Evidence map›Paper›PMID 42412773›Full record

ArticlePloS one2026

Plasma cell-free DNA measured prior to renal replacement therapy initiation is not associated with incident adverse outcomes, hospitalizations or malignancies in chronic kidney disease stage 4-5 patients.

Niilo Liuhto, Jenni Tuominen, Noora Manni, Markus Hakamäki, Roosa Lankinen, Tomi Toukola, Jonna Virtanen, Kaj Metsärinne, Mikko J Järvisalo, Tapio Hellman

Abstract read
In one paragraph

Article in PloS one, 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

10 authors.

Niilo LiuhtoKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.ORCID https://orcid.org/0009-0004-2380-6901
Jenni TuominenDepartment of Genomics, Turku University Hospital and University of Turku, Turku, Finland.
Noora ManniKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.
Markus HakamäkiKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.
Roosa LankinenKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.
Tomi ToukolaDepartment of Nephrology, Vaasa Central Hospital, Vaasa, Finland.
Jonna VirtanenKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.
Kaj MetsärinneKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.
Mikko J JärvisaloDepartment of Internal Medicine, Wellbeing services county of Satakunta, Pori, Finland.
Tapio HellmanKidney Centre, Turku University Hospital and University of Turku, Turku, Finland.ORCID https://orcid.org/0000-0001-9453-5687

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is an inherent feature of advanced chronic kidney disease (CKD) and associated with adverse outcomes. Several inflammatory biomarkers have been shown to be associated with mortality in CKD. Cell-free DNA (cfDNA) is a novel biomarker for inflammation which has not been previously examined in patients with CKD stage 4-5 not undergoing dialysis. cfDNA was extracted from plasma and quantified with Qubit Flex Fluorometer using dsDNA High Sensitivity kit in 138 patients with CKD stage 4-5 not undergoing dialysis at baseline and at a control time point of median 2.7 years of follow-up. A ratio of control and baseline measurement adjusted for an increment of one year of follow-up was calculated. Associations between cfDNA at baseline and all-cause mortality, major adverse cardiovascular and cerebrovascular events (MACCE, defined as a composite outcome of acute myocardial infarction, coronary revascularization, ischemic or hemorrhagic stroke and cardiovascular death), emergency room (ER) visits, hospitalizations or incident malignancies were assessed. Within a median follow-up of 6.2 years, no associations were observed between cfDNA and mortality, MACCEs, ER visits, hospitalizations or incident malignancies. cfDNA control measurement and cfDNA delta ratio was available in 101 patients. Patients who had received a kidney transplant by the control cfDNA measurement had significantly higher cfDNA delta ratio compared to patients not on renal replacement therapy (RRT) and those undergoing dialysis (p < 0.001 for both comparisons). Patients undergoing dialysis at the time of the control cfDNA measurement had higher cfDNA delta ratio (p = 0.003) compared to patients not on RRT. The present study is the first to show that cfDNA is not associated with adverse outcomes in patients with advanced CKD not undergoing dialysis at baseline. Furthermore, our results provide unique data on the evolution of cfDNA levels in predialysis CKD stage 4-5 patients transitioning to different modalities of RRT.

Indexed as

Cell-Free Nucleic AcidsNeoplasmsRenal Insufficiency, ChronicRenal Replacement TherapyAgedBiomarkersCardiovascular DiseasesFemaleHospitalizationHumansMaleMiddle AgedBiomarkersCell-Free Nucleic Acids

Identifiers

PMID42412773
PMCPMC13340856

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.