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Male Circumcision and the Risk of HIV Infection

Joseph Inungu, MD, DrPH; Eilen MaloneBeach, PhD; Jeffrey Betts, PhD
AIDS Read. 2005; 15 (3): 130-135. ©2005 Cliggott Publishing, Division of CMP Healthcare Media

Abstract and Introducion

Abstract

Epidemiologic data have suggested that male circumcision is a major protective factor against male heterosexual HIV transmission and may explain the significant geographic differences in the prevalence of HIV observed within sub-Saharan Africa. To assess the evidence of the protective effect of male circumcision, African studies on its association with HIV infection were reviewed. These studies' systematic lack of control of important confounding factors makes the assessment of the association between male circumcision and HIV transmission very difficult and raises doubt about the validity of the current findings. Randomized trials are needed to determine the true strength of the association. Until then, a decision to recommend mass male circumcision to prevent HIV transmission in sub-Saharan Africa is premature and risky.

Introduction

Of the estimated 38 million persons living with HIV infection worldwide, 75% live in sub-Saharan Africa.[1] The majority of them do not have access to antiretroviral therapy, which is known to prolong the lives of HIV-positive persons in industrialized countries. Without an AIDS vaccine or curative treatment, and given the difficulty in getting persons at risk to adopt healthy sexual behaviors, alternative approaches to curb the spread of HIV infection are urgently needed.
Reports about the potential protective effect of male circumcision (the removal of the penis foreskin) against HIV transmission have energized policy makers, health care prac titioners, and researchers alike to further examine this claim.[2-6] Circumcision has been shown to protect against urinary tract infection,[7-10] sexually transmitted diseases (STDs),[11-13] and cervical and penile carcinoma.[14-16] However, other studies have challenged the protective effect of male circumcision against cervical cancer[17] and penile carcinoma.[18] Despite these health benefits, only 25% of the male world population is circumcised.[6] On the other hand, female circumcision, widely practiced among Muslims, Christians, and Animists in countries in or near Africa, is associated with an increased risk of HIV transmission.[19]
The origin of circumcision is shrouded in antiquity.[20] Many nations practice it either as a ritual to initiate male adolescents into adulthood (eg, among the Bantu people in Africa) or as a religious practice (among Jews and Muslims).[21,22] Neonatal circumcision is currently done for medical reasons, such as phimosis or acute balanoposthitis.[7-10,21]
This study was undertaken to determine whether mass prophy lactic circumcision in sub-Saharan Africa to prevent HIV infection is justified in light of the current state of knowledge about the association between male circumcision and risk of HIV infection. Specifically, this review will address the following research questions: What is the evidence that supports the protective effe ct of circumcision against HIV transmission? Is the evidence sufficient to justify mass prophylactic circumcision as a public health strategy to prevent the spread of HIV in sub-Saharan Africa?
The claim that circumcision reduces the risk of HIV infection is based essentially on what is known from epidemiologic studies, from ob servational studies, and from biologic mechanisms.

Epidemiologic Studies

Since the onset of the HIV epidemic, significant geographic differences in the prevalence of HIV infection have been observed among countries and within neighboring regions in the same country.[6,23-25] Data from Africa showed that countries (such as Zimbabwe, Botswana, and Zambia) with a low level of male circumcision (less than 20%) experience a high prevalence of HIV infection (greater than 19%), whereas countries (such as Cameroon, Gabon, and Ghana) with a high level of male circumcision (greater than 80%) have a lower prevalence of HIV infection.[26]
Buve[27] assessed the geographic difference in the prevalence of HIV disease between 2 African cities with a relatively low HIV prevalence (Cotonou in Benin and Yaounde in Cameroon) and 2 other cities with a high HIV prevalence (Kisumu in Kenya and Ndola in Zambia). Given that these cities were similar with regar d to HIV-related risk factors (mode of HIV transmission, number of sexual partners, and so on), the difference in the prevalence of HIV could only be explained by other factors, such as the level of male circumcision and the type of HIV.
Although reports about a strong negative correlation between male circumcision and the prevalence of HIV appear convincing,[26-28] they could not be replicated in industrialized countries. Despite having the highest proportion of circumcised men (80%) among industrialized countries, the United States also has a high prevalence of HIV infection compared with its counterparts.[29] In addition, after plotting the 1995 AIDS prevalence data from the World Health Organization with the estimated circumcision rates, Van Howe[30] found a positive correlation between male circumcision and AIDS prevalence.

