PT - JOURNAL ARTICLE AU - Xu, Yiwang AU - Miremadi, Ahmad AU - Link, Alexander AU - Malfertheiner, Peter AU - Fitzgerald, Rebecca C AU - Bornschein, Jan TI - Feasibility of combined screening for upper gastrointestinal adenocarcinoma risk by serology and Cytosponge testing: the SUGAR study AID - 10.1136/jclinpath-2019-205700 DP - 2019 Dec 01 TA - Journal of Clinical Pathology PG - 825--829 VI - 72 IP - 12 4099 - http://jcp.bmj.com/content/72/12/825.short 4100 - http://jcp.bmj.com/content/72/12/825.full SO - J Clin Pathol2019 Dec 01; 72 AB - Aims Aim was to assess the feasibility of serum markers to identify individuals at risk for gastro-oesophageal adenocarcinoma to reduce the number of individuals requiring invasive assessment by endoscopy.Methods Blood samples from 56 patients with Barrett’s oesophagus and 202 non-Barrett controls who previously took part in a trial assessing the accuracy of the Cytosponge for Barrett’s oesophagus were assessed for serum pepsinogen (PG) 1 and 2, gastrin-17, trefoil factor 3 (TFF3) and Helicobacter pylori infection.Results PG1 was pathological (<50 ng/mL) in 26 patients (10.1%), none of whom had Barrett’s oesophagus (p<0.001). Smoking and drinking had no influence on these results. Pathological PG1 was associated with stomach pain (p=0.029), disruption of sleep (p=0.027) and disruption of diet by symptoms (p=0.019). Serum TFF3 was not associated with any clinical parameter.Conclusions Assessment of serum PG1 could be combined with a test for Barrett’s oesophagus to identify additional patients requiring endoscopy.