Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
Diabetes Metab Res Rev. 2021 Nov;37(8):e3452. doi: 10.1002/dmrr.3452. Epub 2021 Apr 9.
The fibrosis-4 index (FIB-4) and NAFLD fibrosis score (NFS) are noninvasive and accessible methods for assessing advanced liver fibrosis risk in primary care. We evaluated the distribution of FIB-4 and NFS scores in primary care patients with clinical signals for nonalcoholic fatty liver disease (NAFLD).
This retrospective cohort study of electronic record data between 2007 and 2018 included adults with at least one abnormal aminotransferase and no known (non-NAFLD) liver disease. We calculated patient-level FIB-4 and NFS scores, the proportion of patients with mean values exceeding advanced fibrosis thresholds (indeterminate risk: FIB-4 > 1.3, NFS > -1.455; high-risk: FIB-4 > 2.67, NFS > 0.676), and the proportion of patients with a NAFLD International Classification of Diseases-9/10 code. Logistic regression models evaluated the associations of metabolic syndrome (MetS) components with elevated FIB-4 and NFS scores.
The cohort included 6506 patients with a median of 6 (interquartile range: 3-13) FIB-4 and NFS scores per patient. Of these patients, 81% had at least two components of MetS, 29% had mean FIB-4 and NFS scores for indeterminate fibrosis risk, and 11% had either mean FIB-4 or NFS scores exceeding the high advanced fibrosis risk thresholds. Regression models identified associations of low high-density lipoprotein, hyperglycemia, Black race and male gender with high-risk FIB-4 and NFS values. Only 5% of patients had existing diagnoses for NAFLD identified.
Many primary care patients have FIB-4 and NFS scores concerning for advanced fibrosis, but rarely a diagnosis of NAFLD. Elevated FIB-4 and NFS scores may provide signals for further clinical evaluation of liver disease in primary care settings.
纤维化 4 指数(FIB-4)和非酒精性脂肪性肝病纤维化评分(NFS)是评估初级保健中晚期肝纤维化风险的非侵入性和可及的方法。我们评估了临床信号提示非酒精性脂肪性肝病(NAFLD)的初级保健患者中 FIB-4 和 NFS 评分的分布情况。
这是一项回顾性队列研究,使用 2007 年至 2018 年的电子病历数据,纳入至少有一次异常转氨酶且无已知(非 NAFLD)肝病的成年人。我们计算了患者水平的 FIB-4 和 NFS 评分、平均数值超过晚期纤维化阈值的患者比例(不确定风险:FIB-4>1.3,NFS>-1.455;高风险:FIB-4>2.67,NFS>0.676),以及有 NAFLD 国际疾病分类第 9/10 编码的患者比例。逻辑回归模型评估了代谢综合征(MetS)成分与升高的 FIB-4 和 NFS 评分之间的关联。
该队列包括 6506 名患者,每名患者的中位数 FIB-4 和 NFS 评分分别为 6(四分位距:3-13)。这些患者中,81%至少有两种 MetS 成分,29%平均 FIB-4 和 NFS 评分处于不确定纤维化风险,11%的平均 FIB-4 或 NFS 评分超过晚期纤维化高风险阈值。回归模型确定了低高密度脂蛋白、高血糖、黑人种族和男性与高危 FIB-4 和 NFS 值的关联。只有 5%的患者有现有的 NAFLD 诊断。
许多初级保健患者的 FIB-4 和 NFS 评分提示晚期纤维化,但很少有 NAFLD 的诊断。升高的 FIB-4 和 NFS 评分可能提示在初级保健环境中进一步临床评估肝脏疾病。