TY - JOUR
T1 - Long-term quantitative hepatitis B surface antigen (HBsAg) trajectories in persons with and without HBsAg loss on tenofovir-containing antiretroviral therapy
AU - Begré, Lorin
AU - Boyd, Anders
AU - Salazar-Vizcaya, Luisa
AU - Suter-Riniker, Franziska
AU - Béguelin, Charles
AU - Rockstroh, J. rgen K.
AU - Günthard, Huldrych F.
AU - Calmy, Alexandra
AU - Cavassini, Matthias
AU - Stöckle, Marcel
AU - Schmid, Patrick
AU - Bernasconi, Enos
AU - Levrero, Massimo
AU - Zoulim, Fabien
AU - Wandeler, Gilles
AU - Rauch, Andri
N1 - Funding Information: This work was supported by an investigator‐initiated trial grant from Gilead Sciences (CO‐SW‐985‐5602), by the NEAT‐ID Foundation, by the Department of Teaching and Research, Inselspital, Bern University Hospital and by the Liquid Biobank Inselspital Bern. This study has been financed within the framework of the Swiss HIV Cohort Study, supported by the Swiss National Science Foundation (grant #201369), by SHCS project #809 and by the SHCS research foundation. The SHCS biobank was supported by the Liquid Biobank Inselspital Bern, and by the Department of Teaching and Research, Inselspital, Bern University Hospital. Lorin Begré was supported by the ‘Young Talents in Clinical Research’ programme of the Swiss Academy of Medical Sciences and G. and J. Bangerter‐Rhyner Foundation (grant YTCR 13/19). Gilles Wandeler was supported by a Professorship from the Swiss National Science Foundation (PP00P3_211025). Fabien Zoulim and Massimo Levrero received public grants overseen by the French National Research Agency (ANR) as part of the second ‘Investissements d'Avenir’ programme (reference: ANR‐17‐RHUS‐0003) and by the European Union (grant EU H2020‐847939‐IP‐cure‐B). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript. Publisher Copyright: © 2023 The Authors. HIV Medicine published by John Wiley & Sons Ltd on behalf of British HIV Association.
PY - 2023
Y1 - 2023
N2 - Objectives: Improving the understanding of the patterns of quantitative hepatitis B surface antigen (qHBsAg) trajectories associated with HBsAg loss is important in light of novel anti-hepatitis B virus agents being developed. We evaluated long-term qHBsAg trajectories in persons with HIV and HBV during tenofovir-containing antiretroviral therapy in the Swiss HIV Cohort Study. Methods: We included 29 participants with and 29 without HBsAg loss, defined as qHBsAg <0.05 IU/mL. We assessed qHBsAg decline during therapy in both groups and used agglomerative hierarchical clustering to identify different qHBsAg trajectory profiles in persons with HBsAg loss. Results: The median follow-up time was 11.9 years (IQR 8.4–14.1), and the median time to HBsAg loss was 48 months (IQR 12–96). Among participants with HBsAg loss, 79% had a qHBsAg decline ≥1 log10 IU/mL 2 years after starting tenofovir. The trajectories in qHBsAg levels during tenofovir therapy were heterogeneous, characterized by five distinct profiles. Among participants without HBsAg loss, only 7% had a qHBsAg decline ≥1 log10 IU/ml after 2 years. Conclusions: Most persons with HIV who experienced HBsAg loss had an early decline in qHBsAg levels, with diverse trajectories during long-term tenofovir therapy. In persons without HBsAg loss, qHBsAg levels remained remarkably stable over time.
AB - Objectives: Improving the understanding of the patterns of quantitative hepatitis B surface antigen (qHBsAg) trajectories associated with HBsAg loss is important in light of novel anti-hepatitis B virus agents being developed. We evaluated long-term qHBsAg trajectories in persons with HIV and HBV during tenofovir-containing antiretroviral therapy in the Swiss HIV Cohort Study. Methods: We included 29 participants with and 29 without HBsAg loss, defined as qHBsAg <0.05 IU/mL. We assessed qHBsAg decline during therapy in both groups and used agglomerative hierarchical clustering to identify different qHBsAg trajectory profiles in persons with HBsAg loss. Results: The median follow-up time was 11.9 years (IQR 8.4–14.1), and the median time to HBsAg loss was 48 months (IQR 12–96). Among participants with HBsAg loss, 79% had a qHBsAg decline ≥1 log10 IU/mL 2 years after starting tenofovir. The trajectories in qHBsAg levels during tenofovir therapy were heterogeneous, characterized by five distinct profiles. Among participants without HBsAg loss, only 7% had a qHBsAg decline ≥1 log10 IU/ml after 2 years. Conclusions: Most persons with HIV who experienced HBsAg loss had an early decline in qHBsAg levels, with diverse trajectories during long-term tenofovir therapy. In persons without HBsAg loss, qHBsAg levels remained remarkably stable over time.
KW - HBsAg
KW - HIV
KW - hepatitis B
KW - tenofovir
KW - trajectories
UR - http://www.scopus.com/inward/record.url?scp=85173754009&partnerID=8YFLogxK
U2 - https://doi.org/10.1111/hiv.13561
DO - https://doi.org/10.1111/hiv.13561
M3 - Article
C2 - 37816492
SN - 1464-2662
JO - HIV medicine
JF - HIV medicine
ER -