Evidence map›Paper›PMID 25781943›Full record

ArticlePloS one2015

Improving reconstituted HDL composition for efficient post-ischemic reduction of ischemia reperfusion injury.

Marie-Claude Brulhart-Meynet, Vincent Braunersreuther, Jonas Brinck, Fabrizio Montecucco, Jean-Christophe Prost, Aurelien Thomas, Katia Galan, Graziano Pelli, Sarah Pedretti, Nicolas Vuilleumier and 4 more

Abstract read
In one paragraph

Article in PloS one, 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
–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

27 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. HDL Composition, Heart Failure, and Its Comorbidities.Frontiers in cardiovascular medicine · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. Advances in HDL: Much More than Lipid Transporters.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Quality Versus Quantity: Making HDL Great Again.Arteriosclerosis, thrombosis, and vascular biology · 2017
    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

14 authors.

Marie-Claude Brulhart-MeynetService of Endocrinology, Diabetology, Hypertension and Nutrition, Department of Internal Medicine, Faculty of Medicine, Geneva, Switzerland.
Vincent BraunersreutherDivision of Cardiology, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland; Service of Laboratory Medicine, Department of Genetics and Laboratory Medicine, Geneva University Hospital, Geneva, Switzerland.
Jonas BrinckService of Endocrinology, Diabetology, Hypertension and Nutrition, Department of Internal Medicine, Faculty of Medicine, Geneva, Switzerland.
Fabrizio MontecuccoDivision of Cardiology, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland; Service of Laboratory Medicine, Department of Genetics and Laboratory Medicine, Geneva University Hospital, Geneva, Switzerland; Department of human protein sciences, Geneva University Hospital, Geneva, Switzerland; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa School of Medicine. IRCCS Azienda Ospedaliera Universitaria San Martino-IST Instituto Nazionale per la Ricerca sul Cancro, Genoa, Italy.
Jean-Christophe ProstUnit of Toxicology, CURML, University of Lausanne, Lausanne, Switzerland.
Aurelien ThomasUnit of Toxicology, CURML, University of Lausanne, Lausanne, Switzerland.
Katia GalanDivision of Cardiology, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland.
Graziano PelliDivision of Cardiology, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland.
Sarah PedrettiHatter Institute for Cardiovascular Research in Africa, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.
Nicolas VuilleumierService of Laboratory Medicine, Department of Genetics and Laboratory Medicine, Geneva University Hospital, Geneva, Switzerland; Department of human protein sciences, Geneva University Hospital, Geneva, Switzerland.
François MachDivision of Cardiology, Department of Internal Medicine, Geneva University Hospital, Geneva, Switzerland.
Sandrine LecourHatter Institute for Cardiovascular Research in Africa, Faculty of Health Science, University of Cape Town, Cape Town, South Africa.
Richard W JamesService of Endocrinology, Diabetology, Hypertension and Nutrition, Department of Internal Medicine, Faculty of Medicine, Geneva, Switzerland.
Miguel A FriasService of Endocrinology, Diabetology, Hypertension and Nutrition, Department of Internal Medicine, Faculty of Medicine, Geneva, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNew evidence shows that high density lipoproteins (HDL) have protective effects beyond their role in reverse cholesterol transport. Reconstituted HDL (rHDL) offer an attractive means of clinically exploiting these novel effects including cardioprotection against ischemia reperfusion injury (IRI). However, basic rHDL composition is limited to apolipoprotein AI (apoAI) and phospholipids; addition of bioactive compound may enhance its beneficial effects.

objectiveThe aim of this study was to investigate the role of rHDL in post-ischemic model, and to analyze the potential impact of sphingosine-1-phosphate (S1P) in rHDL formulations. METHODS AND

resultsThe impact of HDL on IRI was investigated using complementary in vivo, ex vivo and in vitro IRI models. Acute post-ischemic treatment with native HDL significantly reduced infarct size and cell death in the ex vivo, isolated heart (Langendorff) model and the in vivo model (-48%, p<0.01). Treatment with rHDL of basic formulation (apoAI + phospholipids) had a non-significant impact on cell death in vitro and on the infarct size ex vivo and in vivo. In contrast, rHDL containing S1P had a highly significant, protective influence ex vivo, and in vivo (-50%, p<0.01). This impact was comparable with the effects observed with native HDL. Pro-survival signaling proteins, Akt, STAT3 and ERK1/2 were similarly activated by HDL and rHDL containing S1P both in vitro (isolated cardiomyocytes) and in vivo.

conclusionHDL afford protection against IRI in a clinically relevant model (post-ischemia). rHDL is significantly protective if supplemented with S1P. The protective impact of HDL appears to target directly the cardiomyocyte.

Indexed as

AnimalsApolipoprotein A-ICells, CulturedLipoproteins, HDLLysophospholipidsMaleMiceMice, Inbred C57BLMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myocardial Reperfusion InjuryMyocytes, CardiacProto-Oncogene Proteins c-aktRatsRats, WistarSphingosineApolipoprotein A-ILipoproteins, HDLLysophospholipidsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Proto-Oncogene Proteins c-aktSphingosinesphingosine 1-phosphateSTAT3 Transcription Factor

Identifiers

PMID25781943
PMCPMC4362758

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Registered trials

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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.