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Appetite ratings and ghrelin concentrations in young adults after administration of a balanced meal. Does sex matter?



Sex-based differences in appetite ratings have been observed previously. Ghrelin is the only known orexigenic peptide hormone. Sex differences in postprandial ghrelin responses may underlie different perceptions of hunger and satiety, but results are conflicting. We conducted a parallel study to evaluate sex differences in postprandial appetite ratings and ghrelin concentration after administration of a physiological meal among students of University of Milan.


Twenty-four healthy, normal weight volunteers (12 men and 12 women) aged 18–35 years were recruited. A balanced mixed meal meeting 40% of the estimated daily energy expenditure and providing 60% of calories from carbohydrates, 25% from lipids and 15% from protein was administrated. Sex differences in appetite ratings (satiety, hunger, fullness and desire to eat) and magnitude of ghrelin suppression during postprandial period (up to 180 min) were determined.


In the fasting state, men and women did not differ in appetite ratings and ghrelin concentrations. After feeding, women tended to reach peak of satiety earlier than men, who in turn reached the nadir of hunger later than women (median: 30 min, interquartile range (IQR): 1; 120 vs. 1 min, IQR 1; 1, p = 0.007). Ghrelin suppression was greater in women (median decremental AUC − 95, IQR − 122; − 66) than in men (median decremental AUC − 47, IQR − 87; − 31, p = 0.041).


These findings suggest sex differences in the postprandial appetite regulation that might be important for nutritional strategy to prevent and treat obesity and eating disorders.


  • After consuming a balanced mixed meal, men have delayed hunger suppression compared with women, who instead experience early satiety.

  • After consuming a balanced mixed meal, ghrelin is suppressed more in women than in men.

  • Sex should be considered in the design of nutritional strategies for the prevention and management of obesity and eating disorders.


Appetite regulation is a complex process involving neural and humoral peripheral signals that interact with the central nervous system, in which the hypothalamus plays a pivotal role [1]. The signaling systems underlying appetite control include peripheral signals of hunger and satiety from the gastrointestinal system, which primarily include gastric motility and peptide release from enteroendocrine cells [2, 3], and signals of adiposity and energy homeostasis that influence eating behavior and food intake [4, 5]. Dysfunction of the signaling network underlying hunger, satiety, and metabolic status has been thought to be involved in the etiology of obesity and eating disorders [6].

Among the gut hormones involved in the appetite regulation, ghrelin is the only known orexigenic peptide hormone. It is produced mainly by cells in the stomach and proximal small intestine [2, 3], and plays a central role in the short-term feeding regulation, given its implication in the hunger perception [7]. Its plasma concentrations increase markedly during fasting and before meals and decrease rapidly during the postprandial phase [8, 9]. Results from an animal study suggest sex differences in the impact of ghrelin on food intake. It has been shown that ghrelin increased food intake significantly more in male and untreated ovariectomized female rats than in female intact and estradiol-treated ovariectomized rats, suggesting that estradiol inhibits the orexigenic action of ghrelin in females and opening up the possibility that higher concentrations of ghrelin are required in females than in males to induce the sensation of hunger [10]. According to this hypothesis, some studies found women having higher ghrelin concentrations than men in fasting state [11,12,13]. It is unclear, instead, whether sex affects the ghrelin response to a physiological meal. Some studies have documented women being more sensitive to overfeeding [14] and perceiving greater satiety and lower hunger after the meal consumption [15,16,17]. Thus, it seems plausible that there is a sex difference in gastrointestinal hormonal signaling of hunger and satiety after meal consumption. Higher postprandial concentrations of cholecystokinin (CCK), a satiety-stimulating gastrointestinal hormone, have been observed in women compared to men [18]. Moreover, changes in plasma CCK concentration were associated with a greater increment in fullness and decrement in hunger in women than in men [19]. We hypothesized that, similarly, there might be greater suppression in ghrelin secretion in women than in men.

