<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rosenfeld A</submitter><funding>Cancer Research UK</funding><funding>Rosetrees Trust</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><pagination>E37-E48</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7056359</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Screening for Barrett's Oesophagus (BE) relies on endoscopy which is invasive and has a low yield. This study aimed to develop and externally validate a simple symptom and risk-factor questionnaire to screen for patients with BE.&lt;h4>Methods&lt;/h4>Questionnaires from 1299 patients in the BEST2 case-controlled study were analysed: 880 had BE including 40 with invasive oesophageal adenocarcinoma (OAC) and 419 were controls. This was randomly split into a training cohort of 776 patients and an internal validation cohort of 523 patients. External validation included 398 patients from the BOOST case-controlled study: 198 with BE (23 with OAC) and 200 controls. Identification of independently important diagnostic features was undertaken using machine learning techniques informati</pubmed_abstract><journal>The Lancet. Digital health</journal><pubmed_title>Development and validation of a risk prediction model to diagnose Barrett's oesophagus (MARK-BE): a case-control machine learning approach.</pubmed_title><pmcid>PMC7056359</pmcid><funding_grant_id>203145Z/16/Z</funding_grant_id><funding_grant_id>16893</funding_grant_id><funding_grant_id>M661</funding_grant_id><funding_grant_id>A12088</funding_grant_id><pubmed_authors>Hagan D</pubmed_authors><pubmed_authors>Winstanley A</pubmed_authors><pubmed_authors>Lovat SJ</pubmed_authors><pubmed_authors>Heifetz EM</pubmed_authors><pubmed_authors>Lovat LB</pubmed_authors><pubmed_authors>Rodriguez Justo M</pubmed_authors><pubmed_authors>BEST2 study group</pubmed_authors><pubmed_authors>Sami SS</pubmed_authors><pubmed_authors>Noiman U</pubmed_authors><pubmed_authors>Wilson A</pubmed_authors><pubmed_authors>Sasieni P</pubmed_authors><pubmed_authors>Jevons S</pubmed_authors><pubmed_authors>Ariza J</pubmed_authors><pubmed_authors>Ahmad OF</pubmed_authors><pubmed_authors>Graham DG</pubmed_authors><pubmed_authors>Ben-Zecharia M</pubmed_authors><pubmed_authors>Rosenfeld A</pubmed_authors><pubmed_authors>Fitzgerald RC</pubmed_authors><pubmed_authors>Novelli M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and validation of a risk prediction model to diagnose Barrett's oesophagus (MARK-BE): a case-control machine learning approach.</name><description>&lt;h4>Background&lt;/h4>Screening for Barrett's Oesophagus (BE) relies on endoscopy which is invasive and has a low yield. This study aimed to develop and externally validate a simple symptom and risk-factor questionnaire to screen for patients with BE.&lt;h4>Methods&lt;/h4>Questionnaires from 1299 patients in the BEST2 case-controlled study were analysed: 880 had BE including 40 with invasive oesophageal adenocarcinoma (OAC) and 419 were controls. This was randomly split into a training cohort of 776 patients and an internal validation cohort of 523 patients. External validation included 398 patients from the BOOST case-controlled study: 198 with BE (23 with OAC) and 200 controls. Identification of independently important diagnostic features was undertaken using machine learning techniques informati</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-22T00:21:44.225Z</modification><creation>2020-05-22T12:09:07Z</creation></dates><accession>S-EPMC7056359</accession><cross_references><pubmed>32133440</pubmed><doi>10.1016/s2589-7500(19)30216-x</doi><doi>10.1016/S2589-7500(19)30216-X</doi></cross_references></HashMap>