
Although there was no solid evidence that Feingold's approach was effective, this strategy has also been applied to autism. Additionally, other diets have been developed with a variety of hypotheses that also lack scientific confirmation. These diets have been applied as treatments for autism as well as for various other disabilities. However, unless a child has a food allergy/intolerance or metabolic condition it is unlikely that dietary changes will affect their disability. Given that a child with an autistic spectrum disorder (ASD) may also have a food allergy and that gastrointestinal difficulties have been suggested as more prevalent in people with autism, it may be useful to determine whether there is any good reason to think that the gastrointestinal system causes autism.
The "gut theory" of autism has been most popularly promoted by Andrew Wakefield. Wakefield and his colleagues (1998) have suggested an association between chronic gastrointestinal difficulties and autism caused by an insult to the gut that occurs as an adverse reaction to the MMR vaccine. Wakefield's research was somewhat suspect in the soundness of the methods used, especially in how cases were identified for inclusion. It has recently come to light that Wakefield was paid a substantial amount of money by the Legal Aid Board to study whether children were harmed by the MMR before conducting his research (Lyall, 2004). The editor who approved the study's publication stated that he would not have published it had this conflict of interest been disclosed (Lyall). Furthermore, this conflict of interest led 10 of the study's co-authors to retract the suggestion of a link between MMR and autism (Mayor, 2004).
Prior to the recent revelation of unacceptable scientific practice, many investigated Wakefield’s claims. Fombonne and Chakrabarti (2001) did an extensive survey of the potential relation between autism and the MMR vaccine and found that there was no evidence for a relation between the vaccine and autism. Several other studies have confirmed that the MMR is not likely to be associated with autism (e.g., D’Souza et al., 2006). Some concern has also been raised about vaccines containing thimerosal producing autism but no sound scientific evidence exists to support this notion. The most definitive study to date was conducted by Danish researchers (Hviid et al., 2003) who studied well over 2 million children that received either a vaccine containing thimerosal or the same vaccine without this preservative and found that the rates of autism were not higher in the group that received vaccines with thimerosal. Some have said that the MMR (or thimerosal) damages the gut, however, Taylor and his colleagues (2002) in a study with nearly 500 children with an autistic spectrum disorder (ASD) found no relation between the MMR and bowel problems. Looking specifically at gut problems in persons with autism, Black, Kaye and Jick (2002) found that children with ASD were no more likely to have a gastrointestinal problem than their age-matched peers. These studies strongly indicate that there is no link between the gut and autism.
Autism is thought by the scientific community to be of genetic origin (e.g., Folstein & Rosen-Sheidly, 2001; IMGSAC, 2001; Muhle, Trentacoste, & Rapin, 2004). It has also come to be well accepted that ASDs are the manifestation of a neurological condition. Acosta and Pearl (2003) posit that the best scientific evidence indicates that autism likely results from "genetically determined prenatal alterations in brain development." Although we are hopeful that empirically validated biological interventions can be developed to treat or perhaps prevent ASDs, it is more likely that the nature of successful therapy will not target the gastrointestinal system.
Nonetheless, it is still unknown whether a dietary intervention could treat autism. Currently, the most popular diet promoted as a cure for autism involves restricting casein and gluten from the child's diet. The unfounded assumption behind recommending that casein and gluten be restricted is that the processing of these substances causes many of the symptoms of autism. Beside the fact that most of the evidence provided as support for casein/gluten theory of autism comes from individuals involved in selling these products or diet-related advice, the lack of scientific acceptance of casein and gluten processing difficulties as a cause of autism is one good reason to be wary of this approach.
Though children with ASD seem no more likely to have gastrointestinal difficulties, including food allergies, than typically developing children, the fact is that both children with ASD and those who are typically developing can have this problem. It is also the case that children are more likely to have food allergies than adults. So food allergies are clearly an appropriate concern. In fact, at times they can involve severe reactions that are life threatening. Food allergies occur because the body develops antibodies specific to the allergen in the offending food. The next time that this substance is ingested, the antibodies then trigger the release of histamine and an allergic reaction occurs. Most children with a significant food allergy appear sickly. They have symptoms that are typical of an allergic reaction, may vomit frequently, and often have abnormal bowel movements. Shortly after the food the child has an allergy to is ingested, symptoms (e.g., diarrhea, tingling/swelling in the mouth area, difficulty breathing, pronounced rashes especially on the face or torso) appear. Most children outgrow their allergies although it is thought that allergies to nuts (and peanuts), fish, and shellfish are likely life-long allergies.
For over a decade I have worked with children with feeding difficulties with and without ASDs and one frequently encountered cause of a child's feeding problem is food allergy. If a child has a documented food allergy then removing the allergen(s) from the child's diet is one necessary component of resolving the problem. However, determining that the child has a food allergy is a critical first step. If a child is suspected of having an allergy because of symptoms, then there are two tests commonly accepted as valid means of diagnosing food allergy. These are the skin prick and RAST (radioallergosorbent) tests. So long as the allergic reaction is not severe, these tests can then combined with information gathered by alternately exposing or restricting access to the suspected allergen and determining whether symptoms respectively appear and dissipate to confirm test results. For the child with a food allergy, the benefit of removing the allergen will be apparent in that the overt symptoms caused by ingestion of the offending substance will dissipate but if the child has a disability as well, the disability will persist. The child who is no longer in discomfort will also likely be more receptive to instruction and have a more positive affect.
