Literature DB >> 24830587

[Advances in the etiology, diagnosis and treatment of central precocious puberty].

Delanie B Macedo1, Priscilla Cukier1, Berenice B Mendonca1, Ana Claudia Latronico1, Vinicius Nahime Brito1.   

Abstract

The onset of puberty is first detected as an increase in the amplitude and frequency of pulses of gonadotropin-releasing hormone (GnRH) after a quiescent period during childhood. The reemergence of pulsatile GnRH secretion leads to increases in the secretion of the gonadotropins, luteinizing hormone (LH), and follicle-stimulating hormone (FSH) by the pituitary gland, and the consequent activation of gonadal function. Early activation of the hypothalamic-pituitary-gonadal axis results in gonadotropin-dependent precocious puberty, also known as central precocious puberty (CPP), which is clinically defined by the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys. Pubertal timing is influenced by complex interactions among genetic, nutritional, environmental, and socioeconomic factors. CPP is diagnosed on the basis of clinical signs of progressive pubertal development before the age of 8 years in girls and 9 years in boys, pubertal basal and/or GnRH-stimulated LH levels, and advanced bone age. Magnetic resonance imaging of the central nervous system is essential for establishing the CPP form as organic or idiopathic. Depot GnRH-analogues represent the first-line of therapy in CPP. Very recently, the genetic component of CPP was demonstrated by the evidence that the deficiency of the MKRN3 gene, located on long arm of chromosome 15, causes familial CPP in humans. In this current review, clinical and therapeutic aspects of the CPP will be discussed, contributing to adequate diagnosis and criterious approach of this relevant condition of pediatric endocrinology.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24830587     DOI: 10.1590/0004-2730000002931

Source DB:  PubMed          Journal:  Arq Bras Endocrinol Metabol        ISSN: 0004-2730


  5 in total

1.  Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case.

Authors:  Monica F Stecchini; Delanie B Macedo; Ana Claudia S Reis; Ana Paula Abreu; Ayrton C Moreira; Margaret Castro; Ursula B Kaiser; Ana Claudia Latronico; Sonir R Antonini
Journal:  Horm Res Paediatr       Date:  2016-07-16       Impact factor: 2.852

2.  High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.

Authors:  Danielle S Bessa; Delanie B Macedo; Vinicius N Brito; Monica M França; Luciana R Montenegro; Marina Cunha-Silva; Leticia G Silveira; Tiago Hummel; Ignacio Bergadá; Debora Braslavsky; Ana Paula Abreu; Andrew Dauber; Berenice B Mendonca; Ursula B Kaiser; Ana Claudia Latronico
Journal:  Neuroendocrinology       Date:  2016-05-26       Impact factor: 4.914

3.  Methylome profiling of healthy and central precocious puberty girls.

Authors:  Danielle S Bessa; Mariana Maschietto; Carlos Francisco Aylwin; Ana P M Canton; Vinicius N Brito; Delanie B Macedo; Marina Cunha-Silva; Heloísa M C Palhares; Elisabete A M R de Resende; Maria de Fátima Borges; Berenice B Mendonca; Irene Netchine; Ana C V Krepischi; Alejandro Lomniczi; Sergio R Ojeda; Ana Claudia Latronico
Journal:  Clin Epigenetics       Date:  2018-11-22       Impact factor: 6.551

4.  Applicability of a novel mathematical model for the prediction of adult height and age at menarche in girls with idiopathic central precocious puberty.

Authors:  Mateus Cavarzan Lopes; Carolina Oliveira Ramos; Ana Claudia Latronico; Berenice B Mendonça; Vinicius N Brito
Journal:  Clinics (Sao Paulo)       Date:  2018-07-26       Impact factor: 2.365

Review 5.  Delayed Puberty-Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries.

Authors:  Sasha R Howard; Leo Dunkel
Journal:  Endocr Rev       Date:  2019-10-01       Impact factor: 19.871

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.