Table 1.
Association between antiretrovirals and incident SARS-CoV-2 infection (AGEhIV COVID-19 substudy) | Association between antiretrovirals and severe COVID-19 (hospitalization and/or death) (ATHENA cohort) | |||||||||
Unadjusted | Adjusteda | Unadjusted | Adjusteda | |||||||
n/Nb | OR (95% CI) | P | OR (95% CI) | P | n/Nb | OR (95% CI) | P | OR (95% CI) | P | |
NRTI backbone | ||||||||||
- Lamivudine only | 0/7 | – | – | – | – | 8/157 | 0.83 (0.38–1.81) | 0.63 | 0.50 (0.21–1.20) | 0.12 |
- Abacavir-based | 2/28 | 0.65 (0.13–3.28) | 0.61 | 0.56 (0.11–2.95) | 0.50 | 35/339 | 1.77 (1.10–2.86) | 0.018 | 1.39 (0.83–2.35) | 0.21 |
- Tenofovir alafenamide-based | 17/107 | 1.61 (0.65–3.94) | 0.30 | 1.33 (0.53–3.38) | 0.55 | 67/946 | 1.18 (0.78–1.77) | 0.43 | 1.01 (0.65–1.56) | 0.96 |
- Tenofovir disoproxil fumarate-based | 8/76 | REF | REF | REF | REF | 39/640 | REF | REF | REF | REF |
- No NRTI | 2/21 | 0.89 (0.18–4.57) | 0.89 | 0.96 (0.18–5.17) | 0.96 | 9/107 | 1.42 (0.67–3.01) | .37 | 0.68 (0.29–1.58) | 0.37 |
INSTI | ||||||||||
- Bictegravir | 6/30 | 2.00 (0.55–7.27) | 0.29 | 2.15 (0.56–8.26) | 0.26 | 21/282 | 0.93 (0.55–1.59) | 0.80 | 0.89 (0.50–1.60) | 0.70 |
- Dolutegravir | 5/45 | REF | REF | REF | REF | 50/626 | REF | REF | REF | REF |
- Elvitegravir/cobicistat | 6/41 | 1.37 (0.38–4.89) | .63 | 0.77 (0.19–3.14) | .72 | 15/349 | 0.52 (0.29–0.94) | .029 | 0.80 (0.43–1.50) | 0.50 |
- Raltegravir | 1/12 | 0.73 (0.08–6.89) | 0.78 | 0.97 (0.10–9.65) | 0.98 | 7/51 | 1.83 (0.79–4.28) | .16 | 1.54 (0.61–3.90) | 0.37 |
- No INSTI | 11/111 | 0.88 (0.29–2.69) | 0.82 | 0.83 (0.26–2.64) | 0.75 | 65/881 | 0.92 (0.63–1.35) | 0.66 | 0.88 (0.58–1.34) | 0.54 |
NNRTI | ||||||||||
- Doravirine | 2/11 | 2.00 (0.24–16.61) | 0.52 | 2.59 (0.27–25.02) | 0.41 | 6/140 | 0.49 (0.18–1.33) | 0.16 | 0.60 (0.20–1.79) | 0.36 |
- Efavirenz | 2/20 | REF | REF | REF | REF | 12/142 | REF | REF | REF | REF |
- Etravirine | 0/1 | – | – | – | – | 1/11 | 1.08 (0.13–9.20) | 0.94 | 0.67 (0.07–6.62) | 0.72 |
- Nevirapine | 4/49 | 0.80 (0.13–4.76) | 0.81 | 0.74 (0.11–5.02) | 0.76 | 18/227 | 0.93 (0.44–2.00) | 0.86 | 0.86 (0.38–1.99) | 0.73 |
- Rilpivirine | 2/13 | 1.64 (0.20–13.34) | 0.65 | 2.22 (0.24–20.23) | 0.48 | 11/172 | 0.74 (0.32–1.73) | 0.49 | 1.07 (0.43–2.65) | 0.89 |
- No NNRTI | 19/145 | 1.36 (0.29–6.32) | 0.70 | 1.15 (0.22–6.03) | 0.87 | 110/1497 | 0.86 (0.46–1.60) | 0.64 | 1.02 (0.51–2.01) | 0.97 |
PI | ||||||||||
- Atazanavir/booster | 1/5 | 5.25 (0.39–71.42) | 0.21 | 9.72 (0.61–155.06) | 0.11 | 2/22 | 0.72 (0.16–3.14) | 0.67 | 0.50 (0.09–2.74) | 0.42 |
- Darunavir/booster | 2/44 | REF | REF | REF | REF | 33/270 | REF | REF | REF | REF |
- Lopinavir/booster | 0/2 | – | – | – | – | 0/5 | – | – | – | – |
- No PI | 26/188 | 3.37 (0.77–14.77) | 0.11 | 3.51 (0.78–15.92) | .10 | 123/1892 | 0.50 (0.33–0.75) | <0.001 | 0.73 (0.47–1.15) | 0.17 |
Values represent odds ratios (OR) with 95% confidence interval using logistic regression.
Adjusted for age, sex at birth, ethnic origin, total comorbidities count, prior AIDS, current CD4+ cell count, and current HIV-1 viral load.
Number of participants with severe COVID-19 (hospitalization and/or death) per total number of participants for each variable category.
CI, confidence interval; INSTI, integrase strand transfer inhibitors; NNRTI, nonnucleoside reverse transcriptase inhibitors; NRTI, nucleoside reverse transcriptase inhibitors; OR, odds ratio; P, P-value; PI, protease inhibitors; REF, reference group.