Center of Health Outcomes Research and Therapeutic Safety (Cohorts), School of Pharmaceutical Sciences, University of Phayao, Phayao, Thailand.
School of Pharmacy, Monash University Malaysia, Selangor, Malaysia.
Liver Int. 2017 Oct;37(10):1535-1543. doi: 10.1111/liv.13413. Epub 2017 Apr 6.
BACKGROUND & AIMS: Non-alcoholic fatty liver disease (NAFLD) can progress from simple steatosis to hepatocellular carcinoma. None of tools have been developed specifically for high-risk patients. This study aimed to develop a simple risk scoring to predict NAFLD in patients with metabolic syndrome (MetS).
A total of 509 patients with MetS were recruited. All were diagnosed by clinicians with ultrasonography-confirmed whether they were patients with NAFLD. Patients were randomly divided into derivation (n=400) and validation (n=109) cohort. To develop the risk score, clinical risk indicators measured at the time of recruitment were built by logistic regression. Regression coefficients were transformed into item scores and added up to a total score. A risk scoring scheme was developed from clinical predictors: BMI ≥25, AST/ALT ≥1, ALT ≥40, type 2 diabetes mellitus and central obesity. The scoring scheme was applied in validation cohort to test the performance.
The scheme explained, by area under the receiver operating characteristic curve (AuROC), 76.8% of being NAFLD with good calibration (Hosmer-Lemeshow χ =4.35; P=.629). The positive likelihood ratio of NAFLD in patients with low risk (scores below 3) and high risk (scores 5 and over) were 2.32 (95% CI: 1.90-2.82) and 7.77 (95% CI: 2.47-24.47) respectively. When applied in validation cohort, the score showed good performance with AuROC 76.7%, and illustrated 84%, and 100% certainty in low- and high-risk groups respectively.
A simple and non-invasive scoring scheme of five predictors provides good prediction indices for NAFLD in MetS patients. This scheme may help clinicians in order to take further appropriate action.
非酒精性脂肪性肝病(NAFLD)可从单纯性脂肪变性进展为肝细胞癌。目前尚无专门针对高危患者的工具。本研究旨在开发一种简单的风险评分系统,以预测代谢综合征(MetS)患者的 NAFLD。
共招募了 509 名 MetS 患者。所有患者均由临床医生通过超声检查确诊是否患有 NAFLD。患者被随机分为推导队列(n=400)和验证队列(n=109)。为了开发风险评分,通过逻辑回归构建了在招募时测量的临床风险指标。回归系数转换为项目得分并加总为总得分。从临床预测因子开发风险评分方案:BMI≥25、AST/ALT≥1、ALT≥40、2 型糖尿病和中心性肥胖。在验证队列中应用评分方案以测试其性能。
该方案通过接受者操作特征曲线下面积(AuROC)解释了 76.8%的 NAFLD,具有良好的校准(Hosmer-Lemeshow χ=4.35;P=.629)。低风险(评分低于 3)和高风险(评分 5 及以上)患者患 NAFLD 的阳性似然比分别为 2.32(95%CI:1.90-2.82)和 7.77(95%CI:2.47-24.47)。当应用于验证队列时,该评分表现出良好的性能,AuROC 为 76.7%,在低风险和高风险组中分别显示出 84%和 100%的确定性。
一个由五个预测因子组成的简单且非侵入性评分方案为 MetS 患者的 NAFLD 提供了良好的预测指标。该方案可能有助于临床医生采取进一步的适当措施。