Noninvasive assessment of liver disease severity in patients with nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes

非酒精性脂肪肝 医学 2型糖尿病 内科学 胃肠病学 疾病 脂肪肝 糖尿病 肝病 内分泌学
作者
Grazia Pennisi,Marco Enea,Vincenzo Falco,Guruprasad P. Aithal,Naaventhan Palaniyappan,Yusuf Yılmaz,Jérôme Boursier,Christophe Cassinotto,Victor de Lédinghen,Wah‐Kheong Chan,Sanjiv Mahadeva,Peter Eddowes,Philip N. Newsome,Thomas Karlas,Johannes Wiegand,Vincent Wai‐Sun Wong,Jörn M. Schattenberg,Christian Labenz,Won Kim,Myoung Seok Lee
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:78 (1): 195-211 被引量:57
标识
DOI:10.1097/hep.0000000000000351
摘要

BACKGROUND AND AIMS: We evaluated the diagnostic accuracy of simple, noninvasive tests (NITs) in NAFLD patients with type 2 diabetes (T2D). METHODS AND RESULTS: This was an individual patient data meta-analysis of 1780 patients with biopsy-proven NAFLD and T2D. The index tests of interest were FIB-4, NAFLD Fibrosis Score (NFS), aspartate aminotransferase-to-platelet ratio index, liver stiffness measurement (LSM) by vibration-controlled transient elastography, and AGILE 3+. The target conditions were advanced fibrosis, NASH, and fibrotic NASH(NASH plus F2-F4 fibrosis). The diagnostic performance of noninvasive tests. individually or in sequential combination, was assessed by area under the receiver operating characteristic curve and by decision curve analysis. Comparison with 2278 NAFLD patients without T2D was also made. In NAFLD with T2D LSM and AGILE 3+ outperformed, both NFS and FIB-4 for advanced fibrosis (area under the receiver operating characteristic curve:LSM 0.82, AGILE 3+ 0.82, NFS 0.72, FIB-4 0.75, aspartate aminotransferase-to-platelet ratio index 0.68; p < 0.001 of LSM-based versus simple serum tests), with an uncertainty area of 12%-20%. The combination of serum-based with LSM-based tests for advanced fibrosis led to a reduction of 40%-60% in necessary LSM tests. Decision curve analysis showed that all scores had a modest net benefit for ruling out advanced fibrosis at the risk threshold of 5%-10% of missing advanced fibrosis. LSM and AGILE 3+ outperformed both NFS and FIB-4 for fibrotic NASH (area under the receiver operating characteristic curve:LSM 0.79, AGILE 3+ 0.77, NFS 0.71, FIB-4 0.71; p < 0.001 of LSM-based versus simple serum tests). All noninvasive scores were suboptimal for diagnosing NASH. CONCLUSIONS: LSM and AGILE 3+ individually or in low availability settings in sequential combination after FIB-4 or NFS have a similar good diagnostic accuracy for advanced fibrosis and an acceptable diagnostic accuracy for fibrotic NASH in NAFLD patients with T2D.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
文静土豆完成签到 ,获得积分10
刚刚
2秒前
maclogos发布了新的文献求助10
2秒前
wsh完成签到 ,获得积分10
2秒前
夏至完成签到 ,获得积分10
4秒前
cobo完成签到,获得积分10
5秒前
ChenGY完成签到,获得积分10
5秒前
水蒸气完成签到,获得积分10
6秒前
七QI完成签到 ,获得积分10
6秒前
传奇3应助hhh采纳,获得10
6秒前
受不了12345完成签到,获得积分10
6秒前
7秒前
111完成签到 ,获得积分10
7秒前
研友_Z7myEL发布了新的文献求助10
7秒前
8秒前
9秒前
13秒前
JamesPei应助研友_Z7myEL采纳,获得10
13秒前
biozy完成签到,获得积分10
13秒前
我避他锋芒完成签到,获得积分10
13秒前
wwqc完成签到,获得积分0
15秒前
闫佳美发布了新的文献求助10
15秒前
畅快的静芙完成签到,获得积分10
16秒前
搞怪元彤完成签到,获得积分10
16秒前
关畅澎完成签到 ,获得积分10
22秒前
Kao应助科研通管家采纳,获得10
22秒前
cdercder应助科研通管家采纳,获得10
22秒前
cdercder应助科研通管家采纳,获得10
22秒前
22秒前
cdercder应助科研通管家采纳,获得10
22秒前
Kao应助科研通管家采纳,获得10
22秒前
甜甜醉波完成签到,获得积分10
22秒前
cdercder应助科研通管家采纳,获得10
23秒前
小水蜜桃完成签到 ,获得积分10
24秒前
贤惠的咖啡完成签到,获得积分10
25秒前
小幼芷完成签到,获得积分10
26秒前
Lion完成签到,获得积分10
28秒前
干饭啦完成签到,获得积分10
29秒前
耍酷的书本完成签到 ,获得积分10
30秒前
fa完成签到,获得积分10
31秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les chinois de jakarta: temples et vie collective 1000
Autoparametric Resonance in Mechanical Systems 1000
基于锂离子电池正极材料回收的绿色溶剂开发及工程化应用研究 800
Social Psychology 600
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 600
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7646173
求助须知:如何正确求助?哪些是违规求助? 9218446
关于积分的说明 19778239
捐赠科研通 7210540
什么是DOI,文献DOI怎么找? 3276969
关于科研通互助平台的介绍 2438624
邀请新用户注册赠送积分活动 2275032