视神经脊髓炎及多发性硬化患者脑部氢质子磁共振波谱分析  被引量:5

Analysis on brain ^1H magnetic resonance spectroscopy characteristics of patients with neuromyelitis optica and multiple sclerosis

在线阅读下载全文

作  者:肖丽[1] 邱伟[1] 陆正齐[1] 陈少琼[2] 胡学强[1] 

机构地区:[1]中山大学附属第三三医院神经内科,510630 [2]中山大学附属第三三医院放射科,510630

出  处:《中国神经免疫学和神经病学杂志》2015年第6期385-388,共4页Chinese Journal of Neuroimmunology and Neurology

摘  要:目的通过氢质子磁共振波谱(^1H magnetic resonance spectroscopy,^1H-MRS)研究视神经脊髓炎(neuromyelitis optica,NMO)及多发性硬化(multiple sclerosis,MS)患者脑部病灶的特征。方法对24例NMO、26例MS患者脑内病灶及其对侧看似正常脑白质(normal appearing white matter,NAWM)进行^1H-MRS扫描,计算并比较各组患者两侧代谢产物〔N-乙酰门冬氨酸/肌酸(NAA/Cr)、胆碱/肌酸(Cho/Cr)、肌醇/肌酸(mI/Cr)〕比值。结果 MS患者脑内病灶NAA/Cr低于对侧NAWM(t=2.232,P=0.03),Cho/Cr(t=1.56,P=0.12)及mI/Cr=(t=0.44,P=0.66)与对侧NAWM比较差异无统计学意义。NMO患者脑内病灶NAA/Cr(t=1.024,P=0.32)、Cho/Cr(t=0.643,P=0.52)及mI/Cr(t=1.267,P=0.23)与其对侧NAWM比较差异均无统计学意义。结论 MS脑内病灶可能存在严重的神经元轴突损害,而NMO脑内病灶可能无明显轴突损害。Objective To investigate ^1H magnetic resonance spectroscopy(^1H-MRS)features of the brain lesions in patients with neuromyelitis optica(NMO)and multiple sclerosis(MS).Methods The clinical data,^1H-MRS features of brain lesions and normal appearing white matter(NAWM)in 24 NMO patients and 26 MS patients were reviewed.The ^1H-MRS features were represented by concentrations of metabolites including the ratios of N-acetyl aspartate to creatine(NAA/Cr),choline-containing compounds to Cr(Cho/Cr)and myoinositol to Cr(mI/Cr).Results Compared with the contralateral NAWM,NAA/Cr ratio of brain lesions in MS patients decreased significantly(t=2.232,P=0.03)while Cho/Cr and mI/Cr ratios increased(t=1.56,0.44,P〉0.05,respectively).Compared with the contralateral NAWM,NAA/Cr,Cho/Cr and mI/Cr ratios of brain lesion in NMO patients decreased(t=1.024,0.643,1.267,P〉0.05,respectively).Conclusions The neuronal/axonal injury may be severe in brain lesions of MS patients,but the neurons and axons of NMO patients may be normal.

关 键 词:视神经脊髓炎 多发性硬化 氢质子磁共振波谱 

分 类 号:R744.51[医药卫生—神经病学与精神病学] R744.52[医药卫生—临床医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象