scholarly journals Airway nitrite is increased in extremely preterm infants with bronchopulmonary dysplasia

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Samuel J. Gentle ◽  
Amelia Freeman ◽  
Rakesh P. Patel ◽  
Namasivayam Ambalavanan ◽  
Charitharth V. Lal
Keyword(s):  
Preterm Infants ◽  
Bronchopulmonary Dysplasia ◽  
Predictive Biomarkers ◽  
University Of Alabama ◽  
Common Complication ◽  
Mortality And Morbidity ◽  
Extremely Preterm ◽  
Extremely Preterm Infants ◽  
The University ◽  
Tracheal Aspirates

Abstract Rationale Bronchopulmonary dysplasia (BPD) is the most common complication of prematurity and significantly contributes to mortality and morbidity with few predictive biomarkers. Given that nitrites have been implicated in pathways associated with lung disease, we hypothesized that nitrite levels would be altered in the airways of premature infants diagnosed with BPD. Methods This was a prospective cohort study of extremely low birth infants (< 28 weeks’ gestation) at the University of Alabama at Birmingham. Nitrite levels from tracheal aspirates (TAs) were compared between intubated and ventilated infants with BPD and gestation matched full term (FT) controls. TA derived nitrite levels from day one after birth were also compared between preterm infants who did and did not develop BPD. Results Infants with BPD were found to have significantly elevated nitrite levels in their tracheal aspirates compared to gestation matched FT controls (p < 0.05). There was a trend for increased nitrite levels on postnatal day one in infants that developed BPD compared to infants that did not develop BPD (p = 0.05). Conclusions In conclusion, nitrite levels are significantly increased in airways of infants with BPD. Data from a larger cohort are needed to further support the utility of nitrite for BPD prediction. Trial registration Not applicable.

scholarly journals MicroRNA Signatures Associated with Bronchopulmonary Dysplasia Severity in Tracheal Aspirates of Preterm Infants

Biomedicines ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 257
Author(s):  
Roopa Siddaiah ◽  
Christiana N. Oji-Mmuo ◽  
Deborah T. Montes ◽  
Nathalie Fuentes ◽  
Debra Spear ◽  
...  
Keyword(s):  
Preterm Infants ◽  
Bronchopulmonary Dysplasia ◽  
Respiratory Infections ◽  
Fetal Lung ◽  
Expression Levels ◽  
Fetal Lung Development ◽  
Extremely Preterm ◽  
Extremely Preterm Infants ◽  
Novel Biomarkers ◽  
Tracheal Aspirates

Bronchopulmonary dysplasia (BPD) is a form of chronic lung disease that develops in neonates as a consequence of preterm birth, arrested fetal lung development, and inflammation. The incidence of BPD remains on the rise as a result of increasing survival of extremely preterm infants. Severe BPD contributes to significant health care costs and is associated with prolonged hospitalizations, respiratory infections, and neurodevelopmental deficits. In this study, we aimed to detect novel biomarkers of BPD severity. We collected tracheal aspirates (TAs) from preterm babies with mild/moderate (n = 8) and severe (n = 17) BPD, and we profiled the expression of 1048 miRNAs using a PCR array. Associations with biological pathways were determined with the Ingenuity Pathway Analysis (IPA) software. We found 31 miRNAs differentially expressed between the two disease groups (2-fold change, false discovery rate (FDR) < 0.05). Of these, 4 miRNAs displayed significantly higher expression levels, and 27 miRNAs had significantly lower expression levels in the severe BPD group when compared to the mild/moderate BPD group. IPA identified cell signaling and inflammation pathways associated with miRNA signatures. We conclude that TAs of extremely premature infants contain miRNA signatures associated with severe BPD. These may serve as potential biomarkers of disease severity in infants with BPD.

