622. Persistent villous atrophy predicts development of complications and mortality in adult patients with coeliac disease: a multicentre longitudinal cohort study and development of a score to identify high-risk patients.
作者: Annalisa Schiepatti.;Stiliano Maimaris.;Suneil A Raju.;Olivia L Green.;Giulia Mantica.;Amelie Therrien.;David Flores-Marin.;Justin Linden.;Fernando Fernández-Bañares.;Maria Esteve.;Daniel Leffler.;Federico Biagi.;David S Sanders.
来源: Gut. 2023年72卷11期2095-2102页
Persistent villous atrophy (pVA) in coeliac disease (CD) despite a gluten-free diet (GFD) has unclear meaning. We aimed to (i) study the relationship between pVA and long-term outcomes and (ii) develop a score to identify patients at risk of pVA.
623. Impact of acute alcohol consumption on circulating microbiome in asymptomatic alcohol-related liver disease.
作者: Mads Israelsen.;Camila Alvarez-Silva.;Bjørn Stæhr Madsen.;Camilla Dalby Hansen.;Nikolaj Christian Torp.;Stine Johansen.;Johanne Kragh Hansen.;Katrine Prier Lindvig.;Jeanlouis Insonere.;Virginie Riviere.;Helene Bæk Juel.;Asker Brejnrod.;Lars Juhl Jensen.;Maja Thiele.;Benjamin Lelouvier.;Torben Hansen.;Manimozhiyan Arumugam.;Aleksander Krag.; .; .
来源: Gut. 2024年73卷6期1041-1044页 624. The first international Rome consensus conference on gut microbiota and faecal microbiota transplantation in inflammatory bowel disease.
作者: Loris Riccardo Lopetuso.;Sara Deleu.;Lihi Godny.;Valentina Petito.;Pierluigi Puca.;Federica Facciotti.;Harry Sokol.;Gianluca Ianiro.;Luca Masucci.;Maria Abreu.;Iris Dotan.;Samuel Paul Costello.;Ailsa Hart.;Tariq H Iqbal.;Sudarshan Paramsothy.;Maurizio Sanguinetti.;Silvio Danese.;Herbert Tilg.;Fabio Cominelli.;Theresa T Pizarro.;Alessandro Armuzzi.;Giovanni Cammarota.;Antonio Gasbarrini.;Séverine Vermeire.;Franco Scaldaferri.
来源: Gut. 2023年72卷9期1642-1650页
Several randomised clinical trials (RCTs) performing faecal microbiota transplantation (FMT) for the management of inflammatory bowel disease (IBD), particularly for ulcerative colitis, have recently been published, but with major variations in study design. These include differences in administered dose, route and frequency of delivery, type of placebo and evaluated endpoints. Although the overall outcomes appear to be promising, they are highly dependent on both donor and recipient factors.
625. Psychological symptoms do not discriminate between reflux phenotypes along the organic-functional refractory GERD spectrum.
作者: Annelies Geeraerts.;Livia Guadagnoli.;Ans Pauwels.;Hannelore Geysen.;Thomas Neyens.;Lukas Van Oudenhove.;Tim Vanuytsel.;Jan Tack.
来源: Gut. 2023年72卷10期1819-1827页
Historically, psychological processes are associated with disorders at the functional end of the gastro-oesophageal reflux disease (GERD) spectrum. However, recent research suggests that psychological symptoms are relevant across the entire GERD spectrum. We aim to investigate whether psychological symptoms are associated with reflux phenotype (True GERD, Borderline GERD, reflux hypersensitivity, functional heartburn) along the GERD spectrum in a cohort of refractory reflux patients.
629. SARS-CoV-2 and the liver: clinical and immunological features in chronic liver disease.
SARS-CoV-2 infection may affect the liver in healthy individuals but also influences the course of COVID-19 in patients with chronic liver disease (CLD). As described in healthy individuals, a strong SARS-CoV-2-specific adaptive immune response is important for the outcome of COVID-19, however, knowledge on the adaptive immune response in CLD is limited.Here, we review the clinical and immunological features of SARS-CoV-2 infection in individuals with CLD. Acute liver injury occurs in many cases of SARS-CoV-2 infection and may be induced by multiple factors, such as cytokines, direct viral infection or toxic effects of COVID-19 drugs. In individuals with CLD, SARS-CoV-2 infection may have a more severe course and promote decompensation and particularly in patients with cirrhosis. Compared with healthy individuals, the SARS-CoV-2-specific adaptive immune responses is impaired in patients with CLD after both, natural infection and vaccination but improves at least partially after booster vaccination.Following SARS-CoV-2 vaccination, rare cases of acute vaccine-induced liver injury and the development of autoimmune-like hepatitis have been reported. However, the concomitant elevation of liver enzymes is reversible under steroid treatment.
631. Ageing trajectory of the gut microbiota is associated with metabolic diseases in a chronological age-dependent manner.
作者: JingXiang Fu.;Wen Qiu.;Huimin Zheng.;Cancan Qi.;Shixian Hu.;Wei Wu.;Huidi Wang.;Guangyan Wu.;Peihua Cao.;Zhenchao Ma.;Chao Zheng.;Wen-Jun Ma.;Hong-Wei Zhou.;Yan He.
来源: Gut. 2023年72卷7期1431-1433页 632. Timing of energy intake and the therapeutic potential of intermittent fasting and time-restricted eating in NAFLD.
