과제정보
이 결과물은 2019년도 대구가톨릭대학교 학술연구비 지원에 의한 것임.
참고문헌
- Adams RD, Fisher CM, Hakim S, Ojemann RG, Sweet WH, Symptomatic Occult Hydrocephalus with "Normal" Cerebrospinal-Fluid Pressure.A Treatable Syndrome. N Engl J Med, 1965;273:117-26. https://doi.org/10.1056/NEJM196507152730301
- Kato T, Sato H, Emi M, Seino T, Arawaka S, Iseki C, Takahashi Y, Wada M, Kawanami, T, Segmental copy number loss of SFMBT1 gene in elderly individuals with ventriculomegaly: a community-based study. Intern Med, 2011;50(4):297-303. https://doi.org/10.2169/internalmedicine.50.4505
- Takahashi Y, Kawanami T, Nagasawa H, Iseki C, Hanyu H, Kato T, Familial normal pressure hydrocephalus (NPH) with an autosomal-dominant inheritance: a novel subgroup of NPH. J Neurol Sci, 2011;308(1-2):149-51. https://doi.org/10.1016/j.jns.2011.06.018
- Bech-Azeddine R, Hogh P, Juhler M, Gjerris F, Waldemar G, Idiopathic normal-pressure hydrocephalus: clinical comorbidity correlated with cerebral biopsy findings and outcome of cerebrospinal fluid shunting. J Neurol Neurosurg Psychiatry, 2007;78(2):157-61. https://doi.org/10.1136/jnnp.2006.095117
- Cabral D, Beach TG, Vedders L, Sue LI, Jacobson S, Myers K, Sabbagh MN, Frequency of Alzheimer's disease pathology at autopsy in patients with clinical normal pressure hydrocephalus. Alzheimers Dement, 2011;7(5):509-13. https://doi.org/10.1016/j.jalz.2010.12.008
- Wikkelso C, Andersson H, Blomstrand C, Lindqvist G, The clinical effect of lumbar puncture in normal pressure hydrocephalus. J Neurol Neurosurg Psychiatry, 1982; 45(1):64-9. https://doi.org/10.1136/jnnp.45.1.64
- Ishikawa M, Hashimoto M, Kuwana N, Mori E, Miyake H, Wachi A, Takeuchi T, Kazui H, Koyama H, Guidelines for management of idiopathic normal pressure hydrocephalus. Neurol Med Chir (Tokyo), 2008;48 Suppl:S1-23. https://doi.org/10.2176/nmc.48.S1
- van Uden CJ, Besser MP, Test-retest reliability of temporal and spatial gait characteristics measured with an instrumented walkway system (GAITRite). BMC Musculoskelet Disord, 2004;5:13. https://doi.org/10.1186/1471-2474-5-13
- McDonough AL, Batavia M, Chen FC, Kwon S, Ziai J, The validity and reliability of the GAITRite system's measurements: A preliminary evaluation. Arch Phys Med Rehabil, 2001;82(3):419-25. https://doi.org/10.1053/apmr.2001.19778
- Nelson AJ, Zwick D, Brody S, Doran C, Pulver L, Rooz G, Sadownick M, Nelson, Rothman J, The validity of the GaitRite and the Functional Ambulation Performance scoring system in the analysis of Parkinson gait. NeuroRehabilitation, 2002;17(3):255-62. https://doi.org/10.3233/nre-2002-17312
- Lim YH, Ko PW, Park KS, Hwang SK, Kim SH, Han J, Yoon U, Lee HW, Kang K, Quantitative Gait Analysis and Cerebrospinal Fluid Tap Test for Idiopathic Normal-pressure Hydrocephalus. Sci Rep, 2019;9(1):16255. https://doi.org/10.1038/s41598-019-52448-3
- Johnston B, Atkins MS, Mackiewich B, Anderson M, Segmentation of multiple sclerosis lesions in intensity corrected multispectral MRI. IEEE Trans Med Imaging, 1996;15(2):154-69. https://doi.org/10.1109/42.491417
- Braak H, Braak E, Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol, 1991;82(4):239-59. https://doi.org/10.1007/BF00308809
- Chetelat G, Landeau B, Eustache F, Mezenge F, Viader F, de la Sayette V, Desgranges B, Baron JC, Using voxel-based morphometry to map the structural changes associated with rapid conversion in MCI: a longitudinal MRI study. Neuroimage, 2005;27(4):934-46. https://doi.org/10.1016/j.neuroimage.2005.05.015
- Worker A, Blain C, Jarosz J, Chaudhuri KR, Barker GJ, Williams SC, Brown R, Leigh PN, Simmons A, Cortical thickness, surface area and volume measures in Parkinson's disease, multiple system atrophy and progressive supranuclear palsy. PLoS One, 2014;9(12):e114167. https://doi.org/10.1371/journal.pone.0114167
- Rimol LM, Nesvag R, Hagler DJ, Jr., Bergmann O, Fennema-Notestine C, Hartberg CB, Haukvik UK, Lange E, Pung CJ, Server A, Melle I, Andreassen OA, Agartz I, Dale AM, Cortical volume, surface area, and thickness in schizophrenia and bipolar disorder. Biol Psychiatry, 2012;71(6):552-60. https://doi.org/10.1016/j.biopsych.2011.11.026
- Seo SW, Ahn J, Yoon U, Im K, Lee JM, Kim ST, Ahn HJ, Chin J, Jeong Y, Na DL, Cortical thinning in vascular mild cognitive impairment and vascular dementia of subcortical type. J Neuroimaging, 2010;20(1):37-45. https://doi.org/10.1111/j.1552-6569.2008.00293.x
- Rosano C, Aizenstein HJ, Studenski S, Newman AB, A regions-of-interest volumetric analysis of mobility limitations in community-dwelling older adults. J Gerontol A Biol Sci Med Sci, 2007;62(9):1048-55. https://doi.org/10.1093/gerona/62.9.1048
- Kang K, Han J, Lee SW, Jeong SY, Lim YH, Lee JM, Yoon U, Abnormal cortical thickening and thinning in idiopathic normal-pressure hydrocephalus. Sci Rep, 2020;10(1):21213. https://doi.org/10.1038/s41598-020-78067-x
- Relkin N, Marmarou A, Klinge P, Bergsneider M, Black PM, Diagnosing idiopathic normal-pressure hydrocephalus. Neurosurgery, 2005;57(3 Suppl):S4-16;discussion ii-v.
- Collins DL, Neelin P, Peters TM, Evans AC, Automatic 3D intersubject registration of MR volumetric data in standardized Talairach space. J Comput Assist Tomogr, 1994;18(2):192-205. https://doi.org/10.1097/00004728-199403000-00005
- Smith SM, Fast robust automated brain extraction. Hum Brain Mapp, 2002;17(3):143-55. https://doi.org/10.1002/hbm.10062
- Sled JG, Zijdenbos AP, Evans AC, A nonparametric method for automatic correction of intensity nonuniformity in MRI data. IEEE Trans Med Imaging, 1998;17(1):87-97. https://doi.org/10.1109/42.668698
- Zijdenbos AP, Forghani R, Evans AC, Automatic "pipeline" analysis of 3-D MRI data for clinical trials: application to multiple sclerosis. IEEE Trans Med Imaging, 2002;21(10):1280-91. https://doi.org/10.1109/TMI.2002.806283
- Tohka J, Zijdenbos A, Evans A, Fast and robust parameter estimation for statistical partial volume models in brain MRI. Neuroimage, 2004;23(1):84-97. https://doi.org/10.1016/j.neuroimage.2004.05.007
- Kim JS, Singh V, Lee JK, Lerch J, Ad-Dab'bagh Y, MacDonald D, Lee JM, Kim SI, Evans AC, Automated 3-D extraction and evaluation of the inner and outer cortical surfaces using a Laplacian map and partial volume effect classification. Neuroimage, 2005;27(1):210-21. https://doi.org/10.1016/j.neuroimage.2005.03.036
- MacDonald D, Kabani N, Avis D, Evans AC, Automated 3-D extraction of inner and outer surfaces of cerebral cortex from MRI. Neuroimage, 2000;12(3):340-56. https://doi.org/10.1006/nimg.1999.0534
