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Editorial: High‐Grade Dysplasia in Colonic Inflammatory Bowel Disease Is Associated With a High Risk of Synchronous or Metachronous Colorectal Cancer 社论:结肠炎性肠病的高度发育不良与同步或异时性结直肠癌的高风险相关
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70442
Alexandra Hickey, Chaonan Dong, Christopher A. Lamb
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引用次数: 0
Letter: Safety and Methodological Considerations for Hepatitis B Immunoglobulin Withdrawal in Hepatitis B Virus Mono‐Infected Liver Transplant Recipients 信函:单乙肝病毒感染肝移植受者停用乙肝免疫球蛋白的安全性和方法学考虑
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70384
Wenying Huang, Wen Zhang, Chang Hu
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引用次数: 0
Editorial: Shingles Risk in IBD —More Evidence to Support Routine Preventive Vaccination? 社论:IBD的带状疱疹风险——更多证据支持常规预防接种?
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70458
Keith Bodger
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引用次数: 0
Editorial: Efficacy of Pharmacological Compared With Dietary Therapy for Patients With Irritable Bowel Syndrome—It Is Nice to Have a Choice 社评:肠易激综合征患者的药理学与饮食疗法的疗效比较——有选择的感觉真好
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70452
Emma P. Halmos, Peter R. Gibson
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引用次数: 0
Letter: Affirming Cardiac Safety While Highlighting Areas for Further Research 信:肯定心脏的安全性,同时强调进一步研究的领域
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70387
Shanshan Huang, Jie Zhou
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引用次数: 0
Editorial: An Important Step Towards Mastering Metabolic Dysfunction-Associated Steatohepatitis-Targeted Therapy in Diabetes 社论:掌握代谢功能障碍相关脂肪性肝炎-糖尿病靶向治疗的重要一步
IF 6.7 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70401
Johnny Yau-Cheung Chang, Chi-Ho Lee
<p>Resmetirom, an oral selective thyroid hormone receptor beta agonist, is the first pharmacological agent approved by the Food and Drug Administration (FDA) of the United States in 2024 for the treatment of non-cirrhotic metabolic dysfunction-associated steatohepatitis (MASH) with liver fibrosis stages F2 and F3. In the ongoing, registrational phase 3 MAESTRO-NASH study, the administration of resmetirom for 52 weeks led to MASH resolution and significant improvement in fibrosis by at least one stage as compared to placebo [<span>1</span>]. However, there remains a dearth of information about combining resmetirom with medications that are recommended for treating comorbidities of metabolic dysfunction-associated steatotic liver disease (MASLD), such as glucagon-like peptide 1 receptor agonists (GLP1RA) and sodium-glucose cotransporter 2 inhibitors (SGLT2i) in type 2 diabetes (T2D) with and without obesity [<span>2, 3</span>]. Notably, around half of T2D patients have MASH [<span>4</span>]. Therefore, the prespecified analysis of MAESTRONASH by Noureddin et al. has provided timely evidence that in T2D patients, the efficacy of resmetirom on MASH end points was not affected by the stable background use of GLP1RA or SGLT2i [<span>5</span>], which are now commonly prescribed due to their established independent cardiovascular and kidney benefits.</p><p>Both GLP1RA and SGLT2i have been shown to resolve and improve MASH in the recent Effect of Semaglutide in Subjects with Non-cirrhotic non-alcoholic steatohepatitis (ESSENCE) and Dapagliflozin Efficacy and Action in Non-alcoholic steatohepatitis (DEAN) trials, respectively, but residual risk remains [<span>6, 7</span>]. Indeed, in around 40% of the T2D participants from the MAESTRONASH trial, at baseline, their MASH remained present despite the use of either GLP1RA or SGLT2i for a reasonable period (median duration 660 days for GLP1RA and 651 days for SGLT2i) [<span>5</span>]. Although the GLP1RA used were mostly liraglutide, dulaglutide and semaglutide 1 mg weekly instead of semaglutide 2.4 mg weekly as in the ESSENCE trial, it reinforces the need to combine pharmacotherapies to target the different pathophysiological pathways in MASH [<span>8</span>].