TY - JOUR
T1 - Exhaled Volatile Organic Compounds for Early Prediction of Bronchopulmonary Dysplasia in Infants Born Preterm
AU - Romijn, Michelle
AU - van Kaam, Anton H.
AU - Fenn, Dominic
AU - Bos, Lieuwe D.
AU - van den Akker, Chris H. P.
AU - Finken, Martijn J. J.
AU - Rotteveel, Joost
AU - Cerullo, Julia
AU - Brinkman, Paul
AU - Onland, Wes
N1 - Funding Information:
This study was supported by an unrestricted grant from Chiesi Onlus, and by the Amsterdam Reproduction and Development research institute. The authors have no conflicts of interest to disclose.
Funding Information:
We thank Dr Abhik Das and his team for providing the equations from the updated NICHD BPD clinical prediction model. We thank everyone who helped collecting exhaled breath samples, in particular Nienke Halbmeijer, PhD student at the Neonatology department of the Emma Children's Hospital Amsterdam University Medical Centers (UMC), and Tessa de Baat, Neonatologist at the Neonatology department of the Emma Children's Hospital Amsterdam UMC. This study was supported by an unrestricted grant from Chiesi Onlus, and by the Amsterdam Reproduction and Development research institute. The authors have no conflicts of interest to disclose.
Publisher Copyright:
© 2023 The Authors
PY - 2023/6
Y1 - 2023/6
N2 - Objective(s): To investigate the predictive performances of exhaled breath volatile organic compounds (VOCs) for development of bronchopulmonary dysplasia (BPD) in infants born preterm. Methods: Exhaled breath was collected from infants born <30 weeks’ gestation at days 3 and 7 of life. Ion fragments detected by gas chromatography–mass spectrometry analysis were used to derive and internally validate a VOC prediction model for moderate or severe BPD at 36 weeks of postmenstrual age. We tested the predictive performance of the National Institute of Child Health and Human Development (NICHD) clinical BPD prediction model with and without VOCs. Results: Breath samples were collected from 117 infants (mean gestation 26.8 ± 1.5 weeks). Thirty-three percent of the infants developed moderate or severe BPD. The VOC model showed a c-statistic of 0.89 (95% CI 0.80-0.97) and 0.92 (95% CI 0.84-0.99) for the prediction of BPD at days 3 and 7, respectively. Adding the VOCs to the clinical prediction model in noninvasively supported infants resulted in significant improvement in discriminative power on both days (day 3: c-statistic 0.83 vs 0.92, P value .04; day 7: c-statistic 0.82 vs 0.94, P value .03). Conclusions: This study showed that VOC profiles in exhaled breath of preterm infants on noninvasive support in the first week of life differ between those developing and not developing BPD. Adding VOCs to a clinical prediction model significantly improved its discriminative performance.
AB - Objective(s): To investigate the predictive performances of exhaled breath volatile organic compounds (VOCs) for development of bronchopulmonary dysplasia (BPD) in infants born preterm. Methods: Exhaled breath was collected from infants born <30 weeks’ gestation at days 3 and 7 of life. Ion fragments detected by gas chromatography–mass spectrometry analysis were used to derive and internally validate a VOC prediction model for moderate or severe BPD at 36 weeks of postmenstrual age. We tested the predictive performance of the National Institute of Child Health and Human Development (NICHD) clinical BPD prediction model with and without VOCs. Results: Breath samples were collected from 117 infants (mean gestation 26.8 ± 1.5 weeks). Thirty-three percent of the infants developed moderate or severe BPD. The VOC model showed a c-statistic of 0.89 (95% CI 0.80-0.97) and 0.92 (95% CI 0.84-0.99) for the prediction of BPD at days 3 and 7, respectively. Adding the VOCs to the clinical prediction model in noninvasively supported infants resulted in significant improvement in discriminative power on both days (day 3: c-statistic 0.83 vs 0.92, P value .04; day 7: c-statistic 0.82 vs 0.94, P value .03). Conclusions: This study showed that VOC profiles in exhaled breath of preterm infants on noninvasive support in the first week of life differ between those developing and not developing BPD. Adding VOCs to a clinical prediction model significantly improved its discriminative performance.
KW - chronic lung disease
KW - exhaled breath
KW - prediction model
KW - preterm infant
UR - https://www.scopus.com/pages/publications/85151379340
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85151379340&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36868304
U2 - 10.1016/j.jpeds.2023.02.014
DO - 10.1016/j.jpeds.2023.02.014
M3 - Article
C2 - 36868304
SN - 0022-3476
VL - 257
SP - 113368
JO - Journal of pediatrics
JF - Journal of pediatrics
M1 - 113368
ER -