Anemia affects 2 billion people worldwide and is a
serious public health problem (1). There are many potential causes of anemia, but
iron deficiency (ID)7 is considered the major underlying nutritional factor.
Nevertheless, it is difficult to quantify the contribution of ID to anemia.
This is especially true in inflammatory conditions such as HIV disease, where
proinflammatory cytokines induce an anemia of inflammation and alter
biochemical indicators of iron status that are commonly used to diagnose
Based on a small number of studies, between 35 and 69%
of HIV-infected pregnant women from sub-Saharan Africa, the geographic region
most heavily affected by the HIVepidemic, are iron deficient (5–7). Although
there are no studies to our knowledge in HIV-infected women of reproductive
age, there is evidence based on HIV-untested women that the prevalence of ID
may be similar to pregnant women. Furthermore, these studies indicate that more
than one-half of anemia may be associated with ID (8,9). The paucity of studies
on iron status in HIV-infected women in sub-Saharan Africa is an important
research gap, as there is
evidence that ID (10), as well as elevated storage
iron, may lead to adverse HIV-related outcomes. The potential risks of ID and
high storage iron are of special relevance for treatment programs recommending
supplemental iron for women of reproductive age (1). To expand the knowledge on
iron status and its relation to anemia as well as HIV disease progression in
sub-Saharan Africa, we conducted an observational study in HIVinfected women of
childbearing age from Dar es Salaam, Tanzania.
Several studies evaluated the association between high
iron status and adverse HIV-related outcomes in sub-Saharan Africa. Among
HIV-infected pregnant women from Zimbabwe, those with severely depleted iron
stores (SF ,6 mg/L) had only 0.27 times the viral load (95% CI ¼ 0.13,0.53)
compared with participants with SF .24 mg/L (11), whereas in HIV-infected pregnant
women from Malawi, sTfR and SF were not associated with CD4 cell count and
viral load (42). In an evaluation from Kenya in 32 HIV-infected adults, 60 mg
elemental iron given twice weekly for 4 mo did not affect viral load (43). Collectively,
the available evidence indicates that among nonpregnant populations from
developed countries, iron overload disorders occur and may lead to adverse
HIV-related outcomes, possibly due to high exposure to iron for extended
periods of time. The risk of iron overload appears to be lower in developing countries
and less evidence links it to adverse outcomes. If you want to read full text
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