Comorbid
I've been meaning to write about this topic for some time but never quite got around to it. Now seems like as good a time as any so here goes.
A lot of people discuss certain medical symptoms and conditions, that may or may not be more common in autistic children, as if these disorders are either linked to the etiology of autism or and integral component of autism. For some reason many parents of autistic children become offended when these symptoms are described as comorbid to autism because they see these things as part of autism. I'm not saying that some autistic children aren't also afflicted with various health issues but let's look at reasons why they are often described as comorbidities and why some would prefer to see these things recognized as symptoms of autism.
First the Definition of Comorbidity
Comorbidity: The coexistence of two or more disease processes.
That's a very simple definition from a medically oriented website but it's a pretty straightforward and more or less accurate definition. The only way this definition works for autism is when one of the two or more diseases is autism. Right there we have a problem because autism cannot accurately be described as a disease. Not with our current knowledge of the biology of autism, it can't.
For the sake of discussion, we'll need to accept that medical professionals will most likely define autism as a medical condition, to some extent, and other medical conditions will be described as co-existing disease processes as long as one doesn't clearly cause the other. That probably won't please many of us but that's the way it usually works.
The definition of comorbidity can also change according to context. In some circles it's perfectly acceptable to describe two or more psychiatric disorders or behaviors as comorbidities.
The presence of multiple disorders in one individual. Pathological gambling has high rates of comorbidity with disorders such as alcoholism and depression.
Unless it becomes widely recognized that drinking causes gambling, gambling causes depression, and depression causes alcoholism, rates of comorbidity will be used to describe the relationship between these conditions. As long as Casinos serve alcohol in attempt to impair gambling decisions, patrons will become depressed after losing money which may cause some to drink. Clinical depression isn't a symptom of gambling losses and alcoholism doesn't promote gambling, for the most part.
The Symptoms of Autism
There's a reason why the DSM-IV description for autism doesn't include things like GI distress, diarrhea, constipation, immune abnormalities, allergies, etc. Autism can be diagnosed in people with any number of other medical or psychiatric conditions and the diagnosis doesn't rely upon physical, medical, or biological parameters. That's one of the reasons we know that autism can be diagnosed more often with Down Syndrome, Fragile-X, Prader Willi Syndrome, Rett Syndrome, etc. Depending on how autism is described, autism itself might be seen as a comorbidity. Autism doesn't cause those other conditions and those conditions can exist without autism.
When Andrew Wakefield decided to investigate GI symptoms in a handful of autistic children, they weren't randomly selected. Parents who were concerned about their autistic child's GI issue sought medical attention from a gastroenterologist. No doubt he saw a strong correlation between autism and GI symptoms. A GI specialist may be more inclined to think that GI inflammation can cause autism in the same way an economist might leap to the conclusion that correlation implies causation. If this particular GI specialist claims to have previously detected the measles virus in the GI tracts of patients with Crohn's Disease, he might be inclined to connect reports of autistic regression with exposure to the measles component of the MMR. It's also likely that these same parents saw a correlation and shared their observations with Dr. Wakefield but we can't be sure.
Whatever the sequence of events, Wakefield reported a relationship between Ileal-lymphoid-nodular hyperplasia, autism, and the presence of the measles virus. Even if he didn't specifically say that one cause the other, he did nothing to dispel the obvious conclusions drawn form his work. One doesn't coin the term autistic enterocolitis and describe the presence of the measles virus only in autistic children without implying a relationship. Of course the relationship was more than implied in the years to follow and we now have a pretty good idea of where he went wrong with the PCR techniques but I don't expect Wakefield will ever come out and admit that he was wrong. We'll probably see more emphasis placed on GI inflammation as he argues that his actions were justified given the circumstances.
Is there a higher rate of GI disturbances and gut inflammation in autistic children? Possibly, maybe even probably. My personal opinion, based on my own observations leads me to believe so but I am willing to accept data from well designed studies if it shows otherwise. So far it looks like there are higher rates but the debate is far from over. Wakefield didn't just claim a relationship between ASD's and GI symptoms. He claimed a relationship between highly specific patterns of GI inflammation, exposure and detection of vaccine strain measles virus, and regressive autism. The presence of all or absence of 1 of 3 could make or break the diagnosis of "new variant inflammatory bowel disease."
