Abstract
Background
Ghrelin, a known orexigenic hormone, has been demonstrated to be produced and released by salivary glands. Obtaining saliva for metabolism studies would be preferable for patients since the procedure is non-invasive.
Methods
The present study examined serum and salivary ghrelin levels in 41 morbidly obese subjects, 45 healthy controls, and 17 patients with metastatic carcinoma by using a commercial radioimmunoassay.
Results
When comparing serum and salivary levels under fasting conditions, ghrelin levels were significantly higher in saliva for morbidly obese and healthy subjects. A significant correlation between salivary and serum ghrelin could only be demonstrated for healthy subjects. Fasting serum ghrelin concentrations in morbidly obese patients were significantly lower compared with healthy controls and cancer patients, however the levels in whole saliva did not differ significantly between all groups. There was only a highly significant inverse correlation between BMI and serum ghrelin. Serum ghrelin correlated positively with age in morbidly obese. There was no significant difference in serum and saliva ghrelin concentrations between men and women. Following the standardized meal, no significant suppression of serum ghrelin levels in morbidly obese was observed, however salivary ghrelin concentrations were significantly decreased.
Conclusions
The results of the present study support the hypothesis that there is an autonomous production of ghrelin in the salivary glands. Further research should focus on factors involved in the regulation of salivary ghrelin. Until the mechanism of regulation is fully understood, the testing of ghrelin levels in saliva is too limited to recommend a switch from serum testing.
Similar content being viewed by others
References
Kojima M, Hosoda H, Date Y, et al. Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature. 1999;402:656–60.
Aydin S, Halifeoglu I, Ozercan IH, et al. A comparison of leptin and ghrelin levels in plasma and saliva of young healthy subjects. Peptides. 2005;26:647–52.
Gröschl M, Topf HG, Bohlender J, et al. Identification of ghrelin in human saliva: production by the salivary glands and potential role in proliferation of oral keratinocytes. Clin Chem. 2005;51:997–1006.
Aydin S, Aydin S, Ozkan Y, et al. Ghrelin is present in human colostrum, transitional and mature milk. Peptides. 2006;27:878–82.
Yoshimoto A, Mori K, Sugawara A, et al. Plasma ghrelin and desacyl ghrelin concentrations in renal failure. J Am Soc Nephrol. 2002;13:2748–52.
Otto B, Spranger J, Benoit SC, et al. The many faces of ghrelin: new perspectives for nutrition research? Br J Nutr. 2005;93:765–71.
Busch P, Wolter S, Rawnaq T, et al. Operative technique and outcome in metabolic surgery: conventional and banded gastric bypass. Zentralbl Chir. 2009;134:32–7.
Tschöp M, Weyer C, Tataranni PA, et al. Circulating ghrelin levels are decreased in human obesity. Diabetes. 2001;50:707–9.
Cummings DE, Purnell JQ, Frayo RS, et al. A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans. Diabetes. 2001;50:1714–19.
Hüttl TP, Obeidat FW, Parhofer KG, et al. Operative techniques and outcomes in metabolic surgery: sleeve gastrectomy. Zentralbl Chir. 2009;134:24–31.
Gröschl M, Topf HG, Rauh M, et al. Postprandial response of salivary ghrelin and leptin to carbohydrate uptake. Gut. 2006;55:433–4.
English PJ, Ghatei MA, Malik IA, et al. Food fails to suppress ghrelin levels in obese humans. J Clin Endocrinol Metab. 2002;87:2984.
le Roux CW, Patterson M, Vincent RP, et al. Postprandial plasma ghrelin is suppressed proportional to meal calorie content in normal-weight but not obese subjects. J Clin Endocrinol Metab. 2005;90:1068–71.
McLaughlin T, Abbasi F, Lamendola C, et al. Plasma ghrelin concentrations are decreased in insulin-resistant obese adults relative to equally obese insulin-sensitive controls. J Clin Endocrinol Metab. 2004;89:1630–5.
