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  • Infectious diseases, Immunology (including allergy), Drugs: cardiovascular system, Headache (including migraine), Pain (neurology), Stroke, Hypertension, Pregnancy, Reproductive medicine, Ischaemic heart disease, Child health, Pain (palliative care), Biological agents, Degenerative joint disease, Drugs: musculoskeletal and joint diseases, Musculoskeletal syndromes, Osteoarthritis, Sexual health, Gastrointestinal surgery, Transplantation, Urological surgery, Poisoning, Artificial and donated transplantation, Occupational and environmental medicine  (1)
  • Open access, Gastroenterology and hepatology  (1)
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  • 1
    Publication Date: 2015-07-11
    Description: When a doctor recommends a new medicine there are questions that a patient would hope to have answered. Will the treatment work for my clinical problem? Are there side effects? How many tablets do I...
    Keywords: Infectious diseases, Immunology (including allergy), Drugs: cardiovascular system, Headache (including migraine), Pain (neurology), Stroke, Hypertension, Pregnancy, Reproductive medicine, Ischaemic heart disease, Child health, Pain (palliative care), Biological agents, Degenerative joint disease, Drugs: musculoskeletal and joint diseases, Musculoskeletal syndromes, Osteoarthritis, Sexual health, Gastrointestinal surgery, Transplantation, Urological surgery, Poisoning, Artificial and donated transplantation, Occupational and environmental medicine
    Topics: Medicine
    Published by BMJ Publishing Group
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  • 2
    Publication Date: 2018-04-28
    Description: Objective To obtain pilot data to evaluate the discriminatory power of biomarkers microRNA-122 (miR-122), high-mobility group box 1 (HMGB1), full-length keratin-18 (flk-18) and caspase-cleaved keratin-18 (cck-18) in plasma to identify potential biliary complications that may require acute intervention. Design An observational biomarker cohort pilot study. Setting In a Scottish University teaching hospital for 12 months beginning on 3 September 2014. Participants Blood samples were collected from adults (≥16 years old) referred with acute biliary-type symptoms who have presented to hospital within 24 hours prior were recruited. Patients unable or refused to give informed consent or were transferred from a hospital outside the National Health Service regional trust were excluded. Primary outcome measures To evaluate whether circulating miR-122, HMGB1, flk-18 and cck-18 can discriminate between people with and without gallstone disease and uncomplicated from complicated gallstone disease during the first 24 hours of hospital admission. Results 300 patients were screened of which 285 patients were included. Plasma miR-122, cck-18 and flk-18 concentrations were increased in patients with gallstones compared with those without (miR-122: median: 2.89 x 10 4 copies/mL vs 0.90 x 10 4 copies/mL (p〈0.001); cck-18: 121.2 U/L vs 103.5 U/L (p=0.031); flk-18: 252.4 U/L vs 145.1 U/L (p〈0.001)). Uncomplicated gallstone disease was associated with higher miR-122 and cck-18 concentrations than complicated disease (miR-122: 5.72 x 10 4 copies/mL vs 2.26 x 10 4 copies/mL (p=0.023); cck-18: 139.7 U/L vs 113.6 U/L (p=0.047)). There was no significant difference in HMGB1 concentration between patients with and without gallstones (p=0.559). Separation between groups for all biomarkers was modest. Conclusion miR-122 and keratin-18 plasma concentrations are elevated in patients with gallstones. However, this result is confounded by the association between biomarker concentrations, age and gender. In this pilot study, miR-122 and keratin-18 were not sufficiently discriminatory to be progressed as clinically useful biomarkers in this context.
    Keywords: Open access, Gastroenterology and hepatology
    Electronic ISSN: 2044-6055
    Topics: Medicine
    Published by BMJ Publishing
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