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Recently, new diagnostic criteria including imaging biomarkers have been proposed for frontotemporal lobar degeneration
(FTLD) in particular for its behavioural variant and language subtypes. These imaging criteria shall enable individual
diagnosis. New imaging criteria were validated by conducting quantitative anatomical likelihood estimate meta-analyses
according to the QUOROM/PRISMA statement across studies published in the literature. These meta-analyses identify the
neural correlates for each of the FTLD subtypes and underline disease-specificity of the imaging criteria. Analyses were
conducted separately for atrophy measured with magnetic resonance imaging (MRI) and glucose metabolism measured
with [F18] fluorodeoxyglucose positron emission tomography (FDG-PET). Both imaging methods revealed specific regional
patterns. Results might open the road to method-specific imaging criteria as already suggested for Alzheimer�s disease. If new
imaging criteria are valid they shall enable early individual diagnosis in single patients. To prove the potential for individual
diagnosis we investigated whether FTLD might be diagnosed with cutting edge pattern classification algorithms in multimodal
imaging data. Support vector machine classification (SVM) with multimodal imaging data (MRI & FDG-PET) enabled
early individual detection of FTLD and discrimination between FTLD and Alzheimer�s disease. Limiting SVM classification
regionally to meta-analytically identified disease networks even improved discrimination accuracy. Analyses were also reliable
in multi-centric data. In conclusion, our results support and refine the application of imaging criteria and suggest that pattern
classification algorithms enable early individual diagnosis and differential diagnosis of FTLD sub types, a precondition for
early intervention strategies.