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哮喘加重的基因特征

Genetic Signatures of Asthma Exacerbation.

作者信息

Park Heung Woo, Tantisira Kelan G

机构信息

Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

The Channing Division of Network Medicine, Department of Medicine, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Allergy Asthma Immunol Res. 2017 May;9(3):191-199. doi: 10.4168/aair.2017.9.3.191.

DOI:10.4168/aair.2017.9.3.191
PMID:28293925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5352570/
Abstract

Asthma exacerbation (AE) usually denotes worsening of asthma symptoms that requires intense management to prevent further deterioration. AE has been reported to correlate with clinical and demographic factors, such as race, gender, and treatment compliance as well as environmental factors, such as viral infection, smoking, and air pollution. In addition, recent observations suggest that there are likely to be genetic factors specific to AE. Understanding genetic factors specific to AE is essential to develop therapy tailored for exacerbation-prone asthma. Here, we summarize the results of studies involving genetic risk factors for AE. To simplify and enhance understanding, we reviewed the studies according to the following categories: hypothesis-driven approaches, hypothesis-free approaches, gene-environment interactions, and pharmacogenetics.

摘要

哮喘急性加重(AE)通常指哮喘症状恶化,需要强化治疗以防止病情进一步恶化。据报道,AE与临床和人口统计学因素相关,如种族、性别和治疗依从性,以及环境因素,如病毒感染、吸烟和空气污染。此外,最近的观察结果表明,可能存在特定于AE的遗传因素。了解特定于AE的遗传因素对于开发针对易加重哮喘的治疗方法至关重要。在此,我们总结了涉及AE遗传危险因素的研究结果。为了简化并增进理解,我们根据以下类别对研究进行了综述:假设驱动方法、无假设方法、基因-环境相互作用和药物遗传学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/5352570/7cd171c7cca7/aair-9-191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/5352570/7cd171c7cca7/aair-9-191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c1/5352570/7cd171c7cca7/aair-9-191-g001.jpg

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Ann Am Thorac Soc. 2016 Mar;13 Suppl 1(Suppl 1):S85-90. doi: 10.1513/AnnalsATS.201507-459MG.
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Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment.儿童哮喘急性发作与精氨酸16β2-肾上腺素能受体基因多态性:一项按治疗分层的荟萃分析
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CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids.
多基因风险评分可识别哮喘和慢性阻塞性肺疾病的异质性。
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Asthma Exacerbations: Patient Features and Potential Long-Term Implications.哮喘恶化:患者特征及潜在长期影响。
Adv Exp Med Biol. 2023;1426:253-263. doi: 10.1007/978-3-031-32259-4_12.
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Polymorphisms in the gene have associations with asthma and chronic obstructive pulmonary disease.该基因中的多态性与哮喘和慢性阻塞性肺疾病有关。
J Thorac Dis. 2023 Feb 28;15(2):589-599. doi: 10.21037/jtd-22-820. Epub 2023 Feb 6.
6
Short-Term Exposure Effect of Ambient Fine Particulate Matter, Ozone and Cold Temperature on Emergency Room Visits for Asthma Patients.环境细颗粒物、臭氧和低温对哮喘患者急诊就诊的短期暴露影响。
Toxics. 2023 Jan 19;11(2):94. doi: 10.3390/toxics11020094.
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J Asthma Allergy. 2022 Aug 24;15:1143-1154. doi: 10.2147/JAA.S376499. eCollection 2022.
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Association of genetic variants of oxidative stress responsive kinase 1 (OXSR1) with asthma exacerbations in non-smoking asthmatics.氧化应激反应激酶 1(OXSR1)的遗传变异与非吸烟哮喘患者哮喘加重的关联。
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