Vedolizumab对非酒精性脂肪肝病程无影响:一项回顾性队列分析

Prabhat Kumar, A. Almomani, Somtochukwu Onwuzo, A. Boustany, Eduard Krishtopaytis, Dana Alshaikh, Almaza a. Albakri, M. Alkhayyat, Tareq Kiwan, Imad Asaad
{"title":"Vedolizumab对非酒精性脂肪肝病程无影响:一项回顾性队列分析","authors":"Prabhat Kumar, A. Almomani, Somtochukwu Onwuzo, A. Boustany, Eduard Krishtopaytis, Dana Alshaikh, Almaza a. Albakri, M. Alkhayyat, Tareq Kiwan, Imad Asaad","doi":"10.46439/gastro.2.013","DOIUrl":null,"url":null,"abstract":"Background and Aim: Non-Alcoholic Fatty Liver Disease (NAFLD) is the commonest cause of chronic liver disease and is a leading cause of liver transplantation in the United States, with no approved medication to halt or reverse its progression. Recent animal-model prospective trial-suggested that drug Vedolizumab leads to improvement and reversal in the NAFLD-related metabolic derangements. Vedolizumab is an α4β7 integrin-inhibitor that is approved for use in IBD patients. Our study aims to understand Vedolizumab's impact on the course of NAFLD in inflammatory bowel disease (IBD) patients.\n\nMethods: We conducted a retrospective cohort analysis of 158 subjects with NAFLD who received Vedolizumab at Cleveland Clinic Foundation (CCF). One cohort of 79 patients with NAFLD who received Vedolizumab were matched with control group of 79 patients. We determined the primary outcome as the response to Vedolizumab measured as Fibrosis-4 (Fib-4) regression to <1.3 points after one year of treatment.\n\nResults: We observed that there was no statistically significant difference response (p= 0.576), progression of the disease (p= 1.000) or change in the number of cirrhosis decompensation episodes (in those with NAFLD cirrhosis) among Vedolizumab recipients.\n\nConclusions: In this retrospective cohort analysis, and unlike in the previous animal model, Vedolizumab was not associated with statistically significant improvement or progression in the Fib-4 score after one year of treatment, and among those with NAFLD-cirrhosis, there was no statistical difference in the complication rates.","PeriodicalId":91025,"journal":{"name":"Journal of clinical and experimental gastroenterology","volume":"353 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Vedolizumab has no effect on the course of non-alcoholic fatty liver disease: A retrospective cohort analysis\",\"authors\":\"Prabhat Kumar, A. Almomani, Somtochukwu Onwuzo, A. Boustany, Eduard Krishtopaytis, Dana Alshaikh, Almaza a. Albakri, M. Alkhayyat, Tareq Kiwan, Imad Asaad\",\"doi\":\"10.46439/gastro.2.013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background and Aim: Non-Alcoholic Fatty Liver Disease (NAFLD) is the commonest cause of chronic liver disease and is a leading cause of liver transplantation in the United States, with no approved medication to halt or reverse its progression. Recent animal-model prospective trial-suggested that drug Vedolizumab leads to improvement and reversal in the NAFLD-related metabolic derangements. Vedolizumab is an α4β7 integrin-inhibitor that is approved for use in IBD patients. Our study aims to understand Vedolizumab's impact on the course of NAFLD in inflammatory bowel disease (IBD) patients.\\n\\nMethods: We conducted a retrospective cohort analysis of 158 subjects with NAFLD who received Vedolizumab at Cleveland Clinic Foundation (CCF). One cohort of 79 patients with NAFLD who received Vedolizumab were matched with control group of 79 patients. We determined the primary outcome as the response to Vedolizumab measured as Fibrosis-4 (Fib-4) regression to <1.3 points after one year of treatment.\\n\\nResults: We observed that there was no statistically significant difference response (p= 0.576), progression of the disease (p= 1.000) or change in the number of cirrhosis decompensation episodes (in those with NAFLD cirrhosis) among Vedolizumab recipients.\\n\\nConclusions: In this retrospective cohort analysis, and unlike in the previous animal model, Vedolizumab was not associated with statistically significant improvement or progression in the Fib-4 score after one year of treatment, and among those with NAFLD-cirrhosis, there was no statistical difference in the complication rates.\",\"PeriodicalId\":91025,\"journal\":{\"name\":\"Journal of clinical and experimental gastroenterology\",\"volume\":\"353 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical and experimental gastroenterology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.46439/gastro.2.013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical and experimental gastroenterology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46439/gastro.2.013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景和目的:非酒精性脂肪性肝病(NAFLD)是慢性肝病的最常见原因,也是美国肝移植的主要原因,目前尚无批准的药物来阻止或逆转其进展。最近的动物模型前瞻性试验表明,Vedolizumab可改善和逆转nafld相关的代谢紊乱。Vedolizumab是一种α4β7整合素抑制剂,已被批准用于IBD患者。我们的研究旨在了解Vedolizumab对炎症性肠病(IBD)患者NAFLD病程的影响。方法:我们对在克利夫兰临床基金会(CCF)接受Vedolizumab治疗的158例NAFLD患者进行了回顾性队列分析。一组79例接受Vedolizumab治疗的NAFLD患者与对照组79例患者相匹配。我们将主要结局确定为对Vedolizumab的反应,在治疗一年后,纤维化-4 (Fib-4)回归到<1.3点。结果:我们观察到,在Vedolizumab接受者中,没有统计学意义上的差异反应(p= 0.576)、疾病进展(p= 1.000)或肝硬化失代偿发作次数(NAFLD肝硬化患者)的变化。结论:在这项回顾性队列分析中,与之前的动物模型不同,Vedolizumab与治疗一年后Fib-4评分的改善或进展没有统计学意义,并且在nafld -肝硬化患者中,并发症发生率没有统计学差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vedolizumab has no effect on the course of non-alcoholic fatty liver disease: A retrospective cohort analysis
Background and Aim: Non-Alcoholic Fatty Liver Disease (NAFLD) is the commonest cause of chronic liver disease and is a leading cause of liver transplantation in the United States, with no approved medication to halt or reverse its progression. Recent animal-model prospective trial-suggested that drug Vedolizumab leads to improvement and reversal in the NAFLD-related metabolic derangements. Vedolizumab is an α4β7 integrin-inhibitor that is approved for use in IBD patients. Our study aims to understand Vedolizumab's impact on the course of NAFLD in inflammatory bowel disease (IBD) patients. Methods: We conducted a retrospective cohort analysis of 158 subjects with NAFLD who received Vedolizumab at Cleveland Clinic Foundation (CCF). One cohort of 79 patients with NAFLD who received Vedolizumab were matched with control group of 79 patients. We determined the primary outcome as the response to Vedolizumab measured as Fibrosis-4 (Fib-4) regression to <1.3 points after one year of treatment. Results: We observed that there was no statistically significant difference response (p= 0.576), progression of the disease (p= 1.000) or change in the number of cirrhosis decompensation episodes (in those with NAFLD cirrhosis) among Vedolizumab recipients. Conclusions: In this retrospective cohort analysis, and unlike in the previous animal model, Vedolizumab was not associated with statistically significant improvement or progression in the Fib-4 score after one year of treatment, and among those with NAFLD-cirrhosis, there was no statistical difference in the complication rates.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信