Evidence map›Paper›PMID 31632171›Full record

ArticleClinical medicine insights. Endocrinology and diabetes2019

Hypercholesterolemia Due to Lipoprotein X: Case Report and Thematic Review.

Laura Kattah, Andrés Gómez, Sebastián Gutiérrez, Kathalina Puerto, Eiman D Moreno-Pallares, Andrés Jaramillo, Carlos O Mendivil

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical medicine insights. Endocrinology and diabetes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Lipidome remodeling in primary biliary cholangitis.Lipids in health and disease · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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 3 institutions in 1 country.

Laura KattahEndocrinology Section, Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Andrés GómezDivision of Gastroenterology, Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Sebastián GutiérrezSchool of Medicine, Universidad de los Andes, Bogotá, Colombia.
Kathalina PuertoSchool of Medicine, Universidad de los Andes, Bogotá, Colombia.
Eiman D Moreno-PallaresDepartment of Internal Medicine, Universidad de Cartagena, Cartagena, Colombia.
Andrés JaramilloEndocrinology Section, Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Carlos O MendivilEndocrinology Section, Fundación Santa Fe de Bogotá, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-5546-4206
Fundación Santa Fe de Bogotá · COUniversidad de Los Andes · COUniversity of Cartagena · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver is a key organ in lipid and lipoprotein metabolism, hence hepatic diseases often manifest as lipid disturbances. Cholestatic liver diseases are frequently associated with an important increase in total cholesterol at the expense of lipoprotein X (LpX), an abnormal lipoprotein isolated and characterized in the 1960s to 1970s in patients with obstructive jaundice. Lipoprotein X is rich in phospholipids, albumin, and free cholesterol, has a density similar to low-density lipoprotein (LDL), and a size similar to very low-density lipoprotein (VLDL), which has hampered its detection through routine laboratory tests. Unlike LDL, LpX has no apoB-100, so it is not removed from circulation via the LDL receptor, and it is not clear whether or not it can be atherogenic. Although LpX was initially described in patients with cholestasis, it has also been found in patients with genetic deficiency of lecithin-cholesterol acyltransferase (LCAT), in patients who receive lipid-rich parenteral nutrition and most recently in patients with graft versus host disease of the liver. In the presence of LpX, plasma total cholesterol can rise up to 1000 mg/dL, which may lead to the development of skin xanthomas and hyperviscosity syndrome. Treatment of LpX-dependent hypercholesterolemia with conventional hypolipidemic drugs is frequently ineffective, and definitive treatment relies on correction of the underlying cause of cholestasis. Here, we present the case of a patient with LpX-dependent hypercholesterolemia in the context of primary biliary cholangitis.

Indexed as

apoBCholestasisgraft-versus-host diseasehypercholesterolemiajaundicelipoprotein X

Identifiers

PMID31632171
PMCPMC6769215
OpenAlexW2977676370

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.