The DOI matches its Crossref record.
Histopathologic correlates of white matter changes on MRI in Alzheimer's disease and normal aging
Abstract
We investigated the histopathologic correlates of white matter changes in Alzheimer's disease (AD) patients (n = 6) and controls (n = 9) using postmortem MRI. White matter changes were rated on a 0 to 3 scale in 51 regions. Histopathologically, we subjectively rated the loss of myelinated axons in the deep and periventricular white matter, denudation of the ventricular ependyma, gliosis, width of the perivascular spaces, and leptomeningeal congophilic angiopathy; we measured structural changes in the walls of the blood vessels in the white matter in micrometers. The AD brains displayed significantly more white matter hyperintensities on MRI than controls. Histopathologically, the denudation of the ventricular ependyma and the gliosis were significantly more severe in AD than in controls, and there was a trend toward more loss of myelinated axons in the deep white matter in the AD brains (p = 0.07). The MRI abnormalities correlated with the loss of myelinated axons in the deep white matter (r' = 0.37; p < 0.01) and with the denudation of the ventricular lining (r' = 0.54; p < 0.01). We could not find any evidence for arteriolosclerosis, but the mean thickness of the adventitia of the arteries of the deep white matter in AD almost doubled the value in control brains (p = 0.0009). We conclude that white matter abnormalities in AD patients and controls consist of loss of myelinated axons, probably caused by arterial changes and breakdown of the ventricular lining. Since imaging/histopathologic correlation was similar in AD patients and controls, these changes probably represent some form of accelerated aging.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“AD subjects show more pervasive white matter change [42–46].”
From Brain aging, Alzheimer's disease, and mitochondria (2011) · cites this paper as [45]
Citations
Cited by
Sorted by citations
A New Rating Scale for Age-Related White Matter Changes Applicable to MRI and CT
Wahlund, L., Barkhof, F., Fazekas, F., Bronge, L., Augustin, M., Sjögren, M., Wallin, A., Adèr, H., Leys, D., Pantoni, L., et al. (2001) · Stroke · doi:10.1161/01.str.32.6.1318 · Cited by 1,838
“Five different regions were rated in the right and left hemispheres separately: (1) the frontal area, which was the frontal lobe anterior to the central sulcus; (2) the parieto-occipital area, which consisted of the parietal and occipital lobes together; (3) the temporal area, which was the temporal lobe (the border b…”
BackgroundSelf-citationLongstreth, W. T., Manolio, T. A., Arnold, A., Burke, G. L., Bryan, N., Jungreis, C. A., Enright, P. L., O'Leary, D., & Fried, L. (1996) · Stroke · doi:10.1161/01.str.27.8.1274 · Cited by 1,464
Pathogenesis of Leukoaraiosis: A Review
Pantoni, L., & Garcia, J. H. (1997) · Stroke · doi:10.1161/01.str.28.3.652 · Cited by 1,225
O'Brien, J. T., Erkinjuntti, T., Reisberg, ., Román, G. C., Pantoni, L., Bowler, J., Ballard, C., DeCarli, C., Gorelick, P., Rockwood, K., et al. (2014) · International Journal of Stroke · doi:10.1111/ijs.12374_18 · Cited by 1,165
Brain atrophy in Alzheimer’s Disease and aging
Pini, L., Pievani, M., Bocchetta, M., Altomare, D., Bosco, P., Cavedo, E., Galluzzi, S., Marizzoni, M., & Frisoni, G. B. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.01.002 · Cited by 836
Heterogeneity of small vessel disease: a systematic review of MRI and histopathology correlations
Gouw, A. A., Seewann, A., van der Flier, W. M., Barkhof, F., Rozemuller, A. M., Scheltens, P., & Geurts, J. J. G. (2011) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.2009.204685 · Cited by 766
Self-citationThe anatomy of mood disorders—review of structural neuroimaging studies
Soares, J. C., & Mann, J. J. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(96)00006-6 · Cited by 760
White matter changes in Alzheimer’s disease: A focus on myelin and oligodendrocytes
Nasrabady, S. E., Rizvi, B., Goldman, J. E., & Brickman, A. M. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0515-3 · Cited by 723
“1) and the loss of myelinated axons, as well as changes in arterial adventitia in deep white matter [68].”
