Noninvasive assessment of liver fibrosis in NAFLD
Open accessAbstract
Nonalcoholic fatty liver disease (NAFLD) has emerged as a leading cause of liver-related morbidity and mortality worldwide, afflicting approximately a billion individuals. NAFLD is a slowly progressive disease that may evolve in a subset of patients toward cirrhosis, hepatocellular carcinoma, and end-stage liver disease. Liver fibrosis severity is the strongest predictor of clinical outcomes. The emergence of effective therapeutics on the horizon highlights the need to identify among patients with NAFLD, those with severe fibrosis or cirrhosis, who are the most at risk of developing complications and target them for therapy. Liver biopsy has been the reference standard for this purpose. However, it is not suitable for large-scale population evaluation, given its well-known limitations (invasiveness, rare but severe complications, and sampling variability). Thus, there have been major efforts to develop simple noninvasive tools that can be used in routine clinical settings and in drug development. Noninvasive approaches are based on the quantification of biomarkers in serum samples or on the measurement of liver stiffness, using either ultrasound- or magnetic resonance-based elastography techniques. This review provides a roadmap for future development and integration of noninvasive tools in clinical practice and in drug development in NAFLD. We discuss herein the principles for their development and validation, their use in clinical practice, including for diagnosis of NAFLD, risk stratification in primary care and hepatology settings, prediction of long-term liver-related and non-liver-related outcomes, monitoring of fibrosis progression and regression, and response to future treatment.
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To date, these surrogates have not been unambiguously linked to true clinical benefits (e.g. liver-related mortality).
“However, to date, these surrogates have not been unambiguously linked to true clinical bene fi ts ( e.g. liver-related mortality). 257”
From EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). (2024) · cites this paper as [257]
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Emerson, S. C., Waikar, S. S., Fuentes, C., Bonventre, J. V., & Betensky, R. A. (2017) · Statistical Methods in Medical Research · doi:10.1177/0962280216689806 · Cited by 12 · see citing works
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Tacke, F., Horn, P., Wai-Sun Wong, V., Ratziu, V., Bugianesi, E., Francque, S., Zelber-Sagi, S., Valenti, L., Roden, M., Schick, F., et al. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2024.04.031 · Cited by 2,210 · see citing works
Epidemiology of metabolic dysfunction-associated steatotic liver disease
Younossi, Z. M., Kalligeros, M., & Henry, L. (2025) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2024.0431 · Cited by 960 · see citing works
(2024) · Obesity Facts · doi:10.1159/000539371 · Cited by 510 · see citing works
Cusi, K. J., Abdelmalek, M. F., Apovian, C. M., Balapattabi, K., Bannuru, R. R., Barb, D., Bardsley, J. K., Beverly, E. A., Corbin, K. D., ElSayed, N. A., et al. (2025) · Diabetes Care · doi:10.2337/dci24-0094 · Cited by 396 · see citing works
Lin, H., Lee, H. W., Yip, T. C.-F., Tsochatzis, E., Petta, S., Bugianesi, E., Yoneda, M., Zheng, M.-H., Hagström, H., Boursier, J., et al. (2024) · JAMA · doi:10.1001/jama.2024.1447 · Cited by 250 · see citing works
Self-citationFibrosis: cross-organ biology and pathways to development of innovative drugs
Rieder, F., Nagy, L. E., Maher, T. M., Distler, J. H. W., Kramann, R., Hinz, B., & Prunotto, M. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01158-9 · Cited by 117 · see citing works
“However, in clinical practice, non-invasive measures of fibrosis are important 326,327 .”
