Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.


Change log
Authors
Grozeva, Detelina 
Carss, Keren 
Spasic-Boskovic, Olivera 
Tejada, Maria-Isabel 
Gecz, Jozef 
Abstract

To identify genetic causes of intellectual disability (ID), we screened a cohort of 986 individuals with moderate to severe ID for variants in 565 known or candidate ID-associated genes using targeted next-generation sequencing. Likely pathogenic rare variants were found in ∼11% of the cases (113 variants in 107/986 individuals: ∼8% of the individuals had a likely pathogenic loss-of-function [LoF] variant, whereas ∼3% had a known pathogenic missense variant). Variants in SETD5, ATRX, CUL4B, MECP2, and ARID1B were the most common causes of ID. This study assessed the value of sequencing a cohort of probands to provide a molecular diagnosis of ID, without the availability of DNA from both parents for de novo sequence analysis. This modeling is clinically relevant as 28% of all UK families with dependent children are single parent households. In conclusion, to diagnose patients with ID in the absence of parental DNA, we recommend investigation of all LoF variants in known genes that cause ID and assessment of a limited list of proven pathogenic missense variants in these genes. This will provide 11% additional diagnostic yield beyond the 10%-15% yield from array CGH alone.

Description
Keywords
Mendelian disease, developmental delay, intellectual disability, next-generation sequencing, Alleles, Cohort Studies, Computational Biology, Female, Genetic Association Studies, High-Throughput Nucleotide Sequencing, Humans, Inheritance Patterns, Intellectual Disability, Male, Mutation, Polymorphism, Single Nucleotide
Journal Title
Hum Mutat
Conference Name
Journal ISSN
1059-7794
1098-1004
Volume Title
36
Publisher
Hindawi Limited
Sponsorship
Wellcome Trust (100140/Z/12/Z)
Wellcome Trust (091310/Z/10/Z)
Action Medical Research (SP4640); the Birth Defect Foundation (RG45448); the Cambridge National Institute for Health Research Biomedical Research Centre (RG64219); the NIHR Rare Diseases BioResource (RBAG163); Wellcome Trust award WT091310; The Cell lines and DNA bank of Rett Syndrome, X-linked mental retardation and other genetic diseases (member of the Telethon Network of Genetic Biobanks (project no. GTB12001); the Genetic Origins of Congenital Heart Disease Study (GO-CHD)- funded by British Heart Foundation (BHF)