So, why not restrict access to casein and gluten just to make sure you are doing everything you can for your child? First, the lack of scientific evidence that casein and gluten cause autism is concerning. This combined with the evidence that gastrointestinal (GI) difficulties and autism are not linked, should cause you to question the plausibility of dietary intervention for this disorder. Then again, most significant in my mind is the fact that children with ASD are prone to selective eating (Ahearn et al., 2001). During our study of the eating habits of children with an ASD, my colleagues and I provided children with a variety of foods across six meals spread out over at least two weeks. Over half of the children we observed presented with some form of selective eating. Though we saw selectivity for various food groups, the food group that our selective eaters were most likely to prefer was starch. Gluten is a constituent of many starches and restricting access to this substance can lead to eliminating the only foods that a child regularly eats.
The course of action that I have followed as a clinician treating selective eating has been to attempt to expand the variety of foods a child eats. I've worked with children who ate only one food and would not eat unless that food was prepared in a specific manner (e.g., macaroni and cheese made with whole milk and butter served straight out of the pan). Going from such selective acceptance of food to eating other foods often takes quite a long time. The only situations in which I would recommend restricting access to food would be if the child had a documented food allergy or excessively consumed food. Several parents have reported to me that they have tried the casein/gluten-free diet and their child would not eat any of the foods presented to them. To be fair, I've also had a number of parents swear to me that this diet was very helpful but none of them answered yes when I asked them if the diet cured their child of autism. It is my opinion that children with an ASD will not benefit from dietary restrictions of any kind unless they also have a food allergy or intolerance. Furthermore, children who are selective eaters are likely to become more selective and may stop eating when their diet is radically restricted. Because children with ASDs are prone to selective eating it is probably a good idea to attempt to expand their diets rather than restrict them.
Acosta, M.T. & Pearl, P.L. (2003). The neurobiology of autism: New pieces of the puzzle. Current Neurology and Neuroscience Reports, 3, 149-156.
Ahearn, W.H., Castine, T., Nault, K., & Green, G. (2001). An assessment of food acceptance in children with autism or pervasive developmental disorder - not otherwise specified. Journal of Autism and Developmental Disorders, 31, 505-512.
Black, C., Kaye,J., & Jick, H. (2002). Relation of childhood GI disorders to autism: Nested case-control study using data from the UK General Practice Research Database. British Medical Journal, 325, 419-421.
Feingold, B.F. (1975). Why your child is hyperactive. New York: Random House.
Folstein, S.E., & Rosen-Sheidley, B. (2001). Genetic of autism: Complex aetiology for a heterogeneous disorder. Nature Reviews: Genetics, 2(12), 943-955.
Fombonne, E. (1999). The epidemiology of autism: A review. Psychological Medicine, 29, 769-786.
Fombonne, E. & Chakrabarti, S. (2001). No evidence for a new variant of measles-mumps-rubella-induced autism. Pediatrics, 108, E58.
Hviid, A., Stellfeld, M., Wohlfahrt, J., & Melbye, M. (2003). Association between thimerosal-containing vaccine and autism. Journal of the American Medical Association, 290, 1763-1766.
International Molecular Genetic Study of Autism Consortium (2001). A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. American Journal of Human Genetics, 69, 570-581.
Lightdale, J.R., Hayer, C., Duer, A., Lind-White, C., Jenkins, S., Siegel, B., Elliot, G.R., & Heyman, M.B. (2001). Effects of intravenous secretin on language and behavior of children with autism and gastrointestinal symptoms: A single-blinded, open-label pilot study. Pediatrics, 108(5). URL:http://www.pediatrics.org/cgi/content/full/108/5/e90.
Lyall, J. (2004). Editor in the eye of the storm. British Medical Journal, 328:528 (28 Feb). doi:10.1136/bmj.328.7438.528.
Mayor, S. (2003). Authors reject interpretation linking autism and MMR vaccine. British Medical Journal, 328:602 (13 Mar). doi:10.1136/bmj.328.7440.602-c.
Muhle, R., Trentacoste, S.V., & Rapin, I. (2004). The genetics of autism. Pediatrics, 113, 472-486.
National Institutes of Health. (1996). NIH Publication No. 96-3572, printed 1994, reprinted 1996. Booklet. 44p. Retrieved September, 1997 from http://www.nimh.nih.gov/publicat/adhd.cfm#adhd6.
Roberts, W., Weaver, L., Brian, J., Bryson, S., Emelianova, S., Griffiths, A., MacKinnon, B., Yim, C., Wolpin, J., & Koren, G. (2001). Repeated doses of porcine secretin in the Treatment of autism: A randomized, placebo-controlled trial. Pediatrics, 107(5). URL:http://www.pediatrics.org/cgi/content/full/107/5/e71.
Ritvo, E.M., & Freeman, B.J. (1978). National society for autistic children definition of the syndrome of autism. Journal of Autism and Childhood Schizophrenia, 8, 162-170.
Taylor, B. et al. (2002). MMR vaccination and bowel problems or developmental regression in children with autism: Population study. British Medical Journal, 324, 393-396.
Wakefield et al. (1998). Ileal-lymphoid-nodular hyperplasia, nonspecific colitis, and pervasive developmental disorder in children: An early report. Lancet, 351, 637-641.
For more sound information about food allergies, go to the National Library of Medicine's food allergy site at: http://www.nlm.nih.gov/medlineplus/foodallergy.html
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