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- Titel:
Disease specific and nonspecific metabolic brain networks in behavioral variant of frontotemporal dementia.
- Dokumenttyp:
- Multicenter Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
- Autor(en):
- Rus, Tomaž; Perovnik, Matej; Vo, An; Nguyen, Nha; Tang, Chris; Jamšek, Jan; Šurlan Popović, Katarina; Grimmer, Timo; Yakushev, Igor; Diehl-Schmid, Janine; Eidelberg, David; Trošt, Maja
- Abstract:
- Behavioral variant of frontotemporal dementia (bvFTD) is common among young-onset dementia patients. While bvFTD-specific multivariate metabolic brain pattern (bFDRP) has been identified previously, little is known about its temporal evolution, internal structure, effect of atrophy, and its relationship with nonspecific resting-state networks such as default mode network (DMN). In this multicenter study, we explored FDG-PET brain scans of 111 bvFTD, 26 Alzheimer's disease, 16 Creutzfeldt-Jakob's disease, 24 semantic variant primary progressive aphasia (PPA), 18 nonfluent variant PPA and 77 healthy control subjects (HC) from Slovenia, USA, and Germany. bFDRP was identified in a cohort of 20 bvFTD patients and age-matched HC using scaled subprofile model/principle component analysis and validated in three independent cohorts. It was characterized by hypometabolism in frontal cortex, insula, anterior/middle cingulate, caudate, thalamus, and temporal poles. Its expression in bvFTD patients was significantly higher compared to HC and other dementia syndromes (p < .0004), correlated with cognitive decline (p = .0001), and increased over time in longitudinal cohort (p = .0007). Analysis of internal network organization by graph-theory methods revealed prominent network disruption in bvFTD patients. We have further found a specific atrophy-related pattern grossly corresponding to bFDRP; however, its contribution to the metabolic pattern was minimal. Finally, despite the overlap between bFDRP and FDG-PET-derived DMN, we demonstrated a predominant role of the specific bFDRP. Taken together, we validated the bFDRP network as a diagnostic/prognostic biomarker specific for bvFTD, provided a unique insight into its highly reproducible internal structure, and proved that bFDRP is unaffected by structural atrophy and independent of normal resting state networks loss.
- Zeitschriftentitel:
- Hum Brain Mapp
- Jahr:
- 2023
- Band / Volume:
- 44
- Heft / Issue:
- 3
- Seitenangaben Beitrag:
- 1079-1093
- Volltext / DOI:
- doi:10.1002/hbm.26140
- PubMed:
- http://view.ncbi.nlm.nih.gov/pubmed/36334269
- Print-ISSN:
- 1065-9471
- TUM Einrichtung:
- Klinik und Poliklinik für Nuklearmedizin
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