• Title of article

    Association Study of the A2M and LRP1 Genes with Alzheimer Disease in the Han Chinese

  • Author/Authors

    Li Bian، نويسنده , , Jian Dong Yang، نويسنده , , Ting Wei Guo، نويسنده , , Yun Duan، نويسنده , , Wei Qin، نويسنده , , Ping-Yun Sun، نويسنده , , Guo Yin Feng، نويسنده , , Lin He، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2005
  • Pages
    7
  • From page
    731
  • To page
    737
  • Abstract
    Background Low-density lipoprotein receptor-related protein 1 (LRP1) and alpha-2-macroglobulin (A2M) are two plausible candidate genes for Alzheimer disease (AD) based on their important biological function and positional information. To date, numerous studies have investigated their possible association with AD but the results are controversial. Methods To investigate the potential genetic contribution of the two genes in the Han Chinese population, we performed a case-control association study using 10 polymorphisms (4 in LRP1 and 6 in A2M) that span approximately the whole corresponding gene. Results Comparison of allele, genotype, and haplotype frequencies for polymorphisms in A2M revealed no significant differences between patients and control subjects. For the LRP1 gene, however, we found an overrepresentation of the CTCG haplotype in the control group (p = .002). The difference was still of statistical significance in the apolipoprotein E (APOE) epsilon 4 negative subjects (pCTCG = .003). Multiple logistic regression analysis did not show any evidence of synergism between A2M, LRP1, and APOE. Conclusions Our results indicate that the CTCG haplotype of LRP1 may reduce the risk of late-onset AD, but A2M is not associated with this disease in the Han Chinese population.
  • Keywords
    A2M (alpha-2-macroglobulin) , Alzheimer disease , association , Haplotype , Linkage Disequilibrium , LRP1 (low-density lipoproteinreceptor-related protein 1)
  • Journal title
    Biological Psychiatry
  • Serial Year
    2005
  • Journal title
    Biological Psychiatry
  • Record number

    502824