To test this hypothesis, we measured postprandial ghrelin concentration and appetite ratings in young men and women after administration of a mixed balanced meal. The meal was standardized on individual daily energy expenditure in order to take into account the different body composition of men and women that may affect ghrelin concentrations [20,21,22]. If confirmed, sex differences in ghrelin response to a meal may explain the different eating behavior observed during mealtime between men and women, and have important implications for nutritional strategies for the prevention and treatment of obesity and eating disorders.

Materials and methods


Twenty-four (12 women and 12 men) volunteers were selected among students of the University of Milan. Recruitment and testing were carried out at the International Center for the Assessment of Nutritional Status (ICANS), University of Milan (Italy), between March and June 2018. Participants had to be aged 18–35 years, normal weight and apparently healthy. History of overweight or obesity, having a diagnosis of anosmia and dysgeusia, endocrine disease (i.e., hyper- or hypothyroidism and diabetes mellitus, polycystic ovary syndrome), eating disorder or any disease causing significant impairment of nutritional status (i.e., Crohn’s disease, neoplasia end-stage renal failure, cirrhosis, congestive heart failure and chronic infection), having consumed drugs affecting endocrine function in the previous 2 months, use of estroprogestinics, recent (< 1 month) occurrence of acute illness or injury and elite athleticism were reasons for exclusion from the study. This study was conducted according to the guidelines laid down in the Declaration of Helsinki. The ethics committee of the University of Milan gave a positive opinion on the study (protocol n. 32/17). Written informed consent was obtained from all participants.

Experimental protocol

In the weeks preceding the study, the volunteers were invited to present themselves fasting at ICANS, in order to undergo a detailed medical examination and anthropometric assessment. Subjects were asked about the type and time spent on physical activity. Women were also asked to report the onset of last menses in order to determine the cycle phase. The volunteers were then organized into eight groups of three people each. The meal test studies were performed in different days distributed over several weeks. Each group participated in one of these study days. Women were allocated to the study days according to the menstrual phase, in order to participate during one of the days corresponding to their follicular phase.

On the evening before the test, we asked the subjects to eat a standardized dinner consisting of rice or pasta with olive oil and/or Parmesan cheese and/or tomato sauce, meat or fish, vegetables with olive oil, bread and fresh fruit, and to finish the dinner by 2100 h. After that time, volunteers were asked to refrain from eating. Water was the only drink allowed.

On the study days, volunteers were asked to report to ICANS at 0830 h in a fasting state. Upon arrival, they were seated in the room prepared for testing, where three stations equipped with everything needed to eat the meal and perform venous samplings had been set up, one for each volunteer in the group. A physician then applied an intravenous catheter into an antecubital vein. Baseline venous blood samples were obtained. A registered dietitian instructed the volunteers on the definitions of hunger, satiety, fullness and desire to eat, and invited them to report their baseline appetite ratings using a 100 mm Visual Analogue Scale (VAS) anchored at either ends with opposite statements (“not all” and “very much”). At 0900 h the test meal was provided and the volunteers were asked to consume the entire meal within 15 min. Venous blood samples were obtained every hour after the meal consumption up to 180 min in order to measure serum ghrelin. Appetite ratings were assessed at the end of the meal and at 30, 60, 90, 120 and 180 min. In order not to influence appetite ratings, volunteers were asked not to talk to each other about how they felt after consuming the meal. Throughout the test, the physician and dietitian remained in the room with the volunteers, managing the timing of blood draws, assisting the volunteers, and ensuring that the meal was entirely consumed on time and that the recommendation not to exchange comments about one's appetite sensations was followed.

Test meal

The test meal consisted of a sandwich of white bread, ham, extra-virgin olive oil and tomato. The meal size was different for each participant, as it had to satisfy 40% of individual daily energy expenditure, estimated multiplying resting energy expenditure, obtained by Harris and Benedict equation [23], for the corresponding physical activity level [24]. The meal had a fixed nutrient composition. Approximately 60% of calories derived from carbohydrates, 25% from lipids and 15% from protein. The meal also provided about 9 g/1000 kcal of dietary fiber. Subjects were asked to consume the entire meal within 15 min.

