J Neurol. 2012 Aug 26. [Epub ahead of print]
Fathinia P, Hermann A, Reuner U, Kassubek J, Storch A, Ludolph AC.
Source
Department of Neurology, University of Ulm, Oberer Eselsberg 45, 89081, Ulm, Germany.
Abstract
Clinical
and neuroimaging data suggest impairment of the nigrostriatal system in
amyotrophic lateral sclerosis (ALS). We thus hypothesized whether
Parkinson's disease (PD)-like midbrain sonography findings are also
present in ALS. Eighty-six patients with the diagnosis of possible or
definite ALS according to revised El Escorial criteria were examined by
transcranial B-mode sonography compared to 76 age- and gender-matched
controls and 33 PD patients. Hyperechogenic areas of the midbrain
representing the substantia nigra were measured planimetrically using
standard protocols. In subjects with sufficient temporal acoustic bone
windows, mean midbrain hyperechogenic areas were significantly higher
in ALS (0.251 ± 0.104 cm(2)) and PD patients (0.286 ± 0.078 cm(2))
compared to controls (0.091 ± 0.054 cm(2)) with no significant
difference between ALS and PD patients (one-way ANOVA: F value = 94.3;
P < 0.0001). Sixty-seven percent (95 % CI 57-78 %) of ALS patients
and 84 % (95 % CI 71-97 %) of PD patients displayed abnormal midbrain
hyperechogenic areas (P = 0.383 for group comparison, χ(2) test). No
correlations of hyperechogenic area sizes in ALS patients were found in
regard to age, gender, ALS subtype (bulbar versus spinal form) or
ALS-FRS-R score. In summary, we observed hyperechogenicity of the
substantia nigra in patients with sporadic ALS with a frequency similar
to that in PD and higher than in all other movement disorders. These
findings are important for the diagnosis and differential diagnosis of
PD and ALS alike.
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