Literature DB >> 22177087

Association of C3435T multi drug resistance gene-1 polymorphism with aspirin resistance in ischemic stroke and its subtypes.

Vandana Sharma1, Subhash Kaul, Amal Al-Hazzani, T Surya Prabha, Polugari Prem Kumar Manohar Rao, Sneha Dadheech, A Jyothy, Anjana Munshi.   

Abstract

Aspirin is the most commonly used antiplatelet drug for treatment of a serious vascular event, most notably myocardial infarction and stroke. Significant fraction of aspirin treated patients is resistant to the antiplatelet effects of the drugs. Previous studies have suggested that a genetic basis for aspirin resistance exists. Therefore the present study was taken up to investigate the role of C3435T polymorphism (rs 1045642) of multiple drug resistance-1 (MDR-1) gene with aspirin resistance in stroke patients. Five hundred and sixty ischemic stroke patients and 560 age and sex matched healthy controls were involved in the study. Baseline clinical data were collected and follow-up telephone interviews were conducted with patients at 3, 6 and 12 months post event to determine stroke outcome. Blood samples were collected and genotypes determined. Significant difference was observed in the genotype distribution and allele frequency between patients and controls. The results were confirmed by a step wise multiple logistic regression analysis controlling all other confounding risk factors [adjusted Odds ratio=3.132 (95% CI; 2.043-4.800; p<0.001)]. There was a significant difference in genotype distribution between drug responders and non-responders. The risk of aspirin resistance was significantly high in patients with TT genotype in comparison to those with CC genotype [(TT vs. CC, χ(2)=6.268; p=0.012, Odds ratio=1.85) (95% CI; 1.142-3.017) (adjusted Odds ratio=2.465; 95% CI; 1.895-4.625 and p<0.001)]. As far as the stroke subtypes are concerned TT genotype associated significantly with aspirin resistance in intracranial large artery atherosclerosis. Our results indicate that the risk of aspirin resistance is more in patients with 3435TT genotype than in those with CC genotype. However, this is a preliminary study and a large study of replication is needed to confirm our results.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22177087     DOI: 10.1016/j.jns.2011.11.027

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

1.  Genetic variation in MDR1, LPL and eNOS genes and the response to atorvastatin treatment in ischemic stroke.

Authors:  Anjana Munshi
Journal:  Hum Genet       Date:  2012-07-19       Impact factor: 4.132

2.  Associations of MDR1, TBXA2R, PLA2G7, and PEAR1 genetic polymorphisms with the platelet activity in Chinese ischemic stroke patients receiving aspirin therapy.

Authors:  Ling-Ling Peng; Yuan-Qi Zhao; Zi-Yi Zhou; Jing Jin; Min Zhao; Xin-Meng Chen; Ling-Yan Chen; Ye-Feng Cai; Jia-Li Li; Min Huang
Journal:  Acta Pharmacol Sin       Date:  2016-09-19       Impact factor: 6.150

3.  Is there a role for MDR1, EPHX1 and protein Z gene variants in modulation of warfarin dosage? a study on a cohort of the Egyptian population.

Authors:  Marianne Samir Makboul Issac; Maggie S El-Nahid; Marian Youssry Wissa
Journal:  Mol Diagn Ther       Date:  2014-02       Impact factor: 4.074

4.  Detailed analysis of gene polymorphisms associated with ischemic stroke in South Asians.

Authors:  Sunaina Yadav; Nazeeha Hasan; Thomas Marjot; Muhammad S Khan; Kameshwar Prasad; Paul Bentley; Pankaj Sharma
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

5.  ABCB1 C3435T polymorphism and response to clopidogrel treatment in coronary artery disease (CAD) patients: a meta-analysis.

Authors:  Jia Su; Jin Xu; Xiaojing Li; Han Zhang; Juwei Hu; Renyuan Fang; Xiaomin Chen
Journal:  PLoS One       Date:  2012-10-09       Impact factor: 3.240

Review 6.  Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases.

Authors:  Nikhil Math; Thang S Han; Irina Lubomirova; Robert Hill; Paul Bentley; Pankaj Sharma
Journal:  Neurol Sci       Date:  2019-07-29       Impact factor: 3.307

  6 in total

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