Observational Studies

To date, a dozen or more cross-sectional studies,[31-43] case-control studies,[44-46] and cohort studies[2,12,47-49] have examined the association between male circumcision and the risk of HIV infection. While the overwhelming majority of these studies showed that the lack of circumcision was associated with an increased risk of HIV infection, the strength of the association varied greatly among studies. This association was found to be strong in studies of high-risk groups (STD clinic attenders, alcohol users, long-haul truck drivers)[48,49] but weak in studies from the general population.[31,33]
Concerns about the validity of the association between male circumcision and the risk of HIV infection have been raised because of methodologic problems (selection bias, misclassification, and lack of control for confounding variables) associated with studies that have evaluated this association. In addition, not all observational studies reported a negative correlation between circumcision and the risk of HIV infection; some studies failed to find a relationship,[31,50] while others found that circumcision increased the risk of HIV infection.[30,33]

Biologic Mechanisms

While the majority of epidemiologic and observational studies suggest an association between circumcision and the risk of HIV infection, they do not explain how the intact foreskin enhances the spread of HIV infection. Five possible mechanisms have been proposed. First, the foreskin contains a high density of Langerhans cells (the prime target for sexual HIV transmission) compared with cervical, vaginal, or rectal mucosa.[50,51] Second, the foreskin increases the risk of ulcerative STDs, which facilitate the transmission of HIV.[4,52] Third, the susceptibility of the foreskin epithelial cells to disruption during intercourse may facilitate HIV transmission.[52] Fourth, the environment under the foreskin (moisture and temperature) may favor microorganism survival and replication.[12] Fifth, a circumcised penis develops a layer of keratin that minimizes the risk of HIV transmission.[53,54]

Discussion

While the majority of existing studies present compelling evidence about the protective effect of male circumcision against the spread of HIV infection, there are lingering concerns about the validity of this finding.
Skepticism about the relationship between circumcision and low risk of HIV infection stems from several factors. First, the inability to rep licate African observations in industrialized countries raises serious concerns. The proportion of circumcised men in Scandinavian countries and Japan is low (less than 1%), yet the prevalence of HIV infection in these countries is also low. The differences in the mode of HIV transmission, the prevalence of STDs, and the level of education between industrialized and developing regions of the world may explain the difficulty in replicating the African experience.
Second, studies conducted to date are limited by several important biases[30,50-53,55-57]: determination of circumcision status was based on self-report. Potential confounding factors, such as age, religion, number of sexual partners, and history of STDs, were not accounted for in many studies. In a survey of 38 sub-Saharan African countries, Gray[58] found that the percentage of Muslims within a country negatively predicted HIV prevalence. Not controlling for the effect of religion was a serious omission. Moreover, the age of persons at the time of circumcision was often overlooked.[55] Participants who had been sexually active before undergoing circumcision may have distorted the findings. In addition, until the results of randomized trials currently under way are available, it is difficult to determine the strength of the association between circumcision and the risk of HIV infection.
Is the call by Halperin and Bailey[26] for mass prophylactic circumcision in sub-Saharan Africa to prevent the spread of HIV infection justified? No, such a call is premature and risky. The publicity surrounding the potential protective effect of circumcision against HIV transmission has contributed to an increased number of persons seeking circumcision in eastern Africa.[59,60] A significant proportion of persons in southern and eastern Africa believe that male circumcision prevents the transmission of STDs and HIV/AIDS and enhances sexual performance.[18,61] Feeling protected and anxious to "try" their new shape, newly circumcised men may embark on risky sexual behavior.[18,62]
Moreover, to meet the high demand for circumcision, traditional healers and unskilled health care workers are performing this operation under unsanitary conditions, placing their "patients" at risk for sepsis, hemorrhage, tetanus, hepatitis B, HIV infection, partial penile amputation, and death.[63-65] Resources and training are needed to make male circumcision safe and widely available at clinics in Africa. The average price for the procedure (currently $30 with a general practitio ner in South Africa) must be lowered to make it affordable.[66]
The devastating impact of AIDS in sub-Saharan Africa requires urgent, effective, and scientifically sound interventions. The evidence that circumcision lowers the risk of HIV infection is not strong enough to make circumcision part of a public health policy in the fight against HIV/AIDS.[31,33,67] Even if ongoing randomized clinical trials confirm the protective effect of circumcision (R. Bailey, unpublished data, 2005; A. Puren, unpublished data, 2005; R. Gray, unpublished data, 2005), this operation can be used only in conjunction with other effective interventions, such as condom use.
Sub-Saharan Africa needs a comprehensive and thoughtful strategy to fight the HIV epidemic. Such a strategy should include the following cardinal elements:
• Provision of a culturally sensitive approach to promote proven, effective interventions (condom use, monogamous relationships, and/or faithfulness in polygamous relationships) and an effort to address the shame and discrimination associated with HIV infection.
• Prevention, diagnosis, and treatment of all STDs in the community.
• Cooperation with local governments to make low-cost antiretroviral therapy available, especially to pregnant women.
• Empowerment of local persons to become more active in the fight against HIV/AIDS.
To make the fight against HIV/AIDS successful and sustainable, African governments must work toward ensuring political stability, avoiding wars, educating their populations (especially women), alleviating poverty, and creating a healthful environment.