Farkas, E., Luiten, P. G. M., & Bari, F. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.01.003 · Cited by 724
“…similar to those identified in post mortem human WM lesions, such as WM rarefaction, demyelination, gliosis, regressive astrocytic changes, and the apoptotic cell death of oligodendrocytes and astrocytes (Kobayashi et al., 2002; Scheltens et al., 1995; Thomas et al., 2002; Tomimoto et al., 1997).”
BackgroundHead, D. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh003 · Cited by 645
Mulkern, R. V., Zengingönül, H. P., Robertson, R. L., Bogner, P., Zou, K. H., Guðbjartsson, H., Guttmann, C. R. G., Holtzman, D. H., Kyriakos, W. E., Jolesz, F. A., et al. (2000) · Magnetic Resonance in Medicine · doi:10.1002/1522-2594(200008)44:2 · Cited by 111
Fernando, M. S., Simpson, J. E., Matthews, F., Brayne, C., Lewis, C. E., Barber, R., Kalaria, R. N., Forster, G., Esteves, F., Wharton, S. B., et al. (2006) · Stroke · doi:10.1161/01.str.0000221308.94473.14 · Cited by 587
Classification of white matter lesions on magnetic resonance imaging in elderly persons
Kim, K. W., MacFall, J. R., & Payne, M. E. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.03.024 · Cited by 539
Ge, Y., Grossman, R. I., Babb, J. S., Rabin, M., Mannon, L. J., & Kolson, D. L. (2002) · PubMed Central · Cited by 528
Anatomical Mapping of White Matter Hyperintensities (WMH)
DeCarli, C. S., Fletcher, E. M., Ramey, V. H., Harvey, D. J., & Jagust, W. J. (2004) · Stroke · doi:10.1161/01.str.0000150668.58689.f2 · Cited by 498
Barber, R., Scheltens, P., Gholkar, A., Ballard, C., McKeith, I., Ince, P., Perry, R., & O'Brien, J. (1999) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.67.1.66 · Cited by 440
“44 Damage to the integrity of the ependymal lining may in turn result in abnormal dynamics of CSF and increased water content.”
BackgroundSelf-citationBlack, S., Gao, F., & Bilbao, J. (2009) · Stroke · doi:10.1161/strokeaha.108.537704 · Cited by 379
Zhan, X., Stamova, B. S., & Sharp, F. R. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00042 · Cited by 361
“(A) Western blots for E. coli K99 pili protein showed K99 protein in 3/3 Alzheimer’s disease (AD) White Matter (WM) samples, 2/3 AD Gray Matter (GM) samples and 0/3 Control GM samples. β-actin was used as loading control.”
BackgroundInfluentialMRI white matter hyperintensities: Three-year follow-up of the Austrian Stroke Prevention Study
Schmidt, R., Fazekas, F., Kapeller, P., Schmidt, H., & Hartung, H.-P. (1999) · Neurology · doi:10.1212/wnl.53.1.132 · Cited by 342
CT and MRI Rating of White Matter Lesions
Fazekas, F., Barkhof, F., Wahlund, L., Pantoni, L., Erkinjuntti, T., Scheltens, P., & Schmidt, R. (2002) · Cerebrovascular Diseases · doi:10.1159/000049147 · Cited by 335
Self-citationHeterogeneity in age-related white matter changes
Schmidt, R., Schmidt, H., Haybaeck, J., Loitfelder, M., Weis, S., Cavalieri, M., Seiler, S., Enzinger, C., Ropele, S., Erkinjuntti, T., et al. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0851-x · Cited by 343
Self-citationKidney Function Is Related to Cerebral Small Vessel Disease
Ikram, M. A., Vernooij, M. W., Albert Hofman, D., Niessen, W. J., van der Lugt, A., & Breteler, M. M. B. (2007) · Stroke · doi:10.1161/strokeaha.107.493494 · Cited by 324
Wen, W., & Sachdev, P. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.12.027 · Cited by 315
Diffusion tensor imaging and aging—A review.
Moseley, M. (2002) · NMR in Biomedicine · doi:10.1002/nbm.785 · Cited by 302
“studies of normal aging.(24) The declines observed in intravoxel coherence with age may reflect tissue status that could result in normal age-related functional decreases.”
