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Multicenter Study
. 2018 May 24;10(1):46.
doi: 10.1186/s13195-018-0376-9.

Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales

Collaborators, Affiliations
Multicenter Study

Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales

Giorgio G Fumagalli et al. Alzheimers Res Ther. .

Abstract

Background: In patients with frontotemporal dementia, it has been shown that brain atrophy occurs earliest in the anterior cingulate, insula and frontal lobes. We used visual rating scales to investigate whether identifying atrophy in these areas may be helpful in distinguishing symptomatic patients carrying different causal mutations in the microtubule-associated protein tau (MAPT), progranulin (GRN) and chromosome 9 open reading frame (C9ORF72) genes. We also analysed asymptomatic carriers to see whether it was possible to visually identify brain atrophy before the appearance of symptoms.

Methods: Magnetic resonance imaging of 343 subjects (63 symptomatic mutation carriers, 132 presymptomatic mutation carriers and 148 control subjects) from the Genetic Frontotemporal Dementia Initiative study were analysed by two trained raters using a protocol of six visual rating scales that identified atrophy in key regions of the brain (orbitofrontal, anterior cingulate, frontoinsula, anterior and medial temporal lobes and posterior cortical areas).

Results: Intra- and interrater agreement were greater than 0.73 for all the scales. Voxel-based morphometric analysis demonstrated a strong correlation between the visual rating scale scores and grey matter atrophy in the same region for each of the scales. Typical patterns of atrophy were identified: symmetric anterior and medial temporal lobe involvement for MAPT, asymmetric frontal and parietal loss for GRN, and a more widespread pattern for C9ORF72. Presymptomatic MAPT carriers showed greater atrophy in the medial temporal region than control subjects, but the visual rating scales could not identify presymptomatic atrophy in GRN or C9ORF72 carriers.

Conclusions: These simple-to-use and reproducible scales may be useful tools in the clinical setting for the discrimination of different mutations of frontotemporal dementia, and they may even help to identify atrophy prior to onset in those with MAPT mutations.

Keywords: Frontotemporal dementia; Genetics; MRI; Visual rating.

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Conflict of interest statement

Ethics approval and consent to participate

Local ethics committees approved the study at each site, and all participants provided written informed consent.

Competing interests

The authors declare that they have no competing interests.

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Figures

Fig. 1
Fig. 1
Mean score of each visual rating scale in each group
Fig. 2
Fig. 2
Representative coronal (for all scales except posterior atrophy scale) and sagittal (posterior atrophy scale) T1-weighted magnetic resonance images of symptomatic carriers of GRN, MAPT, and C9ORF72 mutations (top three rows). Voxel-based morphometric analysis showing areas of significant negative correlation between the scales and grey matter. Maps showing z-scores were rendered on a study-specific template in MNI (Montreal Neurological Institute) space (bottom row). Images are shown with the left hemisphere on the left side of the figure

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