References

1. UNAIDS. A global overview of the AIDS epi demic. Available at: http://www.unaids.org/ bangkok2004/GAR2004_html/GAR2004_00_en.htm. Accessed February 3, 2005.
2. Cameron DW, Simonsen JN, D'Costa LJ, et al. Female to male transmission of human immunodeficiency virus type 1: risk factors for seroconversion in men. Lancet. 1989;2:403-407.
3. Bongaarts J, Reining P, Way P, Conant F. The relationship between male circumcision and HIV infection in African populations. AIDS. 1989;3:373-377.
4. Simonsen JN, Cameron DW, Gakinya MN, et al. Human immunodeficiency virus infection among men with sexually transmitted diseases. Experience from a center in Africa. N Engl J Med. 1988;319:274-278.
5. Moses S, Bradley JE, Nagelkerke NJ, et al. Geographical patterns of male circumcision practices in Africa: association with HIV seroprevalence. Int J Epidemiol. 1990;19:693-697.
6. Carael M, Van de Perre PH, Lepage PH, et al. Human immunodeficiency virus transmission among heterosexual couples in Central Africa. AIDS. 1988;2:201-205.
7. Wiswell TE, Enzenauer RW, Holton ME, et al. Declining frequency of circumcision: implications for changes in the absolute incidence and male to female sex ratio of urinary tract infections in early infancy. Pediatrics. 1987;79:338-342.
8. Wiswell TE, Roscelli JD. Corroborative evidence for the decreased incidence of urinary tract infections in circumcised male infants. Pediatrics. 1986;78:96-99.
9. Schoen EJ, Colby CJ, Ray GT. Newborn circumcision decreases incidence and costs of urinary tract infections during the first year of life. Pediatrics. 2000; 105:789-793.
10. Schoen EJ. Benefits of newborn circumcision: is Europe ignoring medical evidence? Arch Dis Child. 1997;77:258-260.
11. Wilson RA. Circumcision and venereal disease.Can Med Assoc J. 1947;56:54-56.
12. Lavreys L, Rakwar JP, Thompson ML, et al. Effect of circumcision on incidence of human immunodeficiency virus type 1 and other sexually transmitted diseases: a prospective cohort study of trucking company employees in Kenya. J Infect Dis. 1999;180:330-336.
13. Nasio JM, Nagelkerke NJ, Mwatha A, et al. Genital ulcer disease among STD clinic attenders in Nairobi: association with HIV-1 and circumcision status. Int J STD AIDS. 1996;7:410-414.
14. Maden C, Sherman KJ, Beckmann AM, et al. History of circumcision, medical conditions, and sexual activity and risk of penile cancer. J Natl Cancer Inst. 1993;85:19-24.
15. Tsen HF, Morgenstern H, Mack T, Peters RK. Risk factors for penile cancer: results of a population-based case-control study in Los Angeles County (United States). Cancer Causes Control. 2001;12:267-277.
16. Castellsague X, Bosch FX, Munoz N, et al. Male circumcision, penile human papillomavirus infection, and cervical cancer in female partners. N Engl J Med. 2002;346:1105-1112.
17. Stern E, Neely PN. Cancer of the cervix in reference to circumcision and marital history. J Am Med Womens Assoc. 1962;17:739-740.
18. Maiche AG. Epidemiological aspects of cancer of the penis in Finland. Eur J Cancer Prev. 1992;1:153-158.
19. Hrdy DB. Cultural practices contributing to the transmission of human immunodeficiency virus in Africa. Rev Infect Dis. 1987;9:1109-1119.
20. Schneider T. Circumcision and ‘uncircumcision.'S Afr Med J. 1976;50:556-558.
21. Rain-Taljaard RC, Lagarde E, et al. Potential for an intervention based on male circumcision in a South African town with high levels of HIV infection. AIDS Care. 2003;15:315-327.
22. Marck J. Aspects of male circumcision in sub-equatorial African culture history. Health Transit Rev. 1997;7(suppl):337-360.