Yip, T. C., Lee, H. W., Lin, H., Tsochatzis, E. A., Petta, S., Bugianesi, E., Yoneda, M., Zheng, M., Hagström, H., Boursier, J., et al. (2025) · Journal of Hepatology · doi:10.1016/j.jhep.2025.01.014 · Cited by 63 · see citing works
Díaz, L. A., Arab, J. P., Idalsoaga, F. J., Perelli, J., Vega, J. A., Dirchwolf, M., Carreño, J., Samith, B., Valério, C. M., Moreira, R. O., et al. (2025) · Annals of Hepatology · doi:10.1016/j.aohep.2025.101903 · Cited by 66 · see citing works
Crudele, L., Matteis, C. D., Novielli, F., Buduo, E. D., Petruzzelli, S., Giorgi, A. D., Antonica, G., Berardi, E., & Moschetta, A. (2024) · Biology of Sex Differences · doi:10.1186/s13293-024-00617-z · Cited by 62 · see citing works
“On the other hand, liver biopsy may not be considered for screening or follow-up, considering its invasiveness, rare but severe complications, sampling variability, and the need for short-term repeated evaluation in MASLD patients [11, 12].”
BackgroundCastéra, L., Garteiser, P., Laouenan, C., Vidal-Trécan, T., Vallet‐Pichard, A., Manchon, P., Paradis, V., Czernichow, S., Roulot, D. M., Larger, É., et al. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2024.03.023 · Cited by 54 · see citing works
Targeting collagen homeostasis for the treatment of liver fibrosis: Opportunities and challenges
Luangmonkong, T., Parichatikanond, W., & Olinga, P. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115740 · Cited by 53 · see citing works
Liu, W., Huang, S., Ji, H., Kim, S. U., Yip, T. C., Wong, G. L., Petta, S., Tsochatzis, E. A., Nakajima, A., Bugianesi, E., et al. (2025) · Gastroenterology · doi:10.1053/j.gastro.2025.02.034 · Cited by 38 · see citing works
The Janus of a disease: Diabetes and metabolic dysfunction-associated fatty liver disease
Francisco Barrera, M., Uribe, J., Olvares, N., Huerta, P., Cabrera, D., & Romero‐Gómez, M. (2024) · Annals of Hepatology · doi:10.1016/j.aohep.2024.101501 · Cited by 36 · see citing works
Biciusca, T., Stan, S. I., Bălteanu, M. A., Cioboată, R., Ghenea, A. E., Dănoiu, S., Bumbea, A. M., & Biciuşcă, V. (2023) · Diagnostics · doi:10.3390/diagnostics13213316 · Cited by 36 · see citing works
“Currently, the most effective screening methods for NAFLD and fibrosis (FLI, HSI, Steatotest, FIB-4) are those based on serum biomarkers, as well as imaging methods such as transient elastography and MRI, although their cost is quite high [33].”
BackgroundHepatic Fibrosis and Cancer: The Silent Threats of Metabolic Syndrome
Friedman, S. L. (2024) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2023.0240 · Cited by 37 · see citing works
“Screening approaches vary based on the country and technologies available to clinicians, but typically include use of a non-invasive score (e.g., fibrosis-4 [FIB-4] or enhanced liver fibrosis [ELF]) combined with liver stiffness (Fibroscan, Echo-sens, Paris, France) [22,23].”
BackgroundStefanakis, K., Mingrone, G., George, J., & Mantzoros, C. S. (2024) · Metabolism · doi:10.1016/j.metabol.2024.156082 · Cited by 36 · see citing works
Wang, Y., Song, S. J., Jiang, Y., Lai, J. C., Wong, G. L., Wong, V. W., & Yip, T. C. (2024) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2024.0246 · Cited by 32 · see citing works
Galectin-3 and Severity of Liver Fibrosis in Metabolic Dysfunction-Associated Fatty Liver Disease
Sotoudeheian, M. (2024) · Protein and Peptide Letters · doi:10.2174/0109298665301698240404061300 · Cited by 32 · see citing works
Mechanism-guided drug development and treatment for liver fibrosis: a clinical perspective
Zeng, X., Huang, D., Zhu, Z., Cai, Q., Yang, Y., Lu, H., & Chen, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1574385 · Cited by 32 · see citing works
Lai, J. C., Yang, B., Lee, H. W., Lin, H., Tsochatzis, E. A., Petta, S., Bugianesi, E., Yoneda, M., Zheng, M., Hagström, H., et al. (2025) · Gut · doi:10.1136/gutjnl-2025-334981 · Cited by 32 · see citing works
Minetti, E. T., Hamburg, N. M., & Matsui, R. (2024) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2024.1469492 · Cited by 30 · see citing works
NAFLD in the 21st Century: Current Knowledge Regarding Its Pathogenesis, Diagnosis and Therapeutics
Kounatidis, D., Vallianou, N., Geladari, E., Panoilia, M.-P., Daskou, A., Stratigou, T., Karampela, I., Tsilingiris, D., & Dalamaga, M. (2024) · Biomedicines · doi:10.3390/biomedicines12040826 · Cited by 32 · see citing works
“The NIS4 has been demonstrated to perform well for the identification of patients with “at-risk NASH” [50,53].”
