Stravitz-Sanyal Institute for Liver Disease and Metabolic Health, Virginia Commonwealth University School of Medicine, Richmond, Virginia, USA.
Biology Department Genfit SA, Loos, France.
Hepatol Commun. 2023 Aug 9;7(9). doi: 10.1097/HC9.0000000000000223. eCollection 2023 Sep 1.
Older patients are at increased risk for at-risk NASH, defined as NASH with NAFLD activity scores (NAS) ≥4 and significant fibrosis (F ≥ 2). The aim of this study was to compare the performance of 2 new blood tests, NIS4® and NIS2+™, with FIB-4, NFS, ELF™, and alanine aminotransferase (ALT) for the diagnosis of at-risk NASH in a cohort of patients aged ≥65 years.
The clinical performance of multiple blood-based tests was assessed for their ability to detect at-risk NASH using the RESOLVE-IT diag cohort, a large population of patients with metabolic risk who were screened for potential inclusion in the RESOLVE-IT phase 3 trial.
The study cohort (n = 2053) included patients with the full histological spectrum of NAFLD, with patients having liver fibrosis stages F0-4 and NAS scores 0-8. NIS4® and NIS2+™ showed similar assay performance in patients who were <65 versus ≥65 years of age (AUROC = 0.80 vs. 0.78, p = 0.47; 0.81 vs. 0.83 p = 0.45, respectively) for the identification of at-risk NASH. In patients ≥65 (n = 410), NIS2+™ exhibited the highest AUROC compared to NIS4®, FIB-4, NFS, ELF™, and ALT (AUROC = 0.83 vs. 0.78, 0.68, 0.58, 0.69, 0.74, respectively; all p ≤ 0.0009). For NIS2+™, the sensitivity and NPV for ruling-out at-risk NASH at the 0.46 cutoff were 90.2% and 86.0%, and the specificity and PPV for ruling-in at-risk NASH at the 0.68 cutoff were81.1% and 76.3%, respectively.
The clinical performance of NIS2+™ was superior for the diagnosis of at-risk NASH in patients ≥65 years of age. These data support the clinical value of this blood-based test for the diagnosis of at-risk NASH in older adults.
老年患者患风险 NASH 的风险增加,风险 NASH 的定义为伴有非酒精性脂肪性肝病活动评分(NAS)≥4 和显著纤维化(F≥2)的非酒精性脂肪性肝炎。本研究旨在比较两种新型血液检测 NIS4®和 NIS2+™与 FIB-4、NFS、ELF™和丙氨酸氨基转移酶(ALT)在年龄≥65 岁的患者队列中诊断风险 NASH 的性能。
使用 RESOLVE-IT diag 队列评估多种基于血液的检测的临床性能,该队列是代谢风险患者的大型人群,他们被筛选以潜在纳入 RESOLVE-IT 第 3 期试验。
研究队列(n=2053)包括具有完整非酒精性脂肪性肝病组织学谱的患者,患者的肝纤维化分期为 F0-4 和 NAS 评分为 0-8。NIS4®和 NIS2+™在年龄<65 岁和≥65 岁的患者中表现出相似的检测性能(AUROC=0.80 对 0.78,p=0.47;0.81 对 0.83,p=0.45,分别),用于识别风险 NASH。在年龄≥65 岁的患者(n=410)中,与 NIS4®、FIB-4、NFS、ELF™和 ALT 相比,NIS2+™表现出最高的 AUROC(AUROC=0.83 对 0.78、0.68、0.58、0.69、0.74,均 p≤0.0009)。对于 NIS2+™,在 0.46 截定点排除风险 NASH 的灵敏度和阴性预测值分别为 90.2%和 86.0%,在 0.68 截定点纳入风险 NASH 的特异性和阳性预测值分别为 81.1%和 76.3%。
NIS2+™在诊断年龄≥65 岁的患者的风险 NASH 方面的临床性能更优。这些数据支持该基于血液的检测在诊断老年人群中风险 NASH 的临床价值。