Influence of SLCO1B1 Polymorphisms on the Pharmacokinetics of Mycophenolic
Acid in Renal Transplant Recipients
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Published:2023-02
Issue:2
Volume:24
Page:114-123
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ISSN:1389-2002
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Container-title:Current Drug Metabolism
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language:en
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Short-container-title:CDM
Author:
Liu Jiawen1, Tan Ruoyun1, Gu Min12, Wang Zijie1, Zhu Yongqian3, Zhang Jiexiu1, Wei Jintao4, Zheng Ming1, Gui Zeping2, Chen Hao1, Sun Li1, Han Zhijian1, Tao Jun1, Ju Xiaobin1
Affiliation:
1. Department of Urology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, 210029, China 2. Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, 210003, China 3. Department of
Medical Quality Management, The First Affiliated Hospital with Nanjing Medical University, Nanjing, 210029, China 4. Department
of Emergency Medicine, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China
Abstract
Aims:
This study was designed to analyze the correlation between single nucleotide polymorphisms
(SNP) related to drug metabolism and pharmacokinetics of mycophenolic acid (MPA) during long-term follow-up.
Materials and Method:
A retrospective cohort study involving 71 renal transplant recipients was designed. Blood
samples were collected to extract total DNAs, followed by target sequencing based on next-generation sequencing
technology. The MPA area under the curve (AUC) was calculated according to the formula established in our center.
The general linear model and linear regression model were used to analyze the association between SNPs and MPA
AUC.
Results:
A total of 689 SNPs were detected in our study, and 90 tagger SNPs were selected after quality control and
linkage disequilibrium analysis. The general linear model analysis showed that 9 SNPs significantly influenced MPA
AUC. A forward linear regression was conducted, and the model with the highest identical degree (r2=0.55) included
4 SNPs (SLCO1B1: rs4149036 [P < 0.0001], ABCC2: rs3824610 [P = 0.005], POR: rs4732514 [P = 0.006], ABCC2:
rs4148395 [P = 0.007]) and 6 clinical factors (age [P < 0.0001], gender [P < 0.0001], the incident of acute rejection
(AR) [P = 0.001], albumin [P < 0.0001], duration after renal transplantation [P = 0.01], lymphocyte numbers [P =
0.026]). The most relevant SNP to MPA AUC in this model was rs4149036. The subgroup analysis showed that
rs4149036 had a significant influence on MPA AUC in the older group (P = 0.02), high-albumin group (P = 0.01),
male group (P = 0.046), and both within-36-month group (P = 0.029) and after-36-month group (P = 0.041). The
systematic review included 4 studies, and 2 of them showed that the mutation in SLCO1B1 resulted in lower MPA
AUC, which was contrary to our study.
Conclusion:
A total of 4 SNPs (rs4149036, rs3824610, rs4148395, and rs4732514) were identified to be significantly
correlated with MPA AUC. Rs4149036, located in SLCO1B1, was suggested to be the most relevant SNP to MPA
AUC, which had a stronger influence on recipients who were elder, male, or with high serum albumin. Furthermore,
6 clinical factors, including age, gender, occurrence of acute rejection, serum albumin, time from kidney transplantation,
and blood lymphocyte numbers, were found to affect the concentration of MPA.
Funder
National Natural Science Foundation of China “333 High-Level Talents Project” in Jiangsu Province Jiangsu Province Natural Science Foundation Program
Publisher
Bentham Science Publishers Ltd.
Subject
Clinical Biochemistry,Pharmacology
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