β-Amyloid, Blood Vessels, and Brain Function

Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B

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Mixed brain pathologies account for most dementia cases in community-dwelling older persons

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Alzheimer’s Dementia

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Brain Infarction and the Clinical Expression of Alzheimer Disease<subtitle>The Nun Study</subtitle>

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Clearance of Alzheimer’s amyloid-β1-40 peptide from brain by LDL receptor–related protein-1 at the blood-brain barrier

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Pathological correlates of late-onset dementia in a multicentre, community-based population in England and Wales

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Synaptic Activity Regulates Interstitial Fluid Amyloid-β Levels In Vivo

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Imaging β-amyloid burden in aging and dementia

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Cerebral amyloid angiopathy. A critical review.

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Clinical diagnosis of cerebral amyloid angiopathy: validation of the Boston criteria

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Brain infarction and the clinical expression of Alzheimer disease. The Nun Study.

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Is Alzheimer's disease a neurodegenerative or a vascular disorder? Data, dogma, and dialectics

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PET of Brain Amyloid and Tau in Mild Cognitive Impairment

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The Lifetime Risk of Stroke

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β-Amyloid-mediated vasoactivity and vascular endothelial damage

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Brain Infarction and the Clinical Expression of Alzheimer Disease-Reply

Snowdon, D. A. (1997) · JAMA · doi:10.1001/jama.1997.03550020046024 · Cited by 683 · see citing works

SYMPOSIUM: Clearance of Aβ from the Brain in Alzheimer's Disease: Perivascular Drainage of Amyloid‐β Peptides from the Brain and Its Failure in Cerebral Amyloid Angiopathy and Alzheimer's Disease

Weller, R. O., Subash, M., Preston, S., Mazanti, I., & Carare, R. O. (2008) · Brain Pathology · doi:10.1111/j.1750-3639.2008.00133.x · Cited by 682 · see citing works

Cerebral Amyloid Angiopathy

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Imaging of amyloid burden and distribution in cerebral amyloid angiopathy

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Preclinical prediction of Alzheimer's disease using SPECT

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Brain Infarction and the Clinical Expression of Alzheimer Disease

Román, G. C. (1997) · JAMA · doi:10.1001/jama.1997.03550020045023 · Cited by 350 · see citing works

Molecular imaging with Pittsburgh Compound B confirmed at autopsy: a case report.

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Cerebral amyloid angiopathy and cognitive function: The HAAS autopsy study

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Nox2-derived radicals contribute to neurovascular and behavioral dysfunction in mice overexpressing the amyloid precursor protein

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Pathological alterations of the cerebral microvasculature in Alzheimer's disease and related dementing disorders

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Prevalence and severity of microbleeds in a memory clinic setting

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PIB is a non-specific imaging marker of amyloid-beta (A ) peptide-related cerebral amyloidosis

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Amyloid Angiopathy–Related Vascular Cognitive Impairment

Greenberg, S. M., Gurol, M. E., Rosand, J., & Smith, E. E. (2004) · Stroke · doi:10.1161/01.str.0000143224.36527.44 · Cited by 298 · see citing works

Cerebrovascular autoregulation is profoundly impaired in mice overexpressing amyloid precursor protein

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Subcortical infarcts, Alzheimer's disease pathology, and memory function in older persons

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Microbleed Topography, Leukoaraiosis, and Cognition in Probable Alzheimer Disease From the Sunnybrook Dementia Study

Pettersen, J. A., Sathiyamoorthy, G., Gao, F., Szilagyi, G. M., Nadkarni, N. K., George‐Hyslop, P. S., Rogaeva, E. A., & Black, S. E. (2008) · Archives of Neurology · doi:10.1001/archneur.65.6.790 · Cited by 262 · see citing works

Altered morphology and 3D architecture of brain vasculature in a mouse model for Alzheimer's disease

Meyer, E. P., Ulmann-Schuler, A., Staufenbiel, M., & Krucker, T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709788105 · Cited by 260 · see citing works

Leukoencephalopathy in diffuse hemorrhagic cerebral amyloid angiopathy

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White matter lesions, cognition, and recurrent hemorrhage in lobar intracerebral hemorrhage

Smith, E. E., Gurol, M. E., Eng, J. A., Engel, C., Nguyen, T. N., Rosand, J. M., & Greenberg, S. M. (2004) · Neurology · doi:10.1212/01.wnl.0000142966.22886.20 · Cited by 252 · see citing works

Cognitive impact of subcortical vascular and Alzheimer’s disease pathology

Chui, H. C., Zarow, C., Mack, W. J., Ellis, W. G., Zheng, L., Jagust, W. J., Mungas, D., Reed, B. R., Kramer, J. H., DeCarli, C. C., et al. (2006) · Annals of Neurology · doi:10.1002/ana.21009 · Cited by 247 · see citing works

NADPH Oxidase-Derived Reactive Oxygen Species Mediate the Cerebrovascular Dysfunction Induced by the Amyloid β Peptide

Park, L., Anrather, J., Zhou, P., Frys, K., Pitstick, R., Younkin, S., Carlson, G. A., & Iadecola, C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5207-04.2005 · Cited by 244 · see citing works

Aβ1–40-related reduction in functional hyperemia in mouse neocortex during somatosensory activation

Niwa, K., Younkin, L. H., Ebeling, C., Turner, S. K., Westaway, D. A., Younkin, S. G., Ashe, K. H., Carlson, G. A., & Iadecola, C. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.17.9735 · Cited by 244 · see citing works

Vascular pathologies and cognition in a population-based cohort of elderly people

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Cerebral Hypoperfusion Generates Cortical Watershed Microinfarcts in Alzheimer Disease

Suter, O.-C., Sunthorn, T., Kraftsik, R., Straubel, J., Pushpa Darekar, B., Khalili, K., & Judith Miklossy, A. (2002) · Stroke · doi:10.1161/01.str.0000024523.82311.77 · Cited by 235 · see citing works

THE NUN STUDY

Shapira, I. L. (2008) · The Journal of the American Dental Association · doi:10.14219/jada.archive.2008.0118 · Cited by 233 · see citing works

AD lesions and infarcts in demented and non‐demented Japanese‐American men

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Alterations in cerebral blood flow and glucose utilization in mice overexpressing the amyloid precursor protein

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The synaptic Aβ hypothesis of Alzheimer disease

Tanzi, R. E. (2005) · Nature Neuroscience · doi:10.1038/nn0805-977 · Cited by 206 · see citing works

Morphometric comparison of hippocampal microvasculature in ageing and demented people: Diameters and densities

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Spatial Distribution of White-Matter Hyperintensities in Alzheimer Disease, Cerebral Amyloid Angiopathy, and Healthy Aging

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 199 · see citing works

The Cerebral β-Amyloid Angiopathies: Hereditary and Sporadic

Zhang-Nunes, S., Maat–Schieman, M. L. C., van Duinen, S. G., Roos, R. A. C., Frosch, M. P., & Greenberg, S. M. (2006) · Brain Pathology · doi:10.1111/j.1750-3639.2006.tb00559.x · Cited by 195 · see citing works

Age-dependent cerebrovascular dysfunction in a transgenic mouse model of cerebral amyloid angiopathy

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Exogenous Aβ1–40 Reproduces Cerebrovascular Alterations Resulting from Amyloid Precursor Protein Overexpression in Mice

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Alzheimer’s disease pathology influences severity and topographical distribution of cerebral amyloid angiopathy

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Altered angioarchitecture in selected areas of brains with Alzheimer's disease

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Only cerebral capillary amyloid angiopathy correlates with Alzheimer pathology?a pilot study

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Mechanism of Cerebral β-Amyloid Angiopathy: Murine and Cellular Models

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The reciprocal risks of stroke and cognitive impairment in an elderly population

Jin, Y., Legge, S. D., Østbye, T., Feightner, J., & Hachinski, V. (2006) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2006.03.006 · Cited by 146 · see citing works

Amyloid � peptide 1?42 highly correlates with capillary cerebral amyloid angiopathy and Alzheimer disease pathology

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Capillary cerebral amyloid angiopathy is associated with vessel occlusion and cerebral blood flow disturbances

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Cerebral Beta Amyloid Angiopathy Is a Risk Factor for Cerebral Ischemic Infarction. A Case Control Study in Human Brain Biopsies

Cadavid, D., Mena, H., Koeller, K. K., & Frommelt, R. A. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.9.768 · Cited by 137 · see citing works

Cerebrovascular amyloidosis with cerebral hemorrhage

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Association between severe cerebral amyloid angiopathy and cerebrovascular lesions in Alzheimer disease is not a spurious one attributable to apolipoprotein E4.

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Microvasculature in brain biopsy specimens from patients with Alzheimer's disease: an immunohistochemical and ultrastructural study.

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Cerebral amyloid angiopathy and cortical microinfarcts as putative substrates of vascular dementia

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Noninvasive Regional Cerebral Blood Flow Measurements in Dementia

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Metabolism of amyloid β peptide and pathogenesis of Alzheimer's disease

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Impaired visual evoked flow velocity response in cerebral amyloid angiopathy

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Clinical Studies of Cerebral Blood Flow in Alzheimer's Disease

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Cerebral Amyloid Angiopathy, White Matter Lesions and Alzheimer Encephalopathy – A Histopathological Assessment

Haglund, M., & Englund, E. M. (2002) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000063606 · Cited by 87 · see citing works

Stereologic Analysis of Microvascular Morphology in the Elderly

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Tissue Microstructural Changes Are Independently Associated With Cognitive Impairment in Cerebral Amyloid Angiopathy

Viswanathan, A., Patel, P. V., Rahman, R. M. A., Nandigam, R. N. K., Kinnecom, C., Bracoud, L., Rosand, J. M., Chabriat, H., Greenberg, S. M., & Smith, E. E. (2008) · Stroke · doi:10.1161/strokeaha.107.509091 · Cited by 80 · see citing works

Kinetics of Cerebral Amyloid Angiopathy Progression in a Transgenic Mouse Model of Alzheimer Disease

Robbins, E. M., Betensky, R. A., Domnitz, S. B., Purcell, S. M., Garcı́a-Alloza, M., Greenberg, C., Rebeck, G. W., Hyman, B. T., Greenberg, S. M., Frosch, M. P., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3854-05.2006 · Cited by 78 · see citing works

Proinflammatory and Vasoactive Effects of Aβ in the Cerebrovasculature

Townsend, K. P., Obregon, D. F., QUADROS, A., Patel, N. S., Volmar, C., Paris, D., & MULLAN, M. J. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04799.x · Cited by 76 · see citing works

White Matter Alterations in Cerebral Amyloid Angiopathy Measured by Diffusion Tensor Imaging

Salat, D. H., Smith, E. E., Tuch, D. S., Benner, T., Pappu, V., Schwab, K. M., Gurol, M. E., Rosas, H. D., Rosand, J. M., & Greenberg, S. M. (2006) · Stroke · doi:10.1161/01.str.0000227328.86353.a7 · Cited by 71 · see citing works

Influence of Galantamine on Vasomotor Reactivity in Alzheimer’s Disease and Vascular Dementia Due to Cerebral Microangiopathy

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Toxicity of Dutch (E22Q) and Flemish (A21G) Mutant Amyloid β Proteins to Human Cerebral Microvessel and Aortic Smooth Muscle Cells

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Cerebral Cortical Arteriolar Angiopathy, Vascular Beta-Amyloid, Smooth Muscle Actin, Braak Stage, and APOE Genotype

Stopa, E. G., Butala, P., Salloway, S., Johanson, C. E., González, L., Tavares, R., Hovanesian, V., Hulette, C. M., Vitek, M. P., & Cohen, R. A. (2008) · Stroke · doi:10.1161/strokeaha.107.493429 · Cited by 60 · see citing works

Cerebral Amyloid Angiopathy and Lobar Intracerebral Hemorrhage

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Capillary beds are decreased in Alzheimer's disease, but not in Binswanger's disease

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Leukoencephalopathy with cerebral amyloid angiopathy: a semiquantitative and morphometric study

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Prevalence and Effects of Lobar Microhemorrhages in Early-Stage Dementia

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The β‐amyloid peptide of Alzheimer's disease decreases adhesion of vascular smooth muscle cells to the basement membrane

Mok, S. S., Lošić, D., Barrow, C. J., Turner, B. J., Masters, C. L., Martin, L. L., & Small, D. H. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03539.x · Cited by 37 · see citing works

PSM08 Poster Session 8 ‐ Myelin and Oligodendrocyte Biology

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Sporadic cerebral amyloid angiopathy revisited: recent insights into pathophysiology and clinical spectrum

Charidimou, A., Gang, Q., & Werring, D. J. (2012) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2011-301308 · Cited by 611 · see citing works

Emerging concepts in sporadic cerebral amyloid angiopathy

Charidimou, A., Boulouis, G., Gurol, M. E., Ayata, C., Bacskai, B. J., Frosch, M. P., Viswanathan, A., & Greenberg, S. M. (2017) · Brain · doi:10.1093/brain/awx047 · Cited by 555 · see citing works

