Cheng H L, Hancock D P, Rooney K B, Steinbeck K S, Griffin H J, O'Connor H T
Discipline of Exercise and Sport Science, Faculty of Health Sciences, The University of Sydney, Lidcombe, NSW, Australia.
School of Molecular Bioscience, The University of Sydney, Lidcombe, NSW, Australia.
Eur J Clin Nutr. 2014 Nov;68(11):1250-2. doi: 10.1038/ejcn.2014.82. Epub 2014 May 7.
Although iron deficiency is common in women especially during dieting, weight management trials rarely examine the longitudinal impact of genetics on iron. This study examined the associations between the TMPRSS6 rs855791 polymorphism and iron indices at baseline and after a 12-month trial comparing two weight loss diets (higher-protein, higher-haem iron (HPHI) vs lower-protein, lower-haem iron (LPLI)). A total of 76 young overweight women (18-25y; BMI⩾27.5 kg/m(2)) were included at baseline, with 27 (HPHI: n=15; LPLI: n=12) completing the 12-month trial. At baseline, C allele homozygotes exhibited higher serum iron (P=0.047) and lower hepcidin (P=0.023) compared with T allele carriers. After 12 months, no genotypic differences were observed for ferritin and soluble transferrin receptor, although C homozygotes on HPHI showed higher serum iron and transferrin saturation (P<0.05). Results indicate that rs855791 can influence iron metabolism to some extent, but its impact on storage and functional iron status is small relative to dietary protein/iron manipulation.
尽管缺铁在女性中很常见,尤其是在节食期间,但体重管理试验很少研究基因对铁的纵向影响。本研究比较了两种减肥饮食(高蛋白、高铁血红素(HPHI)与低蛋白、低铁血红素(LPLI)),检测了TMPRSS6 rs855791基因多态性与基线及12个月试验后的铁指标之间的关联。共有76名年轻超重女性(18 - 25岁;BMI⩾27.5 kg/m(2))纳入基线研究,其中27名(HPHI组:n = 15;LPLI组:n = 12)完成了12个月的试验。在基线时,与T等位基因携带者相比,C等位基因纯合子血清铁水平较高(P = 0.047),而铁调素水平较低(P = 0.023)。12个月后,铁蛋白和可溶性转铁蛋白受体未观察到基因型差异,尽管HPHI组的C纯合子血清铁和转铁蛋白饱和度较高(P < 0.05)。结果表明,rs855791在一定程度上可影响铁代谢,但相对于饮食中蛋白质/铁的调控,其对铁储存和功能性铁状态的影响较小。