Clinical efficacy of a next‐generation sequencing gene panel for primary immunodeficiency diagnostics. Issue 3 (2nd February 2018)

• Record Type: Journal Article
• Authors: Rae, W.; Ward, D.; Mattocks, C.; Pengelly, R.J.; Eren, E.; Patel, S.V.; Faust, S.N.; Hunt, D.; Williams, A.P.
• Is Part Of: Clinical genetics. Volume 93:Issue 3(2018)
• Page Start: 647
• Page End: 655
• Publication Date: 2018-02-02
• Subjects: clinical diagnostics -- human phenotype ontology -- next‐generation sequencing -- primary immunodeficiency; Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.13163
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract : Human phenotype ontology terms assigned across the 27 participants of primary immunodeficiency cohort. Abstract : Primary immunodeficiencies (PIDs) are rare monogenic inborn errors of immunity that result in impairment of functions of the human immune system. PIDs have a broad phenotype with increased morbidity and mortality, and treatment choices are often complex. With increased accessibility of next‐generation sequencing (NGS), the rate of discovery of genetic causes for PID has increased exponentially. Identification of an underlying monogenic diagnosis provides important clinical benefits for patients with the potential to alter treatments, facilitate genetic counselling, and pre‐implantation diagnostics. We investigated a NGS PID panel of 242 genes within clinical care across a range of PID phenotypes. We also evaluated Phenomizer to predict causal genes from human phenotype ontology (HPO) terms. Twenty‐seven participants were recruited, and a total of 15 reportable variants were identified in 48% (13/27) of the participants. The panel results had implications for treatment in 37% (10/27) of participants. Phenomizer identified the genes harbouring variants from HPO terms in 33% (9/27) of participants. This study shows the clinical efficacy that genetic testing has in the care of PID. However, it also highlights some of the disadvantages of gene panels in the rapidly moving field of PID genomics and current challenges in HPO term assignment for PID.