• 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

新型工具检测慢性胆汁淤积症:角蛋白 7 染色肝组织标本的自动化分析。

Chronic cholestasis detection by a novel tool: automated analysis of cytokeratin 7-stained liver specimens.

机构信息

Department of Pathology, University of Helsinki and Helsinki University Hospital, Haartmaninkatu 3, 00290, Helsinki, Finland.

Aiforia Technologies Oy, Tukholmankatu 8, 000290, Helsinki, Finland.

出版信息

Diagn Pathol. 2021 May 6;16(1):41. doi: 10.1186/s13000-021-01102-6.

DOI:10.1186/s13000-021-01102-6
PMID:33957930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8101247/
Abstract

BACKGROUND

The objective was to build a novel method for automated image analysis to locate and quantify the number of cytokeratin 7 (K7)-positive hepatocytes reflecting cholestasis by applying deep learning neural networks (AI model) in a cohort of 210 liver specimens. We aimed to study the correlation between the AI model's results and disease progression. The cohort of liver biopsies which served as a model of chronic cholestatic liver disease comprised of patients diagnosed with primary sclerosing cholangitis (PSC).

METHODS

In a cohort of patients with PSC identified from the PSC registry of the University Hospital of Helsinki, their K7-stained liver biopsy specimens were scored by a pathologist (human K7 score) and then digitally analyzed for K7-positive hepatocytes (K7%area). The digital analysis was by a K7-AI model created in an Aiforia Technologies cloud platform. For validation, values were human K7 score, stage of disease (Metavir and Nakunuma fibrosis score), and plasma liver enzymes indicating clinical cholestasis, all subjected to correlation analysis.

RESULTS

The K7-AI model results (K7%area) correlated with the human K7 score (0.896; p < 2.2e). In addition, K7%area correlated with stage of PSC (Metavir 0.446; p < 1.849e and Nakanuma 0.424; p < 4.23e) and with plasma alkaline phosphatase (P-ALP) levels (0.369, p < 5.749e).

CONCLUSIONS

The accuracy of the AI-based analysis was comparable to that of the human K7 score. Automated quantitative image analysis correlated with stage of PSC and with P-ALP. Based on the results of the K7-AI model, we recommend K7 staining in the assessment of cholestasis by means of automated methods that provide fast (9.75 s/specimen) quantitative analysis.

摘要

背景

本研究旨在建立一种新的自动化图像分析方法,通过应用深度学习神经网络(AI 模型)在 210 例肝标本中定位和量化反映胆汁淤积的角蛋白 7(K7)阳性肝细胞数量。我们旨在研究 AI 模型结果与疾病进展的相关性。该肝活检队列作为慢性胆汁淤积性肝病模型,由赫尔辛基大学医院原发性硬化性胆管炎(PSC)登记处诊断的患者组成。

方法

在赫尔辛基大学医院 PSC 登记处鉴定的 PSC 患者队列中,他们的 K7 染色肝活检标本由病理学家(人类 K7 评分)进行评分,然后进行 K7 阳性肝细胞(K7%area)的数字分析。数字分析由 Aiforia 技术云平台创建的 K7-AI 模型完成。为了验证,对人类 K7 评分、疾病分期(Metavir 和 Nakunuma 纤维化评分)和指示临床胆汁淤积的血浆肝酶进行相关性分析。

结果

K7-AI 模型结果(K7%area)与人类 K7 评分(0.896;p<2.2e)相关。此外,K7%area 与 PSC 分期(Metavir 0.446;p<1.849e 和 Nakunuma 0.424;p<4.23e)和血浆碱性磷酸酶(P-ALP)水平(0.369,p<5.749e)相关。

结论

基于人工智能的分析准确性可与人类 K7 评分相媲美。自动化定量图像分析与 PSC 分期和 P-ALP 相关。基于 K7-AI 模型的结果,我们建议在评估胆汁淤积时使用 K7 染色,通过提供快速(9.75s/specimen)定量分析的自动化方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f60acc94889e/13000_2021_1102_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f79dbd96a095/13000_2021_1102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/46ba9f9557a8/13000_2021_1102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/a4db3456f884/13000_2021_1102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f24848e4931e/13000_2021_1102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/2d7760202863/13000_2021_1102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f60acc94889e/13000_2021_1102_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f79dbd96a095/13000_2021_1102_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/46ba9f9557a8/13000_2021_1102_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/a4db3456f884/13000_2021_1102_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f24848e4931e/13000_2021_1102_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/2d7760202863/13000_2021_1102_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff36/8101247/f60acc94889e/13000_2021_1102_Fig6_HTML.jpg

