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Urinary gonadotropin measurements by enhanced luminometric assays (LIA) for the evaluation of pubertal development

  • And Demir EMAIL logo , Adem Aydın , Atilla Büyükgebiz , Ulf-Håkan Stenman and Matti Hero
Published/Copyright: April 29, 2021

Abstract

Objectives

Determination of LH in urine has proved to be a reliable method for evaluation of pubertal development. The human LH assay based on time-resolved immunofluorometric (IFMA) technology (AutoDELFIA, PerkinElmer, Wallac) has been found to be suitable for this purpose thanks to its high sensitivity but other assays have not been evaluated. We have analyzed our data obtained by another potentially sensitive detection technique, enhanced luminometric assay (LIA) with the objective of finding a viable alternative to IFMA since these may not be available in the future.

Methods

LIA was used to measure LH and FSH in serum and urine samples from 100 healthy subjects of each Tanner stage and both genders, whose pubertal development has been determined.

Results

Urinary gonodotropin concentrations measured by LIA correlated well with Tanner stage [(r=0.93 for girls, r=0.81 for boys; p<0.01 for LH) and (r=0.81 for girls, r=0.73 for boys; p<0.01 for FSH)]. LIA determinations revealed the increase in U-LH concentrations during the transition from Tanner stage 1–2 in both girls and boys (p<0.001), whereas U-FSH and S-LH were able to detect the increase from Tanner stage 1–2 only in boys or girls, respectively (both p<0.001).

Conclusions

Measurement of urinary gonadotropin concentrations by LIA may be useful for the evaluation of overall pubertal development and also in the detection of transition from prepuberty to puberty.


Corresponding author: Dr. And Demir, New Childrenʼs Hospital, Pediatric Research Center, University of Helsinki, Helsinki University Hospital, Biomedicum II, 6th floor, Tukholmankatu 8 A, FIN-00290, Helsinki, Finland, Phone: +358 50 3119100, Fax: +358 50 3119109, E-mail:

Acknowledgments

The authors would like to express gratitude to the patients and their parents or custodians for their understanding and cooperation in this study.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all parents or custodians as well as children of 6 years age or above.

  5. Ethical approval: The study protocol was approved by the ethics committee of the hospital. The study has complied with the World Medical Association Declaration of Helsinki regarding ethical conduct of research involving human subjects.

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Received: 2020-10-17
Accepted: 2021-03-16
Published Online: 2021-04-29
Published in Print: 2021-07-27

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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