BackgroundBrain aging, Alzheimer's disease, and mitochondria
Swerdlow, R. H. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.08.012 · Cited by 306
Garde, E., Mortensen, E. L., Krabbe, K., Rostrup, E., & Larsson, H. B. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02604-0 · Cited by 307
Neuropathological basis of magnetic resonance images in aging and dementia
Jagust, W. J., Zheng, L., Harvey, D. J., Mack, W. J., Vinters, H. V., Weiner, M. W., Ellis, W. G., Zarow, C., Mungas, D., Reed, B. R., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21296 · Cited by 302
Visual Rating of Age-Related White Matter Changes on Magnetic Resonance Imaging
Kapeller, P., Barber, R., Vermeulen, R. J., Adèr, H. J., Scheltens, P., Freidl, W., Almkvist, O., Moretti, M., del Ser, T., Vaghfeldt, P., et al. (2003) · Stroke · doi:10.1161/01.str.0000049766.26453.e9 · Cited by 304
Self-citationMild cognitive impairment and Alzheimer disease: regional diffusivity of water
Kantarci, K., Jack, C. R., Xu, Y. C., Campeau, N. G., O’Brien, P. C., Smith, G. E., Ivnik, R. J., Boeve, B. F., Kokmen, E., Tangalos, E. G., et al. (2001) · Radiology · doi:10.1148/radiology.219.1.r01ap14101 · Cited by 300
Draganski, B., Ashburner, J., Hutton, C., Kherif, F., Frackowiak, R. S. J., Helms, G., & Weiskopf, N. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.052 · Cited by 306
“, 2005) with an additional reduction in focal WM hyper-intensities (Scheltens et al., 1995).”
BackgroundGouw, A. A., Seewann, A., Vrenken, H., van der Flier, W. M., Rozemuller, J. M., Barkhof, F., Scheltens, P., & Geurts, J. J. G. (2008) · Brain · doi:10.1093/brain/awn265 · Cited by 281
Self-citationHu, H., Ou, Y., Shen, X., Qu, Y., Ma, Y., Wang, Z.-T., Dong, Q., Tan, L., & Yu, J. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.007 · Cited by 299
Regional and global changes in cerebral diffusion with normal aging.
Nusbaum, A. O., Tang, C. Y., Buchsbaum, M. S., Wei, T. C., & Atlas, S. W. (2001) · PubMed Central · Cited by 252
Vascular pathologies and cognition in a population-based cohort of elderly people
Fernando, M. S., & Ince, P. G. (2004) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2004.09.004 · Cited by 239
“These MRI WMLs have shown variable associations with dementia or other neurological or psychiatric disease in general clinical practice and their significance and origin are disputed [16–18].”
BackgroundFully automatic segmentation of white matter hyperintensities in MR images of the elderly
Behloul, F., van den Heuvel, D. M. J., Olofsen, H., van Osch, M. J. P., van der Grond, J., van Buchem, M. A., & Reiber, J. H. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.061 · Cited by 231
Huang, J., Friedland, R. P., & Auchus, A. P. (2007) · American Journal of Neuroradiology · doi:10.3174/ajnr.a0700 · Cited by 220
“Although neuroimaging and pathoanatomic studies have confirmed both macroscopic and microscopic white matter changes in patients with AD and MCI, controversy exists regarding the clinical relevance of these changes and the mechanisms underlying them.(4-7) By taking advantage of the anisotropic nature of water diffusio…”
BackgroundThe enigma of vascular cognitive disorder and vascular dementia
Jellinger, K. A. (2007) · Acta Neuropathologica · doi:10.1007/s00401-006-0185-2 · Cited by 166
“on MRI correlated well with the severity of demyelination and astrogliosis, which were often associated with small lacunar infarcts in both the white matter and basal ganglia, suggesting a common pathophysiology, particularly arteriosclerosis of the penetrating artereries [24, 68, 150, 155, 188, 224, 355, 437, 503, 50…”
BackgroundSimpson, J. E., Fernando, M. S., Clark, L., Ince, P. G., Matthews, F., Forster, G., O'Brien, J. T., Barber, R., Kalaria, R. N., Brayne, C., et al. (2007) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2007.00828.x · Cited by 215
Wen, W., Sachdev, P. S., Li, J. J., Chen, X., & Anstey, K. J. (2009) · Human Brain Mapping · doi:10.1002/hbm.20586 · Cited by 210
“Postmortem examination confirms that WMHs are correlated with histopathologic changes [Fazekas et al., 1993; Scheltens et al., 1995; Smith et al., 2000; Takao et al., 1999].”
