Liver stiffness measurement predicts clinical outcomes in autoimmune hepatitis

Liver stiffness measurement (LSM) has been shown to adequately predict outcomes in patients with liver disease. However, the value of LSM as a predictor of disease progression in autoimmune hepatitis (AIH) remains to be determined. This study aimed to evaluate the role of LSM as a predictor of disea...

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Veröffentlicht in:JHEP reports 2024-11, Vol.6 (11), p.101213, Article 101213
Hauptverfasser: Olivas, Ignasi, Arvaniti, Pinelopi, Gabeta, Stella, Torres, Sonia, Del Barrio, Maria, Díaz-González, Alvaro, Esteban, Paula, Riveiro-Barciela, Mar, Mauro, Ezequiel, Rodríguez-Tajes, Sergio, Zachou, Kalliopi, Dalekos, George N., Londoño, María-Carlota
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Sprache:eng
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Zusammenfassung:Liver stiffness measurement (LSM) has been shown to adequately predict outcomes in patients with liver disease. However, the value of LSM as a predictor of disease progression in autoimmune hepatitis (AIH) remains to be determined. This study aimed to evaluate the role of LSM as a predictor of disease progression and decompensation of cirrhosis in patients with AIH. This multicentre cohort study included 439 patients with histologically confirmed AIH and at least one LSM during follow-up. The association between the first LSM performed at least 6 months after treatment initiation (baseline LSM [BLSM]) and cirrhosis development and poor outcomes (decompensation, liver transplantation, and/or liver-related death) was assessed using Cox regression and its discriminating capacity with a receiver-operating characteristic curve. Most patients were female (n = 301, 70%), with a median age of 52 years. BLSM performed after a median of 2.18 (1.19-4.68) years had a median value of 6 kPa (4.5-8.5). At the time of BLSM, 332 (76%) patients had achieved a biochemical response and 57 (13%) had cirrhosis. During follow-up, eight patients (2%) presented with poor outcomes and 26 (7%) developed cirrhosis. BLSM was higher among patients with poor outcomes (13.5 kPa vs. 6 kPa; p
ISSN:2589-5559
2589-5559
DOI:10.1016/j.jhepr.2024.101213