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Abstract Details

Diagnostic Utility of Volumetric Brain MRI Quantification for Distinguishing Frontotemporal Dementia from Alzheimer’s Disease
Aging, Dementia, and Behavioral Neurology
P10 - Poster Session 10 (5:30 PM-6:30 PM)
10-004

The purpose of this work was to determine the extent to which automated quantitative volumetric MR neuroimaging can distinguish persons with behavioral variant frontotemporal dementia (bvFTD) from the more common Alzheimer’s diseases (AD).

The ability of volumetric brain MRI to be utilized clinically would be better realized if objective data could demonstrate its ability to distinguish common forms of dementia from one another. As bvFTD must often be distinguished from AD, the most common neurodegenerative dementia, applying this question to these disorders has a high potential to affect future clinical practice.

A total of 95 cognitive neurology patients were evaluated by a behavioral neurologist of which 16 met Consensus Criteria for bvFTD and 79 met established criteria for clinically probable AD. All participants received a sagittal T1 weighted volumetric acquisition on a 3T MR scanner and were analyzed by the Neuroreader software to compute brain volumes. Volumes for lobar structures and limbic areas were inputted into a discriminant analysis in SPSS with leave one out cross validation. This analysis produced an ROC and feature selection was also done separately.

Persons with bvFTD were younger (mean age = 60.6 ± 10.3 years) compared to those with AD (mean age = 67.2 ± 11.8 years) (t = 2.1, p = .04). There were no statistically significant differences in gender. The Neuroreader volumes distinguished bvFTD from AD with an AUC of 94%, a sensitivity of 99%, and a specificity of 98%. The three most predictive features from the volumetric analysis were i) Right frontal lobe ii) Right temporal lobe iii) left parietal lobe.

Clinically available, quantitative volumetric MR neuroimaging combined with a predictive analytic approach can distinguish bvFTD from AD with a high level of accuracy, sensitivity and specificity. Future work will evaluate such features in distinguishing other possible etiologies of dementia.

Authors/Disclosures
Somayeh Meysami, MD (Pacific Neuroscience Institute, Providence Saint Johns Health Center)
PRESENTER
Dr. Meysami has nothing to disclose.
Cyrus A. Raji, MD, PhD (Washington University in St Louis) Prof. Raji has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Brainreader ApS. Prof. Raji has received personal compensation in the range of $10,000-$49,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Apollo Health . Prof. Raji has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for Neurevolution Medicine.
Mario F. Mendez, MD, PhD, FÂé¶¹´«Ã½Ó³»­ (VA Greater Los Angeles Healthcare System and UCLA) Dr. Mendez has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Medical Âé¶¹´«Ã½Ó³»­ Speakers' Bureau. Dr. Mendez has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for UpToDate. The institution of Dr. Mendez has received research support from NIH. Dr. Mendez has received publishing royalties from a publication relating to health care.