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  • Johansson, Annica,1969Gothenburg University,Göteborgs universitet,Institutionen för klinisk neurovetenskap, Sektionen för psykiatri,Institute of Clinical Neurosciences, Section of Psychiatry (author)

Genetic association of CDC2 with cerebrospinal fluid tau in Alzheimer's disease

  • Article/chapterEnglish2005

Publisher, publication year, extent ...

  • 2005-11-17
  • S. Karger AG,2005

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/80163
  • https://gup.ub.gu.se/publication/80163URI
  • https://doi.org/10.1159/000088634DOI
  • https://lup.lub.lu.se/record/898726URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:1931802URI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • We have recently reported that a polymorphism in the cell division cycle <i>(CDC2) </i>gene, designated Ex6 + 7I/D, is associated with Alzheimer’s disease (AD). The <i>CDC2</i> gene is located on chromosome 10q21.1 close to the marker D10S1225 linked to AD. Active cdc2 accumulates in neurons containing neurofibrillary tangles (NFT), a process that can precede the formation of NFT. Therefore, <i>CDC2 </i>is a promising candidate susceptibility gene for AD. We investigated the possible effects of the <i>CDC2</i> polymorphism on cerebrospinal fluid (CSF) biomarkers in AD patients. <i>CDC2</i> genotypes were evaluated in relation to CSF protein levels of total tau, phospho-tau and β-amyloid<sub>(1–42)</sub> in AD patients and control individuals, and in relation to the amount of senile plaques and NFT in the frontal cortex and in the hippocampus in patients with autopsy-proven AD and controls. The <i>CDC2</i> Ex6 + 7I allele was associated with a gene dose-dependent increase of CSF total tau levels (F<sub>2, 626</sub> = 7.0, p = 0.001) and the homozygous <i>CDC2</i> Ex6 + 7II genotype was significantly more frequent among AD patients compared to controls (p = 0.006, OR = 1.57, 95% CI 1.13–2.17). Our results provide further evidence for an involvement of cdc2 in the pathogenesis of AD.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Zetterberg, Henrik,1973Gothenburg University,Göteborgs universitet,Institutionen för klinisk neurovetenskap, Sektionen för laborativ neurovetenskap,Institute of Clinical Neurosciences, Section of Experimental Neuroscience(Swepub:gu)xzethe (author)
  • Hampel, Harald (author)
  • Buerger, Katharina (author)
  • Prince, Jonathan A. (author)
  • Minthon, LennartLund University,Lunds universitet,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Clinical Memory Research,Lund University Research Groups(Swepub:lu)psyk-lmi (author)
  • Wahlund, Lars-OlofKarolinska Institutet (author)
  • Blennow, Kaj,1958Gothenburg University,Göteborgs universitet,Institutionen för klinisk neurovetenskap, Sektionen för laborativ neurovetenskap,Institute of Clinical Neurosciences, Section of Experimental Neuroscience(Swepub:gu)xbleka (author)
  • Göteborgs universitetInstitutionen för klinisk neurovetenskap, Sektionen för psykiatri (creator_code:org_t)

Related titles

  • In:Dementia and Geriatric Cognitive Disorders: S. Karger AG20:6, s. 367-3741420-80081421-9824

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