Showing posts with label thyroid. Show all posts
Showing posts with label thyroid. Show all posts

Friday, 1 June 2018

Depression and anxiety *associated* with autoimmune thyroiditis

The results of the systematic review and meta-analysis published by Eva-Maria Siegmann and colleagues [1] provide some further welcome peer-reviewed inspection of the idea that autoimmunity and psychiatric issues are not necessarily separate and independent.

Their specific focus on autoimmune thyroiditis - where the body fails to recognise 'self' as self and mounts an immune response against the thyroid and it's products - and depression and anxiety, is something that has been discussed previously on this blog (see here).

As per the 'systematic review and meta-analysis' status of this paper, the name of the research game was to collect up the relevant peer-reviewed science literature on this topic and produce a coherent 'where we're at' statement. Researchers trawled the various science portals "from inception through December 5, 2017" and eventually arrived at 19 studies fulfilling their criteria: "Case-control studies that reported the association between AIT [autoimmune thyroiditis] and either depression or anxiety disorders." The combined participant number was just over 36,000 people - "(35 168 for depression and 34 094 for anxiety)".

Results: "We found that the chance of developing symptoms of depression that were of clinical relevance is 3.5 times higher among patients with hypothyroidism compared with healthy controls." And: "We found that the chance of developing anxiety disorders is more than 2 times higher among patients with hypothyroidism compared with healthy controls." Hypothyroidism by the way, refers to when the thyroid doesn't produce enough hormones, and is typically the end-result of autoimmune thyroiditis.

The authors also put their findings into some kind of population perspective: "3% of the US population (approximately 9.7 million people) has depression and 5.4% of the US population (approximately 17.5 million people) has anxiety disorders concomitantly with AIT. Thus, 45.5% of depressive disorders and 29.8% of anxiety disorders are associated with this endocrine disease." I don't mind telling you that, based on the currently available research data, those statistics seem to be pretty important. Not least that as and when depression and/or anxiety are diagnosed, physicians could do well to screen their patient for such thyroid-related issues as a first measure.

Of course, there is more to do in this area as the authors note. Not least is some further investigation with regards to the possible biological mechanism(s) through which AIT might act upon the presentation of such psychiatric issues and whether treating/managing AIT could impact on the presentation of depression and/or anxiety.

But yet again, we have further evidence that the [various] actions and effects of the immune system seem to have some important effects on behaviour, mood and wellbeing.

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[1] Siegmann E-M. et al. Association of Depression and Anxiety Disorders With Autoimmune Thyroiditis. JAMA Psychiatry. 2018. May 2.

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Saturday, 26 May 2018

"CFS symptoms resemble a hypothyroid state" but...

I am a little late getting to the paper published by Begoña Ruiz-Núñez and colleagues [1] observing that, at least for some diagnosed with chronic fatigue syndrome (CFS), clinical findings related to thyroid function might "resemble a mild form of “non-thyroidal illness syndrome” and “low T3 syndrome” experienced by a subgroup of hypothyroid patients receiving T4 monotherapy." But I did get here eventually. Before heading into this paper, I'm gonna link to one of the 'already prepared' discussions on the Ruiz-Núñez findings (see here). My analysis is pretty similar but not entirely the same...

So: "We studied 98 CFS patients (21–69 years, 21 males) and 99 age- and sex-matched controls (19–65 years, 23 males)" was the starting point, as participants provided blood samples and 24-hour urine samples onward to various analyses being carried out. This included: "the measurement of routine hematological parameters [Hb, hematocrit, WBC, red blood cells (RBC), and thrombocytes]" and more specifically: "parameters of thyroid function, low-grade inflammation and gut wall integrity..., together with secondary markers of inflammation." Those 'parameters of thyroid function' included various measures of free and total levels of T3 and T4 required to ascertain the presence of "low-T3 syndrome." I was impressed to see that a measure of gut wall integrity was also on the research menu in the form of plasma zonulin levels being included (albeit analysed via ELISA and bearing in mind the issues that have emerged with that particular method).

Results: "Chronic fatigue syndrome patients exhibited lower FT3, TT4, TT3, %TT3, SPINA-GD, and SPINA-GT, lower ratios of TT3/TT4, FT3/FT4, TT3/FT3, and TT4/FT4; and higher %rT3 and rT3/TT3 ratio." These findings were based on 'group' comparisons with those sex-matched not-CFS controls, and point to some 'issues' with thyroid function in general. Coupled to other thyroid related findings, the Ruiz-Núñez suggest that lower levels of thyroid hormones were detected but "distinct from thyroidal disease" typical levels of thyroid-stimulating hormone (TSH) were also reported. TSH is the stuff that tells the thyroid gland to make thyroid hormone (thyroxine (T4)), where T4 is, in effect, the starting material for T3 (triiodothyronine). Where there are suitable levels of TSH but lower levels of T4 and/or T3, one gets the impression that it's more about what's 'happening' to T3 and T4 over and above issues with their production. Indeed, the collected findings led authors to talk about that 'low T3 [triiodothyronine]syndrome' as being potentially pertinent to their findings in relation to CFS. Going back to those plasma zonulin findings, and there is just a sentence from Ruiz-Núñez and colleagues: "Zonulin, a parameter of intestinal permeability... was lower in CFS patients as compared to controls" but not much else.

I'm not particularly au fait with all the details of low T3 syndrome in the context of CFS or anything else so can't really add too much more. From what I gather, this is not a CFS-exclusive condition but does seemingly tap into talk about CFS being reflective of a "hypometabolic state" (see here). Questions about how to 'treat' such thyroid-related issues in the context of CFS remain unanswered, despite authors talking about "trials with, e.g., T3 and iodide supplements" being potentially indicated. I say this bearing in mind that the focus on biochemistry in the Ruiz-Núñez paper could perhaps, have been complemented by a little more on the presentation of clinical symptoms too.

In short, quite a bit more investigation in this area is indicated...

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[1] Ruiz-Núñez B. et al. Higher Prevalence of “Low T3 Syndrome” in Patients With Chronic Fatigue Syndrome: A Case–Control Study. Front. Endocrinol. 2018. Mar 20.

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Friday, 26 January 2018

"maternal hypothyroidism is associated with an increased risk of ASD in children"

The quote heading this post comes from the findings reported by Darios Getahun and colleagues [1] who "used electronic medical records (EMRs) from the Kaiser Permanente Southern California (KPSC) system to evaluate whether maternal hypothyroidism is associated with increased risk of ASD [autism spectrum disorder] in children and whether this risk is modified by race–ethnicity, fetal sex, and timing of exposure."

Hypothyroidism by the way, refers to a clinical state where the thyroid gland is underactive and produces less thyroid hormone than is required. Symptoms such as fatigue/tiredness, depression, weight gain and constipation can follow. Pregnancy hypothyroidism can impact both mother and offspring health and development; at one extreme potentially leading to an increased risk of miscarriage, but also contributing to psychomotor issues and beyond in exposed offspring. Autism has been previously mentioned as a possible *outcome* linked to maternal hypothyroidism (see here) as part of a larger suite of research on the thyroid and offspring developmental outcomes (see here).

Based on a cohort number approaching 400,000 children with some 6,400 children diagnosed with an autism spectrum disorder (ASD), authors observed that: "Children of hypothyroid women had higher rates of ASD than children of women without the diagnosis (2.14 vs. 1.62‰; HR, 1.45; 95% CI, 1.25–1.68)." Maternal hypothyroidism was defined in this study as a formal (ICD-9) diagnosis together with reported details of medication used to treat said hypothyroidism. Researchers also had access to blood test results too: "Blood levels of TSH (>90.4 pmol/ml) and free thyroxine (fT4, <10.45 pmol/ml) obtained from women with a clinical diagnosis of hypothyroidism (99.4% of women with the diagnosis) were used to determine how biochemical hypothyroidism may affect the risk of ASD diagnosis." And as for the autism diagnosis in the current trial.. well, gold-standard springs to mind: "In the KPSC system, the clinical diagnosis of ASD was largely based on definitive diagnosis by a child/adolescent psychiatrist, developmental/behavioral pediatrician, child psychologist, or neurologist who adhered to a standard protocol (Autism Diagnostic Observation Schedule)."

There are a few other important details mentioned in the Getahun study: "Autism diagnoses occurred at younger ages for children born to mothers with hypothyroidism diagnosis than those born to mothers without the diagnosis" and: "Compared with white children, prenatal hypothyroidism was associated with an increased risk of ASD in children of Hispanics... and women of other/mixed race–ethnicity." These findings also require quite a bit more investigation, particularly the idea that there may be a difference in age of presentation of autism when hypothyroidism is potentially implicated.

