Functional Medicine Day: Autism Spectrum Disorder
Welcome to the Functional Medicine day. Today we are welcoming functional medicine doctors and interested health care consumers to discuss this cutting-edge approach to medicine. I am posting this interesting case to get the conversation started. [Note to visitors: To learn more about functional medicine, you can download this PDF file: What is functional medicine?]
Autism is a growing concern, with increasing numbers of children being diagnosed, especially boys. Incidence of autism is now about 1/166, which represents about a tenfold increase in the past 2 decades, although the numbers vary according to researcher. The causes are not yet fully determined, but we do know that, as typical of most diseases, autism is multifactorial.
The main causes appear to be mitochondrial dysfunction, detoxification dysfunction and intestinal fungal overgrowth. This latter cause, according to autism expert Sid Baker, MD, occurs in about 1/3 of cases with aggressive antifungal therapy resulting in complete remission in many.1 Nutrients reported to help autistic children include magnesium, vitamins B2 and A, and medium chain fatty acids. There have been reports that many autistic children have problems eliminating heavy metals, especially mercury.
Case Study
This child, now seven, was first brought to see me at age two. His mother reported that she had seen some symptoms at age 1 (repetitive behaviors), but they disappeared when they removed nuts from his diet. He was growing normally and apparently meeting milestones until age two when he started to get physically weak. This was first noticed when he became unable to climb the gym set at the park which he had climbed with no problems many times before.
Relevant family history is that his parents (mother 49, father 55) were supposedly infertile ( >12 known miscarriages). Unexpectedly, his mother maintained her pregnancy and successfully vaginally delivered him and his fraternal twin. His problems are not surprising considering the history of unsuccessful pregnancies and parents' age well beyond optimal. His fraternal brother is relatively normal, although he does suffer from migraine headaches and food allergies.
Screening blood tests (which showed elevated serum lactic acid) and evaluation of developmental landmarks by a pediatrician resulted in a presumptive diagnosis of autistic spectrum disorder. Conventional care offered little hope, so his parents sought help elsewhere. An elevated lactic acid can be an indication of mitochondrial deficit, so I initially put him on high levels of vitamin B2 and modest levels vitamin B1, Mg, creatine, acetyl-L-carnitine, NAC, glutathione, lipoic acid, and CoQ10 -- a combination of nutrients that would promote energy metabolism while bolstering mitochondrial antioxidant defenses. Later, after doing a urinary organic acids profile, we refined his supplement program and had his mother start giving him medium chain fatty acids (two grams per day). These fatty acids from coconut oil are more easily metabolized by the mitochondria for energy production. The results were remarkable: he became much stronger, and his autistic symptoms all resolved.
Although he is not cured, his metabolic function has been much improved; however, if he stops taking the supplements, he quickly starts to deteriorate. Activation of his mitochondria requires 100 mg/d of B2 (about 50 times the RDI).
His health is not perfect; he is still somewhat physically fragile, and I know we haven't found or fixed all his problems. But if you met and talked with him, you would only see a bright, engaging boy, a bit small for his age.
Interestingly, in reviewing this with his mother before posting his story on the blog, she now feels that his apparent developmental deficiencies were all due to muscle weakness rather than mental issues. Her comment:
The problem with an autism spectrum disorder diagnosis is that there is no specific confirmatory lab test--it is more a diagnosis by exclusion. If we had not caught this early and normalized his mitochondrial function, it is highly likely it would have resulted in (further?) neurological damage and converted his presumptive diagnosis into full manifestation.
Regardless of the diagnosis, Brent clearly has a significant mitochondrial defect that resulted in serious problems, most all of which we were able to resolve with a sophisticated nutritional intervention.
Related Topics:
1 Editor's Note: The successes reported by Dr. Baker as a result of alternative treatments have not yet been supported by scientific studies.
