ArticleItalian journal of pediatrics2025
The relationship between the expression of serum PTEN and TLR4 and the severity and prognosis of neonatal sepsis.
Article in Italian journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
backgroundTo investigate the relationship between the expression of serum PTEN and TLR4 and the severity and prognosis of neonatal septicemia and the guiding significance of management strategy.
methods116 newborns with sepsis admitted to the neonatal department of our hospital from March 2021 to June 2023 were recruited as research subjects. According to the Sequential Organ Failure Assessment (SOFA) scoring system, newborns with scores of 1 to 18 were set into the mild sepsis group (n = 64), newborns with scores from 19 to 24 were set into the severe sepsis group (n = 52), and 8 patients died in the severe sepsis group (death group), 44 cases survived (survival group). During the same period, 50 newborns with normal physical examination were selected as the control group. All patient guardians signed informed consent before inclusion in the study. The inflammation level of the newborns was detected by enzyme-linked immunosorbent assay and automated blood cell counter. The serum Phosphatase and Tensin Homolog (PTEN) and Toll-like Receptor 4 (TLR4) levels of the newborns were tested by enzyme-linked immunosorbent assay. The serum PTEN and TLR4 levels of newborns with severe sepsis were compared between the death group and the survival group. The correlation between PTEN, TLR4 and inflammatory indicators Procalcitonin (PCT), C-Reactive Protein (CRP), Heparin-Binding Protein (HBP), and White Blood Cell Count (WBC) was analyzed by Pearson correlation. The value of biomarkers on the condition and prognosis of newborns was analyzed through Receiver Operating Characteristic (ROC) curves.
resultsThe levels of PCT, CRP, HBP and WBC in the severe sepsis group and mild sepsis group were higher than control group (p < 0.05). The levels of PCT, CRP, HBP and WBC in the severe sepsis group were higher than mild sepsis group (p < 0.05). The PTEN levels in the severe sepsis group and mild sepsis group were lower than control group (p < 0.05), and the PTEN levels in the severe sepsis group were lower than mild sepsis group (p < 0.05). The TLR4 levels in the severe sepsis group and mild sepsis group were higher than control group (p < 0.05), and the TLR4 levels in the severe sepsis group were higher than mild sepsis group (p < 0.05). The PCT, CRP, HBP and WBC levels of newborns in the death group were higher than survival group (p < 0.05). The PTEN level in the death group was lower than survival group (p < 0.05), and the serum TLR4 level in the death group was higher than survival group (p < 0.05). PTEN was negatively correlated with PCT, CRP, HBP and WBC (p < 0.05), that is, the increase in PTEN levels may be related to the reduction of inflammatory response. TLR4 is positively correlated with PCT, CRP, HBP and WBC indicators (p < 0.05), indicating that when TLR4 levels increase, the levels of PCT, CRP, HBP and WBC also tend to increase. Compared with other biomarkers, PTEN and TLR4 showed high diagnostic accuracy, with Area Under the Curve (AUC) values of 0.846 and 0.857 respectively, indicating that PTEN and TLR4 are more effective than other indicators in distinguishing the health status and prognosis of newborns with sepsis (p < 0.05).
conclusionSerum PTEN and TLR4 expression levels go hand in hand to the severity and prognosis of newborns with sepsis, and can be used as early predictors of severe sepsis and death in newborns with severe sepsis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.