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Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction

An increased awareness on neonatal pain-associated complications has led to the development of pain scales adequate to assess the level of pain experienced by newborns such as the ABC score. A commonly used analgesic procedure is to administer a 33% oral dextrose solution to newborns prior to the pa...

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Autores principales: Erbi, Ilaria, Ciantelli, Massimiliano, Farinella, Riccardo, Tuoni, Cristina, Gentiluomo, Manuel, Moscuzza, Francesca, Rizzato, Cosmeri, Bedini, Alice, Faraoni, Maddalena, Giusfredi, Stefano, Tavanti, Arianna, Ghirri, Paolo, Campa, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184594/
https://www.ncbi.nlm.nih.gov/pubmed/32341423
http://dx.doi.org/10.1038/s41598-020-63790-2
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author Erbi, Ilaria
Ciantelli, Massimiliano
Farinella, Riccardo
Tuoni, Cristina
Gentiluomo, Manuel
Moscuzza, Francesca
Rizzato, Cosmeri
Bedini, Alice
Faraoni, Maddalena
Giusfredi, Stefano
Tavanti, Arianna
Ghirri, Paolo
Campa, Daniele
author_facet Erbi, Ilaria
Ciantelli, Massimiliano
Farinella, Riccardo
Tuoni, Cristina
Gentiluomo, Manuel
Moscuzza, Francesca
Rizzato, Cosmeri
Bedini, Alice
Faraoni, Maddalena
Giusfredi, Stefano
Tavanti, Arianna
Ghirri, Paolo
Campa, Daniele
author_sort Erbi, Ilaria
collection PubMed
description An increased awareness on neonatal pain-associated complications has led to the development of pain scales adequate to assess the level of pain experienced by newborns such as the ABC score. A commonly used analgesic procedure is to administer a 33% oral dextrose solution to newborns prior to the painful intervention. Although this procedure is very successful, not in all subjects it reaches complete efficacy. A possible explanation for the different response to the treatment could be genetic variability. We have investigated the genetic variability of the OPRM1 gene in 1077 newborns in relation to non-pharmacologic pain relief treatment. We observed that the procedure was successful in 966 individuals and there was no association between the genotypes and the analgesic efficacy when comparing individuals that had an ABC score = 0 and ABC score >0. However, considering only the individuals with ABC score>0, we found that the homozygous carriers of the G allele of the missense variant SNP rs1799971 (A118G) showed an interesting association with higher ABC score. We also observed that individuals fed with formula milk were more likely to not respond to the analgesic treatment compared to those that had been breastfed.
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spelling pubmed-71845942020-04-29 Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction Erbi, Ilaria Ciantelli, Massimiliano Farinella, Riccardo Tuoni, Cristina Gentiluomo, Manuel Moscuzza, Francesca Rizzato, Cosmeri Bedini, Alice Faraoni, Maddalena Giusfredi, Stefano Tavanti, Arianna Ghirri, Paolo Campa, Daniele Sci Rep Article An increased awareness on neonatal pain-associated complications has led to the development of pain scales adequate to assess the level of pain experienced by newborns such as the ABC score. A commonly used analgesic procedure is to administer a 33% oral dextrose solution to newborns prior to the painful intervention. Although this procedure is very successful, not in all subjects it reaches complete efficacy. A possible explanation for the different response to the treatment could be genetic variability. We have investigated the genetic variability of the OPRM1 gene in 1077 newborns in relation to non-pharmacologic pain relief treatment. We observed that the procedure was successful in 966 individuals and there was no association between the genotypes and the analgesic efficacy when comparing individuals that had an ABC score = 0 and ABC score >0. However, considering only the individuals with ABC score>0, we found that the homozygous carriers of the G allele of the missense variant SNP rs1799971 (A118G) showed an interesting association with higher ABC score. We also observed that individuals fed with formula milk were more likely to not respond to the analgesic treatment compared to those that had been breastfed. Nature Publishing Group UK 2020-04-27 /pmc/articles/PMC7184594/ /pubmed/32341423 http://dx.doi.org/10.1038/s41598-020-63790-2 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Erbi, Ilaria
Ciantelli, Massimiliano
Farinella, Riccardo
Tuoni, Cristina
Gentiluomo, Manuel
Moscuzza, Francesca
Rizzato, Cosmeri
Bedini, Alice
Faraoni, Maddalena
Giusfredi, Stefano
Tavanti, Arianna
Ghirri, Paolo
Campa, Daniele
Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title_full Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title_fullStr Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title_full_unstemmed Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title_short Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction
title_sort role of oprm1, clinical and anthropometric variants in neonatal pain reduction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184594/
https://www.ncbi.nlm.nih.gov/pubmed/32341423
http://dx.doi.org/10.1038/s41598-020-63790-2
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