Evidence map›Paper›PMID 39081873›Full record

ArticleJournal of inflammation research2024

Hsa_circ_0001359 in Serum Exosomes: A Promising Marker to Predict Bronchopulmonary Dysplasia in Premature Infants.

Yan Guo, Jing-Jing Pan, Wen Zhu, Mu-Zi Wang, Tian-Yu Liu, Xiao-Xin Wang, Qian-Qian Wu, Yi-Xin Cheng, Yi-Sen Qian, Xiao-Guang Zhou and 1 more

Abstract read
In one paragraph

Article in Journal of inflammation research, 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
–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

2 citing papers in PubMed.

  1. Article
  2. Review
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

11 authors.

Yan Guo *Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Jing-Jing Pan *Department of Neonatology, The First Affiliated Hospital, Nanjing Medical University, Nanjing, People's Republic of China.
Wen ZhuDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Mu-Zi WangDepartment of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, People's Republic of China.
Tian-Yu LiuDepartment of Neonatology, The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, People's Republic of China.
Xiao-Xin WangDepartment of Pediatrics, Shandong Tumor Hospital, Jinan, People's Republic of China.
Qian-Qian WuDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Yi-Xin ChengDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Yi-Sen QianDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Xiao-Guang ZhouDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
Yang YangDepartment of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.ORCID 0000-0002-0610-7197

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This prospective study is to explore the role of specific circRNAs in predicting the development of bronchopulmonary dysplasia (BPD). Methods: From July 1, 2021 to December 1, 2021, peripheral blood samples were collected from 62 premature infants with gestational age (GA) ≤32 weeks on the 7th, 14th, and 28th day after birth. Then, on the 28th day, the included infants were divided into the BPD group and the non-BPD group according to the definition of BPD. Serum exosomal circRNAs from peripheral blood were identified, sequenced, and compared between the BPD and non-BPD groups at different time points. Specific differentially expressed circRNAs were further verified from another 42 enrolled premature infants (GA ≤32 weeks). The classical lung biological markers in serum were also measured simultaneously. Results: Hsa_circ_0001359 in serum exosomes showed continuous differential expression between the BPD group and the non-BPD group on the 7th, 14th, and 28th day. Compared with that, classical lung biological markers like IL-6, IL-33, KL-6, and ET-1 did not exhibit continuous differences. Moreover, the expression of hsa_circ_0001359 on day 7 had a higher predictive value in predicting BPD (area under curve:0.853, 95% CI:0.738-0.968; adjusted odds ratio:6.033, 95% CI:2.373-13.326). The calibration curve further showed the mean absolute error = 0.033, mean squared error = 0.00231, and quantile of absolute error = 0.058. Conclusion: Hsa_circ_0001359 in serum exosomes is a promising marker for predicting BPD in preterm infants with gestational age ≤32 weeks.

Indexed as

bronchopulmonary dysplasiacircular RNAshigh-throughput sequencingpreterm infants

Identifiers

PMID39081873
PMCPMC11287472

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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.