Evidence map›Paper›PMID 37384330›Full record

ArticleFree neuropathology2023

Postmortem changes in brain cell structure: a review.

Margaret M Krassner, Justin Kauffman, Allison Sowa, Katarzyna Cialowicz, Samantha Walsh, Kurt Farrell, John F Crary, Andrew T McKenzie

Open access · greenAbstract read
In one paragraph

Article in Free neuropathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  11. Effects of Postmortem Intervals on Quantitative MRI in Unfixed and Fixed Swine Brain: Implications for Ex Vivo MRI Applications.Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine · 2026
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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 3 institutions in 1 country.

Margaret M KrassnerDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Justin KauffmanDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Allison SowaMicroscopy and Advanced Bioimaging Core, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Katarzyna CialowiczMicroscopy and Advanced Bioimaging Core, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Samantha WalshHunter College Libraries, CUNY Hunter College, New York, NY.
Kurt FarrellDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
John F CraryDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Andrew T McKenzieDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Allen Institute for Brain Science · USIcahn School of Medicine at Mount Sinai · USHunter College · US

Funding

Research Education ComponentP30AG066514 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Carolyn Wei Zhu · 2020 to 2026
$31.0M
NIA NIH HHS P30 AG066514
6 · The paper itself

Abstract

Brain cell structure is a key determinant of neural function that is frequently altered in neurobiological disorders. Following the global loss of blood flow to the brain that initiates the postmortem interval (PMI), cells rapidly become depleted of energy and begin to decompose. To ensure that our methods for studying the brain using autopsy tissue are robust and reproducible, there is a critical need to delineate the expected changes in brain cell morphometry during the PMI. We searched multiple databases to identify studies measuring the effects of PMI on the morphometry (i.e. external dimensions) of brain cells. We screened 2119 abstracts, 361 full texts, and included 172 studies. Mechanistically, fluid shifts causing cell volume alterations and vacuolization are an early event in the PMI, while the loss of the ability to visualize cell membranes altogether is a later event. Decomposition rates are highly heterogenous and depend on the methods for visualization, the structural feature of interest, and modifying variables such as the storage temperature or the species. Geometrically, deformations of cell membranes are common early events that initiate within minutes. On the other hand, topological relationships between cellular features appear to remain intact for more extended periods. Taken together, there is an uncertain period of time, usually ranging from several hours to several days, over which cell membrane structure is progressively lost. This review may be helpful for investigators studying human postmortem brain tissue, wherein the PMI is an unavoidable aspect of the research.

Indexed as

AutolysisBrain mappingOncotic necrosisPostmortem changesSpecies differencesStaining methods

Identifiers

PMID37384330
PMCPMC10294569
OpenAlexW4382502498

What OpenQuestion holds

Textmetadata
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.