دورية أكاديمية

Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism

التفاصيل البيبلوغرافية
العنوان: Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism
المؤلفون: Vera Dias, V Ribeiro
المصدر: Journal of Pharmacy and Bioallied Sciences, Vol 3, Iss 3, Pp 453-459 (2011)
بيانات النشر: Wolters Kluwer Medknow Publications, 2011.
سنة النشر: 2011
المجموعة: LCC:Pharmacy and materia medica
LCC:Analytical chemistry
مصطلحات موضوعية: Cholesterol 7α-hydroxylase, drug metabolizing enzymes, oxysterol 7α-hydroxylase, sterol 27-hydroxylase, Pharmacy and materia medica, RS1-441, Analytical chemistry, QD71-142
الوصف: It is well known that drug disposition and response are greatly determined by the activities of drug metabolizing enzymes, which are polymorphic. Some of these polymorphisms are clinically relevant and presented an ethnic-dependent pattern of distribution. The characterization of the genetic distribution of different populations allows the selection of therapeutic options in accordance with the genetic background, with the objective to avoid adverse reactions and inefficacy of the treatment. In this work, we studied selected genetic polymorphisms in drug metabolizing enzymes in three different ethnic groups - Portugal, Mozambique and Colombia. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) genotyping methods were developed for drug metabolizing enzymes, namely, cholesterol 7α-hydroxylase (CYP7A1) (−203A>C, −346C>T, −496C>T, N233S, G347S), sterol 27-hydroxylase (CYP27A1) (R164W, A169V, D273N, V400A) and oxysterol 7α-hydroxylase (CYP7B1) (−116C>G, R324H, 1774C>T) to characterize the allelic distribution of these polymorphisms among three different ethnic/geographic origins. A total of 12 CYP7A1, CYP27A1 and CYP7B1 genetic variants were genotyped in a sample of 92 Portuguese, 151 Mozambican and 91 Colombian subjects. The variants N233S in CYP7A1 and 1774C>T in CYP7B1 were not detected in any population studied. The promoter polymorphisms in CYP7A1 (−203A>C, −346C>T, −496C>T) had high frequency in the three ethnic groups. G347S (CYP7A1), R164W, A169V and V400A (CYP27A1) were present in a low frequency but with a similar distribution in the three ethnic groups. Significant differences were observed for D273N (CYP27A1), −346C>T (CYP7A1), −116C>G and R324H (CYP7B1)Our results demonstrate a high variability of drug metabolizing enzymes between the different populations analyzed, indicating that at least some of these polymorphisms are ethnic specific.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0975-7406
0976-4879
العلاقة: http://www.jpbsonline.org/article.asp?issn=0975-7406;year=2011;volume=3;issue=3;spage=453;epage=459;aulast=DiasTest; https://doaj.org/toc/0975-7406Test; https://doaj.org/toc/0976-4879Test
DOI: 10.4103/0975-7406.84465
الوصول الحر: https://doaj.org/article/cb8c77d82d55496999f43382fb879c5cTest
رقم الانضمام: edsdoj.b8c77d82d55496999f43382fb879c5c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:09757406
09764879
DOI:10.4103/0975-7406.84465