Flavin-containing monooxygenase 3 polymorphisms in 13 ethnic populations from Europe, East Asia and sub-Saharan Africa: frequency and linkage analysis

被引:0
|
作者
Mao, Mao [1 ]
Matimba, Alice [2 ,3 ]
Scordo, Maria G. [1 ,4 ]
Gunes, Arzu [1 ,5 ]
Zengil, Hakan [5 ]
Yasui-Furukori, Norio [6 ]
Masimirembwa, Collen [3 ]
Dahl, Marja-Liisa [4 ]
机构
[1] Univ Uppsala Hosp, Dept Med Sci, SE-75185 Uppsala, Sweden
[2] Univ Cape Town, IIDMM, ZA-7700 Rondebosch, South Africa
[3] African Inst Biomed Sci & Technol, Harare, Zimbabwe
[4] Univ Messina, Messina, Italy
[5] Gazi Univ, Ankara, Turkey
[6] Hirosaki Univ, Hirosaki, Aomori, Japan
基金
瑞典研究理事会;
关键词
FMO3; genetic linkage; pharmacogenetics; polymorphisim; population diversity; sub-Saharan Africans; FAMILIAL ADENOMATOUS POLYPOSIS; FMO3; GENE; S-OXYGENATION; N-OXIDATION; IN-VIVO; VARIANTS; METABOLISM; FLAVIN-CONTAINING-MONOOXYGENASE-3; FLAVIN-MONOOXYGENASE-3; IDENTIFICATION;
D O I
10.2217/PGS.09.77
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: To investigate intra- and inter-ethnic differences in three widespread (E158K, V257M and E308G) and two African-specific (D132H and L360P) flavin-containing monooxygenase 3 (FMO3) polymorphisms. Materials & methods: Allele frequencies were determined by TaqMan (R) allelic discrimination assay in 2152 healthy volunteers from Europe (Swedes, Italians and Turks), East Asia (Japanese) and sub-Saharan Africa (nine ethnic groups covering eastern, southern and western regions), followed by haplotype and linkage analysis. Results: Significant subpopulation differences (p < 0.001) in allele frequencies were found for E158K, V257M and E308G in Europeans and regional differences (p < 0.01) for D132H among Africans. No carrier of P360 was identified. Cis-linkage between G308 and K158 was confirmed with the compound variant (K158/G308) being found in a high proportion (12.0-38.3%) of non-African subjects, but rarely (1.3%) among Africans. Conclusions: Distribution of functionally relevant FMO3 polymorphisms varies not only between ethnicities but also within. The K158/G308 variant may have potential clinical importance primarily in non-African populations due to its low prevalence in Africa.
引用
收藏
页码:1447 / 1455
页数:9
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