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共有 3428 条符合本次的查询结果, 用时 3.0795933 秒

381. Drug targets for haemorrhoidal disease: proteome-wide Mendelian randomisation and colocalisation analyses.

作者: Shifang Li.;Meijiao Gong.
来源: Gut. 2024年73卷11期e31页

382. Ebastine for the treatment of irritable bowel syndrome: old drug, new tricks?

作者: Alexander C Ford.
来源: Gut. 2024年73卷3期393-394页

383. Early-life diet and risk of inflammatory bowel disease: a pooled study in two Scandinavian birth cohorts.

作者: Annie Guo.;Johnny Ludvigsson.;Anne Lise Brantsæter.;Sofia Klingberg.;Malin Östensson.;Ketil Størdal.;Karl Mårild.
来源: Gut. 2024年73卷4期590-600页
We assessed whether early-life diet quality and food intake frequencies were associated with subsequent IBD.

384. Inflammatory bowel diseases: are we ready to recommend a preventive diet for infants?

作者: Ashwin N Ananthakrishnan.
来源: Gut. 2024年73卷4期559-560页

385. Optimal age to discontinue long-term surveillance of intraductal papillary mucinous neoplasms: comparative cost-effectiveness of surveillance by age.

作者: Tsuyoshi Hamada.;Hiroki Oyama.;Ataru Igarashi.;Yoshikuni Kawaguchi.;Mihye Lee.;Hiroki Matsui.;Nobuaki Michihata.;Yousuke Nakai.;Kiyohide Fushimi.;Hideo Yasunaga.;Mitsuhiro Fujishiro.
来源: Gut. 2024年73卷6期955-965页
Current guidelines recommend long-term image-based surveillance for patients with low-risk intraductal papillary mucinous neoplasms (IPMNs). This simulation study aimed to examine the comparative cost-effectiveness of continued versus discontinued surveillance at different ages and define the optimal age to stop surveillance.

386. eCura and W-eCura: different scores, different populations, same goal.

作者: Rui Morais.;Diogo Libanio.;João Santos-Antunes.; .
来源: Gut. 2024年73卷11期e29页

387. Long-term follow-up study of necrotising pancreatitis: interventions, complications and quality of life.

作者: Robbert A Hollemans.;Hester C Timmerhuis.;Marc G Besselink.;Stefan A W Bouwense.;Marco Bruno.;Peter van Duijvendijk.;Erwin-Jan van Geenen.;Muhammed Hadithi.;Sybrand Hofker.;Jeanin E Van-Hooft.;Liesbeth M Kager.;Eric R Manusama.;Jan-Werner Poley.;Rutger Quispel.;Tessa Römkens.;George P van der Schelling.;Matthijs P Schwartz.;Bernhard W M Spanier.;Martijn Stommel.;Adriaan Tan.;Niels G Venneman.;Frank Vleggaar.;Roy L J van Wanrooij.;Thomas L Bollen.;Rogier P Voermans.;Robert C Verdonk.;Hjalmar C van Santvoort.; .
来源: Gut. 2024年73卷5期787-796页
To describe the long-term consequences of necrotising pancreatitis, including complications, the need for interventions and the quality of life.

388. Proton pump inhibitors alter gut microbiota by promoting oral microbiota translocation: a prospective interventional study.

作者: Xue Xiao.;Xian Zhang.;Jin Wang.;Yuqiang Liu.;Hailin Yan.;Xiaocun Xing.;Jinlin Yang.
来源: Gut. 2024年73卷7期1098-1109页
The mechanism by which proton pump inhibitors (PPIs) alter gut microbiota remains to be elucidated. We aimed to learn whether PPI induced gut microbiota alterations by promoting oral microbial translocation.

389. Impact of power consumption and power saving for GI endoscopy (power on study) on reducing CO2 emissions.

作者: Anna Fichtl.;Veronika Tacheva.;Niklas Sturm.;Karim Hamesch.;Doerte Wichmann.;Benjamin Mayer.;Martin Müller.;Martin Wagner.;Thomas Seufferlein.;Benjamin M Walter.
来源: Gut. 2024年73卷6期892-896页

390. A mucus production programme promotes classical pancreatic ductal adenocarcinoma.

作者: Claudia Tonelli.;Georgi N Yordanov.;Yuan Hao.;Astrid Deschênes.;Juliene Hinds.;Pascal Belleau.;Olaf Klingbeil.;Erin Brosnan.;Abhishek Doshi.;Youngkyu Park.;Ralph H Hruban.;Christopher R Vakoc.;Alexander Dobin.;Jonathan Preall.;David A Tuveson.
来源: Gut. 2024年73卷6期941-954页
The optimal therapeutic response in cancer patients is highly dependent upon the differentiation state of their tumours. Pancreatic ductal adenocarcinoma (PDA) is a lethal cancer that harbours distinct phenotypic subtypes with preferential sensitivities to standard therapies. This study aimed to investigate intratumour heterogeneity and plasticity of cancer cell states in PDA in order to reveal cell state-specific regulators.

391. Glucagon-like peptide-1 receptor agonists and risk of major adverse liver outcomes in patients with chronic liver disease and type 2 diabetes.

作者: Axel Wester.;Ying Shang.;Emilie Toresson Grip.;Anthony A Matthews.;Hannes Hagström.
来源: Gut. 2024年73卷5期835-843页
Phase II trials suggest glucagon-like peptide-1 receptor (GLP1) agonists resolve metabolic dysfunction-associated steatohepatitis but do not affect fibrosis regression. We aimed to determine the long-term causal effect of GLP1 agonists on the risk of major adverse liver outcomes (MALO) in patients with any chronic liver disease and type 2 diabetes.

