Absence of A673T amyloid-β precursor protein variant in alzheimer's disease and other neurological diseases

Simon Kang Seng Ting, Mei Sian Chong, Nagaendran Kandiah, Shahul Hameed, Louis Tan, Wing Lok Au, Kumar M. Prakash, Ratnagopal Pavanni, Tih Shih Lee, Jia Nee Foo, Jin Xin Bei, Xue Qing Yu, Jian Jun Liu, Yi Zhao, Wei Ling Lee, Eng King Tan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

The rare variant A673T in the amyloid-β precursor protein (APP) gene has been shown to reduce the risk of cognitive impairment. We genotyped the variant in 8721 Asian individuals comprising 552 with Alzheimer's disease and vascular dementia, 790 with Parkinson's disease, and 7379 controls. The A673T variant was absent in all of the subjects. Our finding suggests that the A673T protective variant is not relevant in our Asian population. Studies in other ethnic populations would clarify whether this variant is specific to specific races/ethnicities.

Original languageEnglish
Pages (from-to)2441.e7-2441.e8
JournalNeurobiology of Aging
Volume34
Issue number10
DOIs
Publication statusPublished - Oct 2013
Externally publishedYes

ASJC Scopus Subject Areas

  • General Neuroscience
  • Ageing
  • Developmental Biology
  • Clinical Neurology
  • Geriatrics and Gerontology

Keywords

  • A673T
  • Amyloid-beta precursor protein
  • Dementia

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