GUEST POST: BY DR. WILLIAM PARKER, The Autism/Acetaminophen Link – Summary of Research

I am leaving for Russia in a little more than a week, to talk about the therapeutic use of helminths in autism at the Autism Challenges and Solutions Conference, in Moscow.  Also speaking there is Dr. William Parker, one of the foremost researchers into the immunological effects of helminths.  I have talked about William many times on this blog.  As you know, I’ve been a fan since first reading his work back in 2010.  William is covering the microbiome/autism connection at the conference so our talks are synergistic, and he actually speaks just prior to me.  He’s promised me a great introduction.  I’ll let you all know how he does!

Anyway, William called me a couple of  nights ago to catch up and chat about our upcoming trip – but we ended up spending a good portion of an hour talking about his latest research, on the toxic effects of acetaminophen.

William asked me to share his summary of that research (see below), which was conducted with colleagues from both Duke and Harvard, and was published last month.  This is simply too important for you not to know, especially if you are thinking of having a baby or have a young child.  Please! – pass this on to anyone you know who may benefit!

I told William this depresses the hell out of me (Alex undoubtedly had a load given him when he was re-hospitalized at 36 hours old – more about that in a future post)…but he told me that now that they are isolating the exact mechanism by which acetaminophen does harm, it’s more likely they can come up with treatments in the future.  Well…I can only live in hope.

_________

By William Parker, PhD

Department of Surgery

Duke University Medical Center

Durham, NC 27710

Mounting data pointing at the potential for acetaminophen exposure during early childhood to induce autism in children. A review from scientists and clinicians at Duke and Harvard.

A summary of the evidence presented in the review recently published in the Journals of International Medical Research (http://journals.sagepub.com/doi/pdf/10.1177/0300060517693423) is presented here. Citations for this information can be found in the review, which is open access and contains 195 references.

  1. The review cites eight peer-reviewed studies (there are more*) which now demonstrate that acetaminophen exposure is neurotoxic to the developing brain of humans. Seven of these studies evaluated the effect on children following exposure in utero. Effects of exposure evaluated by various groups included lowered IQ, autism, and behavioral problems. The only study to evaluate the effect of exposure after birth found more than a 60-fold greater risk (literally) of developing autism following exposure after birth than studies looking at the risk of exposure before birth.
  2. A very wide range of factors, all of which are associated with inflammation and oxidative stress, are in turn associated with an increased risk of autism. Thus, it appears that whatever is inducing the epidemic of autism probably acts in concert with inflammation and oxidative stress. This conclusion is consistent with the hypothesis that acetaminophen exposure to infants and children after birth is a leading cause of autism.
  3. Laboratory animals develop permanent brain damage characterized by problems with social function when they are exposed to acetaminophen during an early period of brain development that corresponds to human infancy.
  4. Margaret McCarthy, chair of Pharmacology at the University of Maryland, has elucidated the mechanism by which acetaminophen damages the developing brain, and has explained why acetaminophen is more dangerous to males than to females. This potentially accounts for the increased propensity for males to acquire autism compared to females.
  5. Acetaminophen substantially alters brain chemistry, and temporarily impairs awareness of social issues in adult humans. Although the drug could naively be considered to be anti-inflammatory, exposure to the drug actually causes inflammation, even in healthy adults, and depletes metabolic components needed to deal with inflammation. Further, the drug is immunosuppressive, blocking an important immune function (the febrile response).
  6. No study has ever shown acetaminophen to be safe for the developing brain of a human or a laboratory animal. A major manufacturer of acetaminophen in the US acknowledges that the drug was never proven safe for brain development when used during pregnancy or in childhood. All safety tests that have been conducted were performed with the assumption that any side effects would be acute in nature (e.g., bleeding or organ damage soon after administration of the drug).
  7. A very wide range of circumstantial evidence** points toward the potential for acetaminophen to be at the root of many if not most cases of autism:

(a)   The epidemiology of autism matches the historic use of acetaminophen, with both rising sharply in the early 1980s following the identification of Reye Syndrome as a possible side effect of aspirin use in children.