相似文献

1
Chronic cholestasis detection by a novel tool: automated analysis of cytokeratin 7-stained liver specimens.新型工具检测慢性胆汁淤积症:角蛋白 7 染色肝组织标本的自动化分析。
Diagn Pathol. 2021 May 6;16(1):41. doi: 10.1186/s13000-021-01102-6.
2
Automated image analysis of keratin 7 staining can predict disease outcome in primary sclerosing cholangitis.角蛋白7染色的自动化图像分析可预测原发性硬化性胆管炎的疾病预后。
Hepatol Res. 2023 Apr;53(4):322-333. doi: 10.1111/hepr.13867. Epub 2022 Dec 27.
3
Keratin 7 expression in hepatic cholestatic diseases.肝胆汁淤积性疾病中的角蛋白 7 表达。
Virchows Arch. 2021 Oct;479(4):815-824. doi: 10.1007/s00428-021-03152-z. Epub 2021 Jul 27.
4
Baseline values and changes in liver stiffness measured by transient elastography are associated with severity of fibrosis and outcomes of patients with primary sclerosing cholangitis.瞬时弹性成像测量的肝硬度的基线值和变化与原发性硬化性胆管炎患者纤维化的严重程度和结局相关。
Gastroenterology. 2014 Apr;146(4):970-9; quiz e15-6. doi: 10.1053/j.gastro.2013.12.030. Epub 2013 Dec 31.
5
Dysregulation of antioxidant responses in patients diagnosed with concomitant Primary Sclerosing Cholangitis/Inflammatory Bowel Disease.原发性硬化性胆管炎/炎症性肠病患者的抗氧化反应失调。
Exp Mol Pathol. 2018 Feb;104(1):1-8. doi: 10.1016/j.yexmp.2017.11.012. Epub 2017 Nov 24.
6
norUrsodeoxycholic acid improves cholestasis in primary sclerosing cholangitis.熊去氧胆酸可改善原发性硬化性胆管炎的胆汁淤积。
J Hepatol. 2017 Sep;67(3):549-558. doi: 10.1016/j.jhep.2017.05.009. Epub 2017 May 18.
7
Collagen proportionate area correlates with histological stage and predicts clinical events in primary sclerosing cholangitis.胶原比例面积与原发性硬化性胆管炎的组织学分期相关,并可预测临床事件。
Liver Int. 2021 Nov;41(11):2681-2692. doi: 10.1111/liv.14979. Epub 2021 Jul 13.
8
Efficacy and safety of immune-modulating therapy for primary sclerosing cholangitis: A systematic review and meta-analysis.免疫调节疗法治疗原发性硬化性胆管炎的疗效和安全性:系统评价和荟萃分析。
Pharmacol Ther. 2022 Sep;237:108163. doi: 10.1016/j.pharmthera.2022.108163. Epub 2022 Mar 7.
9
Short-term prognostic factors for primary sclerosing cholangitis.原发性硬化性胆管炎的短期预后因素。
J Hepatobiliary Pancreat Sci. 2015 Jun;22(6):486-90. doi: 10.1002/jhbp.238. Epub 2015 Mar 31.
10
An Imaging Biomarker for Assessing Hepatic Function in Patients With Primary Sclerosing Cholangitis.原发性硬化性胆管炎患者肝功能评估的影像学生物标志物。
Clin Gastroenterol Hepatol. 2019 Jan;17(1):192-199.e3. doi: 10.1016/j.cgh.2018.05.011. Epub 2018 Jul 11.

引用本文的文献

1
A magnetic resonance image-based deep learning radiomics nomogram for hepatocyte cytokeratin 7 expression: application to predict cholestasis progression in children with pancreaticobiliary maljunction.基于磁共振成像的深度学习影像组学列线图用于预测肝内胆管细胞角蛋白7表达:在预测胰胆管合流异常患儿胆汁淤积进展中的应用
Pediatr Radiol. 2025 Apr 5. doi: 10.1007/s00247-025-06225-2.
2
Deep learning assisted quantitative analysis of Aβ and microglia in patients with idiopathic normal pressure hydrocephalus in relation to cognitive outcome.深度学习辅助分析特发性正常压力脑积水患者 Aβ 和小胶质细胞与认知结局的关系。
J Neuropathol Exp Neurol. 2024 Nov 1;83(11):967-978. doi: 10.1093/jnen/nlae083.
3

