The power of neuroimaging biomarkers for screening frontotemporal dementia
Year: 2014
Type: article
Study design: Observational Study
Abstract: Frontotemporal dementia (FTD) is a clinically and pathologically heterogeneous neurodegenerative disease that can result from either frontotemporal lobar degeneration (FTLD) or Alzheimer's disease (AD) pathology. It is critical to establish statistically powerful biomarkers that can achieve substantial cost-savings and increase the feasibility of clinical trials. We assessed three broad categories of neuroimaging methods to screen underlying FTLD and AD pathology in a clinical FTD series: global measures (e.g., ventricular volume), anatomical volumes of interest (VOIs) (e.g., hippocampus) using a standard atlas, and data-driven VOIs using Eigenanatomy. We evaluated clinical FTD patients (N = 93) with cerebrospinal fluid, gray matter (GM) magnetic resonance imaging (MRI), and diffusion tensor imaging (DTI) to assess whether they had underlying FTLD or AD pathology. Linear regression was performed to identify the optimal VOIs for each method in a training dataset and then we evaluated classification sensitivity and specificity in an independent test cohort. Power was evaluated by calculating minimum sample sizes required in the test classification analyses for each model. The data-driven VOI analysis using a multimodal combination of GM MRI and DTI achieved the greatest classification accuracy (89% sensitive and 89% specific) and required a lower minimum sample size (N = 26) relative to anatomical VOI and global measures. We conclude that a data-driven VOI approach using Eigenanatomy provides more accurate classification, benefits from increased statistical power in unseen datasets, and therefore provides a robust method for screening underlying pathology in FTD patients for entry into clinical trials.
Source: Human Brain Mapping
DOI: 10.1002/hbm.22515
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G1400371317, G181261680, G234895681, Age, Hearing Loss, and Sentence Comprehension: Neural Correlates, G3919444319, Alzheimer's Disease Core Center, Frontotemporal Dementias: Genotypes and Phenotypes, G4849756124, G7457190523, G7527168623, G8061420933, G8714196310, TDP-43 Proteinopathies in ALS-Dementia, Neural Basis of Generalized Quantifiers, G9000033698, G9000159269, G9000161801, G9000305149
OpenAlex ID: W2124263729
