Evidence map›Paper›PMID 31481666›Full record

ArticleScientific reports2019

Human cardiac myosin light chain 4 (MYL4) mosaic expression patterns vary by sex.

Tony Y Wang, Dan E Arking, Joseph J Maleszewski, Karen Fox-Talbot, Tim O Nieuwenhuis, Lakshmi Santhanam, Renu Virmani, Avi Z Rosenberg, Marc K Halushka

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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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 at 3 institutions in 1 country.

Tony Y WangDivision of Cardiovascular Pathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Dan E ArkingMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Joseph J MaleszewskiDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Karen Fox-TalbotDivision of Cardiovascular Pathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Tim O NieuwenhuisDivision of Cardiovascular Pathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Lakshmi SanthanamDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Renu VirmaniCVPath Institute, Gaithersburg, Maryland, USA.
Avi Z RosenbergDivision of Renal Pathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-2356-950X
Marc K HalushkaDivision of Cardiovascular Pathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. mhalush1@jhmi.edu.ORCID http://orcid.org/0000-0002-7112-7389
Johns Hopkins University · USCVPath Institute · USMayo Clinic · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Predoctoral Training Program in Human GeneticsT32GM007814 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 1985 to 2021
$10.6M
Mitochondrial DNA Copy Number and Genetic Variation in Coronary Heart DiseaseR01HL131573 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI ARKING, DAN E · 2016 to 2019
$3.2M
Fine Dissection of Atherosclerosis Microenvironment RNA ExpressionR01HL137811 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HALUSHKA, MARC K · 2017 to 2020
$2.4M
xMD-miRNA-Seq estimates cell-specific miRNA expressionR01GM130564 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI HALUSHKA, MARC K · 2018 to 2021
$1.2M
NCI NIH HHS P30 CA006973NHLBI NIH HHS R01 HL131573NHLBI NIH HHS R01 HL137811NIGMS NIH HHS R01 GM130564NIGMS NIH HHS T32 GM007814
6 · The paper itself

Abstract

Sex disparities modulate cardiac function, although the proteins and mechanisms remain to be elucidated. We recently demonstrated a mosaic pattern of protein expression in the heart for over 100 proteins. Here we investigate one of these proteins, myosin light chain 4 (MYL4), which is important for contractile functions by increasing force production. We assayed the expression pattern of MYL4 across 756 ventricular myocardial samples from 668 individuals utilizing a semi-automated Cell Profiler method on five tissue microarrays (TMAs) of cardiac tissues across a diverse set of diseases. The percentage of MYL4 positive cells was significantly higher in male subjects independently across all five TMAs, regardless of disease state (p = 8.66e-15). Higher MYL4 expression was also modestly associated with hypertrophic cardiomyopathy (p = 6.3e-04). MYL4 expression did not associate with sudden cardiac death or other cardiomyopathies. This study demonstrates a new mosaic pattern of protein expression that underlies sex disparities in the human heart.

Indexed as

AdultAgedCardiomyopathy, HypertrophicCoronary Artery DiseaseDeath, Sudden, CardiacFemaleHeart VentriclesHumansLinear ModelsMaleMiddle AgedMyocardiumMyosin Light ChainsSex FactorsTissue Array AnalysisMYL4 protein, humanMyosin Light Chains

Identifiers

PMID31481666
PMCPMC6722118
OpenAlexW2972057048

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.