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Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants

BACKGROUND: The aim of the study was to determine the rate of cytomegalovirus virolactia in the human milk (HM) of mothers of VLBW infants, compare the CMV infection rates and the changes in CMV DNA viral load and nutrient profile among different HM preparation methods. METHODS: A prospective random...

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Autores principales: Chung, Mi Lim, Sung, Heungsup, Jung, Euiseok, Lee, Byong Sop, Kim, Ki Soo, Kim, Ellen Ai-Rhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193732/
https://www.ncbi.nlm.nih.gov/pubmed/37202724
http://dx.doi.org/10.1186/s12887-023-04044-8
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author Chung, Mi Lim
Sung, Heungsup
Jung, Euiseok
Lee, Byong Sop
Kim, Ki Soo
Kim, Ellen Ai-Rhan
author_facet Chung, Mi Lim
Sung, Heungsup
Jung, Euiseok
Lee, Byong Sop
Kim, Ki Soo
Kim, Ellen Ai-Rhan
author_sort Chung, Mi Lim
collection PubMed
description BACKGROUND: The aim of the study was to determine the rate of cytomegalovirus virolactia in the human milk (HM) of mothers of VLBW infants, compare the CMV infection rates and the changes in CMV DNA viral load and nutrient profile among different HM preparation methods. METHODS: A prospective randomized controlled study was performed in infants with gestational age < 32 weeks or birth-weight < 1500 g admitted to neonatal intensive care unit of Asan Medical Center and Haeundae Paik Hospital who were given mother’s own milk. Enrolled infants were randomized into three groups according to the HM preparation methods: freezing-thawing (FT), FT + low-temperature Holder pasteurization (FT + LP), and FT + high-temperature short-term pasteurization (FT + HP). Urine CMV culture and PCR were obtained at birth and at 4, 8, and 12 weeks. HM CMV culture and PCR were obtained at birth and at 3, 6, 9, and 12 weeks. Changes in macronutrients in HM was obtained at 4 ~ 6 weeks. RESULTS: Of 564 infants, 217 mothers (38.5%) produced CMV PCR positive milk. After exclusion, a total of 125 infants were randomized into the FT (n = 41), FT + LP (n = 42), and FT + HP (n = 42) groups, whose rate of HM-acquired CMV infection was 4.9% (n = 2), 9.5% (n = 4), and 2.4% (n = 1), respectively. Out of seven CMV infected infants, two infants fed with FT + LP HM developed CMV infection- associated symptoms. Ages at diagnoses were earlier (28.5 days after birth) and at younger post conceptional age (< 32 weeks) in comparison to infants with asymptomatic CMV infection. CMV DNA viral load significantly decreased after pasturizations, especially in FT + HP group. CONCLUSIONS: HM-acquired symptomatic CMV infection rate is low and its impact on clinical course was not serious in our VLBW infants. However, evidences showing poor neurodevelopmental outcome in later life, we need to generate a guideline to protect VLBW infant form HM transmitted CMV infection. Based on our small sized study, we did not find any superiority in pasteurizing HM with frequently used LP in comparison to frozen or HP HM. More research is needed to determine the method and duration of pasteurization to reduce the HM-acquired CMV infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-023-04044-8.
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spelling pubmed-101937322023-05-19 Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants Chung, Mi Lim Sung, Heungsup Jung, Euiseok Lee, Byong Sop Kim, Ki Soo Kim, Ellen Ai-Rhan BMC Pediatr Research BACKGROUND: The aim of the study was to determine the rate of cytomegalovirus virolactia in the human milk (HM) of mothers of VLBW infants, compare the CMV infection rates and the changes in CMV DNA viral load and nutrient profile among different HM preparation methods. METHODS: A prospective randomized controlled study was performed in infants with gestational age < 32 weeks or birth-weight < 1500 g admitted to neonatal intensive care unit of Asan Medical Center and Haeundae Paik Hospital who were given mother’s own milk. Enrolled infants were randomized into three groups according to the HM preparation methods: freezing-thawing (FT), FT + low-temperature Holder pasteurization (FT + LP), and FT + high-temperature short-term pasteurization (FT + HP). Urine CMV culture and PCR were obtained at birth and at 4, 8, and 12 weeks. HM CMV culture and PCR were obtained at birth and at 3, 6, 9, and 12 weeks. Changes in macronutrients in HM was obtained at 4 ~ 6 weeks. RESULTS: Of 564 infants, 217 mothers (38.5%) produced CMV PCR positive milk. After exclusion, a total of 125 infants were randomized into the FT (n = 41), FT + LP (n = 42), and FT + HP (n = 42) groups, whose rate of HM-acquired CMV infection was 4.9% (n = 2), 9.5% (n = 4), and 2.4% (n = 1), respectively. Out of seven CMV infected infants, two infants fed with FT + LP HM developed CMV infection- associated symptoms. Ages at diagnoses were earlier (28.5 days after birth) and at younger post conceptional age (< 32 weeks) in comparison to infants with asymptomatic CMV infection. CMV DNA viral load significantly decreased after pasturizations, especially in FT + HP group. CONCLUSIONS: HM-acquired symptomatic CMV infection rate is low and its impact on clinical course was not serious in our VLBW infants. However, evidences showing poor neurodevelopmental outcome in later life, we need to generate a guideline to protect VLBW infant form HM transmitted CMV infection. Based on our small sized study, we did not find any superiority in pasteurizing HM with frequently used LP in comparison to frozen or HP HM. More research is needed to determine the method and duration of pasteurization to reduce the HM-acquired CMV infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-023-04044-8. BioMed Central 2023-05-18 /pmc/articles/PMC10193732/ /pubmed/37202724 http://dx.doi.org/10.1186/s12887-023-04044-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Chung, Mi Lim
Sung, Heungsup
Jung, Euiseok
Lee, Byong Sop
Kim, Ki Soo
Kim, Ellen Ai-Rhan
Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title_full Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title_fullStr Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title_full_unstemmed Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title_short Prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
title_sort prevention of human milk-acquired cytomegalovirus infection in very-low-birth-weight infants
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193732/
https://www.ncbi.nlm.nih.gov/pubmed/37202724
http://dx.doi.org/10.1186/s12887-023-04044-8
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