Anthropometric measurements

International standard procedures were followed to measure anthropometric measurements [25]. Body weight, height, circumferences and skinfolds were measured on subjects wearing only light underwear. Body weight was measured by a Column scale (Seca 700 balance, Seca Corporation, Hanover, MD, USA) to 100 g. Body height was measured to the nearest 0.1 cm using a vertical stadiometer. Body mass index was then calculated. Waist circumference was measured with a non-stretch tape applied horizontally midway between the lower rib margin and the superior anterior iliac spine taken to the nearest 0.5 cm. Bicipital, tricipital, subscapular and suprailiac skinfold thicknesses were measured by Holtain Tanner/Whitehouse skinfold calliper (Holtain Ltd, Crymych, Wales). Each skinfold-thickness measurement was taken 3 times and a mean was calculated [25]. Body density and fat mass were then calculated by the Durnin and Womersley method [26] and by the Siri’s formula [27], respectively.

Laboratory analysis

Circulating ghrelin concentrations were measured at baseline and every 60 min up to 3 h using an enzymatic immunoassay kit (BioVendor, Cat. No. RA194063400R, RRID: AB_2895669). This assay is based on a double-antibody sandwich technique. The wells of the plate are coated with a monoclonal antibody specific to the C-terminal part of ghrelin. The acetylcholinesterase (AChE)–Fab’ conjugate (Tracer) which recognizes the N-terminal part of unacylated ghrelin is also added to the wells. Intra- and inter-assay variations were 6.3% and 7.0%, respectively. The limit of determination of this assay is 0.2 pg/ml.

Statistical analysis

Sample size calculation was based on a preliminary analysis of previously published data [28], where we found that, after administration of the same meal we used here, men and women had a ghrelin suppression at 60 min of 0.31 ± 0.18 ng/ml and 0.49 ± 0.16 ng/ml, respectively. With 80% power and a 5% significance level, it was estimated that a sample of 24 volunteers (12 women and 12 men) was sufficient to detect a high effect (Cohen’s d = 1.06) in postprandial ghrelin responses among the sexes.

Continuous variables are presented as median and interquartile range (IQR), as several variables did not follow a normal distribution. Two-sample comparisons between men and women were made by rank-sum test. To test sex differences in the postprandial variations of ghrelin concentrations and appetite ratings, mixed-effects linear regression models were used. Sex (0 = woman, 1 = man), time and sex*time interaction were included as fixed-effect predictors and the patient as random effect. A P value < 0.05 was considered statistically significant. Statistical analysis was performed using STATA version 12.0 (StataCorp).



A total of 12 men and 12 women (median age: 24 years, IQR 22; 26 years; median BMI: 21.9 kg/m2, IQR 20.3; 23.1 kg/m2) were involved in the study, and their characteristics are reported in Table 1. Men and women did not differ for age and BMI. As expected, waist circumference was greater in men, whereas the opposite was found for the percentage of body fat. Men had a greater daily energy expenditure than women.

Table 1 Characteristics of the volunteers

Appetite ratings

Appetite ratings over time according to sex are reported in Fig. 1.

Fig. 1
figure 1

Appetite ratings (mean ± standard error) observed in men and women after ingestion of a balanced mixed meal

Men and women had a similar perception of satiety, hunger, desire to eat and fullness at baseline (Table 2). In women, satiety and fullness peaked immediately after the consumption of the meal, increasing from baseline by 85 mm (95% CI 75; 94) and 76 mm (95% CI 65; 86), respectively. On the contrary, hunger reached the nadir immediately after the consumption of the meal, decreasing by 64 mm (95% CI 55; 74). Finally, the desire to eat reached the nadir at 30 min, decreasing by 65 mm (95% CI 56; 74). All appetite ratings were significantly different from baseline for the whole duration of the study. In men, appetite ratings changes over time from basal were not significantly different from those observed in women (sex*time interactions p > 0.05). Additional file 1: Table S1 shows the meal effect on appetite rating using men as reference.

