|
Do hormonal contraceptives affect the acquisition and transmission of
sexually transmitted infections (STIs), including HIV? If so, what are the
implications for the provision of these methods, which are among the
world's most widely used contraceptives?
Research is conflicting, largely due to study design difficulties.
However, it is clear that hormonal contraceptives do not protect against
HIV or other STIs. Thus, providers should counsel women at high risk of
HIV/STIs to use a condom during each act of intercourse, even if they are
already using a hormonal method.
In the absence of conclusive research that use of hormonal
contraception increases STI risks, providers should also continue to
promote hormonal contraception when it is appropriate for family planning.
The World Health Organization's contraceptive eligibility guidelines place
no restrictions on the use of any hormonal method by women who are at
increased risk of HIV or other STIs.1
If further research shows hormonal contraception increases STI risks,
providers likely will have several counseling options, says Dr. Charles
Morrison, an FHI epidemiologist and principal investigator for a large
study in Zimbabwe, Thailand and Uganda of the impact of oral contraceptive
and injectable depot-medroxyprogesterone acetate (DMPA) use on HIV
acquisition.
"First, women not exposed to HIV/STIs could continue to use any
form of hormonal contraception that is appropriate for their family
planning needs," he says. "Second, if a strong association were
found between one of the hormonal methods and HIV (but not between another
hormonal method and HIV), clients in countries with high HIV prevalence
could obviously be counseled to use the method that does not present an
increased risk."
If a strong association were found between HIV and both the pill and
DMPA, women could be counseled to consider other effective contraceptives,
such as intrauterine devices. For a woman still choosing hormonal
contraception, it would be essential to counsel condom use for disease
protection in addition to use of the hormonal method. Also, any risk
associated with hormonal contraception would have to be carefully weighed
against the risks of rejecting reliable contraception, and the risks
associated with pregnancy itself, says Dr. Morrison.
Widely used methods
The most widely used hormonal contraceptives are oral contraceptives
(which use a progestin alone or a combination of a progestin and an
estrogen) and progestin-only injectables, primarily DMPA. Oral
contraceptives, used by more than 100 million women worldwide in 2000,2
are the most common modern contraceptive method used in sub-Saharan
Africa, where rates of new HIV infections are high even among
"low-risk" family planning clients. In Southeast Asia and India
-- where the HIV epidemic is growing -- a quarter and a half,
respectively, of those women using a modern contraceptive method use the
pill.3 Progestin-only injectables are used by some 12 million
women worldwide.4
Theoretically, these hormonal contraceptives have the potential to
increase the risk of STI acquisition in a number of ways, since both
estrogen and progestins affect the female genital tract. Oral
contraceptives can cause cervical ectopy, a condition in which a specific
type of cell that lines the inside of the cervical canal extends onto the
outer surface of the cervix, where exposure to sexually transmitted
pathogens is greater. Cervical ectopy appears to increase vulnerability to
some STIs,5 which, in turn, increases a woman's risk of HIV
infection.6 Hormones in the pill and injectables have been
associated with changes in the immune system and, theoretically, could
weaken it.7 Also, use of progestins alone thins the lining of
the vagina, possibly leaving it more susceptible to tears or abrasions
through which STI pathogens could enter the body. Finally, while
progestins alone may inhibit infection by thickening cervical mucus,8they
can decrease vaginal acidity, a condition that facilitates infection.
Research suggests that oral contraceptive users are more likely to
become infected with chlamydia than are non-users.9 Whether
cervical ectopy is directly associated with chlamydial infection, however,
is unknown. Data also are conflicting as to whether hormonal contraception
enhances infection with other STIs, such as gonorrhea. To address such
gaps in knowledge, FHI is conducting among 1,000 U.S. women a prospective
study of the association between DMPA or pill use, the development of
cervical ectopy, and subsequent chlamydial and gonococcal infection.
Results are expected in 2001.
