Motor cortex glutathione deficit in ALS measured in vivo with the J-editing technique

被引:95
作者
Weiduschat, N. [1 ]
Mao, X. [1 ]
Hupf, J. [2 ]
Armstrong, N. [2 ]
Kang, G. [1 ]
Lange, D. J. [3 ]
Mitsumoto, H. [2 ]
Shungu, D. C. [1 ]
机构
[1] Weill Cornell Med Coll, Dept Radiol, New York, NY 10021 USA
[2] Columbia Univ, Dept Neurol, New York, NY 10032 USA
[3] Hosp Special Surg, Dept Neurol, New York, NY 10021 USA
关键词
Magnetic resonance spectroscopy; Amyotrophic lateral sclerosis; Glutathione; Oxidative stress; Neurodegeneration; Biomarker; AMYOTROPHIC-LATERAL-SCLEROSIS; OXIDATIVE STRESS; NEURONS; DEGENERATION; DEPLETION;
D O I
10.1016/j.neulet.2014.04.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study compared in vivo levels of the antioxidant glutathione (GSH) in the motor cortex of 11 ALS patients with those in 11 age-matched healthy volunteers (HV). Using the standard J-edited spin-echo difference MRS technique, GSH spectra were recorded on a 3.0T GE MR system from a single precentral gyrus voxel. GSH levels expressed as ratios to the unsuppressed voxel tissue water (W) were 31% lower in ALS patients than in HV (p =.005), and 36% lower in ALS than in HV (p =.02) when expressed as ratios to the total creatine peak (tCr), supporting a role for oxidative stress in ALS. Levels of the putative neuronal marker N-acetylaspartate (NAA) relative to W did not differ between ALS and HV (p =.26), but were lower by 9% in ALS than in HV (p =.013) when expressed as ratios relative to tCr. This discrepancy is attributed to small but opposite changes in NAA and tCr in ALS that, as a ratio, resulted in a statistically significant group difference, further suggesting caution in using tCr as an internal reference under pathological conditions. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:102 / 107
页数:6
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