Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/42242
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dc.contributor.authorLeón-Justel, Antonioen_US
dc.contributor.authorMadrazo-Atutxa, Ainaraen_US
dc.contributor.authorAlvarez-Rios, Ana I.en_US
dc.contributor.authorInfantes-Fontán, Rocioen_US
dc.contributor.authorGarcia-Arnés, Juan A.en_US
dc.contributor.authorLillo-Muñoz, Juan A.en_US
dc.contributor.authorAulinas, Annaen_US
dc.contributor.authorUrgell-Rull, Eulàliaen_US
dc.contributor.authorBoronat, Mauroen_US
dc.contributor.authorSánchez-De-Abajo, Anaen_US
dc.contributor.authorFajardo-Montañana, Carmenen_US
dc.contributor.authorOrtuño-Alonso, Marioen_US
dc.contributor.authorSalinas-Vert, Isabelen_US
dc.contributor.authorGranada, María L.en_US
dc.contributor.authorCano, David A.en_US
dc.contributor.authorLeal-Cerro, Alfonsoen_US
dc.date.accessioned2018-10-24T11:37:17Z-
dc.date.available2018-10-24T11:37:17Z-
dc.date.issued2016en_US
dc.identifier.issn0021-972Xen_US
dc.identifier.urihttp://hdl.handle.net/10553/42242-
dc.description.abstractContext: Cushing's syndrome (CS) is challenging to diagnose. Increased prevalence of CS in specific patient populations has been reported, but routine screening for CS remains questionable. To decrease the diagnostic delay and improve disease outcomes, simple new screening methods for CS in at-risk populations are needed. Objective: To develop and validate a simple scoring system to predict CS based on clinical signs and an easy-to-use biochemical test. Design: Observational, prospective, multicenter. Setting: Referral hospital. Patients: A cohort of 353 patients attending endocrinology units for outpatient visits. Interventions: All patients were evaluated with late-night salivary cortisol (LNSC) and a low-dose dexamethasone suppression test for CS. Main Outcome Measures: Diagnosis or exclusion of CS. Results: Twenty-six cases of CS were diagnosed in the cohort. A risk scoring system was developed by logistic regression analysis, and cutoff values were derived from a receiver operating characteristic curve. This risk score included clinical signs and symptoms (muscular atrophy, osteoporosis, and dorsocervical fat pad) and LNSC levels. The estimated area under the receiver operating characteristic curve was 0.93, with a sensitivity of 96.2% and specificity of 82.9%. Conclusions: We developed a risk score to predict CS in an at-risk population. This score may help to identify at-risk patients in non-endocrinological settings such as primary care, but external validation is warranted.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Clinical Endocrinology and Metabolismen_US
dc.sourceJournal of Clinical Endocrinology and Metabolism[ISSN 0021-972X],v. 101, p. 3747-3754en_US
dc.subject3205 Medicina internaen_US
dc.subject320502 Endocrinologíaen_US
dc.subject.otherCushing’s syndromeen_US
dc.titleA probabilistic model for cushing's syndrome screening in at-risk populations: a prospective multicenter studyen_US
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1210/jc.2016-1673
dc.identifier.scopus84991594371-
dc.identifier.isi000390849800030
dc.contributor.authorscopusid24465619800
dc.contributor.authorscopusid36653044900
dc.contributor.authorscopusid37070328300
dc.contributor.authorscopusid57191573432
dc.contributor.authorscopusid6603445517
dc.contributor.authorscopusid6505711618
dc.contributor.authorscopusid42560893700
dc.contributor.authorscopusid6504434399
dc.contributor.authorscopusid7003952293
dc.contributor.authorscopusid8503270400
dc.contributor.authorscopusid6507871833
dc.contributor.authorscopusid36457161000
dc.contributor.authorscopusid6505891436
dc.contributor.authorscopusid15070430000
dc.contributor.authorscopusid7003981266
dc.contributor.authorscopusid7004614140
dc.description.lastpage3754-
dc.identifier.issue10-
dc.description.firstpage3747-
dc.relation.volume101-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid1645769
dc.contributor.daisngid3174071
dc.contributor.daisngid2454689
dc.contributor.daisngid26868782
dc.contributor.daisngid788415
dc.contributor.daisngid7393884
dc.contributor.daisngid1542826
dc.contributor.daisngid20844842
dc.contributor.daisngid673494
dc.contributor.daisngid6099754
dc.contributor.daisngid4980199
dc.contributor.daisngid12274490
dc.contributor.daisngid9777698
dc.contributor.daisngid366151
dc.contributor.daisngid554439
dc.contributor.daisngid923928
dc.contributor.wosstandardWOS:Leon-Justel, A
dc.contributor.wosstandardWOS:Madrazo-Atutxa, A
dc.contributor.wosstandardWOS:Alvarez-Rios, AI
dc.contributor.wosstandardWOS:Infantes-Fontan, R
dc.contributor.wosstandardWOS:Garcia-Arnes, JA
dc.contributor.wosstandardWOS:Lillo-Munoz, JA
dc.contributor.wosstandardWOS:Aulinas, A
dc.contributor.wosstandardWOS:Urgell-Rull, E
dc.contributor.wosstandardWOS:Boronat, M
dc.contributor.wosstandardWOS:Sanchez-de-Abajo, A
dc.contributor.wosstandardWOS:Fajardo-Montanana, C
dc.contributor.wosstandardWOS:Ortuno-Alonso, M
dc.contributor.wosstandardWOS:Salinas-Vert, I
dc.contributor.wosstandardWOS:Granada, ML
dc.contributor.wosstandardWOS:Cano, DA
dc.contributor.wosstandardWOS:Leal-Cerro, A
dc.date.coverdateOctubre 2016
dc.identifier.ulpgces
dc.description.sjr2,768
dc.description.jcr5,455
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUIBS: Diabetes y endocrinología aplicada-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0001-8535-8543-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameBoronat Cortés, Mauro-
crisitem.author.fullNameSanchez De Abajo,Ana-
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