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Mortality in members of HIV-1 serodiscordant couples in Africa and implications for antiretroviral therapy initiation: Results of analyses from a multicenter randomized trial
© de Bruyn et al.; licensee BioMed Central Ltd. 2012
Received: 5 April 2012
Accepted: 24 September 2012
Published: 30 October 2012
The risk of HIV-1 related mortality is strongly related to CD4 count. Guidance on optimal timing for initiation of antiretroviral therapy (ART) is still evolving, but the contribution of HIV-1 infection to excess mortality at CD4 cell counts above thresholds for HIV-1 treatment has not been fully described, especially in resource-poor settings. To compare mortality among HIV-1 infected and uninfected members of HIV-1 serodiscordant couples followed for up to 24 months, we conducted a secondary data analysis examining mortality among HIV-1 serodiscordant couples participating in a multicenter, randomized controlled trial at 14 sites in seven sub-Saharan African countries.
Predictors of death were examined using Cox regression and excess mortality by CD4 count and plasma HIV-1 RNA was computed using Poisson regression for correlated data.
Among 3295 HIV serodiscordant couples, we observed 109 deaths from any cause (74 deaths among HIV-1 infected and 25 among HIV-1 uninfected persons). Among HIV-1 infected persons, the risk of death increased with lower CD4 count and higher plasma viral levels. HIV-1 infected persons had excess mortality due to medical causes of 15.2 deaths/1000 person years at CD4 counts of 250 – 349 cells/μl and 8.9 deaths at CD4 counts of 350 – 499 cells/μl. Above a CD4 count of 500 cells/μl, mortality was comparable among HIV-1 infected and uninfected persons.
Among African serodiscordant couples, there is a high rate of mortality attributable to HIV-1 infection at CD4 counts above the current threshold (200 – 350 cells/μl) for ART initiation in many African countries. These data indicate that earlier initiation of treatment is likely to provide clinical benefit if further expansion of ART access can be achieved.
HIV-1-related mortality increases as the CD4 count in peripheral blood decreases . Initiation of antiretroviral therapy (ART) at a CD4 count above 200 cells/μl reduces mortality of HIV-1 infected persons compared to therapy that is delayed until CD4 count declines below 200 cells/μl , and adopting an even higher CD4 threshold for initiating ART may further reduce mortality [3–5]. Recently, evidence from a clinical trial demonstrated that initiation of ART at a CD4 count between 350 and 550 cells/μl results in clinical benefits and reduces transmission to HIV-uninfected partners . World Health Organization (WHO) guidelines recommend that therapy be initiated when an HIV-1 infected person’s CD4 count falls to 350 cells/μl . Currently, the CD4 threshold is 200 –250 cells/μl in most African countries, and 350 cells/μl in others, where the WHO guidelines have been adopted.
However, controversy remains regarding the ideal CD4 threshold at which ART should be initiated [3–5, 8], and data to inform guidelines are still limited, especially from resource-poor settings. A large proportion of excess adult mortality in sub-Saharan Africa is HIV-1-related . Excess HIV-1-related mortality has been shown to be related to several clinical factors, such as use of ART, CD4 count, clinical stage of disease, as well as demographic factors, including migration, level of educational attainment, age, and economic status [9–15]. Differential HIV-related mortality, based on access to care and socioeconomic status, has been observed in developed countries . The impact of these factors may be accentuated in developing countries, where access to health care is more limited in general.
We compared mortality among HIV-1 infected and uninfected partners in African HIV-1 serodiscordant couples participating in the Partners in Prevention HSV/HIV Transmission Study, a clinical trial of acyclovir for HSV-2 suppression among HSV-2/HIV-1 dually-infected persons for prevention of HIV-1 transmission to their HIV-1 uninfected partners. As reported previously, acyclovir suppression did not reduce HIV-1 transmission to uninfected partners in spite of a 0.25 log10 reduction in plasma HIV-1 levels , but modestly delayed progression in HIV-1 infected persons . Because most participating couples were cohabiting, the HIV-1 uninfected partners comprised an excellent control group for determining mortality attributable to HIV-1 infection, while accounting for shared exposures such as a common environment, socioeconomic status, diet, exposure to infectious diseases, and access to care.
