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Article type: Research Article
Authors: Kaneko, M.* | Sato, M. | Ogasawara, K. | Imamura, T. | Hashimoto, K. | Momoi, N. | Hosoya, M.
Affiliations: Department of Pediatrics, Fukushima Medical University School of Medicine, Fukushima City, Fukushima, Japan
Correspondence: [*] Address for correspondence: Masatoshi Kaneko, Department of Pediatrics, Fukushima Medical University, Hikarigaoka 1, Fukushima City, Fukushima 960-1295, Japan. Tel.: +81 24 547 1295; Fax: +81 24 548 6578; E-mail: mkhope2001@yahoo.co.jp.
Abstract: OBJECTIVE: To investigate the relationships between serum cytokine concentrations and chorioamnionitis (CAM) and CAM-related bronchopulmonary dysplasia (BPD) in premature infants. METHODS: Serum was collected at 0 and 7 days after birth from 36 premature infants born at <32 weeks of gestation. We examined the relationships between 30 cytokine concentrations and CAM, BPD, and other perinatal factors. RESULTS: On day 0, GM-CSF, IL-15, IL-17, IL-2, IL-2R, VEGF, and MIG concentrations were significantly higher in the CAM group (n = 17) than in the non-CAM group (n = 19). These concentrations had decreased by day 7 and were similar in both groups. The IL-12p70 concentration on day 0 was significantly lower in the BPD group (n = 16) than in the non-BPD group (n = 15). BPD incidence was similar between the CAM and non-CAM groups. CONCLUSIONS: These data support the hypothesis that intrauterine inflammation is not a primary risk factor for BPD. The immunological environment at birth or soon after, rather than intrauterine fetal inflammation (e.g., CAM), is a primary risk factor for BPD onset in preterm infants. Decreased inflammatory responses are particularly relevant, as indicated by the relationship between BPD and low serum IL-12p70 concentrations on day 0.
Keywords: Cytokines, inflammation, interleukin-12, neonatal prematurity
DOI: 10.3233/NPM-171669
Journal: Journal of Neonatal-Perinatal Medicine, vol. 10, no. 2, pp. 147-155, 2017
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