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Novelty in the gut: a review of the gastrointestinal manifestations of syphilis. 肠道中的新奇事物:梅毒胃肠道表现综述。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-14 DOI: 10.1080/00365521.2024.2429676
Lefika Bathobakae, Joseph Russo, Rammy Bashir, Angela Vidreiro, Phenyo Phuu, Tyler Wilkinson, Nischal Sharma, Ruhin Yuridullah, Kamal Amer, Keith Siau

Syphilis is a systemic infection caused by the spirochete Treponema pallidum. It is transmitted during pregnancy or through sexual contact. Signs and symptoms vary depending on the clinical stage of the disease. Syphilis has been well-studied, and the introduction of penicillin has resulted in a decline in the number of new cases and deaths. Recently, however, there has been a surge in new cases in young people, especially those with human immunodeficiency virus (HIV). This epidemiological shift has been attributed to increased sexual activity, risky sexual behaviors, and immunodeficiency. There is a paucity of data on gastrointestinal (GI) manifestations of syphilis owing to its rarity and lack of physician awareness. T. pallidum can seed to any part of the GI tract, resulting in esophagitis, gastritis, hepatitis, pancreatitis, or proctocolitis. Depending on the affected part of the GI tract, syphilis can present with nausea, vomiting, painless esophageal ulcers, dysphagia, abdominal pain, weight loss due to early satiety, diarrhea, melena, hematochezia, dyschezia, or anorectal ulcers. Given its indolent clinical course and vague presentation, GI syphilis can mimic other GI disorders, which can delay diagnosis and treatment. A detailed medical history, physical examination, serological tests, and endoscopy can provide a definitive diagnosis. Syphilis and its GI complications are usually treated with long-acting intramuscular penicillin benzathine, and rarely with a 14-day course of intravenous penicillin. Herein, we describe the clinical features, etiopathogenesis, diagnosis, and treatment of GI syphilis. This primer should aid clinicians in timely diagnosis and treatment of various presentations of GI syphilis.

梅毒是由苍白螺旋体引起的一种全身性感染。它可在怀孕期间或通过性接触传播。体征和症状因疾病的临床阶段而异。梅毒已被充分研究,青霉素的引入导致新发病例和死亡人数下降。但最近,年轻人,尤其是感染了人类免疫缺陷病毒(HIV)的年轻人的新病例激增。这种流行病学上的变化被归因于性活动、危险的性行为和免疫缺陷的增加。由于梅毒罕见且缺乏医生意识,有关梅毒胃肠道(GI)表现的数据很少。苍白螺旋体可播散到消化道的任何部位,导致食道炎、胃炎、肝炎、胰腺炎或直肠结肠炎。根据受影响的消化道部位不同,梅毒可表现为恶心、呕吐、无痛性食道溃疡、吞咽困难、腹痛、早饱导致的体重减轻、腹泻、便血、排便困难或肛门直肠溃疡。由于消化道梅毒的临床病程缓慢,表现模糊,可能会模仿其他消化道疾病,从而延误诊断和治疗。详细的病史、体格检查、血清学检测和内窥镜检查可提供明确诊断。梅毒及其消化道并发症通常采用长效苄星青霉素肌肉注射治疗,很少采用青霉素静脉注射 14 天的疗程。在此,我们将介绍消化道梅毒的临床特征、发病机制、诊断和治疗。这本入门指南应有助于临床医生及时诊断和治疗各种表现的消化道梅毒。
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引用次数: 0
High neutrophil-to-lymphocyte ratio at Helicobacter pylori eradication increases the risk of eradication failure and post-eradication gastric cancer. 根除幽门螺杆菌时中性粒细胞与淋巴细胞的比率过高会增加根除失败和根除后患胃癌的风险。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-14 DOI: 10.1080/00365521.2024.2428280
Takeshi Yasuda, Nobuaki Yagi, Tatsushi Omatsu, Hiroaki Kitae, Yuki Nakahata, Yuriko Yasuda, Naoyuki Sakamoto, Akihiro Obora, Yoshiki Murakami, Takao Kojima

Introduction: Vonoprazan has been known to have a high Helicobacter pylori (H. pylori) eradication rate since its launch in 2015. Yet, the risk factors for eradication failure and development of post-eradication gastric cancer (GC) using VPZ regimen remain unclear.

Methods: This single-center cohort study included 934 consecutive patients who underwent H. pylori eradication using VPZ between February 2015 and June 2017 and were followed up for five years by the end of 2022. We examined several indicators of systemic immune, inflammatory, and nutritional status at the time of eradication to identify those indicators could predict eradication success, risk of post-eradication GC development, and long-term prognosis.

