Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico

• Published in: PloS one 2014-09, Vol.9 (9), p.e108204-e108204
• Main Authors: Ballester, Veroushka, Guo, Xiuqing, Vendrell, Roberto, Haritunians, Talin, Klomhaus, Alexandra M, Li, Dalin, McGovern, Dermot P B, Rotter, Jerome I, Torres, Esther A, Taylor, Kent D
• Format: Article
• Language: English
• Subjects: Adult; Biology and Life Sciences; Continents; Descent; Disease control; Female; Genes; Genetic Association Studies; Genetic Predisposition to Disease; Genetics; Genome-Wide Association Study; Genomes; Genomics; Haplotypes; Humans; Inflammatory bowel disease; Inflammatory bowel diseases; Inflammatory Bowel Diseases - genetics; Intestine; Male; Medicine and Health Sciences; Middle Aged; NOD2 protein; Nod2 Signaling Adaptor Protein - genetics; Polymorphism, Single Nucleotide; Population studies; Populations; Puerto Rico; Quantitative Trait Loci; Receptors, Interleukin - genetics; Risk Factors; Rodents; Single-nucleotide polymorphism; Studies; Ulcerative colitis; Young Adult
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0108204

The Puerto Rico population may be modeled as an admixed population with contributions from three continents: Sub-Saharan Africa, Ancient America, and Europe. Extending the study of the genetics of inflammatory bowel disease (IBD) to an admixed population such as Puerto Rico has the potential to shed light on IBD genes identified in studies of European populations, find new genes contributing to IBD susceptibility, and provide basic information on IBD for the care of US patients of Puerto Rican and Latino descent. In order to study the association between immune-related genes and Crohn's disease (CD) and ulcerative colitis (UC) in Puerto Rico, we genotyped 1159 Puerto Rican cases, controls, and family members with the ImmunoChip. We also genotyped 832 subjects from the Human Genome Diversity Panel to provide data for estimation of global and local continental ancestry. Association of SNPs was tested by logistic regression corrected for global continental descent and family structure. We observed the association between Crohn's disease and NOD2 (rs17313265, 0.28 in CD, 0.19 in controls, OR 1.5, p = 9×10-6) and IL23R (rs11209026, 0.026 in CD, 0.0.071 in controls, OR 0.4, p = 3.8×10-4). The haplotype structure of both regions resembled that reported for European populations and "local" continental ancestry of the IL23R gene was almost entirely of European descent. We also observed suggestive evidence for the association of the BAZ1A promoter SNP with CD (rs1200332, 0.45 in CD, 0.35 in controls, OR 1.5, p = 2×10-6). Our estimate of continental ancestry surrounding this SNP suggested an origin in Ancient America for this putative susceptibility region. Our observations underscored the great difference between global continental ancestry and local continental ancestry at the level of the individual gene, particularly for immune-related loci.