Technorati Tags: functional medicine, autism, autism spectrum disorder, integrative medicine, alternative medicine
Autism is a growing concern, with increasing numbers of children being diagnosed, especially boys. Incidence of autism is now about 1/166, which represents about a tenfold increase in the past 2 decades, although the numbers vary according to researcher. The causes are not yet fully determined, but we do know that, as typical of most diseases, autism is multifactorial.
The main causes appear to be mitochondrial dysfunction, detoxification dysfunction and intestinal fungal overgrowth. This latter cause, according to autism expert Sid Baker, MD, occurs in about 1/3 of cases with aggressive antifungal therapy resulting in complete remission in many.1 Nutrients reported to help autistic children include magnesium, vitamins B2 and A, and medium chain fatty acids. There have been reports that many autistic children have problems eliminating heavy metals, especially mercury.
Case Study
This child, now seven, was first brought to see me at age two. His mother reported that she had seen some symptoms at age 1 (repetitive behaviors), but they disappeared when they removed nuts from his diet. He was growing normally and apparently meeting milestones until age two when he started to get physically weak. This was first noticed when he became unable to climb the gym set at the park which he had climbed with no problems many times before.
Relevant family history is that his parents (mother 49, father 55) were supposedly infertile ( >12 known miscarriages). Unexpectedly, his mother maintained her pregnancy and successfully vaginally delivered him and his fraternal twin. His problems are not surprising considering the history of unsuccessful pregnancies and parents' age well beyond optimal. His fraternal brother is relatively normal, although he does suffer from migraine headaches and food allergies.
Screening blood tests (which showed elevated serum lactic acid) and evaluation of developmental landmarks by a pediatrician resulted in a presumptive diagnosis of autistic spectrum disorder. Conventional care offered little hope, so his parents sought help elsewhere. An elevated lactic acid can be an indication of mitochondrial deficit, so I initially put him on high levels of vitamin B2 and modest levels vitamin B1, Mg, creatine, acetyl-L-carnitine, NAC, glutathione, lipoic acid, and CoQ10 -- a combination of nutrients that would promote energy metabolism while bolstering mitochondrial antioxidant defenses. Later, after doing a urinary organic acids profile, we refined his supplement program and had his mother start giving him medium chain fatty acids (two grams per day). These fatty acids from coconut oil are more easily metabolized by the mitochondria for energy production. The results were remarkable: he became much stronger, and his autistic symptoms all resolved.
Although he is not cured, his metabolic function has been much improved; however, if he stops taking the supplements, he quickly starts to deteriorate. Activation of his mitochondria requires 100 mg/d of B2 (about 50 times the RDI).
His health is not perfect; he is still somewhat physically fragile, and I know we haven't found or fixed all his problems. But if you met and talked with him, you would only see a bright, engaging boy, a bit small for his age.
Interestingly, in reviewing this with his mother before posting his story on the blog, she now feels that his apparent developmental deficiencies were all due to muscle weakness rather than mental issues. Her comment:
Brent (not his name) was having problems learning to read, and he would ask me, "Mom is that an "i" or an "l", or is that an "h" or an "n", and I was very concerned thinking he was slipping mentally, as he should have known this without any problem at this stage. But I would notice at other times he could read words easily, especially if they were listed rather than in sentence form. I also noticed the longer he tried to read a book, the worse his word recognition or decoding became. I was talking with a counselor at his school, and she explained it is much harder for the eyes to track horizontally between each small word and that the eye muscles have to develop the coordination and strength. When she said muscle strength, I knew immediately Brent's problem was eye muscle weakness, not loss of mental function. I explained the problem to him; we changed how he reads, and he got his self confidence back and is now decoding and reading quite well. So, he obviously has muscle weakness throughout his body. The other very obvious place being his swallowing difficulties.I can understand how a mother would not want her child to be diagnosed as autistic. And autism syndrome covers a wide range of dysfunction, ranging from mild to severe. She may be right that most, if not all, of Brent's developmental problems could be explained by muscle weakness secondary to mitochondrial dysfunction. As we progressively restored his mitochondrial function, his muscles began developing again, and his physical and mental deficiencies eventually resolved.
