Evidence map›Paper›PMID 32070676›Full record

ArticleJournal of neuroscience methods2020

Design-Based stereology and binary image histomorphometry in nerve assessment.

Daniel A Hunter, Deng Pan, Matthew D Wood, Alison K Snyder-Warwick, Amy M Moore, Eva L Feldman, Susan E Mackinnon, Michael J Brenner

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Trial
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  4. Gene therapy ameliorates neuromuscular pathology in CLN3 disease.Acta neuropathologica communications · 2025
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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.

Daniel A HunterDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine in Saint Louis, St Louis, MO, 63110, USA. Electronic address: hunterd@wustl.edu.
Deng PanDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine in Saint Louis, St Louis, MO, 63110, USA. Electronic address: pandeng@wustl.edu.
Matthew D WoodDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine in Saint Louis, St Louis, MO, 63110, USA. Electronic address: woodmd@wustl.edu.
Alison K Snyder-WarwickDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine in Saint Louis, St Louis, MO, 63110, USA. Electronic address: snydera@wustl.edu.
Amy M MooreDepartment of Plastic and Reconstructive Surgery, The Ohio State University, Wexner Medical Center, 915 Olentangy River Rd, Suite 2100, Columbus, OH, 43212, USA. Electronic address: mooream@wustl.edu.
Eva L FeldmanDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA. Electronic address: efeldman@med.umich.edu.
Susan E MackinnonDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine in Saint Louis, St Louis, MO, 63110, USA. Electronic address: mackinnons@wustl.edu.
Michael J BrennerDepartment of Otolaryngology - Head and Neck Surgery, University of Michigan, Ann Arbor, MI, 48109, USA. Electronic address: mbren@med.umich.edu.

Funding

THE ROLE OF SCHWANN CELL SENESCENCE IN PERIPHERAL NERVE REGENERATIONR01NS086773 · NINDS · WASHINGTON UNIVERSITY · PI MACKINNON, SUSAN E · 2015 to 2019
$2.1M
T cell roles in regeneration across nerve graft alternativesR01NS115960 · NINDS · WASHINGTON UNIVERSITY · PI WOOD, MATTHEW D. · 2020 to 2024
$1.8M
Mechanisms of Cochlear Oxidative Stress Injury and Strategies to Protect HearingK08DC012535 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRENNER, MICHAEL J. · 2012 to 2016
$1.2M
Investigation of Terminal Schwann Cell Function in Homeostasis and InjuryK08NS096232 · NINDS · WASHINGTON UNIVERSITY · PI SNYDER-WARWICK, ALISON K · 2017 to 2020
$717k
NIDCD NIH HHS K08 DC012535NINDS NIH HHS K08 NS096232NINDS NIH HHS R01 NS086773NINDS NIH HHS R01 NS115960
6 · The paper itself

Abstract

backgroundStereology and histomorphometry are widely used by investigators to quantify nerve characteristics in normal and pathological states, including nerve injury and regeneration. While these methods of analysis are complementary, no study to date has systematically compared both approaches in peripheral nerve. This study investigated the reliability of design-based stereology versus semi-automated binary imaging histomorphometry for assessing healthy peripheral nerve characteristics. NEW

methodStereological analysis was compared to histomorphometry with binary image analysis on uninjured sciatic nerves to determine nerve fiber number, nerve area, neural density, and fiber distribution.

resultsSciatic nerves were harvested from 6 male Lewis rats, aged 8-12 weeks for comprehensive analysis of 6 nerve specimens. From each animal, sciatic nerve specimens were fixed, stained, and sectioned for analysis by light and electron microscopy. Both histomorphometry and stereological peripheral nerve analyses were performed on all specimens by two blinded and independent investigators who quantified nerve fiber count, fiber width, density, and related distribution parameters. COMPARISON WITH EXISTING

methodsHistomorphometry and stereological analysis provided similar outcomes in nerve fiber number and total nerve area. However, the light microscopy, but not electron microscopy, stereological analysis yielded higher nerve fiber area compared to histomorphometry or manual measurement.

conclusionBoth methods measure similar fiber number and overall nerve fiber area; however, stereology with light microscopy quantified higher fiber area. Histomorphometry optimizes throughput and comprehensive analysis but requires user thresholding.

Indexed as

Nerve FibersSciatic NerveAnimalsMaleMicroscopy, ElectronNerve RegenerationRatsRats, Inbred LewReproducibility of ResultsBinary image analysisDesign-Based stereologyElectron microscopyNerve injuryNerve regenerationQuantitative histomorphometry

Identifiers

PMID32070676
PMCPMC8045463

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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.