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The Dangers of Acetaminophen for Neurodevelopment Outweigh Scant Evidence for Long-Term Benefits
William Parker1,2,3, Lauren G Anderson2, John P Jones2
1Department of Psychology and Neuroscience, University of North Carolina, Chapel Hill, NC 27599, USA.
Insights
Acetaminophen (paracetamol) exposure in babies and children is linked to autism spectrum disorder (ASD). Early postpartum exposure poses the greatest risk, potentially causing over 90% of ASD cases.
Area of Science:
- Neuroscience
- Developmental Pediatrics
- Toxicology
Background:
- Acetaminophen (paracetamol) is widely used for pain and fever relief in children.
- Emerging evidence suggests potential neurodevelopmental risks associated with acetaminophen exposure.
- Autism spectrum disorder (ASD) prevalence has increased, prompting investigation into environmental factors.
Purpose of the Study:
- To evaluate the evidence linking acetaminophen exposure to autism spectrum disorder (ASD).
- To estimate the proportion of ASD cases potentially induced by acetaminophen.
- To identify critical neurodevelopmental periods for acetaminophen-induced risks.
Main Methods:
- Review of existing data including animal studies, human observations, temporal correlations, and toxicological data.
- Analysis of acetaminophen's effect on social awareness in adults.
- Estimation of ASD cases induced by acetaminophen during different neurodevelopmental stages.
Main Results:
- Strong evidence suggests acetaminophen exposure induces many ASD cases.
- The early postpartum period is identified as the highest-risk window for acetaminophen-induced ASD.
- Acetaminophen use during early development may account for over 90% of ASD cases.
- Frequent overuse and administration without clear benefit are noted in pediatric populations.
Conclusions:
- Acetaminophen poses a significant risk to neurodevelopment and is linked to autism spectrum disorder.
- The widespread use of acetaminophen in early development warrants a re-evaluation of its pediatric application.
- There is no demonstrated long-term benefit for pediatric use that outweighs the neurodevelopmental risks.
Abstract:
Based on available data that include approximately 20 lines of evidence from studies in laboratory animal models, observations in humans, correlations in time, and pharmacological/toxicological considerations, it has been concluded without reasonable doubt and with no evidence to the contrary that exposure of susceptible babies and children to acetaminophen (paracetamol) induces many, if not most, cases of autism spectrum disorder (ASD). However, the relative number of cases of ASD that might be induced by acetaminophen has not yet been estimated. Here, we examine a variety of evidence, including the acetaminophen-induced reduction of social awareness in adults, the prevalence of ASD through time, and crude estimates of the relative number of ASD cases induced by acetaminophen during various periods of neurodevelopment. We conclude that the very early postpartum period poses the greatest risk for acetaminophen-induced ASD, and that nearly ubiquitous use of acetaminophen during early development could conceivably be responsible for the induction in the vast majority, perhaps 90% or more, of all cases of ASD. Despite over a decade of accumulating evidence that acetaminophen is harmful for neurodevelopment, numerous studies demonstrate that acetaminophen is frequently administered to children in excess of currently approved amounts and under conditions in which it provides no benefit. Further, studies have failed to demonstrate long-term benefits of acetaminophen for the pediatric population, leaving no valid rationale for continued use of the drug in that population given its risks to neurodevelopment.
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