The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients

Masaki Ikeda, Vikram Sharma, S. Mark Sumi, Ekaterina A. Rogaeva, Parvoneh Poorkaj, Robin Sherrington, Linda Nee, Takehide Tsuda, Nobuhito Oda, Mitsunori Watanabe, Masashi Aoki, Mikio Shoji, Koji Abe, Yasuto Itoyama, Shunsaku Hirai, Gerard D. Schellenberg, Thomas D. Bird, P. H. St George-Hyslop

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Abstract

We report the clinical and neuropathologic phenotypes associated with two different missense mutations in the presenilin 1 (PS-1) gene in Japanese patients with early-onset familial Alzheimer's disease (FAD). In the AM/JPN1 pedigree a missense mutation (C→T) was found at nucleotide 1102, which is predicted to cause an alanine-to-valine missense substitution at codon 260. In this family, the disease had a mean age of onset of 40.3 years and an indolent course (range, 8-19 years). Neuropathologic studies in 3 members of this pedigree showed widespread senile plaques, neurofibrillary tangles, and neuronal loss, as well as abundant perivascular subpial amyloid deposits in the Virchow-Robin spaces and the presence of Pick-like intraneuronal inclusions in the dentate gyrus. In the second pedigree, transmitting a C→T nucleotide substitution at position 1027, leading to the missense mutation of alanine to valine at codon 285, the disease had a later onset (mean, 51 years) but a more rapid course. Comparison of the disease phenotypes associated with other missense mutations in exon 9 of PS-1 reveals no clinical or pathological phenotype, which uniquely distinguishes Alzheimer's disease associated with PS-1 mutations from other forms of early-onset FAD, implying that direct mutation screening is required to identify these cases.

Original languageEnglish
Pages (from-to)912-917
Number of pages6
JournalAnnals of Neurology
Volume40
Issue number6
DOIs
Publication statusPublished - Dec 1996
Externally publishedYes

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Presenilins
Missense Mutation
Presenilin-1
Pedigree
Phenotype
Alzheimer Disease
Amyloid Plaques
Valine
Codon
Alanine
Genes
Nucleotides
Mutation
Neurofibrillary Tangles
Songbirds
Dentate Gyrus
Age of Onset
Exons

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Ikeda, M., Sharma, V., Sumi, S. M., Rogaeva, E. A., Poorkaj, P., Sherrington, R., ... St George-Hyslop, P. H. (1996). The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. Annals of Neurology, 40(6), 912-917. https://doi.org/10.1002/ana.410400614

The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. / Ikeda, Masaki; Sharma, Vikram; Sumi, S. Mark; Rogaeva, Ekaterina A.; Poorkaj, Parvoneh; Sherrington, Robin; Nee, Linda; Tsuda, Takehide; Oda, Nobuhito; Watanabe, Mitsunori; Aoki, Masashi; Shoji, Mikio; Abe, Koji; Itoyama, Yasuto; Hirai, Shunsaku; Schellenberg, Gerard D.; Bird, Thomas D.; St George-Hyslop, P. H.

In: Annals of Neurology, Vol. 40, No. 6, 12.1996, p. 912-917.

Research output: Contribution to journalArticle

Ikeda, M, Sharma, V, Sumi, SM, Rogaeva, EA, Poorkaj, P, Sherrington, R, Nee, L, Tsuda, T, Oda, N, Watanabe, M, Aoki, M, Shoji, M, Abe, K, Itoyama, Y, Hirai, S, Schellenberg, GD, Bird, TD & St George-Hyslop, PH 1996, 'The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients', Annals of Neurology, vol. 40, no. 6, pp. 912-917. https://doi.org/10.1002/ana.410400614
Ikeda M, Sharma V, Sumi SM, Rogaeva EA, Poorkaj P, Sherrington R et al. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. Annals of Neurology. 1996 Dec;40(6):912-917. https://doi.org/10.1002/ana.410400614
Ikeda, Masaki ; Sharma, Vikram ; Sumi, S. Mark ; Rogaeva, Ekaterina A. ; Poorkaj, Parvoneh ; Sherrington, Robin ; Nee, Linda ; Tsuda, Takehide ; Oda, Nobuhito ; Watanabe, Mitsunori ; Aoki, Masashi ; Shoji, Mikio ; Abe, Koji ; Itoyama, Yasuto ; Hirai, Shunsaku ; Schellenberg, Gerard D. ; Bird, Thomas D. ; St George-Hyslop, P. H. / The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. In: Annals of Neurology. 1996 ; Vol. 40, No. 6. pp. 912-917.
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