• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血清YKL-40水平作为肝纤维化患者的一种非侵入性潜在生物标志物:一项系统评价和荟萃分析

Serum YKL-40 Levels as a Non-Invasive Potential Biomarker for Liver Fibrosis Patients: A Systematic Review and Meta-Analysis.

作者信息

Li Hong, Xu Xiaoli, Yan Tong

机构信息

Department of Integrated Traditional Chinese and Western Medicine Hepatology, Changzhou Third People's Hospital, Changzhou City, Jiangsu Province, 213000, China.

出版信息

Iran J Public Health. 2025 May;54(5):939-950. doi: 10.18502/ijph.v54i5.18629.

DOI:10.18502/ijph.v54i5.18629
PMID:40765790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12319455/
Abstract

BACKGROUND

This research's comprehensive review and meta-analysis seek to offer additional non-invasive techniques for diagnosing and monitoring liver fibrosis, thereby serving as a dependable resource for clinical practice and scientific investigation.

METHODS

To find pertinent research on the use of serum YKL-40 levels in liver fibrosis patients, databases including PubMed, Web of Science, WILEY ONLINE LIBRARY, Scopus, Embase, Cochrane Library, Science Direct, CNKI, Wanfang Data, VIP Information, and the China Biology Medicine Library System were searched. The search was conducted up to May 2024.

RESULTS

In studies comparing serum YKL-40 levels in patients with hepatic fibrosis and controls, the overall combined difference was 1.37 (0.66, 2.08), with the Chinese subgroup showing high heterogeneity, while the Egyptian study did not show heterogeneity. A total of 17 studies, including 2554 patients, were included. The combined sensitivity for diagnosing advanced fibrosis and severe fibrosis was 0.80 and 0.78 respectively, with specificities of 0.88 and 0.82. The AUC for advanced fibrosis and severe fibrosis were 0.91 and 0.87 respectively.

CONCLUSION

Serum YKL-40 shows potential value in diagnosis of liver fibrosis, but further clinical research is needed to confirm and improve its utility.

摘要

背景

本研究的综合综述和荟萃分析旨在提供额外的非侵入性技术用于诊断和监测肝纤维化,从而为临床实践和科学研究提供可靠资源。

方法

为查找关于肝纤维化患者血清YKL-40水平应用的相关研究,检索了包括PubMed、科学网、WILEY ONLINE LIBRARY、Scopus、Embase、Cochrane图书馆、Science Direct、中国知网、万方数据、维普资讯和中国生物医学文献数据库系统在内的数据库。检索截至2024年5月。

结果

在比较肝纤维化患者和对照组血清YKL-40水平的研究中,总体合并差异为1.37(0.66,2.08),中国亚组显示出高度异质性,而埃及的研究未显示出异质性。共纳入17项研究,包括2554例患者。诊断晚期纤维化和重度纤维化的合并敏感性分别为0.80和0.78,特异性分别为0.88和0.82。晚期纤维化和重度纤维化的AUC分别为0.91和0.87。

结论

血清YKL-40在肝纤维化诊断中显示出潜在价值,但需要进一步的临床研究来证实并提高其效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/4b43ff537df2/IJPH-54-939-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/a1da411f6057/IJPH-54-939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/e8cbf07c037d/IJPH-54-939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/3c03daab8dd5/IJPH-54-939-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/7fb2cf2b5e04/IJPH-54-939-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/25aff5d249c2/IJPH-54-939-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/4b43ff537df2/IJPH-54-939-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/a1da411f6057/IJPH-54-939-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/e8cbf07c037d/IJPH-54-939-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/3c03daab8dd5/IJPH-54-939-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/7fb2cf2b5e04/IJPH-54-939-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/25aff5d249c2/IJPH-54-939-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea1/12319455/4b43ff537df2/IJPH-54-939-g006.jpg