Study population and procedures
Between November 2004 and April 2007, 3408 HIV-1 serodiscordant couples in 7 African countries (Botswana, Kenya, Rwanda, South Africa, Tanzania, Uganda, and Zambia) were enrolled into a randomized, double-blind, placebo-controlled trial of twice daily 400 mg acyclovir in HIV-1/HSV-2 dually infected partners to prevent HIV-1 transmission to the uninfected partner. HIV-1-infected partners were required to be 18 years of age or older, seropositive for HIV-1 and HSV-2, and have a CD4 count ≥250 cells/μl. Persons who had a prior AIDS-defining diagnosis, reported taking ART, had prior adverse reactions to acyclovir or planned use of anti-HSV antivirals, or were pregnant were excluded. For HIV-1 infected participants, CD4 counts were measured at enrolment and 6 month intervals and plasma viral load at enrolment, 3, 6, 12 months, and study exit. Those meeting national criteria for ART initiation during follow-up were offered ART through referral to local clinics or at the study site. HIV-1-infected participants were followed monthly for up to 24 months after enrolment, and HIV-1-uninfected partners were seen quarterly. Study procedures have been detailed elsewhere [17–20].
Medical monitoring and assignment of causes of death
For participants who died during follow-up, information on the putative cause of death was obtained from the surviving partner, family members, and/or medical records, if available. The cause of death was classified as a medical death or traumatic death, such as traffic collisions or assault. The study medical monitor (AW) assigned the medical cause of death to one of the following broad categories based on information provided by the local site: pneumonia or other respiratory illness; malaria; tuberculosis; gastrointestinal infections and other disorders; other infections; or other medical causes.
HIV-1 serostatus was determined by dual rapid tests with confirmatory EIA and HSV-2 serostatus by HerpeSelect-2 EIA (Focus Technologies, Cypress, CA). HIV-1 and HSV-2 serostatus were confirmed in batch by the University of Washington Western blot and only those who were confirmed were included in the analysis . CD4 testing was performed at study sites using standard flow cytometry (BD Biosciences, San Jose, CA), under an external quality assurance program. Plasma HIV-1 RNA was quantified in acid citrate dextrose (ACD) using the 96-test COBAS AmpliPrep/COBAS TaqMan HIV-1 RNA assay, version 1.0 (Roche Diagnostics, Indianapolis, IN) at the University of Washington, with a limit of quantification of 240 copies/mL.
The University of Washington Human Subjects Review Committee and ethical review committees at each local and collaborating institution approved the study protocol. All participants provided written informed consent.
Data were analyzed using SAS (version 9.2, SAS, Cary, NC). Incidence rates were computed by summing the time at risk within each range of predictors. Participants contributed follow-up time to more than one category of CD4 count, plasma HIV-1 RNA and WHO HIV stage, as their condition changed over time. Participants who were HIV-1 infected at enrolment were analyzed separately from their partners to examine potential time-varying predictors of death. Follow-up time for HIV-1 seronegative partners was censored at HIV-1 seroconversion. We compared the proportion dying while on study within couples using McNemar’s test. Paired Cox regression was used to examine baseline predictors of death within couples. Ties were handled using the Efron method and each analysis was stratified by site. Final, multivariate models were determined using backward selection from all predictors significant in univariate analysis at the p < 0.1 level. Because of strong associations with CD4 and HIV viral load, WHO HIV stage was excluded from multivariate analysis. Treatment arm (acyclovir versus placebo) and gender were retained to determine associations after adjustment for other predictors included in the final model. Of note, ART use did not include antiretrovirals used for prevention of mother-to-child transmission of HIV-1.
To evaluation simultaneously the influence of HIV-1 status and, among those HIV-1-seropositive, time-varying measures of immune suppression, generalized estimating equations (GEE) were performed with a Poisson link, an exchangeable correlation structure, and log(time) as an offset . This method took advantage of the paired nature of study participants and allowed appropriate handling of the association between couples, while also permitting generalization of subsequent inference to between-person differences in HIV-1 status. The Poisson link in these GEE models provided risk ratios for the incidence of death, and permitted computation of excess mortality attributable to HIV-1 via transformation of regression coefficients. The delta-method was used to compute the variability of excess mortality (see Additional file 1: Methods) . Our primary analyses examined the risk for death from a medical cause; to assess the robustness of our findings, sensitivity analyses were performed.
