Evaluation of plasma microRNA-122, high-mobility group box 1 and keratin-18 concentrations to stratify acute gallstone disease: a pilot observational cohort study in an emergency general surgery unit

ObjectiveTo 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 interventio...

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Veröffentlicht in:BMJ open 2018-04, Vol.8 (4), p.e020061-e020061
Hauptverfasser: Th’ng, Francesca, Vliegenthart, Bastiaan, Lea, Jonathan D, Antoine, Daniel J, Dear, James W, Mole, Damian J
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Sprache:eng
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Zusammenfassung:ObjectiveTo 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.DesignAn observational biomarker cohort pilot study.SettingIn a Scottish University teaching hospital for 12 months beginning on 3 September 2014.ParticipantsBlood 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 measuresTo 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.Results300 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: 2.89×104 copies/mL vs 0.90×104 copies/mL (p
ISSN:2044-6055
2044-6055
DOI:10.1136/bmjopen-2017-020061