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dc.contributor.authorPena-Bello, Lara
dc.contributor.authorSeoane-Pillado, Teresa
dc.contributor.authorSangiao-Alvarellos, Susana
dc.contributor.authorOuteiriño-Blanco, Elena
dc.contributor.authorVarela-Rodríguez, Bárbara María
dc.contributor.authorJuiz-Valiña, Paula
dc.contributor.authorCordido, María
dc.contributor.authorCordido, Fernando
dc.date.accessioned2017-10-31T11:12:13Z
dc.date.issued2017-06-09
dc.identifier.citationPena-Bello L, Seoane-Pillado T, Sangiao-Alvarellos S, et al. Oral glucose-stimulated growth hormone (GH) test in adult GH deficiency patients and controls: potential utility of a novel test. Eur J Intern Med. 2017;44:55-61es_ES
dc.identifier.issn0953-6205
dc.identifier.issn1879-0828
dc.identifier.urihttp://hdl.handle.net/2183/19669
dc.description.abstract[Abstract] Context. The diagnosis of adult GH deficiency requires confirmation with a GH stimulation test. Oral glucose (OG) administration affects GH secretion, initially decreasing and subsequently stimulating GH secretion. Objective. The aim of this study was to investigate the diagnostic efficacy and safety of a long OG test (LOGT) as a stimulus of GH secretion for the diagnosis of adult GH deficiency (AGHD). Design. Prospective experimental cross-sectional study. Settings. The study was conducted at the Endocrinology department of the University Hospital of a Coruña, Spain. Participants and methods. We included 60 (40 women) AGHD patients (15) and controls (45) paired 1:3, of similar age, sex and BMI. The area under the curve (AUC) and peak were calculated for GH. The Mann-Whitney test was used to compare the different groups. ROC curve analyses were used. p-Values < 0.05 were considered as statistically significant. Interventions. The intervention consisted of orally administering 75 g oral glucose administration; GH was obtained every 30 min for a total of 300 min. Main outcome measurement. Peak GH area under receiver operating characteristic curve (ROC-AUC) following LOGT. Results. Peak GH (μg/L) levels were lower in the AGHD patients (0.26 ± 0.09) than in the controls (4.00 ± 0.45), p < 0.001. After LOGT, with the ROC plot analysis the best peak GH cut-point was 1.0 μg/L, with 100% sensitivity, 78% specificity, ROC-AUC of 0.9089 and 81.82% accuracy. There were no relevant adverse events during any of the LOGT. Conclusions. The LOGT could be a cheap, safe, convenient and effective test for the diagnosis of AGHD.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III; PI13/00322es_ES
dc.description.sponsorshipInstituto de Salud Carlos III; PI16/00884es_ES
dc.description.sponsorshipXunta de Galicia; 10CSA916014PRes_ES
dc.language.isoenges_ES
dc.publisherElsevier para European Federation of Internal Medicinees_ES
dc.relation.urihttp://dx.doi.org/10.1016/j.ejim.2017.06.004es_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectGHes_ES
dc.subjectGlucosees_ES
dc.subjectStimulationes_ES
dc.subjectTestes_ES
dc.titleOral glucose-stimulated growth hormone (GH) test in adult GH deficiency patients and controls: potential utility of a novel testes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/embargoedAccesses_ES
dc.date.embargoEndDate2018-06-09es_ES
dc.date.embargoLift2018-06-09
UDC.journalTitleEuropean Journal of Internal Medicinees_ES
UDC.volume44es_ES
UDC.startPage55es_ES
UDC.endPage61es_ES


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