Evidence map›Paper›PMID 26449834›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2016

PET Imaging of Copper Trafficking in a Mouse Model of Alzheimer Disease.

Julia Baguña Torres, Erica M Andreozzi, Joel T Dunn, Muhammad Siddique, Istvan Szanda, David R Howlett, Kavitha Sunassee, Philip J Blower

Open access · bronzeAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Copper homeostasis and cuproptosis in Alzheimer's disease (Review).International journal of molecular medicine · 2025
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Teaching the chemical elements in biochemistry: Elemental biology and metallomics.Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. Retinal Vasculopathy in Alzheimer's Disease.Frontiers in neuroscience · 2021
    Review
  17. Review
  18. Review
  19. Imaging of changes in copper trafficking and redistribution in a mouse model of Niemann-Pick C disease using positron emission tomography.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2019
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Julia Baguña TorresKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
Erica M AndreozziKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
Joel T DunnKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
Muhammad SiddiqueKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
Istvan SzandaKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
David R HowlettKing's College London, Wolfson Centre for Age-Related Diseases, London, United Kingdom.
Kavitha SunasseeKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and.
Philip J BlowerKing's College London, Division of Imaging Sciences and Biomedical Engineering, St. Thomas' Hospital, London, United Kingdom; and philip.blower@kcl.ac.uk.
King's College London · GBSt Thomas' Hospital · GB

Funding

Cancer Research UK 16463Cancer Research UK A16463Wellcome Trust 084052Wellcome Trust 088641
6 · The paper itself

Abstract

unlabelledAlzheimer disease (AD) is a fatal neurodegenerative disorder characterized by progressive neuronal loss and cognitive decline. The lack of reliable and objective diagnostic markers for AD hampers early disease detection and treatment. Growing evidence supports the existence of a dysregulation in brain copper trafficking in AD. The aim of this study was to investigate brain copper trafficking in a transgenic mouse model of AD by PET imaging with (64)Cu, to determine its potential as a diagnostic biomarker of the disorder.

methodsBrain copper trafficking was evaluated in 6- to 8-mo-old TASTPM transgenic mice and age-matched wild-type controls using the (64)Cu bis(thiosemicarbazone) complex (64)Cu-GTSM (glyoxalbis(N(4)-methyl-3-thiosemicarbazonato) copper(II)), which crosses the blood-brain barrier and releases (64)Cu bioreductively into cells. Animals were intravenously injected with (64)Cu-GTSM and imaged at 0-30 min and 24-25 h after injection. The images were analyzed by atlas-based quantification and texture analysis. Regional distribution of (64)Cu in the brain 24 h after injection was also evaluated via ex vivo autoradiography and compared with amyloid-β plaque deposition in TASTPM mice.

resultsCompared with controls, in TASTPM mice PET image analysis demonstrated significantly increased (by a factor of ~1.3) brain concentration of (64)Cu at 30 min (P < 0.01) and 24 h (P < 0.05) after injection of the tracer and faster (by a factor of ~5) (64)Cu clearance from the brain (P < 0.01). Atlas-based quantification and texture analysis revealed significant differences in regional brain uptake of (64)Cu and PET image heterogeneity between the 2 groups of mice. Ex vivo autoradiography showed that regional brain distribution of (64)Cu at 24 h after injection did not correlate with amyloid-β plaque distribution in TASTPM mice.

conclusionThe trafficking of (64)Cu in the brain after administration of (64)Cu-GTSM is significantly altered by AD-like pathology in the TASTPM mouse model, suggesting that (64)Cu-GTSM PET imaging warrants clinical evaluation as a diagnostic tool for AD and possibly other neurodegenerative disorders.

Indexed as

Positron-Emission TomographyAlzheimer DiseaseAnimalsAutoradiographyBiological TransportBrainCopperCopper RadioisotopesDisease Models, AnimalMiceSolventsTissue DistributionCopperCopper RadioisotopesSolvents64CuAlzheimer’s diseasecopper traffickingpositron emission tomography

Identifiers

PMID26449834
PMCPMC6207347
OpenAlexW2227586783

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.