Evidence map›Paper›PMID 34961784›Full record

ArticlePediatric research2022

Can serum periostin predict bronchopulmonary dysplasia in premature infants?

Hayato Go, Junya Ono, Hitoshi Ohto, Kenneth E Nollet, Kenichi Sato, Yohei Kume, Hajime Maeda, Mina Chishiki, Kentaro Haneda, Hirotaka Ichikawa and 8 more

Abstract read
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In one paragraph

Article in Pediatric research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  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

18 authors at 2 institutions in 1 country.

Hayato GoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan. gohayato2525@gmail.com.
Junya OnoShino-Test Co., Ltd., Sagamihara, Japan.
Hitoshi OhtoFukushima Medical University, Fukushima, Japan.
Kenneth E NolletDepartment of Blood Transfusion and Transplantation Immunology, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kenichi SatoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yohei KumeDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hajime MaedaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Mina ChishikiDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kentaro HanedaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Hirotaka IchikawaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Nozomi KashiwabaraDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Yuji KanaiDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Kei OgasawaraDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Maki SatoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Koichi HashimotoDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Satoshi NunomuraDivision of Medical Biochemistry, Department of Biomolecular Sciences, Saga Medical School, Saga, Japan.
Kenji IzuharaDivision of Medical Biochemistry, Department of Biomolecular Sciences, Saga Medical School, Saga, Japan.
Mitsuaki HosoyaDepartment of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan.
Fukushima Medical University · JPSaga Medical School Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBronchopulmonary dysplasia (BPD) is the most common morbidity complicating preterm birth and affects long-term respiratory outcomes. The objectives of this study were to establish whether serum periostin at birth, day of life (DOL) 28, and corrected 36 weeks' gestational age could be potential biomarkers for BPD.

methodsA total of 98 preterm Japanese infants born at <32 weeks and comparing 41 healthy controls born at term, were divided into BPD (n = 44) and non-BPD (n = 54) cohorts. Serum periostin levels were measured using an enzyme-linked immunosorbent assay.

resultsAmong 98 preterm infants, the median serum periostin levels at birth were higher with BPD (338.0 ng/mL) than without (275.0 ng/mL, P < 0.001). Multivariate analysis revealed that serum periostin levels at birth were significantly associated with BPD (P = 0.013). Serum periostin levels at birth with moderate/severe BPD (345.0 ng/mL) were significantly higher than those with non-BPD/mild BPD (283.0 ng/mL, P = 0.006).

conclusionsSerum periostin levels were significantly correlated with birth weight and gestational age, and serum periostin levels at birth in BPD infants were significantly higher than that in non-BPD infants. IMPACT: This study found higher serum periostin levels at birth in preterm infants subsequently diagnosed with bronchopulmonary dysplasia. It also emerged that serum periostin levels at birth significantly correlated with gestational age and birth weight. The mechanism by which serum periostin is upregulated in BPD infants needs further investigation.

Indexed as

Bronchopulmonary DysplasiaInfant, Premature, DiseasesPremature BirthBiomarkersBirth WeightFemaleHumansInfantInfant, NewbornInfant, PrematureBiomarkers

Identifiers

PMID34961784
OpenAlexW4200060293

What OpenQuestion holds

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Registered trials

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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.