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Butyrylcholinesterase K variant and cerebral amyloid angiopathy.

AbstractBACKGROUND AND PURPOSE:
Cholinesterases are found histochemically in the vessels affected with cerebral amyloid angiopathy (CAA). A gene for the K variant of butyrylcholinesterase (BCHE-K) may be associated with late-onset Alzheimer's disease (AD). In search of genetic risk factors for CAA, we investigated the association of BCHE-K with CAA.
METHODS:
The association between the severity of CAA and BCHE-K was investigated in 155 autopsy cases of the elderly, including 48 patients with AD.
RESULTS:
There was no significant association of BCHE-K with the severity of CAA in the total, AD, or non-AD cases. Status of the epsilon4 allele of apolipoprotein E gene did not influence the results.
CONCLUSIONS:
Our results may suggest that BCHE-K is not a definitive risk factor for CAA in the elderly, although further study with larger samples is necessary to confirm this.
AuthorsM Yamada, N Sodeyama, Y Itoh, N Suematsu, E Otomo, M Matsushita, H Mizusawa
JournalStroke (Stroke) Vol. 29 Issue 12 Pg. 2488-90 (Dec 1998) ISSN: 0039-2499 [Print] United States
PMID9836756 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Apolipoprotein E4
  • Apolipoproteins E
  • Isoenzymes
  • Butyrylcholinesterase
Topics
  • Aged
  • Aged, 80 and over
  • Alleles
  • Alzheimer Disease (enzymology, genetics)
  • Apolipoprotein E4
  • Apolipoproteins E (genetics)
  • Butyrylcholinesterase (genetics, metabolism)
  • Cerebral Amyloid Angiopathy (enzymology, genetics)
  • Gene Frequency
  • Genetic Variation
  • Humans
  • Isoenzymes (metabolism)
  • Middle Aged

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