Table 2 Meal effect on appetite rating according sex and time

However, we observed women reached the peak of satiety marginally earlier than men (p = 0.053, Cohen’s d = 0.83). Almost all women (92%) reported the highest satiety rating immediately after eating the meal, whereas 42% of men reported the peak of satiety at 30 min or later. On the contrary, the nadir of hunger was delayed in men (30 min, IQR 1; 120) than in women (1 min, IQR 1; 1, p = 0.007, Cohen’s d = 1.12) (Table 3).

Table 3 Postprandial appetite ratings parameters


Postprandial ghrelin concentrations according sex are reported in Fig. 2.

Fig. 2
figure 2

Ghrelin concentrations (mean ± standard error) observed in men and women after ingestion of a balanced mixed meal

Fasting ghrelin concentrations were similar between men (1.1 ng/ml, IQR 0.28; 1.7) and women (1.4 ng/ml, IQR 1.2; 1.9; p = 0.406) (Table 4). In women, ghrelin significantly decreased from baseline by 0.56 ng/ml (95% CI − 0.68; − 0.44) at 60 min, by 0.70 ng/ml (95% CI − 0.82; − 0.58) at 120 min, and by 0.58 ng/ml (95% CI − 0.70; − 0.46) at 180 min (η2 time = 0.78), displaying a slight rebound increment. In men, ghrelin changes overtime from basal were significantly different from those observed in women (sex*time interaction p = 0.005, η2 = 0.18). The decrement was more accentuated in women than in men at each time point [0.21 ng/ml (95% CI − 0.38; − 0.04) greater suppression at 60 min, 0.29 ng/ml (95% CI − 0.45; − 0.12) at 120 min, and 0.23 ng/ml (95% CI − 0.39; − 0.06) at 180 min]. Additional file 1: Table S2 shows the meal effect on ghrelin concentrations using men as reference.

Table 4 Meal effect on ghrelin secretion according sex and time

Moreover, median decremental area over ghrelin response curve was greater in women than in men (− 95, IQR − 122; − 66 vs. − 47, IQR − 87; − 31, p = 0.041, Cohen’s d = 0.94) (Table 5).

Table 5 Parameters of postprandial ghrelin response


Our results show that men, after consuming a balanced mixed meal, have delayed hunger suppression compared with women, who instead experience early satiety. This result is supported, at least in part, by a greater reduction in circulating ghrelin concentrations in the three hours following meal consumption in women then in men, although there were no statistically significant sex differences in fasting ghrelin concentrations. Compared with previous studies that observed higher fasting ghrelin concentrations in women than in men [11,12,13], we observed no sex differences. This may be due to the fact that we conducted the study with women in the follicular phase of the cycle, when estrogen concentrations are low, and lesser could be the modulatory activity they have on ghrelin concentration [29, 30]. Our results also show that men and women experienced different subjective perceptions of hunger and satiety although the mean ghrelin values at the various times were similar. Currently, it is not possible to associate absolute levels of ghrelin concentration with subjective measures of appetite. In addition, ghrelin levels are confounded by many factors. The result is a large inter-subject variability in ghrelin levels that may not be associated with different perceptions of hunger and satiety. On the contrary, rapid variations in ghrelin within the individual provide a strong physiological signal related to subjective measures of satiety.

Our results in postprandial appetite ratings are in agreement with previous findings showing women to experience a greater satiety than men after an ad libitum consumption of a liquid or solid balanced mixed meal [15,16,17]. Several mechanisms have been proposed to explain this result. First, female sex hormones, particularly estrogen, are known to be implicated in the regulation of food intake, as they modulate responsiveness to anorectic hormones such as leptin, cholecystokinin, GLP-1, and peptide YY, both at the level of vagal afferent neurons and at the level of nuclei in the central nervous system [31], and therefore may have contributed to more rapid suppression of appetite in women. Second, it is possible that the meal resulted in a greater increment in CCK in women than in men [18]. The increase in postprandial CCK also appears to be associated with a greater increase in fullness and greater decrease in hunger in women than in men [19]. Note that these results were obtained by administering meals having 20–30% of calories from fat, similarly to the meal we provided. Third, several studies observed sex-specific brain areas activation in response to hunger and satiation [17, 32], as well as in response to food stimuli [17, 33], suggesting sex-specific differences in the cognitive and emotional processing of hunger and satiation. Additionally, our data show sex-related difference in postmeal ghrelin decrement which may furtherly explain the differences between men and women in the appetite regulation. This difference does not appear to be influenced by a different postprandial glucose metabolism between sexes. Insulin is known to influence circulating ghrelin levels. However, we recently found that men and women had the same glycemic, insulinemic, and C-peptidemic response by administering the same meal protocol presented in this study [34].

