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Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants

BACKGROUND AND AIM: Human milk has potential protective effects against bronchopulmonary dysplasia (BPD). However, studies on the association between the dose of human milk and BPD in China are limited. This study aimed to evaluate the dose-dependent effects of human milk on BPD and other neonatal m...

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Autores principales: Xu, Yan, Yu, Zhangbin, Li, Qianqian, Zhou, Jinjun, Yin, Xiaoguang, Ma, Yuelan, Yin, Yujie, Jiang, Shanyu, Zhu, Rongping, Wu, Yue, Han, Liangrong, Gao, Yan, Xue, Mei, Qiao, Yu, Zhu, Lingling, Tu, Wenjuan, Wu, Mingfu, Wan, Jun, Wang, Weiyuan, Deng, Xiaoyi, Li, Shuangshuang, Wang, Sannan, Chen, Xiaoqing, Zhou, Qin, Wang, Jinxiu, Cheng, Rui, Wang, Jun, Han, Shuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666971/
https://www.ncbi.nlm.nih.gov/pubmed/33190629
http://dx.doi.org/10.1186/s12887-020-02394-1
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author Xu, Yan
Yu, Zhangbin
Li, Qianqian
Zhou, Jinjun
Yin, Xiaoguang
Ma, Yuelan
Yin, Yujie
Jiang, Shanyu
Zhu, Rongping
Wu, Yue
Han, Liangrong
Gao, Yan
Xue, Mei
Qiao, Yu
Zhu, Lingling
Tu, Wenjuan
Wu, Mingfu
Wan, Jun
Wang, Weiyuan
Deng, Xiaoyi
Li, Shuangshuang
Wang, Sannan
Chen, Xiaoqing
Zhou, Qin
Wang, Jinxiu
Cheng, Rui
Wang, Jun
Han, Shuping
author_facet Xu, Yan
Yu, Zhangbin
Li, Qianqian
Zhou, Jinjun
Yin, Xiaoguang
Ma, Yuelan
Yin, Yujie
Jiang, Shanyu
Zhu, Rongping
Wu, Yue
Han, Liangrong
Gao, Yan
Xue, Mei
Qiao, Yu
Zhu, Lingling
Tu, Wenjuan
Wu, Mingfu
Wan, Jun
Wang, Weiyuan
Deng, Xiaoyi
Li, Shuangshuang
Wang, Sannan
Chen, Xiaoqing
Zhou, Qin
Wang, Jinxiu
Cheng, Rui
Wang, Jun
Han, Shuping
author_sort Xu, Yan
collection PubMed
description BACKGROUND AND AIM: Human milk has potential protective effects against bronchopulmonary dysplasia (BPD). However, studies on the association between the dose of human milk and BPD in China are limited. This study aimed to evaluate the dose-dependent effects of human milk on BPD and other neonatal morbidities in very low birth weight (VLBW) infants. METHODS: This retrospective cohort study of preterm infants was conducted on preterm infants of gestational age ≤ 34 weeks and birth weight < 1500 g admitted to the multicenter clinical research database for breastfeeding quality improvement in Jiangsu province. The multivariate analysis was performed to compare the effect outcomes of daily graded doses [1–24 mL/(kg · day), 25–49 mL/(kg · day), and ≥ 50 mL/(kg · day) of body weight] of human milk on neonatal outcomes throughout the first 4 weeks of life versus a reference group receiving no human milk. The models were adjusted for potential confounding variables. RESULTS: Of 964 included infants, 279 (28.9%) received exclusive preterm formula, 128 (13.3%) received 1–24 ml/(kg · day), 139 (14.4%) received 25–49 ml/(kg · day), and 418 (43.4%) received ≥50 ml/(kg · day) human milk for the first 4 weeks of life. Compared with infants receiving exclusive formula, those receiving the highest volume of human milk daily [≥50 mL/(kg · day)] had lower incidences of BPD [27.5% in ≥50 mL/(kg · day) vs 40.1% in 0 mL/(kg · day) human milk, P = 0.001)], moderate and severe BPD [8.9% in ≥50 mL/(kg · day) vs 16.1% in 0 mL/(kg · day), P = 0.004], necrotizing enterocolitis [NEC; 3.8% in ≥50 mL/(kg · day) vs 10.8% in 0 mL/(kg · day), P = 0.001], late-onset sepsis [LOS; 9.3% in ≥50 mL/(kg · day) vs 19.7% in 0 mL/(kg · day), P <0.01], and extrauterine growth retardation [EUGR; 38.5% in ≥50 mL/(kg · day) vs 57.6% in 0 mL/(kg · day), P <0.01)]. The logistic regression indicated that those receiving ≥50 ml/kg · day human milk had lower odds of BPD [adjusted odds ratio (AOR) 0.453; 95% confidence interval (CI): 0.309, 0.666], moderate and severe BPD (AOR 0.430; 95% CI: 0.249, 0.742), NEC (AOR 0.314; 95% CI: 0.162, 0. 607), LOS (AOR 0.420; 95% CI: 0.263, 0.673), and EUGR (AOR 0.685; 95% CI: 0.479, 0.979). CONCLUSIONS: A daily threshold amount of ≥50 ml/(kg · day) human milk in the first 4 weeks of life was associated with lower incidence of BPD as well as NEC, LOS, and EUGR in VLBW infants. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03453502. Registration date: March 5, 2018. This study was retrospectively registered. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s12887-020-02394-1.
