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Hsa_circ_0001359 in Serum Exosomes: A Promising Marker to Predict Bronchopulmonary Dysplasia in Premature Infants.
Guo, Yan; Pan, Jing-Jing; Zhu, Wen; Wang, Mu-Zi; Liu, Tian-Yu; Wang, Xiao-Xin; Wu, Qian-Qian; Cheng, Yi-Xin; Qian, Yi-Sen; Zhou, Xiao-Guang; Yang, Yang.
Afiliação
  • Guo Y; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Pan JJ; Department of Neonatology, The First Affiliated Hospital, Nanjing Medical University, Nanjing, People's Republic of China.
  • Zhu W; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Wang MZ; Department of Neonatology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, People's Republic of China.
  • Liu TY; Department of Neonatology, The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, People's Republic of China.
  • Wang XX; Department of Pediatrics, Shandong Tumor Hospital, Jinan, People's Republic of China.
  • Wu QQ; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Cheng YX; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Qian YS; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Zhou XG; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
  • Yang Y; Department of Neonatology, Children's Hospital of Nanjing Medical University, Nanjing, People's Republic of China.
J Inflamm Res ; 17: 5025-5037, 2024.
Article em En | MEDLINE | ID: mdl-39081873
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 curve0.853, 95% CI0.738-0.968; adjusted odds ratio6.033, 95% CI2.373-13.326). 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Inflamm Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Inflamm Res Ano de publicação: 2024 Tipo de documento: Article
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