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通过纤维化模式分析来描述与酒精相关和代谢功能障碍相关的脂肪性肝病肝硬化。

Characterizing alcohol-related and metabolic dysfunction-associated steatotic liver disease cirrhosis via fibrotic pattern analysis.

机构信息

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki City, Nagasaki, 852-8501, Japan.

Department of Histology and Cell Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

Sci Rep. 2024 Oct 10;14(1):23679. doi: 10.1038/s41598-024-73739-4.

Abstract

This study aimed to address the diagnostic challenges in distinguishing between alcohol-related liver disease (ALD) and metabolic dysfunction-associated steatotic liver disease (MASLD). We utilized whole-slide imaging technology to conduct a comprehensive digital analysis of liver specimens collected from patients undergoing transplantation. This study included 36 and 17 patients with ALD and MASLD cirrhosis, respectively, who underwent transplantation at our institution. Digital slides were analyzed for fibrosis patterns using FibroNest™. Patient background characteristics were comparable between ALD (n = 36) and MASLD (n = 17) groups, except for sex. The ALD group exhibited thicker collagen per strand, longer and more flexural fibrosis, and a more heterogeneous distribution than the MASLD group. In patients with ALD and concomitant metabolic dysfunction, fiber distribution became relatively uniform, resembling MASLD. Application of the phenotypic fibrosis composite score achieved 100% sensitivity and specificity for ALD/MASLD diagnosis. Digital pathological analysis of the fibrosis patterns showed morphological differences between ALD and MASLD. This approach holds promise for histological differentiation, providing valuable insights beyond the current definitions based solely on alcohol intake. This study emphasizes the potential of digital pathology in refining the diagnostic criteria for hepatic disorders.

摘要

本研究旨在解决酒精性肝病 (ALD) 和代谢功能障碍相关脂肪性肝病 (MASLD) 鉴别诊断中的难题。我们利用全玻片成像技术对我院移植患者的肝组织标本进行了全面的数字分析。本研究共纳入 36 例 ALD 肝硬化和 17 例 MASLD 肝硬化患者,两组患者的基本特征相似,除性别外。与 MASLD 组相比,ALD 组的每条胶原纤维束更厚,纤维化更长、更弯曲,分布更不均匀。在伴有代谢功能障碍的 ALD 患者中,纤维分布变得相对均匀,类似于 MASLD。表型纤维化综合评分的应用对 ALD/MASLD 诊断的灵敏度和特异性均达到 100%。纤维化模式的数字病理分析显示出 ALD 和 MASLD 之间存在形态学差异。这种方法有望实现组织学上的鉴别,提供超越单纯基于酒精摄入的现有定义的有价值的见解。本研究强调了数字病理学在细化肝脏疾病诊断标准方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/849d/11466976/b5a190de0b9c/41598_2024_73739_Fig1_HTML.jpg

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