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Sex Hormones and Adrenal Steroids : Biological Variation Estimated Using Direct and Indirect Methods

Roys, Eirik Åsen (author)
Haukeland Hosp, Norway
Guldhaug, Nora Alicia (author)
Haukeland Hosp, Norway
Viste, Kristin (author)
Haukeland Hosp, Norway
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Jones, Graham Dallas (author)
St Vincents Hosp, Australia; Univ New SouthWales, Australia
Alaour, Bashir (author)
Kings Coll London, England
Sylte, Marit Sverresdotter (author)
Haukeland Hosp, Norway
Torsvik, Janniche (author)
Haukeland Hosp, Norway
Kellmann, Ralf (author)
Haukeland Hosp, Norway
Strand, Heidi (author)
Akershus Univ Hosp, Norway
Theodorsson, Elvar (author)
Linköpings universitet,Avdelningen för klinisk kemi och farmakologi,Medicinska fakulteten,Region Östergötland, Klinisk kemi
Marber, Michael (author)
Kings Coll London, England
Omland, Torbjorn (author)
Univ Oslo, Norway; Akershus Univ Hosp, Norway
Aakre, Kristin Moberg (author)
Haukeland Hosp, Norway; Haukeland Hosp, Norway; Univ Bergen, Norway; Haukeland Hosp, Norway
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 (creator_code:org_t)
2022-11-14
2023
English.
In: Clinical Chemistry. - : Oxford University Press. - 0009-9147 .- 1530-8561. ; 69:1, s. 100-109
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background Biological variation (BV) data may be used to develop analytical performance specifications (APS), reference change values (RCV), and support the applicability of population reference intervals. This study estimates within-subject BV (CVI) for several endocrine biomarkers using 3 different methodological approaches. Methods For the direct method, 30 healthy volunteers were sampled weekly for 10 consecutive weeks. Samples were analyzed in duplicate for 17-hydroxyprogesterone (17-OHP), androstenedione, cortisol, cortisone, estradiol, follicle-stimulating hormone (FSH), luteinizing hormone (LH), sex hormone-binding globulin (SHBG), and testosterone. A CV-ANOVA with outlier removal and a Bayesian model were applied to derive the CVI. For estradiol, FSH and LH, only the male subgroup was included. In the indirect method, using the same analytes and groups, pairs of sequential results were extracted from the laboratory information system. The total result variation for individual pairs was determined by identifying a central gaussian distribution in the ratios of the result pairs. The CVI was then estimated by removing the effect of analytical variation. Results The estimated CVI from the Bayesian model (mu CVP(i)) in the total cohort was: 17-OHP, 23%; androstenedione, 20%; cortisol, 18%; cortisone, 11%; SHBG, 7.4%; testosterone, 16%; and for the sex hormones in men: estradiol, 14%; FSH, 8%; and LH, 26%. CVI-heterogeneity was present for most endocrine markers. Similar CVI data were estimated using the CV-ANOVA and the indirect method. Conclusions Similar CVI data were obtained using 2 different direct and one indirect method. The indirect approach is a low-cost alternative ensuring implementation of CVI data applicable for local conditions.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Medicinteknik -- Medicinsk laboratorie- och mätteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering -- Medical Laboratory and Measurements Technologies (hsv//eng)

Keyword

quality control; LC-MS; adrenal; steroids and steroid hormones; testosterone

Publication and Content Type

ref (subject category)
art (subject category)

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