Author:
Wu Hai-Yan,Li Nai-Shi,Song Yu-Li,Bai Chun-Mei,Wang Qiang,Zhao Yu-Pei,Xiao Yu,Yu Shuang,Li Ming,Chen Yuan-Jia
Abstract
Abstract
Background
Insulinoma is a subtype of pancreatic neuroendocrine tumors. Many patients with insulinoma are obese due to frequent food intake. Ghrelin is associated with obesity and blood levels of insulin. It is not clear if plasma levels of ghrelin in insulinoma patients correlate with hyperinsulinemia and obesity. Expression of ghrelin and its receptor has not been well demonstrated in insulinoma.
Objective
To study if plasma levels of ghrelin is associated with obesity and hyperinsulinemia or hyperproinsulinemia in patients with insulinoma, and to detect the expression of ghrelin and its receptor in insulinoma.
Methods
Plasma levels of acylated ghrelin, insulin, and proinsulin were measured in 37 patients with insulinoma and 25 controls by ELISA. Expression of ghrelin and its receptor GHS-R1A was examined in 20 insulinoma and paired pancreatic specimens by immunostaining. P ≤ 0.05 was considered significant.
Results
The plasma levels of acylated ghrelin in patients with insulinoma were significantly lower than that in the controls (median 15 pg/ml vs. 19 pg/ml, respectively, P = 0.016). The reduced plasma levels of acylated ghrelin in patients were significantly correlated with obesity, hyperinsulinemia, and hyperproinsulinemia (P = 0.029 and P = 0.028, respectively). Expression of ghrelin and its receptor GHS-R1A was shown in the majority of insulinoma specimens. The expression of GHS-R1A was positively correlated with ghrelin expression in insulinoma (P = 0.014).
Conclusions
Plasma levels of acylated ghrelin decreased in patients with insulinoma, probably due to the hyperinsulinemia and obesity in the patients. Expression of both ghrelin and its receptor is common in insulinoma.
Funder
Chinese Academy of Medical Sciences (CAMS) Initiative for Innovative Medicine
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference49 articles.
1. Y.M. Jonkers, F.C. Ramaekers, E.J. Speel, Molecular alterations during insulinoma tumorigenesis. Biochim Biophys. Acta 1775, 313–332 (2007). https://doi.org/10.1016/j.bbcan.2007.05.004
2. M.G. House, R.D. Schulick, Endocrine tumors of the pancreas. Curr. Opin. Oncol. 18, 23–29 (2006)
3. R. Arnold, A. Rinke, M. Anlauf, Persistent hyperinsulinemic hypoglycemia (PHH) in adults: insulinoma and nesidioblastosis. In A Century of Advances in Neuroendocrine Tumor Biology and Treatment, ed. by I.M. Modlin and K. Oberg (Felsenstein, C.C.C.P, Montreaux, 2008), p. 76–85
4. A. Mathur, P. Gorden, S.K. Libutti, Insulinoma. Surg. Clin. North Am. 89, 1105–1121 (2009). https://doi.org/10.1016/j.suc.2009.06.009
5. W. Bonfig, P. Kann, M. Rothmund, H.P. Schwarz, Recurrent hypoglycemic seizures and obesity: delayed diagnosis of an insulinoma in a 15 year-old boy-final diagnostic localization with endosonography. J. Pediatr. Endocrinol. Metab. 20, 1035–1038 (2007)
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