Skip to main content

Advertisement

Log in

Possible increased risk for Alzheimer's disease associated with neprilysin gene

  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Summary.

Neprilysin has recently been reported to be the major physiological Aβ-degradating enzyme. In this study we describe a new biallelic polymorphism in the 3′UTR of the neprilysin gene in a representative population sample. The *159C/C genotype was found to be associated with an increased risk for Alzheimer's disease in an age-dependent manner. Adjusting for sex and APOE status, an odds ratio of 2.74 (p < 0.05) was observed among patients under 75 years old.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received October 2, 2002; accepted December 9, 2002 Published online February 19, 2003

Acknowledgements We would like to thank A. Andrés, F. Calafell (Universitat Pompeu Fabra), and B. Cormand (Universitat de Barcelona) for useful comments and fruitful discussion. We also thank M. Vallés for technical assistance and the ACE staff for their invaluable help. This study was supported by grants from DGICT (PB98-1064, and BOS2001-0794) and by the Generalitat de Catalunya, Grup de Recerca Consolidat 2001SGR00285.

Authors' address: Dr. D. Comas, Unitat de Biologia Evolutiva, Universitat Pompeu Fabra, C/ Doctor Aiguader 80, Barcelona 08003, Catalonia, Spain, e-mail: david.comas@cexs.upf.es

Rights and permissions

Reprints and permissions

About this article

Cite this article

Clarimón, J., Muñoz, F., Boada, M. et al. Possible increased risk for Alzheimer's disease associated with neprilysin gene. J Neural Transm 110, 651–657 (2003). https://doi.org/10.1007/s00702-002-0807-3

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00702-002-0807-3

Navigation