Exclusive
early breast-feeding is associated
with a lower rate of mother-to-child HIV transmission
compared with mixed feeding in developing countries, and use of antiretroviral
therapy may further reduce the risk, according to 2 recently published studies.
Currently,
in developed countries where clean water and a reliable supply of safe infant
formula can be assured, HIV positive women are advised not to breast-feed. However,
in resource-limited settings, the World Health Organization (WHO) recommends breast-feeding,
especially during the first 6 months, unless formula-feeding is acceptable, feasible,
affordable, sustainable, and safe.
Exclusive
Breast-feeding
As
reported in the March 31, 2007 issue of The Lancet, researchers with the
Africa Center for Health and Population Studies assessed the risk of HIV transmission
and infant survival associated with exclusive breast-feeding and other types of
infant feeding. This non-randomized intervention cohort study included 1372 HIV
positive and 1345 HIV negative pregnant women attending prenatal clinics in KwaZulu
Natal, South Africa. For 6 months, infant feeding data were obtained every week
from the mothers (who kept feeding diaries) and blood samples from infants were
drawn monthly to assess HIV infection status.
Results
83% of infants born to HIV
positive mothers were exclusively breast-fed from birth, 8% received exclusive
replacement feeding, and 3% started with a mix of breast-feeding plus other fluids
or solid foods.
For
1276 infants with complete feeding data, the median duration of exclusive breast-feeding
was 159 days.
14.1%
of exclusively breast-fed infants were infected with HIV by 6 weeks of age, and
19.5% by 6 months.
The
estimated risk of HIV infection at 6 months of age was 4.04%.
Breast-fed
infants who received solid foods in addition to breast milk were significantly
more likely to acquire HIV than exclusively breast-fed babies (HR 10.87), as were
infants who received both breast milk and formula (HR 1.82).
The
cumulative 3-month mortality among exclusively breast-fed infants was 6.1%, compared
with 15.1% for infants who received breast milk plus solid foods or formula (HR
2.06).
The
risk on infant HIV infection was significantly associated with maternal CD4 cell
count below 200 cells/mm3 (HR 3.79) and birth weight less than 2500 g (HR 1.81).
Based
on these findings, the authors concluded, "The association between mixed
breast-feeding and increased HIV transmission risk, together with evidence that
exclusive breast-feeding can be successfully supported in HIV-infected women,
warrant revision of the present UNICEF, WHO, and UNAIDS infant feeding guidelines." Accumulating
evidence - such as that provided by a recent outbreak of diarrhea among formula-fed
infants in Botswana "Formula-feeding Linked to Infant Diarrhea Outbreak in
Botswana" - suggests that for HIV positive women in developing countries,
the benefits of breast-feeding may outweigh the risk of HIV transmission (about
1% per month). Furthermore, studies reported at the recent 14th
Conference on Retroviruses and Opportunistic Infections showed that early
weaning before 6 months was not associated with a decreased risk of HIV transmission
compared with continued breast-feeding.
Antiretroviral
Therapy
The
authors of the South African study suggested that "initiation of [antiretroviral]
treatment should be an overriding priority" for HIV positive pregnant
women.
This recommendation
is supported by another recent study reported in the March 1, 2007 Journal
of Acquired Immune Deficiency Syndromes. Italian researchers assessed the
effect of antiretroviral treatment on breast milk viral load and determined plasma
and breast milk drug concentrations in pregnant women taking part in the Drug
Resource Enhancement Against AIDS and Malnutrition (DREAM) program in Mozambique.
The study included
40 women receiving combination therapy with AZT
(zidovudine; Retrovir), 3TC (lamivudine;
Epivir), and nevirapine (Viramune)
from 28 weeks of gestation to 1 month postpartum, and 40 untreated pregnant women.
Infants received a single dose of nevirapine within 72 hours of birth; mothers
agreed not to breast-feed and were provided free formula.
Results
Women in the treated group received a median of 85 days of therapy before delivery.
At
delivery, the median plasma viral load was 2.2 log in the treated group compared
with 4.8 log in the untreated group.
At
delivery, in the treated group, the median viral load was higher in breast milk
than plasma (2.3 vs 2.2 log), while the reverse was true in the untreated group
(3.4 vs 4.8 log).
By
day 7, median breast milk viral loads were lower than plasma HIV RNA levels in
both groups.
HIV
RNA levels in breast milk were significantly lower in the treated group compared
with the untreated group:
- At delivery: median 2.3 vs 3.4 log (P <
0.001); - 7 days post-partum: 1.9 vs 3.6 log (P < 0.001).
Among
women with detectable viral loads at delivery, median breast milk concentrations
of nevirapine, AZT, and 3TC were 0.6, 1.1, 1.8, and 1.1 times higher than maternal
plasma concentrations, respectively.
10%
of women had detectable nevirapine in breast milk but not in plasma, suggesting
the drug may be eliminated more slowly from breast milk.
"Antiretroviral
drugs administered during the last trimester of pregnancy and after delivery reach
levels similar to or higher than plasma concentrations in breast milk and can
significantly reduce HIV RNA levels," the authors concluded. "Our data
support the potential role of maternal HAART prophylaxis in reducing the risk
of breast-feeding-associated transmission."
04/10/07
References
HM
Coovadia, NC Rollins, RM Bland, and others. Mother-to-child transmission of HIV-1
infection during exclusive breastfeeding in the first 6 months of life: an intervention
cohort study. Lancet 369(9567): 1107-1116. March 31, 2007.
M Giuliano,
G Guidotti, M Andreotti, and others. Triple Antiretroviral Prophylaxis Administered
During Pregnancy and After Delivery Significantly Reduces Breast Milk Viral Load:
A Study Within the Drug Resource Enhancement Against AIDS and Malnutrition Program.
JAIDS 44(3): 286-291. March 1, 2007.
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