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Search: L773:2352 8729 > (2018) > Amyloid β peptides ...

  • Toombs, J. (author)

Amyloid β peptides are differentially vulnerable to preanalytical surface exposure, an effect incompletely mitigated by the use of ratios

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-03-22
  • Wiley,2018

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/267446
  • https://gup.ub.gu.se/publication/267446URI
  • https://doi.org/10.1016/j.dadm.2018.02.005DOI

Supplementary language notes

  • Language:English

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

Notes

  • Introduction: We tested the hypothesis that the amyloid β (Aβ) peptide ratios are more stable than Aβ42 alone when biofluids are exposed to two preanalytical conditions known to modify measurable Aβ concentration. Methods: Human cerebrospinal fluid (CSF) and culture media (CM) from human cortical neurons were exposed to a series of volumes and polypropylene surfaces. Aβ42, Aβ40, and Aβ38 peptide concentrations were measured using a multiplexed electrochemiluminescence immunoassay. Data were analyzed using mixed models in R. Results: Decrease of measurable Aβ peptide concentrations was exaggerated in longer peptides, affecting the Aβ42:Aβ40 and Aβ42:Aβ38 ratios. However, the effect size of surface treatment was reduced in Aβ peptide ratios versus Aβ42 alone. For Aβ42:Aβ40, the effect was reduced by approximately 50% (volume) and 75% (transfer) as compared to Aβ42 alone. Discussion: Use of Aβ ratios, in conjunction with concentrations, may mitigate confounding factors and assist the clinical diagnostic process for Alzheimer's disease.

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

  • Foiani, M. S. (author)
  • Wellington, H. (author)
  • Paterson, R. W. (author)
  • Arber, C. (author)
  • Heslegrave, A. (author)
  • Lunn, M. P. (author)
  • Schott, J. M. (author)
  • Wray, S. (author)
  • Zetterberg, Henrik,1973Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry(Swepub:gu)xzethe (author)
  • Göteborgs universitetInstitutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi (creator_code:org_t)

Related titles

  • In:Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring: Wiley10, s. 311-3212352-8729

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