Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases

Introduction: The arachidonic acid (AA) pathway plays a crucial role in allergic inflammatory diseases; however, the functional roles of allergy-associated single nucleotide polymorphisms (SNPs) in this pathway remain incompletely illustrated. Methods: This study belongs to a part of an ongoing Sing...

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Main Authors: Sio, Yang Yie, Shi, Ping, Matta, Sri Anusha, Fok, Rachel Yu Ting, Chiang, Wen Chin, Say, Yee-How, Chew, Fook Tim
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/174277
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-174277
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Medicine, Health and Life Sciences
Asthma
Allergic rhinitis
spellingShingle Medicine, Health and Life Sciences
Asthma
Allergic rhinitis
Sio, Yang Yie
Shi, Ping
Matta, Sri Anusha
Fok, Rachel Yu Ting
Chiang, Wen Chin
Say, Yee-How
Chew, Fook Tim
Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
description Introduction: The arachidonic acid (AA) pathway plays a crucial role in allergic inflammatory diseases; however, the functional roles of allergy-associated single nucleotide polymorphisms (SNPs) in this pathway remain incompletely illustrated. Methods: This study belongs to a part of an ongoing Singapore/Malaysia cross-sectional genetics and epidemiological study (SMCSGES). We performed population genotyping on n = 2,880 individuals from the SMCSGES cohort to assess the associations of SNPs in the AA pathway genes with asthma and allergic rhinitis (AR). Spirometry assessments were performed to identify associations between SNPs and lung function among n = 74 pediatric asthmatic patients from the same cohort. Allergy-associated SNPs were functionally characterized using in vitro promoter luciferase assay, along with DNA methylome and transcriptome data of n = 237 peripheral blood mononuclear cell (PBMC) samples collected from a subset of the SMCSGES cohort. Results: Genetic association analysis showed 5 tag-SNPs from 4 AA pathway genes were significantly associated with asthma (rs689466 at COX2, rs35744894 at hematopoietic PGD2 synthase (HPGDS), rs11097414 at HPGDS, rs7167 at CRTH2, and rs5758 at TBXA2R, p < 0.05), whereas 3 tag-SNPs from HPGDS (rs35744894, rs11097414, and rs11097411) and 2 tag-SNPs from PTGDR (rs8019916 and rs41312470) were significantly associated with AR (p < 0.05). The asthma-associated rs689466 regulates COX2 promoter activity and associates with COX2 mRNA expression in PBMC. The allergy-associated rs1344612 was significantly associated with poorer lung function, increased risks of asthma and AR, and increased HPGDS promoter activity. The allergy-associated rs8019916 regulates PTGDR promoter activity and DNA methylation levels of cg23022053 and cg18369034 in PBMC. The asthma-associated rs7167 affects CRTH2 expression by regulating the methylation level of cg19192256 in PBMC. Conclusions: The present study identified multiple allergy-associated SNPs that modulate the transcript expressions of key genes in the AA pathway. The development of a "personalized medicine" approach with consideration of genetic influences on the AA pathway may hopefully result in efficacious strategies to manage and treat allergic diseases.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Sio, Yang Yie
Shi, Ping
Matta, Sri Anusha
Fok, Rachel Yu Ting
Chiang, Wen Chin
Say, Yee-How
Chew, Fook Tim
format Article
author Sio, Yang Yie
Shi, Ping
Matta, Sri Anusha
Fok, Rachel Yu Ting
Chiang, Wen Chin
Say, Yee-How
Chew, Fook Tim
author_sort Sio, Yang Yie
title Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
title_short Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
title_full Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
title_fullStr Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
title_full_unstemmed Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
title_sort functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases
publishDate 2024
url https://hdl.handle.net/10356/174277
_version_ 1795375047279378432
