Background: Studies have shown that
transmission of HIV strains resistant to antiretroviral drugs may increase as
therapy becomes more widespread.
Methods: We prospectively evaluated
the prevalence of antiretroviral drug resistance (ARVDR) among recently
diagnosed untreated individuals with HIV (not AIDS) sequentially enrolled in 10
U.S. cities.
Plasma specimens were analyzed using conventional sequencing. To identify persons infected within 4-6
months, specimens were tested with a modification of an HIV-1 enzyme
immunoassay (3A11, Abbott).
Results: Of 923 persons enrolled in 1998-2000, 74.7% were
male, 45.4% were African Americans, 23.6% were Hispanic, 44.0% were men who
have sex with men, 10.6% were heterosexual injecting drug users, and 45.4%
reported only heterosexual exposure.
Mutations associated with ARVDR were seen in 8.3% overall. Of the 695 specimens so far tested with 3A11,
12.5% had evidence of recent infection.
The prevalence of ARVDR mutations in the recently infected group was
8.1%. When analysis was restricted to
the 5 cities participating in all 3 years (n=723), ARVDR prevalence increased
significantly between 1998 and1999 (p=0.01 by Fisher’s exact test), but did not
change significantly between 1999-2000 (see Table). A similar (non-significant) trend was seen
among the recently infected (data not shown).
No significant changes in proportions of gender, race, risk group, or
recently infected persons were seen among these years. A non-significant increase in ARVDR
prevalence between 1998 and 1999 was seen in each of the 3 drug classes.
Presence
of ARVDR mutations to: 1998 1999 2000
(N=238) (N=240) (N=245)
Any
drug class 9 (3.8%) 24 (10.0%) 22
(9.0%)
Nucleoside
reverse transcriptase inhibitors
8
(3.4%) 20 (8.3%) 17 (6.9%)
Non-nucleoside
reverse transcriptase inhibitors 1 (0.4%) 5
(2.1%) 3 (1.2%)
Protease
inhibitors 0 (0%) 4
(1.7%) 5 (2.0%)
More
than one drug class 0 (0%) 4
(1.7%) 3 (1.2%)
Conclusions:
An increase
in ARVDR prevalence among persons with newly diagnosed HIV was observed between
1998 and 1999 in 5 cities. Transmission of ARVDR-resistant
strains may increase as treatment becomes more common, although prevalence will
also vary depending on treatment outcomes and the success of risk reduction
measures. Further multiyear studies in
the same geographic areas are needed to evaluate whether the increase will
continue or stabilize.