AZT in Babies- Terrible Risk, Zero Benefit
AZT treatment strategy is based on a number of beliefs. One is that certain biological signals, such as elevated "viral load" and "HIV" antibodies, signify HIV infection. Another is that HIV infection is the cause of AIDS. If either or both of those suppositions are untrue, as some scientists argue [see adjoining article], then all mothers and babies treated in this way are being uselessly exposed to an unquestionably dangerous chemical.
AZT's proven toxicities include severe muscle pain, weakness, and atrophy; heart muscle changes and malfunction; bone marrow suppression, with consequent anemia and loss of all types of blood cells; liver failure; and broad-ranging and sometimes irreversible loss and poisoning of mitochondria, the energy "factories" within our cells. The drug also leads to permanent DNA damage, and studies in mice and monkeys have raised concerns that babies exposed to AZT in the womb will face an increased risk of cancer when they grow up.1
A minority of infants born to HIV-positive mothers show elevated levels of HIV antibodies. Among that minority, many lose their HIV-positive status within about 18 months and are judged not to have been infected, but simply to have inherited the elevated levels of antibodies from their mothers. A European collaborative study by researchers from the Department of Paediatric Epidemiology at London's Institute of Child Health found a natural transmission rate of only 12.9 percent in 372 children, with the researchers declaring, "Estimates in many earlier studies may have been biased upwards."2
So even by conventional reckoning, nearly nine out of ten babies born to HIV-positive mothers cannot receive any benefit from being exposed to AZT.
Screening mothers for HIV and treating both mother and baby with AZT and other antivirals does reduce the proportion of babies who test positive--to as low as 1 or 2 percent in some studies where more than one drug has been used. But this may simply be a result of general suppression of the immune system by the drugs, with resulting reduction in the signals thought to represent HIV positivity. Since there are huge question marks over the validity of the tests, over bias in the interpretation of results, and over what a positive test result means, the crucial question is: What happens to the babies afterwards? Do the antiviral drugs really help children live longer or healthier lives?
The answer appears to be that they don't. US scientist David Rasnick, a member of the South African Government's Advisory Panel on AIDS, told the inquiry in July 2000 that he had "scoured the literature" for evidence of such benefit but was unable to find any. On the contrary, the evidence points in the opposite direction. In June 2000, researchers reported that "rapid disease progression" (defined as occurrence of an AIDS-defining disease or AIDS-related death before 18 months of age) was three times more likely to occur in babies born to mothers treated with AZT than when the mother was untreated. This was despite a halving in the purported infection rate in the AZT-exposed babies.3
Similarly, an Italian study involving more than 200 HIV-positive children found that at three years old, those born to mothers treated with AZT during pregnancy were significantly more likely to have developed severe disease than children whose mothers were not treated. They also had a higher death rate.4 In France, researchers found mitochondrial damage in eight children exposed to AZT in the womb and after birth. Two of the eight died and the others had severe biological and neurological abnormalities.5 Four of the eight had been exposed to AZT and another antiviral drug, lamivudine, and four to AZT alone; none was judged "HIV infected." The findings led the UK's Committee on Safety of Medicines to issue a warning about the risk to babies, in advance of publication of the French study.6
The study also prompted formation of the US Perinatal Safety Review Working Group in February 1999. This group reviewed 353 deaths in more than 20,000 children with and without antiviral drug exposure, and in September the same year reported that it had identified no deaths similar to those reported from France.7 That would be reassuring, were it not for clear evidence from animal and other human studies that AZT and similar drugs are toxic to mitochondria.8 Moreover, the French researchers stated that the symptoms in the children in their study were only identified through a specific search for mitochondrial damage, "and may therefore have not been identified as toxic effects of treatments. Prospective studies designed to investigate this effect are essential."
Long-term consequences of exposing babies to AZT are unknown. In a 1999 study, American researchers found that the chemical becomes incorporated into the DNA of most patients, "including infants exposed to the drug in utero."9 They commented that the biological significance of the immediate damage to DNA, "and potential subsequent events, such as mutagenicity, should be further investigated in large cohorts of HIV-positive individuals." The same authors reported that AZT is "a moderate to strong transplacental carcinogen in mice," leading to tumors in the lungs, liver, and female reproductive organs; that it is readily incorporated into the human placenta; and that "infants exposed to AZT even for short periods of time during gestation may sustain genotoxic damage."1
Increasing the number of drugs used in pregnancy increases the risk to the baby. In New York, an HIV-negative baby whose positive mother received AZT and two other antivirals was born with congestive heart failure secondary to profound, life-threatening anemia. Doctors said the cause was suppression of the baby's bone marrow "by one or more of the antiretroviral agents administered to the mother."11 AZT damage to bone marrow can be long lasting, too. A year after the drug was approved, a 1988 report stated, "Bone marrow changes in patients on zidovudine seem not to be readily reversed when the drug is withdrawn. These findings have serious implications for the use of zidovudine in HIV positive but symptom-free individuals."12 In December 1998, Swiss researchers reported, "Following combination antiretroviral therapy administered during pregnancy, most HIV-positive mothers and about half of their children developed one or more adverse events." Of 30 babies, "the most common adverse event was prematurity (10 infants), followed by anemia (eight)." Two babies had skin tumors, two developed brain hemorrhage, one had a bile duct abnormality, and one had transient hepatitis.13
Some studies have shown high rates of abnormalities in babies exposed to AZT alone. Out of 80 babies born alive to AZT-treated mothers at a hospital in India, 10 percent had birth defects including holes in the chest, abnormal indentations at the base of the spine, misplaced ears, misshapen faces, heart defects, extra digits, and albinism.14 These were probably poor, malnourished babies already at risk of abnormal development. But a New York study showed higher risk of birth anomalies in AZT-exposed babies than in those born to HIV-positive mothers who were not prescribed AZT.15
To cap all of this, a 30,000-word review of the molecular pharmacology of AZT, published in June 1999, presents evidence that AZT's claimed mode of antiviral action cannot be as the manufacturers have proposed, rendering it incapable of exerting anti-HIV effects. On the other hand, the authors conclude, "A number of biochemical mechanisms…predicate the likelihood of widespread, serious toxicity for the use of this drug."16 According to South African lawyer Anthony Brink, this "withering indictment" of AZT "ought to sound its death knell in clinical practice. No doctor whose adult or infant patient sickens or dies on AZT will be safe from damages actions founded on medical negligence after this."17
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