(b)   The qualitative nature of autism apparently shifted from infantile to regressive at the same time that acetaminophen use in infants and children became more popular, in the early to mid-1980s. Other than post-birth acetaminophen exposure as a major inducer of autism, no other plausible explanation for this observation is known to exist.

(c)   A wide range of inflammatory conditions that affect the potential to tolerate oxidative stress are associated with autism. It is expected that these conditions will adversely affect metabolism of acetaminophen. A notable exception is cystic fibrosis, a condition of oxidative stress not known to be associated with autism. Cystic fibrosis is also unusual as a condition of oxidative stress that actually enhances rather than impairs metabolism of acetaminophen. Other than post-birth acetaminophen exposure as a major inducer of autism, no other plausible explanation for this observation is known to exist.

(d)  The number of possible environmental suspects for the induction of autism at a level that would account for the epidemic is dwindling, leaving acetaminophen use in infants and small children as one of the few remaining suspects. A good suspect is one which is newly (since 1980) and widely introduced into the population, and which should be associated with a profoundly large (10-fold or greater) increase in risk of autism. Most suspects tested to date have shown moderate and sometimes variable (dependent on the population studied) associations with autism.

(e)   Genetic variants associated with autism, many associated with oxidative stress, likely influence the metabolism of acetaminophen.

(f)   Circumcision has been identified as a significant risk factor for autism, and the only reasonable explanation put forth for this observation is that acetaminophen use during the procedure is probably inducing autism.

(g)  History demonstrates to us that it is a mistake to ignore the observations of parents when it pertains to autism. Many parents who have historically blamed vaccines for their child’s autism may have actually observed the effects of acetaminophen. In the 1990s, vaccination was advertised as the number one indication for use of acetaminophen. Other than post-birth acetaminophen exposure as a major inducer of autism, no other plausible explanation for this observation is known to exist.

(h)  The idea that acetaminophen use, particularly in infants and small children, is responsible for many if not most cases of autism is an attractive hypothesis, as it satisfies Occam’s Razor in being a simple explanation that explains a wide range of observations.

Conclusions of the review:

  1. There are several unknowns: We have almost no idea just how much benefit that acetaminophen actually provides. (That was never tested.) Perhaps it can be easily replaced by non-pharmaceutical means of reducing fevers, and perhaps not. Second, we don’t know exactly how much neurological damage acetaminophen causes when administered to infants and children.
  2. Despite unknowns, given the preponderance of evidence described above, we conclude that parents and doctors should know all available facts so that they can make informed decisions about use of acetaminophen.
  3. An incisive study needs to be done as quickly as possible, with all available resources at its disposal. Despite the fact that acetaminophen is the most popular drug used in infants, children, and pregnant women, neither the benefits nor the risks of using the drug in those populations have been thoroughly evaluated.
  4. The cost of an incisive study would cost less than the cost of raising and caring for three individuals with autism. Just three.

* Our review cites 8 papers, but there are others, and more on the way.

  • Skovlund and colleagues found that acetaminophen use but not opioid use during pregnancy is associated with a reduction in communication skills. (https://www.ncbi.nlm.nih.gov/pubmed/28168770)
  • A study by Liew et al (Epidemiology 2016; 27: 912–918) showing lower IQ associated with acetaminophen use during pregnancy is cited in our review but not counted as one of the 8 studies listed as showing neurotoxic effects of acetaminophen during development.
  • Vlenterie and colleagues found communication problems and delayed motor milestone attainment associated with acetaminophen use during pregnancy. (https://www.ncbi.nlm.nih.gov/pubmed/27585674)

** Additional circumstantial evidence exists, but was not cited in our review. For example, the unexplained and unusually high prevalence of autism in South Korea (https://www.ncbi.nlm.nih.gov/pubmed/21558103) just happens to occur in a country where children’s acetaminophen capsules were inadvertently overloaded with active ingredient (http://www.saul.com/sites/default/files/3591_WCW062513tcgmp.pdf).


One thought on “GUEST POST: BY DR. WILLIAM PARKER, The Autism/Acetaminophen Link – Summary of Research

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s