Results: The successful eradication rates were 92.6% (intention-to-treat) and 98.7% (per-protocol). Multivariate analysis showed that only a high peripheral blood neutrophil-to-lymphocyte ratio (NLR) was significantly associated with eradication failure. The 5-year GC incidence rate was 1.67%, and all GCs were stage IA. The mean (standard deviation [SD]) time from eradication to diagnosis was 40.5 (6.1) months. Multivariate analysis showed that high NLR and history of GC and hypertension were significantly associated with GC development. Patients with elevated NLR post-eradication had a higher risk of newly developed GC. Twelve patients died during the study period, and a high NLR was associated with a significantly higher mortality rate.

Conclusions: NLR has the potential to be a biomarker that predicts the failure of eradication and development of post-eradication GC. High NLR was also associated with poor long-term prognosis after H. pylori eradication.

导言:据了解,沃诺普拉赞自2015年上市以来,具有较高的幽门螺杆菌(H. pylori)根除率。然而,使用 VPZ 方案根除失败和根除后胃癌(GC)发生的风险因素仍不清楚:这项单中心队列研究纳入了 2015 年 2 月至 2017 年 6 月间使用 VPZ 根除幽门螺杆菌的 934 例连续患者,并在 2022 年底前进行了为期 5 年的随访。我们检查了根除时全身免疫、炎症和营养状况的几项指标,以确定哪些指标可以预测根除成功率、根除后发生 GC 的风险以及长期预后:根除成功率为 92.6%(意向治疗)和 98.7%(按协议)。多变量分析显示,只有高外周血中性粒细胞与淋巴细胞比值(NLR)与根除失败显著相关。5年GC发病率为1.67%,所有GC均为IA期。从根除到确诊的平均(标准差 [SD])时间为 40.5 (6.1) 个月。多变量分析表明,高NLR、GC病史和高血压与GC的发生显著相关。根除后NLR升高的患者新发GC的风险更高。研究期间有12名患者死亡,NLR高的患者死亡率明显更高:结论:NLR有可能成为预测根除失败和根除后发生GC的生物标志物。高NLR也与幽门螺杆菌根除后的长期预后不良有关。
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引用次数: 0
Effects of an anti-inflammatory diet (AID) on maternal and neonatal health outcomes in pregnant Chinese patients with inflammatory bowel disease treated with infliximab (IFX). 抗炎饮食(AID)对接受英夫利昔单抗(IFX)治疗的中国炎症性肠病孕妇和新生儿健康结果的影响。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-09 DOI: 10.1080/00365521.2024.2423828
Yong-Mei Ye, Mei-Hao Wei, Kai-Ni Lv, Xiao-Hui Xue, Rui Shen, Jing-Han Liu

Objective: This study aimed to evaluate the effects of an anti-inflammatory diet (AID) combined with Infliximab (IFX) therapy on maternal and neonatal health outcomes in pregnant Chinese patients with inflammatory bowel disease (IBD).

Methods: IBD patients treated with steady IFX maintenance therapy at the time of conception were randomly assigned to either the IBD-AID group (n = 49), which received an anti-inflammatory diet intervention during the third trimester, or the habitual diet group (n = 49). Primary outcomes included assessments of disease activity, inflammatory markers, and neonatal health. Secondary outcomes included health-related quality of life (HRQoL) in patients and functional gastrointestinal disorders (FGIDs) in infants.

Results: The IBD-AID intervention significantly reduced disease activity scores in IBD patients at 4 weeks post-intervention and 1 month postpartum compared to the habitual diet group, and also improved HRQoL. Serum C-reactive protein (CRP) and fecal calprotectin (FC) levels were significantly lower in the IBD-AID group at these times, with a trend towards lower levels at 6 months postpartum. Birth weight and Apgar scores were higher in the IBD-AID group but did not reach statistical significance. The incidence of at least one FGID in infants was significantly lower in the IBD-AID group (24.5%) compared to the habitual diet group (46.9%, p = 0.034).

Conclusion: The IBD-AID intervention combined with IFX therapy significantly improved disease activity, inflammatory markers, and QoL in maternal IBD patients, and was associated with a lower incidence of FGIDs in infants, indicating benefits for both maternal and neonatal health.

