Evidence map›Paper›PMID 42143126›Full record

ArticleScientific reports2026

Plasma circulating free DNA in chronic schizophrenia: a case-control study.

Kamila Meca, Łukasz Czogalik, Piotr Lewandowski, Marcin Rojek, Szymon Florek, Piotr Gorczyca, Magdalena Piegza

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Kamila MecaStudent Science Club, Department of Psychiatry, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Pyskowicka 49, Tarnowskie Góry, 42-612, Poland. kamilameca01@gmail.com.
Łukasz CzogalikStudent Science Club, Department of Psychiatry, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Pyskowicka 49, Tarnowskie Góry, 42-612, Poland.
Piotr LewandowskiDepartment of Histology and Cell Pathology, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Jordana 19, Zabrze, 41-808, Poland.
Marcin RojekDepartment of Histology and Cell Pathology, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Jordana 19, Zabrze, 41-808, Poland.
Szymon FlorekDepartment of Psychoprophylaxis, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Pyskowicka 49, Tarnowskie Góry, 42-612, Poland.
Piotr GorczycaDepartment of Psychiatry, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Pyskowicka 49, Tarnowskie Góry, 42-612, Poland.
Magdalena PiegzaDepartment of Psychiatry, Medical University of Silesia, Faculty of Medical Sciences in Zabrze, Pyskowicka 49, Tarnowskie Góry, 42-612, Poland.

Funding

Ministry of Education and Science of the Republic of Poland (MEiN) SKN/SP/570134/2023
6 · The paper itself

Abstract

Circulating cell-free DNA (cf-DNA) reflects ongoing cell injury and inflammation, but its role in schizophrenia remains unclear. We conducted a case-control study of 33 clinically stabilized patients with chronic schizophrenia and 30 healthy volunteers. Plasma cf-DNA was quantified by fluorometry and droplet digital PCR (ddPCR) targeting nuclear (cf-nucDNA) and mitochondrial (cf-mtDNA) genomes. In unadjusted analyses, patients showed higher cf-nucDNA than controls (p = 0.020), while cf-mtDNA did not differ. After adjusting for age, sex, and smoking, the case-control difference was no longer significant; however, this result should be interpreted with caution due to substantial confounding between disease status, male sex, and smoking habits within our cohort. No associations were found between cf-DNA and symptom severity, despite a predominance of negative symptoms in the study group. These findings suggest that the observed variance in cf-DNA levels is heavily influenced by demographic and lifestyle factors, which complicates the isolation of a distinct disease-specific biological signal in this study group. While ddPCR is a sensitive tool for psychiatric research, current results do not support the routine clinical application of cf-DNA as a biomarker.

Indexed as

Cell-Free Nucleic AcidsSchizophreniaAdultBiomarkersCase-Control StudiesChronic DiseaseDNA, MitochondrialFemaleHumansMaleMiddle AgedBiomarkersCell-Free Nucleic AcidsDNA, MitochondrialBiomarkersChronic schizophreniaCirculating free DNA

Identifiers

PMID42143126
PMCPMC13376766

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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.