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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Neuropsychobiologyarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Neuropsychobiology
Article . 2004 . Peer-reviewed
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Association Analysis of Brain-Derived Neurotrophic Factor Val66Met Polymorphisms with Alzheimer’s Disease and Age of Onset

Authors: Hsiu-Chih Liu; Li-En Hsu; Tsung-Yun Liu; Shih-Jen Tsai; Chen-Jee Hong; Ching-Hua Lin;

Association Analysis of Brain-Derived Neurotrophic Factor Val66Met Polymorphisms with Alzheimer’s Disease and Age of Onset

Abstract

Because of a decrease in central brain-derived neurotrophic factor (BDNF) levels in Alzheimer’s disease (AD) and the important role of BDNF in neuronal survival, <i>BDNF</i> may represent a candidate gene conferring susceptibility to AD. Recently, a functional <i>BDNF</i> Val66Met polymorphism has been associated with AD in an Italian population. In the present study, we investigated a possible role of this <i>BDNF</i> polymorphism in the susceptibility of AD or AD onset in a Chinese population. Comparing AD patients and controls, the distribution of the <i>BDNF</i> genotypes and alleles did not differ significantly. The onset age was not significantly different comparing the three <i>BDNF</i> genotype groups. Our negative findings suggest that it is unlikely that the <i>BDNF</i> Val66Met polymorphism plays a major role in the pathogenesis of AD in the Chinese population and do not support previous findings that homozygosity for the 66Val allele confers an increased risk for AD. Further studies with genetic variations in <i>BDNF</i> relating either to AD-associated depression or to the AD treatment response are suggested.

Keywords

Male, Polymorphism, Genetic, Brain-Derived Neurotrophic Factor, DNA Mutational Analysis, Valine, Methionine, Gene Frequency, Alzheimer Disease, Case-Control Studies, Humans, Female, Age of Onset, Alleles, Aged

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
77
Top 10%
Top 10%
Top 10%