Demographic and clinical characteristics, by partner type
HIV-1 infected partner
(N = 3295)
(N = 3295)
(n = 1073)
(n = 2222)
(n = 2222)
(n = 1073)
Age, median (IQR)
30 (25, 35)
35 (30, 42)
31 (25, 38)
Married to study partner
Cohabiting with study partner
>8 years of education completed
CD4, median, cells/mm3 (IQR)
426 (334, 571)
481 (354, 664)
394 (276, 544)
437 (312, 617)
HIV-1 plasma RNA, median, log10 copies/mL (IQR)
4.2 (3.5, 4.8)
3.8 (3.0, 4.4)
4.4 (3.6, 5.0)
4.0 (3.2, 4.7)
Ever on ART over follow up
Highest WHO stage of HIV-1
Mortality among HIV-1 infected participants
Univariate and multivariate Cox regression models of predictors of death attributed to medical causes among HIV-1 infected participants
CD4 cell count
2.7 (1.2, 5.6)
2.2 (1.0, 4.9)
4.1 (1.9, 8.6)
2.6 (1.2, 5.9)
8.0 (3.6, 17.7)
3.5 (1.4, 8.5)
Plasma HIV-1 RNA
10 K-50 K
0.5 (0.2, 1.2)
0.5 (0.2, 1.3)
50 K-100 K
1.7 (0.7, 4.1)
1.4 (0.6, 3.6)
5.7 (3.2, 10.0)
†5.8 (2.9, 11.4)
5.6 (2.7, 11.5)
†9.8 (4.1, 23.8)
WHO HIV Stage
3.1 (1.8, 5.1)
15.7 (6.3, 39.4)
0.7 (0.4, 1.1)
0.9 (0.6, 1.5)
1.2 (0.5, 2.6)
1.7 (0.8, 3.6)
Type of housing
1.6 (1.0, 2.7)
0.8 (0.5, 1.3)
1.0 (0.6, 1.6)
Two hundred and ninety persons initiated ART. ART use accounted for 3.8% of follow-up time of HIV-1 seropositive partners (197 of 5170 person-years). Median CD4 count when last measured in clinic prior to ART initiation was 221 (range 11 – 1618). Median time between most recent CD4 count measurement at clinic and first report of ART initiation was 4 months (range 0 – 10). Eleven persons died following ART initiation: six died within three months of ART initiation and an additional four persons died between four and six months after initiation. The crude incidence rate of death prior to ART use was 63 per 4972 person year,s or 13 per 1000, while the incidence following ART initiation was 11 in 197 person years, or 56 per 1000. These rates can be further broken down into 6 in 69 person years (87 per 1000) within six months of ART initiation and 5 in 128 person-years (39 per 1000) at least six months after initiation.
Comparison of mortality within couples
The number of deaths from medical causes was higher among HIV-1 infected participants than HIV-1 uninfected participants (71 vs. 18 deaths, p <0.001, respectively). In sensitivity analyses, these differences remained significant when we restricted the analysis to married couples who reported living together (55 vs. 14, p < 0.001), or to deaths that occurred within the first year of follow up (38 vs. 14, p = 0.001), or all-cause mortality, including trauma (74 vs. 25, p < 0.001).
Comparison of death rates by partner type and gender
Mortality per 1000 PY
Hazard Ratio (95%CI)
3.7 (2.2, 6.2)
1.0 (0.7, 1.6)
0.4 (0.1, 1.3)
0.7 (0.4, 1.1)
2.8 (1.8, 4.4)
0.9 (0.6, 1.3)
0.3 (0.1, 0.9)
0.7 (0.4, 1.0)
Causes of death
Causes of death by partner type
HIV-1 infected (%)
HIV-1 uninfected (%)
Trauma or Injury
Pneumonia and other respiratory illness
Gastrointestinal infections and related disorders
Excess mortality according to CD4 cell count and plasma HIV-1 RNA category among HIV-1 infected participants, after adjusting for ART use
Incidence ofmedical death
Estimated excess mortality per 1000 person-years (95% CI)
Number needed to treat per year (95% CI) to avert 1 death
10.2 (6.9, 13.5)
CD4 cell count
1.2 (−1.8, 4.2)
8.9 (3.8, 14.0)
15.2 (8.1, 22.2)
29.3 (13.9, 44.7)
HIV-1 <10 K
2.0 (−1.1, 5.0)
10 K-50 K
−0.6 (−3.4, 2.3)
50 K-100 K
6.7 (−0.6, 14.0)
43.0† (29.6, 56.4)
Furthermore, persons with a high plasma HIV-1 RNA experienced excess deaths in comparison to HIV-1 uninfected persons, with 43.0 excess deaths/1000 person-years (95%CI: 29.6 – 56.4) for HIV-1 infected persons with viral load greater than 100,000 (among those not taking ART). An interaction term between ART and high HIV viral load (>100 K) was present in the model. No excess mortality was found to be associated with plasma HIV-1 RNA prior to initiating ART for those who began ART (p = 0.58).
