TY - JOUR
T1 - Cohort profile of the PRoteomic Evaluation and Discovery in an IBD Cohort of Tri-service Subjects (PREDICTS) study
T2 - Rationale, organization, design, and baseline characteristics
AU - PREDICTS study team
AU - Porter, Chad K.
AU - Riddle, Mark S.
AU - Gutierrez, Ramiro L.
AU - Princen, Fred
AU - Strauss, Rick
AU - Telesco, Shannon E.
AU - Torres, Joana
AU - Choung, Rok Seon
AU - Laird, Renee M.
AU - Leon, Francisco
AU - Colombel, Jean Frédéric
AU - Murray, Joseph A.
N1 - Funding Information:
This study is coordinated and executed through a Steering Committee (SC) and supported by project management, regulatory, biospecimen and data archival support functions under a Navy Cooperative Research and Development Agreement (CRADA# NMR-11-3920, Antimicrobial Antibodies as Predictors of Inflammatory Bowel Diseases) ( ). The primary function of the SC is to oversee research efforts conducted under the PREDICTS protocols and CRADA. The SC and PREDICTS Study is governed by a written charter (Supplemental Files) which includes specific guidance, policies and procedures for handling data and serum utilization requests, publication and presentation clearance, data sharing, as well as appeal processes to handle disputes. In addition to managing these procedural functions, the SC reviews and monitors all research efforts and provides guidance and direction for future research. The SC provides a stabilizing influence among vested stakeholders so organizational concepts and directions are established and maintained with a mission-oriented view. The SC provides insight on long-term strategies in support of research objectives. Members of the SC ensure objectives are adequately addressed and projects remain under appropriate control and oversight. The SC is also charged with the responsibility of advocating for the Study and identifying new partnerships and opportunities. Fig. 2
Funding Information:
Dr Murray has received grant funding from Alba Therapeutics and Alvine Pharmaceuticals, Inc., has served on an advisory board for Alvine Pharmaceuticals, Inc., and has served as a consultant for AMAG Pharmaceuticals, BioLineRx, Glenmark, UCB Pharma, Takeda, Celimmune and GlaxoSmithKline. J-F Colombel has served as consultant or advisory board member for Abbvie, ABScience, Amgen, Bristol-Myers Squibb, Celltrion, Danone, Ferring, Genentech, Giuliani SPA, Given Imaging, Janssen, Immune Pharmaceuticals, Eli Lilly, Medimmune, Merck & Co., Millenium Pharmaceuticals Inc., Neovacs, Nutrition Science Partners Ltd., Pfizer Inc. Prometheus Laboratories, Protagonist, Receptos, Sanofi, Schering Plough Corporation, Second Genome, Shire, Takeda, Teva Pharmaceuticals, Tigenix, UCB Pharma, Vertex, Dr. August Wolff GmbH & Co. J-F Colombel has served as a speaker for Abbvie, Ferring, Janssen, Merck & Co., Nutrition Science Partners Ltd., Takeda. Joana Torres received consulting fees from Takeda and support from Abbvie to travel to conferences. Fred Princen, Thomas P. Stockfisch, and Sharat Singh are employees of Prometheus Laboratories. Francisco Leon was employee of Janssen R&D. The remaining author discloses no conflicts.
Funding Information:
Funding and support of the PREDICTS study platform was provided through a Cooperative and Research Development Agreement with direct contributions by Janssen Pharmaceuticals, Prometheus Laboratories and the Naval Medical Research Center (NCRADA number NMR-11-3920 ).
Publisher Copyright:
© 2019
PY - 2019/6
Y1 - 2019/6
N2 - Purpose: The etiology of Inflammatory Bowel Disease (IBD) remains currently unknown but evidence would suggest that it results from a complex interplay between genetic susceptibility genes, the intestinal microbiome and the environment, resulting in an increased response towards microbial and self-antigens, followed by the development of pre-clinical intestinal inflammation as a precursor to overt clinical disease. Efforts are needed to provide insights into the characterization of the disease, the possible prediction of complications, and the detection of a pre-clinical disease state where, through early screening and intervention, disease course can be reversed, attenuated or even prevented. A consortium of academic, industry and governmental organization investigators initiated this study to enable an assessment of pre-disease biomarkers in patients newly diagnosed with Crohn's disease (CD) and ulcerative colitis (UC). Participants: A retrospective cohort of 1000 UC and 1000 CD cases with 500 matched controls was drawn from an active duty US military personnel population with relevant inclusion criteria with three associated pre-disease and a single disease-associated archived serum samples. Findings to date: The PREDICTS study has been established as a biorepository platform study to perform novel discovery and analysis efforts in the field of IBD and proteomic systems biology. Future plans: This study is poised to enable the assessment of novel biomarkers within the serum compartment to be analyzed with the goal of identifying pre-disease signals that ultimately predict disease risk, and further elucidate disease pathogenesis in the early stages of the disease process, and identify novel exposures that increase disease risk.
AB - Purpose: The etiology of Inflammatory Bowel Disease (IBD) remains currently unknown but evidence would suggest that it results from a complex interplay between genetic susceptibility genes, the intestinal microbiome and the environment, resulting in an increased response towards microbial and self-antigens, followed by the development of pre-clinical intestinal inflammation as a precursor to overt clinical disease. Efforts are needed to provide insights into the characterization of the disease, the possible prediction of complications, and the detection of a pre-clinical disease state where, through early screening and intervention, disease course can be reversed, attenuated or even prevented. A consortium of academic, industry and governmental organization investigators initiated this study to enable an assessment of pre-disease biomarkers in patients newly diagnosed with Crohn's disease (CD) and ulcerative colitis (UC). Participants: A retrospective cohort of 1000 UC and 1000 CD cases with 500 matched controls was drawn from an active duty US military personnel population with relevant inclusion criteria with three associated pre-disease and a single disease-associated archived serum samples. Findings to date: The PREDICTS study has been established as a biorepository platform study to perform novel discovery and analysis efforts in the field of IBD and proteomic systems biology. Future plans: This study is poised to enable the assessment of novel biomarkers within the serum compartment to be analyzed with the goal of identifying pre-disease signals that ultimately predict disease risk, and further elucidate disease pathogenesis in the early stages of the disease process, and identify novel exposures that increase disease risk.
UR - http://www.scopus.com/inward/record.url?scp=85063696907&partnerID=8YFLogxK
U2 - 10.1016/j.conctc.2019.100345
DO - 10.1016/j.conctc.2019.100345
M3 - Article
AN - SCOPUS:85063696907
SN - 2451-8654
VL - 14
JO - Contemporary Clinical Trials Communications
JF - Contemporary Clinical Trials Communications
M1 - 100345
ER -