs: The uncracked potential for improving maternal and young child nutrition among the world’s poor. Nutr. Rev. 2014, 72, 355–368. [Google Scholar] [CrossRef] [PubMed]
  15. Ratliff, J.; Leite, J.O.; de Ogburn, R.; Puglisi, M.J.; van Heest, J.; Fernandez, M.L. Consuming eggs for breakfast influences plasma glucose and ghrelin, while reducing energy intake during the next 24 h in adult men. Nutr. Res. 2010, 30, 96–103. [Google Scholar] [CrossRef] [PubMed]
  16. Rueda, J.M.; Khosla, P. Impact of breakfasts (with or without eggs) on body weight regulation and blood lipids in university students over a 14-week semester. Nutrients 2013, 5, 5097–5113. [Google Scholar] [CrossRef] [PubMed]
  17. Kral, T.V.E.; Bannon, A.L.; Chittams, J.; Moore, R.H. Comparison of the satiating properties of egg- versus cereal grain-based breakfasts for appetite and energy intake control in children. Eat. Behav. 2016, 20, 14–20. [Google Scholar] [CrossRef] [PubMed]
  18. Weigle, D.S.; Breen, P.A.; Matthys, C.C.; Callahan, H.S.; Meeuws, K.E.; Burden, V.R.; Purnell, J.Q. 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, 41–48. [Google Scholar] [PubMed]
  19. Laurila, M.; Santaniemi, M.; Kesäniemi, Y.A.; Ukkola, O. Peptides High plasma ghrelin protects from coronary heart disease and Leu72Leu polymorphism of ghrelin gene from cancer in healthy adults during the 19 years follow-up study. Peptides 2014, 61, 122–129. [Google Scholar] [CrossRef] [PubMed]
  20. Chou, C.-C.; Bai, C.-H.; Tsai, S.-C.; Wu, M.-S. Low serum acylated ghrelin levels are associated with the development of cardiovascular disease in hemodialysis patients. Intern. Med. 2010, 49, 2057–2064. [Google Scholar] [CrossRef] [PubMed]
  21. Mao, Y.; Tokudome, T.; Kishimoto, I. Ghrelin as a treatment for cardiovascular diseases. Hypertension 2014, 64, 450–454. [Google Scholar] [CrossRef] [PubMed]
  22. Greenberg, A.S.; Obin, M.S. Obesity and the role of adipose tissue in inflammation and metabolism. Am. J. Clin. Nutr. 2006, 83, 461–465. [Google Scholar]
  23. Moran, L.J.; Noakes, M.; Clifton, P.M.; Wittert, G.A.; Tomlinson, L.; Galletly, C.; Luscombe, N.D.; Norman, R.J. Ghrelin and measures of satiety are altered in polycystic ovary syndrome but not differentially affected by diet composition. J. Clin. Endocrinol. Metab. 2004, 89, 3337–3344. [Google Scholar] [CrossRef] [PubMed]
  24. Otto, B.; Heldwein, W.; Otto, C.; Huptas, S.; Parhofer, K.G. Effect of a high-fat meal on the postprandial ghrelin response. Am. J. Clin. Nutr. 2006, 84, 664–665. [Google Scholar] [PubMed]
  25. Zakhari, J.S.; Zorrilla, E.P.; Zhou, B.; Mayorov, A.V.; Janda, K.D. Oligoclonal antibody targeting ghrelin increases energy expenditure and reduces food intake in fasted mice. Mol. Pharm. 2013, 9, 281–289. [Google Scholar] [CrossRef] [PubMed]
  26. American Heart Association. Whole Grains. Available online: http://www.heart.org/HEARTORG/Encyclopedia/Heart-Encyclopedia_UCM_445084_Encyclopedia.jsp?levelSelected=17&title=whole grains (accessed on 11 January 2016).
  27. Davy, B.M.; Davy, K.P.; Ho, R.C.; Beske, S.D.; Davrath, L.R.; Melby, C.L. High-fiber oat cereal compared with wheat cereal consumption favorably alters LDL-cholesterol subclass and particle numbers in middle-aged and older men. Am. J. Clin. Nutr. 2002, 76, 351–358. [Google Scholar] [PubMed]
  28. Fukuyama, N.; Homma, K.; Wakana, N.; Kudo, K.; Suyama, A.; Ohazama, H.; Tsuji, C.; Ishiwata, K.; Eguchi, Y.; Nakazawa, H.; et al. Validation of the Friedewald Equation for Evaluation of Plasma LDL-Cholesterol. J. Clin. Biochem. Nutr. 2008, 43, 1–5. [Google Scholar] [CrossRef] [PubMed]
  29. Chung, H.-Y.; Rasmussen, H.M.; Johnson, E.J. Lutein bioavailability is higher from lutein-enriched eggs than from supplements and spinach in men. J. Nutr. 2004, 134, 1887–1893. [Google Scholar] [PubMed]
  30. USDA Dietary Guidelines for Americans 2015–2020. 2015. Available online: https://health.gov/dietaryguidelines/ (accessed on 15 November 2016).
  31. Van Der Wulp, M.Y.M.; Verkade, H.J.; Groen, A.K. Regulation of cholesterol homeostasis. Mol. Cell. Endocrinol. 2013, 368, 1–16. [Google Scholar] [CrossRef] [PubMed]
  32. Fernandez, M.L. Effects of eggs on plasma lipoproteins in healthy populations. Food Funct. 2010, 1, 156–160. [Google Scholar] [CrossRef] [PubMed]
  33. Ratliff, J.; Mutungi, G.; Puglisi, M.J.; Volek, J.S.; Fernandez, M.L. Carbohydrate restriction (with or without additional dietary cholesterol provided by eggs) reduces insulin resistance and plasma leptin without modifying appetite hormones in adult men. Nutr. Res. 2009, 29, 262–268. [Google Scholar] [CrossRef] [PubMed]
