MicroRNA Expression Aberration Associated with Bronchopulmonary Dysplasia in Preterm Infants: A Preliminary Study.

BACKGROUND: Because environmental insults and genetic factors account for the variance in the risk of bronchopulmonary dysplasia (BPD) in very low birth weight (VLBW, birth weight< 1,500 g) preterm infants, the search for BPD biomarkers has begun to focus on the regulators of non-coding RNA such as...

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Publicado en:Respiratory Care Vol. 58; no. 9; pp. 1527 - 1536
Autores principales: Yen-Tzu Wu, Wei J. Chen, Wu-Shiun Hsieh, Po-Nien Tsao, Sung-Liang Yu, Chi-Yu Lai, Wen-Chung Lee, Suh-Fang Jeng
Formato: equations & formulas pictorial research tables/charts Journal Article
Publicado: Mary Ann Liebert, Inc. Sep2013
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Mary Ann Liebert, Inc.
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        atl: MicroRNA Expression Aberration Associated with Bronchopulmonary Dysplasia in Preterm Infants: A Preliminary Study.
      aug:
        au:
          Yen-Tzu Wu
          Wei J. Chen
          Wu-Shiun Hsieh
          Po-Nien Tsao
          Sung-Liang Yu
          Chi-Yu Lai
          Wen-Chung Lee
          Suh-Fang Jeng
        affil: School and Graduate Institute of Physical Therapy, National Taiwan University Hospital College of Medicine, Taipei, Taiwan.
      sug:
        subj:
          Bronchopulmonary Dysplasia Familial and Genetic
          Gene Expression
          Human
          Biological Markers
          Case Control Studies
          Male
          Female
          Wilcoxon Signed Rank Test
          Fisher's Exact Test
          Wilcoxon Rank Sum Test
          Descriptive Statistics
          Data Analysis Software
          Infant, Very Low Birth Weight
          Funding Source
          Male
          Female
      ab: BACKGROUND: Because environmental insults and genetic factors account for the variance in the risk of bronchopulmonary dysplasia (BPD) in very low birth weight (VLBW, birth weight< 1,500 g) preterm infants, the search for BPD biomarkers has begun to focus on the regulators of non-coding RNA such as microRNAs (miRNAs). Therefore, this study aimed to identify potential miRNAs involved in the pathogenesis of BPD in VLBW preterm infants. METHODS: A case-control study (15 subjects with BPD and 15 sex-matched control subjects without BPD) was conducted to investigate the expression profiles of 365 miRNAs in the peripheral blood of VLBW preterm infants at 36 weeks post-menstrual age (called the older-age set). The expression levels of identified miRNAs were further evaluated in a subsample of blood collected during the first 2 weeks post-natal age (called the younger-age set). Possible biological functions and pathways implicated in the target genes regulated by the miRNAs were explored using database predictions. RESULTS: A 4-miRNA signature (miR-152, miR-30a-3p, miR-133b, and miR-7) with aberrant expression levels at 36 weeks, derived from a supervised classification with internal cross-validation, discriminated the subjects with BPD from those without BPD with an accuracy of 0.91. The discriminative accuracy of the 4 miRNAs was supported by random permutations of either the disease status or the number of miRNAs selected (both P < .001). A down-regulation change of miR-152 and miR-30a-3p expression levels and an up-regulation change of miR-133b and miR-7 expression levels were found in the older-age set, compared to the younger-age set. CONCLUSIONS: This is the first study to identify blood-based miRNAs associated with BPD. The findings provide information regarding the roles of these biomarkers in the development of BPD in VLBW preterm infants.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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