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Plasma KL-6 as a Potential Biomarker for Bronchopulmonary Dysplasia in Preterm Infants. | LitMetric

Plasma KL-6 as a Potential Biomarker for Bronchopulmonary Dysplasia in Preterm Infants.

Crit Care Res Pract

Department of Obstetrics and Gynecology, Medical University of Sofia, Zdrave 2 Street, Sofia 1431, Bulgaria.

Published: January 2024

AI Article Synopsis

Article Abstract

Background: KL-6 is a biomarker of interstitial lung injury and increases during repair.

Aim: Our aim was to determine the predictive value of plasma KL-6 for the development of bronchopulmonary dysplasia (BPD) in preterm infants.

Methods: Ninety-five extremely preterm infants (EPIs), born at <28 gestational age (GA), were divided into two main BPD groups as follows: the moderate/severe and the no/mild group. KL-6 was analyzed on days 7 and 14. Binary logistic regression analyses and ROC curve analyses were performed.

Results: Infants <26 + 0 weeks' GA have higher mean KL-6 than infants >25 + 6 weeks' GA on 7 and 14 days (335 vs. 286 U/ml and 378 vs. 260 U/ml; = 0.005 and 0.018, respectively). In the binary regression model at KL-6 day 7, three of the prognostic factors remained significant-mechanical ventilation OR: 10.38 (95% CI: 3.57-30.14), PDA OR: 6.39 (95% CI: 0.87-46.74), and KL-6 OR: 4.98 (95% CI: 1.54-16.08). The AUC was 0.86 with a sensitivity and specificity of 79% at a cutoff value ≥0.34. In the binary regression model at KL-6 day 14, six of the prognostic factors were significant-PDA OR: 23.34 (95% CI: 2.14-254.24), KL-6 OR: 13.59 (95% CI: 3.19-57.96), GA OR: 4.58 (95% CI: 1.16-18.06), mechanical ventilation OR: 4.45 (95% CI: 1.23-16.16), antenatal steroids OR: 0.19 (95% CI: 0.04-0.95), and gender (female OR: 0.30 (95% CI 0.08-1.12)). The AUC was 0.91, and the sensitivity and accuracy for a cutoff ≥0.37 were 89% and 85%, respectively.

Conclusion: KL-6 could be a useful screening biomarker for early detection of infants at increased risk for developing BPD.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10846922PMC
http://dx.doi.org/10.1155/2024/3623948DOI Listing

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