And then the next question: how could hypothyroid exposure during pregnancy *cause* autism in offspring? The authors detail a few important points that could be relevant to such a question; many of which talk about a role for environmental (non-genetic) influences. So: "Hypothyroidism may be the result of a number of conditions such as inflammatory disease, autoimmune disorders, or iodine deficiencies." Various inflammatory and/or autoimmune conditions have been talked about in the context of autism risk (see here and see here for examples). The observation that most of the cases of hypothyroidism identified in the Getahun data were "because of autoimmune thyroiditis or iatrogenic ablation" adds to the feeling that the immune system / immune function could be an important variable with regards to aetiology. The iodine connection is based on the usefulness of this compound in the production of thyroid hormones.

Finally: "Management of maternal hypothyroidism may ameliorate the risk of ASD." I'm a little bit cautious about such a statement at the current time given (a) the relatively low rate of hypothyroidism picked up in the sample: "the prevalence of chronic hypothyroidism was 2.2%", and (b) the small (but significant) difference in autism rates in cases of maternal hypothyroidism vs. no diagnosis ("2.14 vs. 1.62%"). That's not to say that there may not be areas to look at, such as a role for vitamin D status on autoimmune disease (including that linked to thyroid status, see here) and/or how autoimmune thyroiditis *might* show some connection to depression (see here) which could be relevant to all that chatter about antidepressant medicine use during pregnancy might also impact on offspring autism risk (see here). But lots more research is indicated before any sweeping generalisations are made.

And, just before I leave you, how about the results of the systematic review and meta-analysis by Thompson and colleagues [2] concluding that whilst: "Maternal hypothyroxinaemia and subclinical hypothyroidism may be associated with intellectual disability in offspring" the "effect on the risk of autism in offspring was unclear"?

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[1] Getahun D. et al. Association between maternal hypothyroidism and autism spectrum disorders in children. Pediatric Res. 2018. Jan 3.

[2] Thompson W. et al. Maternal thyroid hormone insufficiency during pregnancy and risk of neurodevelopmental disorders in offspring: A systematic review and meta-analysis. Clin Endocrinol (Oxf). 2018 Jan 11.

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Monday, 10 April 2017

"Predisposition" to autoimmunity and inflammatory activation linked to autistic regression?

The paper by Ori Scott and colleagues [1] provides some very welcome interest in the concept of regression in relation to autism. As I've indicated quite a few times on this blog, regression accompanying cases of autism has [finally] been accepted by the research community at large (see here for example) but there is still some way to go with regards to the hows-and-whys of regression. There are some clues (see here) but more data is required. What the evidence available so far suggests is that sweeping generalisations about autism exclusively occurring/appearing during very early infancy or even before, are probably not as accurate as many people might realise (see here)...

So, starting from the idea that autistic regression might have an important 'immune-related' component to it, the authors set about reviewing the medical charts/records of some 240 children diagnosed with an autism spectrum disorder (ASD). A small but significant proportion of the cohort presented with an "autistic regression variant". Researchers looked at various potentially important facets of those medical charts in relation to things like "febrile illness preceding initial parental concern" (in relation to autistic features) and "possible non-immune precipitants such as pregnancy and postnatal complications." Another important feature of the study was to look-see whether various autoimmune disease/conditions were a feature of the immediate family in regressing and non-regressing cases.

Results: well, febrile illness did seem to be quite a lot more apparent in those children who experienced autistic regression. Indeed the figures went something like 30% in those with autistic regression and 0% in those without. Wow. Researchers also reported that rates of autoimmune disease in the immediate family were quite a bit higher in the regression group compared with non-regressing participants (33% vs. 12%). Further: "Type 1 diabetes and autoimmune thyroiditis were both more common in families with children with autistic regression." The authors conclude: "Our findings suggest that predisposition to autoimmunity, and immune/inflammatory activation, may be associated with autistic regression."

