Analysis of luteinizing hormone (LH) : validation of a commercial ELISA kit for LH analysis and quantification in doping control samples

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Deutscher übersetzter Titel:Analyse des luteinisierenden Hormons (LH) : Validierung eines kommerziellen ELISA-Kits für die LH-Analyse und -Quantifizierung in Dopingproben
Autor:Mäkelä, Riika; Leinonen, Antti; Suominen, Tina
Erschienen in:Drug testing and analysis
Veröffentlicht:12 (2020), 2, S. 239-246, Lit.
Format: Literatur (SPOLIT)
Publikationstyp: Zeitschriftenartikel
Medienart: Elektronische Ressource (online) Gedruckte Ressource
Sprache:Englisch
ISSN:1942-7603, 1942-7611
DOI:10.1002/dta.2716
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Erfassungsnummer:PU202201000531
Quelle:BISp

Abstract des Autors

Luteinizing hormone (LH) is a dimeric glycoprotein produced and secreted by the pituitary gland, with a molecular weight of approximately 30 000 Da. The main clinical use for exogenous LH-administration is typically linked to the treatment of infertility, in both men and women. The desired effect of LH misuse in sport is due to the enhancement of testicular production of testosterone. Elevated LH levels may also indicate the usage of gonadotropin-releasing factors or estrogen blockers. Therefore, LH is listed by the World Anti-Doping Agency (WADA) as a prohibited substance in male athletes, and according to the WADA technical document, laboratories should determine the the total LH concentrations in urine. The TD lists two different assays that are suitable for measuring total LH in urine, Delfia and Siemens Immulite. Other fit-for-purpose assays can be used, as long as they are capable of detecting total LH in urine. In case an assay not listed in the TD will be used, population-based reference values have to be determined in the validation procedure.