Evidence map›Paper›PMID 32486376›Full record

ArticleDiagnostics (Basel, Switzerland)2020

Growth Plate Pathology in the Mucopolysaccharidosis Type VI Rat Model-An Experimental and Computational Approach.

Johana M Guevara-Morales, Michael Frohbergh, Hector Castro-Abril, Juan J Vaca-González, Luis A Barrera, Diego A Garzón-Alvarado, Edward Schuchman, Calogera Simonaro

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Rat models of musculoskeletal lysosomal storage disorders and their role in pre-clinical evaluation of gene therapy approaches.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
  2. Article
  3. Article
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  5. Maternal alloxan exposure induces damage in rat offspring lumbar vertebrae and protective role of arachidonic acid.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

8 authors at 5 institutions in 2 countries.

Johana M Guevara-MoralesInstitute for the Study of Inborn Errors of Metabolism, (IEIM), Pontificia Universidad, Javeriana, Bogotá 4665684, Colombia.
Michael FrohberghExponent Inc., Philadelphia, PA 19104, USA.ORCID 0000-0002-0167-116X
Hector Castro-AbrilNumerical Methods and Modeling Research Group (GNUM)-Biomimetics Laboratory, Universidad Nacional de Colombia, Bogotá 4665684, Colombia.
Juan J Vaca-GonzálezNefertiti, Wellness and New Technologies Group, School of Health and Sports Sciences, Fundación Universitaria del Área Andina, Bogotá 4665684, Colombia.
Luis A BarreraInstitute for the Study of Inborn Errors of Metabolism, (IEIM), Pontificia Universidad, Javeriana-Clinic for Inborn Errors of Metabolism (CEIM)-Hospital Universitario San Ignacio, Bogotá 4665684, Colombia.
Diego A Garzón-AlvaradoNumerical Methods and Modeling Research Group (GNUM)-Biomimetics Laboratory, Universidad Nacional de Colombia, Bogotá 4665684, Colombia.
Edward SchuchmanDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Calogera SimonaroDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Icahn School of Medicine at Mount Sinai · USPontificia Universidad Javeriana · COUniversidad Nacional de Colombia · COExponent (United States) · USFundación Universitaria del Área Andina · CO

Funding

Pontificia Universidad Javeriana 5633
6 · The paper itself

Abstract

backgroundMucopolysaccharidoses (MPS) are a group of inherited metabolic diseases caused by impaired function or absence of lysosomal enzymes involved in degradation of glycosaminoglycans. Clinically, MPS are skeletal dysplasias, characterized by cartilage abnormalities and disturbances in the process of endochondral ossification. Histologic abnormalities of growth cartilage have been reported at advanced stages of the disease, but information regarding growth plate pathology progression either in humans or in animal models, as well as its pathophysiology, is limited.

methodsHistological analyses of distal femur growth plates of wild type (WT) and mucopolysaccharidosis type VI (MPS VI) rats at different stages of development were performed, including quantitative data. Experimental findings were then analyzed in a theoretical scenario.

resultsHistological evaluation showed a progressive loss of histological architecture within the growth plate. Furthermore, in silico simulation suggest the abnormal cell distribution in the tissue may lead to alterations in biochemical gradients, which may be one of the factors contributing to the growth plate abnormalities observed, highlighting aspects that must be the focus of future experimental works.

conclusionThe results presented shed some light on the progression of growth plate alterations observed in MPS VI and evidence the potentiality of combined theoretical and experimental approaches to better understand pathological scenarios, which is a necessary step to improve the search for novel therapeutic approaches.

Indexed as

columnar arrangementgrowth plate computational modelgrowth plate histologymucopolysaccharidosis type VIskeletal dysplasia

Identifiers

PMID32486376
PMCPMC7344727
OpenAlexW3030782725

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.