- Lerch JP, Pruessner JC, Zijdenbos A, Hampel H, Teipel SJ, Evans AC, Focal decline of cortical thickness in Alzheimer's disease identified by computational neuroanatomy. Cereb Cortex, 2005;15(7):995-1001. https://doi.org/10.1093/cercor/bhh200
- Hagler DJ, Jr., Saygin AP, Sereno MI, Smoothing and cluster thresholding for cortical surface-based group analysis of fMRI data. Neuroimage, 2006;33(4):1093-103. https://doi.org/10.1016/j.neuroimage.2006.07.036
- Lyttelton O, Boucher M, Robbins S, Evans A, An unbiased iterative group registration template for cortical surface analysis. Neuroimage, 2007;34(4):1535-44. https://doi.org/10.1016/j.neuroimage.2006.10.041
- Hilal S, Xin X, Ang SL, Tan CS, Venketasubramanian N, Niessen WJ, Vrooman H, Wong TY, Chen C, Ikram MK, Risk Factors and Consequences of Cortical Thickness in an Asian Population. Medicine (Baltimore), 2015;94(23):e852. https://doi.org/10.1097/MD.0000000000000852
- Espeseth T, Westlye LT, Fjell AM, Walhovd KB, Rootwelt H, Reinvang I, Accelerated age-related cortical thinning in healthy carriers of apolipoprotein E epsilon 4. Neurobiol Aging, 2008;29(3):329-40. https://doi.org/10.1016/j.neurobiolaging.2006.10.030
- Fortea J, Sala-Llonch R, Bartres-Faz D, Bosch B, Llado A, Bargallo N, Molinuevo JL, Sanchez-Valle R, Increased cortical thickness and caudate volume precede atrophy in PSEN1 mutation carriers. J Alzheimers Dis, 2010;22(3):909-22. https://doi.org/10.3233/JAD-2010-100678
- Ishii K, Hashimoto M, Hayashida K, Hashikawa K, Chang CC, Nakagawara J, Nakayama T, Mori S, Sakakibara R, A multicenter brain perfusion SPECT study evaluating idiopathic normal-pressure hydrocephalus on neurological improvement. Dement Geriatr Cogn Disord, 2011;32(1):1-10. https://doi.org/10.1159/000328972
- Mataro M, Matarin M, Poca MA, Pueyo R, Sahuquillo J, Barrios M, Junque C, Functional and magnetic resonance imaging correlates of corpus callosum in normal pressure hydrocephalus before and after shunting. J Neurol Neurosurg Psychiatry, 2007;78(4):395-8.
- Gao Z, Zhu Q, Zhang Y, Zhao Y, Cai L, Shields CB, Cai J, Reciprocal modulation between microglia and astrocyte in reactive gliosis following the CNS injury. Mol Neurobiol, 2013;48(3):690-701. https://doi.org/10.1007/s12035-013-8460-4
- Vargas-Sanchez K, Mogilevskaya M, Rodriguez-Perez J, Rubiano MG, Javela JJ, Gonzalez-Reyes RE, Astroglial role in the pathophysiology of status epilepticus: an overview. Oncotarget, 2018;9(42):26954-26976. https://doi.org/10.18632/oncotarget.25485
- Gaist D, Hougaard A, Garde E, Reislev NL, Wiwie R, Iversen P, Madsen CG, Blaabjerg M, Nielsen HH, Kroigard T, Ostergaard K, Kyvik KO, Hjelmborg J, Madsen K, Siebner HR, Ashina M, Migraine with visual aura associated with thicker visual cortex. Brain, 2018;141(3):776-785. https://doi.org/10.1093/brain/awx382
- Baril AA, Gagnon K, Brayet P, Montplaisir J, De Beaumont L, Carrier J, Lafond C, L'Heureux F, Gagnon JF, Gosselin N, Gray Matter Hypertrophy and Thickening with Obstructive Sleep Apnea in Middle-aged and Older Adults. Am J Respir Crit Care Med, 2017;195(11):1509-1518. https://doi.org/10.1164/rccm.201606-1271oc
- Miller JM, McAllister JP, 2nd, Reduction of astrogliosis and microgliosis by cerebrospinal fluid shunting in experimental hydrocephalus. Cerebrospinal Fluid Res, 2007;4:5. https://doi.org/10.1186/1743-8454-4-5