To the best of our knowledge, this is the first study reporting sex differences in ghrelin concentrations after consuming a balanced mixed meal. Previous studies regarding this topic were limited and the results conflicting. Carroll et al. [35] did not detect sex difference in ghrelin concentrations in the first 60 min after administration of an ad libitum liquid mixed meal with fixed nutrients amounts. Differently, Greenman et al. [36] observed higher ghrelin concentrations in women compared with men after administration of an oral load of glucose and lipids, but not protein. Our results differ from those reported in these studies and the first reason for this discrepancy may be in the meal administration protocol. It has been reported that men are more likely to overeat when asked to consume an ad libitum meal, whereas women are more likely to maintain an isocaloric intake [17]. The different amounts of food consumed may have influenced the pattern of postprandial hormones, preventing detection of sex differences. On the other hand, the standardization on individual energy needs of a whole mixed meal to be consumed, allows to study the postprandial physiological response of hormones influencing hunger and satiety. In addition, the effect observed by ingesting solutions containing single nutrients might not reflect the effect of nutrients within a complex matrix, as is the case of a meal. It has been observed that the ingestion of isocaloric beverages with one prevailing nutrient led to different results from those observed after single-nutrient oral load [37]. In the present study, we administer a meal complying the nutritional recommendations for a healthy, balanced meal [24] and therefore the results can be considered representative of reality. However, it cannot be excluded that a meal with a very different nutritional composition, or a vegetarian or vegan meal, which would contribute to higher fiber intake, may lead to different results. Finally, standardizing on individual energy expenditure controls for sex-related differences in body composition that could affect ghrelin concentrations. The second reason that might explain the discrepancy with previous studies is the homogeneity, in terms of age and nutritional status, of the subjects involved in the present study. Both appetite ratings and ghrelin concentrations have been found to change between age and BMI classes [15, 21, 38, 39]. Therefore, recruitment of subjects homogeneous in age and nutritional status allowed us to limit variability due to these factors.

Despite the peculiarities and strengths just described, we recognize that the present study is not without its limitations. Although the sample size calculation suggested that recruitment of 24 subjects was sufficient to detect a significant difference, this is still a small sample size. Although homogeneous recruitment by age and nutritional status limited the variability among subjects, this limits the generalizability of the results. It is not possible to transfer the results presented here to older or overweight or obese subjects without prior confirmation. A further limitation of the generalizability of these results is the recruitment of Caucasian subjects only. Indeed, ethnicity-related differences in postprandial ghrelin suppression have been reported [40], and thus these results need confirmation in subjects of non-Caucasian ethnicity. A further limitation of the study is that resting energy expenditure was estimated using the Harris & Benedict formula. However, we recently showed good agreement and low percent bias between predicted and measured resting energy expenditure in normal weight individuals [41]. A final limitation is that we did not measure leptin and other gastrointestinal hormones involved in the regulation of appetite, as well as we did not measure sex hormones. However, to reduce the variability associated with different concentrations of female sex hormones during different phases of the cycle, the study was conducted when the women were in the follicular phase of the menstrual cycle. Nevertheless, it should be reminded that estradiol levels vary significantly between each individual woman even within the same menstrual phase.

Perspectives and significance

The sexual dimorphism observed in appetite perception and ghrelin suppression underlines the importance of potentially studying men and women as separate groups and of considering sex in the design of nutritional strategies for the prevention and management of obesity and eating disorders. Future studies on this issue that consider other population groups (elderly, obese, etc.) are strongly required.