</p><p>The authors also demonstrated that resmetirom-treated participants who had weight loss ≥ 5%, as compared to those without, showed higher rates of MASH resolution and fibrosis improvement [<span>5</span>]. Further studies should be conducted to investigate if the sequence of initiating these MASH pharmacotherapies matters, for instance, whether starting GLP1RA after resmetirom can enhance its effect through inducing weight loss. Moreover, as several new incretin co-agonists such as tirzepatide, a GLP1- and glucose-dependent insulinotropic polypeptide (GIP) receptors co-agonist, as well as survodutide, a GLP1- and glucagon receptors co-agonist, with more potent weight-reducing effects, have also been shown to improve MASH in phase 2 trials [<span>9,
Resmetirom是一种口服选择性甲状腺激素受体激动剂,是美国食品和药物管理局(FDA)于2024年批准的首个用于治疗伴有肝纤维化F2和F3期的非肝硬化代谢功能障碍相关脂肪性肝炎(MASH)的药物。在正在进行的注册3期MAESTRO-NASH研究中,与安慰剂相比,雷司替米治疗52周导致MASH缓解和纤维化至少一个阶段的显着改善。然而,关于雷司替康与推荐用于治疗伴有或不伴有肥胖的2型糖尿病(T2D)的代谢功能障碍相关脂肪变性肝病(MASLD)合并症的药物(如胰高血糖素样肽1受体激动剂(GLP1RA)和钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)联合用药的信息仍然缺乏[2,3]。值得注意的是,大约一半的T2D患者有MASH bb0。因此,Noureddin等人对MAESTRONASH预先指定的分析及时提供了证据,证明在T2D患者中,雷美替罗对MASH终点的疗效不受GLP1RA或SGLT2i[5]的稳定背景使用的影响,这两种药物目前因其独立的心血管和肾脏益处而被广泛使用。在最近的塞马鲁肽对非肝硬化非酒精性脂肪性肝炎(ESSENCE)和达格列净对非酒精性脂肪性肝炎(DEAN)的疗效和作用试验中,GLP1RA和SGLT2i分别被证明可以缓解和改善MASH,但仍然存在残留风险[6,7]。事实上,在MAESTRONASH试验中,大约40%的T2D参与者,在基线时,尽管使用GLP1RA或SGLT2i一段合理的时间(GLP1RA的中位持续时间为660天,SGLT2i的中位持续时间为651天),他们的MASH仍然存在。尽管GLP1RA主要使用利拉鲁肽、dulaglutide和semaglutide,每周1mg,而不是像ESSENCE试验中使用semaglutide每周2.4 mg,但这加强了联合药物治疗的必要性,以针对MASH bb0中不同的病理生理途径。作者还证明,接受雷美替龙治疗的体重减轻≥5%的受试者,与未接受治疗的受试者相比,表现出更高的MASH消退率和纤维化改善率。这些MASH药物治疗的启动顺序是否有影响,例如雷司替罗后启动GLP1RA是否可以通过诱导体重减轻来增强其效果,还需要进一步的研究。此外,由于几种新的肠促胰岛素共激动剂,如tizepatide (GLP1-和葡萄糖依赖性胰岛素多肽(GIP)受体共激动剂)和survodutide (GLP1-和胰高血糖素受体共激动剂)具有更强的减肥作用,在2期试验中也被证明可以改善MASH[9,10],它们与雷司替罗联合使用的疗效也值得进一步研究。与GLP1RA和SGLT2i相比,resmetirom显然是一个新来者,目前仅在美国上市。预计当雷司美康广泛应用时,许多合并MASLD的T2D患者将已经接受SGLT2i和/或glp1为基础的治疗。因此,从事后分析中发现,这些药物与雷司替龙联合使用安全有效,是临床重要的结果,也是掌握mash靶向治疗糖尿病的关键一步。张耀昌:构思,写作-原稿。李志浩:构思、写作、审编、督导。获得阿斯利康、奥斯迈、拜耳、勃林格殷格翰、礼来、吉利德、葛兰素史克、诺和诺德、赛诺菲安万特的顾问委员会和讲座酬金。剩下的作者没有利益冲突。这篇文章链接到Noureddin等人的论文。要查看这篇文章,请访问https://doi.org/10.1111/apt.70382.Data分享不适用于这篇文章,因为在目前的研究中没有生成或分析数据集。
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引用次数: 0
Letter on ‘Meta‐Analysis: Mortality Trends and Risk Factors in Severe Alcohol‐Associated Hepatitis’ 关于“荟萃分析:严重酒精相关性肝炎的死亡率趋势和危险因素”的信函
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70441
Chao Zhao
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引用次数: 0
Editorial: High‐Grade Dysplasia in Colonic Inflammatory Bowel Disease Is Associated With a High Risk of Synchronous or Metachronous Colorectal Cancer—Authors' Reply 社论:结肠炎性肠病的高度发育不良与同步或异时性结直肠癌的高风险相关
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70473
Monica E. W. Derks, Frank Hoentjen
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引用次数: 0
Editorial: Efficacy of Pharmacological Compared With Dietary Therapy for Patients With Irritable Bowel Syndrome—It Is Nice to Have a Choice. Authors' Reply 社评:肠易激综合征患者的药理学与饮食疗法的疗效比较——有选择的感觉真好。作者的回复
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70469
Kee Huat Chuah, Qing Yuan Loo, Audrey Joe Chii Loh, Jing Yi Leong, Wah Loong Chan, Xin Hui Khoo, Kim Leng Wong, Sarala Panirsheeluam, Vicraman Natarajan, Ai Kah Ng, Hazreen Abdul Majid, Sanjiv Mahadeva
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引用次数: 0
Letter: Reinterpreting the Role of Microbiota‐Driven Nitric Oxide in Cirrhotic Portal Hypertension—A Maladaptive Compensatory Response? 信:重新解释微生物群驱动的一氧化氮在肝硬化门脉高压中的作用——一种适应不良代偿反应?
IF 7.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2025-11-25 DOI: 10.1111/apt.70411
Meiyu Yang, Tiantian Zhang, Susu Zhang
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引用次数: 0
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