  34. Spence, J.D.; Jenkins, D.J.A.; Davignon, J. Dietary cholesterol and egg yolks: Not for patients at risk of vascular disease. Can. J. Cardiol. 2010, 26, e336–e339. [Google Scholar] [CrossRef]
  35. Lewis, G.F.; Rader, D.J. New insights into the regulation of HDL metabolism and reverse cholesterol transport. Circ. Res. 2005, 96, 1221–1232. [Google Scholar] [CrossRef] [PubMed]
  36. Yancey, P.G.; de La Llera-Moya, M.; Swarnakar, S.; Monzo, P.; Klein, S.M.; Connelly, M.A.; Johnson, W.J.; Williams, D.L.; Rothblat, G.H. High density lipoprotein phospholipid composition is a major determinant of the bi-directional flux and net movement of cellular free cholesterol mediated by scavenger receptor BI. J. Biol. Chem. 2000, 275, 36596–36604. [Google Scholar] [CrossRef] [PubMed]
  37. Andersen, C.J.; Blesso, C.N.; Lee, J.; Barona, J.; Shah, D.; Thomas, M.J.; Fernandez, M.L. Egg consumption modulates HDL lipid composition and increases the cholesterol-accepting capacity of serum in metabolic syndrome. Lipids 2013, 48, 557–567. [Google Scholar] [CrossRef] [PubMed]
  38. Shin, J.; Xun, P.; Nakamura, Y.; He, K. Egg consumption in relation to risk of cardiovascular disease and diabetes: A systematic review and meta-analysis. Am. J. Clin. Nutr. 2013, 98, 146–159. [Google Scholar] [CrossRef] [PubMed]
  39. Rong, Y.; Chen, L.; Zhu, T.; Song, Y.; Yu, M.; Shan, Z.; Sands, A.; Hu, F.B.; Liu, L. Egg consumption and risk of coronary heart disease and stroke: Dose-response meta-analysis of prospective cohort studies. BMJ 2013, 346, e8539. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Nutrition Data Glycemic Index, Glycemic Load. Available online: http://nutritiondata.self.com/topics/glycemic-index (accessed on 25 October 2016).
  41. Blesso, C.N.; Andersen, C.J.; Barona, J.; Volk, B.; Volek, J.S.; Fernandez, M.L. Effects of carbohydrate restriction and dietary cholesterol provided by eggs on clinical risk factors in metabolic syndrome. J. Clin. Lipidol. 2013, 7, 463–471. [Google Scholar] [CrossRef] [PubMed]
  42. Venn, B.J.; Green, T.J. Glycemic index and glycemic load: Measurement issues and their effect on diet-disease relationships. Eur. J. Clin. Nutr. 2007, 61 (Suppl. 1), S122–S131. [Google Scholar] [CrossRef] [PubMed]
  43. Tschop, M.; Weyer, C.; Tataranni, P.A.; Devanarayan, V.; Ravussin, E.; Heiman, M.L. Circulating ghrelin levels are decreased in obesity. Diabetes 2001, 50, 707–709. [Google Scholar] [CrossRef] [PubMed]
  44. Liu, A.G.; Puyau, R.S.; Han, H.; Johnson, W.D.; Greenway, F.L.; Dhurandhar, N.V. The Effect of an Egg Breakfast on Satiety in Children and Adolescents: A Randomized Crossover Trial. J. Am. Coll. Nutr. 2015, 34, 37–54. [Google Scholar] [CrossRef] [PubMed]
  45. Martens, M.J.I.; Rutters, F.; Lemmens, S.G.T.; Born, J.M.; Westerterp-Plantenga, M.S. Effects of single macronutrients on serum cortisol concentrations in normal weight men. Physiol. Behav. 2010, 101, 563–567. [Google Scholar] [CrossRef] [PubMed]
  46. Rodríguez, A. Novel molecular aspects of ghrelin and leptin in the control of adipobiology and the cardiovascular system. Obes. Facts 2014, 7, 82–95. [Google Scholar] [CrossRef] [PubMed]
  47. Shiiya, T.; Nakazato, M.; Mizuta, M.; Date, Y.; Mondal, M.S.; Tanaka, M.; Nozoe, S.-I.; Hosoda, H.; Kangawa, K.; Matsukura, S. Plasma Ghrelin Levels in Lean and Obese Humans and the Effect of Glucose on Ghrelin Secretion. J. Clin. Endocrinol. Metab. 2009, 87, 240–244. [Google Scholar] [CrossRef] [PubMed]
  48. Nakazato, M.; Murakami, N.; Date, Y.; Kojima, M.; Matsuo, H.; Kangawa, K.; Matsukura, S. A role for ghrelin in the central regulation of feeding. Nature 2001, 409, 194–198. [Google Scholar] [CrossRef] [PubMed]
  49. Gerstein, D.E.; Woodward-Lopez, G.; Evans, A.E.; Kelsey, K.; Drewnowski, A. Clarifying concepts about macronutrients’ effects on satiation and satiety. J. Am. Diet. Assoc. 2004, 104, 1151–1153. [Google Scholar] [CrossRef] [PubMed]
  50. Clark, L.C.; Byer, H.; Murlin, J.R. Relative to egg biological values and replacement values of some cereal proteins in human subjects. J. Nutr. 1949, 38, 405–420. [Google Scholar] [PubMed]
Nutrients 09 00089 g001 550
Figure 1. Flow chart of the study design. Forty-eight of 50 participants completed the study, as they did not meet requirements for oatmeal consumption during that arm of the intervention.