BackgroundMethodInfluentialLiver fibrosis as a barometer of systemic health by gauging the risk of extrahepatic disease
Lonardo, A., Ballestri, S., Baffy, G., & Weiskirchen, R. (2024) · Metabolism and Target Organ Damage · doi:10.20517/mtod.2024.42 · Cited by 29 · see citing works
Misra, A., Kumar, A., Kuchay, M. S., Ghosh, A., Gulati, S., Choudhary, N. S., Dutta, D., Sharma, P., Vikram, N. K., Rastogi, A., et al. (2025) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2025.103209 · Cited by 27 · see citing works
Diagnosis and non‐invasive assessment of MASLD in type 2 diabetes and obesity
Chan, W., Petta, S., Noureddin, M., Goh, G. B., & Wong, V. W. (2024) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.17866 · Cited by 25 · see citing works
“74 In addition, features of two-dimensional shear wave elastography may reflect lobular inflammation and other properties of MASH.”
BackgroundMAFLD in adults: non-invasive tests for diagnosis and monitoring of MAFLD
Chan, W., Wong, V. W., Adams, L. A., & Nguyen, M. H. (2024) · Hepatology International · doi:10.1007/s12072-024-10661-x · Cited by 24 · see citing works
“In particular, its negative predictive value in excluding advanced fibrosis is high at over 90%, especially in low-prevalence settings such as primary care [24].”
Wan, Q., Liu, X., Xu, J., Zhao, R., Yang, S., Feng, J., Cao, Z., Li, J., He, X., Chen, H., et al. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13605 · Cited by 20 · see citing works
Țâru, M.-G., Tefas, C., Neamți, L., Minciună, I., Țâru, V., Maniu, A., Rusu, I., Petrushev, B., Procopciuc, L. M., Leucuta, D., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0303971 · Cited by 20 · see citing works
Advances in Noninvasive Biomarkers for Nonalcoholic Fatty Liver Disease
Gîlcă-Blanariu, G.-E., Budur, D. S., Mitrică, D., Gologan, E., Timofte, O., Bălan, G. G., OLTEANU, V.-A., & Ștefănescu, G. (2023) · Metabolites · doi:10.3390/metabo13111115 · Cited by 21 · see citing works
“The risk of developing a hepatocellular carcinoma from NAFLD can be assessed using the Polygenic Risk Score-5, which combines PNPLA3, TM6SF2, GCKR, and MBOAT7 [184].”
