Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia; Centre for Liver Disease Research, University of Queensland, Brisbane, Australia.
Centre for Liver Disease Research, University of Queensland, Brisbane, Australia.
Clin Gastroenterol Hepatol. 2020 Mar;18(3):710-718.e4. doi: 10.1016/j.cgh.2019.07.036. Epub 2019 Jul 25.
BACKGROUND & AIMS: There is limited knowledge regarding the longitudinal utility of biomarkers of fibrosis, such as the nonalcoholic fatty liver disease (NAFLD) fibrosis score (NFS) or the fibrosis-4 score (FIB-4) score. We examined longitudinal changes in the NFS and the FIB-4 score in patients with NAFLD, with and without clinically significant fibrosis (CSF).
We performed a retrospective study of 230 patients with NAFLD, collecting clinical and laboratory records to calculate NFS and FIB-4 scores at 6 monthly intervals for 5 years before hepatology assessment of fibrosis. Linear mixed models with random intercept and slope and adjusted for age at baseline were used to assess the progression of NFS and log-transformed FIB-4 scores over time in subjects with and without CSF, determined by liver stiffness measurements of 8.2 kPa or greater.
Patients had a median of 11 (minimum, 10; maximum, 11) retrospective observations over a median time period of 5 years (minimum, 4.5 y; maximum, 5 y). Of patients with low baseline NFS and FIB-4 scores, 31.11% and 37.76%, respectively, had CSF at the time of hepatology assessment. There was a correlation between NFS and log FIB-4 over time (repeated measure r = 0.55; 95% CI, 0.52-0.59). The rate of increase in NFS and log FIB-4 was significantly higher in patients with than without CSF (both P < .001). Predicted NFS increased by 0.17 and 0.06 units per year in subjects with and without CSF, respectively. Predicted log FIB-4 score increased by 0.032 and 0.0003 units per year in subjects with and without CSF, respectively.
Noninvasively measured fibrosis scores increase progressively in patients with NAFLD and CSF. Further studies are needed to determine whether repeated measurements can identify patients at risk for CSF.
关于纤维化生物标志物(如非酒精性脂肪性肝病纤维化评分[NFS]或纤维化-4 评分[FIB-4])的纵向效用,我们知之甚少。本研究旨在检查非酒精性脂肪性肝病(NAFLD)患者中无临床显著纤维化(CSF)和有 CSF 的患者的 NFS 和 FIB-4 评分的纵向变化。
我们对 230 例 NAFLD 患者进行了回顾性研究,收集临床和实验室记录,以在肝纤维化评估前每 6 个月计算一次 NFS 和 FIB-4 评分,时间跨度为 5 年。采用具有随机截距和斜率的线性混合模型,并根据基线时的年龄进行调整,以评估无 CSF 和有 CSF 的患者的 NFS 和对数转化 FIB-4 评分随时间的进展,通过 8.2 kPa 或更大的肝硬度测量值确定有无 CSF。
患者中位随访时间为 5 年(最小随访时间为 4.5 年,最大随访时间为 5 年),中位数有 11 次(最小 10 次,最大 11 次)回顾性观察。在基线时 NFS 和 FIB-4 评分较低的患者中,分别有 31.11%和 37.76%在肝纤维化评估时有 CSF。NFS 和对数 FIB-4 之间存在时间相关性(重复测量 r=0.55;95%CI,0.52-0.59)。有 CSF 的患者的 NFS 和对数 FIB-4 增加率显著高于无 CSF 的患者(均 P <.001)。有 CSF 和无 CSF 的患者的预测 NFS 分别每年增加 0.17 和 0.06 单位,预测对数 FIB-4 评分分别每年增加 0.032 和 0.0003 单位。
患有 NAFLD 和 CSF 的患者的非侵入性纤维化评分逐渐增加。需要进一步的研究来确定重复测量是否可以识别有 CSF 风险的患者。