研究目的本研究旨在评估抗炎饮食(AID)联合英夫利西单抗(IFX)治疗对中国妊娠期炎症性肠病(IBD)患者的孕产妇和新生儿健康结果的影响:受孕时接受稳定的IFX维持治疗的IBD患者被随机分配到IBD-AID组(49人)或习惯饮食组(49人),前者在怀孕的第三个月接受抗炎饮食干预。主要结果包括疾病活动、炎症指标和新生儿健康评估。次要结果包括患者的健康相关生活质量(HRQoL)和婴儿的功能性胃肠道紊乱(FGIDs):结果:与习惯饮食组相比,IBD-AID 干预疗法能明显降低 IBD 患者在干预后 4 周和产后 1 个月的疾病活动评分,同时还能改善 HRQoL。IBD-AID干预组的血清C反应蛋白(CRP)和粪便钙蛋白(FC)水平在这些时间明显降低,并有在产后6个月降低的趋势。IBD-AID 组的出生体重和阿普加评分较高,但未达到统计学意义。与习惯饮食组(46.9%,P = 0.034)相比,IBD-AID 组婴儿至少一种 FGID 的发生率(24.5%)明显降低:IBD-AID干预联合IFX治疗可明显改善IBD孕产妇的疾病活动性、炎症指标和QoL,并降低婴儿FGID的发病率,对孕产妇和新生儿的健康均有益处。
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引用次数: 0
Pyloric index, a new parameter: predicting perioperative prognosis in neonates with hypertrophic pyloric stenosis. 幽门指数,一个新参数:预测患有肥厚性幽门狭窄的新生儿围手术期的预后。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-08 DOI: 10.1080/00365521.2024.2425982
Başak Kaya, Hasan Akduman, Dilek Dilli, Cem Geyik, Ayşe Karaman, Özlem Balcı, Hasibe Gökçe Çınar, Nurdan Dinlen Fettah, Ayşegül Zenciroğlu

Purpose: Delays in the diagnosis and treatment of infantile hypertrophic pyloric stenosis (IHPS) may lead to laboratory and clinical decompensation in infants. The aim of this study was to determine whether pyloric measurement parameters can be effectively used in the clinical prognosis of IHPS by evaluating the relationship between pyloric dimensions on ultrasonographic evaluation at the time of presentation and clinical and laboratory parameters in infants with pyloric stenosis.

Methods: A retrospective observational study was conducted on 122 infants who were followed up with the diagnosis of IHPS in our neonatal clinic and operated on by a pediatric surgeon between January 2005 and December 2020.

Results: The mean pyloric dimensions of the infants were pyloric length 20 mm (17-22), pyloric thickness 5 mm (4-5.8), and pyloric index 96.5 (72.2-124). Babies with preoperative laboratory values of hypokalemia, hypochloremia and metabolic alkalosis had statistically higher pyloric thickness >5 mm (4.1-6) and pyloric index >100 (86-130) parameters.

Conclusion: Pyloric thickness and pyloric index parameters can predict clinical prognosis in babies diagnosed with IHPS in the perioperative period.

目的:婴儿肥厚性幽门狭窄(IHPS)的诊断和治疗延误可能会导致婴儿出现实验室和临床失代偿。本研究的目的是通过评估幽门狭窄婴儿发病时超声评估的幽门尺寸与临床和实验室参数之间的关系,确定幽门测量参数是否可有效用于 IHPS 的临床预后:对2005年1月至2020年12月期间在我院新生儿门诊诊断为IHPS并由儿科医生进行手术的122名婴儿进行了回顾性观察研究:婴儿幽门的平均尺寸为:幽门长 20 毫米(17-22),幽门厚 5 毫米(4-5.8),幽门指数 96.5(72.2-124)。据统计,术前化验值为低钾血症、低氯血症和代谢性碱中毒的婴儿幽门厚度>5 毫米(4.1-6),幽门指数>100(86-130):结论:幽门厚度和幽门指数参数可预测围手术期被诊断为 IHPS 的婴儿的临床预后。
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引用次数: 0
Forty years of successful national research collaboration in liver disease - the Swedish experience. 四十年成功的国家肝病研究合作--瑞典的经验。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 DOI: 10.1080/00365521.2024.2421824
Annika Bergquist, Mattias Ekstedt, Hannes Hagström, Gunnar Järnerot, Stefan Lindgren, Emma Nilsson, Nils Nyhlin, Fredrik Rorsman, Per Stål, Mårten Werner, Stergios Kechagias

Aim: Sweden has historically provided a fruitful arena for research in clinical medicine. We here share 40 years of experience of collaboration in the Swedish hepatology research group (SWEHEP) (https://www.swehep.se).

Methods: We describe the way the Swedish hepatology pioneers started the group and how the network continuously developed over the years. Successful projects such as thorough studies of natural history and various clinical aspects of autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, and steatosis are described.

Results: Over the years, more than 80 publications have been published by the group. A summary of new and ongoing research programs includes the randomized placebo-controlled trial of simvastatin in PSC (PiSCATIN), the prospective BIGMAP (Biochemical and genetic markers for the assessment and prognostication of liver cirrhosis) initiative in patients with liver cirrhosis, and the DETECT-HCC, a prospective multicenter cohort study comparing abbreviated MRI and ultrasound for surveillance of hepatocellular carcinoma every six months over two years. The group philosophy, success factors for the longstanding collaboration as well as experience of failures are shared.

Conclusion: The success of hepatology research in Sweden is based on longstanding collaboration over generations of hepatologists, where everyone contributes, regular research meetings, mutual trust, and perseverance.

