Case-control study reveals glymphatic activity correlates with synaptic vesicle cycle metabolites in behavioral variant frontotemporal dementia, highlighting synaptic pathways as therapeutic targets.
Emerging evidence implicating glymphatic dysfunction contributes to the pathogenesis of frontotemporal dementia (FTD). However, the pathway correlated to glymphatic function in FTD remains poorly understood. We aimed to explore potential underlying metabolic pathways associated with glymphatic dysfunction in FTD. We enrolled 37 behavior FTD (bvFTD) patients and 40 healthy controls. Glymphatic activity was assessed using diffusion tensor imaging data. Plasma metabolomic profiling was performed to identify glymphatic-associated metabolites, followed by pathway enrichment analysis. Additionally, the plasma biomarker was tested in a subset of 25 patients to validate the metabolite findings. Patients with bvFTD exhibited significantly altered metabolite profiles compared to controls. The glymphatic-associated metabolites were predominantly enriched in the synaptic vesicle cycle pathway (FDR p < 0.05). Furthermore, plasma neuropentraxin-2 (NPTX2) levels positively correlated with anterior glymphatic indices ( r = 0.46, p = 0.027). Our findings demonstrate the association between the glymphatic system and synaptic function in bvFTD. • Significant metabolic profile differences between bvFTD patients and controls. • Glymphatic-associated metabolites enriched in synaptic pathways. • Plasma NPTX2 levels positively correlate with anterior glymphatic indices. • Metabolite changes highlight potential therapeutic targets for FTD.
No takes yet. Share an insight, caveat, or question.
Chu et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: