Evidence map›Paper›PMID 40569531›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2025

Metabolomic profiling of renal cyst fluid in advanced ADPKD: insights from dialysis and transplantation cohorts.

Simon Heckscher, Nicolas A Ihlo, Jan Schueler, Fabian Kellermeier, Jens M Werner, Barbara Nuebel, Verena Gross, Matthias May, Bernd Wullich, Martin Kammerl and 13 more

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

23 authors.

Simon Heckscher *Institute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Nicolas A Ihlo *Faculty of Informatics and Data Science, University of Regensburg, Regensburg, Germany.
Jan SchuelerInstitute for Molecular and Cellular Anatomy, University of Regensburg, Regensburg, Germany.
Fabian KellermeierInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Jens M WernerDepartment of Surgery, University Hospital Regensburg, 93053, Regensburg, Germany.
Barbara NuebelDepartment of Urology and Pediatric Urology, University Hospital Erlangen, Erlangen, Germany.
Verena GrossDepartment of Urology, St. Elisabeth Hospital Straubing, Brothers of Mercy Hospital, Straubing, Germany.
Matthias MayDepartment of Urology, St. Elisabeth Hospital Straubing, Brothers of Mercy Hospital, Straubing, Germany.
Bernd WullichDepartment of Urology and Pediatric Urology, University Hospital Erlangen, Erlangen, Germany.
Martin KammerlFaculty of Applied Healthcare Science, Deggendorf Institute of Technology, Deggendorf, Germany.
Carsten GnewuchInstitute for Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Ralph BurkhardtInstitute for Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Björn BuchholzDepartment of Nephrology and Hypertension, University Hospital Erlangen, Erlangen, Germany.
Eric PionInstitute for Molecular and Cellular Anatomy, University of Regensburg, Regensburg, Germany.
Thiha AungInstitute for Molecular and Cellular Anatomy, University of Regensburg, Regensburg, Germany.
Miriam BanasDepartment of Nephrology, University Hospital Regensburg, Regensburg, Germany.
Hans J SchlittDepartment of Surgery, University Hospital Regensburg, 93053, Regensburg, Germany.
Peter J OefnerInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Katja DettmerInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Wolfram GronwaldInstitute of Functional Genomics, University of Regensburg, Regensburg, Germany.
Merle BehrFaculty of Informatics and Data Science, University of Regensburg, Regensburg, Germany.
Silke HaerteisInstitute for Molecular and Cellular Anatomy, University of Regensburg, Regensburg, Germany. silke.haerteis@ur.de.
Katharina M SchmidtDepartment of Surgery, University Hospital Regensburg, 93053, Regensburg, Germany. katharina.schmidt@ukr.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder characterized by progressive renal cyst formation, often leading to end-stage kidney disease (ESKD). In contrast to the urinary metabolome in ADPKD, the composition of renal cyst fluid remains largely unexplored.

methodsWe conducted a comprehensive metabolomic analysis of renal cyst fluid from 26 ADPKD patients (20 on dialysis, six with kidney transplants) using ¹H-NMR spectroscopy and liquid chromatography-mass spectrometry (LC-MS). Cysts were clustered based on metabolite profiles, and differences were analyzed across groups defined by renal function status (dialysis vs. transplant), cyst volume, and cyst fluid sodium concentrations.

resultsDialysis patients and transplant recipients differed significantly in their renal cyst fluid metabolomes. The former exhibited higher concentrations of myoinositol, creatinine, sucrose, τ-methylhistidine, trigonelline, and sarcosine, while the latter showed increased levels of leucine, isoleucine, valine and alanine. Remarkably, metabolites of the immunosuppressive prodrug mycophenolate mofetil were detected in renal cyst fluids after kidney transplantation. Despite intra- and interindividual variability, cyst fluid from the same patient displayed greater homogeneity. Interestingly, metabolomic profiles were not altered by cyst size.

conclusionThis first systematic metabolomic analysis of renal cyst fluid in advanced ADPKD reveals distinct metabolic signatures linked to renal function status. The data provides novel insights into the pathophysiology of ADPKD and highlight the potentials of renal cyst fluid metabolomics for identifying biomarkers and therapeutic targets.

Indexed as

Cyst FluidKidney TransplantationMetabolomicsPolycystic Kidney, Autosomal DominantAdultAgedChromatography, LiquidCohort StudiesFemaleHumansMaleMass SpectrometryMetabolomeMiddle AgedRenal DialysisADPKDCyst fluidMass spectrometryMetabolomicsNMR spectroscopyPatient clustering

Identifiers

PMID40569531
PMCPMC12202516

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.