目的:瑞典历来为临床医学研究提供了一个硕果累累的舞台。我们在此分享瑞典肝病研究小组 (SWEHEP) 40 年来的合作经验 (https://www.swehep.se)。方法:我们介绍了瑞典肝病学先驱们如何创立该研究小组,以及该网络多年来是如何不断发展的。我们介绍了一些成功的项目,如对自身免疫性肝炎、原发性胆汁性胆管炎、原发性硬化性胆管炎和脂肪肝的自然史和各种临床问题的深入研究:多年来,该研究小组共发表了 80 多篇论文。新的和正在进行的研究项目包括辛伐他汀治疗原发性胆汁性胆管炎的随机安慰剂对照试验(PiSCATIN)、针对肝硬化患者的前瞻性 BIGMAP(肝硬化评估和预后的生化和遗传标记)计划以及 DETECT-HCC(一项前瞻性多中心队列研究,比较简略 MRI 和超声波在两年内每六个月对肝细胞癌的监测)。研究小组的理念、长期合作的成功因素以及失败的经验都得到了分享:瑞典肝病学研究的成功基于几代肝病学家的长期合作,每个人都做出了贡献,定期召开研究会议,相互信任,坚持不懈。
{"title":"Forty years of successful national research collaboration in liver disease - the Swedish experience.","authors":"Annika Bergquist, Mattias Ekstedt, Hannes Hagström, Gunnar Järnerot, Stefan Lindgren, Emma Nilsson, Nils Nyhlin, Fredrik Rorsman, Per Stål, Mårten Werner, Stergios Kechagias","doi":"10.1080/00365521.2024.2421824","DOIUrl":"https://doi.org/10.1080/00365521.2024.2421824","url":null,"abstract":"<p><strong>Aim: </strong>Sweden has historically provided a fruitful arena for research in clinical medicine. We here share 40 years of experience of collaboration in the Swedish hepatology research group (SWEHEP) (https://www.swehep.se).</p><p><strong>Methods: </strong>We describe the way the Swedish hepatology pioneers started the group and how the network continuously developed over the years. Successful projects such as thorough studies of natural history and various clinical aspects of autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, and steatosis are described.</p><p><strong>Results: </strong>Over the years, more than 80 publications have been published by the group. A summary of new and ongoing research programs includes the randomized placebo-controlled trial of simvastatin in PSC (PiSCATIN), the prospective BIGMAP (Biochemical and genetic markers for the assessment and prognostication of liver cirrhosis) initiative in patients with liver cirrhosis, and the DETECT-HCC, a prospective multicenter cohort study comparing abbreviated MRI and ultrasound for surveillance of hepatocellular carcinoma every six months over two years. The group philosophy, success factors for the longstanding collaboration as well as experience of failures are shared.</p><p><strong>Conclusion: </strong>The success of hepatology research in Sweden is based on longstanding collaboration over generations of hepatologists, where everyone contributes, regular research meetings, mutual trust, and perseverance.</p>","PeriodicalId":21461,"journal":{"name":"Scandinavian Journal of Gastroenterology","volume":" ","pages":"1-8"},"PeriodicalIF":1.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142558691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
'Does this fecal microbiota transplant work?' Quality assurance of capsule based fecal microbiota transplant production. 粪便微生物群移植有用吗?基于胶囊的粪便微生物群移植生产的质量保证。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI: 10.1080/00365521.2024.2401460
Emil Ainsworth Jochumsen, Maja Skov Kragsnaes, Anna Christine Nilsson, Kristina Fruerlund Rasmussen, Torkell Ellingsen, Mie Agerbaek Juul, Jens Kjeldsen, Dorte Kinggaard Holm

Background: Fecal Microbiota Transplant (FMT) is an effective treatment for recurring Clostridioides Difficile Infections (rCDI). FMT administered via oral capsules (caFMT) offers several practical advantages to conventional liquid FMT. We began using caFMT in 2021 imported from an external institution. Based on similar production methods, we began our own caFMT production in 2022. We aimed to evaluate the quality of our caFMT.

Study design and methods: We created a database of all FMT treatments (n = 180) provided by our institution. Quality of all FMT was evaluated by treatment success rates. We compared our caFMT to the imported caFMT.

Results: Our caFMT yielded similar success rates compared to that of the imported caFMT, 65% (CI 95% 58-72%) and 72% (CI 95% 66-79%) respectively. FMT administered via colonoscopy had a significantly higher success rate, 79% (CI 95% 73-85%) than own our caFMT and other routes of administration. The combined success rate of treatments increased notably for all routes of administration when repeating FMT after prior failure.

Discussion: The fact that our caFMT compared similarly to the imported caFMT was viewed as a success in terms of quality assurance. Our caFMT had a slightly lower success rates compared to data from other studies, but could be affected by several other factors than our FMT-production methods. A lower success rate of caFMT compared to FMT via colonoscopy is acceptable due to the practical advantages offed by caFMT. Our study serves as a practical example, proving that of the standardization of caFMT production is indeed viable.

