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Central precocious puberty in Boston boys: A 10-year single center experience
OBJECTIVE: Recent studies in the US and abroad suggest that boys are undergoing puberty at a younger age. It is unknown if this secular trend extends to boys with central precocious puberty (CPP), who sit at the extreme end of the pubertal spectrum, and if neuroimaging should remain a standard diagn...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021063/ https://www.ncbi.nlm.nih.gov/pubmed/29949619 http://dx.doi.org/10.1371/journal.pone.0199019 |
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author | Topor, Lisa Swartz Bowerman, Kimberly Machan, Jason T. Gilbert, Courtney L. Kangarloo, Tairmae Shaw, Natalie D. |
author_facet | Topor, Lisa Swartz Bowerman, Kimberly Machan, Jason T. Gilbert, Courtney L. Kangarloo, Tairmae Shaw, Natalie D. |
author_sort | Topor, Lisa Swartz |
collection | PubMed |
description | OBJECTIVE: Recent studies in the US and abroad suggest that boys are undergoing puberty at a younger age. It is unknown if this secular trend extends to boys with central precocious puberty (CPP), who sit at the extreme end of the pubertal spectrum, and if neuroimaging should remain a standard diagnostic tool. STUDY DESIGN: Retrospective chart review of all boys with CPP seen by Endocrinology at a US pediatric hospital from 2001–2010. RESULTS: Fifty boys had pubertal onset at an average age of 7.31 years (95CI 6.83–7.89), though many did not present until nearly one year thereafter, by which time 30% were mid-to-late pubertal. Boys were predominantly non-Hispanic White and 64% were overweight/obese. The majority (64%) of boys had neurogenic CPP (CNS-CPP) with neurofibromatosis type I being the most common diagnosis. Diagnosis of CPP led to discovery of a neurogenic lesion in only 3 of 32 (9%) CNS-CPP cases. The remaining boys, with idiopathic CPP (36%), were indistinguishable from those with CNS-CPP aside from four boys who endorsed a family history of PP (22% vs. 0% among CNS-CPP cases). Importantly, there was no change in the incidence of male CPP after accounting for the increase in clinic volume during this time period. CONCLUSION: In this contemporary Boston-based cohort of 50 boys with CPP, most cases were neurogenic, consistent with older literature. Several idiopathic cases had a family history of PP but were otherwise indistinguishable from CNS-CPP cases. Thus, neuroimaging remains a critical diagnostic tool. We find no evidence for an increase in the prevalence of male CPP. |
format | Online Article Text |
id | pubmed-6021063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60210632018-07-07 Central precocious puberty in Boston boys: A 10-year single center experience Topor, Lisa Swartz Bowerman, Kimberly Machan, Jason T. Gilbert, Courtney L. Kangarloo, Tairmae Shaw, Natalie D. PLoS One Research Article OBJECTIVE: Recent studies in the US and abroad suggest that boys are undergoing puberty at a younger age. It is unknown if this secular trend extends to boys with central precocious puberty (CPP), who sit at the extreme end of the pubertal spectrum, and if neuroimaging should remain a standard diagnostic tool. STUDY DESIGN: Retrospective chart review of all boys with CPP seen by Endocrinology at a US pediatric hospital from 2001–2010. RESULTS: Fifty boys had pubertal onset at an average age of 7.31 years (95CI 6.83–7.89), though many did not present until nearly one year thereafter, by which time 30% were mid-to-late pubertal. Boys were predominantly non-Hispanic White and 64% were overweight/obese. The majority (64%) of boys had neurogenic CPP (CNS-CPP) with neurofibromatosis type I being the most common diagnosis. Diagnosis of CPP led to discovery of a neurogenic lesion in only 3 of 32 (9%) CNS-CPP cases. The remaining boys, with idiopathic CPP (36%), were indistinguishable from those with CNS-CPP aside from four boys who endorsed a family history of PP (22% vs. 0% among CNS-CPP cases). Importantly, there was no change in the incidence of male CPP after accounting for the increase in clinic volume during this time period. CONCLUSION: In this contemporary Boston-based cohort of 50 boys with CPP, most cases were neurogenic, consistent with older literature. Several idiopathic cases had a family history of PP but were otherwise indistinguishable from CNS-CPP cases. Thus, neuroimaging remains a critical diagnostic tool. We find no evidence for an increase in the prevalence of male CPP. Public Library of Science 2018-06-27 /pmc/articles/PMC6021063/ /pubmed/29949619 http://dx.doi.org/10.1371/journal.pone.0199019 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Topor, Lisa Swartz Bowerman, Kimberly Machan, Jason T. Gilbert, Courtney L. Kangarloo, Tairmae Shaw, Natalie D. Central precocious puberty in Boston boys: A 10-year single center experience |
title | Central precocious puberty in Boston boys: A 10-year single center experience |
title_full | Central precocious puberty in Boston boys: A 10-year single center experience |
title_fullStr | Central precocious puberty in Boston boys: A 10-year single center experience |
title_full_unstemmed | Central precocious puberty in Boston boys: A 10-year single center experience |
title_short | Central precocious puberty in Boston boys: A 10-year single center experience |
title_sort | central precocious puberty in boston boys: a 10-year single center experience |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021063/ https://www.ncbi.nlm.nih.gov/pubmed/29949619 http://dx.doi.org/10.1371/journal.pone.0199019 |
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