- Kaas JH, Evolution of somatosensory and motor cortex in primates. Anat Rec A Discov Mol Cell Evol Biol, 2004; 281(1):1148-56. https://doi.org/10.1002/ar.a.20120
- Rosso AL, Studenski SA, Chen WG, Aizenstein HJ, Alexander NB, Bennett DA, Black, SE, Camicioli R, Carlson MC, Ferrucci L, Guralnik JM, Hausdorff JM, Kaye J, Launer LJ, Lipsitz LA, Verghese J, Rosano C, Aging, the central nervous system, and mobility. J Gerontol A Biol Sci Med Sci, 2013; 68(11):1379-86. https://doi.org/10.1093/gerona/glt089
- Fukuyama H, Ouchi Y, Matsuzaki S, Nagahama Y, Yamauchi H, Ogawa M, Kimura J, Shibasaki H, Brain functional activity during gait in normal subjects: a SPECT study. Neurosci Lett, 1997;228(3):183-6. https://doi.org/10.1016/S0304-3940(97)00381-9
- Drew T, Prentice S, Schepens B, Cortical and brainstem control of locomotion. Prog Brain Res, 2004;143:251-61. https://doi.org/10.1016/S0079-6123(03)43025-2
- Takakusaki K, Neurophysiology of gait: from the spinal cord to the frontal lobe. Mov Disord, 2013;28(11):1483-91. https://doi.org/10.1002/mds.25669
- Jahn K, Deutschlander A, Stephan T, Strupp M, Wiesmann M, Brandt T, Brain activation patterns during imagined stance and locomotion in functional magnetic resonance imaging. Neuroimage, 2004;22(4):1722-31. https://doi.org/10.1016/j.neuroimage.2004.05.017
- Rosano C, Aizenstein H, Brach J, Longenberger A, Studenski S, Newman AB, Special article: gait measures indicate underlying focal gray matter atrophy in the brain of older adults. J Gerontol A Biol Sci Med Sci, 2008;63(12):1380-8. https://doi.org/10.1093/gerona/63.12.1380
- Regnaux JP, Pradon D, Roche N, Robertson J, Bussel B, Dobkin B, Effects of loading the unaffected limb for one session of locomotor training on laboratory measures of gait in stroke. Clin Biomech (Bristol, Avon), 2008;23(6):762-8. https://doi.org/10.1016/j.clinbiomech.2008.01.011
- Stolze H, Kuhtz-Buschbeck JP, Drucke H, Johnk K, Diercks C, Palmie S, Mehdorn HM, Illert M, Deuschl G, Gait analysis in idiopathic normal pressure hydrocephalus--which parameters respond to the CSF tap test? Clin Neurophysiol, 2000;111(9):1678-86. https://doi.org/10.1016/S1388-2457(00)00362-X
- Stolze H, Kuhtz-Buschbeck JP, Drucke H, Johnk K, Illert M, Deuschl G, Comparative analysis of the gait disorder of normal pressure hydrocephalus and Parkinson's disease. J Neurol Neurosurg Psychiatry, 2001;70(3):289-97. https://doi.org/10.1136/jnnp.70.3.289
- Mackenzie TN, Bailey AZ, Mi PY, Tsang P, Jones CB, Nelson AJ, Human area 5 modulates corticospinal output during movement preparation. Neuroreport, 2016;27(14):1056-60. https://doi.org/10.1097/wnr.0000000000000655
- Lacquaniti F, Guigon E, Bianchi L, Ferraina S, Caminiti R, Representing spatial information for limb movement: role of area 5 in the monkey. Cereb Cortex, 1995;5(5):391-409. https://doi.org/10.1093/cercor/5.5.391
- Anderson TJ, Jenkins IH, Brooks DJ, Hawken MB, Frackowiak RS, Kennard C, Cortical control of saccades and fixation in man. A PET study. Brain, 1994;117(Pt 5):1073-84. https://doi.org/10.1093/brain/117.5.1073
- Fink GR, Frackowiak RS, Pietrzyk U, Passingham RE, Multiple nonprimary motor areas in the human cortex. J Neurophysiol, 1997;77(4):2164-74. https://doi.org/10.1152/jn.1997.77.4.2164