dc.contributor.author | Madsen, Andre | |
dc.contributor.author | Almås, Bjørg | |
dc.contributor.author | Bruserud, Ingvild Særvold | |
dc.contributor.author | Oehme, Ninnie Helen Bakken | |
dc.contributor.author | Nielsen, Christopher Sivert | |
dc.contributor.author | Roelants, Mathieu | |
dc.contributor.author | Hundhausen, Thomas Eckhard | |
dc.contributor.author | Ljubicic, Marie Lindhardt | |
dc.contributor.author | Bjerknes, Robert | |
dc.contributor.author | Mellgren, Gunnar | |
dc.contributor.author | Sagen, Jørn V. | |
dc.contributor.author | Juliusson, Pétur Benedikt | |
dc.contributor.author | Viste, Kristin | |
dc.date.accessioned | 2022-05-23T06:36:14Z | |
dc.date.available | 2022-05-23T06:36:14Z | |
dc.date.issued | 2022-03-17 | |
dc.description.abstract | Context: Hormone reference intervals in pediatric endocrinology are traditionally partitioned by age and lack the framework for benchmarking
individual blood test results as normalized z-scores and plotting sequential measurements onto a chart. Reference curve modeling is applicable
to endocrine variables and represents a standardized method to account for variation with gender and age.<p>
<p>Objective: We aimed to establish gender-specifc biomarker reference curves for clinical use and benchmark associations between hormones,
pubertal phenotype, and body mass index (BMI).
<p>Methods: Using cross-sectional population sample data from 2139 healthy Norwegian children and adolescents, we analyzed the pubertal
status, ultrasound measures of glandular breast tissue (girls) and testicular volume (boys), BMI, and laboratory measurements of 17 clinical biomarkers modeled using the established “LMS” growth chart algorithm in R.
<p>Results: Reference curves for puberty hormones and pertinent biomarkers were modeled to adjust for age and gender. Z-score equivalents
of biomarker levels and anthropometric measurements were compiled in a comprehensive beta coeffcient matrix for each gender. Excerpted
from this analysis and independently of age, BMI was positively associated with female glandular breast volume (β = 0.5, P < 0.001) and leptin
(β = 0.6, P < 0.001), and inversely correlated with serum levels of sex hormone-binding globulin (SHBG) (β = −0.4, P < 0.001). Biomarker z-score
profles differed signifcantly between cohort subgroups stratifed by puberty phenotype and BMI weight class.
<p<Conclusion: Biomarker reference curves and corresponding z-scores provide an intuitive framework for clinical implementation in pediatric
endocrinology and facilitate the application of machine learning classifcation and covariate precision medicine for pediatric patients. | en_US |
dc.identifier.citation | Madsen, Almås, Bruserud, Oehme, Nielsen, Roelants, Hundhausen, Ljubicic, Bjerknes, Mellgren, Sagen, Juliusson, Viste. Reference curves for pediatric endocrinology: leveraging biomarker z-scores for clinical classifications. Journal of Clinical Endocrinology and Metabolism (JCEM). 2022:1-12 | en_US |
dc.identifier.cristinID | FRIDAID 2025889 | |
dc.identifier.doi | 10.1210/clinem/dgac155 | |
dc.identifier.issn | 0021-972X | |
dc.identifier.issn | 1945-7197 | |
dc.identifier.uri | https://hdl.handle.net/10037/25245 | |
dc.language.iso | eng | en_US |
dc.publisher | Oxford University Press | en_US |
dc.relation.journal | Journal of Clinical Endocrinology and Metabolism (JCEM) | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2022 The Author(s) | en_US |
dc.title | Reference curves for pediatric endocrinology: leveraging biomarker z-scores for clinical classifications | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |