Association of SORL1 gene variants with Alzheimer's disease

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Item Type:	Article
Title:	Association of SORL1 gene variants with Alzheimer's disease
Creators Name:	Koelsch, H., Jessen, F., Wiltfang, J., Lewczuk, P., Dichgans, M., Teipel, S.J., Kornhuber, J., Froelich, L., Heuser, I., Peters, O., Wiese, B., Kaduszkiewicz, H., van den Bussche, H., Huell, M., Kurz, A., Ruether, E., Henn, F.A. and Maier, W.
Abstract:	SORL1 gene variants were described as risk factor of Alzheimer's disease (AD) additionally SORL1 gene variants were associated with altered Abeta(42) CSF levels in AD patients. In the present study we investigated the association of SORL1 gene variants (rs2070045 (SNP19), SORL1-18ex26 (SNP21), rs3824968 (SNP23), rs1010159 (SNP25)) with AD risk by using Cox proportional hazard model and Kaplan-Meier survival analysis in 349 AD patients and 483 controls, recruited from a multicenter study of the German Competence Network Dementias. The SNP21G-allele and a SORL1 haplotype consisting of the SNP19 T-allele, SNP21 G-allele and SNP23 A-allele (T/G/A) were associated with increased hazard ratios and an earlier age at onset of AD (SNP21: p=0.002; T/G/A haplotype: p=0.007). This effect was most pronounced in carriers of an additional APOE4 allele (SNP21: p=0.003; T/G/A haplotype: p=0.005). In conclusion, we found SORL1 gene variants located in the 3' region of the gene to be associated with increased AD risk and an earlier age at onset of AD in our Central-European population. Thus, our data support a role of SORL1 polymorphisms in AD.
Keywords:	Alzheimer Dementia, SORL1, Association, Age at Onset
Source:	Brain Research
ISSN:	0006-8993
Publisher:	Elsevier
Volume:	1264
Page Range:	1-6
Date:	6 April 2009
Official Publication:	https://doi.org/10.1016/j.brainres.2009.01.044
PubMed:	View item in PubMed

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