Sharon E. Cooke
Townsville Hospital
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Featured researches published by Sharon E. Cooke.
PLOS ONE | 2011
A. James M. Daveson; Dianne Jones; Soraya Gaze; Henry J. McSorley; Andrew D. Clouston; Andrew Pascoe; Sharon E. Cooke; Richard Speare; Graeme A. Macdonald; Robert P. Anderson; James S. McCarthy; Alex Loukas; John Croese
Background and Aims The association between hygiene and prevalence of autoimmune disease has been attributed in part to enteric helminth infection. A pilot study of experimental infection with the hookworm Necator americanus was undertaken among a group of otherwise healthy people with celiac disease to test the potential of the helminth to suppress the immunopathology induced by gluten. Methods In a 21-week, double-blinded, placebo-controlled study, we explored the effects of N. americanus infection in 20 healthy, helminth-naïve adults with celiac disease well controlled by diet. Staged cutaneous inoculations with 10 and 5 infective 3rd stage hookworm larvae or placebo were performed at week-0 and -12 respectively. At week-20, a five day oral wheat challenge equivalent to 16 grams of gluten per day was undertaken. Primary outcomes included duodenal Marsh score and quantification of the immunodominant α-gliadin peptide (QE65)-specific systemic interferon-γ-producing cells by ELISpot pre- and post-wheat challenge. Results Enteric colonisation with hookworm established in all 10 cases, resulting in transiently painful enteritis in 5. Chronic infection was asymptomatic, with no effect on hemoglobin levels. Although some duodenal eosinophilia was apparent, hookworm-infected mucosa retained a healthy appearance. In both groups, wheat challenge caused deterioration in both primary and several secondary outcomes. Conclusions Experimental N. americanus infection proved to be safe and enabled testing its effect on a range of measures of the human autoimmune response. Infection imposed no obvious benefit on pathology. Trial Registration ClinicalTrials.gov NCT00671138
Journal of Crohns & Colitis | 2013
Ian C. Lawrance; Kevin Murray; Birol Batman; Richard B. Gearry; Rachel Grafton; Krupa Krishnaprasad; Jane M. Andrews; Ruth Prosser; Peter A. Bampton; Sharon E. Cooke; Gillian Mahy; Graham L. Radford-Smith; Anthony Croft; Katherine Hanigan
BACKGROUND Smoking increases CD risk. The aim was to determine if smoking cessation at, prior to, or following, CD diagnosis affects medication use, disease phenotypic progression and/or surgery. METHODS Data on CD patients with disease for ≥5 yrs were collected retrospectively including the Montreal classification, smoking history, CD-related abdominal surgeries, family history, medication use and disease behaviour at diagnosis and the time when the disease behaviour changed. RESULTS 1115 patients were included across six sites (mean follow-up-16.6 yrs). More non-smokers were male (p=0.047) with A1 (p<0.0001), L4 (p=0.028) and perianal (p=0.03) disease. Non-smokers more frequently received anti-TNF agents (p=0.049). (p=0.017: OR 2.5 95%CI 1.18-5.16) and those who ceased smoking prior to diagnosis (p=0.045: OR 2.3 95%CI 1.02-5.21) progressed to complicated (B2/B3) disease as compared to those quitting at diagnosis. Patients with uncomplicated terminal ileal disease at diagnosis more frequently developed B2/B3 disease than isolated colonic CD (p<0.0001). B2/B3 disease was more frequent with perianal disease (p<0.0001) and if i.v. steroids (p=0.004) or immunosuppressants (p<0.0001) were used. 49.3% (558/1115) of patients required at least one intestinal surgery. More smokers had a 2nd surgical resection than patients who quit at, or before, the 1st resection and non-smokers (p=0.044: HR=1.39 95%CI 1.01-1.91). Patients smoking >3 cigarettes/day had an increased risk of developing B2/B3 disease (p=0.012: OR 3.8 95%CI 1.27-11.17). CONCLUSION Progression to B2/B3 disease and surgery is reduced by smoking cessation. All CD patients regardless of when they were diagnosed, or how many surgeries, should be strongly encouraged to cease smoking.
Alimentary Pharmacology & Therapeutics | 2017
James D. Doecke; F. Hartnell; P. Bampton; Sally Bell; Gillian Mahy; Zubin Grover; Peter Lewindon; Lee Jones; Karen Sewell; Krupa Krishnaprasad; Ruth Prosser; D. Marr; J. Fischer; G. Thomas; Jane V. Tehan; Nik S. Ding; Sharon E. Cooke; K. Moss; Alexandra Sechi; P. De Cruz; Rachel Grafton; Susan J. Connor; Ian C. Lawrance; Richard B. Gearry; Jane M. Andrews; Graham L. Radford-Smith
Maintenance anti‐tumour necrosis factor‐α (anti‐TNFα) treatment for Crohns disease is the standard of care for patients with an inadequate response to corticosteroids and immunomodulators.
