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Impact of 14 types of genetic polymorphisms on antihypertensive efficacy of felodipine in healthy Chinese subjects .
- Source :
-
International journal of clinical pharmacology and therapeutics [Int J Clin Pharmacol Ther] 2020 Jul; Vol. 58 (7), pp. 375-386. - Publication Year :
- 2020
-
Abstract
- Objective: This study evaluated different influences of 14 single nucleotide polymorphisms (SNPs) and demographic factors leading to individual differences in the antihypertensive efficacy of felodipine in healthy Chinese subjects.<br />Materials and Methods: 24 subjects were sequenced for candidate SNPs. Plasma samples were obtained as clinical trial protocol, and were determined by a HPLC-MS/MS method. Pharmacokinetic parameters were calculated by WinNonlin 6.0. Statistical analysis was mainly performed by SPSS 22.0. A multiple linear regression model provided different weight coefficients of different demographic and genetic factors.<br />Results: The trend of C <subscript>max</subscript> is almost consistent with AUC <subscript>ss</subscript> increase, but t <subscript>max</subscript> of individuals is different; the antihypertensive effect of felodipine is individually different. A significant association was observed between systolic blood pressure decrease (ΔSBP) and SNPs of CACNA1C , CACNA1D , GNB3 respectively, while CACNA1C and CACNA1 were associated with diastolic blood pressure decrease (ΔDBP). CYP3A5 rs766746 and CYP3A4 rs2242480 were linked with C <subscript>max</subscript> and AUC <subscript>ss</subscript> , and ABCB1 rs1045642 was associated with T <subscript>1/2</subscript> . Significant relationships were shown between AUC <subscript>ss</subscript> and ΔSBP (p = 0.022) as well as C <subscript>max</subscript> and ΔSBP (p = 0.015).<br />Conclusion: The efficacy of felodipine is individually different, influenced especially by CACNA1C rs1051375 and ABCB1 rs1045642. ΔDBP is associated with ΔSBP in multiple-dosing of felodipine in healthy Chinese subjects.
Details
- Language :
- English
- ISSN :
- 0946-1965
- Volume :
- 58
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- International journal of clinical pharmacology and therapeutics
- Publication Type :
- Academic Journal
- Accession number :
- 32301702
- Full Text :
- https://doi.org/10.5414/CP203686