BackgroundVidal-Trécan, T., Julla, J., Khoury, T. E., Venteclef, N., Riveline, J., Paradis, V., Valla, D. C., Gautier, J., & Castéra, L. (2025) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2025.02.018 · Cited by 20 · see citing works
Addissouky, T. A. (2024) · Discover Medicine · doi:10.1007/s44337-024-00083-x · Cited by 16 · see citing works
Wong, V. W., Neff, G. W., Bisceglie, A. M. D., Bai, R., Cheng, J., Meng, Y., Liberman, A., Liu, L., & Gunn, N. (2025) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2025.0145 · Cited by 15 · see citing works
Suárez, M., Martínez, R., Torres, A., Ramón, A., Blasco, P., & Mateo, J. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12206489 · Cited by 15 · see citing works
Noninvasive assessment of liver fibrosis and portal hypertension
Duarte‐Rojo, A., Patel, K., & Rockey, D. C. (2024) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000001019 · Cited by 16 · see citing works
The biochemical pattern defines MASLD phenotypes linked to distinct histology and prognosis
Ampuero, J., Aller, R., Gallego‐Durán, R., Crespo, J., Calleja, J. L., García‐Monzón, C., Gómez‐Camarero, J., Caballería, J., Iacono, O. L., Ibáñez, L., et al. (2024) · Journal of Gastroenterology · doi:10.1007/s00535-024-02098-8 · Cited by 17 · see citing works
A Pragmatic Management Approach for Metabolic Dysfunction-Associated Steatosis and Steatohepatitis
Shah, N., & Sanyal, A. J. (2024) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000003215 · Cited by 15 · see citing works
Țâru, M.-G., & Lupșor‐Platon, M. (2023) · Cancers · doi:10.3390/cancers15164097 · Cited by 13 · see citing works
Lin, R., Zhou, J., Sun, Q., Xin, X., Hu, Y., Zheng, M., & Feng, Q. (2024) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.17889 · Cited by 12 · see citing works
Feng, Q., Izzi‐Engbeaya, C. N., Manousou, P., & Woodward, M. (2025) · BMC Gastroenterology · doi:10.1186/s12876-025-04079-4 · Cited by 12 · see citing works
“Consequently, various non-invasive assessments have been developed and adopted in international guidelines for MASLD management [7, 8].”
Guzmán, C., Bautista-Ubaldo, M. G., Campos-Espinosa, A., Romero-Bello, I. I., Vargas, Á. D. S., & Gutiérrez‐Reyes, G. (2024) · Medicina · doi:10.3390/medicina60030429 · Cited by 12 · see citing works
“Non-alcoholic fatty liver disease (NAFLD) is the most prevalent hepatic disease world-wide, and it is highly associated with metabolic disorders, including obesity, insulin resistance, diabetes, and metabolic syndrome [1–3].”
GLP-1RAs regulate lipid metabolism and induce autophagy through AMPK/SIRT1 pathway to improve NAFLD
Zhang, Q., Wang, J., Hu, X., Lu, W., Cao, Y., Niu, C.-Y., & Yue, H. (2025) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2025.106987 · Cited by 11 · see citing works
The importance of patient engagement in the multimodal treatment of MASLD
Boeckmans, J., Hagström, H., Cryer, D. R. H., & Schattenberg, J. M. (2025) · Communications Medicine · doi:10.1038/s43856-025-00871-1 · Cited by 14 · see citing works
Song, S. J., Nogami, A., Liang, L. Y., Yoneda, M., Leung, H. H. W., Nakajima, A., Lai, J. C., Wong, G. L., Shu, S. S., Wong, V. W., et al. (2024) · Liver International · doi:10.1111/liv.15862 · Cited by 11 · see citing works
Jin, X., Yip, T. C., Wong, G. L., Wong, V. W., & Lai, J. C. (2025) · ULTRASONOGRAPHY · doi:10.14366/usg.24219 · Cited by 10 · see citing works
From NAFLD to MASLD: transforming steatotic liver disease diagnosis and management
Iruzubieta, P., Jiménez-González, C., Cabezas, J., & Crespo, J. (2025) · Metabolism and Target Organ Damage · doi:10.20517/mtod.2024.143 · Cited by 9 · see citing works
Research and application of medicines for treating liver fibrosis: current status and prospects
Chen, S., Wu, Z., Zhang, J., Lin, Y., Xie, J., Yin, D., & Zhu, Y. H. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1582258 · Cited by 10 · see citing works
Non-invasive tests for MetALD and alcohol-related liver disease
Johansen, S., Thiele, M. S., & Krag, A. A. (2025) · JHEP Reports · doi:10.1016/j.jhepr.2025.101569 · Cited by 10 · see citing works
“20,21 In this review, we examine current knowledge on the use of NITs for the diagnosis and prognostication of ALD and Met-ALD, as well as emerging data on tools for monitoring disease progression.”
