The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil

Acetylsalicylic acid (ASA) or aspirin is a pro-drug of salicylates which has significant effect in reducing the cardiovascular events. Potential polymorphic enzymes responsible for the pharmacokinetic variations of ASA include cyclooxygenase-l (COX-1) UDP—glucuronosyltransferase (UGT1A6) and P450 (C...

Full description

Bibliographic Details
Main Author: Abdul Jalil, Nur Jalinna
Format: Thesis
Language:English
Published: 2014
Subjects:
Online Access:http://ir.uitm.edu.my/id/eprint/27272/
http://ir.uitm.edu.my/id/eprint/27272/1/TM_NUR%20JALINNA%20ABDUL%20JALIL%20PH%2014_5.pdf
id uitm-27272
recordtype eprints
spelling uitm-272722020-01-15T01:36:06Z http://ir.uitm.edu.my/id/eprint/27272/ The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil Abdul Jalil, Nur Jalinna Pharmaceutical dosage forms Acetylsalicylic acid (ASA) or aspirin is a pro-drug of salicylates which has significant effect in reducing the cardiovascular events. Potential polymorphic enzymes responsible for the pharmacokinetic variations of ASA include cyclooxygenase-l (COX-1) UDP—glucuronosyltransferase (UGT1A6) and P450 (CYP) (CYP2C9). The main objective of this study is to determine the types and frequencies of variants of genes encoding COX-1 (A-842G), UGT1A6 (UGT1A6*2; A541G and UGT1A6*3; A522C and CYP2C9 (CYP2C9*3; A1075C) in the three major ethnic groups in Malaysian population (Malays, Chinese and Indian). The relevance of those polymorphisms in patients with cardiovascular disease was investigated. The project was approved by relevant Research Ethics Committee, A total of 165 patients with cardiovascular disease who were treated with 75-150 mg daily dose of aspirin and 300 healthy volunteer participants were recruited. DNA was extracted from the blood samples and genotyped for the single nucleotide polymorphisms (SNPs) using allele specific polymerase chain reaction (AS-PCR). All statistical analysis was performed using SPSS software version 2.0. P-values ≤ 0.05 were considered statistically significant. The association between genotype and adverse effect of aspirin therapy was estimated using odd ratio (OR). For UGT1A6, the pair-wise of both SNPs linkage disequilibrium (LD) was computed using Haploview. The variants frequencies for UGT1A6*2,*3 and CYP2C9*3 were 22.83%, 30.0% and 6.50%, respectively; while COX-1 (A-842G) was absent. We found that the genotype for both polymorphisms in UGT1A6 and CYP2C9*3 were significantly different between Indians, Malays and Chinese ethnic. The level of bilirubin and triglyceride of patients with different genotypes of UGT1A6 and CYP2C9*3 were significantly different (p-value < 0.05), respectively. In addition, CYP2C9*3 was found associated with gastritis events with odd ratio (OR) 6.8 (95 % Cl: 1.39 — 33.19; P = 0.033), SNPs of A541G and A522C among the Indians show swung linkage disequilibrium with D‘ value of 1.0. This study had identified significant association of genetic polymorphisms of UGTIA6 and CYP2C9*3 with gastritis event, level of bilirubin and triglyceride, Screening of patients with defective genetic variants could be of relevance in the clinical setting in identifying patients at risk of aspirin induced adverse effect. However, a iiiandomized, clinical study of bigger sample size would be needed before it is translated m clinical routine. 2014 Thesis NonPeerReviewed text en http://ir.uitm.edu.my/id/eprint/27272/1/TM_NUR%20JALINNA%20ABDUL%20JALIL%20PH%2014_5.pdf Abdul Jalil, Nur Jalinna (2014) The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil. Masters thesis, Universiti Teknologi MARA.
repository_type Digital Repository
institution_category Local University
institution Universiti Teknologi MARA
building UiTM Institutional Repository
collection Online Access
language English
topic Pharmaceutical dosage forms
spellingShingle Pharmaceutical dosage forms
Abdul Jalil, Nur Jalinna
The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
description Acetylsalicylic acid (ASA) or aspirin is a pro-drug of salicylates which has significant effect in reducing the cardiovascular events. Potential polymorphic enzymes responsible for the pharmacokinetic variations of ASA include cyclooxygenase-l (COX-1) UDP—glucuronosyltransferase (UGT1A6) and P450 (CYP) (CYP2C9). The main objective of this study is to determine the types and frequencies of variants of genes encoding COX-1 (A-842G), UGT1A6 (UGT1A6*2; A541G and UGT1A6*3; A522C and CYP2C9 (CYP2C9*3; A1075C) in the three major ethnic groups in Malaysian population (Malays, Chinese and Indian). The relevance of those polymorphisms in patients with cardiovascular disease was investigated. The project was approved by relevant Research Ethics Committee, A total of 165 patients with cardiovascular disease who were treated with 75-150 mg daily dose of aspirin and 300 healthy volunteer participants were recruited. DNA was extracted from the blood samples and genotyped for the single nucleotide polymorphisms (SNPs) using allele specific polymerase chain reaction (AS-PCR). All statistical analysis was performed using SPSS software version 2.0. P-values ≤ 0.05 were considered statistically significant. The association between genotype and adverse effect of aspirin therapy was estimated using odd ratio (OR). For UGT1A6, the pair-wise of both SNPs linkage disequilibrium (LD) was computed using Haploview. The variants frequencies for UGT1A6*2,*3 and CYP2C9*3 were 22.83%, 30.0% and 6.50%, respectively; while COX-1 (A-842G) was absent. We found that the genotype for both polymorphisms in UGT1A6 and CYP2C9*3 were significantly different between Indians, Malays and Chinese ethnic. The level of bilirubin and triglyceride of patients with different genotypes of UGT1A6 and CYP2C9*3 were significantly different (p-value < 0.05), respectively. In addition, CYP2C9*3 was found associated with gastritis events with odd ratio (OR) 6.8 (95 % Cl: 1.39 — 33.19; P = 0.033), SNPs of A541G and A522C among the Indians show swung linkage disequilibrium with D‘ value of 1.0. This study had identified significant association of genetic polymorphisms of UGTIA6 and CYP2C9*3 with gastritis event, level of bilirubin and triglyceride, Screening of patients with defective genetic variants could be of relevance in the clinical setting in identifying patients at risk of aspirin induced adverse effect. However, a iiiandomized, clinical study of bigger sample size would be needed before it is translated m clinical routine.
format Thesis
author Abdul Jalil, Nur Jalinna
author_facet Abdul Jalil, Nur Jalinna
author_sort Abdul Jalil, Nur Jalinna
title The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
title_short The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
title_full The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
title_fullStr The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
title_full_unstemmed The implication of the polymorphism of COX-1, UGT1A6, and CYP2C9 among cardiovascular disease (CVD) patients treated with aspirin / Nur Jalinna Abdul Jalil
title_sort implication of the polymorphism of cox-1, ugt1a6, and cyp2c9 among cardiovascular disease (cvd) patients treated with aspirin / nur jalinna abdul jalil
publishDate 2014
url http://ir.uitm.edu.my/id/eprint/27272/
http://ir.uitm.edu.my/id/eprint/27272/1/TM_NUR%20JALINNA%20ABDUL%20JALIL%20PH%2014_5.pdf
first_indexed 2023-09-18T23:18:09Z
last_indexed 2023-09-18T23:18:09Z
_version_ 1777419251285491712