Evidence map›Paper›PMID 30808683›Full record

ArticleJournal of lipid research2019

Plasma lipoprotein-X quantification on filipin-stained gels: monitoring recombinant LCAT treatment ex vivo.

Lita A Freeman, Robert D Shamburek, Maureen L Sampson, Edward B Neufeld, Masaki Sato, Sotirios K Karathanasis, Alan T Remaley

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 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
1.9field-weighted citation impact, top 14% 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, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. Lipid Profile Rather Than theJournal of clinical medicine · 2019
    Article
  13. Hypercholesterolemia Due to Lipoprotein X: Case Report and Thematic Review.Clinical medicine insights. Endocrinology and diabetes · 2019
    Article
  14. 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 2 institutions in 1 country.

Lita A FreemanTranslational Vascular Medicine Branch National Institutes of Health, Bethesda, MD. Electronic address: litaf@mail.nih.gov.
Robert D ShamburekCardiovascular Branch National Heart, Lung, and Blood Institute National Institutes of Health, Bethesda, MD.
Maureen L Sampsonthe NIH Clinical Center National Institutes of Health, Bethesda, MD.
Edward B NeufeldTranslational Vascular Medicine Branch National Institutes of Health, Bethesda, MD.
Masaki SatoTranslational Vascular Medicine Branch National Institutes of Health, Bethesda, MD.
Sotirios K KarathanasisCardiovascular and Metabolic Disease Section, MedImmune, Gaithersburg, MD.
Alan T RemaleyTranslational Vascular Medicine Branch National Institutes of Health, Bethesda, MD; the NIH Clinical Center National Institutes of Health, Bethesda, MD.
National Institutes of Health · USNational Institutes of Health Clinical Center · US

Funding

Development of recombinant Lecithin Cholesterol Acyltransferase as a therapeuticZIAHL006092 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI REMALEY, ALAN THOMAS · 2010 to 2021
$13.0M
6 · The paper itself

Abstract

Familial LCAT deficiency (FLD) patients accumulate lipoprotein-X (LP-X), an abnormal nephrotoxic lipoprotein enriched in free cholesterol (FC). The low neutral lipid content of LP-X limits the ability to detect it after separation by lipoprotein electrophoresis and staining with Sudan Black or other neutral lipid stains. A sensitive and accurate method for quantitating LP-X would be useful to examine the relationship between plasma LP-X and renal disease progression in FLD patients and could also serve as a biomarker for monitoring recombinant human LCAT (rhLCAT) therapy. Plasma lipoproteins were separated by agarose gel electrophoresis and cathodal migrating bands corresponding to LP-X were quantified after staining with filipin, which fluoresces with FC, but not with neutral lipids. rhLCAT was incubated with FLD plasma and lipoproteins and LP-X changes were analyzed by agarose gel electrophoresis. Filipin detects synthetic LP-X quantitatively (linearity 20-200 mg/dl FC; coefficient of variation <20%) and sensitively (lower limit of quantitation <1 mg/ml FC), enabling LP-X detection in FLD, cholestatic, and even fish-eye disease patients. rhLCAT incubation with FLD plasma ex vivo reduced LP-X dose dependently, generated HDL, and decreased lipoprotein FC content. Filipin staining after agarose gel electrophoresis sensitively detects LP-X in human plasma and accurately quantifies LP-X reduction after rhLCAT incubation ex vivo.

Indexed as

BiomarkersFilipinGelsHumansLecithin Cholesterol Acyltransferase DeficiencyLipoproteinsLipoprotein-XPhosphatidylcholine-Sterol O-AcyltransferaseRecombinant ProteinsBiomarkersFilipinGelsLipoproteinsLipoprotein-XPhosphatidylcholine-Sterol O-AcyltransferaseRecombinant Proteinscholesterolfamilial lecithin:cholesterol acyltransferase deficiencyfish-eye diseasehigh density lipoproteinkidneylecithin:cholesterol acyltransferasephospholipids

Identifiers

PMID30808683
PMCPMC6495165
OpenAlexW2916684631

What OpenQuestion holds

Textmetadata
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.