BackgroundCerebral Perfusion and Cerebrovascular Reactivity Are Reduced in White Matter Hyperintensities
Marstrand, J. R., Garde, E., Rostrup, E., Ring, P., Rosenbaum, S., Mortensen, E. L., & Larsson, H. B. W. (2002) · Stroke · doi:10.1161/01.str.0000012808.81667.4b · Cited by 215
Neuropathology of white matter changes in Alzheimer’s disease and vascular dementia
Englund, E. (1998) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000051183 · Cited by 213
Age-related regional variations of the corpus callosum identified by diffusion tensor tractography
Lebel, C., Caverhill-Godkewitsch, S., & Beaulieu, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.072 · Cited by 209
“At older ages, loss of myelinated fibers and decreased axonal density would lead to increasingλ⊥ and lower FAvalues (Moseley, 2002; Scheltens et al., 1995), while greater water content associated with atrophy in the aging brain could cause increased λ// and thus increasing MD (Moseley, 2002).”
BackgroundVoxel-based detection of white matter abnormalities in mild Alzheimer disease
Xie, S., Xiao, J., Gong, G., Zang, Y., Wang, Y., Wu, H., & Jiang, X. X. (2006) · Neurology · doi:10.1212/01.wnl.0000219625.77625.aa · Cited by 208
Holland, C. M., Smith, E. E., Csapo, I., Gurol, M. E., Brylka, D. A., Killiany, R., Blacker, D., Albert, M., Guttmann, C. R. G., & Greenberg, S. M. (2008) · Stroke · doi:10.1161/strokeaha.107.497438 · Cited by 204
Pathophysiologic Mechanisms in the Development of Age-Related White Matter Changes of the Brain
Fazekas, F., Schmidt, R., & Scheltens, P. (1998) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000051182 · Cited by 189
Self-citationFarkas, E., Donka, G., de Vos, R. A. I., Mihály, A., Bari, F., & Luiten, P. G. M. (2004) · Acta Neuropathologica · doi:10.1007/s00401-004-0864-9 · Cited by 191
van Norden, A. G., de Laat, K. F., Gons, R. A. R., van Uden, I. W., van Dijk, E. J., van Oudheusden, L. J. B., Esselink, R. A. J., Bloem, B. R., van Engelen, B. G. M., Zwarts, M. J., et al. (2011) · BMC Neurology · doi:10.1186/1471-2377-11-29 · Cited by 193
“As conventional MRI is not sensitive to early loss of microstructural integrity in the normal appearing white matter (NAWM), possible changes in this largest part of the white matter cannot be assessed [14,15].”
BackgroundImpact of White Matter Changes on Clinical Manifestation of Alzheimer’s Disease
Hirono, N., Kitagaki, H., Kazui, H., Hashimoto, M., & Mori, E. (2000) · Stroke · doi:10.1161/01.str.31.9.2182 · Cited by 186
Schuff, N. W., Ezekiel, F., Gamst, A. C., Amend, D. L., Capizzano, A. A., Maudsley, A. A., & Weiner, M. W. (2001) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1119 · Cited by 183
Regenold, W. T., Phatak, P., Marano, C. M., Gearhart, L., Viens, C. H., & Hisley, K. C. (2007) · Psychiatry Research · doi:10.1016/j.psychres.2006.12.019 · Cited by 178
Song, S.-K., Kim, J. H., Lin, S.-J., Brendza, R. P., & Holtzman, D. M. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.12.003 · Cited by 170
“Neuropathological and biochemical studies on white matter from AD subjects have demonstrated dramatic loss of myelin and axons (Bronge et al., 2002; Scheltens et al., 1995), DNA fragmentation (Forloni et al., 1993; Ivins et al., 1999; Jen et al., 1998; Yuan and Yankner, 2000), and selective loss of…”
BackgroundWhite matter abnormalities in mobility-impaired older persons
Guttmann, C. R. G., Benson, R. R., Warfield, S. K., Wei, X., Anderson, M. C., Hall, C. B., Abu‐Hasaballah, K., Mugler, J. P., & WOLFSON, L. I. (2000) · Neurology · doi:10.1212/wnl.54.6.1277 · Cited by 169
Capizzano, A. A. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2003.019273 · Cited by 160
Voxel-based assessment of gray and white matter volumes in Alzheimer's disease
Guo, X., Wang, Z., Li, K., Li, Z., Qi, Z., Jin, Z. H., Yao, L., & Chen, K. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.10.086 · Cited by 164
“Its pathological feature is primarily the loss or disconnection of fiber tracts [20].”
BackgroundIs late onset depression a prodrome to dementia?
Schweitzer, I., Tuckwell, V., O'Brien, J. T., & Ames, D. J. (2002) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.525 · Cited by 167
Imaging of White Matter Lesions
Barkhof, F., & Scheltens, P. (2002) · Cerebrovascular Diseases · doi:10.1159/000049146 · Cited by 162
Self-citationPostmortem MRI and Histopathology of White Matter Changes in Alzheimer Brains
Bronge, L., Bogdanović, N., & Wahlund, L. (2002) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000057698 · Cited by 157
Gootjes, L., Teipel, S. J., Zebuhr, Y., Schwarz, R., Leinsinger, G., Scheltens, P., Möller, H. ‐., & Hampel, H. J. (2004) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000079199 · Cited by 161
Self-citationBrain tissue volumes in relation to cognitive function and risk of dementia
Ikram, M. A., Vrooman, H. A., Vernooij, M. W., den Heijer, T., Albert Hofman, D., Niessen, W. J., van der Lugt, A., Koudstaal, P. J., & Breteler, M. M. B. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.04.008 · Cited by 156
Paola, M. D., Spalletta, G., & Caltagirone, C. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1370 · Cited by 152
“: +39 06 51501215; Fax: +39 06 51501213; E-mail: m.dipaola@hsantalucia. it. generation, a number of investigations have also documented a general white matter (WM) pathology associated with AD [1] [2] [3] [4] [5] [6].”
Assessment of white matter tract damage in mild cognitive impairment and Alzheimer's disease
Pievani, M., Agosta, F., Pagani, E., Canu, E., Sala, S., Absinta, M., Geroldi, C., Ganzola, R., Frisoni, G. B., & Filippi, M. (2010) · Human Brain Mapping · doi:10.1002/hbm.20978 · Cited by 152
“Pathological correlates of WMHs included myelin and axonal loss, reduction of olygodentrocytes, microglial activation, astrogliosis, and dilated perivascular spaces [Fazekas et al., 1991, 1993; Scheltens et al., 1995].”
BackgroundAge-related changes in the central auditory system
Ouda, L., Profant, O., & Syka, J. (2015) · Cell and Tissue Research · doi:10.1007/s00441-014-2107-2 · Cited by 153
“Another factor related to cortical ageing is WM lesions (WML; hyperintensities on T2-weighted MRI) that correspond to loss of myelinated axons, gliosis, enlarged perivascular spaces and small vessel disease (Grafton et al. 1991; Scheltens et al. 1995), thus representing a risk factor of subcortical and cortical brain…”
BackgroundBot, J., Blezer, E. L. A., Kamphorst, W., Nijeholt, G. J. L. À., Adèr, H. J., Castelijns, J. A., Nicolay, K., Bergers, E., Ravid, R., Polman, C. H., et al. (2004) · Radiology · doi:10.1148/radiol.2332031572 · Cited by 147
Self-citationPost-mortem assessment in vascular dementia: advances and aspirations
McAleese, K. E., Alafuzoff, I. I., Charidimou, A., Reuck, J. D., Grinberg, L. T., Hainsworth, A. H., Hortobágyi, T., Ince, P. G., Jellinger, K. A., Gao, J., et al. (2016) · BMC Medicine · doi:10.1186/s12916-016-0676-5 · Cited by 144
Combined Plasma Biomarkers for Diagnosing Mild Cognition Impairment and Alzheimer’s Disease
Chiu, M., Yang, S., Horng, H. E., Yang, C., Chen, T., Chieh, J.-J., Chen, H.-H., Chen, T.-C., Ho, C.-S., Chang, S.-F., et al. (2013) · ACS Chemical Neuroscience · doi:10.1021/cn400129p · Cited by 136
White matter volumes and periventricular white matter hyperintensities in aging and dementia
Smith, C. D., Snowdon, D. A., Wang, H., & Markesbery, W. R. (2000) · Neurology · doi:10.1212/wnl.54.4.838 · Cited by 137
Fernando, M. S., O'Brien, J. T., Perry, R. H., English, P. T., Forster, G., McMeekin, W., Slade, J. Y., Golkhar, A., Matthews, F. E., Barber, R., et al. (2004) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2004.00550.x · Cited by 137
Brain Lesions on MRI in Elderly Patients with Type 2 Diabetes Mellitus
van Harten, B., Oosterman, J. M., van Loon, B. J. P., Scheltens, P., & Weinstein, H. C. (2006) · European Neurology · doi:10.1159/000098054 · Cited by 135
Self-citationSuridjan, I., Pollock, B. G., Verhoeff, N. P. L. G., Voineskos, A. N., Chow, T., Rusjan, P. M., Lobaugh, N. J., Houle, S., Mulsant, B. H., & Mizrahi, R. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.1 · Cited by 132
Proton magnetic resonance spectroscopy can differentiate Alzheimer's disease from normal aging
Parnetti, L., Tarducci, R., Presciutti, O., Lowenthal, D. T., Pippi, M., Palumbo, B., Gobbi, G., Pelliccioli, G. P., & Senin, U. (1997) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(97)01877-0 · Cited by 130
Is Hypertension Associated With an Accelerated Aging of the Brain?
Tzourio, C., Laurent, S., & Debette, S. (2014) · Hypertension · doi:10.1161/hypertensionaha.113.00147 · Cited by 136
White matter is altered with parental family history of Alzheimer's disease
Bendlin, B. B., Ries, M. L., Canu, E., Sodhi, A., Lazar, M., Alexander, A. L., Carlsson, C. M., Sager, M. A., Asthana, S., & Johnson, S. C. (2010) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2009.11.003 · Cited by 130
“Postmortem assessment of white matter in AD has revealed several pathologic differences compared with control, such as denudation of the ventricular ependyma, gliosis, and loss of myelinated axons in the deep white matter [71].”
BackgroundWolf, H., Ecke, G. M., Bettin, S., Dietrich, J., & Gertz, H. (2000) · International Journal of Geriatric Psychiatry · doi:10.1002/1099-1166(200009)15:9 · Cited by 1
Wen, W. X., Sachdev, P. S., Chen, X., & Anstey, K. J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.057 · Cited by 122
“The caps and lines of PVWMH are neuropathologically related to myelin pallor or rarefaction without other convincing evidence of ischemia (Fazekas et al., 1993; Scheltens et al., 1995).”
White matter lesions and brain gray matter volume in cognitively normal elders
Raji, C. A., López, O. L., Kuller, L. H., Carmichael, O. T., Longstreth, W. T., Jr., Gach, H. M., Boardman, J., Bernick, C. B., Thompson, P. M., & Becker, J. T. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.08.010 · Cited by 123
“Increased WML burden corresponds to loss of myelinated axons, gliosis, enlarged perivascular spaces, and small vessel disease (SVD) (Grafton et al., 1991; Kobari et al., 1990; Scheltens et al., 1995).”
BackgroundHaller, S., Kövari, E., Herrmann, F. R., Cuvinciuc, V., Tomm, A.-M., Zulian, G. B., Lövblad, K., Giannakopoulos, P., & Bouras, C. (2013) · Acta Neuropathologica Communications · doi:10.1186/2051-5960-1-14 · Cited by 124
“[21], the severity of periventricular and deep WM demyelination was assessed on a 4-level semi-quantitative scale, where 0 corresponded to absent; 1 to mild; 2 to moderate and 3 to severe demyelination.”