Journal of Crohns & Colitis | 2012
Krupa Krishnaprasad; Jane M. Andrews; Ian C. Lawrance; Timothy H. Florin; Richard B. Gearry; Rupert W. Leong; Gillian Mahy; Peter A. Bampton; Ruth Prosser; Peta Leach; Laurie Chitti; Charles Cock; Rachel Grafton; Anthony Croft; Sharon E. Cooke; James D. Doecke; Graham L. Radford-Smith
BACKGROUND Crohns disease (CD) exhibits significant clinical heterogeneity. Classification systems attempt to describe this; however, their utility and reliability depends on inter-observer agreement (IOA). We therefore sought to evaluate IOA using the Montreal Classification (MC). METHODS De-identified clinical records of 35 CD patients from 6 Australian IBD centres were presented to 13 expert practitioners from 8 Australia and New Zealand Inflammatory Bowel Disease Consortium (ANZIBDC) centres. Practitioners classified the cases using MC and forwarded data for central blinded analysis. IOA on smoking and medications was also tested. Kappa statistics, with pre-specified outcomes of κ>0.8 excellent; 0.61-0.8 good; 0.41-0.6 moderate and ≤0.4 poor, were used. RESULTS 97% of study cases had colonoscopy reports, however, only 31% had undergone a complete set of diagnostic investigations (colonoscopy, histology, SB imaging). At diagnosis, IOA was excellent for age, κ=0.84; good for disease location, κ=0.73; only moderate for upper GI disease (κ=0.57) and disease behaviour, κ=0.54; and good for the presence of perianal disease, κ=0.6. At last follow-up, IOA was good for location, κ=0.68; only moderate for upper GI disease (κ=0.43) and disease behaviour, κ=0.46; but excellent for the presence/absence of perianal disease, κ=0.88. IOA for immunosuppressant use ever and presence of stricture were both good (κ=0.79 and 0.64 respectively). CONCLUSION IOA using MC is generally good; however some areas are less consistent than others. Omissions and inaccuracies reduce the value of clinical data when comparing cohorts across different centres, and may impair the ability to translate genetic discoveries into clinical practice.
British Journal of Radiology | 2002
Nick A Maskell; Sharon E. Cooke; Dj Meecham Jones; Jg Prior; Rj Butland
Gastroenterology | 2012
Graham L. Radford-Smith; F. Hartnell; Lee Jones; Krupa Krishnaprasad; Ruth Prosser; Debbie Marr; Rachel Grafton; Sharon E. Cooke; Jesse Fischer; Gareth R. Thomas; Zubin Grover; Peter Lewindon; Jane V. Tehan; Nik S. Ding; Kerrie Moss; Sally Bell; Peter De Cruz; Gillian Mahy; Karen Sewell; Anthony Croft; Peter O'Rourke; Ian C. Lawrance; Peter A. Bampton; Jane M. Andrews; Richard B. Gearry
Gastroenterology | 2011
Ian C. Lawrance; Birol Batman; Richard B. Gearry; Rachel Grafton; Krupa Krishnaprasad; Jane M. Andrews; Ruth Prosser; Peter A. Bampton; Sharon E. Cooke; Gillian Mahy; Graham L. Radford-Smith; Anthony Croft; Katherine Hanigan
The Australian Journal of Medical Science | 2008
Richard Speare; Wayne Melrose; Sharon E. Cooke; John Croese
Journal of Crohns & Colitis | 2018
Samba Siva Reddy Pulusu; Ashish Srinivasan; Krupa Krishnaprasad; D Cheng; Tamara Mogilevski; Emma Flanagan; C Keung; C Wu; Ruth Prosser; Elise Sawyer; Q U A Rizvi; Heidi Y. Su; Wai K. Leung; A Edmundson; Sharon E. Cooke; Gillian Mahy; Lena W. Y. Thin; Graham L. Radford-Smith; M. Sparrow; Jane M. Andrews; Susan J. Connor; P. Bampton; Simon Ghaly; D. R. Van Langenberg; S.J. Bell; P. De Cruz; Jakob Begun; Siew C. Ng; Simon Travis; Ian C. Lawrance
Gastroenterology | 2018
Samba Siva Reddy Pulusu; Ashish Srinivasan; Krupa Krishnaprasad; Daniel Cheng; Tamara Mogilevski; Emma Flanagan; Charlotte Keung; Yang Wu; Ruth Prosser; Elise Sawyer; Quart-Ul-Ain Rizvi; Heidi Y. Su; Wai K. Leung; Aleksandra Edmundson; Sharon E. Cooke; Gillian Mahy; Lena W. Y. Thin; Graham L. Radford-Smith; Miles Sparrow; Jane M. Andrews; Susan J. Connor; Peter A. Bampton; Ghaly Simon; Daniel R. van Langenberg; Sally Bell; Peter De Cruz; Jakob Begun; Siew C. Ng; Simon Travis; Ian C. Lawrance