Longitudinal assessment of liver stiffness using ARFI technique does not support increased risk of fibrosis in rheumatoid arthritis patients on methotrexate
- PMID: 38227146
- PMCID: PMC12145398
- DOI: 10.1007/s40477-023-00843-y
Longitudinal assessment of liver stiffness using ARFI technique does not support increased risk of fibrosis in rheumatoid arthritis patients on methotrexate
Abstract
Aims: To assess the liver stiffness in patients with rheumatoid arthritis treated with methotrexate monotherapy using non-invasive, ultrasound-based elastography (acoustic radiation force impulse (ARFI) imaging) in a longitudinal approach.
Methods: In total, 23 MTX-naive patients were longitudinally assessed using acoustic radiation force impulse (ARFI) imaging. Baseline assessments were carried out between July 2018 and April 2019, and the follow-up evaluations took place after an average of 2.6 years. The main outcome variable was the mean shear wave velocity as measured by the ARFI method. It was calculated from 10 valid ARFI measurements for each patient. Inferential statistical analyses (within-group comparisons) were performed using t-tests for dependent samples or suitable nonparametric procedures.
Results: The main finding was that observed ARFI shear wave velocities did not increase during the observation period. In fact, this parameter decreased over time from 1.07 m/s (SD = 0.23) at baseline without MTX exposure to 0.97 m/s (SD = 0.16) at follow-up after a mean of 2.6 years (P = 0.013). Moreover, the magnitude of the change in shear wave velocity could not be predicted by indicators of inflammation or disease activity, BMI, age, sex or NSAR intake (corresponding regression analysis: corrected R2 = 0.344; P = 0.296).
Conclusions: No increased risk of liver fibrosis was found in RA patients treated with MTX monotherapy during observation period.
Keywords: ARFI; Arthritis, Rheumatoid; Disease modifying antirheumatic drugs; Fibroscan; Fibrosis, Liver; Methotrexate.
© 2024. Società Italiana di Ultrasonologia in Medicina e Biologia (SIUMB).
Conflict of interest statement
Declarations. Conflict of interest: Dr. Schäfer reports personal fees from Amgen, AstraZeneca, Novo Nordisk Pharma GmbH, outside the submitted work. Dr. Kovacs has nothing to disclose. Dr. Eder has nothing to disclose. Dr. Nigg has nothing to disclose. Dr. Feuchtenberger reports personal fees from AbbVie, personal fees from Novartis, personal fees from Roche, and personal fees from UCB outside of the submitted work. All authors disclose financial or non-financial interests that are directly or indirectly related to the work submitted for publication. Ethical approval: The study was approved by the Ethics Committee of the University of Würzburg, Würzburg, Germany, on 12 July 2018 (2/18-me). Informed consent: All patients provided written informed consent for blood analysis, study participation and publication of data.
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