2025-10-15 カロリンスカ研究所(KI)
<関連情報>
- https://news.ki.se/new-brain-imaging-technique-can-detect-early-frontotemporal-dementia
- https://www.nature.com/articles/s41380-025-03280-x
遺伝性前頭側頭型認知症における皮質微細構造は疾患の重症度および臨床進行と関連している:GENFI研究 Cortical microstructure is associated with disease severity and clinical progression in genetic frontotemporal dementia: a GENFI study
Elena Rodriguez-Vieitez,Melissa T. Rydell,Abbe Ullgren,Victor Montal,Ignacio Illán-Gala,Juan Fortea,Vesna Jelic,Arabella Bouzigues,Lucy L. Russell,Phoebe H. Foster,Eve Ferry-Bolder,John C. van Swieten,Lize C. Jiskoot,Harro Seelaar,Raquel Sanchez-Valle,Robert Laforce,Daniela Galimberti,Rik Vandenberghe,Alexandre de Mendonça,Pietro Tiraboschi,Isabel Santana,Alexander Gerhard,Johannes Levin,Sandro Sorbi,on behalf of the Genetic Frontotemporal Dementia Initiative (GENFI)
Molecular Psychiatry
Abstract
The study of genetic frontotemporal dementia (FTD) allows investigating its earliest presymptomatic stages. Using cross-sectional T1-weighted and diffusion-weighted MRI, we test the hypothesis that cortical microstructural alterations, quantified as cortical mean diffusivity (cMD), are detectable earlier and are more strongly associated with clinical progression than cortical thickness (CTh). The sample comprised n = 710 individuals (47.8 ± 13.5 years, 56.6% female, 14.1 ± 3.3 years of education), including 118 symptomatic carriers and 305 presymptomatic carriers with mutations in C9orf72, GRN or MAPT genes, and 287 non-carriers, collected from 24 GENFI sites. A subset of n = 453 individuals (289 carriers, 164 non-carriers) were investigated across Clinical Dementia Rating (CDR) = 0, 0.5 and ≥1 stages. Two subsets had longitudinal clinical outcome measures, including n = 403 individuals (239 carriers, 164 non-carriers) with Cambridge Behavioural Inventory-Revised scores during 2.8 ± 1.6 years, and n = 261 individuals (164 carriers, 97 non-carriers) with CDR Sum-of-Boxes scores during 2.0 ± 0.8 years. Regional cMD and CTh were entered into linear mixed-effects models incorporating age, sex and education as covariates; site, and individual nested within site were random intercepts. The results demonstrated that cMD is more sensitive than CTh to track early cortical injury, with elevated cMD first observed at CDR = 0 in C9orf72 carriers, followed by MAPT carriers (from CDR = 0.5 stage), and by GRN carriers (beginning at CDR ≥ 1). At all stages, cortical microstructural injury had stronger effect size and was more widespread than cortical thinning. In all mutation carrier types, cMD was more strongly associated than CTh with subsequent clinical progression. Cortical microstructure is a promising biomarker to identify at-risk individuals before atrophy and clinical progression, with utility in therapeutic trials.