spelling sg-ntu-dr.10356-1742772024-03-31T15:40:12Z Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases Sio, Yang Yie Shi, Ping Matta, Sri Anusha Fok, Rachel Yu Ting Chiang, Wen Chin Say, Yee-How Chew, Fook Tim Lee Kong Chian School of Medicine (LKCMedicine) Medicine, Health and Life Sciences Asthma Allergic rhinitis Introduction: The arachidonic acid (AA) pathway plays a crucial role in allergic inflammatory diseases; however, the functional roles of allergy-associated single nucleotide polymorphisms (SNPs) in this pathway remain incompletely illustrated. Methods: This study belongs to a part of an ongoing Singapore/Malaysia cross-sectional genetics and epidemiological study (SMCSGES). We performed population genotyping on n = 2,880 individuals from the SMCSGES cohort to assess the associations of SNPs in the AA pathway genes with asthma and allergic rhinitis (AR). Spirometry assessments were performed to identify associations between SNPs and lung function among n = 74 pediatric asthmatic patients from the same cohort. Allergy-associated SNPs were functionally characterized using in vitro promoter luciferase assay, along with DNA methylome and transcriptome data of n = 237 peripheral blood mononuclear cell (PBMC) samples collected from a subset of the SMCSGES cohort. Results: Genetic association analysis showed 5 tag-SNPs from 4 AA pathway genes were significantly associated with asthma (rs689466 at COX2, rs35744894 at hematopoietic PGD2 synthase (HPGDS), rs11097414 at HPGDS, rs7167 at CRTH2, and rs5758 at TBXA2R, p < 0.05), whereas 3 tag-SNPs from HPGDS (rs35744894, rs11097414, and rs11097411) and 2 tag-SNPs from PTGDR (rs8019916 and rs41312470) were significantly associated with AR (p < 0.05). The asthma-associated rs689466 regulates COX2 promoter activity and associates with COX2 mRNA expression in PBMC. The allergy-associated rs1344612 was significantly associated with poorer lung function, increased risks of asthma and AR, and increased HPGDS promoter activity. The allergy-associated rs8019916 regulates PTGDR promoter activity and DNA methylation levels of cg23022053 and cg18369034 in PBMC. The asthma-associated rs7167 affects CRTH2 expression by regulating the methylation level of cg19192256 in PBMC. Conclusions: The present study identified multiple allergy-associated SNPs that modulate the transcript expressions of key genes in the AA pathway. The development of a "personalized medicine" approach with consideration of genetic influences on the AA pathway may hopefully result in efficacious strategies to manage and treat allergic diseases. Published version Fook Tim Chew has received research support from the National University of Singapore, Singapore Ministry of Education Academic Research Fund, Singapore Immunology Network, National Medical Research Council (NMRC) (Singapore), Biomedical Research Council (BMRC) (Singapore), National Research Foundation (NRF) (Singapore), Singapore Food Agency (SFA), and the Agency for Science Technology and Research (A*STAR) (Singapore); Grant No.: N-154-000-038-001, R-154-000-191-112, R-154-000-404-112, R-154-000-553-112, R-154-000-565-112, R-154-000-630-112, R-154-000-A08-592, R-154-000-A27-597, R-154-000-A91-592, R-154-000-A95-592, R-154-000-B99-114, BMRC/01/1/21/18/077, BMRC/04/1/21/19/315, BMRC/APG2013/108, SIgN-06-006, SIgN-08-020, NMRC/1150/2008, OFIRG20nov-0033, NRF-MP-2020-0004, SFS_RND_SUFP_001_04, W22W3D0006, H17/01/a0/008, and APG2013/108. Yang Yie SIO has received research support from the NUS Resilience & Growth Postdoctoral Fellowships with Grant No.: R-141-000-036-281. 2024-03-25T05:43:38Z 2024-03-25T05:43:38Z 2023 Journal Article Sio, Y. Y., Shi, P., Matta, S. A., Fok, R. Y. T., Chiang, W. C., Say, Y. & Chew, F. T. (2023). Functional polymorphisms of the arachidonic acid pathway associate with risks and clinical outcomes of allergic diseases. International Archives of Allergy and Immunology, 184(6), 609-623. https://dx.doi.org/10.1159/000530393 1018-2438 https://hdl.handle.net/10356/174277 10.1159/000530393 37231900 2-s2.0-85163199719 6 184 609 623 en International Archives of Allergy and Immunology © 2023 The Author(s). Published by S. Karger AG, Basel. This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. application/pdf