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Heterogeneity of behavioural and language deficits in FTD-MND
Zhe Long1,2,3, Muireann Irish3,4,5, David Foxe3,4
1Department of Neurology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Objective:
To comprehensively examine the clinical presentation of patients diagnosed with frontotemporal dementia-motor neuron disease (FTD-MND) compared to FTD subtypes. To clarify the heterogeneity of behavioural and language deficits in FTD-MND using a data-driven approach.
Methods:
Patients with FTD-MND (n = 31), behavioural variant FTD (n = 119), non-fluent variant primary progressive aphasia (n = 47), semantic variant primary progressive aphasia (n = 42), and controls (n = 127) underwent comprehensive clinical, cognitive and behavioural assessments. Two-step cluster analysis examined patterns of behavioural and language impairment. Voxel-based morphometry and tract-based spatial statistics were used to investigate differences across the subgroups that emerged from cluster analysis.
Results:
More than half of FTD-MND patients initially presented with variable combinations of deficits (e.g., mixed behaviour/cognitive, mixed behaviour/cognitive/motor deficits), with 74% of them meeting criteria for FTD-MND within 24 months with a median of 12 months. The frequency and severity of behavioural and language abnormalities in FTD-MND lie between that seen in the three FTD phenotypes. Cluster analysis identified three patterns of behavioural and language impairment in FTD-MND. The three FTD-MND subgroups demonstrated different profiles of white matter tract disruption, but did not differ in age at onset, disease duration or patterns of cortical atrophy.
Conclusions:
While highly heterogeneous, in terms of behavioural and language deficits, and disease severity, the presentation of FTD-MND may be distinct to that of FTD. Distinct white matter degeneration patterns may underpin heterogeneous clinical profiles in FTD-MND. FTD presenting with mixed behavioural-language disturbances should be monitored closely for at least 12-24 months for the emergence of MND symptoms/signs.
Insights
Frontotemporal dementia-motor neuron disease (FTD-MND) presents heterogeneously, often with mixed deficits. Distinct white matter changes may explain varied clinical profiles in FTD-MND patients.
Area of Science:
- Neuroscience
- Neurology
- Clinical Medicine
Background:
- Frontotemporal dementia-motor neuron disease (FTD-MND) is a complex neurodegenerative disorder.
- Understanding its clinical heterogeneity is crucial for diagnosis and management.
- FTD-MND shares features with frontotemporal dementia (FTD) subtypes, necessitating comparative studies.
Purpose of the Study:
- To compare the clinical presentation of FTD-MND with FTD subtypes.
- To identify distinct patterns of behavioural and language deficits in FTD-MND using a data-driven approach.
- To investigate the neuroanatomical correlates of these clinical profiles.
Main Methods:
- A cohort of FTD-MND patients (n=31), FTD subtypes (n=208), and controls (n=127) underwent comprehensive assessments.
- Two-step cluster analysis was employed to identify patterns of behavioural and language impairment.
- Voxel-based morphometry and tract-based spatial statistics analyzed neuroimaging data.
Main Results:
- Over half of FTD-MND patients initially presented with mixed deficits, with 74% meeting FTD-MND criteria within 24 months.
- FTD-MND showed intermediate behavioural and language abnormalities compared to FTD subtypes.
- Cluster analysis revealed three distinct FTD-MND subgroups with differing white matter degeneration patterns.
Conclusions:
- FTD-MND exhibits a distinct, albeit heterogeneous, clinical presentation compared to FTD subtypes.
- Specific white matter degeneration patterns may underlie the diverse clinical profiles observed in FTD-MND.
- FTD patients with mixed behavioural-language disturbances require close monitoring for emerging motor neuron disease symptoms.
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