In conclusion, our results support the hypothesis of different appetite regulation between men and women, in part due to different postprandial ghrelin regulation. When a balanced mixed meal is ingested, women present a greater satiety immediately after the meal consumption, whereas men exhibit delayed hunger suppression, supported by a smaller decrease in postprandial ghrelin.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.


  1. Hainerová IA, Lebl J. Mechanisms of appetite regulation. J Pediatr Gastroenterol Nutr. 2010;51:1213–2124.

    Article  Google Scholar 

  2. Dhillo WS, Bloom SR. Gastrointestinal hormones and regulation of food intake. Horm Metab Res. 2004;36(11–12):846–51.

    Article  CAS  PubMed  Google Scholar 

  3. Freire RH, Alvarez-Leite JI. Appetite control: hormones or diet strategies? Curr Opin Clin Nutr Metab Care. 2020;23(5):328–35.

    Article  CAS  PubMed  Google Scholar 

  4. Yu JH, Kim M-S. Molecular mechanisms of appetite regulation. Diabetes Metab J. 2012;36(6):391–8.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Camilleri M. Peripheral mechanisms in appetite regulation. Gastroenterology. 2015;148(6):1219–33.

    Article  CAS  PubMed  Google Scholar 

  6. Geliebter A, Ochner CN, Aviram-Friedman R. Appetite-related gut peptides in obesity and binge eating disorder. Am J Lifestyle Med. 2008;2(4):305–14.

    Article  PubMed  Google Scholar 

  7. Mihalache L, Gherasim A, Niţă O, Ungureanu MC, Pădureanu SS, Gavril RS, et al. Effects of ghrelin in energy balance and body weight homeostasis. Hormones (Athens). 2016;15(2):186–96.

    Article  Google Scholar 

  8. Pradhan G, Samson SL, Sun Y. Ghrelin: much more than a hunger hormone. Curr Opin Clin Nutr Metab Care. 2013;16(6):619–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Cummings DE, Purnell JQ, Frayo RS, Schmidova K, Wisse BE, Weigle DS. A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans. Diabetes. 2001;50(8):1714–9.

    Article  CAS  PubMed  Google Scholar 

  10. Clegg DJ, Brown LM, Zigman JM, Kemp CJ, Strader AD, Benoit SC, et al. Estradiol-dependent decrease in the orexigenic potency of ghrelin in female rats. Diabetes. 2007;56(4):1051–8.

    Article  CAS  PubMed  Google Scholar 

  11. Makovey J, Naganathan V, Seibel M, Sambrook P. Gender differences in plasma ghrelin and its relations to body composition and bone - an opposite-sex twin study. Clin Endocrinol (Oxf). 2007;66(4):530–7.

    Article  CAS  Google Scholar 

  12. Beasley JM, Ange BA, Anderson CA, Miller Iii ER, Holbrook JT, Appel LJ. Characteristics associated with fasting appetite hormones (obestatin, ghrelin, and leptin). Obesity (Silver Spring). 2009;17(2):349–54.

    Article  CAS  Google Scholar 

  13. Tai K, Visvanathan R, Hammond AJ, Wishart JM, Horowitz M, Chapman IM. Fasting ghrelin is related to skeletal muscle mass in healthy adults. Eur J Nutr. 2009;48(3):176–83.

    Article  CAS  PubMed  Google Scholar 

  14. Cornier MA, Grunwald GK, Johnson SL, Bessesen DH. Effects of short-term overfeeding on hunger, satiety, and energy intake in thin and reduced-obese individuals. Appetite. 2004;43(3):253–9.

