Dr. Sami Ulus Obstetrics and Pediatrics Training and Research Hospital, Division of Pediatrics, Ankara, Turkey.
Dr. Sami Ulus Obstetrics and Pediatrics Training and Research Hospital, Division of Pediatrics, Department of Pediatric Endocrinology, Ankara, Turkey.
Diabetes Res Clin Pract. 2019 Mar;149:64-68. doi: 10.1016/j.diabres.2019.01.027. Epub 2019 Jan 30.
An increase in reactive oxygen species leads to formation of covalent bonds between sulfur atoms, thus thiol/disulfide homeostasis shifts towards the disulfide direction and oxidative damage occurs. We aimed to determine thiol/disulfide homeostasis in children with T1DM.
Thiol/disulfide homeostasis was evaluated in 30 patients with T1DM and 30 age, gender matched healthy controls. Thiol/disulfide homeostasis parameters were measured using a novel automated measurement method and correlation between demographic data and parameters was measured.
There weren't any significant differences in age or gender between the T1DM and control groups. T1DM group, findings were as follows: native thiol: 388.3 ± 76.7 µmol/L, total thiol: 426.2 ± 87 µmol/L, disulfide: 18.9 ± 7 µmol/L, control group findings were as follows: native thiol: 423.1 ± 45.2 µmol/L, total thiol: 455.7 ± 49.9 µmol/L, disulfide: 16.2 ± 5.6 µmol/L. The disulfide/native thiol and disulfide/total thiol ratios were significantly higher in the T1DM group (p = 0.005 and p = 0.004, respectively), whereas the native thiol level and the native thiol/total thiol ratio were significantly lower in the T1DM group than in the control group (p = 0.036 and p = 0.015, respectively). There wasn't significant correlation between demographic data and thiol/disulfide homeostasis parameters.
This study shows that dynamic thiol/disulfide homeostasis in children with T1DM shifts towards the disulfide direction. We think that this shift is caused by oxidative damage in β-cells. Additional research on thiol/disulfide homeostasis in children with T1DM might provide techniques for early detection of oxidative damage in β-cells.
活性氧的增加导致硫原子之间形成共价键,从而使硫醇/二硫键的动态平衡向二硫键方向移动,并发生氧化损伤。我们旨在确定 T1DM 患儿的硫醇/二硫键动态平衡。
使用新的自动测量方法评估 30 例 T1DM 患儿和 30 例年龄、性别匹配的健康对照者的硫醇/二硫键动态平衡。测量硫醇/二硫键动态平衡参数,并测量与人口统计学数据之间的相关性。
T1DM 组和对照组在年龄或性别上无显著差异。T1DM 组的发现如下:天然硫醇:388.3±76.7µmol/L,总硫醇:426.2±87µmol/L,二硫键:18.9±7µmol/L,对照组的发现如下:天然硫醇:423.1±45.2µmol/L,总硫醇:455.7±49.9µmol/L,二硫键:16.2±5.6µmol/L。T1DM 组的二硫键/天然硫醇和二硫键/总硫醇比值明显较高(p=0.005 和 p=0.004),而 T1DM 组的天然硫醇水平和天然硫醇/总硫醇比值明显低于对照组(p=0.036 和 p=0.015)。人口统计学数据与硫醇/二硫键动态平衡参数之间无显著相关性。
本研究表明,T1DM 患儿的动态硫醇/二硫键平衡向二硫键方向移动。我们认为这种转变是由β细胞的氧化损伤引起的。对 T1DM 患儿的硫醇/二硫键动态平衡进行进一步研究可能为β细胞氧化损伤的早期检测提供技术。