Table 2. Factors associated with HBV DNA suppression after 48 weeks of treatment stratified by baseline HBV DNA.
| Baseline HBV DNA <20,000 IU/ml | |||||
|---|---|---|---|---|---|
| HBV DNA Suppression rate at week 48 [n/N (%)] | Crude RR (95%CI) | P | Adjusted RR(95%CI) | P | |
| cART | |||||
| 3TC-based | 30/31 (96.8) | Reference | Reference | ||
| TDF+3TC-based | 50/51 (98.0) | 1.01 (0.94-1.09) | 0.74 | 1.01 (0.93-1.11) | 0.78 |
| CD4 cell count | |||||
| ≤200 cells/μl | 35/37 (94.6) | Reference | Reference | ||
| >200 cells/μl | 45/45 (100.0) | 1.06 (0.98-1.14) | 0.16 | 1.03 ( 0.98-1.09) | 0.22 |
| Baseline HIV RNA (per 1 log copy/ml increase) | Not applicable | 0.97 (0.91-1.03) | 0.28 | ||
| Baseline HBV DNA (per 1 logIU/ml increase) | Not applicable | 1.00 (0.97-1.03) | 0.83 | 1.00 (0.97-1.03) | 0.99 |
| CD4 count at week 48 (cells/μL) | |||||
| ≤350 | 35/37 (94.6) | Reference | |||
| >350 | 45/45 (100.0) | 1.06 (0.98-1.14) | 0.16 | ||
| Baseline HBV DNA ≥20,000 IU/ml | |||||
| HBV DNA Suppression rate at week 48 [n/N (%)] | Crude RR (95%CI) | P | Adjusted RR(95%CI) | P | |
| cART | |||||
| 3TC-based | 10/29 (34.5) | Reference | Reference | ||
| TDF+3TC-based | 29/40 (72.5) | 2.10 (1.22-3.61) | 0.007 | 1.98 (1.18-3.34) | 0.010 |
| CD4 cell count | |||||
| ≤200 cells/μl | 23/39 (59.0) | Reference | |||
| >200 cells/μl | 16/30 (53.3) | 0.90 (0.59-1.39) | 0.65 | 0.66 (0.46-0.96) | 0.028 |
| Baseline HIV RNA (per 1 log copy/ml) increase | Not applicable | 1.12 (0.85-1.48) | 0.43 | ||
| Baseline HBV DNA (per 1 log IU/ml increase) | Not applicable | 0.74 (0.65-0.85) | <0.001 | 0.74 (0.63-0.87) | <0.001 |
| CD4 count at week 48 (cells/μL) | |||||
| ≤350 | 20/37 (54.1) | Reference | |||
| >350 | 19/32 (59.4) | 1.10 (0.72-1.66) | 0.66 | ||
RR, relative risk; cART, combination antiretroviral therapy; 3TC, lamivudine; TDF, tenofovir.
Since baseline CD4 cell count were not balanced in two treatment groups, we also adjusted for baseline CD4 cell count in multivariate models.
Sex, age and routes of transmission were also adjusted for in multivariate analyses. Of note, they were not significantly associated with HBV DNA suppression in univariate analysis. cART regimens (3TC-based or TDF+3TC-based), baseline HBV DNA and baseline CD4 cell count were forced into the multivariate models; other factors with P values<0.15 in univariate models were also included in the multivariate models.