Sanchez-Ibarra Hector E, Reyes-Cortes Luisa M, Jiang Xian-Li, Luna-Aguirre Claudia M, Aguirre-Trevino Dionicio, Morales-Alvarado Ivan A, Leon-Cachon Rafael B, Lavalle-Gonzalez Fernando, Morcos Faruck, Barrera-Saldaña Hugo A
Molecular Genetics Laboratory, Vitagénesis, S.A. de C.V., Monterrey, Mexico.
Evolutionary Information Laboratory, Department of Biological Sciences, University of Texas at Dallas, Richardson, TX, United States.
Front Pharmacol. 2018 Apr 6;9:320. doi: 10.3389/fphar.2018.00320. eCollection 2018.
The treatment of Type 2 Diabetes Mellitus (T2DM) consists primarily of oral antidiabetic drugs (OADs) that stimulate insulin secretion, such as sulfonylureas (SUs) and reduce hepatic glucose production (e.g., biguanides), among others. The marked inter-individual differences among T2DM patients' response to these drugs have become an issue on prescribing and dosing efficiently. In this study, fourteen polymorphisms selected from Genome-wide association studies (GWAS) were screened in 495 T2DM Mexican patients previously treated with OADs to find the relationship between the presence of these polymorphisms and response to the OADs. Then, a novel association screening method, based on global probabilities, was used to globally characterize important relationships between the drug response to OADs and genetic and clinical parameters, including polymorphisms, patient information, and type of treatment. Two polymorphisms, -Ala1369Ser and -Glu23Lys, showed a significant impact on response to SUs. Heterozygous -Ala1369Ser variant (A/C) carriers exhibited a higher response to SUs compared to homozygous -Ala1369Ser variant (A/A) carriers (-value = 0.029) and to homozygous wild-type genotypes (C/C) (-value = 0.012). The homozygous -Glu23Lys variant (C/C) and wild-type (T/T) genotypes had a lower response to SUs compared to heterozygous (C/T) carriers (-value = 0.039). The screening of OADs response related genetic and clinical factors could help improve the prescribing and dosing of OADs for T2DM patients and thus contribute to the design of personalized treatments.
2型糖尿病(T2DM)的治疗主要包括口服抗糖尿病药物(OADs),如刺激胰岛素分泌的磺脲类药物(SUs)以及减少肝脏葡萄糖生成的药物(如双胍类)等。T2DM患者对这些药物的反应存在显著的个体差异,这已成为有效处方和给药的一个问题。在本研究中,对495名先前接受过OADs治疗的墨西哥T2DM患者进行了全基因组关联研究(GWAS)中筛选出的14种多态性检测,以寻找这些多态性的存在与对OADs反应之间的关系。然后,使用一种基于全局概率的新型关联筛选方法,全面表征对OADs的药物反应与遗传和临床参数之间的重要关系,这些参数包括多态性、患者信息和治疗类型。两种多态性,-Ala1369Ser和-Glu23Lys,对磺脲类药物的反应有显著影响。杂合-Ala1369Ser变体(A/C)携带者与纯合-Ala1369Ser变体(A/A)携带者相比,对磺脲类药物的反应更高(P值 = 0.029),与纯合野生型基因型(C/C)相比也是如此(P值 = 0.012)。与杂合(C/T)携带者相比,纯合-Glu23Lys变体(C/C)和野生型(T/T)基因型对磺脲类药物的反应较低(P值 = 0.039)。筛选与OADs反应相关的遗传和临床因素有助于改善T2DM患者OADs的处方和给药,从而有助于个性化治疗方案的设计。