Number needed to treat
Assuming that ART can effectively reverse immunosuppression and result in a life expectancy similar to that of HIV-1 uninfected persons, as has been observed in resource-rich countries that have ART initiation guidelines with higher CD4 counts, we calculated the number of HIV-1infected persons needed to treat with ART per year to avert a death at each stratum of CD4 cell count and HIV-1 viral load. At CD4 counts less than 250 cells/μl, 34 persons need to receive ART per year to avert one death attributable to HIV infection in this cohort with a median follow-up of 20 months. At CD4 counts in the range 250 – 349 cells/μl and 350 – 499 cells/μl, 66 and 113 persons, respectively, need to be treated to avert one death.
Our study shows that among African HIV-1 serodiscordant couples, who likely share many determinants of health such as socioeconomic status, nutrition and infectious disease exposures, mortality was higher in the HIV-1 infected partner at all but the highest levels of CD4 cell count (>500 cells/μl). We calculated the excess mortality within CD4 cell categories and found that appreciable excess mortality remains, even above CD4 cell counts that prompt initiation of ART according to current WHO guidelines (CD4 ≤ 350 cells/μl), or as currently implemented in many African countries (CD4 ≤ 250 or 200 cells/μl). Given that the excess mortality attributable to HIV-1 is noted at all but the highest levels of CD4 count, aligning the goal of reducing HIV-1-related mortality to revisions of treatment guidelines will likely require further increases in the CD4 threshold for ART initiation.
Few studies have examined the impact of HIV-1 infection with CD4 counts above 200 cells/μl in sub-Saharan Africa. A recent multicohort analysis examining mortality according to CD4 count at which ART was initiated did not include cohorts from Africa . Analyses from the International epidemiological Databases to Evaluate (IeDEA) collaboration examining cohort data from West Africa and Southern Africa indicate that persons initiating ART with CD4 counts above 200 cells/μl have a residual excess mortality of 10.0 (for persons with less advanced clinical staging) to 35.9 deaths per 1000 person-years (for those with more advanced clinical disease) up to 24 months on therapy, compared to country-level estimates of HIV-free mortality . The ART-LINC collaboration reported that mortality in the first year of ART was 6.4% in programs with active retention strategies, with mortality in the period immediately following initiation of therapy being higher than after six months . However, only a small minority of subjects in that analysis were enrolled with a baseline CD4 count above 350 cells/μl, and those that were initiated therapy due to clinical progression or other conditions indicating advanced immunosuppression.
In our analysis, ART use was associated with a significantly increased risk of death. It is likely that this reflects confounding by indication , as ART is initiated in patients with the highest risk of mortality due to advanced HIV-1 disease. Further, since ART was prescribed outside of the study and there was a time lag between laboratory measures performed at study clinics and drug prescription, those on ART are likely to be at lower CD4 count than assessed in clinic; therefore, the observed associations between mortality and CD4 count are also likely to be conservatively biased. We observed that the risk of death fell after six months of therapy. In patients with low CD4 count, initiation of ART is associated with a substantial mortality from immune reconstitution inflammatory syndrome, which may have contributed to this finding . Even though the final model included a number of factors that serve as indicators for ART initiation, we retained ART in the final model to fully describe factors associated with mortality.
In our study, both low CD4 count and high plasma HIV RNA level were independently predictive of poorer survival. This mirrors other studies from developed countries demonstrating an additional predictive role for measure of viremia [26, 27]. Translation of this finding to a useful clinical stratification tool has been more complex. In African treatment programs, treatment initiation is guided by clinical findings and CD4 count, with rare or no measurement of viral load prior to ART. A clinical trial evaluating a combination HIV prevention strategy in Botswana will use viral load as an eligibility criterion  (NCT01583439).
Our findings add to the prior evidence of the prognostic significance of increased HIV-1 RNA levels for a given CD4 count. The association of level of viremia with mortality would also provide support for those advocating for increased use of viral load monitoring, while recognizing the success of African treatment programs has largely rested on their public health orientation, and that cost is a major factor for limited use. An additional consideration supporting wider use of viral load monitoring is that plasma HIV-1 RNA also predicts risk of transmission, and thus remains an important measure of the likelihood of further transmission of HIV-1 in the community [29, 30].
Our study has several strengths. The observations are drawn from a large cohort of HIV-1 serodiscordant couples in Africa. Active outreach efforts to track those with loss to follow-up resulted in excellent retention, and it is likely that few or no deaths were not identified or reported. The diversity of 14 rural and urban sites in seven East and Southern African countries included participants living in a broader range of socioeconomic conditions than might be seen in highly localized study populations, such as demographic surveillance sites. The paired nature of the data provided a comparison group that can more carefully account for many of the socio-economic determinants of health than may be possible through a general community or country-level comparison.
