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在退伍军人健康管理局中识别非酒精性脂肪性肝病的肝纤维化程度。

Identifying Nonalcoholic Fatty Liver Disease Advanced Fibrosis in the Veterans Health Administration.

机构信息

Department of Medicine, Duke University Medical Center, Durham Veterans Administration Medical Center, Box 3913, Durham, NC, 27710, USA.

Sanford School of Public Policy, Duke University, Durham, NC, USA.

出版信息

Dig Dis Sci. 2018 Sep;63(9):2259-2266. doi: 10.1007/s10620-018-5123-3. Epub 2018 May 19.

Abstract

BACKGROUND

Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease. Severe NAFLD with advanced fibrosis results in substantial morbidity and mortality. Associated with metabolic syndrome, NAFLD is often initially clinically silent, yet intensive lifestyle intervention with 7% or greater weight loss can improve or resolve NAFLD. Using a Veterans Health Administration (VHA) liver biopsy cohort, we evaluated simple noninvasive fibrosis scoring systems to identify NAFLD with advanced fibrosis (or severe disease) to assist providers.

METHODS

In our retrospective study of a national VHA sample of patients with biopsy-proven NAFLD or normal liver (2005-2015), we segregated patients by fibrosis stage (0-4). Non-NAFLD liver disease was excluded. We evaluated the diagnostic accuracy of the NAFLD fibrosis score (NFS), fibrosis-4 calculator (FIB-4), aspartate aminotransferase-to-alanine aminotransferase ratio (AST/ALT ratio), AST-to-platelet ratio index (APRI), and body mass index, AST/ALT ratio, and diabetes (BARD) score by age groups.

RESULTS

We included 329 patients with well-defined liver histology (296 NAFLD and 33 normal controls without fibrosis), in which 92 (28%) had advanced (stage 3-4) fibrosis. Across all age groups, NFS and FIB-4 best predicted advanced fibrosis (NFS with 0.676 threshold: AUROC 0.71-0.76, LR + 2.30-22.05, OR 6.00-39.58; FIB-4 with 2.67 threshold: AUROC of 0.62-0.80, LR + 4.70-27.45, OR 16.34-59.65).

CONCLUSIONS

While NFS and FIB-4 scores exhibit good diagnostic accuracy, FIB-4 is optimal in identifying NAFLD advanced fibrosis in the VHA. Easily implemented as a point-of-care clinical test, FIB-4 can be useful in directing patients that are most likely to have advanced fibrosis to GI/hepatology consultation and follow-up.

摘要

背景

非酒精性脂肪性肝病(NAFLD)是最常见的慢性肝病病因。伴有晚期纤维化的严重 NAFLD 可导致较高的发病率和死亡率。NAFLD 常与代谢综合征相关,通常在临床上最初无明显症状,但通过 7%或更大幅度的减重进行强化生活方式干预可改善或消除 NAFLD。我们利用退伍军人健康管理局(VHA)的肝活检队列,评估了简单的非侵入性纤维化评分系统,以识别伴有晚期纤维化(或严重疾病)的 NAFLD,从而为医务人员提供帮助。

方法

在对 2005 年至 2015 年间 VHA 活检证实的 NAFLD 或正常肝脏患者进行的全国性样本回顾性研究中,我们根据纤维化分期(0-4 期)将患者分组。排除非 NAFLD 肝脏疾病。我们评估了 NAFLD 纤维化评分(NFS)、纤维化-4 计算器(FIB-4)、天门冬氨酸氨基转移酶/丙氨酸氨基转移酶比值(AST/ALT 比值)、AST 与血小板比值指数(APRI)和体重指数、AST/ALT 比值和糖尿病(BARD)评分在各年龄组的诊断准确性。

结果

我们纳入了 329 例具有明确肝脏组织学特征的患者(296 例 NAFLD 和 33 例无纤维化的正常对照),其中 92 例(28%)存在晚期(3-4 期)纤维化。在所有年龄组中,NFS 和 FIB-4 对晚期纤维化的预测效果最佳(NFS 以 0.676 为阈值时:AUROC 为 0.71-0.76,LR+为 2.30-22.05,OR 为 6.00-39.58;FIB-4 以 2.67 为阈值时:AUROC 为 0.62-0.80,LR+为 4.70-27.45,OR 为 16.34-59.65)。

结论

虽然 NFS 和 FIB-4 评分具有良好的诊断准确性,但 FIB-4 更适合在 VHA 中识别 NAFLD 晚期纤维化。FIB-4 作为一种易于实施的床边临床检测手段,可用于指导最有可能存在晚期纤维化的患者进行胃肠病学/肝脏病学咨询和随访。

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