脂肪性肝炎
生物标志物
非酒精性脂肪性肝炎
医学
内科学
生物信息学
脂肪肝
生物
疾病
遗传学
非酒精性脂肪肝
作者
Xiang Zhang,Ming‐Hua Zheng,Dehua Liu,Yufeng Lin,Sherlot Juan Song,Eagle Siu‐Hong Chu,Dabin Liu,Seema Singh,Michael R. Berman,Harry Cheuk-Hay Lau,Hongyan Gou,Grace Lai‐Hung Wong,Ni Zhang,Hai‐Yang Yuan,Rohit Loomba,Vincent Wai‐Sun Wong,Jun Yu
标识
DOI:10.1016/j.cmet.2024.10.008
摘要
The current diagnosis of metabolic dysfunction-associated steatotic liver disease (MASLD) and its severe form, metabolic dysfunction-associated steatohepatitis (MASH), is suboptimal. Here, we recruited 700 individuals, including 184 from Hong Kong as a discovery cohort and 516 from San Diego, Wenzhou, and Hong Kong as three validation cohorts. A panel of 3 parameters (C-X-C motif chemokine ligand 10 [CXCL10], cytokeratin 18 fragments M30 [CK-18], and adjusted body mass index [BMI]) was formulated (termed N3-MASH), which discriminated patients with MASLD from healthy controls with an area under the receiver operating characteristic (AUROC) of 0.954. Among patients with MASLD, N3-MASH could identify patients with MASH with an AUROC of 0.823, achieving 90.0% specificity, 62.9% sensitivity, and 88.6% positive predictive value. The diagnostic performance of N3-MASH was confirmed in three validation cohorts with AUROC of 0.802, 0.805, and 0.823, respectively. Additionally, N3-MASH identifies patients with MASH improvement with an AUROC of 0.857. In summary, we developed a robust blood-based panel for the non-invasive diagnosis of MASH, which might help clinicians reduce unnecessary liver biopsies.
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