| Literature DB >> 26410278 |
Gareth Huw Jones1, Martin John Walshaw2.
Abstract
Cystic fibrosis is primarily considered a respiratory disease with superadded pancreatic dysfunction; however the underlying genetic mutation results in the abnormal function of cells throughout the body - including tissues involved in reproduction. Practically all males and up to 50% of females with CF will suffer fertility issues - the causes of which are multifactorial and could be improved by treatments that target the underlying physiological deficit, such as ivacaftor. We consider the mechanisms by which the rapidly developing field of systemic treatments for CF could impact on the fertility of this group and review the available real world evidence.Entities:
Keywords: CFTR modulators; Cystic fibrosis; Fertility
Mesh:
Substances:
Year: 2015 PMID: 26410278 DOI: 10.1016/j.prrv.2015.07.013
Source DB: PubMed Journal: Paediatr Respir Rev ISSN: 1526-0542 Impact factor: 2.726