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dc.rights.licenseopenen_US
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorBROSSAUD, Julie
dc.contributor.authorCHARRET, Lea
dc.contributor.authorDE ANGELI, Delia
dc.contributor.authorHAISSAGUERRE, Magalie
dc.contributor.authorFERRIERE, Amandine
dc.contributor.authorPUERTO, Marie
dc.contributor.authorGATTA-CHERIFI, Blandine
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorCORCUFF, Jean-Benoit
IDREF: 058708154
dc.contributor.authorTABARIN, Antoine
dc.date.accessioned2021-10-20T12:42:56Z
dc.date.available2021-10-20T12:42:56Z
dc.date.issued2021
dc.identifier.issn0804-4643en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/112842
dc.description.abstractEnObjective: Hair cortisol (HF) and cortisone (HE) measurements reflect tissular exposure to cortisol over months and are increased in overt Cushing’s syndrome (CS). No data is available in mild CS. We compared the diagnostic performance of HF and HE between patients with overt or mild CS. Design: Single centre retrospective study. Methods: HF&HE were measured by LC-MS/MS in 48 consecutive adult females with Cushing’s disease (CD), ectopic ACTH syndrome, secreting adenomas and carcinomas, and adrenal incidentalomas. All had impaired dexamethasone suppression tests. Overt CS (n = 25) was diagnosed in front of specific symptoms, a mean UFC (>1.5 ULN) and increased midnight serum cortisol or salivary cortisol. Mild CS (n = 23) was diagnosed in patients lacking specific symptoms and displaying at least one additional biological abnormality including mildly increased UFC (≤1.5 ULN), increased midnight serum cortisol or salivary cortisol and suppressed plasma ACTH in patients with adrenal tumours. In this study, 84 healthy subjects and obese patients served as controls. Results: HF and HE showed roughly similar performance in overt CS (92 and 100% sensitivity, 91 and 99% specificity, respectively). HF and HE were lower in mild CS but higher than in controls (P < 0.01). HE was correlated with midnight serum cortisol (P < 0.02) and volume of adrenal incidentalomas (P < 0.04) but not with UFC. HF and HE had 59% and 68% sensitivity, and 79 and 94% specificity, respectively, for the diagnosis of mild CS. Contrary to UFC, both HF and HE were in the range of overt CS in 11/23 patients with mild CS. Patients with mild CS and increased HE required more antihypertensive treatments and showed worser lipid profiles than patients with normal HE. Conclusions: HF and HE measurement performed better in overt than in mild CS but is a useful adjunct to diagnose mild CS and to identify adrenocortical incidentalomas responsible for excessive cortisol exposure.
dc.language.isoENen_US
dc.title.enHair cortisol and cortisone measurements for the diagnosis of overt and mild Cushing's syndrome
dc.typeArticle de revue
dc.identifier.doi10.1530/EJE-20-1127en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed33449913en_US
bordeaux.journalEuropean Journal of Endocrinologyen_US
bordeaux.page445-454en_US
bordeaux.volume184en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.institutionINSERM
bordeaux.teamNutrition, mémoire et glucocorticoïdesen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03388522
hal.version1
hal.date.transferred2021-10-20T12:43:55Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=European%20Journal%20of%20Endocrinology&amp;rft.date=2021&amp;rft.volume=184&amp;rft.issue=3&amp;rft.spage=445-454&amp;rft.epage=445-454&amp;rft.eissn=0804-4643&amp;rft.issn=0804-4643&amp;rft.au=BROSSAUD,%20Julie&amp;CHARRET,%20Lea&amp;DE%20ANGELI,%20Delia&amp;HAISSAGUERRE,%20Magalie&amp;FERRIERE,%20Amandine&amp;rft.genre=article


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