23. Eyer-Silva WA. Male circumcision and HIV heterosexual transmission. Rev Saude Publica. 2003;37: 678-686.
24. Drain PK, Smith JS, Hughes JP, et al. Correlates of national HIV seroprevalence: an ecologic analysis of 122 developing countries. J Acquir Immune Defic Syndr. 2004;35:407-420.
25. Jansen HA, Morison L, Mosha F, et al. Geographical variations in the prevalence of HIV and other sexually transmitted infections in rural Tanzania. Int J STD AIDS. 2003;14:274-280.
26. Halperin DT, Bailey RC. Male circumcision and HIV infection: 10 years and counting. Lancet. 1999; 354:1813-1815.
27. Buve A. HIV epidemics in Africa: what explains the variations in HIV prevalence? IUBMB Life. 2002; 53:193-195.
28. Boerma JT, Gregson S, Nyamukapa C, Urassa M. Understanding the uneven spread of HIV within Africa: comparative study of biologic, behavioral, and contextual factors in rural populations in Tanzania and Zimbabwe. Sex Transm Dis. 2003;30:779-787.
29. Provisional working estimates of adult HIV prevalence as of end 1994, by country. Wkly Epidemiol Rec. 1995;70:355-357.
30. Van Howe RS. Circumcision and HIV infection: review of the literature and meta-analysis. Int J STD AIDS. 1999;10:8-16.
31. Barongo LR, Borgdorff MW, Mosha FF, et al. The epidemiology of HIV-1 infection in urban areas, roadside settlements and rural villages in Mwanza Region, Tanzania. AIDS. 1992;6:1521-1528.
32. Barongo LR, Borgdorff MW, Newell JN, et al. Intake of a cohort study of urban factory workers in northwest Tanzania. Risk factors for HIV-1 infection. Trop Geogr Med. 1994;46:157-162.
33. Grosskurth H, Mosha F, Todd J, et al. A community trial of the impact of improved sexually transmitted disease treatment on the HIV epidemic in Tanzania: 2. Baseline survey results. AIDS. 1995;9:927-934.
34. Auvert B, Buve A, Ferry B, et al. Ecological and individual level analysis of risk factors for HIV infection in four urban populations in sub-Saharan Africa with different levels of HIV infection. AIDS. 2001;15(suppl 4):S15-S30.
35. Kelly R, Kiwanuka N, Wawer MJ, et al. Age of male circumcision and risk of prevalent HIV infection in rural Uganda. AIDS. 1999;13:399-405.
36. Lankoande S, Meda N, Sangare L, et al. HIV infection in truck drivers in Burkina Faso: a seroprevalence survey [in French]. Med Trop. 1998;58:41-46.
37. Mehendale SM, Shepherd ME, Divekar AD, et al. Evidence for high prevalence & rapid transmission of HIV among individuals attending STD clinics in Pune, India. Indian J Med Res. 1996;104:327-335.
38. Greenblatt RM, Lukehart SA, Plummer FA, et al. Genital ulceration as a risk factor for human immunodeficiency virus infection. AIDS. 1988;2:47-50.
39. Gilks CF, Otieno LS, Brindle RJ, et al. The presentation and outcome of HIV-related disease in Nairobi. Q J Med. 1992;82:25-32.
40. Diallo MO, Ackah AN, Lafontaine MF, et al. HIV-1 and HIV-2 infections in men attending sexually transmitted disease clinics in Abidjan, Cote d'Ivoire. AIDS. 1992;6:581-585.
41. Bwayo J, Plummer F, Omari M, et al. Human immunodeficiency virus infection in long-distance truck drivers in east Africa. Arch Intern Med. 1994; 154:1391-1396.
42. Tyndall MW, Ronald AR, Agoki E, et al. Increased risk of infection with human immunodeficiency virus type 1 among uncircumcised men presenting with genital ulcer disease in Kenya. Clin Infect Dis. 1996;23:449-453.
43. Pepin J, Quigley M, Todd J, et al. Association between HIV-2 infection and genital ulcer diseases among male sexually transmitted disease patients in The Gambia. AIDS. 1992;6:489-493.
44. Pison G, Le Guenno B, Lagarde E, et al. Seasonal migration: a risk factor for HIV infection in rural Senegal. J Acquir Immune Defic Syndr. 1993;6:196-200.
