Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2
- 31 August 2004
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 56 (3) , 444-447
- https://doi.org/10.1002/ana.20220
Abstract
We assessed maximal saccade velocity (MSV) in 82 spinocerebellar ataxia type 2 (SCA2) patients and 80 controls, correlating it to disease duration, polyglutamine expansion size, age at onset, ataxia score, age, and sex. Little overlap with normal values was found even at earliest stages. Stepwise linear regression analysis showed that 60‐degree MSV was strongly influenced by polyglutamine size and less by disease duration, whereas the reverse was found for ataxia score. Saccade velocity thus is a sensitive, quite specific, and objective endophenotype, useful to search polyglutamine modifier genes. Ann Neurol 2004;56:444–447Keywords
Funding Information
- Heinrich and Erna Schaufler-Stiftung in Frankfurt/Main
- Deutsch Forschungsgemeinschaft (KL782/8-1)
This publication has 18 references indexed in Scilit:
- Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell deathHuman Molecular Genetics, 2003
- Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevanceBrain, 2003
- Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar ataxia type 7.Annals of Neurology, 2001
- Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene.Archives of Neurology, 2000
- Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsiesActa Neuropathologica, 1999
- A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosisBrain, 1998
- Oculomotor testing in the differential diagnosis of degenerative ataxic disorders.Archives of Neurology, 1998
- Spinocerebellar Ataxia Type 2Archives of Neurology, 1997
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2Nature Genetics, 1996
- Autosomal dominant cerebellar ataxiaNeurology, 1990