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What Are the Neural Correlates of Meta-cognition and Anosognosia in Alzheimer's Disease? A Systematic Review

Overview
Journal Neurobiol Aging
Publisher Elsevier
Date 2020 Jul 18
PMID 32679396
Citations 26
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Abstract

Awareness of one's own cognitive processes (metacognition) or of one's own illness or deficits (anosognosia) can be impaired in people with Alzheimer's disease (AD). The neural correlates of anosognosia within AD remain inconclusive. Understanding anosognosia is of importance because of its impact on carer burden and increased institutionalization. A systematic review of structural and functional neuroimaging studies was conducted to identify specific brain regions associated with anosognosia within AD. Thirty-two studies were included in the systematic review. Reduced gray matter density, cerebral blood flow, and hypometabolism in 8 key regions were significantly associated with increased anosognosia scores in people with AD. The most frequently associated regions were the inferior frontal gyrus, anterior cingulate cortex, and medial temporal lobe. Other key regions include the superior frontal gyrus, medial frontal gyrus, orbitofrontal cortex, posterior cingulate cortex, and the insula. Identifying brain regions associated with anosognosia can aid understanding and identification of anosognosia in people with AD and potentially facilitate improvements in care.

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References
1.
Turro-Garriga O, Garre-Olmo J, Rene-Ramirez R, Calvo-Perxas L, Gascon-Bayarri J, Conde-Sala J . Consequences of Anosognosia on the Cost of Caregivers' Care in Alzheimer's Disease. J Alzheimers Dis. 2016; 54(4):1551-1560. DOI: 10.3233/JAD-160419. View

2.
Hornberger M, Yew B, Gilardoni S, Mioshi E, Gleichgerrcht E, Manes F . Ventromedial-frontopolar prefrontal cortex atrophy correlates with insight loss in frontotemporal dementia and Alzheimer's disease. Hum Brain Mapp. 2012; 35(2):616-26. PMC: 6869805. DOI: 10.1002/hbm.22200. View

3.
Cosentino S, Metcalfe J, Cary M, de Leon J, Karlawish J . Memory Awareness Influences Everyday Decision Making Capacity about Medication Management in Alzheimer's Disease. Int J Alzheimers Dis. 2011; 2011:483897. PMC: 3109698. DOI: 10.4061/2011/483897. View

4.
Ma Y, Eidelberg D . Functional imaging of cerebral blood flow and glucose metabolism in Parkinson's disease and Huntington's disease. Mol Imaging Biol. 2007; 9(4):223-33. PMC: 4455550. DOI: 10.1007/s11307-007-0085-4. View

5.
Leech R, Braga R, Sharp D . Echoes of the brain within the posterior cingulate cortex. J Neurosci. 2012; 32(1):215-22. PMC: 6621313. DOI: 10.1523/JNEUROSCI.3689-11.2012. View