Genome-wide association study in patients with pulmonary Mycobacterium avium complex disease

• Published in: The European respiratory journal Vol. 58; no. 2; p. 1902269
• Main Authors: Namkoong, Ho, Omae, Yosuke, Asakura, Takanori, Ishii, Makoto, Suzuki, Shoji, Morimoto, Kozo, Kawai, Yosuke, Emoto, Katsura, Oler, Andrew J, Szymanski, Eva P, Yoshida, Mitsunori, Matsuda, Shuichi, Yagi, Kazuma, Hase, Isano, Nishimura, Tomoyasu, Sasaki, Yuka, Asami, Takahiro, Shiomi, Tetsuya, Matsubara, Hiroaki, Shimada, Hisato, Hamamoto, Junko, Jhun, Byung Woo, Kim, Su-Young, Huh, Hee Jae, Won, Hong-Hee, Ato, Manabu, Kosaki, Kenjiro, Betsuyaku, Tomoko, Fukunaga, Koichi, Kurashima, Atsuyuki, Tettelin, Hervé, Yanai, Hideki, Mahasirimongkol, Surakameth, Olivier, Kenneth N, Hoshino, Yoshihiko, Koh, Won-Jung, Holland, Steven M, Tokunaga, Katsushi, Hasegawa, Naoki
• Format: Journal Article
• Language: English
• Published: England 01.08.2021
• ISSN: 0903-1936; 1399-3003
• DOI: 10.1183/13993003.02269-2019

Nontuberculous mycobacteria (NTM) are environmental mycobacteria that can cause a chronic progressive lung disease. Although epidemiological data indicate potential genetic predisposition, its nature remains unclear. We aimed to identify host susceptibility loci for complex (MAC), the most common NTM pathogen. This genome-wide association study (GWAS) was conducted in Japanese patients with pulmonary MAC and healthy controls, followed by genotyping of candidate single-nucleotide polymorphisms (SNPs) in another Japanese cohort. For verification by Korean and European ancestry, we performed SNP genotyping. The GWAS discovery set included 475 pulmonary MAC cases and 417 controls. Both GWAS and replication analysis of 591 pulmonary MAC cases and 718 controls revealed the strongest association with chromosome 16p21, particularly with rs109592 (p=1.64E-13, odds ratio=0.54), which is in an intronic region of the calcineurin like EF-hand protein 2 ( ). Expression quantitative trait loci analysis demonstrated an association with lung CHP2 expression. CHP2 was expressed in the lung tissue in pulmonary MAC disease. This SNP was associated with the nodular bronchiectasis subtype. This SNP was also significantly associated with the disease in patients of Korean (p=2.18E-12, odds ratio=0.54) and European (p=5.12E-03, odds ratio=0.63) ancestry. We identified rs109592 in the locus as a susceptibility marker for pulmonary MAC disease.