Evidence mapPaperPMID 41746789Full record

ArticleKidney3602026

Plasma Metabolites Associated with CKD Stage in Autosomal Dominant Tubulointerstitial Kidney Disease.

Dita Mušálková, Martin Radina, Kendrah Kidd, Hana Hartmannová, Helena Trešlová, Kateřina Hodaňová, Petr Vyleťal, Alena Vrbacká, Miroslav Votruba, Antonio Sanchez and 9 more

Abstract read
In one paragraph

Article in Kidney360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Dita MušálkováResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Martin RadinaResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0009-0001-0027-8665
Kendrah KiddResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0003-3771-0949
Hana HartmannováResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0001-7787-832
Helena TrešlováResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Kateřina HodaňováResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Petr VyleťalResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0002-9357-1237
Alena VrbackáResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0003-4640-1646
Miroslav VotrubaResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Antonio SanchezSection on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.ORCID 0009-0005-9852-0868
Lauren MartinSection on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.ORCID 0009-0003-6450-5411
Abbigail TaylorSection on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Alice KimSection on Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Lucie Rudl KulhaváInstitute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0003-2432-6075
Jiří HrickoInstitute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0009-0000-3295-3226
Tomáš ČajkaInstitute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0002-9728-3355
Martina ŽivnáResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Anthony J BleyerResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0002-2804-5273
Stanislav KmochResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0002-6239-707

Funding

e-INFRA CZ project 90254European Union MULTIOMICS_CZ (Program Johannes Amos Comenius, ID Project CZ.02.01.01/00/23_020/0008540)NCATS NIH HHS Wake Forest Clinical and Translational Science Award (UL1TR001420)Next Generation EU National Institute for Research of Metabolic and Cardiovascular Diseases (Program EXCELES, ID Project No. LX22NPO5104)NIDDK NIH HHS R21 DK106584NIDDK NIH HHS U01 DK103225The National Center for Medical Genomics LM2023067Univerzita Karlova v Praze UNCE 24/MED/022 and CooperatioU.S. Food and Drug Administration 75F40124C00106
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CKDmetabolomicstubulointerstitial disease

Identifiers

PMID41746789
PMCPMC12935368

What Socratic 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 Socratic graph.