Liver and Bile

JHEP Rep. 2025;7(11):101562

Díaz-González Á, Schregel I, Carballo L, Álvarez-Navascués C, Frisancho-Morales E, Miquel M, Retortillo MG, Gómez J, Horta D, Mateos B, Engel B, Volmer F, Barrio MD, Rodríguez-Tajes S, Olivas I, Hartl J, González CA, Hernández-Guerra M, Castello I, Pérez-Medrano I, González-Santiago JM, Arencibía A, Gómez A, Rodríguez-Perálvarez M, Crespo J, Sala M, Salcedo M, Barreira-Díaz A, Riveiro-Barciela M, Taubert R, Schramm C, Londoño MC; ColHai Registry

Isolated IgG elevation in patients with persistently normal transaminases does not affect the outcome of autoimmune hepatitis


Background and aims: The goal of treatment for autoimmune hepatitis is to achieve a complete biochemical response, defined as normalization of transaminases and immunoglobulin G (IgG) levels. Recent data suggest that IgG normalization does not significantly affect survival. The authors evaluated the impact of persistently elevated IgG levels (IgGe) and IgG flares (IgGf) on fibrosis progression and cirrhosis development.
Methods: This retrospective multicenter cohort study included 493 patients with autoimmune hepatitis and persistently normal transaminase levels during follow-up. The inverse probability of treatment weighting (IPTW) propensity score method was used to balance the cohorts.
Results: 349 (70.8%) patients had persistently normal IgG (IgGn) levels, 89 (18.1%) had IgGe, and 55 (11.1%) had IgGf during follow-up. After a median follow-up of 6.2 years (IQR, 4.1–10.1 years) with normal transaminase levels, median liver stiffness measurement (LSM) values remained stable, with no significant differences between groups. During the follow-up, 24 patients developed cirrhosis. Predictive factors for cirrhosis were age (hazard ratio [HR] = 1.10, p < 0.001), albumin (HR = 0.20, p < 0.001), IgG (HR = 1.00, p = 0.001), and platelet count (HR = 0.99, p = 0.001) at diagnosis; LSM (HR = 1.30, p < 0.001) at transaminase normalization; and transaminase normalization at 6 months (HR = 0.24, p = 0.025). In the multivariate analysis, only LSM was independently associated with a higher risk of developing cirrhosis. After IPTW application, elevated IgG (IgGe or IgGf) did not affect fibrosis progression (p = 0.275) or cirrhosis development (p = 0.211).

Conclusions: Persistent or temporary serum IgG elevation in patients with normal transaminase levels did not significantly affect autoimmune hepatitis disease progression, thus challenging the current definition of complete biochemical response.

M.-C. Londoño, Liver Unit, Hospital Clínic Barcelona, Barcelona, Spain, e-mail: mlondono@clinic.cat

or

Á. Díaz-González, Gastroenterology and Hepatology Department, Clinical and Translational Research in Digestive Diseases Group, Valdecilla Research Institute (IDIVAL), Marqués de Valdecilla University Hospital, Santander, Spain, e-mail: alvaro.diaz@scsalud.es

DOI:  10.1016/j.jhepr.2025.101562

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