Accepting that this was research based on chart reviews (and indeed chart reviews in 2014) and the relatively small group numbers presenting with autistic regression, these are potentially important findings. Familial autoimmune conditions/disease *correlating* with autism is by no means a new thing (see here). Type 1 diabetes - the one where the pancreas don't produce any insulin as a result of the body failing to recognise self as self - has some history in relation to offspring autism risk (see here). Autoimmune thyroiditis, or at least some of the biological markers of this disease, also has some research history (see here). Interestingly, autoimmune thyroid disease also might have some connection to cases of depression too (see here) which could pose some intriguing questions in relation to the body of research talking about antidepressant use being potentially important to offspring autism too (see here). It would be a brave person to say there is no possibility of a connection between these and other familial autoimmune conditions and offspring autism...

The febrile illness stats produced by Scott and colleagues in relation to the regression group are really very interesting. Febrile illness denoting fever and corresponding symptoms in relation to autism onset is an area crying out for further research. Yes, febrile illness can affect onset of things like seizures and/or epilepsy and it would be rather intriguing to see whether this might play a role in the onset of some autism bearing in mind the epilepsy connection posed so far (see here). But more than that are the numerous voices talking about fever being a facet of symptoms onset under quite a few circumstances [2]. The words 'post-encephalitic' spring to mind and with it, quite a bit more scientific inquiry being indicated. And there is also another area that might benefit from some additional scrutiny in relation to developmental regression 'plus' other factors accompanying cases of autism [3]...

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[1] Scott O. et al. Clinical clues for autoimmunity and neuroinflammation in patients with autistic regression. Dev Med Child Neurol. 2017 Apr 6.

[2] Mankoski RE. et al. Etiologies of autism in a case-series from Tanzania. J Autism Dev Disord. 2006 Nov;36(8):1039-51.

[3] Poling JS. et al. Developmental regression and mitochondrial dysfunction in a child with autism. J Child Neurol. 2006 Feb;21(2):170-2.

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ResearchBlogging.org Scott O, Shi D, Andriashek D, Clark B, & Goez HR (2017). Clinical clues for autoimmunity and neuroinflammation in patients with autistic regression. Developmental medicine and child neurology PMID: 28383115

Wednesday, 8 March 2017

Blocking FRAAs and thyroid function in autism (continued)

Readers of this post are advised to check out a previous blogging occasion describing how 'FRAAs - folate receptor alpha autoantibodies - may correlate with reduced thyroid function in cases of autism' before heading into this entry on the recent paper published by Richard Frye and colleagues [1].

You're back already? OK, well just in case you didn't read that last entry (😉), it's worthwhile first noting that: "Folate receptor α (FRα) autoantibodies (FRAAs) are prevalent in autism spectrum disorder (ASD). They disrupt the transportation of folate across the blood-brain barrier by binding to the FRα. Children with ASD and FRAAs have been reported to respond well to treatment with a form of folate known as folinic acid, suggesting that they may be an important ASD subgroup to identify and treat." Those are author words not mine (as is the clinical intervention mention).

The 'thyroid' addition to their recent paper follows that previous paper by the authors [2] stating that: "blocking FRAAs are associated with reduced thyroid function and suggest that thyroid function should be examined in children with ASD who are positive for the blocking FRAAs."

This time around the authors examined "blocking and binding FRAAs and thyroid stimulating hormone (TSH), free T4 (FT4), total T3 (TT3), reverse T3 (rT3), thyroid releasing hormone (TRH) and other metabolites" in 87 children diagnosed with an ASD. Some of their cohort had more than one measure of FRAAs, TSH and FT4.

Results: "TSH, TT3 and rT3 were above the normal range in 7%, 33% and 51% of the participants and TRH was below the normal range in 13% of the participants." Further: "TSH concentration was positively and the FT4/TSH, TT3/TSH and rT3/TSH ratios were inversely related to blocking FRAA titers." The observation that levels of thyroid stimulating hormone (TSH) were positively correlated with blocking FRAA titers follows the same pattern as the previous findings reported by authors. Elevations in TSH normally imply that the 'thyroid is struggling' and potentially leaning towards hypothyroidism; the correlation with FRAA titers *could* imply that those blocking antibodies might be part and parcel of why the thyroid is struggling. Ergo: "This study suggests that thyroid dysfunction in ASD may be related to the blocking FRAA."

Accepting that 'FRAA autism' (if I can call it that) is not a universal label to be applied to the autism spectrum (see here) the combined results in this area (with and without the thyroid bit added on) make for interesting reading. Not only do they offer yet another strand to the saying 'an autism diagnosis is the starting not finishing point' when it comes to assessments, but the possible intervention angle also comes to the forefront (see here).

