Longitudinal diffusion tensor imaging in amyotrophic lateral sclerosis
- Equal contributors
1 Department of Neurology, Jena University Hospital, Erlanger Allee 101, Jena, 07747, Germany
2 Department of Psychiatry and Psychotherapy, Medical School Hannover, Carl-Neuberg-Strasse 1, Hannover, 30625, Germany
3 Department of Neurology and Clinical Neurophysiology, Medical School Hannover, Carl-Neuberg-Str.1, Hannover, 30625, Germany
Citation and License
BMC Neuroscience 2012, 13:141 doi:10.1186/1471-2202-13-141Published: 8 November 2012
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder, caused by progressive loss of motor neurons. Changes are widespread in the subcortical white matter in ALS. Diffusion tensor imaging (DTI) detects pathological changes in white matter fibres in vivo, based on alterations in the degree (diffusivity, ADC) and directedness (fractional anisotropy, FA) of proton movement.
24 patients with ALS and 24 age-matched controls received 1.5T DTI. FA and ADC were analyzed using statistical parametric mapping. In 15 of the 24 ALS patients, a second DTI was obtained after 6 months.
Decreased FA in the corticospinal tract (CST) and frontal areas confirm existing results. With a direct comparison of baseline and follow-up dataset, the progression of upper motor neuron degeneration, reflected in FA decrease, could be captured along the CST and in frontal areas. The involvement of cerebellum in the pathology of ALS, as suspected from functional MRI studies, could be confirmed by a reduced FA (culmen, declive). These structural changes correlated well with disease duration, ALSFRS-R, and physical and executive functions.
DTI detects changes that are regarded as prominent features of ALS and thus, shows promise in its function as a biomarker. Using the technique herein, we could demonstrate DTI changes at follow-up which correlated well with clinical progression.