The transition from NAFLD to MASLD: implications for Diagnosis, Prognosis, and Clinical Management
Acierno, C., Nevola, R., Barletta, F., Zielińska, K., Rinaldi, L., Sasso, F. C., Conte, C., Adinolfi, L. E., & Caturano, A. (2025) · Exploration of Medicine · doi:10.37349/emed.2025.1001365 · Cited by 11 · see citing works
Zhao, Y., Hu, D., Cheng, J., Cao, H., Wang, X., He, J., Zhu, Y., & Li, J. (2025) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-025-02069-w · Cited by 9 · see citing works
Yang, C., Chen, S., Feng, B., Lu, Y., Wang, Y., Liao, W., Wu, S., & Wang, L. (2024) · Maturitas · doi:10.1016/j.maturitas.2024.108148 · Cited by 8 · see citing works
Hashim, M. M. A., Khan, M. A. M., Ashraf, M. U., Mohsin, S., Zahoor, K., Niazi, J., Khan, A., Muzaffar, S., Makhdumi, M., Ibad, O. A., et al. (2025) · Cureus · doi:10.7759/cureus.86963 · Cited by 8 · see citing works
Zhou, G., Han, W., Luan, J., & Ma, B. (2025) · BMC Gastroenterology · doi:10.1186/s12876-025-04117-1 · Cited by 8 · see citing works
“…paradigms confront dual limitations: reliance on imperfect diagnostic modalities (ultrasound, MRI, or biopsy) with inherent sensitivity constraints [8, 9], therapeutic options are currently limited to lifestyle interventions, as no approved disease-modifying pharmacologic agents exist [10, 11].”
Noureddin, M., Wei, L., Castéra, L., & Tsochatzis, E. A. (2023) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2023.09.034 · Cited by 8 · see citing works
“One of the most intriguing developments arising from this renaming process is the recognition of the impact of moderate alcohol consumption on the natural history and response to therapies in NAFLD/MASLD.”
Rigor, J., MARTINS, M. E., Passos, B., Oliveira, R., & Martins‐Mendes, D. (2024) · Minerva Medica · doi:10.23736/s0026-4806.24.09290-5 · Cited by 7 · see citing works
Ogawa, Y., Tomeno, W., Imamura, Y., Baba, M., Ueno, T., Kobayashi, T., Iwaki, M., Nogami, A., Kessoku, T., Honda, Y., et al. (2024) · Hepatology Research · doi:10.1111/hepr.14117 · Cited by 7 · see citing works
Jiang, H., Yu, H., Hu, C., Huang, Y., Yang, B., Xi, X., Lei, Y., Wu, B., & Yang, Y. (2025) · Annals of Hepatology · doi:10.1016/j.aohep.2025.101788 · Cited by 7 · see citing works
Arvaniti, P. (2023) · Annals of Gastroenterology · doi:10.20524/aog.2023.0841 · Cited by 7 · see citing works
“Accordingly, MASLD fibrosis score (MFS), a simple and easily accessible online score, has been proved useful for the determination of advanced disease in MASLD patients, who are at high risk for presenting advanced fibrosis and/or cirrhosis [14,15].”
Using NIS2+™ to identify at-risk MASH in clinical trials
Lai, J. C., & Wong, V. W. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.11.009 · Cited by 7 · see citing works
Fang, X., Yin, Y., Zhao, H., Wang, C., Li, H., Shang, Y., Li, J., Gao, Y., Méndez‐Sánchez, N., & Qi, X. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1481051 · Cited by 6 · see citing works
Ye, D., Ji, X., Ma, Y.-M., Shi, J., Wang, J.-F., Chen, J., Hu, X.-N., & Bao, Z.-J. (2025) · Population Health Metrics · doi:10.1186/s12963-025-00378-w · Cited by 6 · see citing works
“Traditional methods for diagnosing ALF, such as liver biopsy, are invasive and carry potential risks [6].”
Wu, L., Tang, R., Liang, Y., Jin, Y., Xu, K., Chen, X., Shi, J., & Li, J. (2025) · Lipids in Health and Disease · doi:10.1186/s12944-025-02728-x · Cited by 6 · see citing works
“Recognized as a significant driver of chronic liver pathology, MASLD may advance to liver cirrhosis and even hepatocellular carcinoma, posing a substantial threat to patients’ over-all health status and daily life quality and exacerbating the burden of the disease [4, 5].”
Feng, Q., Manousou, P., Izzi‐Engbeaya, C. N., Loomba, R. S., Thursz, M. R., & Woodward, M. (2025) · Liver International · doi:10.1111/liv.70485 · Cited by 6 · see citing works
Barriers to care linkage and educational impact on unnecessary MASLD referrals
Lee, J., Yoon, E. L., Oh, J. H., Kim, K., Ahn, S. B., & Jun, D. W. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1407389 · Cited by 6 · see citing works
Algorithms for Early Detection of Silent Liver Fibrosis in the Primary Care Setting
Bech, K., Lindvig, K. P., Thiele, M. S., & Castéra, L. (2024) · Seminars in Liver Disease · doi:10.1055/s-0043-1778127 · Cited by 6 · see citing works
Trinks, J., Mascardi, M. F., Gadano, A. C., & Marciano, S. (2024) · World Journal of Gastroenterology · doi:10.3748/wjg.v30.i14.1982 · Cited by 6 · see citing works
Sotoudeheian, M. (2024) · Current Protein and Peptide Science · doi:10.2174/0113892037315931240618085529 · Cited by 6 · see citing works
Exosome-based liquid biopsy for rare and complex diseases
Li, J., Peng, J., Guo, H., Zheng, W., Chen, R., Miao, C., Wang, J., Chen, Z., & Tang, C. (2025) · International Journal of Surgery · doi:10.1097/js9.0000000000003951 · Cited by 5 · see citing works
Noninvasive liver fibrosis assessment in metabolic dysfunction-associated steatotic liver disease
Ribeiro, T. C. R., Soares, V. D. P. B., Fabri, J. C., & Ramos, L. E. D. A. (2026) · World Journal of Hepatology · doi:10.4254/wjh.v18.i1.111534 · Cited by 5 · see citing works
Sharma, S., Choudhury, A. K., Thadikemalla, V. S. G., Rastogi, A., Gandhi, T. K., & Sarin, S. K. (2025) · Journal of Clinical and Experimental Hepatology · doi:10.1016/j.jceh.2025.103438 · Cited by 5 · see citing works
Immunological mechanisms underlying fibrotic diseases via single-cell technologies
Koda, Y., Nakamoto, N., & Kanai, T. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1720047 · Cited by 4 · see citing works
Choudhary, N. S., Kuchay, M. S., Dhampalwar, S., Singh, K. A., Singh, M. K., Singh, G., Saraf, N., & Duseja, A. K. (2026) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2026.103380 · Cited by 4 · see citing works
Lim, N., Devuni, D., German, M. N., Guy, J. E., Rabiee, A., Sharma, P., Shingina, A., Shroff, H., & Pillai, A. A. (2024) · Hepatology · doi:10.1097/hep.0000000000001036 · Cited by 5 · see citing works
Jasty, V. S. J., Urias, E., Tiong, K. L. A., Aboona, M. B., Song, M. W., Faulkner, C., Devan, P., Neo, J. E., Wijarnpreecha, K., Wong, Y. J., et al. (2024) · Digestive Diseases and Sciences · doi:10.1007/s10620-024-08635-y · Cited by 4 · see citing works
“Non-invasive tests (NITs) for diagnosing advanced fibrosis and predicting LRE have largely replaced invasive measure for risk stratification in routine practice [8–10].”
Ma, X., Liu, G., Liu, L., Dou, Z., He, X. M., & Chen, X. (2025) · The FASEB Journal · doi:10.1096/fj.202501627r · Cited by 3 · see citing works
Ouranos, K., Michael, M., Mylona, E. K., Shehadeh, F., Kalligeros, M., Teng, M. L. P., Muthiah, M. D., Siddiqui, M. S., Kodali, S., Basra, T., et al. (2026) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2025.12.021 · Cited by 3 · see citing works
Bakay, U., Duran, T. İ., Bakay, Ö. S. K., & Ekmekçioğlu, R. (2026) · Dermatology Practical & Conceptual · doi:10.5826/dpc.1601a6746 · Cited by 3 · see citing works
“Some observational studies have reported improvements in noninvasive fibrosis indices, including the Fibrosis-4 (FIB-4) index and NAFLD fibrosis score, following IL-17 inhibitor therapy [13,14], whereas others have found no significant change [15,16].”
