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皮质类固醇药物遗传学:CRHR1基因序列变异与吸入皮质类固醇治疗的哮喘患者肺功能改善的关联

Corticosteroid pharmacogenetics: association of sequence variants in CRHR1 with improved lung function in asthmatics treated with inhaled corticosteroids.

作者信息

Tantisira Kelan G, Lake Stephen, Silverman Eric S, Palmer Lyle J, Lazarus Ross, Silverman Edwin K, Liggett Stephen B, Gelfand Erwin W, Rosenwasser Lanny J, Richter Brent, Israel Elliot, Wechsler Michael, Gabriel Stacey, Altshuler David, Lander Eric, Drazen Jeffrey, Weiss Scott T

机构信息

Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

出版信息

Hum Mol Genet. 2004 Jul 1;13(13):1353-9. doi: 10.1093/hmg/ddh149. Epub 2004 May 5.

Abstract

Corticosteroids mediate a variety of immunological actions and are commonly utilized in the treatment of a wide range of diseases. Unfortunately, therapy with this class of medications is associated with a large proportion of non-responders and significant side effects. Inhaled corticosteroids are the most commonly used asthma controller therapy. However, asthmatic response to corticosteroids also varies widely between individuals. We investigated the genetic contribution to the variation in response to inhaled corticosteroid therapy in asthma. The association of longitudinal change in lung function and single nucleotide polymorphisms from candidate genes crucial to the biologic actions of corticosteroids were evaluated in three independent asthmatic clinical trial populations utilizing inhaled corticosteroids as the primary therapy in at least one treatment arm. Variation in one gene, corticotropin-releasing hormone receptor 1 (CRHR1) was consistently associated with enhanced response to therapy in each of our three populations. Individuals homozygous for the variants of interest manifested a doubling to quadrupling of the lung function response to corticosteroids compared with lack of the variants (P-values ranging from 0.006 to 0.025 for our three asthmatic populations). As the primary receptor mediating the release of adrenocorticotropic hormone, which regulates endogenous cortisol levels, CRHR1 plays a pivotal, pleiotropic role in steroid biology. These data indicate that genetic variants in CRHR1 have pharmacogenetic effects influencing asthmatic response to corticosteroids, provide a rationale for predicting therapeutic response in asthma and other corticosteroid-treated diseases, and suggests this gene pathway as a potential novel therapeutic target.

摘要

皮质类固醇介导多种免疫作用,常用于治疗多种疾病。不幸的是,这类药物治疗伴随着很大比例的无反应者和显著的副作用。吸入性皮质类固醇是最常用的哮喘控制疗法。然而,哮喘患者对皮质类固醇的反应在个体之间也有很大差异。我们研究了基因对哮喘患者吸入性皮质类固醇治疗反应差异的影响。在三个独立的哮喘临床试验人群中,评估了肺功能的纵向变化与对皮质类固醇生物学作用至关重要的候选基因单核苷酸多态性之间的关联,这些人群中至少有一个治疗组将吸入性皮质类固醇作为主要治疗方法。在我们的三个人群中,一个基因促肾上腺皮质激素释放激素受体1(CRHR1)的变异始终与治疗反应增强相关。与缺乏相关变异的个体相比,携带感兴趣变异的纯合子个体对皮质类固醇的肺功能反应增加了一倍至四倍(我们的三个哮喘人群的P值范围为0.006至0.025)。作为介导促肾上腺皮质激素释放的主要受体,促肾上腺皮质激素调节内源性皮质醇水平,CRHR1在类固醇生物学中起着关键的、多效性的作用。这些数据表明,CRHR1基因变异具有影响哮喘患者对皮质类固醇反应的药物遗传学效应,为预测哮喘和其他皮质类固醇治疗疾病的治疗反应提供了理论依据,并表明该基因途径是一个潜在的新型治疗靶点。

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