Research on serum uric acid (UA) trajectories in HIV/AIDS patients receiving integrase strand transfer inhibitor (INSTI)-based antiretroviral therapy (ART) remains limited. This retrospective cohort study included 212 patients categorized by ART exposure into four groups: continuous non-INSTI, non-INSTI to INSTI switch, continuous INSTI, and INSTI to non-INSTI switch groups. After 1:1 matching, linear mixed-effects models were used to assess longitudinal UA changes and hyperuricemia (HUA) probability. Baseline UA consistently predicted UA trajectories. A significant three-way interaction (regimen × time × baseline UA) was observed only in the continuous non-INSTI versus non-INSTI-to-INSTI switch comparison, indicating that in the group switching from non-INSTI-to-INSTI, the patients with high baseline UA presented a more pronounced decrease in UA levels than patients with normal baseline UA. Baseline UA was also correlated with HUA probability during follow-up. These findings indicate that baseline UA is an important predictor of long-term UA patterns and longitudinal probability of HUA during follow-up, whereas the INSTI-associated changes in UA trajectory are preliminary observations that require further validation.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: