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PMID: 11281447 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Lack of association between alpha2-macroglobulin polymorphisms and Alzheimer's disease.

Human genetics ·Vol. 108 ·No. 2 ·2001-02-00 ·Pages 105-8

Wang X, Luedecking EK, Minster RL, Ganguli M, DeKosky ST, Kamboh MI

Abstract

This study was undertaken to investigate the role of two alpha2-macroglobulin (A2M) polymorphisms, an intronic 5-bp deletion and Ile1000Val, in the development of Alzheimer's disease (AD) and to evaluate the interaction between the apolipoprotein E (APOE) and A2M polymorphisms. The A2M polymorphisms were screened by using polymerase-chain-reaction-based assays in 555 white late-onset AD cases and 446 controls. The gentoype distributions of the 5-bp deletion and Ile1000Val polymorphisms were comparable between cases and controls (P = 0.158 and P = 0.148, respectively). Likewise, there was no significant difference in allele frequencies of each polymorphism among cases and controls (P = 0.361 and P = 0.062, respectively). The stratification of data by APOE*4 status also did not yield any significant association. In conclusion, we observed no association between either the intronic deletion polymorphism or the Ile1000Val polymorphism of A2M and AD in our case-control cohort.

MeSH Terms
Aged Aged, 80 and over Alzheimer Disease/genetics Apolipoproteins E/genetics Female Genotype Humans Male Polymerase Chain Reaction Polymorphism, Genetic alpha-Macroglobulins/genetics
Chemicals
Apolipoproteins E alpha-Macroglobulins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wang X
Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, PA 15261, USA.
Luedecking E K
Minster R L
Ganguli M
DeKosky S T
Kamboh M I
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
2001-02-00
Pages
105-8
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
Grants
NIA NIH HHS · AG 05133 · United States
NIA NIH HHS · AG 07562 · United States
NIA NIH HHS · AG 13672 · United States
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