Chinese Medical Sciences Journal ›› 2018, Vol. 33 ›› Issue (2): 100-106.doi: 10.24920/11812
• Original Article • Previous Articles Next Articles
Chen Zhiye1, Liu Mengqi1, Ma Lin2, *()
Received:
2017-07-17
Published:
2018-06-30
Online:
2018-05-28
Contact:
Ma Lin
E-mail:cjr.malin@vip.163.com
Chen Zhiye, Liu Mengqi, Ma Lin. Cortical Thinning Pattern of Bulbar- and Spinal-onset Amyotrophic Lateral Sclerosis: a Surface-based Morphometry Study[J].Chinese Medical Sciences Journal, 2018, 33(2): 100-106.
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Cluster | Anatomic region | MNI-space | K value | Pvalue | tvalue | ||
---|---|---|---|---|---|---|---|
X | Y | Z | |||||
ALS vs. NC | |||||||
1 | Left precentral gyrus | -9 | -24 | 76 | 619 | 0.000 | 4.15 |
2 | Left postcentral gyrus | -56 | -9 | 19 | 293 | 0.000 | 3.70 |
3 | Right gyrus rectus | 4 | 43 | -22 | 150 | 0.000 | 3.41 |
4 | Right medial precentral gyrus | 6 | -22 | 73 | 191 | 0.000 | 3.37 |
ALS-bulbar vs. NC | |||||||
5 | Left precentral gyrus | -25 | -16 | 68 | 154 | 0.000 | 4.20 |
6 | Righ SMC | 8 | -8 | 69 | 219 | 0.000 | 4.45 |
ALS-spinal vs. NC | |||||||
7 | Left posterior insula | -36 | -13 | -5 | 264 | 0.000 | 3.85 |
8 | Right gyrus rectus | 5 | 42 | -24 | 210 | 0.000 | 3.51 |
Figure 3.
Brain regions with decreased cortical thickness in the ALS-bulbar patients and in the ALS-spinal patients compared with the NC group. A. Decreased cortical thickness in ALS-bulbar located in the left precentral gyrus and the right supplementary motor cortex. B. Decreased cortical thickness in the ALS-spinal located in the left posterior insula and the right gyrus rectus. Color bar represent t value."
"
Brain regions | Cortical thickness (mm) | Disease duration | ALSFRS-R score | |||
---|---|---|---|---|---|---|
r | Pvalue | r | Pvalue | |||
ALS vs. NC | ||||||
Left precentral gyrus | 2.77±0.22 | 0.003 | 0.979 | 0.245 | 0.053 | |
Left postcentral gyrus | 2.26±0.19 | -0.052 | 0.684 | 0.126 | 0.326 | |
Right gyrus rectus | 3.31±0.19 | -0.311 | 0.013 | -0.018 | 0.886 | |
Right precentral gyrus | 2.88±0.15 | -0.081 | 0.528 | 0.271 | 0.032 | |
ALS-spinal vs. NC | ||||||
Left insula | 3.95±0.35 | -0.409 | 0.004 | -0.011 | 0.943 | |
Right gyrus rectus | 3.34±0.19 | -0.351 | 0.014 | -0.022 | 0.881 | |
ALS-bulbar vs. NC | ||||||
Left precentral gyrus | 2.70±0.22 | -0.226 | 0.458 | 0.224 | 0.461 | |
Right supplementary motor cortex | 2.19±0.14 | 0.071 | 0.818 | 0.204 | 0.505 |
1. |
Chou SM, Norris FH . Amyotrophic lateral sclerosis: lower motor neuron disease spreading to upper motor neurons. Muscle Nerve 1993; 16(8):864-9. doi: 10.1002/mus.880160810.
doi: 10.1002/mus.880160810 |
2. |
van der Graaff MM, de Jong JM, Baas F , et al. Upper motor neuron and extra-motor neuron involvement in amyotrophic lateral sclerosis: a clinical and brain imaging review. Neuromuscul Disord 2009; 19(1):53-8. doi: 10.1016/j.nmd.2008.10.002.
doi: 10.1016/j.nmd.2008.10.002 pmid: 19070491 |
3. |
Pringle CE, Hudson AJ, Munoz DG , et al. Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria. Brain 1992; 115(Pt2):495-520. doi: 10.1093/brain/115.2.495.