Cerebral amyloid angiopathy pathology and cognitive domains in older persons

Arvanitakis, Z., Leurgans, S. E., Wang, Z., Wilson, R. S., Bennett, D. A., & Schneider, J. A. (2011) · Annals of Neurology · doi:10.1002/ana.22112 · Cited by 383 · see citing works

CSF biomarkers of neuroinflammation and cerebrovascular dysfunction in early Alzheimer disease

Janelidze, S., Mattsson, N., Stomrud, E., Lindberg, O., Palmqvist, S., Zetterberg, H., Blennow, K., & Hansson, O. (2018) · Neurology · doi:10.1212/wnl.0000000000006082 · Cited by 359 · see citing works

Fibrinogen and β-Amyloid Association Alters Thrombosis and Fibrinolysis: A Possible Contributing Factor to Alzheimer's Disease

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Emerging roles of innate and adaptive immunity in Alzheimer’s disease

Chen, X., & Holtzman, D. M. (2022) · Immunity · doi:10.1016/j.immuni.2022.10.016 · Cited by 297 · see citing works

Cerebral hypoperfusion accelerates cerebral amyloid angiopathy and promotes cortical microinfarcts

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Cholinesterase targeting by polyphenols: A therapeutic approach for the treatment of Alzheimer’s disease

Jabir, N. R., Khan, F. R., & Tabrez, S. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12971 · Cited by 187 · see citing works

Associations Between Cerebral Small-Vessel Disease and Alzheimer Disease Pathology as Measured by Cerebrospinal Fluid Biomarkers

Kester, M. I., Goos, J. D. C., Teunissen, C. E., Benedictus, M. R., Bouwman, F. H., Wattjes, M. P., Barkhof, F., Scheltens, P., & van der Flier, W. M. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.754 · Cited by 161 · see citing works

Alzheimer’s disease, cerebrovascular disease, and the β-amyloid cascade

Honjo, K., Black, S. E., & Verhoeff, N. P. L. G. (2012) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100015547 · Cited by 152 · see citing works

Blood-brain barrier leakage in Alzheimer’s disease: From discovery to clinical relevance

Nehra, G., Bauer, B., & Hartz, A. M. S. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108119 · Cited by 127 · see citing works

Taxifolin inhibits amyloid-β oligomer formation and fully restores vascular integrity and memory in cerebral amyloid angiopathy

Saito, S., Yamamoto, Y., Maki, T., Hattori, Y., Ito, H., Mizuno, K., Harada-Shiba, M., Kalaria, R. N., Fukushima, M., Takahashi, R., et al. (2017) · Acta Neuropathologica Communications · doi:10.1186/s40478-017-0429-5 · Cited by 110 · see citing works

Cerebral white matter lesions – associations with Aβ isoforms and amyloid PET

van Westen, D., Lindqvist, D., Blennow, K., Minthon, L., Nägga, K., Stomrud, E., Zetterberg, H., & Hansson, O. (2016) · Scientific Reports · doi:10.1038/srep20709 · Cited by 66 · see citing works

Cerebral small vessel disease in aging and <scp>A</scp>lzheimer's disease: a comparative study using <scp>MRI</scp> and <scp>SPECT</scp>

Makedonov, I., Black, S. E., & MacIntosh, B. J. (2013) · European Journal of Neurology · doi:10.1111/j.1468-1331.2012.03785.x · Cited by 62 · see citing works

Cerebral Amyloid Angiopathy Limits Treatment of Stroke

GAVALLER, M. D., GAVALLER, M. D., & Oh, H. (2019) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2019.01.045

Does Cerebral Amyloid Angiopathy Affect Cognition

Rosand, J. M. (2002) · Journal watch · doi:10.1056/jn200209060000002

Prevalence of Cerebral Amyloid Angiopathy Pathology and Strictly Lobar Microbleeds in East-Asian Versus Western Populations: A Systematic Review and Meta-Analysis

de Kort, A. M., Verbeek, M. M., Schreuder, F. H. B. M., Klijn, C. J. M., & Jäkel, L. (2024) · Journal of Stroke · doi:10.5853/jos.2023.04287 · Cited by 17 · see citing works

Neuroimaging Demonstration of Evolving Small Vessel Ischemic Injury in Cerebral Amyloid Angiopathy

Menon, R. S., & Kidwell, C. S. (2009) · Stroke · doi:10.1161/strokeaha.109.552935 · Cited by 38 · see citing works

Cortical Superficial Siderosis Is Associated with Worse Outcomes in Patients with Cerebral Amyloid Angiopathy

Kim, A. (2019) · Journal watch · doi:10.1056/nejm-jw.na48446