UCD Institute of Food & Health, University College Dublin, Belfield, D04 V1W8 Dublin, Ireland.
Institute for Global Food Security, Queens University Belfast, Belfast BT7 1NN, UK.
Nutrients. 2021 May 2;13(5):1539. doi: 10.3390/nu13051539.
Excessive adiposity is associated with several metabolic perturbations including disturbances in iron homeostasis. Increased systemic inflammation in obesity stimulates expression of the iron regulatory hormone hepcidin, which can result in a maldistribution of bodily iron, which may be implicated in metabolic dysfunction. This study aimed to investigate the effect of adiposity and any associated inflammation on iron homeostasis and the potential implications of dysregulated iron metabolism on metabolic health. Analyses are based on a subsample from the cross-sectional Irish National Adult Nutrition Survey (2008-2010) ( = 1120). Ferritin status and risk of iron overload were determined based on established WHO ferritin ranges. Participants were classed as having a healthy % body fat or as having overfat or obesity based on age- and gender-specific % body fat ranges as determined by bioelectrical impedance. Biomarkers of iron status were examined in association with measures of body composition, serum adipocytokines and markers of metabolic health. Excessive % body fat was significantly associated with increased serum hepcidin and ferritin and an increased prevalence of severe risk of iron overload amongst males independent of dietary iron intake. Elevated serum ferritin displayed significant positive associations with serum triglycerides and markers of glucose metabolism, with an increased but non-significant presentation of metabolic risk factors amongst participants with overfat and obesity at severe risk of iron overload. Increased adiposity is associated with dysregulations in iron homeostasis, presenting as increased serum hepcidin, elevated serum ferritin and an increased risk of iron overload, with potential implications in impairments in metabolic health.
肥胖与多种代谢紊乱有关,包括铁稳态紊乱。肥胖症中系统性炎症增加会刺激铁调节激素铁调素的表达,从而导致体内铁的分布不均,这可能与代谢功能障碍有关。本研究旨在探讨肥胖和任何相关炎症对铁稳态的影响,以及铁代谢失调对代谢健康的潜在影响。分析基于横断面爱尔兰国家成人营养调查(2008-2010 年)的一个亚样本(n = 1120)。根据世界卫生组织(WHO)的铁蛋白范围确定铁蛋白状况和铁过载风险。根据生物电阻抗法确定的年龄和性别特异性体脂%范围,将参与者分为健康体脂%或超重或肥胖。将铁状态的生物标志物与身体成分、血清脂肪细胞因子和代谢健康标志物进行关联检查。过多的体脂%与男性血清铁调素和铁蛋白升高以及严重铁过载风险的患病率增加独立于膳食铁摄入有关。血清铁蛋白升高与血清甘油三酯和葡萄糖代谢标志物呈显著正相关,在严重铁过载风险的超重和肥胖参与者中,代谢危险因素的出现增加但无统计学意义。肥胖与铁稳态失调有关,表现为血清铁调素升高、血清铁蛋白升高和铁过载风险增加,可能对代谢健康造成损害。