doi: 10.1093/brain/115.2.495 |
4. |
Pamphlett R, Kril J, Hng TM . Motor neuron disease: a primary disorder of corticomotoneurons? Muscle Nerve 1995; 18(3):314-8. doi: 10.1002/mus.880180308.
doi: 10.1002/mus.880180308 |
5. |
Abrahams S, Goldstein LH, Suckling J , et al. Frontotemporal white matter changes in amyotrophic lateral sclerosis. J Neurol 2005; 252(3):321-31. doi: 10.1007/s00415-005-0646-x.
doi: 10.1007/s00415-005-0646-x pmid: 15739047 |
6. |
Ashburner J, Friston KJ . Voxel-based morphometry—the methods. Neuroimage 2000; 11(6 Pt 1):805-21. doi: 10.1006/nimg.2000.0582.
doi: 10.1006/nimg.2000.0582 |
7. |
Thivard L, Pradat PF, Lehéricy S , et al. Diffusion tensor imaging and voxel based morphometry study in amyotrophic lateral sclerosis: relationships with motor disability. J Neurol Neurosurg Psychiatry 2007; 78(8):889-92. doi: 10.1136/jnnp.2006.101758.
doi: 10.1136/jnnp.2006.101758 pmid: 2117724 |
8. |
Grosskreutz J, Kaufmann J, Fr?drich J , et al. Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis. BMC Neurol 2006; 6(17):1-10. doi: 10.1186/1471-2377-6-17.
doi: 10.1186/1471-2377-6-17 |
9. |
Shen D, Cui L, Fang J , et al. Voxel-wise meta-analysis of gray matter changes in amyotrophic lateral sclerosis. Front Aging Neurosci 2016; 8(64):1-12. doi: 10.3389/fnagi.2016.00064.
doi: 10.3389/fnagi.2016.00064 pmid: 4811926 |
10. |
Sheng L, Ma H, Zhong J , et al. Motor and extra-motor gray matter atrophy in amyotrophic lateral sclerosis: quantitative meta-analyses of voxel-based morphometry studies. Neurobiol Aging 2015; 36(12):3288-99. doi: 10.1016/j.neurobiolaging.2015.08.018.
doi: 10.1016/j.neurobiolaging.2015.08.018 pmid: 26362941 |
11. |
Fornito A, Yücel M, Wood SJ , et al. Surface-based morphometry of the anterior cingulate cortex in first episode schizophrenia. Hum Brain Mapp 2008; 29(4):478-89. doi: 10.1002/hbm.20412.
doi: 10.1002/hbm.20412 |
12. |
Chen Z, Ma L . Grey matter volume changes over the whole brain in amyotrophic lateral sclerosis: A voxel-wise meta-analysis of voxel based morphometry studies. Amyotroph Lateral Scler 2010; 11(6):549-54. doi: 10.3109/17482968.2010.516265.
doi: 10.3109/17482968.2010.516265 pmid: 20929296 |
13. |
Kim H, Kim JH, Possin KL , et al. Surface-based morphometry reveals caudate subnuclear structural damage in patients with premotor Huntington disease. Brain Imaging Behav 2016; 11(5):1365-72. doi: 10.1007/s11682-016-9616-4.
doi: 10.1007/s11682-016-9616-4 pmid: 27730480 |
14. |
Huang P, Lou Y, Xuan M , et al. Cortical abnormalities in Parkinson’s disease patients and relationship to depression: A surface-based morphometry study. Psychiatry Res Neuroimaging 2016; 250:24-8. doi: 10.1016/j.pscychresns.2016.03.002.
doi: 10.1016/j.pscychresns.2016.03.002 pmid: 27107157 |
15. |
Lu H, Ma SL, Chan SS , et al. The effects of apolipoprotein epsilon 4 on aging brain in cognitively normal Chinese elderly: a surface-based morphometry study. Int Psychogeriatr 2016; 28(9):1503-11. doi: 10.1017/S1041610216000624.
doi: 10.1017/S1041610216000624 pmid: 27097839 |
16. | Butman JA, Floeter MK . Decreased thickness of primary motor cortex in primary lateral sclerosis. Am J Neuroradiol 2007; 28(1):87-91. |
17. |
Roccatagliata L, Bonzano L, Mancardi G , et al. Detection of motor cortex thinning and corticospinal tract involvement by quantitative MRI in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2009; 10(1):47-52. doi: 10.1080/17482960802267530.