Figure 1. Flow chart of the study design. Forty-eight of 50 participants completed the study, as they did not meet requirements for oatmeal consumption during that arm of the intervention.
Nutrients 09 00089 g001
Nutrients 09 00089 g002 550
Figure 2. Results from satiety VAS completed prior to each meal during OATS (white bars) and EGGS (black bars) periods; n = 48. (a) Participants consuming two eggs per day felt more satisfied prior to eating dinner; (b) Participants consuming two eggs per day wanted something sweet for breakfast as compared to lunch and dinner; (c) Participants consuming two eggs did not prefer something salty as compared to oatmeal; (d) Participants wanted something less savory following the consumption of two eggs per day; * different from oatmeal at p < 0.05 and ** different from oatmeal at p < 0.01.
Figure 2. Results from satiety VAS completed prior to each meal during OATS (white bars) and EGGS (black bars) periods; n = 48. (a) Participants consuming two eggs per day felt more satisfied prior to eating dinner; (b) Participants consuming two eggs per day wanted something sweet for breakfast as compared to lunch and dinner; (c) Participants consuming two eggs did not prefer something salty as compared to oatmeal; (d) Participants wanted something less savory following the consumption of two eggs per day; * different from oatmeal at p < 0.05 and ** different from oatmeal at p < 0.01.
Nutrients 09 00089 g002
Nutrients 09 00089 g003 550
Figure 3. Fasting plasma ghrelin concentrations for subjects after the oatmeal (577.8 ± 219.7 pg/mL) and eggs (553.0 ± 181.5 pg/mL) periods, * p < 0.05. Participants (n = 48) had lower circulating total ghrelin following consumption of two eggs.
Figure 3. Fasting plasma ghrelin concentrations for subjects after the oatmeal (577.8 ± 219.7 pg/mL) and eggs (553.0 ± 181.5 pg/mL) periods, * p < 0.05. Participants (n = 48) had lower circulating total ghrelin following consumption of two eggs.
Nutrients 09 00089 g003
Nutrients 09 00089 g004 550
Figure 4. Correlation between fasting plasma ghrelin and body mass index (BMI) following the consumption of two eggs for breakfast; participants (n = 48), r = −0.47, p < 0.01.
Figure 4. Correlation between fasting plasma ghrelin and body mass index (BMI) following the consumption of two eggs for breakfast; participants (n = 48), r = −0.47, p < 0.01.
Nutrients 09 00089 g004
Table
Table 1. Baseline characteristics of subjects 1.
Table 1. Baseline characteristics of subjects 1.
ParameterValues
Age (years)23.3 ± 3.1
Gender (n = F/M)26/24
BMI (kg/m2)23.2 ± 2.1
WC (cm)81.3 ± 6.5
Systolic BP (mmHg)112.1 ± 12.4
Diastolic BP (mmHg)72.7 ± 7.0
Total Cholesterol (mmol/L)3.9 ± 0.7
LDL-C (mmol/L)1.9 ± 0.6
HDL-C (mmol/L)1.7 ± 0.5
LDL-C/HDL-C1.2 ± 0.07
Triglycerides (mmol/L)0.9 ± 0.04
Glucose (mmol/L)5.1 ± 0.3
CRP (mg/dL)0.2 ± 0.8
1 Values are presented as mean ± SD; n = 50.
Table
Table 2. Dietary intake during eggs and oatmeal periods 1.
Table 2. Dietary intake during eggs and oatmeal periods 1.
ParameterEggsOatmeal
Weight (kg)68.2 ± 11.268.2 ± 11.1
Energy (kcal)1937 ± 6302016 ± 1461
Protein (%)19.2 ± 4.417.6 ± 4.1
Carbohydrate (%)41.4 ± 6.2 **48.9 ± 8.2
Total Fat (%)37.2 ± 5.1 **32.2 ± 6.7
SFA (g/day)27.3 ± 11.9 **21.1 ± 8.1
MUFA (g/day)30.4 ± 11.6 **23.2 ± 9.6
PUFA (g/day)16.6 ± 7.415.7 ± 11.5
Total Fiber (g/day)18.3 ± 7.020.9 ± 11.4
Soluble Fiber (g/day)5.6 ± 2.6 *7.0 ± 4.0
Insoluble Fiber (g/day)12.7 ± 7.413.9 ± 8.0
Cholesterol (mg/day)546.1 ± 96.6 **173.1 ± 90.6
Lutein + Zeaxanthin (µg/day)2820 ± 34432327 ± 3997
Glycemic Index59.0 ± 5.959.9 ± 6.0
Glycemic Load109.9 ± 42.4 *122.6 ± 49.1
1 Values are presented as mean ± SD; n = 48; * p < 0.025, ** p < 0.001.
Table
Table 3. Anthropometrics, blood pressure, plasma lipids, glucose, and liver enzymes after the eggs and oatmeal breakfasts 1.
Table 3. Anthropometrics, blood pressure, plasma lipids, glucose, and liver enzymes after the eggs and oatmeal breakfasts 1.
ParameterEggsOatmeal
BMI (kg/m2)23.2 ± 2.222.7 ± 2.6
WC (cm)81.9 ± 6.482.6 ± 6.6
Systolic BP (mmHg)110.3 ± 10.1111.2 ± 11.7
Diastolic BP (mmHg)74.4 ± 6.473.4 ± 6.3
Total cholesterol (mmol/L)4.2 ± 0.7 *4.0 ± 0.7
LDL cholesterol (mmol/L)2.1 ± 0.7 *1.9 ± 0.6
HDL cholesterol (mmol/L)1.71 ± 0.48 *1.62 ± 0.47
LDL-C/HDL-C1.35 ± 0.621.30 ± 0.56
Triglycerides (mmol/L)0.89 ± 0.370.91 ± 0.41
Glucose (mmol/L)5.1 ± 0.45.0 ± 0.4
ALT (U/L)18.2 ± 7.917.6 ± 6.0
AST (U/L)24.5 ± 7.824.5 ± 8.8
1 Values are presented as mean ± SD; n = 48; * p < 0.025.