We assumed that economic resources and access to care were shared equally within the couple. Such an assumption may not be correct in all cases, as the man may control a disproportionate amount of resources available within the family. Women have a marginalized status in some African societies . Should such marginalization undermine our assumption of equitable access to resources and limit access to care, we might have expected to observe higher mortality among women participating in the trial. Our findings suggest otherwise, in that we observed a higher rate of all-cause death among men, once stratified by HIV-status, albeit not a statistically significant finding. Thus we found no reason to infer that power differentials related to gender were significantly impeding women’s access to care, or if present, were overshadowed by differential healthcare seeking behaviour [32, 33]. Furthermore, the couples that chose to participate in a discordant couples’ trial may not reflect couples in a general population. The increased mortality among men has been noted in HIV-1/TB co-infected patients attending care in Soweto . Other studies have also noted higher mortality among men related to trauma . There is a need to investigate barriers to men accessing care and understand factors associated with higher mortality in men.
HIV-1 is also known to have deleterious impacts on the socioeconomic status of households . It is not clear what effect, if any, such a phenomenon might have had in this cohort, and whether any negative impacts would have more significantly impacted the HIV-1 infected or HIV-1 uninfected participant. Most sites conducted the study in or adjacent to a health care facility, which may have also skewed the distribution of socio-economic status of study participants. Differences in socio-economic status between facility-based and community-based patient samples attending HIV-1 care have been noted in the African context .
In summary, our data confirm the large contribution from HIV-1 to mortality in adults in the African setting. Our data also indicate that the excess mortality was highest in those with CD4 counts below 250 cells/μl, although a significant excess remained at all CD4 categories below 500 cells/μl. Thus, our results support increasing the CD4 threshold for treatment initiation, together with expanding HIV testing for asymptomatic persons in the community, if the goal of reducing HIV-1-related excess mortality is to be achieved. Determination of plasma HIV-1 RNA measures may further aid in identifying those individuals at higher risk of rapid disease progression and HIV-1 transmission.
Bill and Melinda Gates Foundation (grant ID #26469); NIH grant AI-30731 (AM, AW) and AI-083034 (JMB, CC).
Partners in Prevention HSV/HIV-1 Transmission Study Team
University of Washington Coordinating Center and Central Laboratories, Seattle, USA: Connie Celum (principal investigator), Anna Wald (protocol co-chair), Jairam Lingappa (medical director), Jared M. Baeten, Mary Campbell, Lawrence Corey, Robert W. Coombs, James P. Hughes, Amalia Magaret, M. Juliana McElrath, Rhoda Morrow, James I. Mullins
Study sites and site principal investigators:
Cape Town, South Africa (University of Cape Town): David Coetzee; Eldoret, Kenya (Moi University, Indiana University): Kenneth Fife, Edwin Were; Gaborone, Botswana (Botswana Harvard Partnership): Max Essex, Joseph Makhema; Kampala, Uganda (Infectious Disease Institute, Makerere University): Elly Katabira, Allan Ronald; Kigali, Rwanda (Rwanda Zambia HIV-1 Research Group, and Emory University): Susan Allen, Kayitesi Kayitenkore, Etienne Karita; Kisumu, Kenya (Kenya Medical Research Institute, University of California San Francisco): Elizabeth Bukusi, Craig Cohen; Kitwe, Zambia (Rwanda Zambia HIV-1 Research Group, and Emory University): Susan Allen, William Kanweka; Lusaka, Zambia (Rwanda Zambia HIV-1 Research Group, and Emory University): Susan Allen, Bellington Vwalika; Moshi, Tanzania (Kilimanjaro Christian Medical College, Harvard University): Saidi Kapiga, Rachel Manongi; Nairobi, Kenya (University of Nairobi, University of Washington): Carey Farquhar, Grace John-Stewart, James Kiarie; Ndola, Zambia (Rwanda Zambia HIV-1 Research Group, and Emory University): Susan Allen, Mubiana Inambao; Orange Farm, South Africa (Reproductive Health Research Unit, University of the Witwatersrand): Sinead Delany-Moretlwe, Helen Rees; Soweto, South Africa (Perinatal HIV-1 Research Unit, University of the Witwatersrand): Guy de Bruyn, Glenda Gray, James McIntyre; Thika, Kenya (University of Nairobi, University of Washington): Nelly Rwamba Mugo.
Data management was provided by DF/Net Research, Inc. (Seattle, USA) and site laboratory oversight was provided by Contract Lab Services (University of the Witwatersrand, Johannesburg, South Africa).
Role of the funding source
The authors designed and undertook the study, had full access to the raw data, did all analyses, wrote the report, and had final responsibility for the decision to submit for publication. The funder had no role in design, data collection, analysis, interpretation, or writing of the report.
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