doi: 10.1080/17482960802267530 pmid: 1862277218622772 |
18. |
Cosottini M, Donatelli G, Costagli M , et al. High-resolution 7T MR imaging of the motor cortex in amyotrophic lateral sclerosis. AJNR Am J Neuroradiol 2016; 37(3):455-61. doi: 10.3174/ajnr.A4562.
doi: 10.3174/ajnr.A4562 |
19. |
d’Ambrosio A, Gallo A, Trojsi F , et al. Frontotemporal cortical thinning in amyotrophic lateral sclerosis. AJNR Am J Neuroradiol 2014; 35(2):304-10. doi: 10.3174/ajnr.A3753.
doi: 10.3174/ajnr.A3753 pmid: 24113470 |
20. |
Chen Z, Liu M, Ma L . Gray matter volume changes over the whole brain in the bulbar- and spinal-onset amyotrophic lateral sclerosis: a voxel-based morphometry study. Chin Med Sci J 2018; 33(1):20-8. doi: 10.24920/11804.
doi: 10.24920/11804 pmid: 29620511 |
21. |
Brooks BR, Miller RG, Swash M , et al. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2000; 1(5):293-9. doi: 10.1080/146608200300079536.
doi: 10.1080/146608200300079536 pmid: 11464847 |
22. |
Ohashi Y, Tashiro K, Itoyama Y , et al. Study of functional rating scale for amyotrophic lateral sclerosis: revised ALSFRS(ALSFRS-R) Japanese version. Brain and nerve 2001; 53(4):346-55. Japanese.
pmid: 11360474 |
23. |
Galea M, Woodward M . Mini-Mental State Examination (MMSE). Aust J Physiother 2005; 51(3):198. doi: 10.1016/S0004-9514(05)70034-9.
doi: 10.1016/S0004-9514(05)70034-9 |
24. |
Dahnke R, Yotter RA, Gaser C . Cortical thickness and central surface estimation. Neuroimage 2013; 65:336-48. doi: 10.1016/j.neuroimage.2012.09.050.
doi: 10.1016/j.neuroimage.2012.09.050 pmid: 23041529 |
25. |
Desikan RS, Ségonne F, Fischl B , et al. An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage 2006; 31(3):968-80. doi: 10.1016/j.neuroimage.2006.01.021.
doi: 10.1016/j.neuroimage.2006.01.021 pmid: 16530430 |
26. |
Hamilton RL, Bowser R . Alzheimer disease pathology in amyotrophic lateral sclerosis. Acta Neuropathol 2004; 107(6):515-22. doi: 10.1007/s00401-004-0843-1.
doi: 10.1007/s00401-004-0843-1 pmid: 15024584 |
27. |
Chen Z, Ma L . Grey matter volume changes over the whole brain in amyotrophic lateral sclerosis: A voxel-wise meta-analysis of voxel based morphometry studies. Amyotroph Lateral Scler 2010; 11(6):549-54. doi: 10.3109/17482968.2010.516265.
doi: 10.3109/17482968.2010.516265 pmid: 20929296 |
28. |
Gredal O, Pakkenberg H, Karlsborg M , et al. Unchanged total number of neurons in motor cortex and neocortex in amyotrophic lateral sclerosis: a stereological study. J Neurosci Methods 2000; 95(2):171-6. doi: 10.1016/S0165-0270(99)00175-2.
doi: 10.1016/S0165-0270(99)00175-2 pmid: 10752488 |
29. |
Kiernan JA, Hudson AJ . Changes in shapes of surviving motor neurons in amyotrophic lateral sclerosis. Brain 1993; 116(Pt 1):203-15. doi: 10.1093/brain/116.1.203.
doi: 10.1093/brain/116.1.203 pmid: 8453457 |
30. |
Nagy D, Kato T, Kushner PD . Reactive astrocytes are widespread in the cortical gray matter of amyotrophic lateral sclerosis. J Neurosci Res 1994; 38(3):336-47. doi: 10.1002/jnr.490380312.
doi: 10.1002/jnr.490380312 pmid: 7523689 |
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