Evidence map›Paper›PMID 23787894›Full record

ArticleNature protocols2013

Studying synapses in human brain with array tomography and electron microscopy.

Kevin R Kay, Colin Smith, Ann K Wright, Alberto Serrano-Pozo, Amy M Pooler, Robert Koffie, Mark E Bastin, Thomas H Bak, Sharon Abrahams, Katherine J Kopeikina and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature protocols, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
9.3field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Altered Molecular Composition of a Specific Subset of Prefrontal Cortical Excitatory Synapses in Schizophrenia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Synaptic resilience is associated with maintained cognition during ageing.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  17. Article
  18. Article
  19. Frontiers in neuroanatomy · 2023
    Article
  20. Review

8 more citing papers are in PubMed but not listed here.

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

15 authors at 4 institutions in 2 countries.

Kevin R KayMassachusetts General Hospital and Harvard Medical School, MassGeneral Institute for Neurodegenerative Disease, Charlestown, MA, USA.
Colin Smith
Ann K Wright
Alberto Serrano-Pozo
Amy M Pooler
Robert Koffie
Mark E Bastin
Thomas H Bak
Sharon Abrahams
Katherine J Kopeikina
Declan McGuone
Matthew P Frosch
Thomas H Gillingwater
Bradley T Hyman
Tara L Spires-Jones
University of Edinburgh · GBHarvard University · USMassachusetts General Hospital · USMaineGeneral Medical Center · US

Funding

THE ROLE OF ADVANCED CAA IN ALZHEIMER'S DEMENTIAP50AG005134 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 1985 to 2018
$42.1M
Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Sudeshna Das · 2019 to 2026
$36.5M
Neurobiology and Neuropyschology of AgingT32AG000277 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MOSS, MARK BARRY · 2001 to 2012
$2.3M
Synaptic loss and plasticity in aging and Alzheimer's diseaseR00AG033670 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI SPIRES-JONES, TARA LEIGH · 2012 to 2013
$481k
Synaptic loss and plasticity in aging and Alzheimer's diseaseK99AG033670 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI SPIRES-JONES, TARA LEIGH · 2009 to 2010
$177k
Medical Research Council G1100616Medical Research Council G110616Medical Research Council MR/L016400/1NIA NIH HHS K99 AG033670NIA NIH HHS P30 AG062421NIA NIH HHS P50 AG005134NIA NIH HHS P50AG05134NIA NIH HHS R00 AG033670NIA NIH HHS R00AG033670NIA NIH HHS T32 AG000277NIA NIH HHS T32AG000277
6 · The paper itself

Abstract

Postmortem studies of synapses in human brain are problematic because of the axial resolution limit of light microscopy and the difficulty in preserving and analyzing ultrastructure with electron microscopy (EM). Array tomography (AT) overcomes these problems by embedding autopsy tissue in resin and cutting ribbons of ultrathin serial sections. Ribbons are imaged with immunofluorescence, allowing high-throughput imaging of tens of thousands of synapses to assess synapse density and protein composition. The protocol takes ~3 d per case, excluding image analysis, which is done at the end of the study. Parallel processing for transmission electron microscopy (TEM) using a protocol modified to preserve the structure in human samples allows complementary ultrastructural studies. Incorporation of AT and TEM into brain banking is a potent way of phenotyping synapses in well-characterized clinical cohorts in order to develop clinicopathological correlations at the synapse level. This will be important for research in neurodegenerative disease, developmental disease and psychiatric illness.

Indexed as

Anatomy, Cross-SectionalAutopsyBrainHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, Electron, TransmissionSynapsesTomography

Identifiers

PMID23787894
PMCPMC3712649
OpenAlexW2090558712

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.