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The Systems Theory of Autistogenesis

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  • J. Patrick Malone

Abstract

The systems theory of autistogenesis accounts for genetic and environmental predisposing factors for pervasive developmental disorders. During development, regions of the brain myelinate differentially, even while neuroinflammatory events induce neurological damage. Incorrect dietary ratios of docosahexaenoic acid (DHA) to arachidonic acid (AA) promote developmental aberration characteristic of autism spectrum disorders (ASD), and commercial infant formulae possesses DHA/AA ratios unsuitable for normal brain development in those predisposed. The aromatase gene regulates DHA/AA metabolism and represents a potential biomarker for ASD. Aromatase converts testosterone to estradiol. Estradiol is neuroprotective and a modulator of oxytocin receptors deficient in autism. Neuroprotective DHA is not well synthesized in males and is regulated by estradiol. Therefore, converging evidence indicates that any disturbance to the autistogenic system linking environment to neurobiology and genetics is capable of inducing developmental disorders with gender disparity.

Suggested Citation

  • J. Patrick Malone, 2012. "The Systems Theory of Autistogenesis," SAGE Open, , vol. 2(2), pages 21582440124, April.
  • Handle: RePEc:sae:sagope:v:2:y:2012:i:2:p:2158244012444281
    DOI: 10.1177/2158244012444281
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    References listed on IDEAS

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    Cited by:

    1. J. Patrick Malone, 2013. "Phenotypic Plasticity, CYP19A1 Pleiotropy, and Maladaptive Selection in Developmental Disorders," SAGE Open, , vol. 3(2), pages 21582440134, May.

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