本文引用的文献

1
Artificial intelligence identifies inflammation and confirms fibroblast foci as prognostic tissue biomarkers in idiopathic pulmonary fibrosis.人工智能识别炎症,并确认成纤维细胞灶为特发性肺纤维化的预后组织生物标志物。
Hum Pathol. 2021 Jan;107:58-68. doi: 10.1016/j.humpath.2020.10.008. Epub 2020 Nov 5.
2
Next generation diagnostic pathology: use of digital pathology and artificial intelligence tools to augment a pathological diagnosis.下一代诊断病理学:利用数字病理学和人工智能工具辅助病理诊断。
Diagn Pathol. 2019 Dec 27;14(1):138. doi: 10.1186/s13000-019-0921-2.
3
Validation, clinical utility and limitations of the Amsterdam-Oxford model for primary sclerosing cholangitis.
A deep-learning-based model for assessment of autoimmune hepatitis from histology: AI(H).
一种基于深度学习的组织学评估自身免疫性肝炎的模型:AI(H)。
Virchows Arch. 2024 Dec;485(6):1095-1105. doi: 10.1007/s00428-024-03841-5. Epub 2024 Jun 15.
4
AI-algorithm training and validation for identification of endometrial CD138+ cells in infertility-associated conditions; polycystic ovary syndrome (PCOS) and recurrent implantation failure (RIF).用于识别不孕相关病症(多囊卵巢综合征(PCOS)和反复种植失败(RIF))中子宫内膜CD138 +细胞的人工智能算法训练与验证
J Pathol Inform. 2024 Apr 29;15:100380. doi: 10.1016/j.jpi.2024.100380. eCollection 2024 Dec.
5
Dynamic changes in AI-based analysis of endometrial cellular composition: Analysis of PCOS and RIF endometrium.基于人工智能的子宫内膜细胞成分分析中的动态变化:多囊卵巢综合征和反复种植失败子宫内膜的分析。
J Pathol Inform. 2024 Feb 1;15:100364. doi: 10.1016/j.jpi.2024.100364. eCollection 2024 Dec.
6
Artificial Intelligence-Based Opportunities in Liver Pathology-A Systematic Review.基于人工智能的肝脏病理学机遇——一项系统综述
Diagnostics (Basel). 2023 May 19;13(10):1799. doi: 10.3390/diagnostics13101799.
7
Deep Learning-Based Image Analysis of Liver Steatosis in Mouse Models.基于深度学习的小鼠模型肝脂肪变性的图像分析。
Am J Pathol. 2023 Aug;193(8):1072-1080. doi: 10.1016/j.ajpath.2023.04.014. Epub 2023 May 24.
8
Update on Hepatobiliary Plasticity.肝胆可塑性研究进展。
Semin Liver Dis. 2023 Feb;43(1):13-23. doi: 10.1055/s-0042-1760306. Epub 2023 Feb 10.
9
Novel histological scoring for predicting disease outcome in primary sclerosing cholangitis.原发性硬化性胆管炎疾病结局预测的新型组织学评分。
Histopathology. 2022 Aug;81(2):192-204. doi: 10.1111/his.14677. Epub 2022 May 31.
原发性硬化性胆管炎阿姆斯特丹-牛津模型的验证、临床实用性和局限性。
J Hepatol. 2019 Nov;71(5):992-999. doi: 10.1016/j.jhep.2019.06.012. Epub 2019 Jul 3.
4
Implementation of deep neural networks to count dopamine neurons in substantia nigra.实现深度神经网络来计数黑质中的多巴胺神经元。
Eur J Neurosci. 2018 Sep;48(6):2354-2361. doi: 10.1111/ejn.14129. Epub 2018 Sep 20.
5
Influence of Progenitor-Derived Regeneration Markers on Hepatitis C Virus-Related Cirrhosis Outcome (ANRS CO12 CirVir Cohort).祖细胞衍生的再生标志物对丙型肝炎病毒相关肝硬化结局的影响(ANRS CO12 CirVir 队列)。
Hepatology. 2018 Oct;68(4):1534-1548. doi: 10.1002/hep.29927.
6
Do orcein-positive copper-binding protein deposits and cytokeratin 7 co-localise in periportal hepatocytes in chronic cholestasis?在慢性胆汁淤积症中,orcein阳性的铜结合蛋白沉积物与细胞角蛋白7是否在汇管区周围肝细胞中共定位?
J Clin Pathol. 2018 Jun;71(6):563-564. doi: 10.1136/jclinpath-2018-205139. Epub 2018 Mar 20.
7
Primary sclerosing cholangitis.原发性硬化性胆管炎。
Lancet. 2018 Jun 23;391(10139):2547-2559. doi: 10.1016/S0140-6736(18)30300-3. Epub 2018 Feb 13.
8
Copper, copper-binding protein and cytokeratin 7 in biliary disorders.铜、铜结合蛋白和细胞角蛋白7在胆道疾病中的作用
Histopathology. 2017 Dec;71(6):1006-1008. doi: 10.1111/his.13314. Epub 2017 Sep 29.
9
Interobserver Variability in Histologic Evaluation of Liver Fibrosis Using Categorical and Quantitative Scores.使用分类和定量评分对肝纤维化进行组织学评估时的观察者间变异性
Am J Clin Pathol. 2017 Apr 1;147(4):364-369. doi: 10.1093/ajcp/aqx011.
10
Validation of the prognostic value of histologic scoring systems in primary sclerosing cholangitis: An international cohort study.原发性硬化性胆管炎组织学评分系统预后价值的验证:一项国际队列研究。
Hepatology. 2017 Mar;65(3):907-919. doi: 10.1002/hep.28963. Epub 2017 Jan 11.