| Literature DB >> 18541377 |
Heike Kölsch1, Frank Jessen, Jens Wiltfang, Piotr Lewczuk, Martin Dichgans, Johannes Kornhuber, Lutz Frölich, Isabella Heuser, Oliver Peters, Jörg B Schulz, Sibylle G Schwab, Wolfgang Maier.
Abstract
SORL1 gene variants were described as risk factors of Alzheimer's disease (AD). We investigated the association of four SORL1 variants with CSF levels of Abeta42 and Abeta40 in 153 AD patients recruited from a multicenter study of the German Competence Net Dementias. Only one SORL1 SNP was associated with altered Abeta42 levels in the single marker analysis (SNP21: p=0.011), the other SNPs did not show an association with Abeta42 or Abeta40 CSF levels. Haplotype analysis identified a three marker SORL1 haplotype consisting of SNP19 T-allele, SNP21 G-allele and SNP23 A-allele (T/G/A) which was associated with reduced Abeta42 CSF levels in AD patients (p=0.003). Abeta40 levels were also lower in carriers of this haplotype; however, this did not reach statistical significance (p=0.15). We found a SORL1 haplotype which was associated with CSF levels of amyloid-beta cleavage products, measured as altered levels of Abeta42. Thus our data suggest that SORL1 gene variants might influence AD pathology.Entities:
Mesh：
Substances：
Year: 2008 PMID： 18541377 DOI： 10.1016/j.neulet.2008.05.049
Source DB: PubMed Journal: Neurosci Lett ISSN： 0304-3940 Impact factor: 3.046