Brain levels of thiamine and its phosphate esters in Friedreich's ataxia and spinocerebellar ataxia type 1

• Published in: Movement disorders Vol. 11; no. 4; p. 437
• Main Authors: Bettendorff, L, Mastrogiacomo, F, LaMarche, J, Dozić, S, Kish, S J
• Format: Journal Article
• Language: English
• Published: United States 01.07.1996
• Subjects: Adolescent; Adult; Cerebellar Cortex - pathology; Cerebral Cortex - pathology; Child; Child, Preschool; Female; Friedreich Ataxia - pathology; Humans; Male; Middle Aged; Reference Values; Spinocerebellar Degenerations - pathology; Thiamine - metabolism; Thiamine Monophosphate - metabolism; Thiamine Pyrophosphate - metabolism
• ISSN: 0885-3185; 1531-8257
• DOI: 10.1002/mds.870110415

Decreased blood and cerebrospinal fluid levels of thiamine have been reported in patients with spinocerebellar ataxia disorders. To determine whether a thiamine deficiency is present in the brain, we measured levels of thiamine and its phosphate esters thiamine monophosphate (TMP) and thiamine diphosphate (TDP), in postmortem cerebellar and cerebral cortices of patients with Friedreich's ataxia (FA) and spinocerebellar ataxia type 1 (SCA1). Brain levels of free (nonphosphorylated) thiamine, TMP, TDP, and total thiamine in FA and SCA1 were, on average, not significantly different from control values. However, a nonsignificant trend was observed for slightly reduced levels of TDP and total thiamine in cerebellar cortex of the SCA1 patients, a finding that might be related to the severe neuronal damage in this brain area. We conclude that in FA, brain thiamine concentrations are normal, whereas in SCA1 the levels are, at most, only slightly reduced.