What else would I like to see in this area? Well, quite a bit more work on thyroid function and autism could be a good starting point, outside of the maternal thyroid function (autoimmunity) and offspring risk bit (see here). Given that also all those thyroid metabolites are reliant on iodine (the number referring to the number of iodine units chemically attached), there could be quite a bit more to see when it comes to iodine and [some] autism too (see here). Then another research question: what happens to thyroid function as and when something like folinic acid is used? Science already has some idea that folinic acid - under double-blind, placebo-controlled conditions - might be useful for aspects of some autism (see here). Could we learn from other studies looking at folinic acid where thyroid function has been mentioned? [3] I daresay we could...

To close, science is great. Especially when it talks about case reports like this...

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[1] Frye RE. et al. Thyroid dysfunction in children with autism spectrum disorder is associated with folate receptor alpha autoimmune disorder. J Neuroendocrinol. 2017 Feb 15.

[2] Frye RE. et al. Folate Receptor Alpha Autoantibodies Modulate Thyroid Function in Autism Spectrum Disorder. NAJ Med Sci. 2014; 7: 53-56.

[3] Blehaut H. et al. Effect of leucovorin (folinic acid) on the developmental quotient of children with Down's syndrome (trisomy 21) and influence of thyroid status. PLoS One. 2010 Jan 11;5(1):e8394.

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ResearchBlogging.org Frye RE, Wynne R, Rose S, Slattery J, Delhey L, Tippett M, Kahler SG, Bennuri SC, Melnyk S, Sequeira JM, & Quadros E (2017). Thyroid dysfunction in children with autism spectrum disorder is associated with folate receptor alpha autoimmune disorder. Journal of neuroendocrinology PMID: 28199771

Saturday, 2 January 2016

Iodine and autism (again)

Welcome back to Questioning Answers in 2016.

Let's continue our travels down the autism peer-reviewed research path by starting with some brief discussion of the findings reported by Anna Błażewicz and colleagues [1] talking about iodine and autism.

With the aim of assessing "the iodine status of Polish boys with severe autism compared to their healthy peers" (authors words not mine), researchers reported results for various iodine and related measures (including metabolites related to thyroid function). They concluded that: "Thyroid hormones were within normal reference ranges in both groups while urinary iodine was significantly lower in autistic boys suggesting that further studies into the nonhormonal role of iodine in autism are required."

I've previously covered the topic of iodine and autism on this blog (see here). That time as this, we are talking about quite a few participants with autism presenting with iodine deficiency keeping in mind that the measurement of iodine in urine is actually quite a good way of ascertaining nutritional iodine status [2]. Błażewicz et al also suggested that various presented symptoms pertinent to autism might 'correlate' with iodine status; something again suggested in previous, independent results [3].

Insofar as the 'nonhormonal' uses of iodine and what deficiency in [some] autism might mean, I'd be minded to point other areas of interest outside of just cognitive effects [4]. The intersection between iodine, selenium and iron is worthwhile mentioning in light of the various co-dependencies of these nutrients in maintaining health and wellbeing. Other research has noted deficiencies in these three nutrients as part of a pattern in some autism [5]. Together with a suite of peer-reviewed literature suggesting that there maybe much more to see when it comes to micronutrient levels in at least some cases of autism, the onus once again is on screening followed by evidence-guided decisions on possible intervention(s).

Music, and as always at this time of year, think Vienna and An der schönen blauen Donau...

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[1] Błażewicz A. et al. Iodine in autism spectrum disorders. Journal of Trace Elements in Medicine and Biology. 2015. Dec 4.

[2] Delange F. et al. Determining median urinary iodine concentration that indicates adequate iodine intake at population level. Bulletin of the World Health Organization. 2002; 80: 633-636.

[3] Hamza RT. et al. Iodine Deficiency in Egyptian Autistic Children and Their Mothers: Relation to Disease Severity. Arch Med Res. 2013 Oct 9. pii: S0188-4409(13)00222-1.

[4] Redman K. et al. Iodine Deficiency and the Brain: Effects and Mechanisms. Crit Rev Food Sci Nutr. 2015 Apr 16:0.

[5] Blaurock-Busch E. et al. Toxic Metals and Essential Elements in Hair and Severity of Symptoms among Children with Autism. Maedica (Buchar). 2012 Jan;7(1):38-48.

