862. Faecal immunochemical testing (FIT) in patients with signs or symptoms of suspected colorectal cancer (CRC): a joint guideline from the Association of Coloproctology of Great Britain and Ireland (ACPGBI) and the British Society of Gastroenterology (BSG).
作者: Kevin J Monahan.;Michael M Davies.;Muti Abulafi.;Ayan Banerjea.;Brian D Nicholson.;Ramesh Arasaradnam.;Neil Barker.;Sally Benton.;Richard Booth.;David Burling.;Rachel Victoria Carten.;Nigel D'Souza.;James Edward East.;Jos Kleijnen.;Michael Machesney.;Maria Pettman.;Jenny Pipe.;Lance Saker.;Linda Sharp.;James Stephenson.;Robert Jc Steele.
来源: Gut. 2022年71卷10期1939-62页
Faecal immunochemical testing (FIT) has a high sensitivity for the detection of colorectal cancer (CRC). In a symptomatic population FIT may identify those patients who require colorectal investigation with the highest priority. FIT offers considerable advantages over the use of symptoms alone, as an objective measure of risk with a vastly superior positive predictive value for CRC, while conversely identifying a truly low risk cohort of patients. The aim of this guideline was to provide a clear strategy for the use of FIT in the diagnostic pathway of people with signs or symptoms of a suspected diagnosis of CRC. The guideline was jointly developed by the Association of Coloproctology of Great Britain and Ireland/British Society of Gastroenterology, specifically by a 21-member multidisciplinary guideline development group (GDG). A systematic review of 13 535 publications was undertaken to develop 23 evidence and expert opinion-based recommendations for the triage of people with symptoms of a suspected CRC diagnosis in primary care. In order to achieve consensus among a broad group of key stakeholders, we completed an extended Delphi of the GDG, and also 61 other individuals across the UK and Ireland, including by members of the public, charities and primary and secondary care. Seventeen research recommendations were also prioritised to inform clinical management.
863. Accurate liquid biopsy for the diagnosis of non-alcoholic steatohepatitis and liver fibrosis.
作者: Giulia Angelini.;Simona Panunzi.;Lidia Castagneto-Gissey.;Francesca Pellicanò.;Andrea De Gaetano.;Maurizio Pompili.;Laura Riccardi.;Matteo Garcovich.;Marco Raffaelli.;Luigi Ciccoritti.;Ornella Verrastro.;Maria Francesca Russo.;Fabio Maria Vecchio.;Giovanni Casella.;James Casella-Mariolo.;Luigi Papa.;Pier Luigi Marini.;Francesco Rubino.;Carel W le Roux.;Stefan Bornstein.;Geltrude Mingrone.
来源: Gut. 2023年72卷2期392-403页
Clinical diagnosis and approval of new medications for non-alcoholic steatohepatitis (NASH) require invasive liver biopsies. The aim of our study was to identify non-invasive biomarkers of NASH and/or liver fibrosis.
864. Regulatory enhancer profiling of mesenchymal-type gastric cancer reveals subtype-specific epigenomic landscapes and targetable vulnerabilities.
作者: Shamaine Wei Ting Ho.;Taotao Sheng.;Manjie Xing.;Wen Fong Ooi.;Chang Xu.;Raghav Sundar.;Kie Kyon Huang.;Zhimei Li.;Vikrant Kumar.;Kalpana Ramnarayanan.;Feng Zhu.;Supriya Srivastava.;Zul Fazreen Bin Adam Isa.;Chukwuemeka George Anene-Nzelu.;Milad Razavi-Mohseni.;Dustin Shigaki.;Haoran Ma.;Angie Lay Keng Tan.;Xuewen Ong.;Ming Hui Lee.;Su Ting Tay.;Yu Amanda Guo.;Weitai Huang.;Shang Li.;Michael A Beer.;Roger Sik Yin Foo.;Ming Teh.;Anders Jacobsen Skanderup.;Bin Tean Teh.;Patrick Tan.
