Share:
Share this content in WeChat
X
Review
Current status of spinal cord MRI study of amyotrophic lateral sclerosis
WANG Juan  ZHENG Senyuan  HUANG Pan 

Cite this article as: Wang J, Zheng SY, Huang P. Current status of spinal cord MRI study of amyotrophic lateral sclerosis. Chin J Magn Reson Imaging, 2020, 11(11): 1048-1050. DOI:10.12015/issn.1674-8034.2020.11.021.


[Abstract] Amyotrophic lateral sclerosis (ALS) is the most common type of motor neuron disease (MND), showing continuous worsen. There is currently no effective treatment. Nursing and respiratory support have significantly improved the patient's quality of life and survival rate. However, due to the heterogeneity of clinical manifestations, the average time from symptom onset to diagnosis is long. In view of this, finding new biomarkers to assist diagnosis and prognosis assessment becomes particularly important. Magnetic resonance imaging is safe, noninvasive, and easy to collect, and is a reasonable choice as a biomarker. The vast majority of current ALS imaging studies focus on cerebral changes, which are limited to upper motor neurons. Spinal cord MRI can study both upper motor neurons and lower motor neurons at the same time, so it may be a sensitive marker for early disease.
[Keywords] amyotrophic lateral sclerosis;spinal cord;magnetic resonance imaging

WANG Juan Department of Neurology, Deyang People's Hospital of Sichuan Province, Deyang 618000, China

ZHENG Senyuan Department of Neurology, Deyang People's Hospital of Sichuan Province, Deyang 618000, China

HUANG Pan* Department of Neurology, Deyang People's Hospital of Sichuan Province, Deyang 618000, China

*Correspondence to: Huang P, E-mail: 1032857970@qq.com

Conflicts of interest   None.

ACKNOWLEDGMENTS  The Science and Technology Project of Health Planning Committee of Sichuan No. 20PJ239
Received  2020-06-02
Accepted  2020-09-28
DOI: 10.12015/issn.1674-8034.2020.11.021
Cite this article as: Wang J, Zheng SY, Huang P. Current status of spinal cord MRI study of amyotrophic lateral sclerosis. Chin J Magn Reson Imaging, 2020, 11(11): 1048-1050. DOI:10.12015/issn.1674-8034.2020.11.021.

