Related Experiment Video
Updated: Oct 6, 2026

Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
Medial temporal lobe metabolic impairment in dementia associated with motor neuron disease
G Garraux1, E Salmon, C Degueldre
1Cyclotron Research Center, Sart Tilman B30, B-4000, Liège, Belgium. garraux@pet.crc.ulg.ac.be
Abstract:
In the course of their disease certain patients with frontotemporal dementia (FTD) develop clinical features compatible with a motor neuron disease (FTD-MND). Previous reports have suggested that the functional pattern is similar in FTD and FTD-MND. However, some neuropathological studies suggest greater involvement of medial temporal regions in FTD-MND than in FTD. Using statistical parametric mapping (SPM96), we compared the metabolic patterns obtained at rest with positron emission tomography in 10 FTD patients and three FTD-MND patients with those obtained from 46 healthy subjects (HS). Mean age, duration of illness and dementia stage did not differ statistically between the FTD and FTD-MND groups. In comparison with HS, both groups showed frontal and anterior temporal hypometabolism at P<0.001. When the FTD-MND group was compared to the FTD group, significant hypometabolism was only observed in bilateral amygdala, bilateral hippocampus, and bilateral enthorinal and parahippocampal regions (Brodmann's areas, BA 28/36) at P<0.005. We found no significant differences in regional glucose uptake when FTD patients were contrasted to FTD-MND patients. Our results suggest statistically comparable frontal and lateral temporal hypometabolism in both conditions but greater impairment of medial temporal lobe activity in FTD-MND. Our results and a review of the literature support the hypothesis that there is a functional continuum between classical motor neuron disease (cMND), FTD-MND, and FTD.
Insights
Patients with frontotemporal dementia (FTD) and FTD-motor neuron disease (FTD-MND) show similar frontal and temporal hypometabolism. However, FTD-MND patients exhibit greater impairment in medial temporal lobe activity, suggesting a functional continuum.
Area of Science:
- Neuroscience
- Neurology
- Medical Imaging
Background:
- Frontotemporal dementia (FTD) can present with motor neuron disease features (FTD-MND).
- Previous studies suggest functional similarities between FTD and FTD-MND, but neuropathology indicates greater medial temporal involvement in FTD-MND.
- Understanding the metabolic patterns in FTD and FTD-MND is crucial for differentiating these conditions and understanding their relationship.
Purpose of the Study:
- To compare the metabolic patterns in patients with FTD and FTD-MND using positron emission tomography (PET).
- To investigate the extent of hypometabolism in medial temporal regions in FTD-MND compared to FTD.
- To explore the hypothesis of a functional continuum between classical motor neuron disease (cMND), FTD-MND, and FTD.
Main Methods:
- Positron emission tomography (PET) was used to measure regional glucose metabolism at rest.
- Statistical parametric mapping (SPM96) was employed to compare metabolic data.
- Ten FTD patients, three FTD-MND patients, and 46 healthy subjects (HS) were included in the study.
Main Results:
- Both FTD and FTD-MND groups showed significant frontal and anterior temporal hypometabolism compared to HS.
- FTD-MND patients exhibited significantly greater hypometabolism in the bilateral amygdala, hippocampus, and entorhinal/parahippocampal regions compared to FTD patients.
- No significant differences in regional glucose uptake were found when directly contrasting FTD patients with FTD-MND patients in all regions.
Conclusions:
- FTD and FTD-MND share comparable frontal and lateral temporal hypometabolism.
- FTD-MND is characterized by a more pronounced impairment of medial temporal lobe activity.
- The findings support a functional continuum linking cMND, FTD-MND, and FTD.
Related Concept Videos
Alzheimer Disease l: Introduction
Alzheimer Disease ll: Pathophysiology
Dementia l: Introduction
Alterations in Muscle Tone lll
Hepatic Encephalopathy