45. MacDonald KS, Malonza I, Chen DK, et al. Vitamin A and risk of HIV-1 seroconversion among Kenyan men with genital ulcers. AIDS. 2001;15:635-639.
46. Sassan-Morokro M, Greenberg AE, Coulibaly IM, et al. High rates of sexual contact with female sex workers, sexually transmitted diseases, and condom neglect among HIV-infected and uninfected men with tuberculosis in Abidjan, Cote d'Ivoire. J Acquir Immune Defic Syndr Hum Retrovirol. 1996;11:183-187.
47. Gray RH, Kiwanuka N, Quinn TC, et al. Male circumcision and HIV acquisition and transmission: cohort studies in Rakai, Uganda. Rakai Project Team. AIDS. 2000;14:2371-2381.
48. Telzak EE, Chiasson MA, Bevier PJ, et al. HIV-1 seroconversion in patients with and without genital ulcer disease. A prospective study. Ann Intern Med. 1993;119:1181-1186.
49. Bloom SS, Urassa M, Isingo R, et al. Community effects on the risk of HIV infection in rural Tanzania. Sex Transm Infect. 2002;78:261-266.
50. Soilleux EJ, Coleman N. Expression of DC-DIGN in human foreskin may facilitate sexual transmission of HIV. J Clin Pathol. 2004;57:77-78.
51. Hussain LA, Lehner T. Comparative investigation of Langerhans' cells and potential receptors for HIV in oral, genitourinary and rectal epithelia. Immunology. 1995;85:475-484.
52. Jessamine PG, Plummer FA, Ndinya Achola JO, et al. Human immunodeficiency virus, genital ulcers and the male foreskin: synergism in HIV-1 transmission. Scand J Infect Dis Suppl. 1990;69:181-186.
53. Nicoll A. Routine male neonatal circumcision and risk of infection with HIV-1 and other sexually transmitted diseases. Arch Dis Child. 1997;77:1994-1995.
54. de Vincenzi I, Mertens T. Male circumcision: a role in HIV prevention? AIDS. 1994;8:153-160.
55. Siegfried N, Muller M, Volmink J, et al. Male circumcision for prevention of heterosexual acquisition of HIV in men. Cochrane Database Syst Rev. 2003;(3): CD003362.
56. O'Farrell N, Egger M. Circumcision in men and the prevention of HIV infection: a ‘meta-analysis' revisited. Int J STD AIDS. 2000;11:137-142.
57. Moses S, Plummer FA, Bradley JE, et al. The association between lack of male circumcision and risk for HIV infection: a review of the epidemiological data. Sex Transm Dis. 1994;21:201-210.
58. Gray PB. HIV and Islam: is HIV prevalence lower among Muslims? Soc Sci Med. 2004;58:1751-1756.
59. Caldwell JC, Caldwell P. The African AIDS epidemic. Sci Am. 1996;274:62-63,66-68.
60. Nnko S, Washija R, Urassa M, Boerma JT. Dynamics of male circumcision practices in northwest Tanzania. Sex Transm Dis. 2001;28:214-218.
61. Lagarde E, Dirk T, Puren A, et al. Acceptability of male circumcision as a tool for preventing HIV infection in a highly infected community in South Africa. AIDS. 2003;17:89-95.
62. Collymore Y. Debate over male circumcision and HIV prompts more research. Population Today. 2001; 29(7):1,4.
63. Menahem S. Complications arising from ritual circumcision: pathogenesis and possible prevention. Isr J Med Sci. 1981;17:45-48.
64. Hiss J, Horowitz A, Kahana T. Fatal haemorrhage following male ritual circumcision. J Clin Forensic Med. 2000;7:32-34.
65. Shenfeld OZ, Ad-El D. Penile reconstruction after complete glans amputation during ritual circumcision [in Hebrew]. Harefuah. 2000;39:352-354, 407.
66. Shillinger K. Male circumcision cited for differing HIV rates among Africans. Available at: http:// www.antipas.org/news/world/circumcision.html. Accessed February 3, 2005.
67. Bailey RC, Plummer FA, Moses S. Male circumcision and HIV prevention: current knowledge and future research directions. Lancet Infect Dis. 2001;1:223-231.