来源: Gut. 2023年72卷2期226-241页
Gastric cancer (GC) comprises multiple molecular subtypes. Recent studies have highlighted mesenchymal-subtype GC (Mes-GC) as a clinically aggressive subtype with few treatment options. Combining multiple studies, we derived and applied a consensus Mes-GC classifier to define the Mes-GC enhancer landscape revealing disease vulnerabilities.
867. Consensus-based development of a causal attribution system for post-ERCP adverse events.
作者: Nauzer Forbes.;B Joseph Elmunzer.;Rajesh N Keswani.;Robert J Hilsden.;Matt Hall.;John T Anderson.;Marianna Arvanitakis.;Yen-I Chen.;Anna Duloy.;Grace H Elta.;Jennifer L Maranki.;Klaus Mergener.;Bret T Petersen.;Amrita Sethi.;Peter D Siersema.;Zachary L Smith.;Jennifer J Telford.;Frances Tse.;Peter B Cotton.;Sachin Wani.
来源: Gut. 2022年 868. Methionine deficiency facilitates antitumour immunity by altering m6A methylation of immune checkpoint transcripts.
作者: Ting Li.;Yue-Tao Tan.;Yan-Xing Chen.;Xiao-Jun Zheng.;Wen Wang.;Kun Liao.;Hai-Yu Mo.;Junzhong Lin.;Wei Yang.;Hai-Long Piao.;Rui-Hua Xu.;Huai-Qiang Ju.
来源: Gut. 2023年72卷3期501-511页
Methionine metabolism is involved in a myriad of cellular functions, including methylation reactions and redox maintenance. Nevertheless, it remains unclear whether methionine metabolism, RNA methylation and antitumour immunity are molecularly intertwined.
869. A novel peptide protects against diet-induced obesity by suppressing appetite and modulating the gut microbiota.
作者: Zhanzhan Li.;Bing Zhang.;Ning Wang.;Zhenqiang Zuo.;Hong Wei.;Fangqing Zhao.
来源: Gut. 2023年72卷4期686-698页
The obesity epidemic and its metabolic complications continue to be a major global public health threat with limited effective treatments, especially drugs that can be taken orally. Peptides are a promising class of molecules that have gained increased interest for their applications in medicine and biotechnology. In this study, we focused on looking for peptides that can be administrated orally to treat obesity and exploring its mechanisms.
870. Autologous T cell responses to primary human colorectal cancer spheroids are enhanced by ectonucleotidase inhibition.
作者: Julie Bonnereau.;Tristan Courau.;Nicolas Asesio.;Delphine Salfati.;Fatiha Bouhidel.;Hélène Corte.;Sarah Hamoudi.;Nassim Hammoudi.;Julie Lavolé.;Justine Vivier-Chicoteau.;Victor Chardiny.;Leon Maggiori.;Mathieu Blery.;Romain Remark.;Cécile Bonnafous.;Pierre Cattan.;Antoine Toubert.;Purnima Bhat.;Matthieu Allez.;Thomas Aparicio.;Lionel Le Bourhis.
来源: Gut. 2023年72卷4期699-709页
T cells are major effectors of the antitumoural immune response. Their activation by tumour-associated antigens can unleash their proliferation and cytotoxic functions, leading to tumour cell elimination. However, tumour-related immunosuppressive mechanisms including the overexpression of immune checkpoints like programmed cell death protein-1 (PD-1), are also engaged, promoting immune escape. Current immunotherapies targeting these pathways have demonstrated weak efficacy in colorectal cancer (CRC). It is thus crucial to find new targets for immunotherapy in this cancer type.
871. British Society of Gastroenterology guidelines on the management of functional dyspepsia.
作者: Christopher J Black.;Peter A Paine.;Anurag Agrawal.;Imran Aziz.;Maria P Eugenicos.;Lesley A Houghton.;Pali Hungin.;Ross Overshott.;Dipesh H Vasant.;Sheryl Rudd.;Richard C Winning.;Maura Corsetti.;Alexander C Ford.