Based on Wakefield's requirements, how many autistic children would be eligible for the diagnosis - Measles-mumps-rubella-induced regressive autism. None, apparently, since no other labs are able to confirm the presence of the measles virus and it's difficult to find a doctor ready and eager to scope children without good reason, autism or not.
Should we include nodular lymphoid hyperplasia in the DSM-V diagnostic criteria for autism? Of course not. Even when it's reported along with Bannayan-Riley-Ruvalcaba syndrome , autism and PTEN mutation. The traits that make this person autistic are still described as autism and comorbid conditions are described with different medical terms. Never will the word autism be used to communicate a broad range of physical medical disorders.
Idiopathic Autism
According to Wikipedia, the word idiopathic means arising spontaneously or from an obscure or unknown cause. Idiopathic Autism has become somewhat of a catch-all phrase where a cause, most often genetic, is unknown. Although the majority of autism falls into this category, this does not mean the majority of autism is the same thing. Before we had the tools to identify genetic and environmental factors, it could be said that all autism was idiopathic autism. Unfortunately, when a cause isn't identified, the void may be filled with any number of less plausible hypotheses. This phenomenon isn't unique to autism but no where else can we witness such a low standard of scientific accountability.
Autism By Any Other Name
I can't count the number of times I've heard it said that one type of autism or autistic-like behaviors aren't the same as this autism, core autism, idiopathic autism, HF, LF, AS, Whatever. Just stop it already. If a person is diagnosed as autistic, that's autism, alright? Whether it's part of Cri du chat syndrome or a creatine transport deficiency, if the label is applied it can't be peeled away by amateur diagnosticians on internet mailing lists. If a diagnosis gets counted under total number of cases which in turn is held up as evidence of an autism epidemic, you don't get to break out individual causes as it serves your agenda.
At this point we haven't found a single thing that causes autism each and ever time. True, there are certain genetic conditions associated with autism, there are several substances and infectious agents that may increase the chances of having an autistic child following prenatal exposure, and there are many suspected prenatal and perinatal risk factors under investigation.
No single gene, environmental factor, combination of genes and/or environment, or other risk factors, can consistently cause autism. I doubt that we will find such a gene or agent but we will most certainly continue to identify new causes, potential treatments, comorbidities, categories, and labels cleaved from the idiopathic autism realm. There's a lot to sort out before we can say that one thing is caused by another so our only option for now is to ignore symptoms that may or may not be associated with being autistic, or continue to discuss these things as potential comorbid conditions. Humans will always sort, catalog, and label all we encounter. We need to exercise great caution when we approach categorizing humans by comorbidities.


11 Comments:
I have noticed also a "trend" in not wanting any co-concurring conditions to be identified in a person with a diagnosis of autism. Too me this seemed odd until I started looking at some of the people who were promoting this. I realized that admitting the possibility of co-concurring conditions (Tourettes, OCD, Bi-polar)have an effect on the idea that autism is caused by mercury only. Because of course the other conditions HAVE been around in medical literature for much longer than 1930 (autism has also but many refuse to acknowledge that).
LB
I haven't heard of that but it makes sense, LB.
On the other side of the issue, many of us have experienced frustrataion when a doctor says something like "Well, that's just part of autism." or medical problems are missed and over looked because the doctor doesn't want to deal with an autistic child.
If a kid is having severe digestive problems and a GP tells the parents, "that's just part of autism," then the GP is part of the problem. Still it's the mercury parent legal strategy to paint autism in the most horrendous terms possible, so we have Lujene Clark apparently telling Bobby Kennedy Jr that _all_ autistic children have these horrific gut pains that cause them to double over when they are in their kindergarten class and writhe in pain on the floor... He wrote that on Huffington Post, didn't he?
What's more shocking than talk about children and "caustic" diarrhea running down their legs? This gets lots of play in Kirby's book because it gets everyone's attention really quickly. "Oh! That's autism! I thought it was just a kid sitting in the corner rocking and staring... I guess this is REALLY bad!" They are tapping into the fear of contamination and the grossness factor.
There are some studies that have found a non-significant difference in gastrointestinal issues between autisit and non-autistic children. See this and also this.
The problem with the case control studies that use parental reports or even medical history is that they are easily confounded by prevailing hype. More rigorous methodology is needed if these correlations are to be believed.
Good explanation of cause vs. comorbidity, BTW.