[1]
Hobson EV, McDermott CJ. Supportive and symptomatic management of amyotrophic lateral sclerosis. Nat Rev Neurol, 2016, 12(9): 526-538. DOI: 10.1038/nrneurol.2016.111
[2]
Robberecht WPhilips T. The changing scene of amyotrophic lateral sclerosis. Nature reviews, Neuroscience, 2013, 14(4): 248-264. DOI: 10.1038/nrn3430
[3]
Paganoni S, Macklin EA, Lee A, et al. Diagnostic timelines and delays in diagnosing amyotrophic lateral sclerosis (ALS). Amyotroph Lateral Scler Frontotemporal Degener, 2014, 15(5-6): 453-456. DOI: 10.3109/21678421.2014.903974
[4]
Ravits JM, La Spada AR. ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration. Neurology, 2009, 73(10): 805-811. DOI: 10.1212/WNL.0b013e3181b6bbbd
[5]
Bede P, Querin G, Pradat PF. The changing landscape of motor neuron disease imaging: the transition from descriptive studies to precision clinical tools. Current Opinion Neurol, 2018. 31(4): 431-438. DOI: 10.1097/WCO.0000000000000569
[6]
Paquin MÊ, El Mendili MM, Gros C, et al. Spinal Cord Gray Matter Atrophy in Amyotrophic Lateral Sclerosis. AJNR. Am J Neuroradiol, 2018. 39(1): 184-192. DOI: 10.3174/ajnr.A5427
[7]
de Albuquerque M, Branco LM, Rezende TJ, et al. Longitudinal evaluation of cerebral and spinal cord damage in Amyotrophic Lateral Sclerosis. NeuroImage, 2017, 14: 269-276. DOI: 10.1016/j.nicl.2017.01.024
[8]
Mendili MM, Cohen-Adad J, Pelegrini-Issac M, et al. Multi-parametric spinal cord MRI as potential progression marker in amyotrophic lateral sclerosis. Plos One, 2014. 9(4): DOI: e95516. DOI: 10.1371/journal.pone.0095516
[9]
Branco LM, De Albuquerque M, De Andrade HM, et al. Spinal cord atrophy correlates with disease duration and severity in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener, 2014, 15(1-2): 93-97. DOI: 10.3109/21678421.2013.852589
[10]
Rasoanandrianina H, Grapperon AM, Taso M, et al. Region-specific impairment of the cervical spinal cord (SC) in amyotrophic lateral sclerosis: a preliminary study using SC templates and quantitative MRI (diffusion tensor imaging/inhomogeneous magnetization transfer). NMR Biomed, 2017, 30(12): DOI: . DOI: 10.1002/nbm.3801
[11]
van der Burgh HK, Westeneng HJ, Meier JM, et al. Cross-sectional and longitudinal assessment of the upper cervical spinal cord in motor neuron disease. NeuroImage, Clinical, 2019, 24: 101984. DOI: 10.1016/j.nicl.2019.101984
[12]
Piaggio N, Pardini M, Roccatagliata L, et al. Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis. Eur Radiol Experal, 2018, 2: 13. DOI: 10.1186/s41747-018-0045-6
[13]
Grolez G, Kyheng M, Lopes R, et al. MRI of the cervical spinal cord predicts respiratory dysfunction in ALS. Scientific reports, 2018, 8(1): 1828. DOI: 10.1038/s41598-018-19938-2
[14]
Niessen HG, Angenstein F, Sander K, et al. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient. Exper Neurol, 2006, 201(2): 293-300. DOI: 10.1016/j.expneurol.2006.04.007
[15]
Ludolph AC. Vacuolization correlates with spin-spin relaxation time in motor brainstem nuclei and behavioural tests in the transgenic G93A-SOD1 mouse model of ALS. Eur J Neurosci, 2007, 26(7): 1895-1901. DOI: 10.1111/j.1460-9568.2007.05831.x
[16]
Cohen-Adad J, Zhao W, Keil B, et al. 7-T MRI of the spinal cord can detect lateral corticospinal tract abnormality in amyotrophic lateral sclerosis. Muscle Nerve, 2013, 47(5): 760-762. DOI: 10.1002/mus.23720
[17]
Wang Y, Liu L, Ma L, et al. Preliminary study on cervical spinal cord in patients with amyotrophic lateral sclerosis using MR diffusion tensor imaging. Acad Radiol, 2014. 21(5): 590-596. DOI: 10.1016/j.acra.2014.01.014
[18]
Patzig M, Bochmann K, Lutz J, et al. Measurement of structural integrity of the spinal cord in patients with amyotrophic lateral sclerosis using diffusion tensor magnetic resonance imaging. PloS One, 2019, 14(10): e0224078. DOI: 10.1371/journal.pone.0224078
[19]
Gatto RG, Li W, Gao J, et al. In vivo diffusion MRI detects early spinal cord axonal pathology in a mouse model of amyotrophic lateral sclerosis. NMR Biomed, 2018, 31(8): e3954. DOI: 10.1002/nbm.3954
[20]
Gatto RG, Li W, Magin RL. Diffusion tensor imaging identifies presymptomatic axonal degeneration in the spinal cord of ALS mice. Brain Research, 2018, 1659: 45-52. DOI: 10.1002/nbm.3954
[21]
Gatto RG, Amin MY, Deyoung D, et al. Ultra-high field diffusion MRI reveals early axonal pathology in spinal cord of ALS mice. Transl Neurodegener, 2018, 7: 20. DOI: 10.1186/s40035-018-0122-z
[22]
Underwood CK, Kurniawan ND, Butler TJ, et al. Non-invasive diffusion tensor imaging detects white matter degeneration in the spinal cord of a mouse model of amyotrophic lateral sclerosis. NeuroImage, 2011, 55(2): 455-461. DOI: 10.1016/j.neuroimage.2010.12.044
[23]
Tariq M, Schneider T, Alexander DC, et al. Bingham-NODDI: mapping anisotropic orientation dispersion of neurites using diffusion MRI. NeuroImage, 2016, 133: 207-223. DOI: 10.1016/j.neuroimage.2016.01.046
[24]
Gatto RG, Mustafi SM, Amin MY, et al. Neurite orientation dispersion and density imaging can detect presymptomatic axonal degeneration in the spinal cord of ALS mice. Funct Neurol, 2018, 33(3): 155-163.
[25]
刘新峰,张体江.磁化传递成像在神经系统疾病的研究现状.磁共振成像, 2013, 4(2): 146-150. DOI: 10.3969/jssn.1674-8034.2013.02.014
[26]
齐德明.磁共振波谱成像的研究进展.影像研究与医学应用, 2017, 1(15): 5-6.
[27]
Carew JD, Nair G, Pineda-Alonso N, et al. Magnetic resonance spectroscopy of the cervical cord in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 2011. 12(3): p. 185-91. DOI: 10.3109/17482968.2010.515223

PREV Advances in research on resting brain network functional magnetic resonance imaging for PD with cognitive impairmente
NEXT Application of resting state fMRI in the study of the obstructive sleep apnea-hypopnea syndrome
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn