Evidence map›Paper›PMID 35453521›Full record

ArticleBiomedicines2022

Determination of Serum Progranulin in Patients with Untreated Familial Hypercholesterolemia.

Bíborka Nádró, Hajnalka Lőrincz, Lilla Juhász, Anita Szentpéteri, Ferenc Sztanek, Éva Varga, Dénes Páll, György Paragh, Mariann Harangi

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. 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

9 authors at 2 institutions in 1 country.

Bíborka NádróDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Hajnalka LőrinczDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Lilla JuhászDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Anita SzentpéteriDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Ferenc SztanekDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Éva VargaDepartment of Internal Medicine and Hematology, Semmelweis University, 1088 Budapest, Hungary.
Dénes PállDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
György ParaghDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Mariann HarangiDepartment of Internal Medicine, Division of Metabolic Disorders, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-9761-9595
University of Debrecen · HUSemmelweis University · HU

Funding

Faculty of Medicine, University of Debrecen Bridging Fund to M.H.GINOP GINOP-2.3.2-15-2016-00062National Research, Development and Innovation Office (NKFIH) K115723
6 · The paper itself

Abstract

backgroundFamilial hypercholesterolemia (FH) is an autosomal dominant trait characterized by elevated LDL-C concentrations and is associated with an increased risk of premature atherosclerosis. Progranulin (PGRN) is a multifunctional protein that is known to have various anti-atherogenic effects. To date, the use of serum PGRN in patients with FH has not been studied.

methodsIn total, 81 untreated patients with heterozygous FH (HeFH) and 32 healthy control subjects were included in this study. Serum PGRN, sICAM-1, sVCAM-1, oxLDL and TNFα concentrations were determined by ELISA. Lipoprotein subfractions were detected by Lipoprint. We diagnosed FH using the Dutch Lipid Clinic Network criteria.

resultsWe could not find a significant difference between the PGRN concentrations of the HeFH patients and controls (37.66 ± 9.75 vs. 38.43 ± 7.74 ng/mL, ns.). We found significant positive correlations between triglyceride, TNFα, sVCAM-1, the ratio of small HDL subfraction and PGRN, while significant negative correlations were found between the ratio of large HDL subfraction and PGRN both in the whole study population and in FH patients. PGRN was predicted by sVCAM-1, logTNFα and the ratio of small HDL subfraction.

conclusionsThe strong correlations between HDL subfractions, inflammatory markers and PGRN suggest that PGRN may exert its anti-atherogenic effect in HeFH through the alteration of HDL composition and the amelioration of inflammation rather than through decreasing oxidative stress.

Indexed as

familial hypercholesterolemiahigh-density lipoprotein subfractioninflammationprogranulintumor necrosis factor alpha

Identifiers

PMID35453521
PMCPMC9032136
OpenAlexW4220717195

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.