Evidence map›Paper›PMID 29149195›Full record

ArticlePloS one2017

Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.

Jason Q Core, Mehrsa Mehrabi, Zachery R Robinson, Alexander R Ochs, Linda A McCarthy, Michael V Zaragoza, Anna Grosberg

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 1 institution in 2 countries.

Jason Q CoreDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.
Mehrsa MehrabiDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.
Zachery R RobinsonDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.
Alexander R OchsDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.
Linda A McCarthyDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.
Michael V ZaragozaPediatrics-Genetics & Genomics Division-School of Medicine, University of California, Irvine, CA, United States of America.
Anna GrosbergDepartments of Biomedical Engineering, University of California, Irvine, CA, United States of America.ORCID http://orcid.org/0000-0002-8878-0843
University of California, Irvine · US

Funding

Cardiac Functional and Structural Implications of Lamin A/C MutationsR01HL129008 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GROSBERG, ANNA, ZARAGOZA, MICHAEL V · 2015 to 2019
$2.1M
Training Program in Cardiovascular Applied Research and EntrepreneurshipT32HL116270 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUGHES, CHRISTOPHER C. W. · 2013 to 2022
$1.6M
NHLBI NIH HHS R01 HL129008NHLBI NIH HHS T32 HL116270
6 · The paper itself

Abstract

Nuclear shape defects are a distinguishing characteristic in laminopathies, cancers, and other pathologies. Correlating these defects to the symptoms, mechanisms, and progression of disease requires unbiased, quantitative, and high-throughput means of quantifying nuclear morphology. To accomplish this, we developed a method of automatically segmenting fluorescently stained nuclei in 2D microscopy images and then classifying them as normal or dysmorphic based on three geometric features of the nucleus using a package of Matlab codes. As a test case, cultured skin-fibroblast nuclei of individuals possessing LMNA splice-site mutation (c.357-2A>G), LMNA nonsense mutation (c.736 C>T, pQ246X) in exon 4, LMNA missense mutation (c.1003C>T, pR335W) in exon 6, Hutchinson-Gilford Progeria Syndrome, and no LMNA mutations were analyzed. For each cell type, the percentage of dysmorphic nuclei, and other morphological features such as average nuclear area and average eccentricity were obtained. Compared to blind observers, our procedure implemented in Matlab codes possessed similar accuracy to manual counting of dysmorphic nuclei while being significantly more consistent. The automatic quantification of nuclear defects revealed a correlation between in vitro results and age of patients for initial symptom onset. Our results demonstrate the method's utility in experimental studies of diseases affecting nuclear shape through automated, unbiased, and accurate identification of dysmorphic nuclei.

Indexed as

MutationAdultAgedAge FactorsAge of OnsetCase-Control StudiesCell NucleusExonsFemaleFibroblastsGene ExpressionHeart DiseasesHumansImage Processing, Computer-AssistedLamin Type AMaleLamin Type ALMNA protein, human

Identifiers

PMID29149195
PMCPMC5693421
OpenAlexW2768390797

What OpenQuestion holds

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LicenceCC BY
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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.