ArticleFrontiers in psychology2025
Behavioral and neural effects of temporoparietal high-definition transcranial direct current stimulation in logopenic variant primary progressive aphasia: a preliminary study.
Article in Frontiers in psychology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03805659 (High-Definition Transcranial Direct Current Stimulation), which is not on this map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
High-Definition Transcranial Direct Current Stimulation (HD-tDCS) in Logopenic Variant Primary Progressive Aphasia (lvPPA): Effects on Language and Neural Mechanisms
Who cites it
2 citing papers in PubMed.
- A multi-modal approach for the treatment of non-fluent/agrammatic variant of Primary Progressive Aphasia.Brain communications · 2025Trial
- Efficacy of Transcranial Magnetic Stimulation and Transcranial Direct-Current Stimulation in Primary Progressive Aphasia Treatment: A Review.Brain sciences · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
Abstract
Background: High-definition-tDCS (HD-tDCS) is a recent technology that allows for localized cortical stimulation, but has not yet been investigated as an augmentative therapy while targeting the left temporoparietal cortex in logopenic variant PPA (lvPPA). The changes in neuronal oscillatory patterns and resting-state functional connectivity in response to HD-tDCS also remains poorly understood. Objective: We sought to investigate the effects of HD-tDCS with phonologic-based language training on language, cognition, and resting-state functional connectivity in lvPPA. Methods: We used a double-blind, within-subject, sham-controlled crossover design with a 4-month between-treatment period in four participants with lvPPA. Participants completed language, cognitive assessments, and imaging with magnetoencephalography (MEG) and resting-state functional MRI (fMRI) prior to treatment with either anodal HD-tDCS or sham targeting the left supramarginal gyrus over 10 sessions. Language and cognitive assessments, MEG, and fMRI were repeated after the final session and at 2 months follow-up. Preliminary data on efficacy was evaluated based on relative changes from baseline in language and cognitive scores. Language measures included metrics derived from spontaneous speech from picture description. Changes in resting-state functional connectivity within the phonological network were analyzed using fMRI. Magnitudes of source-level evoked responses and hemispheric laterality indices from language task-based MEG were used to assess changes in cortical engagement induced by HD-tDCS. Results: All four participants were retained across the 4-month between-treatment period, with satisfactory blinding of participants and investigators throughout the study. Anodal HD-tDCS was well tolerated with a side effect profile that did not extend past the immediate treatment period. No benefit of HD-tDCS over sham on language and cognitive measures was observed in this small sample. Functional imaging results using MEG and fMRI indicated an excitatory effect of anodal HD-tDCS compared to sham and suggested that greater temporoparietal activation and connectivity was positively associated with language outcomes. Conclusion: Anodal HD-tDCS to the inferior parietal cortex combined with language training appears feasible and well tolerated in participants with lvPPA. Language outcomes may be explained by regression to the mean, and to a lesser degree, by ceiling effects and differences in baseline disease severity. The intervention has apparent temporoparietal correlates, and its clinical efficacy should be further studied in larger trials. Clinical trial registration: ClinicalTrials.gov, Number NCT03805659.
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