4.4 Article

The A118G single-nucleotide polymorphism in OPRM1 is a risk factor for asthma severity

Journal

ALLERGOLOGY INTERNATIONAL
Volume 71, Issue 1, Pages 55-65

Publisher

JAPANESE SOC ALLERGOLOGY
DOI: 10.1016/j.alit.2021.08.006

Keywords

Allergic asthma; A118G; OPRM1; Polymorphism; Th2 cell differentiation

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [25461164, 17K09624, 16K19608, 19K17913]
  2. Japanese Society of Allergology

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This study found that asthma patients carrying the OPRM1 GG genotype exhibit enhanced airway hyperresponsiveness in the absence of forced stress exposure, possibly due to enhanced Th2 cell differentiation in regional lymph nodes. Naloxone methiodide injection can reduce Th2 cell increase and eosinophil elevation in GG mice, bringing them back to the levels seen in AA mice.
Background: Although population studies have implicated emotional burden in asthma severity, the underlying genetic risk factors are not completely understood. We aimed to evaluate the genetic influence of a functional single-nucleotide polymorphism (SNP) in the stress-related m-opioid receptor gene (OPRM1; A118G SNP, rs1799971) on asthma severity. Methods: We initially assessed disease severity in asthmatic outpatients carrying A118G. Using an ovalbumin-induced experimental asthma rodent model harboring the functionally equivalent SNP, we investigated the mechanism by which this SNP influences the allergic immune response. Results: Among 292 outpatients, 168 underwent airway hyperresponsiveness (AHR) to methacholine testing. Compared with patients carrying the AA and AG genotypes, those carrying the GG genotype exhibited enhanced AHR. The stress levels were presumed to be moderate among patients and were comparable among genotypes. Compared with Oprm1 AA mice, GG mice demonstrated aggravated asthma-related features and increased pulmonary interleukin-4thornCD4thorn effector and effector memory T cells under everyday life stress conditions. Intraperitoneal naloxone methiodide injection reduced effector CD4thorn T cell elevation associated with increased eosinophil numbers in bronchoalveolar lavage fluid of GG mice to the levels in AA mice, suggesting that elevated Th2 cell generation in the bronchial lymph node (BLN) of GG mice induces enhanced eosinophilic inflammation. Conclusions: Without forced stress exposure, patients with asthma carrying the OPRM1 GG genotype exhibit enhanced AHR, attributable to enhanced Th2 cell differentiation in the regional lymph node. Further research is necessary to elucidate the role of the OPRM1 A118G genotype in the Th2 cell differentiation pathway in the BLN. Copyright (c) 2021, Japanese Society of Allergology. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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