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首页> 外文期刊>Indian Journal of Medical and Paediatric Oncology >Interethnic differences in single and haplotype structures of folylpolyglutamate synthase and gamma-glutamyl hydrolase variants and their influence on disease susceptibility to acute lymphoblastic leukemia in the Indian population: An exploratory study
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Interethnic differences in single and haplotype structures of folylpolyglutamate synthase and gamma-glutamyl hydrolase variants and their influence on disease susceptibility to acute lymphoblastic leukemia in the Indian population: An exploratory study

机译:叶酸聚谷氨酸合酶和γ-谷氨酰水解酶变体的单一和单倍型结构的种族间差异及其对印度人群急性淋巴细胞白血病疾病易感性的影响:一项探索性研究

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Aim: We aim to establish the genotype and haplotype frequencies of folylpolyglutamate synthase (FPGS rs10106 and rs1544105) and gamma-glutamyl hydrolase (GGH rs3758149 and rs11545078) variants in the South Indian population (SI) and to study the association of these variants with susceptibility to acute lymphoblastic leukemia (ALL). We also aim to compare the genotype and haplotype frequencies of studied variants with those of superpopulations from the 1000 Genomes Project collected in phase-3 and other published studies in the literature. Materials and Methods: A total of 220 unrelated healthy volunteers and 151 patients with ALL of both sexes were recruited for the study. Extracted DNA was subjected to genotyping by allelic discrimination using quantitative real-time-polymerase chain reaction. Genotype details of the studied variants in other ethnicities were obtained from 1000 genomes project Phase 3 data. Haploview software was used to construct haplotypes. Results: In our study, the frequencies of FPGS rs1006'G' and rs1544105'A' alleles were found to be 37% and 37.2%, respectively, and the frequencies of GGH rs3758149'T' and GGH rs11545078'T' alleles were found to be 29.8% and 16.7%, respectively. Among the studied variants, FPGS rs1544105'AA' genotype carriers were found to be susceptible to the risk of ALL (odds ratio: 2.16; 95% confidence interval [CI]: 1.15–4.07; P = 0.02). Haplotype structures of FPGS and GGH variants in SI population were significantly different from other ethnicities (P Conclusion: FPGS rs1544105'AA' genotype was found to influence the risk for ALL. Intra and interethnic differences exist in the distribution of studied variants. Therefore, the impact of each variant on the susceptibility and outcome of diseases may differ between populations.
机译:目的:我们旨在确定南印度人口(SI)中叶酰聚谷氨酸合酶(FPGS rs10106和rs1544105)和γ-谷氨酰水解酶(GGH rs3758149和rs11545078)的基因型和单倍型频率,并研究这些变体与易感性的关系急性淋巴细胞白血病(ALL)。我们还旨在比较研究的变体的基因型和单倍型频率与在第三阶段和文献中其他已发表的研究中收集的1000个基因组计划的超种群的基因型和单倍型频率。材料和方法:总共招募了220名无关的健康志愿者和151名患有ALL的男女患者进行研究。使用定量实时聚合酶链反应通过等位基因鉴别对提取的DNA进行基因分型。可从1000个基因组计划的第3阶段数据中获得其他种族中已研究变体的基因型详细信息。使用Haploview软件构建单倍型。结果:在我们的研究中,发现FPGS rs1006'G'和rs1544105'A'等位基因的频率分别为37%和37.2%,并且发现了GGH rs3758149'T'和GGH rs11545078'T'等位基因的频率分别为29.8%和16.7%。在研究的变体中,发现FPGS rs1544105'AA'基因型携带者易患ALL风险(比值:2.16; 95%置信区间[CI]:1.15-4.07; P = 0.02)。 SI人群中FPGS和GGH变异的单倍型结构与其他种族有显着差异(P结论:发现FPGS rs1544105'AA'基因型影响ALL的风险。研究变异的内部和种族间存在差异。每个变体对疾病易感性和结果的影响在人群之间可能有所不同。

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