背景:粪便微生物群移植(FMT)是治疗复发性艰难梭菌感染(rCDI)的有效方法。与传统的液体 FMT 相比,通过口服胶囊(caFMT)给药的 FMT 具有一些实际优势。2021 年,我们开始使用从外部机构进口的 caFMT。基于类似的生产方法,我们于 2022 年开始自己生产 caFMT。我们的目的是评估我们的 caFMT 质量:我们建立了本机构提供的所有 FMT 治疗(n = 180)的数据库。根据治疗成功率评估所有 FMT 的质量。我们将我们的 caFMT 与进口的 caFMT 进行了比较:结果:与进口 caFMT 相比,我们的 caFMT 成功率相似,分别为 65% (CI 95% 58-72%) 和 72% (CI 95% 66-79%)。通过结肠镜进行 FMT 治疗的成功率为 79%(CI 95% 73-85%),明显高于我们的 caFMT 和其他给药途径。在先前治疗失败后再次进行 FMT 治疗时,所有给药途径的综合治疗成功率都明显提高:讨论:从质量保证的角度来看,我们的 caFMT 与进口的 caFMT 相比具有相似性,这被视为一种成功。与其他研究的数据相比,我们的 caFMT 成功率略低,但这可能受到 FMT 生产方法以外的其他一些因素的影响。与通过结肠镜进行 FMT 相比,caFMT 的成功率较低是可以接受的,因为 caFMT 具有实际优势。我们的研究是一个实践范例,证明了 caFMT 生产标准化确实可行。
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引用次数: 0
Obstructive sleep apnoea is independently associated with non-alcoholic fatty pancreatic disease. 阻塞性睡眠呼吸暂停与非酒精性脂肪性胰腺疾病密切相关。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 Epub Date: 2024-09-26 DOI: 10.1080/00365521.2024.2406559
Jiaojiao Lin, Han Wang, Xiaoyang Chen, Lina Han, Zhibin Huang, Guorong Lyu, Shilin Li

Purpose: This study investigated the prevalence of non-alcoholic fatty pancreatic disease (NAFPD) in patients with obstructive sleep apnoea (OSA) and analysed the correlation between them.

Materials and methods: Patients who underwent polysomnography and modified abdominal ultrasound examinations were continuously enrolled and divided into OSA and control groups. The OSA group was further divided into NAFPD and non-NAFPD groups. Differences in various indicators were compared. Binary logistic regression analyses were conducted to identify factors influencing NAFPD.

Results: A total of 210 participants were included in the study, including 178 in the OSA group and 32 in the control group. The prevalence of NAFPD, weight, body mass index (BMI), and other indicators were significantly higher in the OSA group than that in the control group (p < 0.05). The above indices, prevalence of hypertension and metabolic associated steatotic liver disease (MASLD), and severity of sleep apnoea were higher in the NAFPD group than that in the non-NAFPD group (p < 0.05). Binary logistic regression analysis showed a 4.4% increased risk of NAFPD for each unit increase in apnea-hypopnea index (AHI) after adjusting for BMI and hypertension.

Conclusion: The prevalence of NAFPD was higher in the OSA group than that in the control group, and chronic intermittent hypoxia was strongly associated with pancreatic fat infiltration; AHI, BMI, and hypertension were independent risk factors for NAFPD. The NAFPD group had a higher prevalence of obesity and some other diseases.

目的:本研究调查了非酒精性脂肪性胰腺疾病(NAFPD)在阻塞性睡眠呼吸暂停(OSA)患者中的患病率,并分析了两者之间的相关性:连续登记接受多导睡眠图和改良腹部超声检查的患者,并将其分为 OSA 组和对照组。OSA 组又分为 NAFPD 组和非 NAFPD 组。比较了各种指标的差异。进行二元逻辑回归分析以确定影响 NAFPD 的因素:研究共纳入 210 名参与者,其中 OSA 组 178 人,对照组 32 人。OSA 组的 NAFPD 患病率、体重、体质指数(BMI)和其他指标均显著高于对照组(POSA 组的 NAFPD 患病率高于对照组,慢性间歇性缺氧与胰腺脂肪浸润密切相关;AHI、BMI 和高血压是 NAFPD 的独立危险因素。NAFPD组肥胖和其他一些疾病的发病率更高。
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引用次数: 0
The risk of cholangiocarcinoma in patients with MASLD is not increased compared to the general population. 与普通人群相比,MASLD 患者罹患胆管癌的风险并没有增加。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 Epub Date: 2024-10-09 DOI: 10.1080/00365521.2024.2412735
Christina Villard, Linnea Widman, Ernesto Sparrelid, Annika Bergquist, Hannes Hagström

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing in prevalence globally. MASLD is associated with an increased rate of comorbidities, including cardiovascular disease, liver cirrhosis, and hepatocellular carcinoma (HCC). While the link between MASLD and HCC is well known, the potential association with biliary tract cancer, including cholangiocarcinoma (CCA) and gallbladder cancer (GBC), is less certain. To evaluate whether individuals with MASLD are at increased risk of developing CCA compared to the general population, we performed a nationwide cohort study investigating the longitudinal association between MASLD and CCA.

