Evidence map›Paper›PMID 25745027›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Dialysis Modalities and HDL Composition and Function.

Michael Holzer, Gernot Schilcher, Sanja Curcic, Markus Trieb, Senka Ljubojevic, Tatjana Stojakovic, Hubert Scharnagl, Chantal M Kopecky, Alexander R Rosenkranz, Akos Heinemann and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 96 citations in OpenAlex.

  1. Trial
  2. Ten tips for the first hemodialysis sessions.Clinical kidney journal · 2026
    Review
  3. Review
  4. Lifestyles, metabolome and diabetic kidney disease: a cohort study.QJM : monthly journal of the Association of Physicians · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. HDL and chronic kidney disease.Atherosclerosis plus · 2023
    Article
  20. Article

2 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Michael HolzerInstitute of Experimental and Clinical Pharmacology.
Gernot SchilcherClinical Division of Nephrology, Department of Internal Medicine.
Sanja CurcicInstitute of Experimental and Clinical Pharmacology.
Markus TriebInstitute of Experimental and Clinical Pharmacology.
Senka LjubojevicClinical Division of Cardiology, Department of Internal Medicine, and.
Tatjana StojakovicClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria; and.
Hubert ScharnaglClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria; and.
Chantal M KopeckyDepartment of Internal Medicine III, Clinical Division of Nephrology and Dialysis, Medical University of Vienna, Vienna, Austria.
Alexander R RosenkranzClinical Division of Nephrology, Department of Internal Medicine.
Akos HeinemannInstitute of Experimental and Clinical Pharmacology.
Gunther MarscheInstitute of Experimental and Clinical Pharmacology, gunther.marsche@medunigraz.at.
Medical University of Graz · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid abnormalities may have an effect on clinical outcomes of patients on dialysis. Recent studies have indicated that HDL dysfunction is a hallmark of ESRD. In this study, we compared HDL composition and metrics of HDL functionality in patients undergoing hemodialysis (HD) or peritoneal dialysis (PD) with those in healthy controls. We detected a marked suppression of several metrics of HDL functionality in patients on HD or PD. Compositional analysis revealed that HDL from both dialysis groups shifted toward a more proinflammatory phenotype with profound alterations in the lipid moiety and protein composition. With regard to function, cholesterol efflux and anti-inflammatory and antiapoptotic functions seemed to be more severely suppressed in patients on HD, whereas HDL-associated paraoxonase activity was lowest in patients on PD. Quantification of enzyme activities involved in HDL metabolism suggested that HDL particle maturation and remodeling are altered in patients on HD or PD. In summary, our study provides mechanistic insights into the formation of dysfunctional HDL in patients with ESRD who are on HD or PD.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseAgedAryldialkylphosphataseCase-Control StudiesCells, CulturedCholesterolCholesterol Ester Transfer ProteinsFemaleHumansKidney Failure, ChronicLipopolysaccharidesLipoprotein LipaseLipoproteins, HDLMacrophagesMaleMiddle Aged1-Alkyl-2-acetylglycerophosphocholine EsteraseAryldialkylphosphataseCETP protein, humanCholesterolCholesterol Ester Transfer ProteinsLipopolysaccharidesLipoprotein LipaseLipoproteins, HDLNF-kappa BPhosphatidylcholine-Sterol O-AcyltransferasePhospholipid Transfer ProteinsPLTP protein, humanTriglyceridescardiovascular diseasehemodialysislipidsperitoneal dialysis

Identifiers

PMID25745027
PMCPMC4552105
OpenAlexW2140455131

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.