TY - JOUR
T1 - Novel Genetic Loci for Nontuberculous Mycobacterial Pulmonary Disease and Potential Protective Effect of Body Mass Index
AU - Park, Kyungtaek
AU - Kim, Hyejin
AU - Huh, Hee Jae
AU - Namkoong, Ho
AU - Hasegawa, Naoki
AU - Nishimura, Tomoyasu
AU - Asakura, Takanori
AU - Morimoto, Kozo
AU - Kurashima, Atsuyuki
AU - Omae, Yosuke
AU - Kawai, Yosuke
AU - Tokunaga, Katsushi
AU - Berghout, Joanne
AU - Fennelly, Kevin P.
AU - Holland, Steven M.
AU - Cho, Jaeyoung
AU - Yim, Jae Joon
AU - Won, Sungho
AU - Jhun, Byung Woo
AU - Won, Hong Hee
N1 - Publisher Copyright:
Copyright © 2025 by the American Thoracic Society. This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/pages/standard-publication-reuse-rights)
PY - 2025/11
Y1 - 2025/11
N2 - Rationale: Although nontuberculous mycobacteria (NTM) are widespread, only some individuals develop NTM pulmonary disease (NTM-PD), suggesting the involvement of host factors. Objectives: To identify the genomic structure of NTM-PD and determine whether a definitive association exists between NTM-PD and nine risk factors. Methods: We performed genome-wide association studies in two independent Korean cohorts involving 1,949 patients with NTM-PD and 2,955 healthy participants. Significantly associated genetic variants were validated in Japanese (1,137 cases, 1,546 controls) and European (243 cases, 570 controls) cohorts, respectively. Genes associated with lead variants were identified and their roles in NTM-PD were supported by single-cell transcriptome datasets. Genetic correlations and Mendelian randomization between NTM-PD and nine risk factors were examined. Measurements and Main Results: We identified two novel loci and replicated a locus associated with NTM-PD: rs60084385 (odds ratio [OR], 1.34; 95% confidence interval [CI], 1.21–1.48; P = 6.97 × 10−9), rs1479595 (OR, 1.40; 95% CI, 1.27–1.55; P = 7.08 × 10−11), and rs194792 (OR, 1.70; 95% CI, 1.50–1.93; P = 1.39 × 10−16). These associations were replicated in the independent cohorts. The three loci were significantly associated with expression of IL1Rs, PDE8B (phosphodiesterase 8B), and PRKCB (protein kinase C β), respectively, whose involvement in the pathogenesis of NTM-PD was further validated. Among the risk factors, only body mass index demonstrated both a significant genetic correlation with NTM-PD (rg, −0.57; false discovery rate, 1.33 × 10−5) and a potential causal relationship (OR, 0.38; 95% CI, 0.24–0.59; false discovery rate, 8.55 × 10−5). Conclusions: Our study identified three genetic loci associated with NTM-PD and a negative association of body mass index with NTM-PD.
AB - Rationale: Although nontuberculous mycobacteria (NTM) are widespread, only some individuals develop NTM pulmonary disease (NTM-PD), suggesting the involvement of host factors. Objectives: To identify the genomic structure of NTM-PD and determine whether a definitive association exists between NTM-PD and nine risk factors. Methods: We performed genome-wide association studies in two independent Korean cohorts involving 1,949 patients with NTM-PD and 2,955 healthy participants. Significantly associated genetic variants were validated in Japanese (1,137 cases, 1,546 controls) and European (243 cases, 570 controls) cohorts, respectively. Genes associated with lead variants were identified and their roles in NTM-PD were supported by single-cell transcriptome datasets. Genetic correlations and Mendelian randomization between NTM-PD and nine risk factors were examined. Measurements and Main Results: We identified two novel loci and replicated a locus associated with NTM-PD: rs60084385 (odds ratio [OR], 1.34; 95% confidence interval [CI], 1.21–1.48; P = 6.97 × 10−9), rs1479595 (OR, 1.40; 95% CI, 1.27–1.55; P = 7.08 × 10−11), and rs194792 (OR, 1.70; 95% CI, 1.50–1.93; P = 1.39 × 10−16). These associations were replicated in the independent cohorts. The three loci were significantly associated with expression of IL1Rs, PDE8B (phosphodiesterase 8B), and PRKCB (protein kinase C β), respectively, whose involvement in the pathogenesis of NTM-PD was further validated. Among the risk factors, only body mass index demonstrated both a significant genetic correlation with NTM-PD (rg, −0.57; false discovery rate, 1.33 × 10−5) and a potential causal relationship (OR, 0.38; 95% CI, 0.24–0.59; false discovery rate, 8.55 × 10−5). Conclusions: Our study identified three genetic loci associated with NTM-PD and a negative association of body mass index with NTM-PD.
KW - BMI
KW - genome-wide association study
KW - NTM-PD
UR - https://www.scopus.com/pages/publications/105039528889
U2 - 10.1164/rccm.202406-1253OC
DO - 10.1164/rccm.202406-1253OC
M3 - Journal article
C2 - 40938630
AN - SCOPUS:105039528889
SN - 1073-449X
VL - 211
SP - 2191
EP - 2202
JO - American Journal of Respiratory and Critical Care Medicine
JF - American Journal of Respiratory and Critical Care Medicine
IS - 11
ER -