Methods: A retrospective cohort study was performed including all patients ≥18 years of age, diagnosed with MASLD, from 1st of January 1987 to 31st of December 2020, through the Swedish National Patient Register. For each patient with MASLD, ten individuals, matched to the MASLD patient on year of diagnosis, age, sex, and municipality were selected as reference individuals. The international Classification of Diseases (ICD) codes were used to define MASLD and incident CCA. Incidence rates were calculated, and regression analyses were performed.

Results: Out of the 11,940 exposed patients with MASLD, 11 developed CCA (0.1%) out of whom three were diagnosed with iCCA (0.03%), during a median follow-up time of  five years. Out of 112,537 reference individuals, 62 were diagnosed with CCA (0.3%), out of whom 15 were diagnosed with iCCA (0.01%). The rate of GBC was not higher compared to the reference population.

Conclusion: This large cohort study found a low incidence of CCA in patients with MASLD, comparable to the general population which can reassure clinicians and patients that no specific vigilance for CCA should be considered in MASLD patients at present.

背景:代谢功能障碍相关性脂肪性肝病(MASLD)在全球的发病率越来越高。代谢功能障碍相关性脂肪性肝病与心血管疾病、肝硬化和肝细胞癌(HCC)等合并症的发病率增加有关。MASLD与HCC之间的联系已众所周知,但与胆道癌(包括胆管癌(CCA)和胆囊癌(GBC))的潜在联系却不太确定。为了评估与普通人群相比,MASLD 患者罹患 CCA 的风险是否会增加,我们在全国范围内开展了一项队列研究,调查 MASLD 与 CCA 之间的纵向关联:我们通过瑞典全国患者登记册,对 1987 年 1 月 1 日至 2020 年 12 月 31 日期间所有年龄≥18 岁、确诊为 MASLD 的患者进行了回顾性队列研究。为每名 MASLD 患者选择了 10 名在诊断年份、年龄、性别和城市方面与 MASLD 患者匹配的人作为参照个体。国际疾病分类(ICD)代码被用来定义MASLD和CCA事件。计算发病率并进行回归分析:结果:在 11,940 名暴露于 MASLD 的患者中,有 11 人罹患 CCA(0.1%),其中 3 人被诊断为 iCCA(0.03%),随访时间中位数为 5 年。在 112,537 名参照个体中,62 人被诊断为 CCA(0.3%),其中 15 人被诊断为 iCCA(0.01%)。与参照人群相比,GBC的发病率并不高:这项大型队列研究发现,MASLD 患者的 CCA 发病率较低,与普通人群相当,这可以让临床医生和患者放心,目前无需考虑对 MASLD 患者的 CCA 给予特别警惕。
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引用次数: 0
Mortality and rate of hospitalization stratified by patients' BMI in a colonoscopy screening - a cross sectional analysis of data from Polish Colonoscopy Screening Platform. 结肠镜筛查中按患者体重指数分层的死亡率和住院率--对波兰结肠镜筛查平台数据的横断面分析。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 Epub Date: 2024-10-04 DOI: 10.1080/00365521.2024.2410795
Piotr Spychalski, Paulina Wieszczy, Katarzyna Połomska, Jarek Kobiela, Jaroslaw Regula, Michal F Kaminski, Nastazja Pilonis

Background: Currently, it remains unknown whether there is an association between body mass index (BMI) and complications during screening colonoscopy; hence, it remains unclear whether BMI should be considered a risk factor in pre-procedural assessments. The aim of this study was to compare mortality and unplanned hospitalization rates before and after colonoscopy stratified by patients' BMI.

Material and methods: This was a retrospective cohort study of individuals who underwent screening colonoscopy as part of the Polish Colonoscopy Screening Program (PCSP). The included individuals were followed up for mortality and hospitalization episodes from 42 days prior to colonoscopy to 30 days after the procedure. Rates for the endpoints were calculated, compared, and adjusted for available data. Weighted averages of stratum-specific rates were calculated. Additional subanalyses were performed for sex and procedure type (screening colonoscopy without biopsy, colonoscopy with biopsy, or colonoscopy with polypectomy).

Results: A total of 55390 individuals who underwent colonoscopy between years 2012-2015 were included. Obese individuals had significantly more hospitalizations than non-obese patients (1.94% versus 0%, p = .038). Analysis of adjusted hospitalization rates stratified by sex revealed that obese males had significantly higher related hospitalizations' rates before or after and after colonoscopy. Unadjusted and adjusted mortality rates after screening colonoscopy did not reveal significant differences between BMI categories.

