Time to Diagnosis and Its Predictors in Syndromes Associated With Frontotemporal Lobar Degeneration

Objectives: Frontotemporal Lobar Degeneration (FTLD) causes a heterogeneous group of neurodegenerative disorders with a wide range of clinical features. This might delay time to diagnosis. The aim of the present study is to establish time to diagnosis and its predictors in patients with FTLD-associated syndromes. Design: Retrospective study. Setting: Tertiary referral center. Participants: A total of 1029 patients with FTLD-associated syndromes (age: 68 [61 - 73] years, females: 46%) from 1999 to 2023 were included in the present study. Measurements: Time to diagnosis was operationalized as the time between symptom onset and the diagnosis of a FTLD-associated syndrome. The associations between time to diagnosis and possible predictors (demographic and clinical variables) were investigated through univariate and multivariate linear models. Results: Median time to diagnosis was 2 [1-3] years. We observed that younger age at onset ( b =-0.03, p < 0.001), having worked as a professional rather than as a blue ( b = 0.52, p = 0.024) or a white ( b = 0.46, p = 0.050) collar, and having progressive supranuclear palsy (p < 0.05) or the semantic variant of primary progressive aphasia (p < 0.05) phenotypes were significantly associated with increased time to diagnosis. No significant changes of time to diagnosis have been observed over 20 years. Conclusions: The identification of predictors of time to diagnosis might improve current diagnostic algorithms, resulting in a timely initiation of symptomatic treatments, early involvement in clinical trials, and more adequate public health policies for patients and theirfamilies.