J Acad Nutr Diet. 2019 Apr;119(4):617-625. doi: 10.1016/j.jand.2018.09.007. Epub 2018 Dec 15.
Excess iron levels can induce oxidative stress and could therefore affect telomere attrition. However, little is known about the impact of body iron status on telomere length.
Our aim was to examine the association between serum ferritin concentrations, an indicator of body iron status, and leukocyte telomere length in US adults.
We conducted a nationwide, population-based, cross-sectional study.
PARTICIPANTS/SETTING: We used data from the National Health and Nutrition Examination Survey (NHANES) 1999-2002. We included 7,336 adults aged 20 years or older who had available data on serum ferritin levels and telomere length. High ferritin levels were defined as a serum ferritin level >200 ng/mL (449.4 pmol/L) in women and >300 ng/mL (674.1 pmol/L) in men. Low ferritin levels were defined as a serum ferritin level <30 ng/mL (67.4 pmol/L).
Leukocyte telomere length was assayed using the quantitative polymerase chain reaction method.
Linear regression with survey weights was performed to estimate the association between serum ferritin levels and telomere length.
The prevalence of adults with high and low serum ferritin levels was 10.9% and 17.6%, respectively. High ferritin levels were inversely associated with telomere length compared to normal ferritin levels. After adjustment for demographic, socioeconomic and lifestyle factors, body mass index, C-reactive protein, and leukocyte cell type composition, the β coefficient for log-transformed telomere length was -0.020 (standard error [SE]=0.009; P=0.047). The association was stronger in adults aged 65 years or older (β coefficient -0.081, SE=0.017; P<0.001) than in adults 20 to 44 years old (β coefficient -0.023, SE=0.019; P=0.24) or adults aged 45 to 64 years old (β coefficient 0.024, SE=0.015; P=0.10) (P for interaction 0.003). Low ferritin levels were not significantly associated with telomere length compared with normal ferritin levels.
In a US nationally representative population, high body iron status was associated with shorter telomeres, especially in adults aged 65 years or older.
过量的铁会引起氧化应激,从而影响端粒损耗。然而,目前人们对体内铁状态对端粒长度的影响知之甚少。
我们旨在研究美国成年人血清铁蛋白浓度(反映体内铁状态的指标)与白细胞端粒长度之间的关系。
我们进行了一项全国性的、基于人群的横断面研究。
参与者/设置:我们使用了 1999-2002 年全国健康与营养调查(NHANES)的数据。我们纳入了 7336 名年龄在 20 岁及以上、有血清铁蛋白水平和端粒长度数据的成年人。高铁蛋白水平定义为女性血清铁蛋白水平>200ng/ml(449.4pmol/L)和男性>300ng/ml(674.1pmol/L)。低铁蛋白水平定义为血清铁蛋白水平<30ng/ml(67.4pmol/L)。
使用定量聚合酶链反应方法检测白细胞端粒长度。
采用带调查权重的线性回归来估计血清铁蛋白水平与端粒长度之间的关系。
高血清铁蛋白水平和低血清铁蛋白水平的成年人患病率分别为 10.9%和 17.6%。与正常铁蛋白水平相比,高铁蛋白水平与端粒长度呈负相关。在调整人口统计学、社会经济和生活方式因素、体重指数、C 反应蛋白和白细胞细胞类型组成后,端粒长度的对数转换β系数为-0.020(标准误[SE]=0.009;P=0.047)。在 65 岁及以上的成年人中,这种关联更强(β系数-0.081,SE=0.017;P<0.001),而在 20-44 岁的成年人中(β系数-0.023,SE=0.019;P=0.24)或 45-64 岁的成年人中(β系数 0.024,SE=0.015;P=0.10),这种关联则较弱(P 交互作用=0.003)。与正常铁蛋白水平相比,低铁蛋白水平与端粒长度无显著相关性。
在美国具有全国代表性的人群中,较高的机体铁含量与较短的端粒长度有关,尤其是在 65 岁及以上的成年人中。