Rationale: Common and rare variants that are associated with the risk of developing idiopathic pulmonary fibrosis (IPF) have been identified predominantly in European ancestry populations. Objective: To better understand the genetic variants that contribute to IPF in individuals with Asian ancestry, we conducted a genome-wide association study of IPF in East Asian populations. Methods: We included 1,026 patients with IPF and compared them to 1,723 unaffected controls of Japanese and Korean ancestry. Genome-wide association analysis was conducted in the Japanese and Korean ancestry cohorts separately and combined using meta-analysis. Restricted maximum likelihood was used to estimate the SNP-based heritability and local ancestry of chromosome 11 was inferred for each subject. Results: We identified loci on chromosomes 4 (FAM13A; rs7690839), 5 (TERT; rs7734992), 6 (DSP; rs2076295), and 11 (MUC5B; rs35705950) that were significantly associated with risk of IPF. Importantly, the sentinel variants in each of these loci are the same as, or in strong linkage disequilibrium with, the risk variants that have been observed in studies of European ancestry populations. In aggregate, common variants (not including the MUC5B promoter variant) account for approximately 25% of the risk of developing IPF in these East Asian ancestry cohorts. Moreover, local ancestry analysis indicates that the presence of MUC5B promoter variant in the East Asian population is not a result of admixture with European ancestry populations. Conclusions: We conclude that the IPF risk loci in East Asian populations are shared with those of European ancestry populations, although their risk allele frequencies and effect sizes differ. These findings indicate shared genetic risk factors of IPF across ancestries.
Peljto, A. L., Furusawa, H., Puthenvedu, D., Lee, J. S., Steele, M. P., Brancato, J., Cardwell, J., Blumhagen, R. Z., De Andrade, J., Bendstrup, E., Blackwell, T. S., Bonella, F., Borie, R., Braybrooke, R., Brown, K. K., Carbone, R. G., Christie, J. D., Costabel, U., Crestani, B., Davidsen, J. R., Dieude, P., Donnelly, S. C., Egan, J., Eickelberg, O., Fernández Pérez, E. R., Fiddler, C. A., Foster, E. E., Gibson, K. F., Gudmundsson, G., Guthridge, J. M., Henry, M. T., Hirani, N., Jenkins, R. G., Kass, D. J., Keane, M. P., Kokturk, N., Kropski, J. A., Lederer, D., Leone, P. M., Linderholm, A. L., Maher, T. M., Mathai, S. K., Mccarthy, C., Mcelroy, A. N., Mogulkoc, N., Molina-Molina, M., Molyneaux, P. L., Montesi, S. B., Nathan, S. D., Noth, I., Olaniyi, J. A., Oldham, J. M., O'Reilly, K. M. A., Palmisciano, A. J., Pardo, A., Parfrey, H., Planas-Cerezales, L., Poletti, V., Porteous, M. K., Puppo, F., Richeldi, L., Rojas, M., Salinas, M., Schluger, N., Selman, M., Shea, B. S., Sterclova, M., Solomon, J. J., Tomassetti, S., Vasakova, M. K., Zhang, Y., Corte, T. J., Dickinson, J. L., Glaspole, I., Moodley, Y. P., Prele, C. M. A., Ryerson, C. J., Wolters, P. J., Jinno, M., Miyata, Y., Akagawa, S., Narumoto, O., Kita, T., Shibayama, T., Li, T., Owan, I., Wakamatsu, K., Arai, T., Hirose, M., Kim, D. S., Ohta, K., Ohta, S., Park, J. S., Park, M. S., Yang, I. V., Fingerlin, T. E., Miyazaki, Y., Okamoto, T., Inoue, Y., Song, J. W., Schwartz, D. A., Idiopathic Pulmonary Fibrosis Risk Loci in East Asian Populations Mirror those of European Populations, <<AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE>>, 2026; 2026 (2026): 1-6. [doi:10.1093/ajrccm/aamag152] [https://hdl.handle.net/10807/338220]
Idiopathic Pulmonary Fibrosis Risk Loci in East Asian Populations Mirror those of European Populations
Richeldi, Luca;
2026
Abstract
Rationale: Common and rare variants that are associated with the risk of developing idiopathic pulmonary fibrosis (IPF) have been identified predominantly in European ancestry populations. Objective: To better understand the genetic variants that contribute to IPF in individuals with Asian ancestry, we conducted a genome-wide association study of IPF in East Asian populations. Methods: We included 1,026 patients with IPF and compared them to 1,723 unaffected controls of Japanese and Korean ancestry. Genome-wide association analysis was conducted in the Japanese and Korean ancestry cohorts separately and combined using meta-analysis. Restricted maximum likelihood was used to estimate the SNP-based heritability and local ancestry of chromosome 11 was inferred for each subject. Results: We identified loci on chromosomes 4 (FAM13A; rs7690839), 5 (TERT; rs7734992), 6 (DSP; rs2076295), and 11 (MUC5B; rs35705950) that were significantly associated with risk of IPF. Importantly, the sentinel variants in each of these loci are the same as, or in strong linkage disequilibrium with, the risk variants that have been observed in studies of European ancestry populations. In aggregate, common variants (not including the MUC5B promoter variant) account for approximately 25% of the risk of developing IPF in these East Asian ancestry cohorts. Moreover, local ancestry analysis indicates that the presence of MUC5B promoter variant in the East Asian population is not a result of admixture with European ancestry populations. Conclusions: We conclude that the IPF risk loci in East Asian populations are shared with those of European ancestry populations, although their risk allele frequencies and effect sizes differ. These findings indicate shared genetic risk factors of IPF across ancestries.
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