| Literature DB >> 12218659 |
M Axel Wollmer1, Andreas Papassotiropoulos, Johannes R Streffer, Luigi M E Grimaldi, Elisabeth Kapaki, Giuliana Salani, George P Paraskevas, Alessia Maddalena, Dominique de Quervain, Claudia Bieber, Daniel Umbricht, Ulrike Lemke, Simone Bosshardt, Nadia Degonda, Katharina Henke, Thomas Hegi, Hans H Jung, Thomas Pasch, Christoph Hock, Roger M Nitsch.
Abstract
Tissue inhibitor of metalloproteinases 1 (TIMP-1) inhibits several proteinases including a disintegrin and metalloproteinase 10 (ADAM10), a major alpha-secretase that cleaves the beta-amyloid precursor protein within its amyloidogenic Abeta domain. The gene encoding TIMP-1 (TIMP 1) maps to the short arm of the X chromosome, in a region previously suggested as conferring genetic susceptibility for Alzheimer's disease (AD). To determine whether genetic variability of TIMP 1 contributes to the pathogenesis of AD, we analysed one single nucleotide polymorphism within TIMP 1 and one single nucleotide polymorphism in the 5'-untranslated region of TIMP 1 in patients with AD and control subjects from two independent and ethnically different populations. We did not observe any association between TIMP 1 genotypes and the diagnosis of AD in men or women. We also measured TIMP-1 protein levels in the cerebrospinal fluid of patients with AD, healthy control subjects, and patients with other neurological disorders. TIMP-1 levels were similar in all groups. In addition, no significant differences were observed after stratification for TIMP 1 genotypes. Our data show that neither genetic variability nor protein levels of TIMP-1 are associated with AD. Copyright 2002 Lippincott Williams & WilkinsEntities:
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Year: 2002 PMID: 12218659 DOI: 10.1097/00041444-200209000-00006
Source DB: PubMed Journal: Psychiatr Genet ISSN: 0955-8829 Impact factor: 2.458