Evidence map›Paper›PMID 38347448›Full record

ArticleBMC pediatrics2024

Combined gestational age and serum fucose for early prediction of risk for bronchopulmonary dysplasia in premature infants.

Liangliang Li, Shimin Xu, Miaomiao Li, Xiangyun Yin, Hongmin Xi, Ping Yang, Lili Ma, Lijuan Zhang, Xianghong Li

Open access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2024. 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
0.4field-weighted citation impact, top 40% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Incidence and factors associated with bronchopulmonary dysplasia: a cohort study in a high-risk Colombian neonatal intensive care unit.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2026
    Observational
  2. Article
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

9 authors at 3 institutions in 1 country.

Liangliang Li *Division of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China.
Shimin Xu *Division of Neonatology, Beijing jingdu Children's Hospital, Beijing, China.
Miaomiao LiDepartment of Medical Genetic, The Affiliated Hospital of Qingdao University, Shandong, China.
Xiangyun YinDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China.
Hongmin XiDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China.
Ping YangDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China.
Lili MaDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China.
Lijuan ZhangDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China. zhanglj@qduhospital.cn.
Xianghong LiDivision of Neonatology, The Affiliated Hospital of Qingdao University, Shandong, China. a18661802398@163.com.
Qingdao University · CNAffiliated Hospital of Qingdao University · CNBeijing Children’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAs the predominant complication in preterm infants, Bronchopulmonary Dysplasia (BPD) necessitates accurate identification of infants at risk and expedited therapeutic interventions for an improved prognosis. This study evaluates the potential of Monosaccharide Composite (MC) enriched with environmental information from circulating glycans as a diagnostic biomarker for early-onset BPD, and, concurrently, appraises BPD risk in premature neonates. MATERIALS AND

methodsThe study incorporated 234 neonates of ≤32 weeks gestational age. Clinical data and serum samples, collected one week post-birth, were meticulously assessed. The quantification of serum-free monosaccharides and their degraded counterparts was accomplished via High-performance Liquid Chromatography (HPLC). Logistic regression analysis facilitated the construction of models for early BPD diagnosis. The diagnostic potential of various monosaccharides for BPD was determined using Receiver Operating Characteristic (ROC) curves, integrating clinical data for enhanced diagnostic precision, and evaluated by the Area Under the Curve (AUC).

resultsAmong the 234 neonates deemed eligible, BPD development was noted in 68 (29.06%), with 70.59% mild (48/68) and 29.41% moderate-severe (20/68) cases. Multivariate analysis delineated several significant risk factors for BPD, including gestational age, birth weight, duration of both invasive mechanical and non-invasive ventilation, Patent Ductus Arteriosus (PDA), pregnancy-induced hypertension, and concentrations of two free monosaccharides (Glc-F and Man-F) and five degraded monosaccharides (Fuc-D, GalN-D, Glc-D, and Man-D). Notably, the concentrations of Glc-D and Fuc-D in the moderate-to-severe BPD group were significantly diminished relative to the mild BPD group. A potent predictive capability for BPD development was exhibited by the conjunction of gestational age and Fuc-D, with an AUC of 0.96.

conclusionA predictive model harnessing the power of gestational age and Fuc-D demonstrates promising efficacy in foretelling BPD development with high sensitivity (95.0%) and specificity (94.81%), potentially enabling timely intervention and improved neonatal outcomes.

Indexed as

Bronchopulmonary DysplasiaInfant, PrematureFemaleFucoseGestational AgeHumansInfantInfant, NewbornMaleMonosaccharidesPregnancyFucoseMonosaccharidesBronchopulmonary dysplasiaHigh-performance liquid chromatographyMonosaccharide composite (MC)Prediction modelSerum monosaccharides

Identifiers

PMID38347448
PMCPMC10860215
OpenAlexW4391753445

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.