| Literature DB >> 26823837 |
Rong Hu1, Min Lin2, Jun Ye3, Bao-Ping Zheng4, Li-Xia Jiang1, Juan-Juan Zhu5, Xiao-Hong Chen1, Mi Lai1, Tian-Yu Zhong1.
Abstract
In southern China, glucose-6-phosphate dehydrogenase (G6PD) deficiency is a significant health problem, and the incidence ranged from 0.5 to 4.08% in different Chinese population. The aims of this study are to investigate the molecular epidemiological characteristic of the G6PD gene among Chinese Hakka in southern Jiangxi province. 2331 unrelated subjects were screened for G6PD deficiency by a fluorescent test. DNA from deficient individuals was analyzed by a gene chip analysis for thirteen common Chinese G6PD mutations. In total, 3.60% (82/2331; 95% CI 2.77-4.27) of the sample were found to be G6PD-deficient. Eight mutations were found from 80 samples. However, mutation(s) for the two remaining samples were unknown. The most common mutations were G6PD Canton (1376 G>T) and G6PD Kaiping (1388 G>A), and the following mutations were 1311 polymorphism (1311 C>T), G6PD Gaohe (95 A>G), G6PD Chinese-5 (1024 C>T), G6PD Maewo (1360 C>T), Shunde (592 C>T), G6PD Viangchan (871 G>A) and Chinese-3 (493 A>G). This is the first report of G6PD deficiency among Chinese Hakka population in Jiangxi province.Entities:
Keywords: Chinese Hakka; G6PD deficiency; gene chip; gene mutation
Mesh:
Year: 2015 PMID: 26823837 PMCID: PMC4713623
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625