Share and Cite

MDPI and ACS Style

Missimer, A.; DiMarco, D.M.; Andersen, C.J.; Murillo, A.G.; Vergara-Jimenez, M.; Fernandez, M.L. Consuming Two Eggs per Day, as Compared to an Oatmeal Breakfast, Decreases Plasma Ghrelin while Maintaining the LDL/HDL Ratio. Nutrients 2017, 9, 89. https://doi.org/10.3390/nu9020089

AMA Style

Missimer A, DiMarco DM, Andersen CJ, Murillo AG, Vergara-Jimenez M, Fernandez ML. Consuming Two Eggs per Day, as Compared to an Oatmeal Breakfast, Decreases Plasma Ghrelin while Maintaining the LDL/HDL Ratio. Nutrients. 2017; 9(2):89. https://doi.org/10.3390/nu9020089

Chicago/Turabian Style

Missimer, Amanda, Diana M. DiMarco, Catherine J. Andersen, Ana Gabriela Murillo, Marcela Vergara-Jimenez, and Maria Luz Fernandez. 2017. "Consuming Two Eggs per Day, as Compared to an Oatmeal Breakfast, Decreases Plasma Ghrelin while Maintaining the LDL/HDL Ratio" Nutrients 9, no. 2: 89. https://doi.org/10.3390/nu9020089

APA Style

Missimer, A., DiMarco, D. M., Andersen, C. J., Murillo, A. G., Vergara-Jimenez, M., & Fernandez, M. L. (2017). Consuming Two Eggs per Day, as Compared to an Oatmeal Breakfast, Decreases Plasma Ghrelin while Maintaining the LDL/HDL Ratio. Nutrients, 9(2), 89. https://doi.org/10.3390/nu9020089

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop