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Diencephalic versus Hippocampal Amnesia in Alzheimer’s Disease: The Possible Confabulation-Misidentification Phenotype

Background: Alzheimer’s disease (AD) is clinically heterogeneous, including the classical-amnesic (CA-) phenotype and some variants. Objective: We aim to describe a further presentation we (re)named confabulation-misidentification (CM-) phenotype. Methods: We performed a retrospective longitudinal c...

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Published in:Journal of Alzheimer's disease 2023-01, Vol.91 (1), p.363-388
Main Authors: Abbate, Carlo, Trimarchi, Pietro D., Fumagalli, Giorgio G., Gallucci, Alessia, Tomasini, Emanuele, Fracchia, Stefania, Rebecchi, Isabella, Morello, Elisabetta, Fontanella, Anna, Parisi, Paola M.R., Tartarone, Federica, Giunco, Fabrizio, Ciccone, Simona, Nicolini, Paola, Lucchi, Tiziano, Arosio, Beatrice, Inglese, Silvia, Rossi, Paolo D.
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cited_by cdi_FETCH-LOGICAL-c438t-4c08d6b6a8e70a0a3defa458f8981f43705ec74f65e27ede8ebb3c9e672cbc263
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container_title Journal of Alzheimer's disease
container_volume 91
creator Abbate, Carlo
Trimarchi, Pietro D.
Fumagalli, Giorgio G.
Gallucci, Alessia
Tomasini, Emanuele
Fracchia, Stefania
Rebecchi, Isabella
Morello, Elisabetta
Fontanella, Anna
Parisi, Paola M.R.
Tartarone, Federica
Giunco, Fabrizio
Ciccone, Simona
Nicolini, Paola
Lucchi, Tiziano
Arosio, Beatrice
Inglese, Silvia
Rossi, Paolo D.
description Background: Alzheimer’s disease (AD) is clinically heterogeneous, including the classical-amnesic (CA-) phenotype and some variants. Objective: We aim to describe a further presentation we (re)named confabulation-misidentification (CM-) phenotype. Methods: We performed a retrospective longitudinal case-series study of 17 AD outpatients with the possible CM-phenotype (CM-ADs). Then, in a cross-sectional study, we compared the CM-ADs to a sample of 30 AD patients with the CA-phenotype (CA-ADs). The primary outcome was the frequency of cognitive and behavioral features. Data were analyzed as differences in percentage by non-parametric Chi Square and mean differences by parametric T-test. Results: Anterograde amnesia (100%) with early confabulation (88.2%), disorientation (88.2%) and non-infrequently retrograde amnesia (64.7%) associated with reduced insight (88.2%), moderate prefrontal executive impairment (94.1%) and attention deficits (82.3%) dominated the CM-phenotype. Neuropsychiatric features with striking misidentification (52.9%), other less-structured delusions (70.6%), and brief hallucinations (64.7%) were present. Marked behavioral disturbances were present early in some patients and very common at later stages. At the baseline, the CM-ADs showed more confabulation (p 
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Objective: We aim to describe a further presentation we (re)named confabulation-misidentification (CM-) phenotype. Methods: We performed a retrospective longitudinal case-series study of 17 AD outpatients with the possible CM-phenotype (CM-ADs). Then, in a cross-sectional study, we compared the CM-ADs to a sample of 30 AD patients with the CA-phenotype (CA-ADs). The primary outcome was the frequency of cognitive and behavioral features. Data were analyzed as differences in percentage by non-parametric Chi Square and mean differences by parametric T-test. Results: Anterograde amnesia (100%) with early confabulation (88.2%), disorientation (88.2%) and non-infrequently retrograde amnesia (64.7%) associated with reduced insight (88.2%), moderate prefrontal executive impairment (94.1%) and attention deficits (82.3%) dominated the CM-phenotype. Neuropsychiatric features with striking misidentification (52.9%), other less-structured delusions (70.6%), and brief hallucinations (64.7%) were present. Marked behavioral disturbances were present early in some patients and very common at later stages. At the baseline, the CM-ADs showed more confabulation (p &lt; 0.001), temporal disorientation (p &lt; 0.02), misidentification (p = 0.013), other delusions (p = 0.002), and logorrhea (p = 0.004) than the CA-ADs. In addition, more social disinhibition (p = 0.018), reduction of insight (p = 0.029), and hallucination (p = 0.03) persisted at 12 months from baseline. Both the CA- and CM-ADs showed anterior and medial temporal atrophy. Compared to HCs, the CM-ADs showed more right fronto-insular atrophy, while the CA-ADs showed more dorsal parietal, precuneus, and right parietal atrophy. Conclusion: We described an AD phenotype resembling diencephalic rather than hippocampal amnesia and overlapping the past-century description of presbyophrenia.</description><identifier>ISSN: 1387-2877</identifier><identifier>ISSN: 1875-8908</identifier><identifier>EISSN: 1875-8908</identifier><identifier>DOI: 10.3233/JAD-220919</identifier><identifier>PMID: 36442200</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Alzheimer Disease - complications ; Alzheimer Disease - psychology ; Alzheimer's disease ; Amnesia ; Amnesia - psychology ; Atrophy ; Cognitive ability ; Confusion ; Cortex (parietal) ; Cross-Sectional Studies ; Disorientation ; Genotype &amp; phenotype ; Hallucinations ; Hippocampus ; Humans ; Memory ; Memory Disorders ; Neurodegenerative diseases ; Neuropsychological Tests ; Phenotypes ; Retrograde amnesia ; Retrospective Studies</subject><ispartof>Journal of Alzheimer's disease, 2023-01, Vol.91 (1), p.363-388</ispartof><rights>2023 – The authors. 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Neuropsychiatric features with striking misidentification (52.9%), other less-structured delusions (70.6%), and brief hallucinations (64.7%) were present. Marked behavioral disturbances were present early in some patients and very common at later stages. At the baseline, the CM-ADs showed more confabulation (p &lt; 0.001), temporal disorientation (p &lt; 0.02), misidentification (p = 0.013), other delusions (p = 0.002), and logorrhea (p = 0.004) than the CA-ADs. In addition, more social disinhibition (p = 0.018), reduction of insight (p = 0.029), and hallucination (p = 0.03) persisted at 12 months from baseline. Both the CA- and CM-ADs showed anterior and medial temporal atrophy. Compared to HCs, the CM-ADs showed more right fronto-insular atrophy, while the CA-ADs showed more dorsal parietal, precuneus, and right parietal atrophy. 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Objective: We aim to describe a further presentation we (re)named confabulation-misidentification (CM-) phenotype. Methods: We performed a retrospective longitudinal case-series study of 17 AD outpatients with the possible CM-phenotype (CM-ADs). Then, in a cross-sectional study, we compared the CM-ADs to a sample of 30 AD patients with the CA-phenotype (CA-ADs). The primary outcome was the frequency of cognitive and behavioral features. Data were analyzed as differences in percentage by non-parametric Chi Square and mean differences by parametric T-test. Results: Anterograde amnesia (100%) with early confabulation (88.2%), disorientation (88.2%) and non-infrequently retrograde amnesia (64.7%) associated with reduced insight (88.2%), moderate prefrontal executive impairment (94.1%) and attention deficits (82.3%) dominated the CM-phenotype. Neuropsychiatric features with striking misidentification (52.9%), other less-structured delusions (70.6%), and brief hallucinations (64.7%) were present. Marked behavioral disturbances were present early in some patients and very common at later stages. At the baseline, the CM-ADs showed more confabulation (p &lt; 0.001), temporal disorientation (p &lt; 0.02), misidentification (p = 0.013), other delusions (p = 0.002), and logorrhea (p = 0.004) than the CA-ADs. In addition, more social disinhibition (p = 0.018), reduction of insight (p = 0.029), and hallucination (p = 0.03) persisted at 12 months from baseline. Both the CA- and CM-ADs showed anterior and medial temporal atrophy. Compared to HCs, the CM-ADs showed more right fronto-insular atrophy, while the CA-ADs showed more dorsal parietal, precuneus, and right parietal atrophy. Conclusion: We described an AD phenotype resembling diencephalic rather than hippocampal amnesia and overlapping the past-century description of presbyophrenia.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>36442200</pmid><doi>10.3233/JAD-220919</doi><tpages>26</tpages><oa>free_for_read</oa></addata></record>
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subjects Alzheimer Disease - complications
Alzheimer Disease - psychology
Alzheimer's disease
Amnesia
Amnesia - psychology
Atrophy
Cognitive ability
Confusion
Cortex (parietal)
Cross-Sectional Studies
Disorientation
Genotype & phenotype
Hallucinations
Hippocampus
Humans
Memory
Memory Disorders
Neurodegenerative diseases
Neuropsychological Tests
Phenotypes
Retrograde amnesia
Retrospective Studies
title Diencephalic versus Hippocampal Amnesia in Alzheimer’s Disease: The Possible Confabulation-Misidentification Phenotype
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