中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2008年
5期
294-298
,共5页
翦凡%崔丽英%管宇宙%潘华%丁则昱
翦凡%崔麗英%管宇宙%潘華%丁則昱
전범%최려영%관우주%반화%정칙욱
肌萎缩侧索硬化%运动神经元%磁共振成像,弥散%磁共振波谱学
肌萎縮側索硬化%運動神經元%磁共振成像,瀰散%磁共振波譜學
기위축측색경화%운동신경원%자공진성상,미산%자공진파보학
Amyotrophie lateral sclerosis%Motor neurons%Diffusion magnetic resonance imaging%Magnetic resonance spectroscopy
目的 研究肌萎缩侧索硬化(ALS)的弥散张量成像(DTI)和磁共振波谱(MRS)特点,并对ALs的病理生理机制进行初步探讨.方法 ALS患者38例,单纯下运动神经元受累疾病患者8例,混合型颈椎病5例和健康对照34名,行常规头颅MRI、DTI和1H-MRS测定.结果 21%(8/38)的ALS患者可见T2 FLAIR序列双侧锥体束走行异常高信号,强度高于皮质灰质.ALS组和健康对照组相比,中央前回(ALS组0.492±0.059,健康对照组0.552 4-0.045,F=17.150,P<0.01)、内囊后肢(分别为0.679 ±0.048、0.727±0.031,F=19.481,P<0.01)、大脑脚(左侧0.740±0.038、0.761±0.024,F=4.290;右侧0.720±0.044、0.746±0.034,F=3.264,均P<0.01)的部分各向异性(FA值)显著降低;ALS组上述部位的N-乙酰大冬氨酸/肌酸(NAA/Cr)值和健康对照组相比亦存在显著降低.AKS组各部位FA值降低百分率分别为10.9%、6.6%、2.8%~3.5%,以中央前回处最为显著;内囊前肢、枕叶处的FA值亦有不同程度降低.结论 DTI和MRS枪测不仪有助于ALS患者:运动神经元高位受累的确认和ALS的诊断和鉴别诊断,而且还可促进对ALS病理机制和病损分布的了解.
目的 研究肌萎縮側索硬化(ALS)的瀰散張量成像(DTI)和磁共振波譜(MRS)特點,併對ALs的病理生理機製進行初步探討.方法 ALS患者38例,單純下運動神經元受纍疾病患者8例,混閤型頸椎病5例和健康對照34名,行常規頭顱MRI、DTI和1H-MRS測定.結果 21%(8/38)的ALS患者可見T2 FLAIR序列雙側錐體束走行異常高信號,彊度高于皮質灰質.ALS組和健康對照組相比,中央前迴(ALS組0.492±0.059,健康對照組0.552 4-0.045,F=17.150,P<0.01)、內囊後肢(分彆為0.679 ±0.048、0.727±0.031,F=19.481,P<0.01)、大腦腳(左側0.740±0.038、0.761±0.024,F=4.290;右側0.720±0.044、0.746±0.034,F=3.264,均P<0.01)的部分各嚮異性(FA值)顯著降低;ALS組上述部位的N-乙酰大鼕氨痠/肌痠(NAA/Cr)值和健康對照組相比亦存在顯著降低.AKS組各部位FA值降低百分率分彆為10.9%、6.6%、2.8%~3.5%,以中央前迴處最為顯著;內囊前肢、枕葉處的FA值亦有不同程度降低.結論 DTI和MRS鎗測不儀有助于ALS患者:運動神經元高位受纍的確認和ALS的診斷和鑒彆診斷,而且還可促進對ALS病理機製和病損分佈的瞭解.
목적 연구기위축측색경화(ALS)적미산장량성상(DTI)화자공진파보(MRS)특점,병대ALs적병리생리궤제진행초보탐토.방법 ALS환자38례,단순하운동신경원수루질병환자8례,혼합형경추병5례화건강대조34명,행상규두로MRI、DTI화1H-MRS측정.결과 21%(8/38)적ALS환자가견T2 FLAIR서렬쌍측추체속주행이상고신호,강도고우피질회질.ALS조화건강대조조상비,중앙전회(ALS조0.492±0.059,건강대조조0.552 4-0.045,F=17.150,P<0.01)、내낭후지(분별위0.679 ±0.048、0.727±0.031,F=19.481,P<0.01)、대뇌각(좌측0.740±0.038、0.761±0.024,F=4.290;우측0.720±0.044、0.746±0.034,F=3.264,균P<0.01)적부분각향이성(FA치)현저강저;ALS조상술부위적N-을선대동안산/기산(NAA/Cr)치화건강대조조상비역존재현저강저.AKS조각부위FA치강저백분솔분별위10.9%、6.6%、2.8%~3.5%,이중앙전회처최위현저;내낭전지、침협처적FA치역유불동정도강저.결론 DTI화MRS창측불의유조우ALS환자:운동신경원고위수루적학인화ALS적진단화감별진단,이차환가촉진대ALS병리궤제화병손분포적료해.
Objective To investigate the diffusion tensor imaging(DTI)and magnetic resonance spectroscopy(MRS)changes in amyotrophic lateral sclerosis(ALS)and to study on the physiopathology of ALS.Methods Thirty-eight AIS patients,8 patients with pure lower motor neuron involvement and 5 patients with mixed-type cervical spondylosis and 34 healthy controls were enrolled and examined with the conventional brain MRI,DTI and 1H-MRS.Results T2-weighted and T2 FLAIR images revealed abnormal high signals in bilateral pyramidal tract positions in 21%(8/38)of ALS patients,which was higher than that in the coaex When compared with the control group,the values of FA in the precentral gyms(0.492±0.059 vs 0.552±0.045,F=17.150,P<0.01),the posterior limb of the internal capsule(0.679±0.048 vs 0.727 4-0.031.F=19.481.P<0.01)and the cerebral peduncle(1eft:0.740 4-0.038 vs 0.761 4±0.024.F=4.290;right:0.720 ±0.044 vs 0.746 ±0.034,F=3.264,both P<0.01)of the ALS group were decreased significantly.so were the values of NAA/Cr.And the FA reduction rate was 10.9%,6.6% and 2.8%-3.5% respectively.There was also a significant decrease in FA in the anterior limb of the internal capsule and the occipital lobe in the ALS group.Conclusion Not only does the application of DTI and MRS help to demonstrate upper motor neuron involvement in the brain and facilitate the diagnosis and differential diagnosis of ALS,but also increases the understanding of the lesion distribution and physiopathology in ALS.