Fecal gelatinase does not predict mortality in patients with alcohol-associated hepatitis.

IF 4.1 3区 生物学 Q2 CELL BIOLOGY Microbial Cell Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.15698/mic2024.08.836
Yongqiang Yang, Phillipp Hartmann, Bernd Schnabl
{"title":"Fecal gelatinase does not predict mortality in patients with alcohol-associated hepatitis.","authors":"Yongqiang Yang, Phillipp Hartmann, Bernd Schnabl","doi":"10.15698/mic2024.08.836","DOIUrl":null,"url":null,"abstract":"<p><p>Alcohol-associated liver disease is highly prevalent worldwide, with alcohol-associated hepatitis as a severe form characterized by substantial morbidity, mortality, and economic burden. Gut bacterial dysbiosis has been linked to progression of alcohol-associated hepatitis. Fecal cytolysin secreted by the pathobiont <i>Enterococcus faecalis</i> (<i>E. faecalis</i>) is associated with increased mortality in patients with alcohol-associated hepatitis. Although gelatinase is considered a virulence factor in <i>E. faecalis</i>, its prevalence and impact on alcohol-associated hepatitis patient outcomes remains unclear. In this study, 20 out of 65 (30.8%) patients with alcohol-associated hepatitis tested positive for gelatinase in their stool. There were no significant differences in 30-day and 90-day mortality between gelatinase-positive and gelatinase-negative patients (p=0.97 and p=0.48, respectively). Fecal gelatinase had a low discriminative ability for 30-day mortality (area under the curve [AUC] 0.50 vs fibrosis-4 Index (FIB-4) 0.75) and 90-day mortality compared with other established liver disease markers (AUC 0.57 vs FIB-4 0.79 or 'age, serum bilirubin, INR, and serum creatinine' (ABIC) score 0.78). Furthermore, fecal gelatinase was not an important feature for 30-day or 90-day mortality per random forest analysis. Finally, gelatinase-positive patients with alcohol-associated hepatitis did not exhibit more severe liver disease compared with gelatinase-negative patients. In conclusion, fecal gelatinase does not predict mortality or disease severity in patients with alcohol-associated hepatitis from our cohort.</p>","PeriodicalId":18397,"journal":{"name":"Microbial Cell","volume":"11 ","pages":"328-338"},"PeriodicalIF":4.1000,"publicationDate":"2024-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11350238/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.15698/mic2024.08.836","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Alcohol-associated liver disease is highly prevalent worldwide, with alcohol-associated hepatitis as a severe form characterized by substantial morbidity, mortality, and economic burden. Gut bacterial dysbiosis has been linked to progression of alcohol-associated hepatitis. Fecal cytolysin secreted by the pathobiont Enterococcus faecalis (E. faecalis) is associated with increased mortality in patients with alcohol-associated hepatitis. Although gelatinase is considered a virulence factor in E. faecalis, its prevalence and impact on alcohol-associated hepatitis patient outcomes remains unclear. In this study, 20 out of 65 (30.8%) patients with alcohol-associated hepatitis tested positive for gelatinase in their stool. There were no significant differences in 30-day and 90-day mortality between gelatinase-positive and gelatinase-negative patients (p=0.97 and p=0.48, respectively). Fecal gelatinase had a low discriminative ability for 30-day mortality (area under the curve [AUC] 0.50 vs fibrosis-4 Index (FIB-4) 0.75) and 90-day mortality compared with other established liver disease markers (AUC 0.57 vs FIB-4 0.79 or 'age, serum bilirubin, INR, and serum creatinine' (ABIC) score 0.78). Furthermore, fecal gelatinase was not an important feature for 30-day or 90-day mortality per random forest analysis. Finally, gelatinase-positive patients with alcohol-associated hepatitis did not exhibit more severe liver disease compared with gelatinase-negative patients. In conclusion, fecal gelatinase does not predict mortality or disease severity in patients with alcohol-associated hepatitis from our cohort.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
粪便明胶酶不能预测酒精相关性肝炎患者的死亡率。
酒精相关性肝病在全球范围内发病率很高,其中酒精相关性肝炎是一种严重的肝病,具有发病率高、死亡率高和经济负担重的特点。肠道细菌失调与酒精相关性肝炎的恶化有关。病原菌粪肠球菌(E. faecalis)分泌的粪便细胞溶解素与酒精相关性肝炎患者死亡率的增加有关。虽然明胶酶被认为是粪肠球菌的毒力因子,但其流行程度及其对酒精相关性肝炎患者预后的影响仍不清楚。在这项研究中,65 名酒精相关性肝炎患者中有 20 人(30.8%)的粪便中检测出明胶酶呈阳性。明胶酶阳性和明胶酶阴性患者的 30 天和 90 天死亡率无明显差异(分别为 p=0.97 和 p=0.48)。与其他已确定的肝病标志物相比,粪便明胶酶对 30 天死亡率(曲线下面积 [AUC] 0.50 vs 纤维化-4 指数 (FIB-4) 0.75)和 90 天死亡率(AUC 0.57 vs FIB-4 0.79 或 "年龄、血清胆红素、INR 和血清肌酐"(ABIC)评分 0.78)的判别能力较低。此外,根据随机森林分析,粪便明胶酶不是 30 天或 90 天死亡率的重要特征。最后,与明胶酶阴性的患者相比,明胶酶阳性的酒精相关性肝炎患者并没有表现出更严重的肝病。总之,粪便明胶酶不能预测我们队列中酒精相关性肝炎患者的死亡率或疾病严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Microbial Cell
Microbial Cell Multiple-
CiteScore
6.40
自引率
0.00%
发文量
32
审稿时长
12 weeks
期刊最新文献
Microwave-assisted preparation of yeast cells for ultrastructural analysis by electron microscopy. Efflux pumps: gatekeepers of antibiotic resistance in Staphylococcus aureus biofilms. A complex remodeling of cellular homeostasis distinguishes RSV/SARS-CoV-2 co-infected A549-hACE2 expressing cell lines. RidA proteins contribute to fitness of S. enterica and E. coli by reducing 2AA stress and moderating flux to isoleucine biosynthesis. Fecal gelatinase does not predict mortality in patients with alcohol-associated hepatitis.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1