Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
BMC Med Genet. 2012 Nov 22;13:112. doi: 10.1186/1471-2350-13-112.
This study investigated variation in NR1I2 and NR1I3 and its effect on plasma efavirenz levels in HIV/AIDS patients. Variability in plasma drug levels has largely led research on identifying causative variants in drug metabolising enzyme (DME) genes, with little focus on the nuclear receptor genes NR1I2 and NR1I3, coding for PXR and CAR, respectively, that are involved in regulating DMEs.
464 Bantu-speaking South Africans comprising of HIV/AIDS patients on efavirenz-based treatment (n=301) and 163 healthy subjects were genotyped for 6 SNPs in NR1I2 and NR1I3. 32 of the 301 patients had their DNA binding domains (DBDs) in NR1I2 and NR1I3 sequenced.
Significantly decreased efavirenz plasma concentrations were observed in patients carrying the NR1I3 rs3003596C/C and T/C genotypes (P=0.015 and P=0.010, respectively). Sequencing resulted in the discovery of a further 13 SNPs, 3 of which are novel variants in the DBD of NR1I2. There were significant differences in the distribution of NR1I2 and NR1I3 SNPs between South Africans when compared to Caucasian, Asian and Yoruba population groups.
For the realisation of personalised medicine, PXR and CAR genetic variation should be taken into consideration because of their involvement in the regulation of DMEs.
本研究调查了 NR1I2 和 NR1I3 的变异及其对 HIV/AIDS 患者中依非韦伦血浆水平的影响。血浆药物水平的变异性在很大程度上导致了研究人员寻找药物代谢酶 (DME) 基因中的致病变异,而很少关注核受体基因 NR1I2 和 NR1I3,它们分别编码 PXR 和 CAR,参与调节 DME。
本研究纳入了 464 名班图语南非人,包括接受依非韦伦为基础治疗的 HIV/AIDS 患者(n=301)和 163 名健康对照者,对 NR1I2 和 NR1I3 中的 6 个 SNP 进行了基因分型。在 301 名患者中,有 32 名患者对 NR1I2 和 NR1I3 的 DNA 结合域 (DBD) 进行了测序。
携带 NR1I3 rs3003596C/C 和 T/C 基因型的患者依非韦伦血浆浓度显著降低(P=0.015 和 P=0.010)。测序发现了另外 13 个 SNP,其中 3 个是 NR1I2 DBD 的新变异。与高加索人、亚洲人和约鲁巴人相比,南非人 NR1I2 和 NR1I3 单核苷酸多态性的分布存在显著差异。
为了实现个体化医学,应该考虑 PXR 和 CAR 遗传变异,因为它们参与了 DME 的调节。