Combination of Fibrosis-4, liver-stiffness measurement, and Fibroscan-AST score to predict liver-related outcomes in nonalcoholic fatty liver disease.


Journal

Hepatology communications
ISSN: 2471-254X
Titre abrégé: Hepatol Commun
Pays: United States
ID NLM: 101695860

Informations de publication

Date de publication:
01 10 2023
Historique:
received: 09 04 2023
accepted: 09 07 2023
medline: 25 9 2023
pubmed: 22 9 2023
entrez: 22 9 2023
Statut: epublish

Résumé

Noninvasive tests, such as Fibrosis-4 (FIB-4), liver-stiffness measurement (LSM) by vibration-controlled transient elastography, and Fibroscan-AST (FAST), are frequently used for risk stratification in NAFLD. The comparative performance of FIB-4 and LSM and FAST to predict clinical outcomes of patients with NAFLD remained unclear. We aim to evaluate the performance of FIB-4, LSM, and FAST scores to predict clinical outcomes in patients with NAFLD. We included consecutive adult patients with NAFLD with transient elastography performed between 2015 and 2022 from the United States and Singapore. Patients with NAFLD stratified based on baseline FIB-4, LSM, and FAST score were followed up until clinical outcomes notably liver-related events (LREs), LREs or death, death, and major adverse cardiac events. A total of 1262 patients with NAFLD (63% with obesity and 37% with diabetes) with vibration-controlled transient elastography were followed up for median 3.5 years. FIB-4 stratified patients with NAFLD into low-risk (<1.3), intermediate-risk (1.3-2.67), and high-risk (>2.67) in 59.4%, 31.5%, and 9.1%, respectively. No LRE occurred with baseline FIB-4 <1.3, regardless of LSM and FAST score. Higher FIB-4 was associated with a higher risk of LREs within each LSM category. FIB-4 had a higher area under the received operating characteristic curve than LSM or FAST score to predict LRE. In this multicenter international study, FIB-4 and LSM synergistically predicted the risk of LRE. In patients with FIB-4 <1.3, vibration-controlled transient elastography may incorrectly classify up to 10% of the patients as high risk. FIB-4 should be incorporated into risk stratification in NAFLD even among patients who underwent VCTE.

Identifiants

pubmed: 37738409
doi: 10.1097/HC9.0000000000000244
pii: 02009842-202310010-00021
pmc: PMC10519529
pii:
doi:

Types de publication

Multicenter Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : K08 DK132312
Pays : United States

Informations de copyright

Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases.

Références

Clin Gastroenterol Hepatol. 2022 Dec;20(12):2809-2817.e28
pubmed: 34890795
J Am Heart Assoc. 2019 Jun 18;8(12):e010541
pubmed: 31185781
Clin Mol Hepatol. 2023 Jan;29(1):135-145
pubmed: 36064306
Clin Gastroenterol Hepatol. 2022 Nov;20(11):2567-2576.e6
pubmed: 34971806
J Hepatol. 2021 Sep;75(3):659-689
pubmed: 34166721
Ann Acad Med Singap. 2022 Nov;51(11):686-694
pubmed: 36453216
Am J Gastroenterol. 2022 Mar 1;117(3):453-461
pubmed: 35041626
Clin Gastroenterol Hepatol. 2016 Feb;14(2):301-8.e1-2
pubmed: 26291667
Hepatology. 2023 May 1;77(5):1797-1835
pubmed: 36727674
Clin Gastroenterol Hepatol. 2023 May;21(5):1293-1302.e5
pubmed: 35842119
Hepatology. 2015 May;61(5):1547-54
pubmed: 25125077
Am J Gastroenterol. 2019 Jun;114(6):916-928
pubmed: 31169533
Aliment Pharmacol Ther. 2021 Aug;54(4):470-480
pubmed: 34152626
J Hepatol. 2022 Apr;76(4):959-974
pubmed: 35120736
BMC Med Res Methodol. 2017 Apr 7;17(1):53
pubmed: 28388943
PLoS One. 2022 Apr 15;17(4):e0266859
pubmed: 35427375
N Engl J Med. 2021 Oct 21;385(17):1559-1569
pubmed: 34670043
Clin Gastroenterol Hepatol. 2021 Mar;19(3):580-589.e5
pubmed: 32531342
J Hepatol. 2021 Oct;75(4):786-794
pubmed: 34090928
Lancet Gastroenterol Hepatol. 2020 Apr;5(4):362-373
pubmed: 32027858
Biometrics. 1988 Sep;44(3):837-45
pubmed: 3203132
Gut. 2022 May;71(5):1006-1019
pubmed: 34001645
Hepatology. 2006 Jun;43(6):1317-25
pubmed: 16729309
Hepatology. 2011 Sep 2;54(3):1082-1090
pubmed: 21618575

Auteurs

Yu Jun Wong (YJ)

Department of Gastroenterology & Hepatology, Changi General Hospital, Singapore.
Duke-NUS Academic Clinical Program, SingHealth, Singapore.
Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Esteban Urias (E)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA.

Michael W Song (MW)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA.

Tanvi Goyal (T)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA.

Wei Xuan Tay (WX)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Nicole Xinrong Han (NX)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Jing Hong Loo (JH)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Tian Yu Qiu (TY)

Department of Gastroenterology & Hepatology, Changi General Hospital, Singapore.

Karn Wijarnpreecha (K)

Department of Medicine, Division of Gastroenterology and Hepatology, University of Arizona College of Medicine, Phoenix, Arizona, USA.

Yiong Huak Chan (YH)

Biostatistics Unit, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Vincent L Chen (VL)

Division of Gastroenterology and Hepatology, University of Michigan, Ann Arbor, Michigan, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH