HIV transmission risks in unprotected sexual relationships vary considerably according to different factors such as type of sexual practice,1 stage of HIV infection,2 presence of sexually transmitted infections,2,3 and plasma viral load in the HIV-infected partner.4-6 Highly active antiretroviral therapy (HAART) has been shown to be highly effective in reducing plasma levels of HIV RNA among infected persons7; therefore, these treatments could diminish the risk of HIV transmission.4 Reduction of infectiousness among individuals who receive antiretroviral therapy has been demonstrated in mother-to-child transmission8 but has not been fully established in sexual transmission, in spite of the important influence it could have on the course of the pandemic.9-12
In the absence of changes in other relevant factors, a reduction in the sexual transmission of HIV after the introduction of HAART would be indicative of the effectiveness of this treatment to prevent new infections. With this aim in mind, we studied first-time HIV testers whose sole risk exposure was having a steady heterosexual partner who was infected. We compared HIV prevalence among those who were recruited during the years before the introduction of HAART and those included during the period when HAART was being used.
PATIENTS AND METHODS
The study was conducted in a clinic in Madrid that launched a specific program for HIV-serodiscordant sexual couples in 1987. To each patient who was diagnosed with HIV infection, it was recommended that his or her sexual partner also visit the clinic for voluntary counseling and testing. With the informed consent of both partners, stable heterosexual couples attending this program were prospectively included in an observational study to analyze HIV sexual transmission risk, determinant factors, and needs related to prevention and reproduction aspects. Couples were recruited when the nonindex partner came to the clinic for his or her first HIV test in the period from January 1991 to December 2003. For the present analysis, 393 couples were selected with the following criteria: ongoing sexual relationship during the past 6 months, in which one of the partners (“index case”) had been diagnosed with HIV-1 with a well-identified probable route of infection and the nonindex partner had not had a previous diagnosis of HIV and where the sexual relationship with the index case was the sole known risk exposure.
Interviews and Laboratory Tests
Both members of each couple were interviewed separately during a medical visit by means of a structured questionnaire before the serologic HIV result for the nonindex partner was known. The information collected for index cases included sociodemographic characteristics, probable route of infection, date of HIV infection diagnosis, AIDS-defining diseases, last CD4+ lymphocyte count, and antiretroviral treatments. Plasma HIV RNA level (Branched-DNA; Bayer Diagnostics, France) was available since 1997. The information concerning nonindex partners contained sociodemographic data, date of the beginning of their relationship as a couple, and frequency of intercourse without a condom in the past 6 months. Women were also asked about pregnancies with their partner. For both members, the history of sexually transmitted diseases and presence of dysuria, genital discharge, ulcers, or warts were obtained through anamnesis and medical examination. Serologic study of syphilis was conducted using the reaginic test, and positive samples were confirmed by Treponema pallidum hemagglutination assay (TPHA) or the fluorescent treponemal antibody absorption test (FTA-ABS). For all participants, blood specimens were tested for HIV by an enzyme-linked immunosorbent assay, and reactive sera were confirmed by Western blot analysis.
The most complete of all antiretroviral therapies received by the index case since the beginning of the couple's relationship was considered in the analyses. For the whole of the period from 1991 through 2003, HIV prevalence among nonindex partners was compared according to index case's antiretroviral regimen (no treatment, mono- or bitherapy, 3 or more drugs).
In accordance with current international guidelines,13 HAART has been available free of charge in Spain to all patients since 1997. With this fact in mind, HIV prevalence among nonindex partners was compared for 3 calendar periods: pre-HAART (1991-1995); early HAART (1996-1998), the transition period; and late HAART (1999-2003), corresponding to the full implementation of this therapy.
A 2-sided χ2 test and the Fisher exact test were used to compare proportions. Differences in continuous variables were tested with the Wilcoxon test and Kruskal-Wallis test. The bivariate analysis was followed by a multivariate logistic regression used to identify the isolated effect of the calendar period, adjusting by confounder covariables. The association between variables was quantified by means of the prevalence odds ratio (OR) and its 95% confidence interval (CI).
Couples' Characteristics According to Enrollment Period
Table 1 shows characteristics of the 393 couples grouped according to the enrollment period. In all 3 periods, the man was the initially HIV-infected partner in most couples and most index cases were infected through risk practices related to injecting drug use, although in the late HAART period, the proportion of individuals infected by a sexual route rose to 35.8% (P = 0.0003). The mean length of the couple relationships was 2.7 years, and 8.7% of women were pregnant at the time of their first visit to the clinic, without any significant variation between periods.
The index case's CD4+ cell count at the time of inclusion in the study remained stable (P = 0.9072); nevertheless, the percentage of those diagnosed with an AIDS-defining disease rose from 9.8% to 19.8% (P = 0.0453), and the proportion of index cases with antiretroviral therapy increased from 6.5% to 49.1% (P < 0.0001). Whereas all patients who were treated during the first period underwent mono- or bitherapy, they all received combinations of 3 or more antiretroviral drugs in the last period.
Among index cases, the frequency of sexually transmitted infections decreased from 9.8% to 0.9% (P = 0.0063). None of the nonindex partners had received postexposure prophylaxis.