来源: Gut. 2022年71卷9期1697-1723页
Functional dyspepsia (FD) is a common disorder of gut-brain interaction, affecting approximately 7% of individuals in the community, with most patients managed in primary care. The last British Society of Gastroenterology (BSG) guideline for the management of dyspepsia was published in 1996. In the interim, substantial advances have been made in understanding the complex pathophysiology of FD, and there has been a considerable amount of new evidence published concerning its diagnosis and classification, with the advent of the Rome IV criteria, and management. The primary aim of this guideline, commissioned by the BSG, is to review and summarise the current evidence to inform and guide clinical practice, by providing a practical framework for evidence-based diagnosis and treatment of patients. The approach to investigating the patient presenting with dyspepsia is discussed, and efficacy of drugs in FD summarised based on evidence derived from a comprehensive search of the medical literature, which was used to inform an update of a series of pairwise and network meta-analyses. Specific recommendations have been made according to the Grading of Recommendations Assessment, Development and Evaluation system. These provide both the strength of the recommendations and the overall quality of evidence. Finally, in this guideline, we consider novel treatments that are in development, as well as highlighting areas of unmet need and priorities for future research.
875. Cold versus hot EMR for large duodenal adenomas.
作者: Alessandro Repici.;Antonio Capogreco.;Marco Spadaccini.;Roberta Maselli.;Piera Alessia Galtieri.;Alessandro Fugazza.;Silvia Carrara.;Matteo Colombo.;Guido Schachschal.;Anna Creutzfeldt.;Shahila Perveen Aslam.;Asma Alkandari.;Pradeep Bhandari.;Alexander Meining.;Cesare Hassan.;Thomas Rösch.
来源: Gut. 2022年71卷9期1763-1765页 876. Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.
作者: Stephan Buch.;Hamish Innes.;Philipp Ludwig Lutz.;Hans Dieter Nischalke.;Jens U Marquardt.;Janett Fischer.;Karl Heinz Weiss.;Jonas Rosendahl.;Astrid Marot.;Marcin Krawczyk.;Markus Casper.;Frank Lammert.;Florian Eyer.;Arndt Vogel.;Silke Marhenke.;Johann von Felden.;Rohini Sharma.;Stephen Rahul Atkinson.;Andrew McQuillin.;Jacob Nattermann.;Clemens Schafmayer.;Andre Franke.;Christian Strassburg.;Marcella Rietschel.;Heidi Altmann.;Stefan Sulk.;Veera Raghavan Thangapandi.;Mario Brosch.;Carolin Lackner.;Rudolf E Stauber.;Ali Canbay.;Alexander Link.;Thomas Reiberger.;Mattias Mandorfer.;Georg Semmler.;Bernhard Scheiner.;Christian Datz.;Stefano Romeo.;Stefano Ginanni Corradini.;William Lucien Irving.;Joanne R Morling.;Indra Neil Guha.;Eleanor Barnes.;M Azim Ansari.;Jocelyn Quistrebert.;Luca Valenti.;Sascha A Müller.;Marsha Yvonne Morgan.;Jean-François Dufour.;Jonel Trebicka.;Thomas Berg.;Pierre Deltenre.;Sebastian Mueller.;Jochen Hampe.;Felix Stickel.
来源: Gut. 2023年72卷2期381-391页
Hepatocellular carcinoma (HCC) often develops in patients with alcohol-related cirrhosis at an annual risk of up to 2.5%. Some host genetic risk factors have been identified but do not account for the majority of the variance in occurrence. This study aimed to identify novel susceptibility loci for the development of HCC in people with alcohol related cirrhosis.
878. Autoimmune gastritis: long-term natural history in naïve Helicobacter pylori-negative patients.
作者: Massimo Rugge.;Ludovica Bricca.;Stefano Guzzinati.;Diana Sacchi.;Marco Pizzi.;Edoardo Savarino.;Fabio Farinati.;Manuel Zorzi.;Matteo Fassan.;Angelo Paolo Dei Tos.;Peter Malfertheiner.;Robert M Genta.;David Y Graham.
来源: Gut. 2023年72卷1期30-38页
Autoimmune gastritis (AIG) is an immunomediated disease targeting parietal cells, eventually resulting in oxyntic-restricted atrophy. This long-term follow-up study aimed at elucidating the natural history, histological phenotype(s), and associated cancer risk of patients with AIG consistently tested H. pylori-negative (naïve H. pylori-negative subjects).
|