TY - JOUR
T1 - Salivary cytokine — A non-invasive predictor for bronchopulmonary dysplasia in premature neonates
AU - Su, Ting Yu
AU - Chen, I. Lun
AU - Yeh, Tsu Fuh
AU - Yu, Hung Ren
AU - Hsu, Ying Lun
AU - Hung, Chih Hsing
AU - Huang, Hsin Chun
N1 - Funding Information:
This study was supported by Kaohsiung Chang Gung Memorial Hospital [grant numbers CMRPG8F0711, CMRPG8G0991]; and [grant number CMRPG8E0971].
Funding Information:
We appreciated the Biostatistics Center, Kaohsiung Chang Gung Memorial Hospital for statistics work. This study was supported by Kaohsiung Chang Gung Memorial Hospital [grant numbers CMRPG8F0711, CMRPG8G0991]; and [grant number CMRPG8E0971].
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/12
Y1 - 2021/12
N2 - Background: To find a less invasive method of cytokine detection for premature neonates, we conducted this cohort study to investigate the salivary cytokines and to analyze their correlations with bronchopulmonary dysplasia (BPD). Methods: Premature neonates younger than 34 weeks of gestational age without maternal or neonatal infection were recruited. Salivary samples were collected on their first (D1) and seventh (D7) days of life. The cytokine levels were detected by MILLPLEX® MAP Human multiplex assay. One-way analysis of variance, the Kruskal-Wallis test, Pearson's chi-square test, and logistic regression were used to analyze the data. Results: Totally 125 neonates were enrolled and separated into four groups: control, mild, moderate, and severe BPD group. The salivary levels of D1 interleukin (IL)-6, IL-8, IL-10, IL-17, interferon (IFN)-γ, and D7 IL-6 (p = 0.001, 0.001, 0.000, 0.043, 0.037 and 0.001, respectively) were significantly higher in the BPD groups than in the control group. After adjusting for the gestational age, acid-base equivalent, and absolute neutrophil count, comparing to the control group, the levels of D7 IL-17 became significantly lower in all three BPD groups (p = 0.032, 0.030, and 0.030, respectively) and that of D7 IFN-α2 became significantly lower in the severe BPD group (p = 0.037). Conclusion: Early-life salivary cytokine levels were correlated with the development of BPD in premature neonates. This study provides a novel method to predict BPD early and non-invasively.
AB - Background: To find a less invasive method of cytokine detection for premature neonates, we conducted this cohort study to investigate the salivary cytokines and to analyze their correlations with bronchopulmonary dysplasia (BPD). Methods: Premature neonates younger than 34 weeks of gestational age without maternal or neonatal infection were recruited. Salivary samples were collected on their first (D1) and seventh (D7) days of life. The cytokine levels were detected by MILLPLEX® MAP Human multiplex assay. One-way analysis of variance, the Kruskal-Wallis test, Pearson's chi-square test, and logistic regression were used to analyze the data. Results: Totally 125 neonates were enrolled and separated into four groups: control, mild, moderate, and severe BPD group. The salivary levels of D1 interleukin (IL)-6, IL-8, IL-10, IL-17, interferon (IFN)-γ, and D7 IL-6 (p = 0.001, 0.001, 0.000, 0.043, 0.037 and 0.001, respectively) were significantly higher in the BPD groups than in the control group. After adjusting for the gestational age, acid-base equivalent, and absolute neutrophil count, comparing to the control group, the levels of D7 IL-17 became significantly lower in all three BPD groups (p = 0.032, 0.030, and 0.030, respectively) and that of D7 IFN-α2 became significantly lower in the severe BPD group (p = 0.037). Conclusion: Early-life salivary cytokine levels were correlated with the development of BPD in premature neonates. This study provides a novel method to predict BPD early and non-invasively.
KW - Bronchopulmonary dysplasia
KW - Interferon-alpha 2 (IFN-α2)
KW - Interleukin-17 (IL-17)
KW - Premature neonates
KW - Salivary biomarker
KW - Salivary cytokine
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U2 - 10.1016/j.cyto.2021.155616
DO - 10.1016/j.cyto.2021.155616
M3 - Article
C2 - 34134911
AN - SCOPUS:85107981152
SN - 1043-4666
VL - 148
JO - Cytokine
JF - Cytokine
M1 - 155616
ER -