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spelling pubmed-76669712020-11-16 Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants Xu, Yan Yu, Zhangbin Li, Qianqian Zhou, Jinjun Yin, Xiaoguang Ma, Yuelan Yin, Yujie Jiang, Shanyu Zhu, Rongping Wu, Yue Han, Liangrong Gao, Yan Xue, Mei Qiao, Yu Zhu, Lingling Tu, Wenjuan Wu, Mingfu Wan, Jun Wang, Weiyuan Deng, Xiaoyi Li, Shuangshuang Wang, Sannan Chen, Xiaoqing Zhou, Qin Wang, Jinxiu Cheng, Rui Wang, Jun Han, Shuping BMC Pediatr Research Article BACKGROUND AND AIM: Human milk has potential protective effects against bronchopulmonary dysplasia (BPD). However, studies on the association between the dose of human milk and BPD in China are limited. This study aimed to evaluate the dose-dependent effects of human milk on BPD and other neonatal morbidities in very low birth weight (VLBW) infants. METHODS: This retrospective cohort study of preterm infants was conducted on preterm infants of gestational age ≤ 34 weeks and birth weight < 1500 g admitted to the multicenter clinical research database for breastfeeding quality improvement in Jiangsu province. The multivariate analysis was performed to compare the effect outcomes of daily graded doses [1–24 mL/(kg · day), 25–49 mL/(kg · day), and ≥ 50 mL/(kg · day) of body weight] of human milk on neonatal outcomes throughout the first 4 weeks of life versus a reference group receiving no human milk. The models were adjusted for potential confounding variables. RESULTS: Of 964 included infants, 279 (28.9%) received exclusive preterm formula, 128 (13.3%) received 1–24 ml/(kg · day), 139 (14.4%) received 25–49 ml/(kg · day), and 418 (43.4%) received ≥50 ml/(kg · day) human milk for the first 4 weeks of life. Compared with infants receiving exclusive formula, those receiving the highest volume of human milk daily [≥50 mL/(kg · day)] had lower incidences of BPD [27.5% in ≥50 mL/(kg · day) vs 40.1% in 0 mL/(kg · day) human milk, P = 0.001)], moderate and severe BPD [8.9% in ≥50 mL/(kg · day) vs 16.1% in 0 mL/(kg · day), P = 0.004], necrotizing enterocolitis [NEC; 3.8% in ≥50 mL/(kg · day) vs 10.8% in 0 mL/(kg · day), P = 0.001], late-onset sepsis [LOS; 9.3% in ≥50 mL/(kg · day) vs 19.7% in 0 mL/(kg · day), P <0.01], and extrauterine growth retardation [EUGR; 38.5% in ≥50 mL/(kg · day) vs 57.6% in 0 mL/(kg · day), P <0.01)]. The logistic regression indicated that those receiving ≥50 ml/kg · day human milk had lower odds of BPD [adjusted odds ratio (AOR) 0.453; 95% confidence interval (CI): 0.309, 0.666], moderate and severe BPD (AOR 0.430; 95% CI: 0.249, 0.742), NEC (AOR 0.314; 95% CI: 0.162, 0. 607), LOS (AOR 0.420; 95% CI: 0.263, 0.673), and EUGR (AOR 0.685; 95% CI: 0.479, 0.979). CONCLUSIONS: A daily threshold amount of ≥50 ml/(kg · day) human milk in the first 4 weeks of life was associated with lower incidence of BPD as well as NEC, LOS, and EUGR in VLBW infants. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03453502. Registration date: March 5, 2018. This study was retrospectively registered. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at 10.1186/s12887-020-02394-1. BioMed Central 2020-11-16 /pmc/articles/PMC7666971/ /pubmed/33190629 http://dx.doi.org/10.1186/s12887-020-02394-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Xu, Yan
Yu, Zhangbin
Li, Qianqian
Zhou, Jinjun
Yin, Xiaoguang
Ma, Yuelan
Yin, Yujie
Jiang, Shanyu
Zhu, Rongping
Wu, Yue
Han, Liangrong
Gao, Yan
Xue, Mei
Qiao, Yu
Zhu, Lingling
Tu, Wenjuan
Wu, Mingfu
Wan, Jun
Wang, Weiyuan
Deng, Xiaoyi
Li, Shuangshuang
Wang, Sannan
Chen, Xiaoqing
Zhou, Qin
Wang, Jinxiu
Cheng, Rui
Wang, Jun
Han, Shuping
Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title_full Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title_fullStr Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title_full_unstemmed Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title_short Dose-dependent effect of human milk on Bronchopulmonary dysplasia in very low birth weight infants
title_sort dose-dependent effect of human milk on bronchopulmonary dysplasia in very low birth weight infants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666971/
https://www.ncbi.nlm.nih.gov/pubmed/33190629
http://dx.doi.org/10.1186/s12887-020-02394-1
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