相似文献

1
Serum YKL-40 Levels as a Non-Invasive Potential Biomarker for Liver Fibrosis Patients: A Systematic Review and Meta-Analysis.血清YKL-40水平作为肝纤维化患者的一种非侵入性潜在生物标志物:一项系统评价和荟萃分析
Iran J Public Health. 2025 May;54(5):939-950. doi: 10.18502/ijph.v54i5.18629.
2
Transient elastography for diagnosis of stages of hepatic fibrosis and cirrhosis in people with alcoholic liver disease.瞬时弹性成像技术用于诊断酒精性肝病患者的肝纤维化和肝硬化分期。
Cochrane Database Syst Rev. 2015 Jan 22;1(1):CD010542. doi: 10.1002/14651858.CD010542.pub2.
3
[Chinese herbal medicine for side effects of transarterial chemoembolization in liver cancer patients: a systematic review and meta-analysis].[中药治疗肝癌患者经动脉化疗栓塞术副作用的系统评价与Meta分析]
Zhong Xi Yi Jie He Xue Bao. 2012 Dec;10(12):1341-62. doi: 10.3736/jcim20121204.
4
Blood biomarkers for the non-invasive diagnosis of endometriosis.用于子宫内膜异位症无创诊断的血液生物标志物。
Cochrane Database Syst Rev. 2016 May 1;2016(5):CD012179. doi: 10.1002/14651858.CD012179.
5
Non-invasive diagnostic assessment tools for the detection of liver fibrosis in patients with suspected alcohol-related liver disease: a systematic review and economic evaluation.疑似酒精性肝病患者肝纤维化无创诊断评估工具的系统评价和经济评估。
Health Technol Assess. 2012;16(4):1-174. doi: 10.3310/hta16040.
6
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.系统性药理学治疗慢性斑块状银屑病:网络荟萃分析。
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.
7
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.慢性斑块状银屑病的全身药理学治疗:一项网状Meta分析。
Cochrane Database Syst Rev. 2020 Jan 9;1(1):CD011535. doi: 10.1002/14651858.CD011535.pub3.
8
Nutritional support for liver disease.肝病的营养支持
Cochrane Database Syst Rev. 2012 May 16;2012(5):CD008344. doi: 10.1002/14651858.CD008344.pub2.
9
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
10
Screening for prostate cancer.前列腺癌筛查
Cochrane Database Syst Rev. 2013 Jan 31;2013(1):CD004720. doi: 10.1002/14651858.CD004720.pub3.

本文引用的文献

1
ACG Clinical Guideline: Alcohol-Associated Liver Disease.ACG 临床指南:酒精相关性肝病。
Am J Gastroenterol. 2024 Jan 1;119(1):30-54. doi: 10.14309/ajg.0000000000002572. Epub 2023 Sep 1.
2
YKL-40 promotes chemokine expression following drug-induced liver injury via TF-PAR1 pathway in mice.YKL-40通过TF-PAR1途径促进小鼠药物性肝损伤后的趋化因子表达。
Front Pharmacol. 2023 Aug 24;14:1205062. doi: 10.3389/fphar.2023.1205062. eCollection 2023.
3
Association of Non-Invasive Markers with Significant Fibrosis in Patients with Nonalcoholic Fatty Liver Disease: A Cross-Sectional Study.
非酒精性脂肪性肝病患者非侵入性标志物与显著肝纤维化的相关性:一项横断面研究。
Diabetes Metab Syndr Obes. 2023 Jul 31;16:2255-2268. doi: 10.2147/DMSO.S417754. eCollection 2023.
4
Hepatic inflammatory responses in liver fibrosis.肝纤维化中的肝脏炎症反应。
Nat Rev Gastroenterol Hepatol. 2023 Oct;20(10):633-646. doi: 10.1038/s41575-023-00807-x. Epub 2023 Jul 3.
5
Prevalence of Liver Steatosis and Fibrosis in the General Population and Various High-Risk Populations: A Nationwide Study With 5.7 Million Adults in China.中国普通人群及各类高危人群中肝脂肪变性和肝纤维化的患病率:一项针对570万成年人的全国性研究。
Gastroenterology. 2023 Oct;165(4):1025-1040. doi: 10.1053/j.gastro.2023.05.053. Epub 2023 Jun 26.
6
Serum CHI3L1 as a Biomarker for Non-invasive Diagnosis of Liver Fibrosis.血清 CHI3L1 作为一种非侵入性诊断肝纤维化的生物标志物。
Discov Med. 2022 Jan-Feb;33(168):41-49.
7
Serum CHI3L1 as a diagnostic marker and risk factor for liver fibrosis in HBeAg-negative chronic hepatitis B.血清几丁质酶3样蛋白1作为HBeAg阴性慢性乙型肝炎肝纤维化的诊断标志物和危险因素。
Am J Transl Res. 2022 Jun 15;14(6):4090-4096. eCollection 2022.
8
The Value of Serum CHI3L1 for the Diagnosis of Chronic Liver Diseases.血清几丁质酶3样蛋白1在慢性肝病诊断中的价值
Int J Gen Med. 2022 Jun 28;15:5835-5841. doi: 10.2147/IJGM.S364602. eCollection 2022.
9
Diagnostic Value of Serum Chitinase-3-Like Protein 1 for Liver Fibrosis: A Meta-analysis.血清几丁质酶-3-样蛋白1对肝纤维化的诊断价值:一项Meta分析
Biomed Res Int. 2022 Mar 20;2022:3227957. doi: 10.1155/2022/3227957. eCollection 2022.
10
Increased Levels of CHI3L1 and HA Are Associated With Higher Occurrence of Liver Damage in Patients With Obstructive Sleep Apnea.几丁质酶3样蛋白1(CHI3L1)和透明质酸(HA)水平升高与阻塞性睡眠呼吸暂停患者肝损伤的高发生率相关。
Front Med (Lausanne). 2022 Feb 25;9:854570. doi: 10.3389/fmed.2022.854570. eCollection 2022.