The problem with an autism spectrum disorder diagnosis is that there is no specific confirmatory lab test--it is more a diagnosis by exclusion. If we had not caught this early and normalized his mitochondrial function, it is highly likely it would have resulted in (further?) neurological damage and converted his presumptive diagnosis into full manifestation.
Regardless of the diagnosis, Brent clearly has a significant mitochondrial defect that resulted in serious problems, most all of which we were able to resolve with a sophisticated nutritional intervention.
Related Topics:
1 Editor's Note: The successes reported by Dr. Baker as a result of alternative treatments have not yet been supported by scientific studies.
Technorati Tags: functional medicine, autism, autism spectrum disorder, integrative medicine, alternative medicine



14 Comments:
Mitochondrial dysfunction has been implicated in other disorders such as migraine, chronic fatigue and fibromyalgia, etc. I wonder if this is caused by excessive oxidant stress, perhaps due to inadequate antioxidant intake from the mother during her child's embryonic and fetal development. Could the mother's mitochondrial DNA have been damaged and passed on to her child?
Some disturbing research suggest mitochondrial dysfunction is far more common than generally realized. Genetics, damage from oxidation and environmental toxins, enzymatic dysfunction from nutrioinal deficiencies--all contribute. Some of these factors can be measured.
Another interesting area that is being explored in the autistic community is methylation defects, either acquired or inherited. Could you speak to the issues of folate and B12 deficiencies and how these may play some role in autistic spectrum disorders?
Dr. Dan, I believe you can speak to methylation defects better than I can!
Joe,
this is not an area of my expertise. However I do know a little of the research, which is quite fascinating. Dr Jill James and her group have been significantly involved in this line of inquiry in autistic children. They measured plasma concentrations of methionine, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), adenosine, homocysteine, cystathionine, cysteine, and oxidized and reduced glutathione in 20 children with autism and in 33 control children. Relative to the control children, the children with autism had significantly lower baseline plasma concentrations of methionine, SAM, homocysteine, cystathionine, cysteine, and total glutathione and significantly higher concentrations of SAH, adenosine, and oxidized glutathione. This metabolic profile is consistent with impaired capacity for methylation (significantly lower ratio of SAM to SAH) and increased oxidative stress (significantly lower redox ratio of reduced glutathione to oxidized glutathione) in children with autism. They concluded that an increased vulnerability to oxidative stress and a decreased capacity for methylation may contribute to the development and clinical manifestation of autism. James followed this study was another where they measured plasma levels of metabolites in methionine transmethylation and transsulfuration pathways in 80 autistic and 73 control children. The metabolic results indicated that plasma methionine and the ratio of S-adenosylmethionine (SAM) to S-adenosylhomocysteine (SAH), an indicator of methylation capacity, were significantly decreased in the autistic children relative to age-matched controls. In addition, plasma levels of cysteine, glutathione, and the ratio of reduced to oxidized glutathione, an indication of antioxidant capacity and redox homeostasis, were significantly decreased. They also found differences in allele frequency for relevant genes encoding the reduced folate carrier (RFC 80G > A), transcobalamin II (TCN2 776G > C), catechol-O-methyltransferase (COMT 472G > A), methylenetetrahydrofolate reductase (MTHFR 677C > T and 1298A > C), and glutathione-S-transferase (GST M1). James and her colleagues proposed that an increased vulnerability to oxidative stress (endogenous or environmental) may contribute to the development and clinical manifestations of autism. A good resource is the Defeat Autism Now group (DAN) for those who want to investigate further.
Please comment on the usefulness of genetic SNP testing to identify these metabolic issues in methylation for example and then the efficacy of oral RNA products that claim to modify the gene errors and improve autism.
I'd also like to congratulate WebMD for supporting functional medicine with this blog and the related member forums.