Conclusions: Overweight and obesity are not clinically relevant risk factors for mortality and hospitalization six weeks before or 30 days after screening colonoscopy. Obese males may be more likely to require hospital care after colonoscopy.

背景:目前,体质指数(BMI)与结肠镜检查并发症之间是否存在关联仍是未知数;因此,在术前评估中是否应将体质指数视为风险因素仍不明确。本研究旨在比较结肠镜检查前后按患者体重指数分层的死亡率和计划外住院率:这是一项回顾性队列研究,研究对象是波兰结肠镜筛查项目(PCSP)中接受结肠镜筛查的患者。从结肠镜检查前 42 天到结肠镜检查后 30 天,对纳入研究的患者的死亡率和住院次数进行了随访。对终点的比率进行了计算、比较,并根据现有数据进行了调整。计算了各层特异性比率的加权平均值。此外,还针对性别和手术类型(无活检的筛查性结肠镜检查、有活检的结肠镜检查或有息肉切除术的结肠镜检查)进行了子分析:共纳入2012-2015年间接受结肠镜检查的55390人。肥胖患者的住院率明显高于非肥胖患者(1.94% 对 0%,P = 0.038)。对按性别分层的调整后住院率进行分析后发现,肥胖男性在结肠镜检查前后的相关住院率明显更高。结肠镜筛查后未调整和调整后的死亡率并未显示出不同体重指数类别之间的显著差异:超重和肥胖不是结肠镜筛查前六周或筛查后 30 天内导致死亡和住院的临床相关风险因素。肥胖男性在结肠镜检查后可能更需要住院治疗。
{"title":"Mortality and rate of hospitalization stratified by patients' BMI in a colonoscopy screening - a cross sectional analysis of data from Polish Colonoscopy Screening Platform.","authors":"Piotr Spychalski, Paulina Wieszczy, Katarzyna Połomska, Jarek Kobiela, Jaroslaw Regula, Michal F Kaminski, Nastazja Pilonis","doi":"10.1080/00365521.2024.2410795","DOIUrl":"10.1080/00365521.2024.2410795","url":null,"abstract":"<p><strong>Background: </strong>Currently, it remains unknown whether there is an association between body mass index (BMI) and complications during screening colonoscopy; hence, it remains unclear whether BMI should be considered a risk factor in pre-procedural assessments. The aim of this study was to compare mortality and unplanned hospitalization rates before and after colonoscopy stratified by patients' BMI.</p><p><strong>Material and methods: </strong>This was a retrospective cohort study of individuals who underwent screening colonoscopy as part of the Polish Colonoscopy Screening Program (PCSP). The included individuals were followed up for mortality and hospitalization episodes from 42 days prior to colonoscopy to 30 days after the procedure. Rates for the endpoints were calculated, compared, and adjusted for available data. Weighted averages of stratum-specific rates were calculated. Additional subanalyses were performed for sex and procedure type (screening colonoscopy without biopsy, colonoscopy with biopsy, or colonoscopy with polypectomy).</p><p><strong>Results: </strong>A total of 55390 individuals who underwent colonoscopy between years 2012-2015 were included. Obese individuals had significantly more hospitalizations than non-obese patients (1.94% versus 0%, <i>p</i> = .038). Analysis of adjusted hospitalization rates stratified by sex revealed that obese males had significantly higher related hospitalizations' rates before or after and after colonoscopy. Unadjusted and adjusted mortality rates after screening colonoscopy did not reveal significant differences between BMI categories.</p><p><strong>Conclusions: </strong>Overweight and obesity are not clinically relevant risk factors for mortality and hospitalization six weeks before or 30 days after screening colonoscopy. Obese males may be more likely to require hospital care after colonoscopy.</p>","PeriodicalId":21461,"journal":{"name":"Scandinavian Journal of Gastroenterology","volume":" ","pages":"1259-1264"},"PeriodicalIF":1.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142372760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Eradication rate and safety of vonoprazan-amoxicillin dual therapy for helicobacter pylori eradication: a randomized controlled trial. 根除幽门螺旋杆菌的沃诺普拉赞-阿莫西林双重疗法的根除率和安全性:随机对照试验。
IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Pub Date : 2024-11-01 Epub Date: 2024-09-22 DOI: 10.1080/00365521.2024.2407898
Guoping Jiang, Mengzhao Luo, Peifen Zheng, Yanqun Cong, Yuliang Feng, Feng Zhou

Background: Helicobacter pylori (H. pylori), prevalent in developing regions, is a key factor in gastrointestinal diseases. Despite the common use of bismuth-based quadruple therapy, its drawbacks have prompted the search for alternatives. Recently, vonoprazan, a novel acid suppressant, has shown promise in combination with antibiotics as a dual therapy for H. pylori eradication. This study aimed to assess the therapeutic outcomes and adverse events of vonoprazan-amoxicillin dual therapy compared to quadruple therapy.

