Evidence map›Paper›PMID 35211826›Full record

ArticleInternational urology and nephrology2022

Midkine release during hemodialysis is predictive of hypervolemia and associates with excess (cardiovascular) mortality in patients with end-stage renal disease: a prospective study.

Sabine Brandt, Anja Fischer, Carla Kreutze, Dorothea Hempel, Xenia Gorny, Florian G Scurt, Delia L Şalaru, Peter Bartsch, Anja Bernhardt, Stefanie M Bode-Böger and 5 more

Open access · hybridAbstract read
In one paragraph

Article in International urology and nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

15 authors at 4 institutions in 2 countries.

Sabine BrandtClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.ORCID http://orcid.org/0000-0003-1912-6941
Anja FischerClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Carla KreutzeClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Dorothea HempelClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Xenia GornyClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Florian G ScurtClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Delia L ŞalaruClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Peter BartschClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Anja BernhardtClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Stefanie M Bode-BögerInstitute of Clinical Pharmacology, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.
Matthias GirndtDepartment of Internal Medicine II, Martin-Luther-University Halle, Halle, Germany.
Roman FiedlerDepartment of Internal Medicine II, Martin-Luther-University Halle, Halle, Germany.
Berend IsermannInstitute of Clinical Chemistry and Pathobiochemistry, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.
Jonathan A LindquistClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Peter R MertensClinic of Nephrology and Hypertension, Diabetes and Endocrinology, Otto-Von-Guericke-University Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany. peter.mertens@med.ovgu.de.
Otto-von-Guericke-Universität Magdeburg · DEMartin Luther University Halle-Wittenberg · DEGrigore T. Popa University of Medicine and Pharmacy · ROUniversity Hospital Leipzig · DE

Funding

Deutsche Forschungsgemeinschaft 97850925 - SFB 854 Project A01Deutsche Forschungsgemeinschaft 97850925 - SFB 854 Project B26NDeutsche Forschungsgemeinschaft GRK 2408 Project 7Deutsche Forschungsgemeinschaft GRK 2408 Project 8Deutsche Forschungsgemeinschaft LI-1031/4-1Deutsche Forschungsgemeinschaft ME-1365/7-2 ME-1365/9-2Saxony-Anhalt and the European Structural and Investment Funds (ESF, 2014-2020) ZS/2016/08/80645
6 · The paper itself

Abstract

backgroundIn end-stage renal disease, a high cardiovascular risk profile and endothelial damage prevails. The heparin-binding growth factor midkine stimulates neo-angiogenesis in ischemic diseases, coordinates neutrophil influx, and raises blood pressure through stimulated angiotensin synthesis.

methodsWe determined changes of midkine serum levels during hemodialysis sessions under the assumption that endothelial cell-derived midkine is released. Periprocedural differences (∆midkine) were calculated and correlated with cardiovacular biomarkers and fluid status (clinical assessment, V. cava collapse, comet tail phenomenon), cardiovascular morbidities, mortality rates. Blood was collected before and after dialysis from hemodialysis patients (n = 171; diabetes: n = 70; hypervolemia: n = 83; both: n = 32).

resultsBaseline midkine levels were ~ fourfold elevated compared to healthy controls (n = 100). Further, on average a tenfold rise was detected during dialysis, the extent of which was partially related to non-fractionated heparin application (r

conclusionThus, for dialysis patients inadequate periprocedural midkine upregulation is linked with hypervolemia and associates with cardiovascular events.

Indexed as

Heart FailureKidney Failure, ChronicWater-Electrolyte ImbalanceBiomarkersHeparinHumansMidkineProspective StudiesRenal DialysisBiomarkersHeparinMidkineCardiovascular disease: biomarkerDiabetesHemodialysisHypervolemiaMidkine

Identifiers

PMID35211826
PMCPMC9372127
OpenAlexW4214587464

What OpenQuestion holds

Textmetadata
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.