Bob Sager MD
Member IFM Forum
Dr. Pizzorno,
I started teaching a functional medicine training program this year, covering the most basic issues, hormones, digestion and detox using a six month teleseminar/webinar format. It has been a good experience for my students and I'd like to present the curriculum to you for your review and comments.
My goal is to teach how to create a successful and profitable functional medicine based practice. I'm very excited about the program as I see the students apply the concepts and do the work.
Best,
Daniel Kalish, DC
dr@drkalish.com
drkalish.com
Good review Dan. One question though, I thought with impaired methylation that homocysteine levels increase? Your note says one study showed lowered levels.
Re genomic testing, I think this diagnostic tool has tremendous potential. However, a few words of caution:
1. Make sure the SNPs you are measuring are sufficiently predictive. There is a problem with patents and costs that appears to result in some SNPs being done because of availability, but they are actually of poor predictive value. I and my team looked at one panel and found that more than half the SNPs being measured had virtually no predictive value. In other words, they showed real genetic variations but those variation had not clinical significance.
2. Be sure to measure SNPs that are actionable, i.e., they are associated with known enzymes and those enzymes can be impacted with nutritional (or other) interventions.
I also thank you and WebMD for supporting Functional Medicine day.
Your article and the forum discussions bring to life the idea that autism appears to be multifactorial. It is perhaps no coincidence that autism, and other modern syndromes and disorders, seems to be on the rise along with the body burden of environmental toxins. We now know that levels of industrial and household chemicals, pesticides and pollutants in infants, children, pregnant women and their breast milk is increased.
While we know that environmental toxins have potential neurologic, endocrine and genetic effects in animal models, the studies in humans are relatively few (but promising).
It seems to me that the "Precautionary Principle" approach to toxin exposure is reasonable. It would be interesting to see studies looking at the relationship between toxin body burdens and mitochondrial and detoxification inefficiencies as we go forward with autism research.
What are your thoughts in relationship to this in the case you presented?
Thank you for your comments Dr. Haiden. I agree with you re the toxic burden and its many damaging effects on health. For this particular child, I've known the family for many years and am pretty confident his toxic exposure is significantly below the norm.
Dear Joe,
What I like most about the discussion around autism is a moving away from the old philosophical approach 'if we do not know the answer, then it does not exist, the condition is therefore idiopathic'. Your approach to integrative and functional medicine moves away from the simplistic model of cause and effect, to a more contextual model of causes, aggravating factors, co-morbid pathologies, abnormal function / dysfunction and complications. It is through this methodology that disease / pathology can better be understood, and functional approaches discovered.
Well said Myron.
Thank you all for your involvement today.
My grandson was diagnosed about 9 years ago with epilepsy. He has had every type of seizure that there is. He has been treated by many of the finest neurologists and his seizures still have not improved. He also was diagnosed with autism. I started researching autism when I heard that some children with autism also have seizure disorders. I believe he should be treated for autism and that treatment will help his seizure disorder. Two things happened to him that would indicate that he might have a missing protein. When he was born he had a fever and had to stay in the hospital several days after being born. The doctor said he got an infection for being in the birth canal too long. For the first year of his life he had GERD. Both of these things I have read will cause a decrease or distruction of this protein. Trying to find a doctor who will even consider this possibility has been up to now impossible. Could I receive some information or guidance from anyone?
The parents of 7-year-old Evan Riggle have been dealing with his autism since he was 1. We have chronicled their search for effective treatments, including rare blood transfusions to boost his immune system.
Evan Riggle
But Evan is far more receptive to an IV of glutathione, an amino acid in your body that neutralizes harmful molecules.
“So, by helping boost their own natural glutathione production, it reduces the oxidative stress in their body and they are less combative, they are more calm and therefore generally more cooperative,” says Emlyn Riggle.
http://www.fox11az.com/news/topstories/stories/kmsb-20070926-whasjc-AutismPkgs.111b2c23c.html
I hope someone can find a use for this info.
Randy Grover
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