inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of...
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Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic
heterogeneity
by Simon Mead, Mark Poulter, Jon Beck, Thomas E. F. Webb, Tracy A. Campbell, Jacqueline M. Linehan, Melanie Desbruslais, Susan Joiner, Jonathan D. F.
Wadsworth, Andrew King, Peter Lantos, and John Collinge
BrainVolume 129(9):2297-2317
August 21, 2006
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Linked microsatellite haplotypes on chromosome 20.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
The UK 6-OPRI prion disease pedigree The smaller pedigree 2 shares the same microsatellite and SNP haplotype background as the larger pedigree.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
(A) Cumulative age of onset and age at death curves; (B) cumulative age of onset curves for the two genotypes at codon 129.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
(A) Age at onset and (B) age at death histograms with curves modelling the data assuming a normal distribution.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Of historical interest is an autopsy report of an individual in the pedigree (III.5) who was admitted in 1897 and died in 1901.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
MRI appearances of 6-OPRI prion disease These show cerebral and cerebellar atrophy (A) Coronal T1 at the level of the hippocampus, (B) Axial T2 at the level of the basal ganglia and (C)
Sagittal T1 (all from patient VII.20).
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Neuropathology from two autopsy cases of 6-OPRI prion disease.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Pearson correlation of age of onset versus duration of disease.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Kaplan–Meier survival curves.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Molecular PrPSc typing in 6-OPRI prion disease (A) Immunoblot with anti-PrP monoclonal antibody 3F4.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]
Heritability of age of onset.
Simon Mead et al. Brain 2006;129:2297-2317
© The Author (2006). Published by Oxford University Press. All rights reserved. For Permissions, please email: [email protected]