    Article  PubMed  Google Scholar 

  15. Gregersen NT, Møller BK, Raben A, Kristensen ST, Holm L, Flint A, et al. Determinants of appetite ratings: the role of age, gender, BMI, physical activity, smoking habits, and diet/weight concern. Food Nutr Res. 2011.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Bédard A, Hudon A-M, Drapeau V, Corneau L, Dodin S, Lemieux S. Gender differences in the appetite response to a satiating diet. J Obes. 2015;2015: 140139.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Cornier MA, Salzberg AK, Endly DC, Bessesen DH, Tregellas JR. Sex-based differences in the behavioral and neuronal responses to food. Physiol Behav. 2010;99(4):538–43.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Nolan LJ, Guss JL, Liddle RA, Pi-Sunyer FX, Kissileff HR. Elevated plasma cholecystokinin and appetitive ratings after consumption of a liquid meal in humans. Nutrition. 2003;19(6):553–7.

    Article  CAS  PubMed  Google Scholar 

  19. Burton-Freeman B, Davis PA, Schneeman BO. Interaction of fat availability and sex on postprandial satiety and cholecystokinin after mixed-food meals. Am J Clin Nutr. 2004;80(5):1207–14.

    Article  CAS  PubMed  Google Scholar 

  20. Delporte C. Structure and physiological actions of ghrelin. Scientifica (Cairo). 2013;2013: 518909.

    Article  CAS  Google Scholar 

  21. Shiiya T, Nakazato M, Mizuta M, Date Y, Mondal MS, Tanaka M, et al. Plasma ghrelin levels in lean and obese humans and the effect of glucose on ghrelin secretion. J Clin Endocrinol Metab. 2002;87(1):240–4.

    Article  CAS  PubMed  Google Scholar 

  22. Bertoli S, Magni P, Krogh V, Ruscica M, Dozio E, Testolin G, et al. Is ghrelin a signal of decreased fat-free mass in elderly subjects? Eur J Endocrinol. 2006;155(2):321–30.

    Article  CAS  PubMed  Google Scholar 

  23. Harris JA, Benedict FG. A biometric study of human basal metabolism. Proc Natl Acad Sci U S A. 1918;4(12):370–3.

    Article  CAS  Google Scholar 

  24. Italian Society of Human Nutrition (SINU). Dietary reference values of nutrients and energy for the Italian population. (2014).

  25. Lohman TG, Roche AF, Martorell R. Anthropometric standardization reference manual. Champaign: Human Kinetics Books; 1988.

    Google Scholar 

  26. Durnin JV, Womersley J. Body fat assessed from total body density and its estimation from skinfold-thickness: measurements on 481 men and women aged from 16 to 72 years. Br J Nutr. 1974;32(1):77–97.

    Article  CAS  Google Scholar 

  27. Siri WE. Body composition from fluid spaces and density: analysis of methods. In: Brozek J, Henschel A, editors. Techniques for measuring body compositon. Washington: National Academy of Sciences - National Research Council; 1961. p. 223–44.

    Google Scholar 

  28. Spadafranca A, Rinelli S, Riva A, Morazzoni P, Magni P, Bertoli S, et al. Phaseolus vulgaris extract affects glycometabolic and appetite control in healthy human subjects. Br J Nutr. 2013;109(10):1789–95.

    Article  CAS  PubMed  Google Scholar 

  29. Kellokoski E, Pöykkö SM, Karjalainen AH, Ukkola O, Heikkinen J, Kesäniemi YA, et al. Estrogen replacement therapy increases plasma ghrelin levels. J Clin Endocrinol Metab. 2005;90(5):2954–63.

    Article  CAS  PubMed  Google Scholar 

  30. Paulo RC, Brundage R, Cosma M, Mielke KL, Bowers CY, Veldhuis JD. Estrogen elevates the peak overnight production rate of acylated ghrelin. J Clin Endocrinol Metab. 2008;93(11):4440–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Huang KP, Raybould HE. Estrogen and gut satiety hormones in vagus-hindbrain axis. Peptides. 2020;133: 170389.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Del Parigi A, Chen K, Gautier JF, Salbe AD, Pratley RE, Ravussin E, et al. Sex differences in the human brain’s response to hunger and satiation. Am J Clin Nutr. 2002;75(6):1017–22.

    Article  PubMed  Google Scholar 

  33. Smeets PA, de Graaf C, Stafleu A, van Osch MJ, Nievelstein RA, van der Grond J. Effect of satiety on brain activation during chocolate tasting in men and women. Am J Clin Nutr. 2006;83(6):1297–305.

    Article  CAS  PubMed  Google Scholar 

  34. Leone A, De Amicis R, Bertoli S, Spadafranca A, De Carlo G, Battezzati A. Absence of a sexual dimorphism in postprandial glucose metabolism after administration of a balanced mixed meal in healthy young volunteers. Nutr Diabetes. 2022;12:6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Carroll JF, Kaiser KA, Franks SF, Deere C, Caffrey JL. Influence of BMI and gender on postprandial hormone responses. Obesity (Silver Spring). 2007;15(12):2974–83.

    Article  CAS  Google Scholar 

  36. Greenman Y, Golani N, Gilad S, Yaron M, Limor R, Stern N. Ghrelin secretion is modulated in a nutrient- and gender-specific manner. Clin Endocrinol (Oxf). 2004;60(3):382–8.

    Article  CAS  Google Scholar 

  37. Foster-Schubert KE, Overduin J, Prudom CE, Liu J, Callahan HS, Gaylinn BD, et al. Acyl and total ghrelin are suppressed strongly by ingested proteins, weakly by lipids, and biphasically by carbohydrates. J Clin Endocrinol Metab. 2008;93(5):1971–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Purnell JQ, Weigle DS, Breen P, Cummings DE. Ghrelin levels correlate with insulin levels, insulin resistance, and high-density lipoprotein cholesterol, but not with gender, menopausal status, or cortisol levels in humans. J Clin Endocrinol Metab. 2003;88(12):5747–52.

    Article  CAS  PubMed  Google Scholar 

  39. Nass R, Farhy LS, Liu J, Pezzoli SS, Johnson ML, Gaylinn BD, et al. Age-dependent decline in acyl-ghrelin concentrations and reduced association of acyl-ghrelin and growth hormone in healthy older adults. J Clin Endocrinol Metab. 2014;99(2):602–8.

    Article  CAS  PubMed  Google Scholar 

  40. Brownley KA, Light KC, Grewen KM, Bragdon EE, Hinderliter AL, West SG. Postprandial ghrelin is elevated in black compared with white women. J Clin Endocrinol Metab. 2004;89(9):4457–63.

    Article  CAS  PubMed  Google Scholar 

  41. Bedogni G, Bertoli S, Leone A, De Amicis R, Lucchetti E, Agosti F, et al. External validation of equations to estimate resting energy expenditure in 14,952 adults with overweight and obesity and 1948 adults with normal weight from Italy. Clin Nutr. 2019;38(1):457–64.

    Article  PubMed  Google Scholar 

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We are indebted to the volunteers for their participation in the study. We thank Angela Spadafranca and the ICANS' laboratory technicians, in particular, Stefano Ravasenghi, Giovanni Fiorillo and Franca Criscuoli for their work.


This research did not receive any specific grant. It was funded by ICANS internal grant. The University of Milan partially covered the open access APC through the APC initiative.

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Authors and Affiliations



AL and AB conceptualized and designed the study; AL, RD, SB and AB conducted the experiment; AL created and managed the database; AL performed the statistical analysis; MP and SR searched for and reviewed literature; AL wrote the original draft; AL, RD, SB and AB reviewed and edited the manuscript. All authors have read and agreed to the published version of the manuscript.

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Correspondence to Alessandro Leone.

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The ethics committee of the University of Milan gave a positive opinion on the study (Protocol No. 32/17). Written informed consent was obtained from all participants.

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The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Table S1.

Meal effect on appetite rating according sex and time (using men as reference). Table S2. Meal effect on ghrelin according sex and time (using men as reference) (DOCX 15 KB)

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Leone, A., De Amicis, R., Pellizzari, M. et al. Appetite ratings and ghrelin concentrations in young adults after administration of a balanced meal. Does sex matter?. Biol Sex Differ 13, 25 (2022).

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