Division of Human Nutrition, Wageningen University, P.O. Box 8129, 6700 EV, Wageningen, The Netherlands.
Genes Nutr. 2015 Jan;10(1):442. doi: 10.1007/s12263-014-0442-2. Epub 2014 Nov 22.
Transmembrane protease, serine 6 (TMPRSS6), is likely to be involved in iron metabolism through its pleiotropic effect on hepcidin concentrations. Recently, genome-wide association studies have identified common variants in the TMPRSS6 gene to be linked to anaemia and low iron status. To get a more precise evaluation of identified TMPRSS6 single nucleotide polymorphism associations with iron status in cohorts of differing continental ancestry, we conducted a systematic review with meta-analyses. We searched the literature using HuGE Navigator, Pubmed and Scopus databases for primarily genome-wide association studies using TMPRSS6 as a free term. Fixed-effects meta-analysis was used to obtain summary estimates of associations. Eleven studies comprised Caucasian populations, four included an Asian population and one study included an African-American population. Differences in minor allele frequencies of 8 TMPRSS6 SNPs (rs855791, rs4820268, rs2111833, rs1421312, rs228921, rs228918, rs228919 and rs575620) across ethnic groups were observed, with the MAF of rs855791 significantly higher in Asian populations than in Caucasians (0.55 vs 0.42, P < 0.0001). In the meta-analysis, the A allele of rs855791 was associated with lower Hb and ferritin concentrations in all populations. This allele was also associated with increased serum transferrin receptor and transferrin concentrations. We observed similar associations for the G allele in rs4820268. Clear disparities in associations were found for the African-American population, although not statistically significant. Associations between TMPRSS6 SNPs and anaemia are consistent across Caucasian and Asian populations. This study highlights the need to conduct studies in African populations where iron deficiency is of utmost public health significance.
跨膜丝氨酸蛋白酶 6(TMPRSS6)可能通过对血红素浓度的多效作用参与铁代谢。最近,全基因组关联研究发现 TMPRSS6 基因中的常见变体与贫血和低铁状态有关。为了更精确地评估不同大陆血统队列中鉴定的 TMPRSS6 单核苷酸多态性与铁状态的关联,我们进行了系统评价和荟萃分析。我们使用 HuGE Navigator、PubMed 和 Scopus 数据库搜索文献,主要使用 TMPRSS6 作为自由术语进行全基因组关联研究。使用固定效应荟萃分析获得关联的综合估计值。11 项研究包括白人群体,4 项研究包括亚洲人群体,1 项研究包括非裔美国人。在不同种族群体中观察到 8 个 TMPRSS6 SNP(rs855791、rs4820268、rs2111833、rs1421312、rs228921、rs228918、rs228919 和 rs575620)的次要等位基因频率存在差异,亚洲人群体的 rs855791 的 MAF 明显高于白人群体(0.55 比 0.42,P < 0.0001)。在荟萃分析中,rs855791 的 A 等位基因与所有人群的 Hb 和铁蛋白浓度降低相关。该等位基因也与血清转铁蛋白受体和转铁蛋白浓度升高相关。我们观察到 rs4820268 中 G 等位基因的类似关联。尽管没有统计学意义,但非裔美国人的群体存在明显的差异。TMPRSS6 SNP 与贫血之间的关联在白人和亚洲人群体中是一致的。本研究强调需要在铁缺乏对公共卫生具有最重要意义的非洲人群体中开展研究。