Aydin S. A comparison of ghrelin, glucose, alpha-amylase and protein levels in saliva from diabetics. J Biochem Mol Biol. 2007;40:29–35.
Ozbay Y, Aydin S, Dagli AF, et al. Obestatin is present in saliva: alterations in obestatin and ghrelin levels of saliva and serum in ischemic heart disease. BMB Rep. 2008;41:55–61.
Dynesen AW, Bardow A, Astrup A, et al. Meal-induced compositional changes in blood and saliva in persons with bulimia nervosa. Am J Clin Nutr. 2008;87:12–22.
Shimizu Y, Nagaya N, Isobe T, et al. Increased plasma ghrelin level in lung cancer cachexia. Clin Cancer Res. 2003;9:774–8.
Garcia JM, Garcia-Touza M, Hijazi RA, et al. Active ghrelin levels and active to total ghrelin ratio in cancer-induced cachexia. J Clin Endocrinol Metab. 2005;90:2920–6.
Cetinkaya Z, Aydin S, Cerrahoglu YZ, et al. Changes in appetite hormone (ghrelin) levels of saliva and serum in acute appendicitis cases before and after operation. Appetite. 2009;52:104–7.
Aygen B, Dogukan A, Dursun FE, et al. Ghrelin and obestatin levels in end-stage renal disease. J Int Med Res. 2009;37:757–65.
Aydin S, Dag E, Ozkan Y, et al. Nesfatin-1 and ghrelin levels in serum and saliva of epileptic patients: hormonal changes can have a major effect on seizure disorders. Mol Cell Biochem. 2009;328:49–56.
Morínigo R, Casamitjana R, Moizé V, et al. Short-term effects of gastric bypass surgery on circulating ghrelin levels. Obes Res. 2004;12:1108–16.
Garcia-Fuentes E, Garrido-Sanchez L, Garcia-Almeida JM, et al. Different effect of laparoscopic Roux-en-Y gastric bypass and open biliopancreatic diversion of Scopinaro on serum PYY and ghrelin levels. Obes Surg. 2008;18:1424–9.
Ariyasu H, Takaya K, Tagami T, et al. Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans. J Clin Endocrinol Metab. 2001;86:4753–8.
Bauer JM, Wirth R, Troegner J, et al. Ghrelin, anthropometry and nutritional assessment in geriatric hospital patients. Z Gerontol Geriatr. 2007;40:31–6.
Rigamonti AE, Pincelli AI, Corrà B, et al. Plasma ghrelin concentrations in elderly subjects: comparison with anorexic and obese patients. J Endocrinol. 2002;175:R1–5.
Marchesini G, Bianchi G, Lucidi P, et al. Plasma ghrelin concentrations, food intake, and anorexia in liver failure. J Clin Endocrinol Metab. 2004;89:2136–41.
Purnell JQ, Weigle DS, Breen P, et al. 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;88:5747–52.
Whitson BA, Leslie DB, Kellogg TA, et al. Entero-endocrine changes after gastric bypass in diabetic and nondiabetic patients: a preliminary study. J Surg Res. 2007;141:31–9.
Barazzoni R, Zanetti M, Ferreira C, et al. Relationships between desacylated and acylated ghrelin and insulin sensitivity in the metabolic syndrome. J Clin Endocrinol Metab. 2007;92:3935–40.
Acknowledgment
We thank Ruma Makarowa, Institute of Clinical Chemistry and Pathobiochemistry, University Magdeburg, for her support in the laboratory.
Conflict of Interest Disclosure
The authors declare that they have no conflict of interest.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Benedix, F., Westphal, S., Patschke, R. et al. Comparison of Serum and Salivary Ghrelin in Healthy Adults, Morbidly Obese, and Patients with Metastatic Carcinoma. OBES SURG 21, 1265–1271 (2011). https://doi.org/10.1007/s11695-010-0161-8
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11695-010-0161-8