BackgroundFactors affecting brain structure in men with HIV disease in the post-HAART era
Becker, J. T., Maruca, V., Kingsley, L., Sanders, J. M., Alger, J. R., Barker, P. B., Goodkin, K., Martin, E. M., Miller, E. N., Ragin, A. B., et al. (2011) · Neuroradiology · doi:10.1007/s00234-011-0854-2 · Cited by 117
Huang, H., Fan, X., Weiner, M., Martin‐Cook, K., Xiao, G., Davis, J., Devous, M. D., Rosenberg, R. N., & Diaz-Arrastia, R. R. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.06.027 · Cited by 122
“Although AD is generally considered to affect primarily gray matter, pathological evidence on white matter damages is also widespread (Scheltens et al., 1995; Smith et al., 2000, Gouw et al., 2008) and are believed to be related to axonal damage and breakdown of oligodendrocytes and myelin (Smith…”
BackgroundMethodInfluentialShape differences of the brain ventricles in Alzheimer's disease
Ferrarini, L., Palm, W. M., Olofsen, H., van Buchem, M. A., Reiber, J. H. C., & Behloul, F. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.048 · Cited by 113
di Paola, M., Luders, E., di Iulio, F., Cherubini, A., Passafiume, D., Thompson, P., Caltagirone, C., Toga, A., & Spalletta, G. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.07.050 · Cited by 111
“…www.e lsev ie r.com/ locate /yn img Callosal atrophy in mild cognitive impairment and Alzheimer's disease: Different effects in different stages Margherita Di Paola a,b,⁎, Eileen Luders c, Fulvia Di Iulio a, Andrea Cherubini a, Domenico Passafiume b, Paul M. Thompson c, Carlo Caltagirone…”
BackgroundSODERLUND, H., Nyberg, L. H., Adolfsson, R., NILSSON, L., & Launer, L. J. (2003) · Cortex · doi:10.1016/s0010-9452(08)70879-7 · Cited by 112
“White matter hyperintensities (WMHs) are common in Alzheimer’s disease (Brun and Englund, 1986; Scheltens et al., 1995) and in other types of dementia (Almkvist et al., 1992; Skoog et al., 1994).”
BackgroundQuantitative MR Imaging in Alzheimer Disease
Ramani, A., Jensen, J. H., & Helpern, J. A. (2006) · Radiology · doi:10.1148/radiol.2411050628 · Cited by 113
Age‐related Brain Changes Associated with Motor Function in Healthy Older People
Camicioli, R. M., Moore, M. M., Sexton, G. J., Howieson, D. B., & Kaye, J. A. (1999) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1999.tb02997.x · Cited by 108
Microstructural white matter changes in metabolic syndrome
Segura, B., Jurado, M. Á., Freixenet, N., Falcón, C., Junqué, C., & Arboix, A. (2009) · Neurology · doi:10.1212/wnl.0b013e3181b163cd · Cited by 104
Pathological Correlates of White Matter Hyperintensities on Magnetic Resonance Imaging
Shim, Y. S., Yang, D. W., Roe, C. M., Coats, M. A., Benzinger, T. L. S., Xiong, C., Galvin, J. E., Cairns, N. J., & Morris, J. C. (2014) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000366411 · Cited by 104
Diffusion-MRI in neurodegenerative disorders
Goveas, J., O’Dwyer, L., Mascalchi, M., Cosottini, M., Diciotti, S., De Santis, S., Passamonti, L., Tessa, C., Toschi, N., & Giannelli, M. (2015) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2015.04.006 · Cited by 104
“axons in deepWM [9–12].”
Murray, M. E., Vemuri, P., Preboske, G. M., Murphy, M. C., Schweitzer, K. J., Parisi, J. E., Jack, C. R., & Dickson, D. W. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e318277387e · Cited by 100
“Alzheimer disease is known to affect axonal density and heighten gliosis in the WM (11, 17, 27), potentially confounding age-related pathologic interpretation of FLAIR signal changes in periventricular and subcortical WMH relative to NAWM.”
Age‐Associated White Matter Lesions: The MRC C ognitive F unction and A geing S tudy
Wharton, S. B., Simpson, J. E., Brayne, C., & Ince, P. G. (2014) · Brain Pathology · doi:10.1111/bpa.12219 · Cited by 105
“WML and Binswanger’s disease where white matter pathology is severe and diffuse, have been associated with increased microglial and macro-glial pathology, including astrogliosis, regressive changes in astrocytes and apoptosis of oligodendrocytes and astrocytes (1, 41, 68).”
