Evidence map›Paper›PMID 40676261›Full record

ArticlePediatric research2026

Preterm functional outcomes are reflected in early postnatal proteome changes.

Magdalena Zasada, Maciej Suski, Natalia Łapińska, Weronika Pogoda, Aleksandra Kowalik, Marta Olszewska, Przemko Kwinta

Abstract read
In one paragraph

Article in Pediatric research, 2026. 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

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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

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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
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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.

Magdalena Zasada *Department of Pediatrics, Jagiellonian University Medical College, Krakow, Poland. magdalena.zasada@uj.edu.pl.
Maciej Suski *Department of Pharmacology, Jagiellonian University Medical College, Faculty of Medicine, Krakow, Poland.
Natalia ŁapińskaDepartment of Pharmaceutical Technology and Biopharmaceutics, Jagiellonian University Medical College, Faculty of Pharmacy, Krakow, Poland.
Weronika PogodaProteomics Laboratory, Centre for the Development of Therapies for Civilization and Age-Related Diseases CDT-CARD, Jagiellonian University Medical College, Krakow, Poland.
Aleksandra KowalikDepartment of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Marta OlszewskaDepartment of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Przemko KwintaDepartment of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvances in omics technologies have enabled precise analysis of protein abundance. This study applies such methods to investigate urinary proteomic quantitative changes associated with prematurity.

methodsUrine samples were collected from very-low-gestational-age (VLGA) infants (n = 29) without premature brain damage, as assessed using the Kidokoro scale and magnetic resonance imaging at term-equivalent age, and from full-term infants (n = 19) on the 1

resultsWe identified 61 proteins that were significantly differentially abundant in urine throughout the study. The regulated urinary proteins were enriched in functional domains related to the immune system, hemostasis, and complement and coagulation cascades, indicating underdevelopment in VLGA infants. Conversely, the augmented pathways included extracellular matrix organization, cholesterol metabolism and PPAR signaling.

conclusionsThe urinary proteome of VLGA infants differed significantly from that of term neonates, revealing protein profiles linked to immune system immaturity and hemostasis, altered metabolism and perturbed extracellular matrix metabolism. This study underscores how prematurity affects the urinary proteome, offering insights into the molecular pathways influenced by premature birth. IMPACT: The urinary proteome of premature newborns differs from the urinary proteome of full-term newborns; analysis of urine proteins indicates the functional consequences of prematurity. In our study, we tested urine on the 1

Indexed as

Infant, PrematureProteomeBiomarkersComputational BiologyFemaleGestational AgeHumansInfant, NewbornMagnetic Resonance ImagingMaleProteomicsBiomarkersProteome

Identifiers

PMID40676261
PMCPMC13021510

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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.