Cited by 17

The DOI matches its Crossref record.

Genetic Deficiency of Plasma Lipoprotein-Associated Phospholipase A2 (PLA2G7 V297F Null Mutation) and Risk of Alzheimer's Disease in Japan

Koshy, Beena, Miyashita, Akinori, St. Jean, Pamela, Stirnadel, Heide, Kaise, Toshihiko, Rubio, Justin P., Mooser, Vincent, Kuwano, Ryozo, Irizarry, Michael C.·2010·Journal of Alzheimer's Disease

Abstract

High plasma lipoprotein phospholipase A2 activity (Lp-PLA2) is reported to be a risk factor for dementia. A loss of function polymorphism in the Lp-PLA2 gene - PLA2G7 V279F - is found almost exclusively in Asians. In 1,952 subjects with late-onset AD and 2,079 non-demented controls recruited from Japan, the PLA2G7 null allele was not associated with risk or age at onset of AD: logistic regression OR 0.98 (95% CI 0.86-1.12, p=0.81) per additional null allele, adjusted for age/age at onset, gender, and APOE ε4. Genetic deficiency of Lp-PLA2 activity is not associated with a reduced risk of AD in the Japanese population.

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Crossref · 10.3233/jad-2010-100513

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Authors
Koshy, B., Miyashita, A., St. Jean, P., Stirnadel, H., Kaise, T., Rubio, J. P., Mooser, V., Kuwano, R., & Irizarry, M. C.
Affiliations
  • Genetics, GlaxoSmithKline, Research Triangle Park, NC, USA
  • Department of Molecular Genetics, Bioresource Science Branch, Center for Bioresources, Brain Research Institute, Niigata University, Niigata, Japan
  • WW Epidemiology, GlaxoSmithKline, Research Triangle Park, NC, USA
  • Epidemiology, GlaxoSmithKline, Tokyo, Japan
Venue
Journal of Alzheimer's Disease
Published
2010-09-02
Volume
21
Issue
3
Pages
775-780
ISSN
  • 1875-8908
  • 1387-2877
Cited by
17
References
0

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