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用于治疗2型糖尿病的胰高血糖素样肽-1激动剂的药物遗传学

Pharmacogenetics of Glucagon-like Peptide-1 Agonists for the Treatment of Type 2 Diabetes Mellitus.

作者信息

Karras Spyridon N, Rapti Eleni, Koufakis Theocharis, Kyriazou Angeliki, Goulis Dimitrios G, Kotsa Kalliopi

机构信息

Division of Endocrinology and Metabolism - Diabetes Center, First Department of Internal Medicine, Medical School, Aristotle University of Thessaloniki, AHEPA University Hospital, Thessaloniki, Greece.

Unit of Reproductive Endocrinology, First Department of Obstetrics and Gynecology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.

出版信息

Curr Clin Pharmacol. 2017;12(4):202-209. doi: 10.2174/1574884713666180221121512.

Abstract

BACKGROUND

Pharmacogenetics is a promising area of medical research, providing methods to identify the appropriate pharmaceutical agent and dosing for each unique patient. Glucagon- like peptide-1 (GLP-1) agonists are a novel therapeutic choice used in the treatment of type 2 diabetes mellitus (T2DM), demonstrating efficacy regarding glycemic control and weight loss. Therapeutic response to GLP-1 agonist treatment is a complex biophenomenon, dependent on a plethora of modifiable (diet, exercise, adherence) and non-modifiable (genetic individual variants, ethnic characteristics) parameters. Ιn this context, it has been hypothesized that genetic polymorphisms of GLP-1 related genes may be associated with the therapeutic response to GLP-1 agonist treatment. This review focuses on the most important polymorphisms of the GLP-1 biological network that could affect clinical response to GLP-1 agonist treatment.

METHODS

Biomedical databases were searched to identify key articles in the field and their results are critically presented in this review.

RESULT

Recent pharmacological and clinical studies demonstrated a significant variation in GLP-1 agonist treatment, in cohorts with homogeneous adherence to diet, exercise and antidiabetic treatment. These studies identified several cases of non-responders to GLP-1 agonist therapy, in association with specific allelic patterns of GLP-1 receptor or other biomolecules implicated in glucose homeostasis.

CONCLUSION

Although the exact DNA sequences that cause the molecular changes leading to a variable response to GLP-1 agonists have not been yet fully identified, these findings underline the importance of an individualized approach in anti-diabetic treatment.

摘要

背景

药物遗传学是医学研究中一个很有前景的领域,它为确定适合每个独特患者的药物及剂量提供了方法。胰高血糖素样肽-1(GLP-1)激动剂是用于治疗2型糖尿病(T2DM)的一种新型治疗选择,在血糖控制和体重减轻方面显示出疗效。对GLP-1激动剂治疗的反应是一种复杂的生物现象,取决于大量可改变的(饮食、运动、依从性)和不可改变的(基因个体变异、种族特征)参数。在这种背景下,有人推测GLP-1相关基因的遗传多态性可能与对GLP-1激动剂治疗的反应有关。本综述重点关注可能影响对GLP-1激动剂治疗临床反应的GLP-1生物网络的最重要多态性。

方法

检索生物医学数据库以识别该领域的关键文章,并在本综述中对其结果进行批判性呈现。

结果

近期的药理学和临床研究表明,在饮食、运动和抗糖尿病治疗依从性相同的队列中,GLP-1激动剂治疗存在显著差异。这些研究确定了几例对GLP-1激动剂治疗无反应的病例,与GLP-1受体或其他参与葡萄糖稳态的生物分子的特定等位基因模式有关。

结论

尽管导致对GLP-1激动剂产生可变反应的分子变化的确切DNA序列尚未完全确定,但这些发现强调了抗糖尿病治疗中个体化方法的重要性。

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