Cerebral amyloid angiopathy-related cognitive impairment: the search for a specific neuropsychological pattern
Abstract
Cerebral amyloid angiopathy is diagnosed in stroke units after lobar intracerebral hemorrhage. CAA can also be diagnosed in memory clinics when patients are referred for cognitive impairment assessment, and may be a reason for admission to emergency or neurology departments because of rapidly progressive cognitive or neurological decline, or a transient focal neurological episode. CAA may even be observed in older community-dwelling individuals. Neuropsychological impairment in CAA has been described over the past 20 years. The symptoms most commonly reported are perceptual speed, episodic memory, semantic memory, attention and executive function, and global cognitive impairments. Psychiatric symptoms, such as personality changes, behavioral disturbances and depression, have been more recently described. CAA is also a risk factor for the development of dementia, and its relationship with Alzheimer's disease has been demonstrated in post-mortem studies. Yet, despite the increase in literature on CAA-related cognitive and psychiatric symptoms, the specific characteristics of symptoms in CAA are difficult to assess because of the substantial prevalence of comorbidities such as small vessel disease due to high blood pressure, Lewy body disease and, of course, AD, all of which act as important confounding factors. Also, within the entity of CAA itself, the additive and perhaps synergistic effects of each lesion on cognition remain to be assessed. In the present paper, the focus is on the latest evidence of neuropsychological impairment observed in CAA patients, and the emergence of a possible specific neuropsychological profile due to CAA is also discussed.
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Neuropathological examination of patient brains harboring APP duplications shows abundant plaque and tangle pathology as well as cerebral amyloid angiopathy (CAA).
“Neuropathological examination of patient brains harboring APP duplications show abundant plaque and tangle pathology as well cerebral amyloid angiopathy (CAA)”
From Genetic architecture of Alzheimer's disease (2020) · cites this paper as [248]
Cites
(2001) · The Lancet · doi:10.1016/s0140-6736(00)03589-3 · Cited by 1,338 · see citing works
Prevalence of superficial siderosis in patients with cerebral amyloid angiopathy
Linn, J., Halpin, A., Demaerel, P., Ruhland, J., Giese, A. D., Dichgans, M., van Buchem, M. A., Bruckmann, H., & Greenberg, S. M. (2010) · Neurology · doi:10.1212/wnl.0b013e3181dad605 · Cited by 914 · see citing works
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
Cerebral amyloid angiopathy and cognitive outcomes in community-based older persons
Boyle, P. A., Yu, L., Nag, S., Leurgans, S., Wilson, R. S., Bennett, D. A., & Schneider, J. A. (2015) · Neurology · doi:10.1212/wnl.0000000000002175 · Cited by 423 · see citing works
Association of Cerebral Microbleeds With Cognitive Decline and Dementia
Akoudad, S., Wolters, F. J., Viswanathan, A., de Bruijn, R. F., van der Lugt, A., Hofman, A., Koudstaal, P. J., Ikram, M. A., & Vernooij, M. W. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.1017 · Cited by 403 · 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
The clinical spectrum of cerebral amyloid angiopathy
Greenberg, S. M., Vonsattel, J. P., Stakes, J. W., Gruber, M., & Finklestein, S. P. (1993) · Neurology · doi:10.1212/wnl.43.10.2073 · Cited by 361 · see citing works
Cerebral amyloid angiopathy and cognitive function: The HAAS autopsy study
Pfeifer, L. A., White, L. R., Ross, G. W., Petrovitch, H., & Launer, L. J. (2002) · Neurology · doi:10.1212/wnl.58.11.1629 · Cited by 338 · see citing works
Dementia risk after spontaneous intracerebral haemorrhage: a prospective cohort study
Moulin, S., Labreuche, J., Bombois, S., Rossi, C., Boulouis, G., Hénon, H., Duhamel, A., Leys, D., & Cordonnier, C. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)00130-7 · Cited by 269 · see citing works
Population studies of sporadic cerebral amyloid angiopathy and dementia: a systematic review
Keage, H. A. D., Carare, R. O., Friedland, R. P., Ince, P. G., Love, S., Nicoll, J. A. R., Wharton, S. B., Weller, R. O., & Brayne, C. (2009) · BMC Neurology · doi:10.1186/1471-2377-9-3 · Cited by 181 · see citing works
Structural network alterations and neurological dysfunction in cerebral amyloid angiopathy
Reijmer, Y. D., Fotiadis, P., Martinez-Ramirez, S., Salat, D. H., Schultz, A., Shoamanesh, A., Ayres, A. M., Vashkevich, A., Rosas, D., Schwab, K., et al. (2015) · Brain · doi:10.1093/brain/awu316 · Cited by 181 · see citing works
Brenowitz, W. D., Nelson, P. T., Besser, L. M., Heller, K., & Kukull, W. A. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.06.028 · Cited by 174 · see citing works
Cerebral Amyloid Angiopathy Is Associated With Executive Dysfunction and Mild Cognitive Impairment
Case, N. F., Charlton, A., Zwiers, A. M., Batool, S. A., McCreary, C. R., Hogan, D. B., Ismail, Z., Zerna, C., Coutts, S. B., Frayne, R., et al. (2016) · Stroke · doi:10.1161/strokeaha.116.012999 · Cited by 134 · see citing works
Diagnostic value of lobar microbleeds in individuals without intracerebral hemorrhage
Martínez‐Ramírez, S., Romero, J., Shoamanesh, A., McKee, A. C., van Etten, E. S., Pontes‐Neto, O. M., Macklin, E. A., Ayres, A. M., Auriel, E., Himali, J. J., et al. (2015) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2015.04.009 · Cited by 133 · see citing works
Neuropsychological outcome after a first symptomatic ischaemic stroke with ‘good recovery’
Planton, M., Peiffer, S., Albucher, J., Barbeau, E. J., Tardy, J., Pastor, J., Januel, A.-C., Bézy, C., Lemesle, B., Puel, M., et al. (2011) · European Journal of Neurology · doi:10.1111/j.1468-1331.2011.03450.x · Cited by 81 · see citing works
Xiong, L., Davidsdottir, S., Reijmer, Y. D., Shoamanesh, A., Roongpiboonsopit, D., Thanprasertsuk, S., Martínez‐Ramírez, S., Charidimou, A., Ayres, A. M., Fotiadis, P., et al. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-150890 · Cited by 62 · see citing works
Deficit of Episodic Memory: Anatomy and Related Patterns in Stroke Patients
Godefroy, O., Roussel, M., Leclerc, X., & Leys, D. (2009) · European Neurology · doi:10.1159/000197107 · Cited by 51 · see citing works
Small vessel disease burden in cerebral amyloid angiopathy without symptomatic hemorrhage
Boulouis, G., Charidimou, A., Jessel, M. J., Xiong, L., Roongpiboonsopit, D., Fotiadis, P., Pasi, M., Ayres, A. M., Merrill, M. E., Schwab, K. M., et al. (2017) · Neurology · doi:10.1212/wnl.0000000000003655 · Cited by 45 · see citing works
Cerebral amyloidal angiopathy—A disease with implications for neurology and psychiatry
Gahr, M., Nowak, D. A., Connemann, B. J., & Schönfeldt‐Lecuona, C. (2013) · Brain Research · doi:10.1016/j.brainres.2013.04.052 · Cited by 43 · see citing works
High prevalence of cognitive impairment after intracerebral hemorrhage
Planton, M., Saint‐Aubert, L., Raposo, N., Branchu, L., Lyoubi, A., Bonneville, F., Albucher, J., Olivot, J., Péran, P., & Pariente, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178886 · Cited by 43 · see citing works
Charidimou, A., Ni, J., Martínez‐Ramírez, S., Vashkevich, A., Ayres, A. M., Rosand, J. M., Gurol, M. E., Greenberg, S. M., & Viswanathan, A. (2016) · Cerebrovascular Diseases · doi:10.1159/000442299 · Cited by 38 · see citing works
Florbetapir imaging in cerebral amyloid angiopathy-related hemorrhages
Raposo, N., Planton, M., Péran, P., Payoux, P., Bonneville, F., Lyoubi, A., Albucher, J. F., Acket, B., Salabert, A., Olivot, J., et al. (2017) · Neurology · doi:10.1212/wnl.0000000000004228 · Cited by 35 · see citing works
Impact of spontaneous intracerebral hemorrhage on cognitive functioning: An update
Planton, M., Raposo, N., Danet, L., Albucher, J., Péran, P., & Pariente, J. (2017) · Revue Neurologique · doi:10.1016/j.neurol.2017.06.010 · Cited by 33 · see citing works
Neuropsychological Effects of Cerebral Amyloid Angiopathy
Schrag, M., & Kirshner, H. S. (2016) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-016-0674-1 · Cited by 25 · see citing works
Verhaltensauffälligkeiten und Persönlichkeitsveränderung bei zerebraler Amyloidangiopathie
Gahr, M., Connemann, B. J., & Schönfeldt‐Lecuona, C. (2012) · Psychiatrische Praxis · doi:10.1055/s-0032-1305119 · Cited by 5 · see citing works
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Genetic architecture of Alzheimer's disease
Neuner, S. M., TCW, J., & Goate, A. M. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104976 · Cited by 126 · see citing works
“Neuropathological examination of patient brains harboring APP duplications show abundant plaque and tangle pathology as well cerebral amyloid angiopathy (CAA), which is characterized by deposition of Aβ in the cerebrovasculature and by hemorrhagic stroke (Planton et al., 2017; Ellis et al., 1996).”
BackgroundRetinal Vasculopathy in Alzheimer’s Disease
Shi, H., Koronyo, Y., Rentsendorj, A., Fuchs, D.-T. S., Sheyn, J., Black, K. L., Mirzaei, N., & Koronyo‐Hamaoui, M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.731614 · Cited by 90 · see citing works
Denver, P., D’Adamo, H., Hu, S., Zuo, X., Zhu, C., Okuma, C., Kim, P., Castro, D., Jones, M. R., Leal, C. D. R., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01269 · Cited by 36 · see citing works
Schoentgen, B., Gagliardi, G. P., & Defontaines, B. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01814 · Cited by 38 · see citing works
Smirnov, D. S., Galasko, D., Hiniker, A., Edland, S. D., & Salmon, D. P. (2021) · Neurology · doi:10.1212/wnl.0000000000011772 · Cited by 25 · see citing works
TDP ‐43 Pathology Exacerbates Cognitive Decline in Primary Age‐Related Tauopathy
Smirnov, D. S., Salmon, D. P., Galasko, D. R., Edland, S. D., Pizzo, D. P., Goodwill, V., & Hiniker, A. O. (2022) · Annals of Neurology · doi:10.1002/ana.26438 · Cited by 26 · see citing works
Distinct brain regional proteome changes in the rTg‐DI rat model of cerebral amyloid angiopathy
Schrader, J. M., Xu, F., & Nostrand, W. E. V. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15463 · Cited by 18 · see citing works
Huang, H., Deng, X., Wang, Y., Shen, S., Wang, S., Hu, M., Liu, S., Su, X., Li, C., Li, T., et al. (2024) · Advanced Science · doi:10.1002/advs.202404096 · Cited by 17 · see citing works
Foidl, B. M., & Humpel, C. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.01.009 · Cited by 16 · see citing works
Longitudinal Cognitive Decline in a Novel Rodent Model of Cerebral Amyloid Angiopathy Type-1
Popescu, D. L., Nostrand, W. E. V., & Robinson, J. K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21072348 · Cited by 16 · see citing works
Malek-Ahmadi, M., Chen, K.-W., Perez, S. E., & Mufson, E. (2018) · Journal of Alzheimer's Disease · doi:10.3233/jad-180765 · Cited by 11 · see citing works
Barucci, E., Salvadori, E., Magi, S., Squitieri, M., Fiore, G. M., Ramacciotti, L., Formelli, B., Pescini, F., & Poggesi, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-55719-w · Cited by 8 · see citing works
Detection of varicella zoster virus antigen and DNA in two cases of cerebral amyloid angiopathy
Mescher, T., Boyer, P. J., Bubak, A. N., Hassell, J. E., & Nagel, M. A. (2021) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2021.117315 · Cited by 7 · see citing works
Quality of life, depression and anxiety in cerebral amyloid angiopathy: A cross‐sectional study
Kaushik, K., Waslam, N. G., van der Zwet, R. G. J., Voigt, S., van Dort, R., van Zwet, E. W., Terwindt, G. M., van Etten, E. S., & Wermer, M. J. H. (2024) · European Journal of Neurology · doi:10.1111/ene.16476 · Cited by 6 · see citing works
Cognition in (pre)symptomatic Dutch‐type hereditary and sporadic cerebral amyloid angiopathy
van Dort, R., Kaushik, K., Rasing, I., van der Zwet, R. G. J., Schipper, M. R., van der Grond, J., van Rooden, S., van Zwet, E. W., Terwindt, G. M., Middelkoop, H. A. M., et al. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.14171 · Cited by 5 · see citing works
Blood Plasma Markers in Depressed Mice under Chronic Social Defeat Stress
Смагин, Д. А., Bezryadnov, D. V., Zavialova, M. G., Abramova, A. Y., Pertsov, S. S., & Kudryavtseva, N. N. (2024) · Biomedicines · doi:10.3390/biomedicines12071485 · Cited by 5 · see citing works
Angiopathie Amyloïde Cérébrale : avancées récentes et perspectives
Raposo, N., Pariente, J., Albucher, J., Olivot, J., Calvière, L., Viguier, A., Bonneville, F., Barbieux‐Guillot, M., & Chollet, F. (2020) · Bulletin de l Académie Nationale de Médecine · doi:10.1016/j.banm.2020.12.005 · Cited by 3 · see citing works
Cerebral Amyloid Angiopathy and Risk of Dementia in Patients With Cognitive Complaint
Raposo, N., Morice-Morand, M., Genin, T., Lepetit, M., Conhoc, J., Bouteloup, V., Mangin, J., Marie Chupin, A., Chêne, G., Dufouil, C., et al. (2026) · Neurology · doi:10.1212/wnl.0000000000218009 · Cited by 3 · see citing works
Hall, C., Chiabotti, P. S., Bommarito, G., Alemán‐Gómez, Y., Carlier, S., Nasuti, M., Damian, D., Jreige, M., Dunet, V., Rouaud, O., et al. (2025) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2025.107892 · Cited by 2 · see citing works
Pizzoni, L., Cavalli, A., Matteo, F. D., & Mancini, G. (2025) · Current Alzheimer Research · doi:10.2174/0115672050390451250808002719 · Cited by 1 · see citing works
Terao, C. M., Erani, F. R., Urias, U. A., Lopez, F., Chang, F., Banks, S. J., Gilbert, P. E., Coughlin, D. G., Bangen, K. J., & Thomas, K. R. (2026) · Alzheimer s Research & Therapy · doi:10.1186/s13195-026-02041-4 · Cited by 1 · see citing works
Angiopatia amiloide cerebrale sporadica
Puy, L., Hochart, A., Moulin, S., & Cordonnier, C. (2020) · EMC - Neurologia · doi:10.1016/s1634-7072(20)44005-x
Hashemilar, M., & Forghani, N. (2021) · Archives of Neuroscience · doi:10.5812/ans.111362
Lombardi, G., Berti, V., Ginestroni, A., Nacmias, B., & Sorbi, S. (2024) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-230183
Neuropsychiatric Symptoms in Cerebral Amyloid Angiopathy: A Significant but Overlooked Association
Prelog, P. R., Zupan, M., & Frol, S. (2025) · Brain Sciences · doi:10.3390/brainsci15090959
- Authors
- Planton, M., Raposo, N., Albucher, J.-F., & Pariente, J.
- Affiliations
- Inserm (FR)
- Corresponding author
- Pariente, J.
- Venue
- Revue Neurologique
- Publisher
- Elsevier BV
- Published
- 2017-11
- Volume
- 173
- Issue
- 9
- Pages
- 562-565
- ISSN
- 0035-3787 (ISSN-L)
- OpenAlex
- W2761588143
- Cited by
- 26
- References
- 25
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 6 · 2022: 2 · 2021: 5 · 2020: 5 · 2019: 2 · 2018: 1
- FWCI
- 1.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Revue Neurologique (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Health Sciences › Medicine › Neurology › Intracerebral and Subarachnoid Hemorrhage Research
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- cerebral amyloid angiopathy, cognitive impairment, neuropsychological profile, episodic memory, semantic memory, executive function, attention, perceptual speed, dementia, Alzheimer's disease, psychiatric symptoms, personality change, behavioral problems, depression, cerebral small vessel disease, Lewy body disease, comorbidities
- MeSH terms
- Alzheimer Disease, Humans, Neuropsychology, Cerebral Amyloid Angiopathy, Cognitive Dysfunction
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