SNAP-II for prediction of mortality and morbidity in extremely preterm infants

2018 ◽  
Vol 32 (16) ◽  
pp. 2694-2701 ◽  
Author(s):  
Marc Beltempo ◽  
Prakesh S. Shah ◽  
Xiang Y. Ye ◽  
Jehier Afifi ◽  
Shoo Lee ◽  
...  
Keyword(s):  
Preterm Infants ◽  
Mortality And Morbidity ◽  
Prediction Of Mortality ◽  
Extremely Preterm ◽  
Extremely Preterm Infants

scholarly journals Admission Temperature and Associated Mortality and Morbidity among Moderately and Extremely Preterm Infants

2018 ◽  
Vol 192 ◽  
pp. 53-59.e2 ◽  
Author(s):  
Abbot R. Laptook ◽  
Edward F. Bell ◽  
Seetha Shankaran ◽  
Nansi S. Boghossian ◽  
Myra H. Wyckoff ◽  
...  
Keyword(s):  
Preterm Infants ◽  
Mortality And Morbidity ◽  
Extremely Preterm ◽  
Extremely Preterm Infants

Bubbly and cystic appearance on chest radiograph of extremely preterm infants with bronchopulmonary dysplasia is associated with wheezing disorder

2019 ◽  
Vol 109 (4) ◽  
pp. 711-719
Author(s):  
Hirokazu Arai ◽  
Masato Ito ◽  
Tomoo Ito ◽  
Syozo Ota ◽  
Tsutomu Takahashi ◽  
...  
Keyword(s):  
Preterm Infants ◽  
Bronchopulmonary Dysplasia ◽  
Chest Radiograph ◽  
Extremely Preterm ◽  
Extremely Preterm Infants

Duration of significant patent ductus arteriosus and bronchopulmonary dysplasia in extremely preterm infants

2019 ◽  
Vol 39 (12) ◽  
pp. 1648-1655 ◽  
Author(s):  
Hussnain Mirza ◽  
Jorge Garcia ◽  
Genevieve McKinley ◽  
Laura Hubbard ◽  
Wendla Sensing ◽  
...  
Keyword(s):  
Patent Ductus Arteriosus ◽  
Preterm Infants ◽  
Bronchopulmonary Dysplasia ◽  
Ductus Arteriosus ◽  
Extremely Preterm ◽  
Extremely Preterm Infants ◽  
Patent Ductus

scholarly journals Tracheal Aspirate miRNA Signatures in Preterm Infants with Severe Bronchopulmonary Dysplasia

2021 ◽  
Author(s):  
Roopa Siddaiah ◽  
Christiana Oji-Mmuo ◽  
Deborah Montes ◽  
Nathalie Fuentes ◽  
Ann Donnelly ◽  
...  
Keyword(s):  
Preterm Infants ◽  
Bronchopulmonary Dysplasia ◽  
Respiratory Infections ◽  
Fetal Lung ◽  
Tracheal Aspirate ◽  
Expression Levels ◽  
Fetal Lung Development ◽  
Extremely Preterm ◽  
Extremely Preterm Infants ◽  
Novel Biomarkers

Bronchopulmonary dysplasia (BPD) is a form of chronic lung disease that develops in neonates as a consequence of preterm birth and arrested fetal lung development. The incidence of BPD remains on the rise, as a result of increasing survival of extremely preterm infants. Severe BPD contributes to significant health care costs and is associated with prolonged hospitalizations, respiratory infections, and neurodevelopmental deficits. In this study, we aimed to detect novel biomarkers of severe BPD. We collected tracheal aspirates (TA) from preterm babies with mild/moderate (n = 8) and severe (n = 17) BPD, and we profiled the expression of 1048 miRNAs using a PCR array. Associations with biological pathways were determined with the Ingenuity Pathway Analysis (IPA) software. We found 31 miRNAs differentially expressed between the two disease groups (2-fold change, FDR &amp;lt; 0.05). Of these, 4 miRNAs displayed significantly higher expression levels, and 27 miRNAs had significantly lower expression levels in the severe BPD vs. the mild/moderate BPD group. IPA identified cell signaling and inflammation pathways associated with miRNA signatures. We conclude that TAs of extreme premature infants contain miRNA signatures associated with severe BPD. These signatures may serve as biomarkers of disease severity in infants with BPD.

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