Evidence map›Paper›PMID 31337804›Full record

ArticleScientific reports2019

Citrate anion improves chronic dialysis efficacy, reduces systemic inflammation and prevents Chemerin-mediated microvascular injury.

Sergio Dellepiane, Davide Medica, Cesare Guarena, Tiziana Musso, Alessandro Domenico Quercia, Gianluca Leonardi, Marita Marengo, Massimiliano Migliori, Vincenzo Panichi, Luigi Biancone and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. High-flux hemodialysis with polymethylmethacrylate membranes reduces soluble CD40L, a mediator of cardiovascular disease in uremia.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Trial
  3. The effect of citrate in cardiovascular system and clot circuit in critically ill patients requiring continuous renal replacement therapy.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2023
    Trial
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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  15. Article
  16. Chemerin as a Driver of Hypertension: A Consideration.American journal of hypertension · 2020
    Review
  17. 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

13 authors at 3 institutions in 1 country.

Sergio DellepianeNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Davide MedicaNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Cesare GuarenaNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Tiziana MussoMicrobiology and Virology Unit, Department of Pathology, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Alessandro Domenico QuerciaNephrology and Kidney Transplantation Unit, Department of Translational Medicine and Center for Autoimmune and Allergic Diseases (CAAD), University of Piemonte Orientale (UPO), "Maggiore della Carità" University Hospital, Novara, Italy.
Gianluca LeonardiNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Marita MarengoNephrology and Dialysis Unit, ASLCN1, Cuneo, Italy.
Massimiliano MiglioriNephrology and Dialysis Unit, "Versilia Hospital", Camaiore, LU, Italy.
Vincenzo PanichiNephrology and Dialysis Unit, "Versilia Hospital", Camaiore, LU, Italy.
Luigi BianconeNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Francesco PizzarelliNephrology and Dialysis Unit, SM Annunziata Hospital, Florence, Italy.
Giovanni CamussiNephrology, Dialysis and Kidney Transplantation Unit, Department of Medical Sciences, University of Torino, "Città della Salute e della Scienza" University Hospital, Torino, Italy.
Vincenzo CantaluppiNephrology and Kidney Transplantation Unit, Department of Translational Medicine and Center for Autoimmune and Allergic Diseases (CAAD), University of Piemonte Orientale (UPO), "Maggiore della Carità" University Hospital, Novara, Italy. vincenzo.cantaluppi@med.uniupo.it.
Ospedale Versilia · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITOspedale SS. Annunziata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic inflammation and uremic toxins (UT) determine the increased cardiovascular mortality observed in chronic hemodialysis (HD) patients. Among UT, the adipokine Chemerin induces vascular dysfunction by targeting both endothelial and vascular smooth muscular cells (EC and VSMC). As Citrate anion modulates oxidative metabolism, systemic inflammation and vascular function, we evaluated whether citrate-buffered dialysis improves HD efficiency, inflammatory parameters and chemerin-mediated microvascular injury. 45 patients were treated in sequence with acetate, citrate and, again, acetate-buffered dialysis solution (3 months per interval). At study admission and after each treatment switch, we evaluated dialysis efficacy and circulating levels of chemerin and different inflammatory biomarkers. In vitro, we stimulated EC and VSMC with patients' plasma and we investigated the role of chemerin as UT. Citrate dialysis increased HD efficacy and reduced plasma levels of CRP, fibrinogen, IL6 and chemerin. In vitro, patients' plasma induced EC and VSMC dysfunction. These effects were reduced by citrate-buffered solutions and paralleled by the decrease of chemerin levels. Consistently, chemerin receptor knockdown reduced EC and VSMC dysfunction. In conclusion, Switching from acetate to citrate improved dialysis efficacy and inflammatory parameters; in vitro, chemerin-induced EC and VSMC injury were decreased by using citrate as dialysis buffer.

Indexed as

ChemokinesCitric AcidC-Reactive ProteinEndothelium, VascularFemaleFibrinogenHemodialysis SolutionsHumansInflammationInterleukin-6MaleMicrovesselsMiddle AgedMuscle, Smooth, VascularRenal DialysisTreatment OutcomeChemokinesCitric AcidC-Reactive ProteinFibrinogenHemodialysis SolutionsInterleukin-6RARRES2 protein, human

Identifiers

PMID31337804
PMCPMC6650610
OpenAlexW2963917021

What OpenQuestion holds

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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.