Ho Brian, Thompson Andrew, Jorgensen Andrea L, Pirmohamed Munir
Wolfson Centre for Personalised Medicine, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Department of Pharmacology and Therapeutics, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
JHEP Rep. 2023 Aug 24;5(12):100896. doi: 10.1016/j.jhepr.2023.100896. eCollection 2023 Dec.
BACKGROUND & AIMS: Population screening for non-alcoholic fatty liver disease (NAFLD) and associated comorbidities remains an unaddressed clinical need. We aimed to assess the utility of the fatty liver index (FLI) for risk stratification of NAFLD and related comorbidities using the UK Biobank.
Electronic health records and liver MRI-proton density fat fraction (PDFF) were used to define NAFLD cases. FLI was calculated and individuals with high alcohol intake and other liver diseases were excluded. Using listwise deletion analysis, the area under receiver-operating characteristic curve (AUROC) of FLI for NAFLD risk was determined. Thereafter, time-dependent covariate-adjusted Cox regression models were used to estimate FLI's risk stratification potential for comorbidities of interest.
FLI was derived for 327,800 individuals with a median age of 58 (IQR 51.5-64.5), of whom 59.8% were females. Using Perspectum Diagnostics and AMRA protocols as references, FLI identified the risk of NAFLD with AUROCs (95% CI, n) of 0.858 (0.848-0.867, n = 7,566) and 0.851 (0.844-0.856, n = 10,777), respectively. Intermediate and high-risk FLI was associated with increased cardiometabolic and malignant disease. In the first 3 years, high-risk FLI conferred an increased risk (adjusted hazard ratio, 95% CI) of ischaemic heart disease (2.14, 1.94-2.36), hypertension (2.84, 2.70-2.98), type 2 diabetes mellitus (4.55, 4.04-5.12), dyslipidaemia (2.48, 2.32-2.64), ischaemic stroke (1.31, 1.20-1.42) and hepatic malignancy (1.69, 1.23-2.30). FLI was not associated with risk of extrahepatic malignancy but was associated with a higher risk of specific cancers (colon, upper gastrointestinal and breast). All-cause mortality was similarly stratified by FLI, independently of non-invasive fibrosis scores.
FLI identifies NAFLD and holds potential for the risk stratification of cardiometabolic and malignant disease outcomes (including some extrahepatic malignancies), as well as all-cause mortality. Its use in population screening for primary and secondary prevention of NAFLD should be considered.
Our analysis using the UK Biobank study shows the potential of the fatty liver index as a risk stratification tool for identifying the risk of developing NAFLD, ischaemic heart disease, ischaemic stroke, type 2 diabetes mellitus, hypertension, hyperlipidaemia, hepatic malignancy, specific metabolism-related malignancies and all-cause mortality. These results suggest that the fatty liver index should be considered as a non-invasive steatosis score that may help guide primary prevention strategies for NAFLD and related outcomes.
对非酒精性脂肪性肝病(NAFLD)及其相关合并症进行人群筛查仍是一项未得到满足的临床需求。我们旨在利用英国生物银行评估脂肪肝指数(FLI)对NAFLD及相关合并症进行风险分层的效用。
利用电子健康记录和肝脏磁共振成像-质子密度脂肪分数(PDFF)来定义NAFLD病例。计算FLI,并排除高酒精摄入量和其他肝脏疾病患者。采用列删除分析确定FLI用于NAFLD风险的受试者工作特征曲线下面积(AUROC)。此后,使用时间依存协变量调整的Cox回归模型来估计FLI对感兴趣合并症的风险分层潜力。
为327,800名中位年龄为58岁(四分位间距51.5 - 64.5)的个体计算了FLI,其中59.8%为女性。以Perspectum诊断公司和AMRA方案为参考,FLI识别NAFLD风险的AUROC(95%CI,n)分别为0.858(0.848 - 0.867,n = 7,566)和0.851((0.844 - 0.856,n = 10,777)。FLI中、高风险与心血管代谢疾病和恶性疾病风险增加相关。在最初3年中,FLI高风险使缺血性心脏病(调整后风险比,95%CI)风险增加(2.14,1.94 - 2.36)、高血压(2.84,2.70 - 2.98)、2型糖尿病(4.55,4.04 - 5.12)、血脂异常(2.48,2.32 - 2.64)、缺血性卒中(1.31,1.20 - 1.42)和肝脏恶性肿瘤(1.69,1.23 - 2.30)风险增加。FLI与肝外恶性肿瘤风险无关,但与特定癌症(结肠癌、上消化道癌和乳腺癌)风险较高相关。全因死亡率也根据FLI进行了类似分层,与非侵入性纤维化评分无关。
FLI可识别NAFLD,并在心血管代谢和恶性疾病结局(包括一些肝外恶性肿瘤)以及全因死亡率的风险分层方面具有潜力。应考虑将其用于NAFLD一级和二级预防的人群筛查。
我们利用英国生物银行研究进行的分析表明,脂肪肝指数作为一种风险分层工具,在识别发生NAFLD、缺血性心脏病、缺血性卒中、2型糖尿病、高血压、高脂血症、肝脏恶性肿瘤、特定代谢相关恶性肿瘤和全因死亡率风险方面具有潜力。这些结果表明,脂肪肝指数应被视为一种非侵入性脂肪变性评分,可能有助于指导NAFLD及相关结局的一级预防策略。