InfluentialCobbold, J. F., Miller, H., Hallsworth, K., Manousou, P., Marjot, T., Allison, M. E. D., Anstee, Q. M., Armstrong, M., Avery, L., Azzu, V., et al. (2026) · The Lancet. Gastroenterology & hepatology · doi:10.1016/s2468-1253(26)00077-4 · Cited by 3 · see citing works
Capuccio, S., Privitera, G., Scilletta, S., Rocca, F. L., Marco, M. D., Scicali, R., Pino, A. D., Piro, S., & Russello, M. (2026) · Liver international (Print) · doi:10.1111/liv.70431 · Cited by 4 · see citing works
“…that combination strategies targeting both THR-β and metabolic pathways may enhance efficacy and allow more personalised treatment approaches [89], Future perspectives involve conducting longitudinal studies to assess long-term outcomes, mechanistic investigations to refine patient…”
Ueda, N., Mokuda, S., Kawaoka, T., Uchikawa, S., Amioka, K., Tsuge, M., Asada, K., Okada, Y., Kobayashi, Y., Ishikawa, M., et al. (2024) · Hepatology Research · doi:10.1111/hepr.14061 · Cited by 3 · see citing works
Liu, Q., Yang, Y., Wang, Y., Wei, S., Yang, L., Liu, T., Yu, Z., Feng, Y., Yao, P., & Zhu, Q. (2025) · Journal of Hepatocellular Carcinoma · doi:10.2147/jhc.s505752 · Cited by 3 · see citing works
Zhang, Y., & Wong, V. W. (2024) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2024.0766 · Cited by 3 · see citing works
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“Oxidative stress occurs in the livers of MASLD patients, and excess folate can lead to an increase in intracellular reactive oxygen species, which promotes MASLD (Sanyal et al., 2023; Tincopa and Loomba, 2023).”
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“[5,6] Existing non-invasive modalities for identifying liver fibrosis and steatosis include ultrasound-based imaging tests such as vibration-controlled transient elastography (VCTE) with liver stiffness measurement (VCTE-LSM) and controlled attenuation parameter (VCTE-CAP).”
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MAFLD/MASLD: Past, Present, and Future
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Non-invasive assessment of MASH resolution
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How to incorporate endohepatology into your bariatric practice
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“10 Several NITs have been suggested for identifying at-risk NASH and advanced fi brosis/cirrhosis (Fig.”
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- Authors
- Sanyal, A. J., Castera, L., & Wong, V. W.-S.
- Affiliations
- Virginia Commonwealth University (US)
- Chinese University of Hong Kong (HK)
- Corresponding author
- Sanyal, Arun J.
- Wong, Vincent Wai-Sun
- Venue
- Clinical Gastroenterology and Hepatology
- Publisher
- Elsevier BV
- Published
- 2023-07
- Volume
- 21
- Issue
- 8
- Pages
- 2026-2039
- ISSN
- 1542-3565 (ISSN-L)
- OpenAlex
- W4365505095
- Cited by
- 157
- References
- 79
- Citations by year
- 2026: 39 · 2025: 57 · 2024: 49 · 2023: 12
- FWCI
- 6.11
- Type
- journal article
- Language
- en
- Update notices
- erratum (2024-03-01)
- Open access
- bronze
- doi.org
- Licence
- Locations
- Clinical Gastroenterology and Hepatology (acceptedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Keywords
- non-alcoholic fatty liver disease, liver fibrosis, noninvasive fibrosis assessment, liver stiffness, elastography, serum biomarkers, liver biopsy limitations, liver cirrhosis, risk stratification, drug development, hepatocellular carcinoma risk
- MeSH terms
- Biopsy, Fibrosis, Humans, Liver Cirrhosis, Liver Neoplasms, Ultrasonography, Elasticity Imaging Techniques, Non-alcoholic Fatty Liver Disease
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