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Liver Stiffness Measurement can Predict Liver Inflammation in Chronic Hepatitis B Patients with Normal Alanine Transaminase

BACKGROUND AND AIMS: To determine whether liver stiffness measurement (LSM) indicates liver inflammation in chronic hepatitis B (CHB) with different upper limits of normal (ULNs) for alanine aminotransferase (ALT). METHODS: We grouped 439 CHB patients using different ULNs for ALT: cohort I, ≤40 U/L...

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Detalles Bibliográficos
Autores principales: Huang, Ling-Ling, Yu, Xue-Ping, Ruan, Qing-Fa, Lin, Yan-Xue, Li, Huan, Jin, Wen, Liu, Rui-Feng, Liang, Yan-Lan, Liu, Yu-Rui, Zhu, Yue-Yong, Jiang, Jia-Ji, Mao, Ri-Cheng, Zeng, Da-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318296/
https://www.ncbi.nlm.nih.gov/pubmed/37408816
http://dx.doi.org/10.14218/JCTH.2022.00329
Descripción
Sumario:BACKGROUND AND AIMS: To determine whether liver stiffness measurement (LSM) indicates liver inflammation in chronic hepatitis B (CHB) with different upper limits of normal (ULNs) for alanine aminotransferase (ALT). METHODS: We grouped 439 CHB patients using different ULNs for ALT: cohort I, ≤40 U/L (439 subjects); cohort II, ≤35/25 U/L (males/females; 330 subjects); and cohort III, ≤30/19 U/L (males/females; 231 subjects). Furthermore, 84 and 96 CHB patients with normal ALT (≤40 U/L) formed the external and prospective validation groups, respectively. We evaluated the correlation between LSM and biopsy-confirmed liver inflammation, and determined diagnostic accuracy using area under the curve (AUC). A noninvasive LSM-based model was developed using multivariate logistic regression. RESULTS: Fibrosis-adjusted LSM values significantly increased with increasing inflammation. The AUCs of LSM in cohorts I, II, and III were 0.799, 0.796, and 0.814, respectively, for significant inflammation (A≥2) and 0.779, 0.767, and 0.770, respectively, for severe inflammation (A=3). Cutoff LSM values in all cohorts for A≥2 and A=3 were 6.3 and 7.5 kPa, respectively. Internal, external, and prospective validations showed high diagnostic accuracy of LSM for A≥2 and A=3, and no significant differences in AUCs among the four groups. LSM and globulin independently predicted A≥2. The AUC of an LSM-globulin model for A≥2 exceeded those of globulin, ALT, and AST, but was similar to that of LSM. CONCLUSIONS: LSM predicted liver inflammation and guided the indication of antiviral therapy for CHB in patients with normal ALT.