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Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia

Objectives: Polycystic ovary syndrome is a common endocrine disease in adolescent females that is usually diagnosed based on clinical and hormonal abnormalities. Female adolescents with poorly controlled congenital adrenal hyperplasia are at increased risk of developing polycystic ovary syndrome. Th...

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Autores principales: Abdelhamed, Marwa H, Al-Ghamdi, Waad M, Al-Agha, Abdulmoein E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787295/
https://www.ncbi.nlm.nih.gov/pubmed/35106235
http://dx.doi.org/10.7759/cureus.20698
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author Abdelhamed, Marwa H
Al-Ghamdi, Waad M
Al-Agha, Abdulmoein E
author_facet Abdelhamed, Marwa H
Al-Ghamdi, Waad M
Al-Agha, Abdulmoein E
author_sort Abdelhamed, Marwa H
collection PubMed
description Objectives: Polycystic ovary syndrome is a common endocrine disease in adolescent females that is usually diagnosed based on clinical and hormonal abnormalities. Female adolescents with poorly controlled congenital adrenal hyperplasia are at increased risk of developing polycystic ovary syndrome. This study aimed to determine the prevalence of polycystic ovary syndrome and assess its relationship with hormonal control among adolescents with congenital adrenal hyperplasia. Methods: This retrospective descriptive study included 40 pubertal female adolescents aged between 12 and 20 years with at least two years after menarche diagnosed with classical congenital adrenal hyperplasia since birth who were screened routinely for polycystic ovary syndrome via pelvic ultrasonography between 2012 and 2020 at King Abdul-Aziz University Hospital, Jeddah, Saudi Arabia. Serum adrenocorticotropic hormone, 17-hydroxy -progesterone, testosterone, dehydroepiandrosterone sulfate, luteinizing hormone, and follicle-stimulating hormone levels were measured. Results: Polycystic ovary syndrome was detected via routine pelvic ultrasonography in 12/40 (30%) females. The median age of the affected females was 16.6 years, with the youngest female aged 12.5 years. The bone age of the patients had advanced ≤3 years. Further, serum adrenocorticotropic hormone was determined to be an independent factor affecting polycystic ovary syndrome development, indicating poor hormonal control (P = 0.005). Conclusion: Polycystic ovary disease is likely a complication of poorly controlled congenital adrenal hyperplasia disease. Therefore, increasing the awareness of polycystic ovary disease among congenital adrenal hyperplasia females via routine ultrasonography screening is advisable to facilitate the early diagnosis and improve disease management.
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spelling pubmed-87872952022-01-31 Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia Abdelhamed, Marwa H Al-Ghamdi, Waad M Al-Agha, Abdulmoein E Cureus Endocrinology/Diabetes/Metabolism Objectives: Polycystic ovary syndrome is a common endocrine disease in adolescent females that is usually diagnosed based on clinical and hormonal abnormalities. Female adolescents with poorly controlled congenital adrenal hyperplasia are at increased risk of developing polycystic ovary syndrome. This study aimed to determine the prevalence of polycystic ovary syndrome and assess its relationship with hormonal control among adolescents with congenital adrenal hyperplasia. Methods: This retrospective descriptive study included 40 pubertal female adolescents aged between 12 and 20 years with at least two years after menarche diagnosed with classical congenital adrenal hyperplasia since birth who were screened routinely for polycystic ovary syndrome via pelvic ultrasonography between 2012 and 2020 at King Abdul-Aziz University Hospital, Jeddah, Saudi Arabia. Serum adrenocorticotropic hormone, 17-hydroxy -progesterone, testosterone, dehydroepiandrosterone sulfate, luteinizing hormone, and follicle-stimulating hormone levels were measured. Results: Polycystic ovary syndrome was detected via routine pelvic ultrasonography in 12/40 (30%) females. The median age of the affected females was 16.6 years, with the youngest female aged 12.5 years. The bone age of the patients had advanced ≤3 years. Further, serum adrenocorticotropic hormone was determined to be an independent factor affecting polycystic ovary syndrome development, indicating poor hormonal control (P = 0.005). Conclusion: Polycystic ovary disease is likely a complication of poorly controlled congenital adrenal hyperplasia disease. Therefore, increasing the awareness of polycystic ovary disease among congenital adrenal hyperplasia females via routine ultrasonography screening is advisable to facilitate the early diagnosis and improve disease management. Cureus 2021-12-25 /pmc/articles/PMC8787295/ /pubmed/35106235 http://dx.doi.org/10.7759/cureus.20698 Text en Copyright © 2021, Abdelhamed et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Endocrinology/Diabetes/Metabolism
Abdelhamed, Marwa H
Al-Ghamdi, Waad M
Al-Agha, Abdulmoein E
Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title_full Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title_fullStr Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title_full_unstemmed Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title_short Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia
title_sort polycystic ovary syndrome among female adolescents with congenital adrenal hyperplasia
topic Endocrinology/Diabetes/Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787295/
https://www.ncbi.nlm.nih.gov/pubmed/35106235
http://dx.doi.org/10.7759/cureus.20698
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