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Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study
The role of anti-Müllerian hormone (AMH), a potential marker of the hypothalamic-pituitary-ovarian axis, is not well established in adolescent females. Most studies use secondary sexual characteristics or chronological age as predictors for AMH. Skeletal maturity, an indicator of bone development, h...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571635/ https://www.ncbi.nlm.nih.gov/pubmed/37841846 http://dx.doi.org/10.21203/rs.3.rs-3342941/v1 |
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author | Ford, McKenzie L Choh, Audrey C Gonzalez, Brandon Lindheim, Steven R Stanczyk, Frank Z McGinnis, Lynda K Czerwinski, Stefan A Lee, Miryoung |
author_facet | Ford, McKenzie L Choh, Audrey C Gonzalez, Brandon Lindheim, Steven R Stanczyk, Frank Z McGinnis, Lynda K Czerwinski, Stefan A Lee, Miryoung |
author_sort | Ford, McKenzie L |
collection | PubMed |
description | The role of anti-Müllerian hormone (AMH), a potential marker of the hypothalamic-pituitary-ovarian axis, is not well established in adolescent females. Most studies use secondary sexual characteristics or chronological age as predictors for AMH. Skeletal maturity, an indicator of bone development, has not been examined to predict AMH. This study sought to examine patterns of change in AMH in relation to skeletal maturity. Demographics, anthropometry, hand-wrist radiographs, and cardiometabolic risk factors from 88 females (212 observations), between the ages of 8 to 18 years from the Fels Longitudinal Study were used in this study. AMH was analyzed using ELISA from stored frozen serum samples. Generalized linear mixed effect modeling was used. In the stepwise regression models, log-transformed AMH (AMHlog) was regressed on relative skeletal age as the skeletal maturity indicator (calculated as chronological age minus skeletal age) and adjusted for chronological age, adiposity, and cardiometabolic risk factors. Skeletal maturity significantly predicted lower AMHlog (β= −0.073, SE=0.032, p=0.023). Glucose was significantly associated with decreases in AMHlog (β= −0.008, SE=0.004, p=0.044). Chronological age modeled as a cubic function was not significant. AMH and skeletal maturity may provide correlated information on growth and pubertal status in adolescent females. |
format | Online Article Text |
id | pubmed-10571635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-105716352023-10-14 Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study Ford, McKenzie L Choh, Audrey C Gonzalez, Brandon Lindheim, Steven R Stanczyk, Frank Z McGinnis, Lynda K Czerwinski, Stefan A Lee, Miryoung Res Sq Article The role of anti-Müllerian hormone (AMH), a potential marker of the hypothalamic-pituitary-ovarian axis, is not well established in adolescent females. Most studies use secondary sexual characteristics or chronological age as predictors for AMH. Skeletal maturity, an indicator of bone development, has not been examined to predict AMH. This study sought to examine patterns of change in AMH in relation to skeletal maturity. Demographics, anthropometry, hand-wrist radiographs, and cardiometabolic risk factors from 88 females (212 observations), between the ages of 8 to 18 years from the Fels Longitudinal Study were used in this study. AMH was analyzed using ELISA from stored frozen serum samples. Generalized linear mixed effect modeling was used. In the stepwise regression models, log-transformed AMH (AMHlog) was regressed on relative skeletal age as the skeletal maturity indicator (calculated as chronological age minus skeletal age) and adjusted for chronological age, adiposity, and cardiometabolic risk factors. Skeletal maturity significantly predicted lower AMHlog (β= −0.073, SE=0.032, p=0.023). Glucose was significantly associated with decreases in AMHlog (β= −0.008, SE=0.004, p=0.044). Chronological age modeled as a cubic function was not significant. AMH and skeletal maturity may provide correlated information on growth and pubertal status in adolescent females. American Journal Experts 2023-09-29 /pmc/articles/PMC10571635/ /pubmed/37841846 http://dx.doi.org/10.21203/rs.3.rs-3342941/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Ford, McKenzie L Choh, Audrey C Gonzalez, Brandon Lindheim, Steven R Stanczyk, Frank Z McGinnis, Lynda K Czerwinski, Stefan A Lee, Miryoung Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title | Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title_full | Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title_fullStr | Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title_full_unstemmed | Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title_short | Anti-Müllerian hormone levels are associated with skeletal maturity in adolescent girls in the Fels Longitudinal Study |
title_sort | anti-müllerian hormone levels are associated with skeletal maturity in adolescent girls in the fels longitudinal study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571635/ https://www.ncbi.nlm.nih.gov/pubmed/37841846 http://dx.doi.org/10.21203/rs.3.rs-3342941/v1 |
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