Using the pill appears to reduce symptoms, as well as the incidence, of
pelvic inflammatory disease (PID), caused by untreated gonococcal and
chlamydial infection. But asymptomatic PID still may damage a woman's
fallopian tubes, leaving her at risk for infertility.
Nearly all of some 30 studies of the association between hormonal
contraception and HIV had major limitations, a team from FHI and the
University of Washington, Seattle, WA, USA, concluded in 1998. A British
researcher who reviewed the data from many of the same studies reached the
same conclusion, noting that "no clear or consistent patterns emerge
from these studies."10 However, a significant association
between pill use and increased HIV risk was found by University of
Washington researchers when they analyzed 28 studies grouped by
methodologic quality. When six of the eight best studies detected the
association, researchers concluded that "for women at risk of HIV
infection, oral contraceptive use for prevention of pregnancy should be
accompanied by condom use for prevention of HIV infection."11
Data from studies of progestin-only injectables and HIV/STI risks also
are conflicting, and no published studies are available on the impact of
Norplant, a progestin-only implant, on HIV acquisition. A 1996 study found
an eight-fold increase in simian immunodeficiency virus (SIV) infection in
SIV-exposed monkeys receiving implants that maintained high progestin
levels in their blood, compared to a group of placebo control monkeys
exposed to SIV at a stage of their menstrual cycle when natural
progesterone levels were low. Researchers noted that enhanced HIV
infection was strikingly correlated with progesterone-related thinning of
the monkeys' vaginal lining.12However, monkeys exposed to SIV
throughout the entire menstrual cycle had a much lower risk of infection,
an important observation since women at risk for HIV infection probably
are exposed to the virus throughout most of the menstrual cycle.13
In a recent study of the effect of one DMPA injection, women did not
experience at one or three months the dramatic vaginal thinning previously
seen in monkeys.14Another recent study showed that DMPA use
among 20 women for two to three years did not affect the thickness of the
vaginal lining.15
At a 1996 meeting, experts reviewed human study data and concluded that
an association between hormonal contraceptive use and HIV infection was
questionable. Obtaining more definitive information requires a large,
prospective study of the impact of oral contraceptive and DMPA use on HIV
infection among women in a low-risk, general population, concluded a 1996
National Institute of Child Health and Human Development (NICHD) panel.
The study that FHI is coordinating in Zimbabwe, Thailand and Uganda has
been carefully designed to avoid many of the methodological pitfalls of
earlier studies. Sponsored by NICHD and expected to be completed in 2003,
the study will follow for 15 to 24 months about 6,000 low-risk,
HIV-negative women seen at family planning, maternal/child health, and STI
clinics. Ancillary studies will investigate whether hormonal contraception
affects acquisition of herpes simplex virus (HSV), human papilloma virus
(HPV) and bacterial vaginosis, and the role of these infections in HIV
acquisition. In addition, FHI will investigate the role of hormonal
contraception and HIV subtype on genital shedding of HIV among women who
become infected during the study.
Use of the pill, use of DMPA, and pregnancy are all associated with
greater cervical shedding of HSV, according to a recent study of 273 women
in Mombasa, Kenya, who were infected with both HIV and HSV. "The
increased frequency of HSV shedding in hormonal contraceptive users and
pregnant women may reflect direct effects of the hormones on virus
replication or effects on the immune system's ability to control virus
reactivation," noted the study's authors.16 However,
results of studies of the association between hormonal contraception and
cervical shedding of HIV are limited and inconclusive.
-- Kim Best
References
- World Health Organization. Improving Access to
Quality Care in Family Planning. Medical Eligibility Criteria for
Contraceptive Use. Geneva: World Health Organization, 1996.
- Oral contraceptives -- an update. Popul Rep
2000;Series A(9):1.
- Levels and Trends of Contraceptive Use as
Assessed in 1994. New York: United Nations Population Division,
1996.
- New era for injectables. Popul Rep 1995;Series
K(5):1.
- Louv WC, Austin H, Perlman J, et al. Oral
contraceptive use and the risk of chlamydial and gonococcal
infections. Am J Obstet Gynecol 1989;160(2):396-402; Critchlow
CW, Wölner-Hanssen P, Eschenbach DA, et al. Determinants of cervical
ectopia and of cervicitis: age, oral contraception, specific cervical
infection, smoking, and douching. Am J Obstet Gynecol 1995;173(2):534-43;
McGregor JA, Hammill HA. Contraception and sexually transmitted
diseases: interactions and opportunities. Am J Obstet Gynecol 1993;168(6
Pt 2):2033-41.
- Grosskurth H, Mosha F, Todd J, et al. Impact of
improved treatment of sexually transmitted diseases on HIV infection
in rural Tanzania: randomised controlled trial. Lancet 1995;346(8974):530-36;
Cohen MS. Sexually transmitted diseases enhance HIV transmission: no
longer a hypothesis. Lancet 1998;351(Suppl III):5-7.
- Sonnex C. Influence of ovarian hormones on
urogenital infection. Sex Transm Inf 1998;74(1):11-19; Styrt B,
Sugarman B. Estrogens and infection. Rev Infect Dis 1991;13(6):1139-50;
Schuurs A, Geurts T, Goorissen E, et al. Immunologic effects of
estrogens, progestins, and estrogen-progestin combinations. In
Goldzieher J, ed. Pharmacology of the Contraceptive Steroids.
(New York: Raven Press, 1994)379-99.
- Daly CC, Helling-Giese GE, Mati JK, et al.
Contraceptive methods and the transmission of HIV: implications for
family planning. Genitourin Med 1994;70(2):110-17.
- Cottingham J, Hunter D. Chlamydia trachomatis and
oral contraceptive use: a quantitative review. Genitourin Med 1992;68(4):209-16;
Louv; Kinghorn GR, Waugh MA. Oral contraceptive use and prevalence of
infection with Chlamydia trachomatis in women. Br J Vener
Dis 1981;57(3):187-90; Avonts D, Sercu M, Heyerick P, et al.
Incidence of uncomplicated genital infections in women using oral
contraception or an intrauterine device: a prospective study. Sex
Transm Dis 1990:17(1):23-29; Hart G. Factors associated with
genital chlamydial and gonococcal infection in females. Genitourin
Med 1992;68(4):217-20; Harrison HR, Costin M, Meder JB, et al.
Cervical Chlamydia trachomatis infection in university women:
relationship to history, contraception, ectopy, and cervicitis. Am
J Obstet Gynecol 1985;153(3):244-51.
- Stephenson JM. Systematic review of hormonal
contraception and risk of HIV transmission: when to resist
meta-analysis. AIDS 1998;12(6):545-53.
- Wang CC, Kreiss JK, Reilly M. Risk of HIV infection
in oral contraceptive pill users: a meta-analysis. J Acq Immune
Defic Syndr 1999;21(1):51-58.
- Marx PA, Spira AI, Gettie A, et al. Progesterone
implants enhance SIV vaginal transmission and early virus load. Nat
Med 1996;2(10):1084-89.
- Duerr A, Warren D, Smith D. Contraceptives and HIV
transmission [letter]. Nat Med 1997;3(2):124.
- Mauck CK, Callahan MM, Baker J, et al. The effect of
one injection of Depo-Provera on the human vaginal epithelium and
cervical ectopy. Contraception 1999;60(1):15-24.
- Bahamondes L, Trevisan M, Andrade L, et al. The
effect upon the human vaginal histology of the long-term use of the
injectable contraceptive Depo-Provera. Contraception 2000;62(1)23-27.
- Mostad SB, Kreiss JK, Ryncarz AJ, et al. Cervical
shedding of herpes simplex virus in human immunodeficiency
virus-infected women: effects of hormonal contraception, pregnancy and
vitamin A deficiency. J Infect Dis 2000;181(1):58-63.
For more information, visit Family Health International's Website at www.fhi.org
Go to FHI's Network |