Choi In-Young, Lee Phil, Hughes Abbey J, Denney Douglas R, Lynch Sharon G
Hoglund Brain Imaging Center and Departments of Molecular & Integrative Physiology and Neurology, University of Kansas Medical Center, Kansas City, KS, USA.
Hoglund Brain Imaging Center and Department of Molecular & Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, USA.
Mult Scler. 2017 Jun;23(7):956-962. doi: 10.1177/1352458516669441. Epub 2016 Sep 12.
Increased oxidative stress leads to loss of glutathione (GSH). We have reported lower cerebral GSH in patients with secondary progressive multiple sclerosis (SPMS), indicating the involvement of oxidative stress in multiple sclerosis (MS) pathophysiology.
This study expanded upon our earlier work by examining longitudinal changes in cerebral GSH in patients with SPMS in relation to their clinical status.
A total of 13 patients with SPMS (Expanded Disability Status Scale (EDSS) = 4.0-6.5; MS duration = 21.2 ± 8.7 years) and 12 controls were studied over 3-5 years. GSH mapping was acquired from frontal and parietal regions using a multiple quantum chemical shift imaging technique at 3 T. Clinical assessments of the patient's disability included EDSS, gait, motor strength, ataxia, tremor, brainstem function and vision changes.
Brain GSH concentrations in patients were lower than those in controls for both baseline and 3- to 5-year follow-ups. Longitudinal GSH changes of patients were associated with their neurologist's blinded appraisal of their clinical progression. Patients judged to have worsening clinical status had significantly greater declines in frontal GSH concentrations than those with stable clinical status.
GSH provides a distinct measure associated with the disease progression in SPMS, possibly due to its dynamic alignment with pathogenic processes of MS related to oxidative stress.
氧化应激增加会导致谷胱甘肽(GSH)流失。我们曾报道继发性进展型多发性硬化症(SPMS)患者脑内GSH水平较低,这表明氧化应激参与了多发性硬化症(MS)的病理生理过程。
本研究通过检测SPMS患者脑内GSH的纵向变化及其与临床状态的关系,对我们早期的工作进行了拓展。
对13例SPMS患者(扩展残疾状态量表(EDSS)=4.0 - 6.5;MS病程=21.2±8.7年)和12名对照者进行了3至5年的研究。使用3T的多量子化学位移成像技术从额叶和顶叶区域获取GSH图谱。对患者残疾情况的临床评估包括EDSS、步态、肌力、共济失调、震颤、脑干功能和视力变化。
在基线以及3至5年的随访中,患者脑内GSH浓度均低于对照者。患者GSH的纵向变化与其神经科医生对其临床进展的盲法评估相关。被判定临床状态恶化的患者额叶GSH浓度下降幅度明显大于临床状态稳定的患者。
GSH为SPMS疾病进展提供了一种独特的衡量指标,这可能是由于它与MS氧化应激相关致病过程的动态关联。