Cerebellar dentate nucleus in Alzheimer's disease with myoclonus

Citation
Y. Fukutani et al., Cerebellar dentate nucleus in Alzheimer's disease with myoclonus, DEMENT G C, 10(2), 1999, pp. 81-88
Citations number
48
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
ISSN journal
14208008 → ACNP
Volume
10
Issue
2
Year of publication
1999
Pages
81 - 88
Database
ISI
SICI code
1420-8008(199903/04)10:2<81:CDNIAD>2.0.ZU;2-R
Abstract
Although myoclonus commonly occurs in a later stage of Alzheimer's disease (AD), the pathological basis of this symptom is still unclear. In order to elucidate the neuropathological substrate of myoclonus in AD, we quantitati vely assessed neuronal density and volume, with a discrimination between sm all and large neurons, at the rostral and caudal parts in the cerebellar de ntate nucleus of 8 AD patients with myoclonus, 10 AD patients without myocl onus and 9 controls, using stereological probes. The neuronal numerical den sity of the large neurons at the rostral part and of total counts (rostral and caudal parts) in the myoclonic AD group were significantly greater than in the nonmyoclonic AD group. There were no significant differences in the density of small neurons between the two AD groups, The ratio of small neu rons to large neurons (S/L ratio) of total counts was significantly lower i n AD with myoclonus than in AD without myoclonus, The mean neuronal volume of the large neurons at the rostral part was significantly greater in myocl onic AD than in nonmyoclonic AD. Conversely, the volume of the small neuron s at the rostral part was significantly lower in myoclonic AD than in nonmy oclonic AD. This study, for the first time, shows an increase in mean volum e of large neurons and a decrease in mean volume of small neurons as well a s a change in the S/L ratio in the dentate nucleus in AD with myoclonus. An im balance in the S/L ratio as well as morphological changes of these neur ons in the dentate nucleus may contribute to the pathological substrate of myoclonus in AD.