Even if we accept the premise that autistic children are more likely to suffer GI distress...and even if we accept the notion that an autistic child's biochemistry is different thus causing such distress...it's still a long way from saying that vaccines cause autism or that post-natal environmental insults play a role in autism.
The problem is that nobody has provided a reasonable mechanism for which a vaccine or combination of "environmental insults" can cause the specific biological differences inherent in autism. (Not even "1,000 Sources Maria".)
Hi NotMercury,
I quite like this post, as a balanced approach to autism and comorbidities. I also agree with the idea that there are probably multiple etiologies. My daughter definitely has GI and absorption issues. I have no issue with them being described as comorbidities until it is proven otherwise. That being said, I still want them treated.
What I would suggest regarding comorbidities is that while autistics may or may not have higher prevalences of various comorbidities, the consequences of those comorbidites may be different than in the background population. As an example, if Dr Casanova’s autistic minicolumn hypothesis (Casanova et al 2002a, Casanova et al 2002b, Casanova 2006) is correct then the minicolumnar differences within the autistic and potentially broader autism phenotype (BAP) brains could lead to increased (or at least altered) vulnerabilities. In addition, autistic (and BAP?) brain growth patterns (faster growth in the first few years) could also increase vulnerabilities, as could altered nutritional and metabolic requirements (potentially higher to fuel the faster brain growth).
I suggested a few hypotheses in a post on Autism and the Evolution of the Brain that may be more or less plausible, depending on one’s viewpoint, that are too long to discuss in a comment (and at >5000 words, maybe too long for a post).
Hi Ian,
There's a new study published in Biological Psychiatry that may interest you.
Gaze-Fixation, Brain Activation, and Amygdala Volume in Unaffected Siblings of Individuals with Autism
Kim M. Dalton, Brendon M. Nacewicz, Andrew L. Alexander, and Richard J. Davidson
Background
The broad autism phenotype includes subclinical autistic characteristics found to have a higher prevalence in unaffected family members of individuals with autism. These characteristics primarily affect the social aspects of language, communication, and human interaction. The current research focuses on possible neurobehavioral characteristics associated with the broad autism phenotype.
Methods
We used a face-processing task associated with atypical patterns of gaze fixation and brain function in autism while collecting brain functional magnetic resonance imaging (fMRI) and eye tracking in unaffected siblings of individuals with autism.
Results
We found robust differences in gaze fixation and brain function in response to images of human faces in unaffected siblings compared with typically developing control individuals. The siblings' gaze fixations and brain activation patterns during the face processing task were similar to that of the autism group and showed decreased gaze fixation along with diminished fusiform activation compared with the control group. Furthermore, amygdala volume in the siblings was similar to the autism group and was significantly reduced compared with the control group.
Conclusions
Together, these findings provide compelling evidence for differences in social/emotional processing and underlying neural circuitry in siblings of individuals with autism, supporting the notion of unique endophenotypes associated with the broad autism phenotype.
Hi NotMercury,
Thanks for letting me know about this study. It is definitely interesting, and I would suggest supportive of the concept of a pre-autistic or proto-autistic brain structure. Although ASD has been 'discovered' (i.e. described and documented) in diminishing order of 'severity', perhaps ASD is the BAP plus something else, rather than the BAP being a lesser form of ASD.
Hi not mercury
Very interesting post.
anonimouse
No, I am not talking about 1000 causes, but specific candidates ones. About potential mechanisms, I have prepared several drafts to discuss/share with several researchers in different fields and I have done this and still and I will with a lot of interesting interactions ( not the most controversial ones I must say).BTW, you never read the drafts I have about Did you? Obviously I accept that you can not be interested. Other people are.
Ian, I really like the BAP analysis that is currently being done. Being in the BAP- following different tests- this kind of studies are really interesting for me.
This is interesting: "The broad autism phenotype includes subclinical autistic characteristics found to have a higher prevalence in unaffected family members of individuals with autism. These characteristics primarily affect the social aspects of language, communication, and human interaction. "
This seems to indicate that my own idea of extremes of developmental difference (from my first MEd paper) is likely to be accurate.
JBJr's taken to posting under other people's names (like Any Mouse's) ... whilst retaining his own discoursive disorder therein. So I've been forced to get a Blogger account just for the purpose of commenting... I'd have for anyone to think that I'd even consider wanting to agree with JBJr.
"I'd have for anyone to think"... "I'd hate for anyone to think"
I need food.
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