392. Response to McAlindon's letter.

作者: Lorenzo Fuccio.;Laura Neilson.;Leonardo Frazzoni.;Colin J Rees.
来源: Gut. 2024年73卷11期e27页

393. Non-linear association of baseline viral load with on-treatment hepatocellular carcinoma risk in chronic hepatitis B: still needs further discussion.

作者: Taiyu He.;Dazhi Zhang.
来源: Gut. 2024年73卷11期e28页

394. New facet of CARs: HBV-specific CARs as inhibitors of virus morphogenesis and release.

作者: Eberhard Hildt.;Jianming Hu.
来源: Gut. 2024年73卷4期566-567页

395. Short-duration selective decontamination of the digestive tract infection control does not contribute to increased antimicrobial resistance burden in a pilot cluster randomised trial (the ARCTIC Study).

作者: Iain Robert Louis Kean.;John A Clark.;Zhenguang Zhang.;Esther Daubney.;Deborah White.;Paloma Ferrando-Vivas.;Gema Milla.;Brian Cuthbertson.;John Pappachan.;Nigel Klein.;Paul Mouncey.;Kathy Rowan.;John Myburgh.;Theodore Gouliouris.;Stephen Baker.;Julian Parkhill.;Nazima Pathan.; Arctic Research Team.
来源: Gut. 2024年73卷6期910-921页
Selective decontamination of the digestive tract (SDD) is a well-studied but hotly contested medical intervention of enhanced infection control. Here, we aim to characterise the changes to the microbiome and antimicrobial resistance (AMR) gene profiles in critically ill children treated with SDD-enhanced infection control compared with conventional infection control.

396. Thyroid hormone receptor-beta agonists: new MASLD therapies on the horizon.

作者: Christopher D Byrne.;Giovanni Targher.;Herbert Tilg.
来源: Gut. 2024年73卷4期573-581页

397. Fibrosis in IBD: from pathogenesis to therapeutic targets.

作者: Florian Rieder.;Pranab K Mukherjee.;William J Massey.;Yan Wang.;Claudio Fiocchi.
来源: Gut. 2024年73卷5期854-866页
Intestinal fibrosis resulting in stricture formation and obstruction in Crohn's disease (CD) and increased wall stiffness leading to symptoms in ulcerative colitis (UC) is among the largest unmet needs in inflammatory bowel disease (IBD). Fibrosis is caused by a multifactorial and complex process involving immune and non-immune cells, their soluble mediators and exposure to luminal contents, such as microbiota and environmental factors. To date, no antifibrotic therapy is available. Some progress has been made in creating consensus definitions and measurements to quantify stricture morphology for clinical practice and trials, but approaches to determine the degree of fibrosis within a stricture are still lacking.

398. Oral bacteria accelerate pancreatic cancer development in mice.

作者: Elias Saba.;Maria Farhat.;Alaa Daoud.;Arin Khashan.;Esther Forkush.;Noam Hallel Menahem.;Hasnaa Makkawi.;Karthikeyan Pandi.;Sarah Angabo.;Hiromichi Kawasaki.;Inbar Plaschkes.;Oren Parnas.;Gideon Zamir.;Karine Atlan.;Michael Elkin.;Lior Katz.;Gabriel Nussbaum.
来源: Gut. 2024年73卷5期770-786页
Epidemiological studies highlight an association between pancreatic ductal adenocarcinoma (PDAC) and oral carriage of the anaerobic bacterium Porphyromonas gingivalis, a species highly linked to periodontal disease. We analysed the potential for P. gingivalis to promote pancreatic cancer development in an animal model and probed underlying mechanisms.

399. MASLD: a systemic metabolic disorder with cardiovascular and malignant complications.

作者: Giovanni Targher.;Christopher D Byrne.;Herbert Tilg.
来源: Gut. 2024年73卷4期691-702页
Non-alcoholic fatty liver disease (NAFLD) has rapidly become the most common chronic liver disease globally and is currently estimated to affect up to 38% of the global adult population. NAFLD is a multisystem disease where systemic insulin resistance and related metabolic dysfunction play a pathogenic role in the development of NAFLD and its most relevant liver-related morbidities (cirrhosis, liver failure and hepatocellular carcinoma) and extrahepatic complications, such as cardiovascular disease (CVD), type 2 diabetes mellitus, chronic kidney disease, and certain types of extrahepatic cancers. In 2023, three large multinational liver associations proposed that metabolic dysfunction-associated steatotic liver disease (MASLD) should replace the term NAFLD; the name chosen to replace non-alcoholic steatohepatitis was metabolic dysfunction-associated steatohepatitis (MASH). Emerging epidemiological evidence suggests an excellent concordance rate between NAFLD and MASLD definitions-that is, ~99% of individuals with NAFLD meet MASLD criteria. In this narrative review, we provide an overview of the literature on (a) the recent epidemiological data on MASLD and the risk of developing CVD and malignant complications, (b) the underlying mechanisms by which MASLD (and factors strongly linked with MASLD) may increase the risk of these extrahepatic complications and (c) the diagnosis and assessment of CVD risk and potential treatments to reduce CVD risk in people with MASLD or MASH.

400. Enhancing the opportunities for cholangiocarcinoma precision therapy.

作者: Reka Toth.;Paul J Brindley.;Javier Vaquero.
来源: Gut. 2024年73卷6期888-889页
共有 3428 条符合本次的查询结果, 用时 3.0795933 秒