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      ABCC2 Polymorphisms and Haplotype are Associated with Drug Resistance in Chinese Epileptic Patients

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          SUMMARY 

          Aims: Some study found that ATP‐binding cassette (ABC) efflux transporters play an important role in antiepileptic drug resistance, especially ABCB1 and ABCC2. The aims of this study were to evaluate the relationship between the genetic polymorphisms of ABCC2 and ABCB1 and the therapeutic efficacy of antiepileptic drugs (AEDs) in Chinese epileptic patients. Methods: ABCB1 rs1045642 (3435C>T) and ABCC2 rs717620 (−24C>T), rs3740066 (3972C>T), and rs2273697 (1249G>A) polymorphisms loci in 537 Chinese epilepsy patients (217 drug resistant patients and 320 drug responders) were genotyped by polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP). Results: ABCC2 rs717620 −24TT genotype was significantly associated with drug resistant epilepsy (odds ratio [OR]= 4.06 [1.79–9.20], P= 0.001). The OR values of ABCC2 rs717620 −24 CT+TT genotypes and ABCC2 rs3740066 (3972C>T) CT+TT genotypes were markedly higher in drug resistant patients (OR = 1.57 [1.08–2.29], P= 0.018; OR = 1.49 [1.02–2.18], P= 0.038, respectively) compared with responsive patients. ABCC2 rs2273697 (1249G>A) and ABCB1 rs1045642 (3435C>T) polymorphisms were not associated with drug resistant epilepsy. Linkage disequilibrium (LD) test showed that the ABCC2 rs717620 were in strong LD with rs2273697 (D’= 0.694) and rs3740066 (D’= 0.699). The frequencies of haplotypes TGT ( ABCC2 −24C>T/ ABCC2 1249G>A/ ABCC2 3972C>T) in resistant patients was significantly higher than those in responsive patients (21.0% vs. 14.2%, P < 0.05). Conclusion: ABCC2−24C>T, 3972C>T polymorphisms and one ABCC2 haplotype is associated with AED resistance; ABCC2 1249G>A and ABCB1 3435C>T polymorphisms are not associated with AED resistance in our study. These data suggest that ABCC2 polymorphisms and haplotype may affect the response of antiepileptic drugs.

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          Author and article information

          Journal
          CNS Neurosci Ther
          CNS Neurosci Ther
          10.1111/(ISSN)1755-5949
          CNS
          CNS Neuroscience & Therapeutics
          Blackwell Publishing Ltd (Oxford, UK )
          1755-5930
          1755-5949
          28 May 2012
          August 2012
          : 18
          : 8 ( doiID: 10.1111/cns.2012.18.issue-8 )
          : 647-651
          Affiliations
          [ 1 ]Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University Xiangya School of Medicine, Changsha, China
          [ 2 ]Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, China
          [ 3 ]Laboratories of Functional Genomics and Proteomics, Creighton University Medical Center, Omaha, NE, USA
          [ 4 ]Department of Orthopaedics, Xiangya Hospital, Central South University, Changsha, China
          [ 5 ]Department of Pharmacy, the Third Hospital of Huaihua City, Huaihua, China
          Author notes
          [*]Zhao‐Qian Liu, Institute of Clinical Pharmacology, Hunan Key Laboratory of pharmacogenetics, Central South University Xiangya School of Medicine, Changsha, Hunan 410078, China.
Tel: +86‐731‐84805380;
Fax: +86‐731‐82354476;
E‐mail: liuzhaoqian63@ 123456126.com
          Article
          PMC6493375 PMC6493375 6493375 CNS336
          10.1111/j.1755-5949.2012.00336.x
          6493375
          22630058
          62b1e8a1-77a1-4afe-8fae-db14368a4e9a
          © 2012 Blackwell Publishing Ltd
          History
          Page count
          Figures: 1, Tables: 4, Equations: 0, References: 38, Pages: 5
          Categories
          Original Articles
          Original Articles
          Custom metadata
          2.0
          August 2012
          Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.2.1 mode:remove_FC converted:02.05.2019

          Haplotypes,Epilepsy, ABCC2 polymorphism, ABCB1 polymorphism

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