Evidence map›Paper›PMID 25071090›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Restoration of renal function does not correct impairment of uremic HDL properties.

Chantal Kopecky, Michael Haidinger, Ruth Birner-Grünberger, Barbara Darnhofer, Christopher C Kaltenecker, Gunther Marsche, Michael Holzer, Thomas Weichhart, Marlies Antlanger, Johannes J Kovarik and 3 more

Open access · bronzeAbstract 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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. The HDL Proteome Watch: Compilation of studies leads to new insights on HDL function.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Review
  6. High-Density Lipoproteins in Kidney Disease.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Kidney as modulator and target of "good/bad" HDL.Pediatric nephrology (Berlin, Germany) · 2019
    Review
  13. Article
  14. Deepening our understanding of HDL proteome.Expert review of proteomics · 2019
    Review
  15. Article
  16. HDL in CKD-The Devil Is in the Detail.Journal of the American Society of Nephrology : JASN · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. Review
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

13 authors at 4 institutions in 2 countries.

Chantal KopeckyDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Michael HaidingerDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Ruth Birner-GrünbergerInstitute of Pathology, Center of Medical Research, Omics Center Graz, and.
Barbara DarnhoferAustrian Center of Industrial Biotechnology, Graz, Austria.
Christopher C KalteneckerDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Gunther MarscheInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria; and.
Michael HolzerInstitute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria; and.
Thomas WeichhartInstitute of Medical Genetics, Medical University of Vienna, Vienna, Austria;
Marlies AntlangerDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Johannes J KovarikDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Johannes WerzowaDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Manfred HeckingDivision of Nephrology and Dialysis, Department of Internal Medicine III, and.
Marcus D SäemannDivision of Nephrology and Dialysis, Department of Internal Medicine III, and marcus.saemann@meduniwien.ac.at.
Medical University of Graz · ATMedical University of Vienna · ATAustrian Centre of Industrial Biotechnology (Austria) · ATBudgetary Health Care Institution of the Omsk Region "Clinical Oncology Center" · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease remains the leading cause of death in renal transplant recipients, but the underlying causative mechanisms for this important problem remain elusive. Recent work has indicated that qualitative alterations of HDL affect its functional and compositional properties in ESRD. Here, we systematically analyzed HDL from stable renal transplant recipients, according to graft function, and from patients with ESRD to determine whether structural and functional properties of HDL remain dysfunctional after renal transplantation. Cholesterol acceptor capacity and antioxidative activity, representing two key cardioprotective mechanisms of HDL, were profoundly suppressed in kidney transplant recipients independent of graft function and were comparable with levels in patients with ESRD. Using a mass spectroscopy approach, we identified specific remodeling of transplant HDL with highly enriched proteins, including α-1 microglobulin/bikunin precursor, pigment epithelium-derived factor, surfactant protein B, and serum amyloid A. In conclusion, this study demonstrates that HDL from kidney recipients is uniquely altered at the molecular and functional levels, indicating a direct pathologic role of HDL that could contribute to the substantial cardiovascular risk in the transplant population.

Indexed as

Kidney TransplantationAdultCase-Control StudiesCholesterol, HDLFemaleHomeostasisHumansKidney Failure, ChronicMaleMiddle AgedProteomicsUremiaCholesterol, HDLcardiovascular diseaseCKDdyslipidemialipidsrenal transplantation

Identifiers

PMID25071090
PMCPMC4341473
OpenAlexW2148923792

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.