| Literature DB >> 30060175 |
Dandi Qiao1, Asher Ameli1,2, Dmitry Prokopenko1, Han Chen3,4, Alvin T Kho5, Margaret M Parker1, Jarrett Morrow1, Brian D Hobbs1,6, Yanhong Liu7, Terri H Beaty8, James D Crapo9, Kathleen C Barnes10, Deborah A Nickerson11, Michael Bamshad12, Craig P Hersh1,6, David A Lomas13, Alvar Agusti14, Barry J Make9, Peter M A Calverley15, Claudio F Donner16, Emiel F Wouters17, Jørgen Vestbo18, Peter D Paré19, Robert D Levy19, Stephen I Rennard20,21, Ruth Tal-Singer22, Margaret R Spitz7, Amitabh Sharma1, Ingo Ruczinski23, Christoph Lange24, Edwin K Silverman1,6, Michael H Cho1,6,25.
Abstract
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.Entities:
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Year: 2018 PMID: 30060175 PMCID: PMC6196654 DOI: 10.1093/hmg/ddy269
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 5.121