Serial Liver Stiffness Measurement and Fibrosis-4 Scores in Metabolic Dysfunction-Associated Steatotic Liver Disease

被引:0
作者
Goyal, Tanvi [1 ]
Song, Michael W. [2 ]
Suresh, Deepika [2 ]
Jasty, Venkata S. J. [2 ]
Urias, Esteban [2 ]
Wijarnpreecha, Karn [3 ,4 ]
Wong, Yu Jun [5 ,6 ]
Chen, Vincent L. [7 ]
机构
[1] Univ Penn, Div Hosp Med, Dept Med, Philadelphia, PA USA
[2] Univ Michigan, Dept Internal Med, Ann Arbor, MI USA
[3] Banner Univ, Med Ctr, Dept Internal Med, Div Gastroenterol & Hepatol, Phoenix, AZ USA
[4] Univ Arizona, Coll Med Phoenix, Dept Med, Div Gastroenterol & Hepatol, Phoenix, AZ USA
[5] Changi Gen Hosp, Dept Gastroenterol & Hepatol, Singapore, Singapore
[6] SingHealth, Duke NUS Acad Clin Program, Singapore, Singapore
[7] Univ Michigan, Dept Internal Med, Div Gastroenterol & Hepatol, 1500 East Med Ctr Dr, Ann Arbor, MI 48109 USA
关键词
Fibroscan; VCTE; Non-invasive test; Dynamics; NAFLD; STEATOHEPATITIS; MANAGEMENT; MORTALITY; STAGE; FIB-4; RISK;
D O I
10.1007/s10620-024-08683-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundIn patients with metabolic dysfunction-associated steatotic liver disease (MASLD), there are limited data on how changes in FIB4 and liver stiffness measurement (LSM) correlate in non-biopsy cohorts. AimsOur objective was to evaluate associations between changes in FIB4 and LSM in MASLD patients. MethodsWe included MASLD patients with serial VCTE from 2015-2022. The primary predictors were change in FIB4 and presence of diabetes, obesity, and high alanine aminotransferase (ALT). The primary outcome, applied only to patients with LSM1 < 8 kPa, was incident significant fibrosis (SF) defined as a >= 20% increase in LSM2 vs. LSM1 and LSM2 >= 8 kPa. A secondary outcome was LSM progression with a similar definition but applied to all participants, not only those with LSM1 < 8 kPa. ResultsOf 285 included patients, 216 had LSM1 < 8 kPa and were included in the primary analysis; of these, 34 (16%) had incident SF. Changes in FIB4 correlated with changes in LSM (R = 0.16, p = 0.016). Independent predictors of incident SF included comorbid diabetes mellitus (OR 2.43, 95% CI 1.04-6.56), obesity (OR 3.88, 95% CI 1.63-9.25), and baseline ALT >= 30 (OR 8.55, 95% CI 1.10-66.29). A model including ALT, diabetes, and obesity outperformed a model with FIB4 change alone. ConclusionAmong patients with MASLD, changes in FIB4 correlated with changes in LSM but more significant correlates of incident significant fibrosis included diabetes mellitus, obesity, and high baseline ALT.
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收藏
页码:4250 / 4258
页数:9
相关论文
共 37 条
[1]   Patient Determinants for Histologic Diagnosis of NAFLD in the Real World: A TARGET-NASH Study [J].
Barritt, A. Sidney ;
Watkins, Stephanie ;
Gitlin, Norman ;
Klein, Samuel ;
Lok, Anna S. ;
Loomba, Rohit ;
Schoen, Cheryl ;
Reddy, K. Rajender ;
Trinh, Huy Ngoc ;
Mospan, Andrea R. ;
Vos, Miriam B. ;
Weiss, L. Michael ;
Cusi, Kenneth ;
Neuschwander-Tetri, Brent A. ;
Sanyal, Arun J. .
HEPATOLOGY COMMUNICATIONS, 2021, 5 (06) :938-946
[2]   Liver stiffness (Fibroscan®) is a predictor of all-cause mortality in people with non-alcoholic fatty liver disease [J].
Braude, Michael ;
Roberts, Stuart ;
Majeed, Ammar ;
Lubel, John ;
Prompen, Jirayut ;
Dev, Anouk ;
Sievert, William ;
Bloom, Stephen ;
Gow, Paul ;
Kemp, William .
LIVER INTERNATIONAL, 2023, 43 (01) :90-99
[3]   Patterns and predictors of mortality and disease progression among patients with non-alcoholic fatty liver disease [J].
Canbay, Ali ;
Kachru, Nandita ;
Haas, Jennifer Scarlet ;
Sowa, Jan-Peter ;
Meise, Dominic ;
Ozbay, Ahmet Burak .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2020, 52 (07) :1185-1194
[4]   Relationship between three commonly used non-invasive fibrosis biomarkers and improvement in fibrosis stage in patients with non-alcoholic steatohepatitis [J].
Chalasani, Naga ;
Abdelmalek, Manal F. ;
Loomba, Rohit ;
Kowdley, Kris, V ;
McCullough, Arthur J. ;
Dasarathy, Srinivasan ;
Neuschwander-Tetri, Brent A. ;
Terrault, Norah ;
Ferguson, Beatrice ;
Shringarpure, Reshma ;
Shapiro, David ;
Sanyal, Arun J. .
LIVER INTERNATIONAL, 2019, 39 (05) :924-932
[5]   PNPLA3 eGenotype and Diabetes Identify Patients With Nonalcoholic Fatty Liver Disease at High Risk of Incident Cirrhosis [J].
Chen, Vincent L. ;
Oliveri, Antonino ;
Miller, Matthew J. ;
Wijarnpreecha, Karn ;
Du, Xiaomeng ;
Chen, Yanhua ;
Cushing, Kelly C. ;
Lok, Anna S. ;
Speliotes, Elizabeth K. .
GASTROENTEROLOGY, 2023, 164 (06) :966-+
[6]   Risk factors for histological progression of non-alcoholic steatohepatitis analyzed from repeated biopsy cases [J].
Daijo, Kana ;
Nakahara, Takashi ;
Inagaki, Yuki ;
Nanba, Maiko ;
Nishida, Yuno ;
Uchikawa, Shinsuke ;
Kodama, Kenichiro ;
Oya, Kazuki ;
Morio, Kei ;
Fujino, Hatsue ;
Ono, Atsushi ;
Murakami, Eisuke ;
Yamauchi, Masami ;
Kawaoka, Tomokazu ;
Miki, Daiki ;
Tsuge, Masataka ;
Hiramatsu, Akira ;
Hayes, C. Nelson ;
Imamura, Michio ;
Aikata, Hiroshi ;
Ochi, Hidenori ;
Chayama, Kazuaki .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2020, 35 (08) :1412-1419
[7]   Baveno VII - Renewing consensus in portal hypertension [J].
de Franchis, Roberto ;
Bosch, Jaime ;
Garcia-Tsao, Guadalupe ;
Reiberger, Thomas ;
Ripoll, Cristina .
JOURNAL OF HEPATOLOGY, 2022, 76 (04) :959-974
[8]   Fibrosis Stage Is the Strongest Predictor for Disease-Specific Mortality in NAFLD After Up to 33 Years of Follow-Up [J].
Ekstedt, Mattias ;
Hagstrom, Hannes ;
Nasr, Patrik ;
Fredrikson, Mats ;
Stal, Per ;
Kechagias, Stergios ;
Hultcrantz, Rolf .
HEPATOLOGY, 2015, 61 (05) :1547-1554
[9]  
European Association for the Study of the Liver
[10]  
European Association for the Study of Diabetes, 2024, J HEPATOL