UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Whole exome sequencing analysis in severe chronic obstructive pulmonary disease

Qiao, D; Ameli, A; Prokopenko, D; Chen, H; Kho, AT; Parker, MM; Morrow, J; ... Cho, MH; + view all (2018) Whole exome sequencing analysis in severe chronic obstructive pulmonary disease. Human Molecular Genetics , 27 (21) pp. 3801-3812. 10.1093/hmg/ddy269. Green open access

[thumbnail of whole exome sequencing paper.pdf]
whole exome sequencing paper.pdf - Accepted Version

Download (529kB) | Preview


Chronic obstructive pulmonary disease (COPD), one of the leading causes of death worldwide, is substantially influenced by genetic factors. Alpha-1 antitrypsin deficiency demonstrates that rare coding variants of large effect can influence COPD susceptibility. To identify additional rare coding variants in patients with severe COPD, we conducted whole exome sequencing analysis in 2543 subjects from two family-based studies (Boston Early-Onset COPD Study and International COPD Genetics Network) and one case-control study (COPDGene). Applying a gene-based segregation test in the family-based data, we identified significant segregation of rare loss of function variants in TBC1D10A and RFPL1 (P-value < 2x10-6), but were unable to find similar variants in the case-control study. In single-variant, gene-based and pathway association analyses, we were unable to find significant findings that replicated or were significant in meta-analysis. However, we found that the top results in the two datasets were in proximity to each other in the protein-protein interaction network (P-value = 0.014), suggesting enrichment of these results for similar biological processes. A network of these association results and their neighbors was significantly enriched in the transforming growth factor beta-receptor binding and cilia-related pathways. Finally, in a more detailed examination of candidate genes, we identified individuals with putative high-risk variants, including patients harboring homozygous mutations in genes associated with cutis laxa and Niemann-Pick Disease Type C. Our results likely reflect heterogeneity of genetic risk for COPD along with limitations of statistical power and functional annotation, and highlight the potential of network analysis to gain insight into genetic association studies.

Type: Article
Title: Whole exome sequencing analysis in severe chronic obstructive pulmonary disease
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1093/hmg/ddy269
Publisher version: https://doi.org/10.1093/hmg/ddy269
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > VP: Health
URI: https://discovery.ucl.ac.uk/id/eprint/10060801
Downloads since deposit
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item