Genetic causes of central precocious puberty

• Published in: Clinical Pediatric Endocrinology Vol. 31; no. 3; pp. 101 - 109
• Main Author: Toshihiro Tajima
• Format: Journal Article
• Language: English; Japanese
• Published: The Japanese Society for Pediatric Endocrinology 01.07.2022
• ISSN: 0918-5739
• DOI: 10.1297/cpe.31.2022-0021

[Highlights] ●The review clarifies new genetic etiologies of CPP. ●The genetic etiologies are useful for a better understanding of the timing of puberty. ●The genetic imprinting plays an important role in the regulation of puberty. [Abstract.] Central precocious puberty (CPP) is a condition in which the hypothalamus-pituitary-gonadal system is activated earlier than the normal developmental stage. The etiology includes organic lesions in the brain ; however, in the case of idiopathic diseases, environmental and/or genetic factors are involved in the development of CPP. A genetic abnormality in KISS1R, that encodes the kisspeptin receptor, was first reported in 2008 as a cause of idiopathic CPP. Furthermore, genetic alterations in KISS1, MKRN3, DLK1, and PROKR2 have been reported in idiopathic and/or familial CPP. Of these, MKRN3 has the highest frequency of pathological variants associated with CPP worldwide ; but, abnormalities in MKRN3 are rare in patients in East Asia, including Japan. MKRN3 and DLK1 are maternal imprinting genes ; thus, CPP develops when a pathological variant is inherited from the father. The mechanism of CPP due to defects in MKRN3 and DLK1 has not been completely clarified, but it is suggested that both may negatively control the progression of puberty. CPP due to such a single gene abnormality is extremely rare, but it is important to understand the mechanisms of puberty and reproduction. A further development in the genetics of CPP is expected in the future.