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β2-肾上腺素能受体基因多态性在哮喘中的意义。

The significance of beta2-adrenergic receptor polymorphisms in asthma.

作者信息

Litonjua Augusto A

机构信息

Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Curr Opin Pulm Med. 2006 Jan;12(1):12-7. doi: 10.1097/01.mcp.0000198068.50457.95.

Abstract

PURPOSE OF REVIEW

The gene that encodes the beta2-adrenergic receptor (ADRB2) is one of the most studied candidate genes in asthma. This review examines recent articles of the relationship between ADRB2 polymorphisms and asthma.

RECENT FINDINGS

Candidate gene association studies of ADRB2 and asthma have been dominated by analyses of the two common non-synonymous coding single nucleotide polymorphisms, Arg16Gly and Glu27Gly. Published studies have yielded inconsistent results. Three recent meta-analyses on the effects of these two polymorphisms have found no associations with asthma, although there were suggestions of associations with other asthma-related phenotypes, such as nocturnal asthma and asthma severity. Other recent studies have investigated other single nucleotide polymorphisms in this gene (i.e. single nucleotide polymorphisms in the promoter region and other single nucleotide polymorphisms in the coding region). These analyses have investigated the association between these single nucleotide polymorphisms (and haplotypes of these polymorphisms) and asthma-related phenotypes such as lung function, airways hyperresponsiveness, and response to a bronchodilator, and have suggested that certain regions of the gene may be associated with different phenotypes. Results from these studies, however, have also been inconsistent.

SUMMARY

Polymorphisms of ADRB2 are not major risk factors for the development of asthma. These polymorphisms are likely to be important, however, in determining drug response. Future studies need to fully characterize all of the variation in the gene and perform comprehensive association studies. Finally, interactions between ADRB2 and other genes in the beta-agonist pathway are an important and active area of research that will shed more light on inter-individual differences in drug response.

摘要

综述目的

编码β2肾上腺素能受体(ADRB2)的基因是哮喘领域研究最多的候选基因之一。本综述探讨了ADRB2基因多态性与哮喘之间关系的近期文章。

近期研究发现

ADRB2与哮喘的候选基因关联研究主要集中在两种常见的非同义编码单核苷酸多态性,即Arg16Gly和Glu27Gly的分析上。已发表的研究结果并不一致。最近三项关于这两种多态性影响的荟萃分析未发现与哮喘有关联,尽管有迹象表明与其他哮喘相关表型有关联,如夜间哮喘和哮喘严重程度。其他近期研究调查了该基因中的其他单核苷酸多态性(即启动子区域的单核苷酸多态性和编码区域的其他单核苷酸多态性)。这些分析研究了这些单核苷酸多态性(以及这些多态性的单倍型)与哮喘相关表型之间的关联,如肺功能、气道高反应性和对支气管扩张剂的反应,并表明该基因的某些区域可能与不同表型有关联。然而,这些研究的结果也不一致。

总结

ADRB2基因多态性不是哮喘发病的主要危险因素。然而,这些多态性可能在决定药物反应方面很重要。未来的研究需要全面表征该基因的所有变异,并进行全面的关联研究。最后,ADRB2与β-激动剂途径中其他基因之间的相互作用是一个重要且活跃的研究领域,将为药物反应的个体差异提供更多的线索。

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