Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease
Version of Record online: 15 DEC 2005
Copyright © 2005 American Neurological Association
Annals of Neurology
Volume 59, Issue 2, pages 298–309, February 2006
How to Cite
Nishioka, K., Hayashi, S., Farrer, M. J., Singleton, A. B., Yoshino, H., Imai, H., Kitami, T., Sato, K., Kuroda, R., Tomiyama, H., Mizoguchi, K., Murata, M., Toda, T., Imoto, I., Inazawa, J., Mizuno, Y. and Hattori, N. (2006), Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease. Ann Neurol., 59: 298–309. doi: 10.1002/ana.20753
- Issue online: 25 JAN 2006
- Version of Record online: 15 DEC 2005
- Manuscript Accepted: 22 OCT 2005
- Manuscript Revised: 19 OCT 2005
- Manuscript Received: 10 AUG 2005
Recently, genomic multiplications of α-synuclein gene (SNCA) have been reported to cause hereditary early-onset parkinsonism. The objective of this study was to assess the frequency of SNCA multiplications among autosomal dominant hereditary Parkinson's disease (ADPD).
We screened 113 ADPD probands and 200 sporadic PD cases by quantitative polymerase chain reaction and confirmed SNCA multiplications by flurorescence in situ hybridization (FISH) and comparative genomic hybridization array.
Two families (two patients from Family A and one from Family B) with SNCA duplication were identified among ADPD patients. Even though they had the same SNCA duplication, one patient had dementia. Because there was exactly the same difference between the regions originated from each patient, the finding suggests that the phenotype of SNCA multiplication may be also influenced by the range of duplication region. We also detected asymptomatic carriers in the families of both patients. Interestingly, the penetrance ratio was 33.3% (2/6) in one kindred, indicating that the ratio was very much lower than expected.
These two newly identified Japanese patients with SNCA duplication and the five previously identified American and European families with SNCA triplication or duplication mutations indicate that the incidence of SNCA multiplication may be more frequent than previously estimated. Ann Neurol 2006