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Pain after upper limb surgery under peripheral nerve block is associated with gut microbiome composition and diversity
Gut microbiota play a role in certain pain states. Hence, these microbiota also influence somatic pain. We aimed to determine if there was an association between gut microbiota (composition and diversity) and postoperative pain. Patients (n = 20) undergoing surgical fixation of distal radius fractur...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404729/ https://www.ncbi.nlm.nih.gov/pubmed/34485761 http://dx.doi.org/10.1016/j.ynpai.2021.100072 |
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author | Brenner, David Cherry, Paul Switzer, Tim Butt, Ihsan Stanton, Catherine Murphy, Kiera McNamara, Brian Iohom, Gabriella O'Mahony, Siobhain M. Shorten, George |
author_facet | Brenner, David Cherry, Paul Switzer, Tim Butt, Ihsan Stanton, Catherine Murphy, Kiera McNamara, Brian Iohom, Gabriella O'Mahony, Siobhain M. Shorten, George |
author_sort | Brenner, David |
collection | PubMed |
description | Gut microbiota play a role in certain pain states. Hence, these microbiota also influence somatic pain. We aimed to determine if there was an association between gut microbiota (composition and diversity) and postoperative pain. Patients (n = 20) undergoing surgical fixation of distal radius fracture under axillary brachial plexus block were studied. Gut microbiota diversity and abundance were analysed for association with: (i) a verbal pain rating scale of < 4/10 throughout the first 24 h after surgery (ii) a level of pain deemed “acceptable” by the patient during the first 24 h following surgery (iii) a maximum self-reported pain score during the first 24 h postoperatively and (iv) analgesic consumption during the first postoperative week. Analgesic consumption was inversely correlated with the Shannon index of alpha diversity. There were also significant differences, at the genus level (including Lachnospira), with respect to pain being “not acceptable” at 24 h postoperatively. Porphyromonas was more abundant in the group reporting an acceptable pain level at 24 h. An inverse correlation was noted between abundance of Collinsella and maximum self-reported pain score with movement. We have demonstrated for the first time that postoperative pain is associated with gut microbiota composition and diversity. Further work on the relationship between the gut microbiome and somatic pain may offer new therapeutic targets. |
format | Online Article Text |
id | pubmed-8404729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84047292021-09-02 Pain after upper limb surgery under peripheral nerve block is associated with gut microbiome composition and diversity Brenner, David Cherry, Paul Switzer, Tim Butt, Ihsan Stanton, Catherine Murphy, Kiera McNamara, Brian Iohom, Gabriella O'Mahony, Siobhain M. Shorten, George Neurobiol Pain Special issue on Microbiome and Pain Gut microbiota play a role in certain pain states. Hence, these microbiota also influence somatic pain. We aimed to determine if there was an association between gut microbiota (composition and diversity) and postoperative pain. Patients (n = 20) undergoing surgical fixation of distal radius fracture under axillary brachial plexus block were studied. Gut microbiota diversity and abundance were analysed for association with: (i) a verbal pain rating scale of < 4/10 throughout the first 24 h after surgery (ii) a level of pain deemed “acceptable” by the patient during the first 24 h following surgery (iii) a maximum self-reported pain score during the first 24 h postoperatively and (iv) analgesic consumption during the first postoperative week. Analgesic consumption was inversely correlated with the Shannon index of alpha diversity. There were also significant differences, at the genus level (including Lachnospira), with respect to pain being “not acceptable” at 24 h postoperatively. Porphyromonas was more abundant in the group reporting an acceptable pain level at 24 h. An inverse correlation was noted between abundance of Collinsella and maximum self-reported pain score with movement. We have demonstrated for the first time that postoperative pain is associated with gut microbiota composition and diversity. Further work on the relationship between the gut microbiome and somatic pain may offer new therapeutic targets. Elsevier 2021-08-18 /pmc/articles/PMC8404729/ /pubmed/34485761 http://dx.doi.org/10.1016/j.ynpai.2021.100072 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Special issue on Microbiome and Pain Brenner, David Cherry, Paul Switzer, Tim Butt, Ihsan Stanton, Catherine Murphy, Kiera McNamara, Brian Iohom, Gabriella O'Mahony, Siobhain M. Shorten, George Pain after upper limb surgery under peripheral nerve block is associated with gut microbiome composition and diversity |
title | Pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
title_full | Pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
title_fullStr | Pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
title_full_unstemmed | Pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
title_short | Pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
title_sort | pain after upper limb surgery under peripheral nerve block is associated
with gut microbiome composition and diversity |
topic | Special issue on Microbiome and Pain |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404729/ https://www.ncbi.nlm.nih.gov/pubmed/34485761 http://dx.doi.org/10.1016/j.ynpai.2021.100072 |
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