Rush to judgment: the STI-treatment trials and HIV in sub-Saharan Africa

被引:12
作者
Stillwaggon, Eileen [1 ]
Sawers, Larry [2 ]
机构
[1] Gettysburg Coll, Dept Econ, Gettysburg, PA 17325 USA
[2] Amer Univ, Dept Econ, Washington, DC 20016 USA
关键词
HIV; AIDS; RCT; STI; sub-Saharan Africa; sexually transmitted disease and HIV; randomized controlled trial; SEXUALLY-TRANSMITTED-DISEASES; FEMALE GENITAL SCHISTOSOMIASIS; IMMUNODEFICIENCY-VIRUS TYPE-1; PUBLIC-HEALTH; BACTERIAL VAGINOSIS; SYNDROMIC TREATMENT; SEX WORKERS; RANDOMIZED TRIAL; VAGINAL FLORA; RISK-FACTORS;
D O I
10.7448/IAS.18.1.19844
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: The extraordinarily high incidence of HIV in sub-Saharan Africa led to the search for cofactor infections that could explain the high rates of transmission in the region. Genital inflammation and lesions caused by sexually transmitted infections (STIs) were a probable mechanism, and numerous observational studies indicated several STI cofactors. Nine out of the ten randomized controlled trials (RCTs), however, failed to demonstrate that treating STIs could lower HIV incidence. We evaluate all 10 trials to determine if their design permits the conclusion, widely believed, that STI treatment is ineffective in reducing HIV incidence. Discussion: Examination of the trials reveals critical methodological problems sufficient to account for statistically insignificant outcomes in nine of the ten trials. Shortcomings of the trials include weak exposure contrast, confounding, non-differential misclassification, contamination and effect modification, all of which consistently bias the results toward the null. In any future STI-HIV trial, ethical considerations will again require weak exposure contrast. The complexity posed by HIV transmission in the genital microbial environment means that any future STI-HIV trial will face confounding, non-differential misclassification and effect modification. As a result, it is unlikely that additional trials would be able to answer the question of whether STI control reduces HIV incidence. Conclusions: Shortcomings in published RCTs render invalid the conclusion that treating STIs and other cofactor infections is ineffective in HIV prevention. Meta-analyses of observational studies conclude that STIs can raise HIV transmission efficiency two-to fourfold. Health policy is always implemented under uncertainty. Given the known benefits of STI control, the irreparable harm from not treating STIs and the likely decline in HIV incidence resulting from STI control, it is appropriate to expand STI control programmes and to use funds earmarked for HIV prevention to finance those programmes.
引用
收藏
页数:9
相关论文
共 78 条
  • [1] Assessing the validity of clinical trials
    Akobeng, Anthony K.
    [J]. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2008, 47 (03) : 277 - 282
  • [2] [Anonymous], COCHRANE DATABASE SY
  • [3] [Anonymous], GLOB BURD DIS EST DE
  • [4] Acute sexually transmitted infections increase human immunodeficiency virus type 1 plasma viremia, increase plasma type 2 cytokines, and decrease CD4 cell counts
    Anzala, AO
    Simonsen, JN
    Kimani, J
    Ball, TB
    Nagelkerke, NJD
    Rutherford, J
    Ngugi, EN
    Bwayo, JJ
    Plummer, FA
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (02) : 459 - 466
  • [5] Association of Oncogenic and Nononcogenic Human Papillomavirus With HIV Incidence
    Auvert, Bertran
    Lissouba, Pascale
    Cutler, Ewalde
    Zarca, Kevin
    Puren, Adrian
    Taljaard, Dirk
    [J]. JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2010, 53 (01) : 111 - 116
  • [6] Human immunodeficiency virus transmission and the role of other sexually transmitted diseases - Measures of association and study design
    Boily, MC
    Anderson, RM
    [J]. SEXUALLY TRANSMITTED DISEASES, 1996, 23 (04) : 312 - 332
  • [7] Cartwright N., 2007, BioSocieties, V2, P11, DOI [10.1017/S1745855207005029, DOI 10.1017/S1745855207005029]
  • [8] Acyclovir and Transmission of HIV-1 from Persons Infected with HIV-1 and HSV-2
    Celum, C.
    Wald, A.
    Lingappa, J. R.
    Magaret, A. S.
    Wang, R. S.
    Mugo, N.
    Mujugira, A.
    Baeten, J. M.
    Mullins, J. I.
    Hughes, J. P.
    Bukusi, E. A.
    Cohen, C. R.
    Katabira, E.
    Ronald, A.
    Kiarie, J.
    Farquhar, C.
    Stewart, G. J.
    Makhema, J.
    Essex, M.
    Were, E.
    Fife, K. H.
    de Bruyn, G.
    Gray, G. E.
    McIntyre, J. A.
    Manongi, R.
    Kapiga, S.
    Coetzee, D.
    Allen, S.
    Inambao, M.
    Kayitenkore, K.
    Karita, E.
    Kanweka, W.
    Delany, S.
    Rees, H.
    Vwalika, B.
    Stevens, W.
    Campbell, M. S.
    Thomas, K. K.
    Coombs, R. W.
    Morrow, R.
    Whittington, W. L. H.
    McElrath, M. J.
    Barnes, L.
    Ridzon, R.
    Corey, L.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (05) : 427 - 439
  • [9] Effect of aciclovir on HIV-1 acquisition in herpes simplex virus 2 seropositive women and men who have sex with men: a randomised, double-blind, placebo-controlled trial
    Celum, Connie
    Wald, Anna
    Hughes, James
    Sanchez, Jorge
    Reid, Stewart
    Delany-Moretlwe, Sinead
    Cowan, Frances
    Casapia, Martin
    Ortiz, Abner
    Fuchs, Jonathan
    Buchbinder, Susan
    Koblin, Beryl
    Zwerski, Sheryl
    Rose, Scott
    Wang, Jing
    Corey, Lawrence
    [J]. LANCET, 2008, 371 (9630) : 2109 - 2119
  • [10] Bacterial Vaginosis Associated with Increased Risk of Female-to-Male HIV-1 Transmission: A Prospective Cohort Analysis among African Couples
    Cohen, Craig R.
    Lingappa, Jairam R.
    Baeten, Jared M.
    Ngayo, Musa O.
    Spiegel, Carol A.
    Hong, Ting
    Donnell, Deborah
    Celum, Connie
    Kapiga, Saidi
    Delany, Sinead
    Bukusi, Elizabeth A.
    [J]. PLOS MEDICINE, 2012, 9 (06) : 18