Evidence map›Paper›PMID 33410136›Full record

ArticleThe Journal of comparative neurology2021

Astrocyte regional heterogeneity revealed through machine learning-based glial neuroanatomical assays.

Jessica Blackburn, Michele Joana Alves, Mehmet Tahir Aslan, Lokman Cevik, Jing Zhao, Catherine M Czeisler, José Javier Otero

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2021. 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
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

7 authors at 1 institution in 1 country.

Jessica BlackburnDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Michele Joana AlvesDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Mehmet Tahir AslanDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Lokman CevikDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Jing ZhaoDepartment of Biomedical Informatics, The Ohio State University College of Medicine, Columbus, OH, USA.
Catherine M CzeislerDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.
José Javier OteroDepartment of Pathology, Division of Neuropathology, The Ohio State University College of Medicine, Columbus, OH, USA.ORCID 0000-0003-0680-4520
The Ohio State University · US

Funding

Mechanisms of Congenital HypoventilationR01HL132355 · NHLBI · OHIO STATE UNIVERSITY · PI CZEISLER, CATHERINE, OTERO, JOSE JAVIER · 2016 to 2020
$2.5M
NHLBI NIH HHS R01 HL132355
6 · The paper itself

Abstract

Evaluation of reactive astrogliosis by neuroanatomical assays represents a common experimental outcome for neuroanatomists. The literature demonstrates several conflicting results as to the accuracy of such measures. We posited that the diverging results within the neuroanatomy literature were due to suboptimal analytical workflows in addition to astrocyte regional heterogeneity. We therefore generated an automated segmentation workflow to extract features of glial fibrillary acidic protein (GFAP) and aldehyde dehydrogenase family 1, member L1 (ALDH1L1) labeled astrocytes with and without neuroinflammation. We achieved this by capturing multiplexed immunofluorescent confocal images of mouse brains treated with either vehicle or lipopolysaccharide (LPS) followed by implementation of our workflows. Using classical image analysis techniques focused on pixel intensity only, we were unable to identify differences between vehicle-treated and LPS-treated animals. However, when utilizing machine learning-based algorithms, we were able to (1) accurately predict which objects were derived from GFAP or ALDH1L1-stained images indicating that GFAP and ALDH1L1 highlight distinct morphological aspects of astrocytes, (2) we could predict which neuroanatomical region the segmented GFAP or ALDH1L1 object had been derived from, indicating that morphological features of astrocytes change as a function of neuroanatomical location. (3) We discovered a statistically significant, albeit not highly accurate, prediction of which objects had come from LPS versus vehicle-treated animals, indicating that although features exist capable of distinguishing LPS-treated versus vehicle-treated GFAP and ALDH1L1-segmented objects, that significant overlap between morphologies exists. We further determined that for most classification scenarios, nonlinear models were required for improved treatment class designations. We propose that unbiased automated image analysis techniques coupled with well-validated machine learning tools represent highly useful models capable of providing insights into neuroanatomical assays.

Indexed as

AstrocytesMachine LearningAnimalsFluorescent Antibody TechniqueGliosisImage Processing, Computer-AssistedMiceMicroscopy, Confocalastrocyteclustering analysisgliosismachine learningneuroanatomyneuroinflammation

Identifiers

PMID33410136
PMCPMC8113076
OpenAlexW3119860444

What OpenQuestion holds

Textmetadata
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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.