TY - JOUR
T1 - Australia IBD Microbiome (AIM) Study
T2 - protocol for a multicentre longitudinal prospective cohort study
AU - Williams, Astrid Jane
AU - Paramsothy, Ramesh
AU - Wu, Nan
AU - Ghaly, Simon
AU - Leach, Steven
AU - Paramsothy, Sudarshan
AU - Corte, Crispin
AU - O'Brien, Claire
AU - Burke, Catherine
AU - Wark, Gabrielle
AU - Samocha-Bonet, Dorit
AU - Lambert, Kelly
AU - Ahlenstiel, Golo
AU - Wasinger, Valerie
AU - Dutt, Shoma
AU - Pavli, Paul
AU - Grimm, Michael
AU - Lemberg, Daniel
AU - Connor, Susan
AU - Leong, Rupert
AU - Hold, Georgina
N1 - Copyright:
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Funding Information:
University of New South Wales is the primary sponsor for the AIM study. This work was supported by Gastroenterology Society of Australia (GESA; Research Collaboration Award 2018), Sydney Children’s Hospital Randwick, St George and Sutherland Medical Research Foundation (SSMRF; Research Grant 2019) and Crohn’s Colitis Australia.
Publisher Copyright:
© 2021 BMJ Publishing Group. All rights reserved.
PY - 2021/2/16
Y1 - 2021/2/16
N2 - INTRODUCTION: Crohn's disease and ulcerative colitis are common chronic idiopathic inflammatory bowel diseases (IBD), which cause considerable morbidity. Although the precise mechanisms of disease remain unclear, evidence implicates a strong multidirectional interplay between diet, environmental factors, genetic determinants/immune perturbations and the gut microbiota. IBD can be brought into remission using a number of medications, which act by suppressing the immune response. However, none of the available medications address any of the underlying potential mechanisms. As we understand more about how the microbiota drives inflammation, much interest has focused on identifying microbial signals/triggers in the search for effective therapeutic targets. We describe the establishment of the Australian IBD Microbiota (AIM) Study, Australia's first longitudinal IBD bioresource, which will identify and correlate longitudinal microbial and metagenomics signals to disease activity as evaluated by validated clinical instruments, patient-reported surveys, as well as biomarkers. The AIM Study will also gather extensive demographic, clinical, lifestyle and dietary data known to influence microbial composition in order to generate a more complete understanding of the interplay between patients with IBD and their microbiota. METHODS: The AIM Study is an Australian multicentre longitudinal prospective cohort study, which will enrol 1000 participants; 500 patients with IBD and 500 healthy controls over a 5-year period. Assessment occurs at 3 monthly intervals over a 24-month period. At each assessment oral and faecal samples are self-collected along with patient-reported outcome measures, with clinical data also collected at baseline, 12 and 24 months. Intestinal tissue will be sampled whenever a colonoscopy is performed. Dietary intake, general health and psychological state will be assessed using validated self-report questionnaires. Samples will undergo metagenomic, transcriptomic, proteomic, metabolomic and culturomic analyses. Omics data will be integrated with clinical data to identify predictive biomarkers of response to therapy, disease behaviour and environmental factors in patients with IBD. ETHICS AND DISSEMINATION: Ethical approval for this study has been obtained from the South Eastern Sydney Local Health District Research Ethics Committee (HREC 2019/ETH11443). Findings will be reported at national and international gastroenterology meetings and published in peer-reviewed journals. TRIAL REGISTRATION NUMBER: ACTRN12619000911190.
AB - INTRODUCTION: Crohn's disease and ulcerative colitis are common chronic idiopathic inflammatory bowel diseases (IBD), which cause considerable morbidity. Although the precise mechanisms of disease remain unclear, evidence implicates a strong multidirectional interplay between diet, environmental factors, genetic determinants/immune perturbations and the gut microbiota. IBD can be brought into remission using a number of medications, which act by suppressing the immune response. However, none of the available medications address any of the underlying potential mechanisms. As we understand more about how the microbiota drives inflammation, much interest has focused on identifying microbial signals/triggers in the search for effective therapeutic targets. We describe the establishment of the Australian IBD Microbiota (AIM) Study, Australia's first longitudinal IBD bioresource, which will identify and correlate longitudinal microbial and metagenomics signals to disease activity as evaluated by validated clinical instruments, patient-reported surveys, as well as biomarkers. The AIM Study will also gather extensive demographic, clinical, lifestyle and dietary data known to influence microbial composition in order to generate a more complete understanding of the interplay between patients with IBD and their microbiota. METHODS: The AIM Study is an Australian multicentre longitudinal prospective cohort study, which will enrol 1000 participants; 500 patients with IBD and 500 healthy controls over a 5-year period. Assessment occurs at 3 monthly intervals over a 24-month period. At each assessment oral and faecal samples are self-collected along with patient-reported outcome measures, with clinical data also collected at baseline, 12 and 24 months. Intestinal tissue will be sampled whenever a colonoscopy is performed. Dietary intake, general health and psychological state will be assessed using validated self-report questionnaires. Samples will undergo metagenomic, transcriptomic, proteomic, metabolomic and culturomic analyses. Omics data will be integrated with clinical data to identify predictive biomarkers of response to therapy, disease behaviour and environmental factors in patients with IBD. ETHICS AND DISSEMINATION: Ethical approval for this study has been obtained from the South Eastern Sydney Local Health District Research Ethics Committee (HREC 2019/ETH11443). Findings will be reported at national and international gastroenterology meetings and published in peer-reviewed journals. TRIAL REGISTRATION NUMBER: ACTRN12619000911190.
KW - Adult gastroenterology
KW - Inflammatory bowel disease
KW - Paediatric gastroenterology
UR - http://www.scopus.com/inward/record.url?scp=85101709314&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2020-042493
DO - 10.1136/bmjopen-2020-042493
M3 - Article
C2 - 33593778
AN - SCOPUS:85101709314
SN - 2044-6055
VL - 11
SP - 1
EP - 8
JO - BMJ Open
JF - BMJ Open
IS - 2
M1 - e042493
ER -