BMC Public Health· 2026Q1
Prevalence and determinants of virological non-suppression at 24 weeks among people living with HIV in Hubei, China
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- Q1SCImago
- 2026year
Short summary
In Hubei, China, 6.81% of newly treated HIV patients showed virological non-suppression at 24 weeks, with higher baseline viral load and illicit drug use infection linked to poorer outcomes.
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Key points
- Overall virological non-suppression rate at 24 weeks was 6.81% among 4535 treatment-naive PLWH in Hubei, China.
- Female sex, higher baseline CD4 counts, and INSTI-based ART regimens were associated with lower non-suppression rates.
- Higher baseline HIV viral load and infection via illicit drug use were associated with higher non-suppression rates.
- The study identified key factors for early identification of patients at risk for suboptimal early virological response.
AI-generated from the title and abstract; the full text is not read.
Abstract
Virological non-suppression at 24 weeks after antiretroviral therapy (ART) initiation suggests a suboptimal early virological response and may help identify patients who require closer monitoring and support. However, real-world evidence on virological non-suppression at 24 weeks and its associated factors among treatment-naive people living with HIV (PLWH) in China remains limited. We conducted a retrospective cohort study using the HIV electronic database of the Hubei Provincial Center for Disease Control and Prevention. Treatment‑naive PLWH who initiated ART between Feb 2022 and Jun 2025 were included. The primary outcome was virological non-suppression at 24 weeks, defined as plasma HIV RNA > 200 copies/mL at the week 24 for HIV viral load (VL) assessment. Logistic regression was used to identify baseline demographic, clinical, and initial treatment factors associated with this outcome. Among 4535 treatment‑naive PLWH, the overall rate of virological non-suppression at 24 weeks during 2022–2025 was 6.81%. In multivariable analysis, female (aOR = 0.65, 95% CI: 0.46–0.93, p = 0.017), higher baseline CD4 count (200–349 vs. < 200: aOR = 0.57, 95% CI: 0.41–0.79, p < 0.001; 350–499 vs. < 200: aOR = 0.54, 95% CI: 0.35–0.85, p = 0.007), and initiation on integrase strand transfer inhibitor (INSTI)‑based regimens (aOR = 0.35, 95% CI: 0.26–0.48, p < 0.001) were associated with lower 24-week virological non-suppression rates. Higher baseline HIV VL (aOR = 1.83, 95% CI:1.57–2.13, p < 0.001) and infection via illicit drug use (aOR = 9.88, 95% CI:2.90–33.60, p < 0.001) were associated with higher 24-week virological non-suppression rate. These findings support early identification of treatment-naive PLWH at higher risk of 24-week virological non-suppression, particularly those with higher baseline VL, lower baseline CD4 count, infection via illicit drug use, and NNRTI-based initial regimens. Closer early VL monitoring and adherence support may help improve early virological response, while regimen optimization should be considered when clinically appropriate and accessible.
The authors' abstract, as published at the source. BMC Public Health, 2026 · DOI ↗
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Field: Infectious Diseases
Infectious DiseasesMedicine