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dc.contributor.authorUeland, Grethe Åstrøm
dc.contributor.authorDahl, Sandra Rinne
dc.contributor.authorMethlie, Paal
dc.contributor.authorHessen, Saleh
dc.contributor.authorHusebye, Eystein Sverre
dc.contributor.authorThorsby, Per Medbøe
dc.date.accessioned2023-01-02T10:08:39Z
dc.date.available2023-01-02T10:08:39Z
dc.date.created2022-09-23T12:36:26Z
dc.date.issued2022
dc.identifier.issn0015-0282
dc.identifier.urihttps://hdl.handle.net/11250/3040240
dc.description.abstractObjective To define liquid chromatography tandem mass spectrometry (LC-MS/MS)–based cutoff levels and panels of steroid hormones, to improve diagnosis of nonclassic congenital adrenal hyperplasia (NCCAH) and other partial enzyme defects in the adrenals. Design Prospective cohort analysis. Setting University hospital-based tertiary endocrine center. Patients One hundred and twenty-one healthy adults and 65 patients evaluated for possible NCCAH (validation cohort). Interventions The LC-MS/MS–determined cutoffs for 11 steroids (basal and cosyntropin-stimulated) were defined by 2.5% and 97.5% percentile in healthy subjects. Validation cohort was used for comparison. Main Outcome Measures Percentage of patients diagnosed with NCCAH among patients with polycystic ovary syndrome (PCOS)-like symptomatology. Evaluation of the defined LC-MS/MS–based cutoff levels for steroid hormones among this patient group. Results Of the 65 PCOS-like patients evaluated for possible NCCAH, 8 (12.5%) were discovered and genetically verified, and 2 had classic congenital adrenal hyperplasia. Cosyntropin-stimulated 17-hydroxyprogesterone (17OHP) showed the best diagnostic accuracy for NCCAH with an area under the curve of 0.95 (0.89–1.0 with a sensitivity of 86% and a specificity of 88%. In homozygote patients, 21-deoxycortisol and 17OHP levels were elevated, in heterozygote patients only 17OHP (basal or stimulated) was raised. Four healthy patients in the validation cohort had 17OHP above the basal cutoff. Conclusions The NCCAH syndrome is frequent in patients with suspected PCOS, and should be considered as a routine screening when assessing infertility. We suggest the use of serum steroid profiling, including 21-deoxycortisol, together with the cosyntropin stimulation test with 17OHP. Our data support a 17OHP cutoff of 8.5 nmol/L (2.8 ng/mL) 60 minutes after cosyntropin stimulation, when measured with LC-MS/MS, significantly lower than current European guidelines.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.urihttps://www.clinicalkey.com/#!/content/playContent/1-s2.0-S0015028222003156?returnurl=https:%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0015028222003156%3Fshowall%3Dtrue&referrer=https:%2F%2Fpub
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAdrenal steroid profiling as a diagnostic tool to differentiate polycystic ovary syndrome from nonclassic congenital adrenal hyperplasia: pinpointing easy screening possibilities and normal cutoff levels using liquid chromatography tandem mass spectrometryen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1016/j.fertnstert.2022.05.012
dc.identifier.cristin2054787
dc.source.journalFertility and Sterilityen_US
dc.source.pagenumber384-391en_US
dc.identifier.citationFertility and Sterility. 2022, 118 (2), 384-391.en_US
dc.source.volume118en_US
dc.source.issue2en_US


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