Publication
Unacylated ghrelin does not seem to influence glucose homeostasis in obese women
dc.contributor.author | Silva-Nunes, José | |
dc.contributor.author | Brito, Miguel | |
dc.contributor.author | Silva, Carina | |
dc.contributor.author | Oliveira, Ana Cebola | |
dc.contributor.author | Veiga, Luísa | |
dc.date.accessioned | 2017-12-11T16:56:10Z | |
dc.date.available | 2017-12-11T16:56:10Z | |
dc.date.issued | 2017-05 | |
dc.description.abstract | Background and Aim: Unacylated ghrelin (UAG) is the major form of circulating ghrelin. Initially considered as a non-functional peptide, soon after UAG has been associated with a negative action on energy balance, suppression of hepatic glucose production and a decrease in circulating levels of insulin. The aim of this study was to analyze the association between the serum levels of UAG and glucose metabolism parameters in obese women, independently from the eventual interference of adiposity. Material and Methods: One hundred lean and 254 obese Caucasian women were studied. Each woman was characterized for total body weight, body mass index (BMI), waist and hip circumferences, glucose at fasting and 2 hours after an oral glucose tolerance test (OGTT), fasting insulin, glycated hemoglobin (HbA1c), and UAG. Insulin resistance was assessed by the homeostasis model assessment (HOMA-IR). Obese women were classified into three glycemic status subgroups (normoglycemia, prediabetes, and diabetes) according to HbA1c and glucose values. Results: When compared with the lean group, significantly lower UAG levels were observed in obese women when compared with the lean group (350.2±251.9 vs 219.2±149.7 pg/ml; P<0.001). However, no significant difference was observed through obesity classes I to III. UAG levels were not significantly different among glycemic status subgroups and did not show any direct association with glucose, insulin, HOMA-IR, or HbA1c values. Conclusions: Although the level of the unacylated form of ghrelin shows an association with anthropometrics it seems not to be involved in glucose homeostasis. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Silva-Nunes J, Brito M, Silva C, Oliveira A, Veiga L. Unacylated ghrelin does not seem to influence glucose homeostasis in obese women. In: 19th European Congress of Endocrinology 2017, 20-23 May 2017, Lisbon (Portugal). Endocr Abs. 2017;49:EP451. | pt_PT |
dc.identifier.doi | 10.1530/endoabs.49.EP451 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.21/7680 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | BioScientifica | pt_PT |
dc.relation.publisherversion | http://www.endocrine-abstracts.org/ea/0049/ea0049ep451.htm | pt_PT |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | pt_PT |
dc.subject | Endocrinology | pt_PT |
dc.subject | Obesity | pt_PT |
dc.subject | Woman | pt_PT |
dc.subject | Glucose homeostasis | pt_PT |
dc.subject | Unacylated ghrelin | pt_PT |
dc.subject | Anthropometrics | pt_PT |
dc.title | Unacylated ghrelin does not seem to influence glucose homeostasis in obese women | pt_PT |
dc.type | conference object | |
dspace.entity.type | Publication | |
oaire.citation.endPage | EP451 | pt_PT |
oaire.citation.startPage | EP451 | pt_PT |
oaire.citation.title | Endocrine Abstracts | pt_PT |
oaire.citation.volume | 49 | pt_PT |
person.familyName | Brito | |
person.familyName | Veiga | |
person.givenName | Miguel | |
person.givenName | Luisa | |
person.identifier.ciencia-id | 231F-F341-7E93 | |
person.identifier.ciencia-id | 9413-918D-DB0E | |
person.identifier.orcid | 0000-0001-6394-658X | |
person.identifier.orcid | 0000-0003-1153-8343 | |
person.identifier.rid | A-7970-2016 | |
person.identifier.rid | L-2730-2013 | |
person.identifier.scopus-author-id | 35224551000 | |
person.identifier.scopus-author-id | 8318978600 | |
rcaap.rights | openAccess | pt_PT |
rcaap.type | conferenceObject | pt_PT |
relation.isAuthorOfPublication | 4252d8e0-800c-4d67-8b13-0b711d860669 | |
relation.isAuthorOfPublication | aac1914a-275f-4be2-819d-ab41d356b45a | |
relation.isAuthorOfPublication.latestForDiscovery | aac1914a-275f-4be2-819d-ab41d356b45a |
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