转铁蛋白饱和度
氧化应激
铁蛋白
医学
转铁蛋白
丙二醛
血清铁
内科学
认知
谷胱甘肽过氧化物酶
胃肠病学
内分泌学
精神科
超氧化物歧化酶
贫血
血清铁蛋白
作者
Elcin E Umur,Çağatay Öktenli,Serkan Çelik,Fatih Tangı,Özkan Sayan,Yavuz Sanısoğlu,Osman Metin İpçioğlu,Hakan Terekeci,Cihan Top,Selim Nalbant,Yaşar Küçükardalı
标识
DOI:10.1111/j.1447-0594.2011.00694.x
摘要
Aim: The aim of this study is to examine the relation between body iron, oxidative stress and cognitive function in elderly. Methods: Eighty‐seven elderly residents from nursing homes were the subjects of our study. Cognitive status was screened by the Mini‐Mental State Examination (MMSE). Of the 87 eligible subjects, 46 patients who obtained 24 or fewer points on the MMSE scale were considered as subjects with cognitive dysfunction. The control group consisted of 41 subjects who obtained more than 24 points on the MMSE. Routine biochemical analyses, parameters of iron metabolism, malondialdehyde (MDA) and glutathione peroxidase (GSH‐Px) were determined in all subjects. Results: There were statistically significant increases in serum iron, transferrin saturation, ferritin and MDA levels; whereas there was a statistically significant decrease in serum GSH‐Px enzyme activity and serum sodium levels in subjects with cognitive dysfunction. A significant negative correlation was found between serum iron, transferrin saturation, ferritin and MMSE score. There was a negative correlation between MMSE score and serum MDA; however, a positive significant correlation was found between MMSE score and both GSH‐Px enzyme activity and serum sodium. Conclusion: Our study provides evidence of increased markers of iron deposition and oxidative stress in patients with cognitive dysfunction. It seems likely that these markers negatively affect the MMSE score. Interestingly, we did not find any correlation between the markers of iron deposition and oxidative stress. Future studies will be required to demonstrate whether diminishing iron and oxidative stress will enhance MMSE score and thereby ameliorate cognitive impairment. Geriatr Gerontol Int 2011; 11: 504–509.
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