Abstract:Forty-two parents of children with autistic disorder, 15 children with autistic disorder, 17 siblings of children with autistic disorder, and 12 unrelated normal adult controls were studied to determine if immunoglobulins isolated from their plasma would inhibit binding of the 5HT1A agonist, [3H]-8-hydroxy-N,N-dipropyl-2-aminotetralin (DPAT) to 5HT1A receptors in human hippocampal membranes. There were no significant differences among the means of percentage inhibition of DPAT binding of parents, children with… Show more
“…Some authors have suggested that individuals with autism and regression might represent a distinct PDD subtype (Rogers 2004). It has also been hypothesised that regression might follow specific environmental triggers (Kurita 1985;Cook et al 1993;Warren et al 1996;van Gent et al 1997). The possibility of 'environmentally mediated' regression has been investigated indirectly by measuring the rate of autism related milder phenotypes (the broader autism phenotype) amongst the parents of children with autism with and without regression.…”
The characteristics of early developmental regression (EDR) were investigated in individuals with ASD from affected relative pairs recruited to the International Molecular Genetic Study of Autism Consortium (IMGSAC). Four hundred and fifty-eight individuals with ASD were recruited from 226 IMGSAC families. Regression before age 36 months occurred in 23.9% of individuals. The observed concordance rate for EDR within sibling pairs (18.9%) was not significantly above the rate expected under independence (13.5%, p = 0.10). The rate of regression in individuals with ASD from multiplex families was similar to that reported in singleton and epidemiological samples. Regression concordance data were not supportive of a separate familial influence on EDR, other than as a part of autism itself.
“…Some authors have suggested that individuals with autism and regression might represent a distinct PDD subtype (Rogers 2004). It has also been hypothesised that regression might follow specific environmental triggers (Kurita 1985;Cook et al 1993;Warren et al 1996;van Gent et al 1997). The possibility of 'environmentally mediated' regression has been investigated indirectly by measuring the rate of autism related milder phenotypes (the broader autism phenotype) amongst the parents of children with autism with and without regression.…”
The characteristics of early developmental regression (EDR) were investigated in individuals with ASD from affected relative pairs recruited to the International Molecular Genetic Study of Autism Consortium (IMGSAC). Four hundred and fifty-eight individuals with ASD were recruited from 226 IMGSAC families. Regression before age 36 months occurred in 23.9% of individuals. The observed concordance rate for EDR within sibling pairs (18.9%) was not significantly above the rate expected under independence (13.5%, p = 0.10). The rate of regression in individuals with ASD from multiplex families was similar to that reported in singleton and epidemiological samples. Regression concordance data were not supportive of a separate familial influence on EDR, other than as a part of autism itself.
“…This could be compatible with a compensatory increase in serotonin production, explaining the increased levels in blood. It has been suggested that antibodies to serotonin receptors may be characteristic of some children with autism, but Cook et al [1993] presented data discounting that theory. Apter et al [1991] have reviewed the research on tryptophan (the dietary precursor of serotonin) in relation to autistic disorder.…”
“…Viral infection, or the immune response to viral infection, has been proposed to result in antibody production to neurotransmitter receptors such as serotonin binding sites [Todd and Ciaranello, 1985;Singh et al, 1997]. The possibility of immunoreactivity at serotonin binding sites is controversial [Yuwiler et al, 1992;Cook et al, 1993]. Prenatal exposures that might alter brain development by immunologic mechanisms have also been proposed.…”
Section: Evidence For Neuroimmune Insult In Asdmentioning
In no area of developmental pediatric practice is there more controversy regarding the choice of treatment than related to children with autistic spectrum disorders (ASD). Complementary and alternative medical therapies (CAM) are often elected because they are perceived as treating the cause of symptoms rather than the symptoms themselves. CAM used for autism can be divided by proposed mechanism: immune modulation, gastrointestinal, supplements that affect neurotransmitter function, and nonbiologic intervention. Secretin as a therapy for autism is discussed as an example of how a clinical observation rapidly grew to a widespread treatment before well-designed studies demonstrated absence of effect. The plausibility for behavioral effect was not substantiated by clinical studies. CAM used for treatment of autism is examined in terms of rationale, evidence of efficacy, side effects, and additional commentary. Families and clinicians need access to well-designed clinical evidence to assist them in choice of therapies.
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