Evidence map›Paper›PMID 31920567›Full record

ArticleFrontiers in neuroanatomy2019

Automated Individualization of Size-Varying and Touching Neurons in Macaque Cerebral Microscopic Images.

Zhenzhen You, Yaël Balbastre, Clément Bouvier, Anne-Sophie Hérard, Pauline Gipchtein, Philippe Hantraye, Caroline Jan, Nicolas Souedet, Thierry Delzescaux

Abstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

9 authors.

Zhenzhen YouCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Yaël BalbastreCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Clément BouvierCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Anne-Sophie HérardCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Pauline GipchteinCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Philippe HantrayeCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Caroline JanCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Nicolas SouedetCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.
Thierry DelzescauxCEA-CNRS-UMR 9199, Laboratoire des Maladies Neurodégénératives, MIRCen, Université Paris-Saclay, Fontenay-aux-Roses, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In biomedical research, cell analysis is important to assess physiological and pathophysiological information. Virtual microscopy offers the unique possibility to study the compositions of tissues at a cellular scale. However, images acquired at such high spatial resolution are massive, contain complex information, and are therefore difficult to analyze automatically. In this article, we address the problem of individualization of size-varying and touching neurons in optical microscopy two-dimensional (2-D) images. Our approach is based on a series of processing steps that incorporate increasingly more information. (1) After a step of segmentation of neuron class using a Random Forest classifier, a novel min-max filter is used to enhance neurons' centroids and boundaries, enabling the use of region growing process based on a contour-based model to drive it to neuron boundary and achieve individualization of touching neurons. (2) Taking into account size-varying neurons, an adaptive multiscale procedure aiming at individualizing touching neurons is proposed. This protocol was evaluated in 17 major anatomical regions from three NeuN-stained macaque brain sections presenting diverse and comprehensive neuron densities. Qualitative and quantitative analyses demonstrate that the proposed method provides satisfactory results in most regions (e.g., caudate, cortex, subiculum, and putamen) and outperforms a baseline Watershed algorithm. Neuron counts obtained with our method show high correlation with an adapted stereology technique performed by two experts (respectively, 0.983 and 0.975 for the two experts). Neuron diameters obtained with our method ranged between 2 and 28.6 μm, matching values reported in the literature. Further works will aim to evaluate the impact of staining and interindividual variability on our protocol.

Indexed as

macaque brainmicroscopic imagesneuron individualizationsize-varying neuronstouching neurons

Identifiers

PMID31920567
PMCPMC6929681

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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.