Jin Li Hua, Kim Bo-Hyung, Lee Ji Hyun, Lee Kidong, Kwack KyuBum, Yim Sung-Vin
Department of Clinical Pharmacology and Therapeutics, College of Medicine, Kyung Hee University, Seoul 02447, Korea.
Department of BioMedical Science, College of Life Science, CHA University, SeongNam 13488, Republic of Korea.
Transl Clin Pharmacol. 2017 Dec;25(4):166-172. doi: 10.12793/tcp.2017.25.4.166. Epub 2017 Dec 20.
Talniflumate is a phthalidyl ester of niflumic acid, which has potent analgesic and anti-inflammatory effects and is widely used to treat inflammatory disorders, such as rheumatoid arthritis. To screen the possible genetic factors affecting the pharmacokinetics (PK) of talniflumate, 23 male Korean volunteers were enrolled from two separate bioequivalence studies. All subjects received 740 mg (two tablets) talniflumate in a standard 2×2 cross-over model in a randomized order. For the genetic study, PK parameters of the reference drug were used. We used Illumina Human610Quad v1.0 DNA Analysis BeadChip for whole genome single nucleotide polymorphism (SNP) analysis and whole genome genotyping data were processed by linear regression analysis for PK parameters. Whole genome analysis revealed 1498 significant SNPs ( < 0.0001) for C, 65 significant SNPs ( < 0.0001) for , and 1491 significant SNPs ( < 0.0001) for For clinical pharmacological purposes, we selected SNPs from drug metabolizing enzymes and transporters, and analyzed the PK parameters of various genotypes. Two SNPs (rs11165069 from ABCA4 (p=0.00002); rs17847036 from CYP2C9 (p=0.000001)) showed significant associations with talniflumate . In the group, two SNPs (rs3787555 from CYP24A1 (p=0.00035); rs2275034 from ABCA4 (p=0.000587)) showed significant associations with talniflumate . In the group, two SNPs (rs11165069 from ABCA4 (p=0.00002); rs12461006 from SLC1A6 (p=0.00008)) exhibited significant associations with talniflumate absorption. These results show that genetic factors could affect the PK parameters, and provide information that may be used in the development of personalized talniflumate therapy.
他尼氟酯是尼氟酸的邻苯二甲酰酯,具有强效镇痛和抗炎作用,广泛用于治疗炎症性疾病,如类风湿性关节炎。为筛选影响他尼氟酯药代动力学(PK)的可能遗传因素,从两项独立的生物等效性研究中招募了23名韩国男性志愿者。所有受试者按照标准的2×2交叉模型,以随机顺序服用740毫克(两片)他尼氟酯。对于基因研究,使用了参比药物的PK参数。我们使用Illumina Human610Quad v1.0 DNA分析微珠芯片进行全基因组单核苷酸多态性(SNP)分析,并通过对PK参数的线性回归分析处理全基因组基因分型数据。全基因组分析显示,C的1498个SNP具有显著意义(<0.0001),AUC的65个SNP具有显著意义(<0.0001),Cmax的1491个SNP具有显著意义(<0.0001)。出于临床药理学目的,我们从药物代谢酶和转运体中选择SNP,并分析了不同基因型的PK参数。两个SNP(ABCA4的rs11165069(p = 0.00002);CYP2C9的rs17847036(p = 0.000001))与他尼氟酯AUC显示出显著关联。在AUC组中,两个SNP(CYP24A1的rs3787555(p = 0.00035);ABCA4的rs2275034(p = 0.000587))与他尼氟酯AUC显示出显著关联。在Cmax组中,两个SNP(ABCA4的rs11165069(p = 0.00002);SLC1A6的rs12461006(p = 0.00008))与他尼氟酯吸收显示出显著关联。这些结果表明遗传因素可能影响PK参数,并提供了可用于他尼氟酯个性化治疗开发的信息。