The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries

• Published in: Chest Vol. 147; no. 2; p. 460
• Main Authors: Peljto, Anna L, Selman, Moises, Kim, Dong Soon, Murphy, Elissa, Tucker, Laura, Pardo, Annie, Lee, Jung Su, Ji, Wonjun, Schwarz, Marvin I, Yang, Ivana V, Schwartz, David A, Fingerlin, Tasha E
• Format: Journal Article
• Language: English
• Published: United States 01.02.2015
• Subjects: Aged; Asian Continental Ancestry Group - genetics; European Continental Ancestry Group - genetics; Female; Genetic Association Studies; Genetic Variation; Humans; Idiopathic Pulmonary Fibrosis - ethnology; Idiopathic Pulmonary Fibrosis - genetics; Intracellular Signaling Peptides and Proteins - genetics; Logistic Models; Male; Mexico; Middle Aged; Mucin-5B - genetics; Republic of Korea; Signal Transduction - genetics; Mexico; Republic of Korea
• ISSN: 1931-3543
• DOI: 10.1378/chest.14-0867

Polymorphisms in the MUC5B promoter, TOLLIP, and nine additional genetic loci have been associated with idiopathic pulmonary fibrosis (IPF) within non-Hispanic white populations. It is unknown whether these variants account for risk of IPF in other racial/ethnic populations. We conducted a candidate single nucleotide polymorphism (SNP) association study in cohorts of Mexican and Korean patients with IPF. We chose 12 SNPs from 11 loci that are associated with IPF among non-Hispanic whites and genotyped these SNPs in cohorts of Mexican (83 patients, 111 control subjects) and Korean (239 patients, 87 control subjects) people. Each SNP was tested for association with IPF, after adjusting for age and sex. The MUC5B promoter SNP rs35705950 was associated with IPF in the Mexican (OR = 7.36, P = .0001), but not the Korean (P = .99) cohort. The SNP in IVD (chromosome15, rs2034650) was significantly associated with pulmonary fibrosis in both the Mexican (OR = 0.40, P = .01) and Korean (OR = 0.13, P = .0008) cohorts. In the Korean cohort, there were no other variants associated with disease. In the Mexican cohort, SNPs on chromosomes 3, 4, and 11 were also associated with disease. The strongest identified genetic risk factor for IPF among the non-Hispanic white population, the MUC5B promoter polymorphism, is also a strong risk factor in a Mexican population, but is very rare in a Korean population. The majority of genetic variants that account for risk of IPF in groups other than non-Hispanic whites are unknown. Hispanic and Asian populations should be studied separately to identify genetic risk loci for IPF.