UGT2B7 c.-161C>T polymorphism frequency in Croatian population

被引:0
|
作者
Bozina, Tamara [1 ]
Karacic, Ena [2 ]
Ganoci, Lana [3 ]
Cukovic-Cavka, Silvija [4 ]
Palic, Jozefina [1 ]
Bozina, Nada [5 ]
Simicevic, Livija [3 ]
机构
[1] Univ Zagreb, Sch Med, Dept Med Chem Biochem & Clin Chem, Zagreb, Croatia
[2] Univ Zagreb, Fac Pharm & Biochem, Zagreb, Croatia
[3] Univ Hosp Ctr Zagreb, Dept Lab Diagnost, Div Pharmacogen & Therapy Individualisat, Zagreb, Croatia
[4] Univ Zagreb, Univ Hosp Ctr Zagreb, Sch Med, Dept Gastroenterol, Zagreb, Croatia
[5] Univ Zagreb, Sch Med, Dept Pharmacol, Zagreb, Croatia
来源
ARHIV ZA HIGIJENU RADA I TOKSIKOLOGIJU-ARCHIVES OF INDUSTRIAL HYGIENE AND TOXICOLOGY | 2022年 / 73卷 / 04期
关键词
allelic variants; genotyping; glucuronidation; pharmacogenetics; uridine diphosphate glucuronosyltransferase-2B7; DIPHOSPHATE-GLUCURONOSYLTRANSFERASE; 2B7; UDP-GLUCURONOSYLTRANSFERASES; -161C-GREATER-THAN-T POLYMORPHISM; UGT2B7; VARIANTS; VALPROIC ACID; GLUCURONIDATION; PHARMACOKINETICS; LAMOTRIGINE; CANCER; ASSOCIATION;
D O I
10.2478/aiht-2022-73-3663
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Uridine diphosphate glucuronosyltransferase-2B7 (UGT2B7), enzyme responsible for the elimination of a number of xenobiotics through glucuronidation, is expressed in the gut, kidneys, intestines, and brain. However, data on the frequency of UGT2B7 polymorphisms in the Croatian population are limited. The aim of this study was to assess the frequency of the UGT2B7 c.-161C > T (rs7668258) polymorphism in the Croatian population and to compare it with reported frequencies in other populations. This polymorphism is in complete linkage disequilibrium with the UGT2B7 c.802C > T (UGT2B7*2, rs7439366) variant, which is important in clinical medicine. The study reports data of 501 participants from University Hospital Centre Zagreb. All data were collected and analysed retrospectively. Genotyping was performed by real-time polymerase chain reaction (PCR) using the TaqMan((R)) Drug Metabolism Genotyping Assay for UGT2B7 c.-161C > T (rs7668258). We found that 120 (23.95 %) participants were carriers of the UGT2B7 c.-161CC genotype and 255 (50.9 %) were heterozygous carriers (UGT2B7 c.-161CT), while 126 (25.15 %) were homozygous carriers of the variant allele (UGT2B7 c.-161TT). The frequency of the variant UGT2B7 c.-161C > T allele in this study was T=0.506. The frequency of the UGT2B7 c.-161C > T allelic variants and genotypes in the Croatian population is similar to other European populations.
引用
收藏
页码:303 / 307
页数:5
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