Montreal Cognitive Assessment vs the Mini-Mental State Examination as a Screening Tool for Patients With Genetic Frontotemporal Dementia.

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Tác giả: Kerala Adams-Carr, Pam Boesjes, Arabella Bouzigues, Rhian S Convery, Liset de Boer, Julie F H De Houwer, Elise G P Dopper, Eve Ferry-Bolder, Phoebe H Foster, Lize C Jiskoot, Jackie M Poos, Jonathan D Rohrer, Lucy L Russell, Harro Seelaar, Tine Swartenbroekx, Najlae Tahboun, Esther Van Den Berg

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Neurology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 91122

BACKGROUND AND OBJECTIVES: With upcoming clinical trials targeting preclinical stages of genetic frontotemporal dementia (FTD), early detection through cognitive screening is crucial. The Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA) have potential as screening instruments for early-stage genetic FTD. However, no comparative evaluation has been performed. We aimed to compare MMSE and MoCA performance among presymptomatic, prodromal, and symptomatic pathogenic variant carriers to analyze which screening test has superior discriminative abilities. METHODS: We used cross-sectional and longitudinal data from 2 longitudinal genetic FTD cohort studies in the Netherlands and the United Kingdom, collected between 2021 and 2024. Participants were either presymptomatic, prodromal, or symptomatic pathogenic variant carriers or healthy controls (first-degree family members without pathogenic variants for FTD). Grouping was based on the global CDR-plus-NACC-FTLD score. Participants were assessed with both MoCA and MMSE. Statistical analyses compared total and subscores between groups and evaluated predictive and classification accuracy of both tests. RESULTS: A total of 243 participants (mean age 49.9 ± 13.1 years, mean education 14.5 ± 3.0 years, 56% female), 157 of whom were pathogenic variant carriers ( DISCUSSION: Its higher sensitivity and better discriminative power make MoCA a more valuable tool for cognitive screening in upcoming clinical trials targeting preclinical FTD. Future studies should aim for larger sample sizes from additional study centers.
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