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Assessing the relationship between cognitive dysfunction and brain atrophy in Alzheimer's disease
Author(s) -
Edison Paul,
Femminella Grazia Daniela,
Nowell Joseph,
Raza Sanara,
Livingston Nicholas R,
Blunt Eleanor G,
Carver Stefan,
Holmes Clive,
Ritchie Craig W,
Lawrence Robert M,
McFarlane Brady,
Tadros George,
Ridha Basil H,
Bannister Carol,
Walker Zuzana,
Archer Hilary,
Coulthard Elizabeth,
Underwood Ben,
Prasanna Aparna,
Koranteng Paul,
Karim Salman,
Junaid Kehinde,
McGuinness Bernadette,
Nilforooshan Ramin,
Macharouthu Ajayverma,
Donaldson Andrew,
Thacker Simon,
Russell Gregor,
Malik Naghma,
Mate Vandana,
Knight Lucy,
Kshemendran Sajeev,
Harrison John E,
Brooks David J,
Passmore Anthony Peter,
Ballard Clive
Publication year - 2020
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1002/alz.046004
Subject(s) - atrophy , temporal lobe , hippocampus , neuropsychology , brain size , medicine , neurodegeneration , psychology , biomarker , alzheimer's disease , cognition , dementia , neuroscience , magnetic resonance imaging , audiology , pathology , disease , radiology , epilepsy , chemistry , biochemistry
Background Brain atrophy can be reliably measured through volumetric analysis of structural MRI and is a valid biomarker of neurodegeneration in Alzheimer’s disease (AD) pathology 1 . The Alzheimer’s Disease Assessment Scale‐Cognitive subscale (ADAS‐Cog12) is a neuropsychological test designed to assess the level of cognitive dysfunction in AD within cognitive domains such as memory 2 . This study aimed to assess the relationship between brain atrophy and ADAS‐Cog12 score in patients with AD. Methods 172 patients with mild‐to‐moderate Alzheimer’s disease (Age range 51‐58, Mean=71, SD=+/‐8) underwent a T1‐weighted MPRAGE MRI scan and neuropsychological testing using the ADAS‐Cog12. Volumetric MRI measures extracted using Freesurfer for the hippocampus, medial temporal lobe, temporal lobe and total grey matter were individually correlated with each patient’s ADAS‐Cog12 score using Pearson’s correlation coefficient following removal of outliers in each data set (+/‐ 2SD from the mean). Results Increasing ADAS‐Cog12 score was significantly correlated with decreasing volume of the hippocampus ( r =‐0.280, p <0.001), medial temporal lobe ( r =‐0.246, p =0.001), temporal lobe ( r =‐0.300, p <0.001) and total grey matter ( r =‐0.236, p =0.002). Conclusions This study demonstrated that the ADAS‐Cog12 correlated with AD‐related regional brain atrophy, suggesting that ADAS‐Cog could be used as an outcome measure in AD trials and reflects underlying neuronal damage along with cognitive function.