HIV Prevalence Among Nonindex Partners
For the nonindex partners, HIV prevalence declined from 10.3% in the pre-HAART period to 6.8% in the early HAART period and to 1.9% in the late HAART period (P = 0.0254). HIV prevalence among partners of index cases who had not received any antiretroviral therapy was 8.6%, whereas no partner was infected in couples in which the index case was being treated with HAART (P = 0.0123). Other variables associated with a higher HIV prevalence among nonindex partners were unprotected coital acts in past 6 months, CD4+ count less than 350 cells/μL in the index case, and pregnancy during that couple's relationship. Moreover, the presence or history of AIDS-defining diseases and high levels of HIV RNA for index cases were close to statistical significance, although this last information was only available for some couples. No association was found with gender, age, length of the relationship, time since HIV diagnosis in the index case, and presence of genital or sexually transmitted infections (Table 2).
The decrease in HIV prevalence among nonindex partners was especially pronounced when index cases had a CD4+ count less than 350 cells/μL and when they took antiretroviral drugs (Table 3). As a consequence, in the late HAART period, there was no difference in HIV prevalence between couples whose index case received HAART (0%) and those whose index case had received no treatment (3.7%; P = 0.4954).
Using logistic regression analysis, we evaluated changes in HIV prevalence between the 3 periods, which corresponded to different levels of HAART availability, adjusting them by possible confusion factors (Table 4). The results confirmed the pronounced decrease in HIV prevalence among nonindex partners recruited during the late HAART period when compared with the prevalence observed among those included during the pre-HAART period (OR = 0.14, 95% CI: 0.03-0.66; P = 0.0127). Other variables independently associated with higher HIV prevalence were CD4+ count less than 350 cells/μL, sexual intercourse without a condom in the previous 6 months, and pregnancy during that couple's relationship. In the multivariate analysis, the gender of the index cases, the length of the couples' relationships, antiretroviral therapy, and the presence or history of AIDS-defining diseases and sexually transmitted infections were not significantly associated with a higher HIV prevalence among nonindex partners. Interaction terms between calendar period and other covariables were not statistically significant.
These results demonstrate an important reduction in the heterosexual transmission of HIV and provide evidence showing that such a reduction can be attributed to HAART. On the one hand, none of the HIV-infected index cases who received HAART had transmitted HIV to his or her partner compared with 8.7% of the index cases who had not received this therapy. On the other hand, HIV prevalence among individuals with a stable heterosexual partner previously diagnosed with HIV infection is 5 times lower since HAART has been widely available than during the period before the introduction of HAART.
Comparison between calendar periods with different levels of HAART availability, once the influence of changes in other variables that affect HIV transmissibility has been excluded, enables us to evaluate the effectiveness of these therapies in reducing transmission when applied under uncontrolled conditions. Antiretroviral therapy is prescribed for patients with worse clinical, immunologic, or virologic states,13 who are thus more infectious toward their sexual partners.2-4 This could help to explain why the impact of HAART on HIV transmission has been important, although only half of the index cases underwent such therapy. With the introduction of HAART, the context in which antiretroviral therapy was prescribed was enlarged, and this could account for the fact that HIV prevalence among partners of index cases who did not receive antiretroviral drugs also decreased.
The inclusion criteria applied in our study allow us to state, with a rather high level of probability, that HIV infections detected among nonindex partners are attributable to heterosexual transmission by their index case partner. The information was collected before the nonindex partner's serologic status was known, which reduces possible biases.
The major limitation of our results is that they do not completely enable us to rule out the effect of factors other than antiretroviral therapy on the reduction of HIV prevalence among the nonindex partners. The proportion of couples who practiced unprotected coital acts decreased as well as the frequency of sexually transmitted infections, which would contribute to a lower transmission rate. In any case, the marked decrease in HIV prevalence of the nonindex partners in the HAART period was maintained after adjusting for all these changes.
Several arguments suggest that antiretroviral therapy can reduce sexual transmission of HIV. The viral load in genital secretions seems to decline, together with the viral load in plasma, after combination therapy.14,15 A prospective study established a link between zidovudine use and a decrease in the rate of HIV transmission from infected men to their partners,16 and another more recent study suggests that homosexual men have lower infectivity after the introduction of HAART.17
As shown by other studies, the fact of having practiced unprotected coitus2,3 and the low levels of CD4+ cell counts were 2 of the major explanatory variables of HIV transmission to the sexual partner. The low levels of CD4+ cell counts can be justified mainly because of the presence of high viral load values and/or a long duration of the infection,18 and both of these circumstances could have contributed to a higher likelihood of HIV transmission. We did not find any association between the presence of sexually transmitted infections and HIV transmission to the partner,2-4 although such an association has been described in various studies.1 Nevertheless, a genital discharge was not present in any of these infections, and only 1 subject had genital ulcers.
Although not a single case of HIV transmission was found when the index case had received HAART, the existence of some risk could not be totally excluded, because the persistence of HIV in genital secretions of patients with HAART has been described.19 Some increases in risky practices have been observed for various population groups and were attributed to a slackening in preventive measures because of HAART.20-23 Other studies have revealed no change24,25 or even a decrease of risky behavior frequency that coincides with HAART introduction, however.26 A rise in risky behavior could thus cancel out or even reverse the preventive effect on sexual transmission obtained though antiretroviral therapies. This is why it is important not to forget that the main preventive measure for HIV sexual transmission remains the avoidance of risky sexual practices.
In conclusion, after the introduction of HAART, an important decrease in HIV transmission has been observed in a thoroughly studied group of steady heterosexual couples, irrespective of any changes in other factors that affect transmission. These results strongly suggest that combined antiretroviral treatments applied according to current guidelines have a great potential for preventing HIV transmission to sexual partners. The accessibility to HAART for HIV-infected people around the world, as long as it is not accompanied by a relaxation of other prevention measures, could greatly contribute to controlling the spread of HIV among similar populations.
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