Evidence map›Paper›PMID 32927635›Full record

ArticleJournal of clinical medicine2020

Characterization of LP-Z Lipoprotein Particles and Quantification in Subjects with Liver Disease Using a Newly Developed NMR-Based Assay.

Shimpi Bedi, Erwin Garcia, Elias J Jeyarajah, Irina Shalaurova, Maria Camila Perez-Matos, Z Gordon Jiang, Robin P F Dullaart, Steven P Matyus, William J Kirk, James D Otvos and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  9. High plasma levels of betaine, a trimethylamine N-Oxide-related metabolite, are associated with the severity of cirrhosis.Liver international : official journal of the International Association for the Study of the Liver · 2023
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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

12 authors at 3 institutions in 2 countries.

Shimpi BediCenter for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237-0507, USA.ORCID 0000-0003-3277-7845
Erwin GarciaLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.ORCID 0000-0002-2956-2715
Elias J JeyarajahLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.
Irina ShalaurovaLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.
Maria Camila Perez-MatosDivision of Gastroenterology & Hepatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Z Gordon JiangDivision of Gastroenterology & Hepatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Robin P F DullaartDepartment of Endocrinology, University of Groningen, University Medical Center Groningen, 9713 Groningen, The Netherlands.
Steven P MatyusLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.
William J KirkLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.
James D OtvosLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.
W Sean DavidsonCenter for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237-0507, USA.
Margery A ConnellyLaboratory Corporation of America Holdings (LabCorp), Burlington, NC 27560, USA.ORCID 0000-0002-3917-592X
Beth Israel Deaconess Medical Center · USUniversity of Cincinnati · USUniversity Medical Center Groningen · NL

Funding

Adenosine deaminase 2 regulates macrophage phenotype and liver fibrosis in nonalcoholic fatty liver diseaseK08DK115883 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI JIANG, ZHENGHUI GORDON · 2018 to 2022
$839k
Gilead Liver Scholar grant from Gilead Science No numbermerican Association for the Study of Liver Diseases Alan Hoffman Clinical and Translational Research grant No numberNIDDK NIH HHS K08 DK115883NIH HHS K08DK115883NIH HHS R01HL104136NIH HHS R01HL67093
6 · The paper itself

Abstract

backgroundLipoprotein particles with abnormal compositions, such as lipoprotein X (LP-X) and lipoprotein Z (LP-Z), have been described in cases of obstructive jaundice and cholestasis. The study objectives were to: (1) develop an NMR-based assay for quantification of plasma/serum LP-Z particles, (2) evaluate the assay performance, (3) isolate LP-Z particles and characterize them by lipidomic and proteomic analysis, and (4) quantify LP-Z in subjects with various liver diseases.

methodsAssay performance was assessed for linearity, sensitivity, and precision. Mass spectroscopy was used to characterize the protein and lipid content of isolated LP-Z particles.

resultsThe assay showed good linearity and precision (2.5-6.3%). Lipid analyses revealed that LP-Z particles exhibit lower cholesteryl esters and higher free cholesterol, bile acids, acylcarnitines, diacylglycerides, dihexosylceramides, lysophosphatidylcholines, phosphatidylcholines, triacylglycerides, and fatty acids than low-density lipoprotein (LDL) particles. A proteomic analysis revealed that LP-Z have one copy of apolipoprotein B per particle such as LDL, but less apolipoprotein (apo)A-I, apoC3, apoA-IV and apoC2 and more complement C3. LP-Z were not detected in healthy volunteers or subjects with primary biliary cholangitis, primary sclerosing cholangitis, autoimmune hepatitis, or type 2 diabetes. LP-Z were detected in some, but not all, subjects with hypertriglyceridemia, and were high in some subjects with alcoholic liver disease.

conclusionsLP-Z differ significantly in their lipid and protein content from LDL. Further studies are needed to fully understand the pathophysiological reason for the enhanced presence of LP-Z particles in patients with cholestasis and alcoholic liver disease.

Indexed as

cholestasislipoproteinsliver diseasenuclear magnetic resonance spectroscopy

Identifiers

PMID32927635
PMCPMC7564541
OpenAlexW3083844534

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.