Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?

To date, the value of fasting plasma acylated ghrelin (AG) and unacylated ghrelin (UAG) as potential novel biomarkers in patients with neuroendocrine tumors (NETs) is unknown.The aims of this study are to (i) compare fasting AG and UAG levels between nonobese, nondiabetic NET patients (N = 28) and a...

Full description

Bibliographic Details
Main Authors: Roxanne C S van Adrichem, Aart Jan van der Lely, Martin Huisman, Richard A Feelders, Patric J D Delhanty, Wouter W de Herder, Piet Kramer
Format: Article
Language:English
Published: Bioscientifica 2016-07-01
Series:Endocrine Connections
Subjects:
Online Access:http://www.endocrineconnections.com/content/5/4/143
id doaj-954857acb1824615afe1e80edf32fd7e
record_format Article
spelling doaj-954857acb1824615afe1e80edf32fd7e2020-11-24T21:39:08ZengBioscientificaEndocrine Connections2049-36142049-36142016-07-015414315110.1530/EC-16-0021Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?Roxanne C S van Adrichem0Aart Jan van der Lely1Martin Huisman2Richard A Feelders3Patric J D Delhanty4Wouter W de Herder5Piet Kramer6Department of Internal Medicine, Sector of Endocrinology, ENETS Centre of Excellence for Neuroendocrine Tumors, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Sector of Endocrinology, ENETS Centre of Excellence for Neuroendocrine Tumors, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Sector of Endocrinology, ENETS Centre of Excellence for Neuroendocrine Tumors, Erasmus MC, Rotterdam, The NetherlandsDepartment of Internal Medicine, Erasmus MC, Rotterdam, The NetherlandsTo date, the value of fasting plasma acylated ghrelin (AG) and unacylated ghrelin (UAG) as potential novel biomarkers in patients with neuroendocrine tumors (NETs) is unknown.The aims of this study are to (i) compare fasting AG and UAG levels between nonobese, nondiabetic NET patients (N = 28) and age- (±3 years) and sex-matched nonobese, nondiabetic controls (N = 28); and (ii) study the relationship between AG, UAG, and AG/UAG ratios and biochemical (chromogranin-A (CgA) and neuron-specific enolase (NSE) levels) and clinical parameters (age at diagnosis, sex, primary tumor location, carcinoid syndrome, ENETS TNM classification, Ki-67 proliferation index, grading, prior incomplete surgery) in NET patients. Fasting venous blood samples (N = 56) were collected and directly stabilized with 4-(2-aminoethyl) benzenesulfonyl fluoride hydrochloride after withdrawal. Plasma AG and UAG levels were determined by ELISA. Expression of ghrelin was examined in tumor tissue by immunohistochemistry. There were no significant differences between NET patients and controls in AG (median: 62.5 pg/mL, IQR: 33.1–112.8 vs median: 57.2 pg/mL, IQR: 26.7–128.3, P = 0.66) and UAG in levels (median: 76.6 pg/mL, IQR: 35.23–121.7 vs median: 64.9, IQR: 27.5–93.1, P = 0.44). No significant correlations were found between AG, UAG, and AG/UAG ratios versus biochemical and clinical parameters in NET patients with the exception of age at diagnosis (AG: ρ = −0.47, P = 0.012; AG/UAG ratio: ρ = −0.50, P = 0.007) and baseline chromogranin-A levels (AG/UAG ratio: ρ = −0.44, P = 0.019). In our view, fasting plasma acylated and unacylated ghrelin appear to have no value as diagnostic biomarkers in the clinical follow-up of patients with NETs.http://www.endocrineconnections.com/content/5/4/143neuroendocrine tumors (NETs)human unacylated ghrelin (UAG)human acylated ghrelin (AG)biomarker
collection DOAJ
language English
format Article
sources DOAJ
author Roxanne C S van Adrichem
Aart Jan van der Lely
Martin Huisman
Richard A Feelders
Patric J D Delhanty
Wouter W de Herder
Piet Kramer
spellingShingle Roxanne C S van Adrichem
Aart Jan van der Lely
Martin Huisman
Richard A Feelders
Patric J D Delhanty
Wouter W de Herder
Piet Kramer
Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
Endocrine Connections
neuroendocrine tumors (NETs)
human unacylated ghrelin (UAG)
human acylated ghrelin (AG)
biomarker
author_facet Roxanne C S van Adrichem
Aart Jan van der Lely
Martin Huisman
Richard A Feelders
Patric J D Delhanty
Wouter W de Herder
Piet Kramer
author_sort Roxanne C S van Adrichem
title Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
title_short Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
title_full Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
title_fullStr Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
title_full_unstemmed Plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
title_sort plasma acylated and plasma unacylated ghrelin: useful new biomarkers in patients with neuroendocrine tumors?
publisher Bioscientifica
series Endocrine Connections
issn 2049-3614
2049-3614
publishDate 2016-07-01
description To date, the value of fasting plasma acylated ghrelin (AG) and unacylated ghrelin (UAG) as potential novel biomarkers in patients with neuroendocrine tumors (NETs) is unknown.The aims of this study are to (i) compare fasting AG and UAG levels between nonobese, nondiabetic NET patients (N = 28) and age- (±3 years) and sex-matched nonobese, nondiabetic controls (N = 28); and (ii) study the relationship between AG, UAG, and AG/UAG ratios and biochemical (chromogranin-A (CgA) and neuron-specific enolase (NSE) levels) and clinical parameters (age at diagnosis, sex, primary tumor location, carcinoid syndrome, ENETS TNM classification, Ki-67 proliferation index, grading, prior incomplete surgery) in NET patients. Fasting venous blood samples (N = 56) were collected and directly stabilized with 4-(2-aminoethyl) benzenesulfonyl fluoride hydrochloride after withdrawal. Plasma AG and UAG levels were determined by ELISA. Expression of ghrelin was examined in tumor tissue by immunohistochemistry. There were no significant differences between NET patients and controls in AG (median: 62.5 pg/mL, IQR: 33.1–112.8 vs median: 57.2 pg/mL, IQR: 26.7–128.3, P = 0.66) and UAG in levels (median: 76.6 pg/mL, IQR: 35.23–121.7 vs median: 64.9, IQR: 27.5–93.1, P = 0.44). No significant correlations were found between AG, UAG, and AG/UAG ratios versus biochemical and clinical parameters in NET patients with the exception of age at diagnosis (AG: ρ = −0.47, P = 0.012; AG/UAG ratio: ρ = −0.50, P = 0.007) and baseline chromogranin-A levels (AG/UAG ratio: ρ = −0.44, P = 0.019). In our view, fasting plasma acylated and unacylated ghrelin appear to have no value as diagnostic biomarkers in the clinical follow-up of patients with NETs.
topic neuroendocrine tumors (NETs)
human unacylated ghrelin (UAG)
human acylated ghrelin (AG)
biomarker
url http://www.endocrineconnections.com/content/5/4/143
work_keys_str_mv AT roxannecsvanadrichem plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT aartjanvanderlely plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT martinhuisman plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT richardafeelders plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT patricjddelhanty plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT wouterwdeherder plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
AT pietkramer plasmaacylatedandplasmaunacylatedghrelinusefulnewbiomarkersinpatientswithneuroendocrinetumors
_version_ 1725932454265487360