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Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study

BACKGROUND: Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis in children, and its cause remains unknown. The Immune-metabolic CONnections to Scoliosis (ICONS) Study was designed to elucidate the potential mechanisms by which immune system-paraspinal muscle crosstalk contrib...

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Autores principales: Rudrapatna, Srikesh, Peterson, Devin, Missiuna, Paul, Aditya, Ishan, Drew, Brian, Sahar, Nicola, Thabane, Lehana, Samaan, M. Constantine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715623/
https://www.ncbi.nlm.nih.gov/pubmed/29225911
http://dx.doi.org/10.1186/s40814-017-0193-0
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author Rudrapatna, Srikesh
Peterson, Devin
Missiuna, Paul
Aditya, Ishan
Drew, Brian
Sahar, Nicola
Thabane, Lehana
Samaan, M. Constantine
author_facet Rudrapatna, Srikesh
Peterson, Devin
Missiuna, Paul
Aditya, Ishan
Drew, Brian
Sahar, Nicola
Thabane, Lehana
Samaan, M. Constantine
author_sort Rudrapatna, Srikesh
collection PubMed
description BACKGROUND: Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis in children, and its cause remains unknown. The Immune-metabolic CONnections to Scoliosis (ICONS) Study was designed to elucidate the potential mechanisms by which immune system-paraspinal muscle crosstalk contributes to the development of AIS. In this report, we document the evaluation of ICONS Study feasibility. METHODS: This study was conducted at a tertiary pediatric academic center in Hamilton, Ontario, Canada. We included boys and girls, aged 10–17 years with a diagnosis of AIS requiring corrective spinal surgery. Exclusion criteria included patients on high-dose steroids, immunosuppressive therapy, anti-thrombotic medications, those with an active infection for 15 days before participation, autoimmune disease, pregnancy, and patients who were unwilling to consent. Pre-determined feasibility criteria included permission to approach participants and recruitment rates of 80%, consenting of at least 80% of participants to provide biological samples, 90% or higher case report form and questionnaire completion, resources to be sufficient in at least 80% of recruitments, and the ability to successfully collect and process 80% or more of the biological samples needed for this study. RESULTS: Between August 2013 and October 2014, we identified 32 potential participants with AIS, but had the resources to approach only 16, of which 12 (75%) agreed to be approached by the research team, and all consented to participate. Of the 12 participants recruited, 11 questionnaire packages and muscle biopsies (91.7% for each objective) were collected, while other biological samples (serum, plasma, whole blood for DNA and RNA processing, urine) were collected from all participants. CONCLUSIONS: The ICONS study protocols and procedures are feasible. However, recruitment rates were less than predicted. For the full study, we plan on prolonging the recruitment phase and the inclusion of additional centers to achieve recruitment targets.
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spelling pubmed-57156232017-12-08 Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study Rudrapatna, Srikesh Peterson, Devin Missiuna, Paul Aditya, Ishan Drew, Brian Sahar, Nicola Thabane, Lehana Samaan, M. Constantine Pilot Feasibility Stud Research BACKGROUND: Adolescent idiopathic scoliosis (AIS) is the most common form of scoliosis in children, and its cause remains unknown. The Immune-metabolic CONnections to Scoliosis (ICONS) Study was designed to elucidate the potential mechanisms by which immune system-paraspinal muscle crosstalk contributes to the development of AIS. In this report, we document the evaluation of ICONS Study feasibility. METHODS: This study was conducted at a tertiary pediatric academic center in Hamilton, Ontario, Canada. We included boys and girls, aged 10–17 years with a diagnosis of AIS requiring corrective spinal surgery. Exclusion criteria included patients on high-dose steroids, immunosuppressive therapy, anti-thrombotic medications, those with an active infection for 15 days before participation, autoimmune disease, pregnancy, and patients who were unwilling to consent. Pre-determined feasibility criteria included permission to approach participants and recruitment rates of 80%, consenting of at least 80% of participants to provide biological samples, 90% or higher case report form and questionnaire completion, resources to be sufficient in at least 80% of recruitments, and the ability to successfully collect and process 80% or more of the biological samples needed for this study. RESULTS: Between August 2013 and October 2014, we identified 32 potential participants with AIS, but had the resources to approach only 16, of which 12 (75%) agreed to be approached by the research team, and all consented to participate. Of the 12 participants recruited, 11 questionnaire packages and muscle biopsies (91.7% for each objective) were collected, while other biological samples (serum, plasma, whole blood for DNA and RNA processing, urine) were collected from all participants. CONCLUSIONS: The ICONS study protocols and procedures are feasible. However, recruitment rates were less than predicted. For the full study, we plan on prolonging the recruitment phase and the inclusion of additional centers to achieve recruitment targets. BioMed Central 2017-12-05 /pmc/articles/PMC5715623/ /pubmed/29225911 http://dx.doi.org/10.1186/s40814-017-0193-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Research
Rudrapatna, Srikesh
Peterson, Devin
Missiuna, Paul
Aditya, Ishan
Drew, Brian
Sahar, Nicola
Thabane, Lehana
Samaan, M. Constantine
Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title_full Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title_fullStr Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title_full_unstemmed Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title_short Understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
title_sort understanding muscle-immune interactions in adolescent idiopathic scoliosis: a feasibility study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715623/
https://www.ncbi.nlm.nih.gov/pubmed/29225911
http://dx.doi.org/10.1186/s40814-017-0193-0
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