1. Academic Validation
  2. Inactivating KISS1 mutation and hypogonadotropic hypogonadism

Inactivating KISS1 mutation and hypogonadotropic hypogonadism

  • N Engl J Med. 2012 Feb 16;366(7):629-35. doi: 10.1056/NEJMoa1111184.
A Kemal Topaloglu 1 Javier A Tello L Damla Kotan Mehmet N Ozbek M Bertan Yilmaz Seref Erdogan Fatih Gurbuz Fatih Temiz Robert P Millar Bilgin Yuksel
Affiliations

Affiliation

  • 1 Faculty of Medicine, Department of Pediatric Endocrinology, Cukurova University, Adana, Turkey. ktopaloglu@cu.edu.tr
Abstract

Gonadotropin-releasing hormone (GnRH) is the central regulator of gonadotropins, which stimulate gonadal function. Hypothalamic neurons that produce kisspeptin and neurokinin B stimulate GnRH release. Inactivating mutations in the genes encoding the human Kisspeptin Receptor (KISS1R, formerly called GPR54), neurokinin B (TAC3), and the neurokinin B receptor (TACR3) result in pubertal failure. However, human kisspeptin loss-of-function mutations have not been described, and contradictory findings have been reported in Kiss1-knockout mice. We describe an inactivating mutation in KISS1 in a large consanguineous family that results in failure of pubertal progression, indicating that functional kisspeptin is important for puberty and reproduction in humans. (Funded by the Scientific and Technological Research Council of Turkey [TÜBİTAK] and Others ).

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