Abstract:Frontotemporal dementia (FTD) is difficult to diagnose, due to its heterogeneous nature and overlap in symptoms with primary psychiatric disorders. Brain MRI for atrophy is a key biomarker but lacks sensitivity in the early stage. Morphometric MRI-based measures and machine learning techniques are a promising tool to improve diagnostic accuracy. Our aim was to review the current state of the literature using morphometric MRI to classify FTD and assess its applicability for clinical practice. A search was compl… Show more
“…MRI allows detection of bvFTD-specific brain atrophy, which includes frontal and anterior temporal volume loss, and shows a good diagnostic accuracy for differentiating FTD from normal subjects and other dementias in clinical practice [38][39][40]. MRI of bvFTD can show severe frontal and anterior temporal atrophy (Figs.…”
Neuroimaging can provide important biomarkers and is very useful for supporting dementia diagnosis. This review summarizes the neuroimaging findings of dementia with Lewy bodies (DLB), frontotemporal lobar degeneration (FTLD), and normal pressure hydrocephalus (NPH). In DLB, medial temporal atrophy is milder than that of Alzheimer's disease. 2-fluoro-2-deoxy-d-glucose-positron emission tomography and brain perfusion single-photon emission computed tomography demonstrate hypometabolism and hypoperfusion in the occipital lobe, in addition to decreased metabolism and perfusion in the parietotemporal, posterior cingulate, precuneus, and frontal association cortices. The cingulate island sign, which shows relatively spared middle-to-posterior cingulate cortex metabolism compared with precuneus hypometabolism, is proposed to detect DLB in 2-fluoro-2-deoxy-d-glucose-positron emission tomography imaging. Reduced uptake in dopamine transporter imaging and reduced myocardial uptake in iodine-123 metaiodobenzylguanidine cardiac scintigraphy are indicative biomarkers for DLB diagnosis. Characteristic findings of FTLD include dominant frontotemporal atrophy, hypometabolism, and hypoperfusion. Most idiopathic NPH cases demonstrate disproportionally enlarged subarachnoid space hydrocephalus findings, including dilated ventricular systems, enlarged Sylvian fissures, tight sulci in the midline, and a high convexity.
“…MRI allows detection of bvFTD-specific brain atrophy, which includes frontal and anterior temporal volume loss, and shows a good diagnostic accuracy for differentiating FTD from normal subjects and other dementias in clinical practice [38][39][40]. MRI of bvFTD can show severe frontal and anterior temporal atrophy (Figs.…”
Neuroimaging can provide important biomarkers and is very useful for supporting dementia diagnosis. This review summarizes the neuroimaging findings of dementia with Lewy bodies (DLB), frontotemporal lobar degeneration (FTLD), and normal pressure hydrocephalus (NPH). In DLB, medial temporal atrophy is milder than that of Alzheimer's disease. 2-fluoro-2-deoxy-d-glucose-positron emission tomography and brain perfusion single-photon emission computed tomography demonstrate hypometabolism and hypoperfusion in the occipital lobe, in addition to decreased metabolism and perfusion in the parietotemporal, posterior cingulate, precuneus, and frontal association cortices. The cingulate island sign, which shows relatively spared middle-to-posterior cingulate cortex metabolism compared with precuneus hypometabolism, is proposed to detect DLB in 2-fluoro-2-deoxy-d-glucose-positron emission tomography imaging. Reduced uptake in dopamine transporter imaging and reduced myocardial uptake in iodine-123 metaiodobenzylguanidine cardiac scintigraphy are indicative biomarkers for DLB diagnosis. Characteristic findings of FTLD include dominant frontotemporal atrophy, hypometabolism, and hypoperfusion. Most idiopathic NPH cases demonstrate disproportionally enlarged subarachnoid space hydrocephalus findings, including dilated ventricular systems, enlarged Sylvian fissures, tight sulci in the midline, and a high convexity.
“…In an effort to address the need for improved diagnostic biomarkers for the behavioural variant frontotemporal dementia (bvFTD), several studies have demonstrated the potential value of morphometric MRI analysis for diagnostic purposes (McCarthy et al., 2018). Here, we performed a deformation-based morphometry (DBM) study of longitudinal MRI changes in bvFTD.…”
HighlightsThe expected atrophy was shown in the frontal lobes and anterior temporal regions.Subcortical structures were notably affected in our bvFTD cohort.Ventricles and sulci within frontotemporal regions were larger in the bvFTD cohort.Ventricles and sulci showed significant enlargement and over a one-year period.Ventricular expansion was the most prominent differentiator of bvFTD from controls.
“…The best AUC was reported by Raamana et al (AUC 0.938, 100% sensitivity and 88% specificity). However, the main limitation of that study is that the bvFTD diagnosis from the validation cohort was based on clinical criteria (39). Contrarily, the bvFTD subjects from our validation cohort are known carriers of a pathogenic mutation and have therefore, definite bvFTD diagnosis.…”
Abbreviations FTD: frontotemporal dementia GRN: progranulin MAPT: microtubule-associated protein tau C9orf72 : chromosome 9 open reading frame 72 bvFTD: behavioural variant of frontotemporal dementia MRI: magnetic resonance imaging CNCs: cognitively normal controls DBM: deformation-based morphometry FTLDNI: frontotemporal lobar degeneration neuroimaging initiative T1-w: T1 weighted GENFI: Genetic frontotemporal dementia initiative MMSE: Mini mental state examination MOCA: Montreal cognitive assessment FTLD-CDR: Frontotemporal lobar degeneration Clinical Dementia Rating score CGI: Clinical global impression FRS: Frontotemporal dementia rating scale FDR: False Discovery Rate PCA: Principal component analysis PCs: Principal components SF: Semantic fluency ROC: Receiver operating characteristic curves AUC: Area under the curve LR+: positive likelihood ratio LR-: negative likelihood ratio Abstract INTRODUCTION: Brain structural imaging is paramount for the diagnosis of behavioral variant of frontotemporal dementia (bvFTD), but it has low sensitivity leading to erroneous or late diagnosis.
METHODS:A total of 515 subjects from two different bvFTD databases (training and validation cohorts) were included to perform voxel-wise deformation-based morphometry analysis to identify regions with significant differences between bvFTD and controls. A random forest classifier was used to individually predict bvFTD from morphometric differences in isolation and together with bedside cognitive scores.
RESULTS:Average ten-fold cross-validation accuracy was 89% (82% sensitivity, 93% specificity) using only MRI and 94% (89% sensitivity, 98% specificity) with the addition of semantic fluency. In a separate validation cohort of genetically confirmed bvFTD, accuracy was 88% (81% sensitivity, 92% specificity) with MRI and 91% (79% sensitivity, 96% specificity) with added cognitive scores.
DISCUSSION:The random forest classifier developed can accurately predict bvFTD at the individual subject level.
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