Evidence map›Paper›PMID 23985995›Full record

ArticleThe Journal of investigative dermatology2014

Anti-psoriatic therapy recovers high-density lipoprotein composition and function.

Michael Holzer, Peter Wolf, Martin Inzinger, Markus Trieb, Sanja Curcic, Lisa Pasterk, Wolfgang Weger, Akos Heinemann, Gunther Marsche

Abstract read
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  16. Oxidized Lipids and Lipoprotein Dysfunction in Psoriasis.Journal of psoriasis and psoriatic arthritis · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Michael HolzerInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Peter WolfDepartment of Dermatology, Medical University of Graz, Graz, Austria. Electronic address: peter.wolf@medunigraz.at.
Martin InzingerDepartment of Dermatology, Medical University of Graz, Graz, Austria.
Markus TriebInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Sanja CurcicInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Lisa PasterkInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Wolfgang WegerDepartment of Dermatology, Medical University of Graz, Graz, Austria.
Akos HeinemannInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.
Gunther MarscheInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria. Electronic address: gunther.marsche@medunigraz.at.

Funding

Austrian Science Fund FWF P 22976
6 · The paper itself

Abstract

Psoriasis is a chronic inflammatory disorder associated with increased cardiovascular mortality. Psoriasis affects high-density lipoprotein (HDL) composition, generating dysfunctional HDL particles. However, data regarding the impact of anti-psoriatic therapy on HDL composition and function are not available. HDL was isolated from 15 psoriatic patients at baseline and after effective topical and/or systemic anti-psoriatic therapy and from 15 age- and sex-matched healthy controls. HDL from psoriatic patients showed a significantly impaired capability to mobilize cholesterol from macrophages (6.4 vs. 8.0% [(3)H]cholesterol efflux, P<0.001), low paraoxonase (217 vs. 350 μM(-1) minute(-1) mg(-1) protein, P=0.011) and increased Lp-PLA2 activities (19.9 vs. 12.1 nM(-1) minute(-1) mg(-1) protein, P=0.028). Of particular interest, the anti-psoriatic therapy significantly improved serum lecithin-cholesterol acyltransferase activity and decreased total serum lipolytic activity but did not affect serum levels of HDL-cholesterol. Most importantly, these changes were associated with a significantly improved HDL-cholesterol efflux capability. Our results provide evidence that effective anti-psoriatic therapy recovers HDL composition and function, independent of serum HDL-cholesterol levels, and support to the emerging concept that HDL function may be a better marker of cardiovascular risk than HDL-cholesterol levels.

Indexed as

PUVA TherapyAdministration, TopicalAdultAgedAntigens, Human PlateletAryldialkylphosphataseCardiovascular DiseasesCholesterolFemaleHumansLipolysisLipoproteins, HDLMacrophagesMaleMiddle AgedPhosphatidylcholine-Sterol O-AcyltransferaseAntigens, Human PlateletAryldialkylphosphataseCholesterolhuman platelet antigen 1bLipoproteins, HDLPhosphatidylcholine-Sterol O-AcyltransferaseTritium

Identifiers

PMID23985995
PMCPMC4178282

What OpenQuestion holds

Textmetadata
LicenceTDM
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.