Methods: A randomized controlled trial (RCT) enrolled H. pylori-infected patients at Zhejiang Hospital. Participants were randomly assigned to dual and quadruple therapy groups. The primary endpoints were H. pylori eradication and adverse events.

Results: Of the 400 patients studied from April 2022 to June 2023, In the intention-to-treat (ITT) analysis, the eradication rates of H. pylori in vonoprazan-amoxicillin dual therapy group and quadruple therapy group were 94.0% and 87.0%, respectively, p = 0.017. In the per-protocol (PP) analysis were 97.9% and 93.0%, p = 0.022. Additionally, the dual therapy group had a significantly lower incidence of adverse events (19%) compared to the quadruple therapy group (53%) (p < 0.001).

Conclusion: Vonoprazan-amoxicillin dual therapy demonstrates superior eradication efficacy and reduced adverse events compared to quadruple therapy in H. pylori-infected patients, suggesting its potential for clinical application and promotion.

背景:幽门螺杆菌(H. pylori)在发展中地区普遍存在,是导致胃肠道疾病的关键因素。尽管以铋为基础的四联疗法很常用,但其缺点促使人们寻找替代疗法。最近,一种新型抑酸剂 vonoprazan 与抗生素联用,作为根除幽门螺杆菌的双重疗法,显示出了良好的前景。本研究旨在评估vonoprazan-阿莫西林双重疗法与四重疗法相比的治疗效果和不良反应:一项随机对照试验(RCT)招募了浙江医院的幽门螺杆菌感染患者。参与者被随机分配到双重疗法组和四重疗法组。主要终点是幽门螺杆菌根除率和不良反应:在2022年4月至2023年6月接受研究的400名患者中,在意向治疗(ITT)分析中,vonoprazan-阿莫西林双重疗法组和四重疗法组的幽门螺杆菌根除率分别为94.0%和87.0%,P = 0.017。在每方案(PP)分析中,分别为 97.9% 和 93.0%,p = 0.022。此外,与四联疗法组(53%)相比,双联疗法组的不良事件发生率(19%)明显较低(P 结论:双联疗法组的不良事件发生率明显低于四联疗法组:在幽门螺杆菌感染患者中,沃诺普拉赞-阿莫西林双重疗法与四联疗法相比,具有更优越的根除疗效并减少了不良反应,这表明其具有临床应用和推广的潜力。
{"title":"Eradication rate and safety of vonoprazan-amoxicillin dual therapy for helicobacter pylori eradication: a randomized controlled trial.","authors":"Guoping Jiang, Mengzhao Luo, Peifen Zheng, Yanqun Cong, Yuliang Feng, Feng Zhou","doi":"10.1080/00365521.2024.2407898","DOIUrl":"10.1080/00365521.2024.2407898","url":null,"abstract":"<p><strong>Background: </strong>Helicobacter pylori (<i>H. pylori</i>), prevalent in developing regions, is a key factor in gastrointestinal diseases. Despite the common use of bismuth-based quadruple therapy, its drawbacks have prompted the search for alternatives. Recently, vonoprazan, a novel acid suppressant, has shown promise in combination with antibiotics as a dual therapy for <i>H. pylori</i> eradication. This study aimed to assess the therapeutic outcomes and adverse events of vonoprazan-amoxicillin dual therapy compared to quadruple therapy.</p><p><strong>Methods: </strong>A randomized controlled trial (RCT) enrolled <i>H. pylori</i>-infected patients at Zhejiang Hospital. Participants were randomly assigned to dual and quadruple therapy groups. The primary endpoints were <i>H. pylori</i> eradication and adverse events.</p><p><strong>Results: </strong>Of the 400 patients studied from April 2022 to June 2023, In the intention-to-treat (ITT) analysis, the eradication rates of H. pylori in vonoprazan-amoxicillin dual therapy group and quadruple therapy group were 94.0% and 87.0%, respectively, <i>p</i> = 0.017. In the per-protocol (PP) analysis were 97.9% and 93.0%, <i>p</i> = 0.022. Additionally, the dual therapy group had a significantly lower incidence of adverse events (19%) compared to the quadruple therapy group (53%) (<i>p</i> < 0.001).</p><p><strong>Conclusion: </strong>Vonoprazan-amoxicillin dual therapy demonstrates superior eradication efficacy and reduced adverse events compared to quadruple therapy in <i>H. pylori</i>-infected patients, suggesting its potential for clinical application and promotion.</p>","PeriodicalId":21461,"journal":{"name":"Scandinavian Journal of Gastroenterology","volume":" ","pages":"1229-1233"},"PeriodicalIF":1.6,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142294383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Scandinavian Journal of Gastroenterology
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