Department of Biochemistry, North West University, Mahikeng 2735, South Africa.
Department of Family Medicine, Walter Sisulu University, East London 5200, South Africa.
Genes (Basel). 2022 Aug 5;13(8):1394. doi: 10.3390/genes13081394.
Objective: This study describes the single nucleotide polymorphisms (SNPs) in amlodipine-associated genes and assesses their correlation with blood pressure control among South African adults with hypertension. Methods: In total, 304 hypertensive patients on amlodipine treatment belonging to the indigenous Swati, Xhosa and Zulu population groups of South Africa were recruited between June 2017 and June 2019. Participants were categorized into: controlled (blood pressure < 140/90 mmHg) and uncontrolled (blood pressure ≥ 140/90 mmHg) hypertension. Thirteen SNPs in amlodipine pharmacogenes with a high PharmGKB evidence base were selected and genotyped using MassArray (Agena BioscienceTM). Logistic regression was fitted to identify significant associations between the SNPs and blood pressure control with amlodipine. Results: The majority of the participants were females (76.6%), older than 45 years (89.1%) and had uncontrolled hypertension (52.3%). Of the 13 SNPs genotyped, five SNPs, rs1042713 (minor allele frequency = 45.9%), rs10494366 (minor allele frequency = 35.3%), rs2239050 (minor allele frequency = 28.7%), rs2246709 (minor allele frequency = 51.6%) and rs4291 (minor allele frequency = 34.4%), were detected among the Xhosa participants, while none were detected among the Swati and Zulu tribal groups. Variants rs1042713 and rs10494366 demonstrated an expression frequency of 97.5% and 79.5%, respectively. Variant TA genotype of rs4291 was significantly associated with uncontrolled hypertension. No association was established between blood pressure response to amlodipine and the remaining four SNPs. Conclusions: This study reports the discovery of five SNPs in amlodipine genes (rs2239050, rs2246709, rs4291, rs1042713 and rs10494366) among the indigenous Xhosa-speaking tribe of South Africa. In addition, the TA genotype of rs4291 was associated with blood pressure control in this cohort. These findings might open doors for more pharmacogenomic studies, which could inform innovations to personalised anti-hypertensive treatment in the ethnically diverse population of South Africa.
本研究描述了氨氯地平相关基因中的单核苷酸多态性(SNPs),并评估了它们与南非高血压成年患者血压控制的相关性。方法:本研究共纳入了 304 名接受氨氯地平治疗的高血压患者,他们属于南非本土的斯瓦蒂、科萨和祖鲁族群,于 2017 年 6 月至 2019 年 6 月期间招募。参与者分为:血压控制良好(血压<140/90mmHg)和血压控制不佳(血压≥140/90mmHg)两组。选择了具有高 PharmGKB 证据基础的氨氯地平药物基因中的 13 个 SNPs,并使用 MassArray(Agena BioscienceTM)进行基因分型。使用逻辑回归来确定 SNPs 与氨氯地平降压治疗之间的显著相关性。结果:大多数参与者为女性(76.6%),年龄大于 45 岁(89.1%),血压控制不佳(52.3%)。在 13 个基因分型的 SNPs 中,有 5 个 SNPs(rs1042713 的等位基因频率为 45.9%、rs10494366 的等位基因频率为 35.3%、rs2239050 的等位基因频率为 28.7%、rs2246709 的等位基因频率为 51.6%和 rs4291 的等位基因频率为 34.4%)在科萨参与者中被检测到,而在斯瓦蒂和祖鲁部落群体中均未检测到。rs1042713 和 rs10494366 的变体表达频率分别为 97.5%和 79.5%。rs4291 的 TA 基因型与血压控制不佳显著相关。在剩余的四个 SNPs 中,未建立血压对氨氯地平反应与 SNP 之间的关联。结论:本研究在南非本土的科萨族中发现了氨氯地平基因中的五个 SNPs(rs2239050、rs2246709、rs4291、rs1042713 和 rs10494366)。此外,rs4291 的 TA 基因型与该队列的血压控制相关。这些发现可能为更多的药物基因组学研究打开大门,这可能为南非多样化种族人群的个体化抗高血压治疗提供创新思路。