BackgroundRisk factors and global cognitive status related to brain arteriolosclerosis in elderly individuals
Ighodaro, E. T., Abner, E. L., Fardo, D. W., Lin, A.-L., Katsumata, Y., Schmitt, F. A., Kryscio, R. J., Jicha, G. A., Neltner, J. H., Monsell, S. E., et al. (2017) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15621574 · Cited by 98
Age-related microvascular degeneration in the human cerebral periventricular white matter
Farkas, E., de Vos, R. A. I., Donka, G., Steur, E. N. H. J., Mihály, A., & Luiten, P. G. M. (2006) · Acta Neuropathologica · doi:10.1007/s00401-005-0007-y · Cited by 102
“Investigations with specific markers have revealed demyelination [50], the loss of fine, myelinated fibers [49], apoptosis of oligodendrocytes [7, 33], gliosis [46], and regressive astrocytic changes [51].”
BackgroundDiffusion-tensor imaging of cognitive performance
Moseley, M. E., Bammer, R., & Illes, J. (2002) · Brain and Cognition · doi:10.1016/s0278-2626(02)00524-9 · Cited by 100
The relation of cerebral magnetic resonance signal hyperintensities to Alzheimer's disease
Fazekas, F., Kapeller, P., Schmidt, R., Offenbacher, H., Payer, F., & Fazekas, G. (1996) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(96)00169-4 · Cited by 99
Fazekas, F., Schmidt, R., Kleinert, R., Kapeller, P., Roob, G., & Flooh, E. (1998) · Journal of neural transmission. Supplementum · doi:10.1007/978-3-7091-6467-9_4 · Cited by 96
Canu, E., McLaren, D. G., Fitzgerald, M. E., Bendlin, B. B., Zoccatelli, G., Alessandrini, F., Pizzini, F. B., Ricciardi, G. K., Beltramello, A., Johnson, S. C., et al. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1295 · Cited by 96
“Although Alzheimer's Disease (AD) is often viewed as a gray matter (GM) disease, white matter (WM) alterations are also commonly observed [1-4].”
STARKSTEIN, S. E., Sabe, L., Vázquez, S., Lorenzo, G. D., Martinez, A., Petracca, G., Teson, A., Chemerinski, E., & Leiguarda, R. C. (1997) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.63.1.66 · Cited by 93
Cognitive Impairment and Cellular/Vascular Changes in the Cerebral White Mattera
Pantoni, L., & García, J. H. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb48463.x · Cited by 94
Bendlin, B. B., Carlsson, C. M., Johnson, S. C., Zetterberg, H., Blennow, K., Willette, A. A., Okonkwo, O. C., Sodhi, A., Ries, M. L., Birdsill, A. C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037720 · Cited by 91
Chowdhury, M. H., Nagai, A., Bokura, H., Nakamura, E., Kobayashi, S., & Yamaguchi, S. (2010) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2009.12.010 · Cited by 91
van Zagten, M., Lodder, J., & Kessels, F. (1998) · Movement Disorders · doi:10.1002/mds.870130119 · Cited by 89
Haglund, M., & Englund, E. M. (2002) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000063606 · Cited by 87
Metadata
- Authors
- Scheltens, P., Barkhof, F., Leys, D., Wolters, E. C., Ravid, R., & Kamphorst, W.
- Affiliations
- From the Departments of Neurology (Drs. Scheltens and Wolters), Diagnostic Radiology (Dr. BarkhoO, and Neuropathology (Dr. Kamphorst), Academisch Ziekenhuis W, and the Netherlands Brain Bank (Dr. Ravid), Amsterdam, the Netherlands; and the Department of Neurology (Dr. Leys), Hospital B, University of Lille, Lille, France.
- Université de Lille (FR)
- Venue
- Neurology
- Published
- 1995-05
- Volume
- 45
- Issue
- 5
- Pages
- 883-888
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W2043592305
- Cited by
- 344
- References
- 0
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 6 · 2023: 6 · 2022: 6 · 2021: 4 · 2020: 10 · 2019: 7 · 2018: 6 · 2017: 9 · 2016: 10 · 2015: 13 · 2014: 22 · 2013: 11 · 2012: 10
- FWCI
- 8.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- Alzheimer's disease, white matter hyperintensities, normal aging, gliosis, arteriolosclerosis, adventitial thickening, postmortem MRI, accelerated aging
- MeSH terms
- Aged, Aged, 80 and over, Aging, Alzheimer Disease, Brain, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review