Next-generation sequencing refines the genetic architecture of Greek GnRH-deficient patients

• Main Authors: M I Stamou, P Varnavas, L Plummer, V Koika, N A Georgopoulos
• Format: Article
• Language: English
• Published: Bioscientifica 2019-04-01
• Series: Endocrine Connections
• Subjects: GnRH; genetics; whole exome sequencing; Kallmann; hypogonadism
• Online Access: https://ec.bioscientifica.com/view/journals/ec/8/5/EC-19-0010.xml

Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is a rare disease with a wide spectrum of reproductive and non-reproductive clinical characteristics. Apart from the phenotypic heterogeneity, IGD is also highly genetically heterogeneous with >35 genes implicated in the disease. Despite this genetic heterogeneity, genetic enrichment in specific subpopulations has been described. We have previously described low prevalence of genetic variation in the Greek IGD cohort discovered with utilization of Sanger sequencing in 14 known IGD genes. Here, we describe the expansion of genetic screening in the largest IGD Greek cohort that has ever been studied with the usage of whole-exome sequencing, searching for rare sequencing variants (RSVs) in 37 known IGD genes. Even though Sanger sequencing detected genetic variation in 21/81 IGD patients in 7/14 IGD genes without any evidence of oligogenicity, whole exome sequencing (WES) revealed that 27/87 IGD patients carried a rare genetic change in a total of 15 genes with 4 IGD cases being oligogenic. Our findings suggest that next-generation sequencing (NGS) techniques can discover previously undetected variation, making them the standardized method for screening patients with rare and/or more common disorders.