Non-alcoholic fatty liver disease (NAFLD) represents a major public health concern and is associated with a substantial global burden of liver-related and cardiovascular-related morbidity and mortality. High total energy intake coupled with unhealthy consumption of ultra-processed foods and saturated fats have long been regarded as major dietary drivers of NAFLD. However, there is an accumulating body of evidence demonstrating that the timing of energy intake across a the day is also an important determinant of individual risk for NAFLD and associated metabolic conditions. This review summarises the available observational and epidemiological data describing associations between eating patterns and metabolic disease, including the negative effects of irregular meal patterns, skipping breakfast and night-time eating on liver health. We suggest that that these harmful behaviours deserve greater consideration in the risk stratification and management of patients with NAFLD particularly in a 24-hour society with continuous availability of food and with up to 20% of the population now engaged in shiftwork with mistimed eating patterns. We also draw on studies reporting the liver-specific impact of Ramadan, which represents a unique real-world opportunity to explore the physiological impact of fasting. By highlighting data from preclinical and pilot human studies, we present a further biological rationale for manipulating timing of energy intake to improve metabolic health and discuss how this may be mediated through restoration of natural circadian rhythms. Lastly, we comprehensively review the landscape of human trials of intermittent fasting and time-restricted eating in metabolic disease and offer a look to the future about how these dietary strategies may benefit patients with NAFLD and non-alcoholic steatohepatitis.
635. Emerging interleukin targets in the tumour microenvironment: implications for the treatment of gastrointestinal tumours.
作者: Lindsay Kathleen Dickerson.;Jason A Carter.;Karan Kohli.;Venu G Pillarisetty.
来源: Gut. 2023年72卷8期1592-1606页
The effectiveness of antitumour immunity is dependent on intricate cytokine networks. Interleukins (ILs) are important mediators of complex interactions within the tumour microenvironment, including regulation of tumour-infiltrating lymphocyte proliferation, differentiation, migration and activation. Our evolving and increasingly nuanced understanding of the cell type-specific and heterogeneous effects of IL signalling has presented unique opportunities to fine-tune elaborate IL networks and engineer new targeted immunotherapeutics. In this review, we provide a primer for clinicians on the challenges and potential of IL-based treatment. We specifically detail the roles of IL-2, IL-10, IL-12 and IL-15 in shaping the tumour-immune landscape of gastrointestinal malignancies, paying particular attention to promising preclinical findings, early-stage clinical research and innovative therapeutic approaches that may properly place ILs to the forefront of immunotherapy regimens.
636. Mature tertiary lymphoid structures are key niches of tumour-specific immune responses in pancreatic ductal adenocarcinomas.
作者: Gabriela Sarti Kinker.;Glauco Akelinghton Freire Vitiello.;Ariane Barros Diniz.;Mariela Pires Cabral-Piccin.;Pedro Henrique Barbosa Pereira.;Maria Letícia Rodrigues Carvalho.;Wallax Augusto Silva Ferreira.;Alexandre Silva Chaves.;Amanda Rondinelli.;Arianne Fagotti Gusmão.;Alexandre Defelicibus.;Gabriel Oliveira Dos Santos.;Warley Abreu Nunes.;Laura Carolina López Claro.;Talita Magalhães Bernardo.;Ricardo Tadashi Nishio.;Adhemar Monteiro Pacheco.;Ana Carolina Laus.;Lidia Maria Rebolho Batista Arantes.;Julia Lima Fleck.;Victor Hugo Fonseca de Jesus.;André de Moricz.;Ricardo Weinlich.;Felipe José Fernandez Coimbra.;Vladmir Cláudio Cordeiro de Lima.;Tiago da Silva Medina.
来源: Gut. 2023年72卷10期1927-1941页
To better understand the immune microenvironment of pancreatic ductal adenocarcinomas (PDACs), here we explored the relevance of T and B cell compartmentalisation into tertiary lymphoid structures (TLSs) for the generation of local antitumour immunity.
639. Autoimmune gastritis may be less susceptible to cancer development than Helicobacter pylori-related gastritis based on histological analysis.
作者: Junya Arai.;Ryota Niikura.;Yoku Hayakawa.;Yoshihiro Hirata.;Tetsuo Ushiku.;Mitsuhiro Fujishiro.
来源: Gut. 2024年73卷6期1037-1038页 640. Eradicating Helicobacter pylori via 13C-urea breath screening to prevent gastric cancer in indigenous communities: a population-based study and development of a family index-case method.
作者: Wei-Yi Lei.;Jian-Yu Lee.;Shu-Ling Chuang.;Ming-Jong Bair.;Chien-Lin Chen.;Jeng-Yih Wu.;Deng-Chyang Wu.;Felice Tien O'Donnell.;Hui-Wen Tien.;Yi-Ru Chen.;Tsung-Hsien Chiang.;Yu-Hsin Hsu.;Tsui-Hsia Hsu.;Pei-Chun Hsieh.;Li-Ju Lin.;Shu-Li Chia.;Chao-Chun Wu.;Yi-Maun Subeq.;Shu-Hui Wen.;Hsiu-Chun Chang.;Yu-Wen Lin.;Kuo-Ping Sun.;Chia-Hsiang Chu.;Ming-Shiang Wu.;David Y Graham.;Hsiu-Hsi Chen.;Yi-Chia Lee.
来源: Gut. 2023年72卷12期2231-2240页
Screening and eradication of Helicobacter pylori help reduce disparities in the incidence of gastric cancer. We aimed to evaluate its acceptability and feasibility in the indigenous communities and develop a family index-case method to roll out this programme.
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