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ResearchBlogging.org Błażewicz, A., Makarewicz, A., Korona-Glowniak, I., Dolliver, W., & Kocjan, R. (2015). Iodine in autism spectrum disorders Journal of Trace Elements in Medicine and Biology DOI: 10.1016/j.jtemb.2015.12.002

Sunday, 20 December 2015

The ties that bind? Comorbidity and autism (again)

"It was found that 92.9% of participants presented with a family history of autoimmune disease."

That was one of the headline findings reported in the paper by Arlene Mannion & Geraldine Leader [1] who conducted a follow-up study to previous work [2] looking at the important issue of comorbidity and autism with a specific focus on whether "comorbid symptoms changed over time."

Fifty-six children and adolescents diagnosed with DSM-IV autism spectrum disorder (ASD) participated in their study, drawn from a previous cohort of 89 involved in previous research by these authors. A range of measures were included for study including a focus on sleep and functional bowel issues.

When it came to describing this smaller cohort two years after their original research participation, examination of current comorbid diagnoses alongside ASD showed a worrying trend insofar as rates of epilepsy, attention-deficit hyperactivity disorder (ADHD) and anxiety disorder. An additional 5 children/young adults presented with ADHD at this second time of study for example. Three participants also presented with an anxiety disorder this time around. These are perhaps not unexpected findings (see here and see here).

Drilling down further into the presented data, a few other trends are present:

  • Sleep issues were prevalent. Nearly 80% of participants showed signs of a sleep problem "classified as a score of 41 or more on the CSHQ [Children's Sleep Habits Questionnaire]."
  • Gastrointestinal (GI) symptoms, as measured on the Gastrointestinal Symptom Inventory from the ATN, were also notable in this cohort. Nearly three-quarters of participants presented with at least on GI symptom within the last 3 months. A smaller group (7%) presented with 5 GI symptoms recently. GI symptoms also persisted in over 80% of participants during the 2-year period before this follow-up study.
  • GI and sleep issues also seemed to go hand-in-hand. Almost two-thirds of the cohort "presented with both sleep problems and gastrointestinal symptoms" as evidenced when specific GI symptoms were analysed (bloating, nausea, abdominal pains, diarrhoea and constipation).
  • Researchers also questioned about family medical history as well as participants. Alongside the figure already presented about familial autoimmune disease, various other "psychological, developmental or medical disorder" were noted.
  • Osteoarthritis, psoriasis and hypothyroidism (Hashimoto's thyroiditis) were the most common familial autoimmune conditions described in this cohort. Mention is however also made about Crohn's disease (n=9) and coeliac disease (n=4) too.

Obviously one has to keep in mind a few salient points before getting to carried away with this information. The participant numbers on the first occasion (N=89) and this time around (N=56) are quite small. The authors also note that the use of "parental report" might also be considered a limitation; balancing that however by making reference to the Phillip Gorrindo paper [3] covered in previous posts (see here) on how: "Parents were sensitive to the existence, although not necessarily the nature, of GID [gastrointestinal dysfunction]".

That all being said, the trends reported by Mannion & Leader are consistent with previous peer-reviewed data on the issue of comorbidity and autism. Sleep problems are pretty widespread (see here) as are functional bowel issues (see here). Indeed, even more pathological bowel issues seem to be 'over-represented' when it comes to a diagnosis of autism (see here). That the two issues might be somehow 'joined together' has also been previously raised in the research literature (see here).

The reports on certain familial health conditions being associated with cases of autism is also not new news. I've long speculated about the role of familial autoimmune conditions and autism on this blog (see here and see here) on the back of research spanning several decades (see here). Talk specifically of a connection between the skin condition psoriasis and autism is included (see here) as is the idea that both inflammatory bowel conditions (see here) and more food-related bowel states (see here) might in some families, show a connection to autism. Much more study is implied including a focus on the N=1 [4].

The idea that autoimmune disease specifically affecting the thyroid might also be a route of further scientific inquiry with autism in mind is something of real interest in light of quite a bit of other research in this area (see here and see here). As I've mentioned in previous posts, the idea that familial autoimmune disease affecting the thyroid might also be related to the onset of presentation of offspring autism [5] is a research topic crying out for further replication. The possibility of an association also opens up a number of other avenues for study based on the idea that autoimmune features might reflect one or more 'types' of autism (see here) or indeed, linked to one or more of the common comorbidities occurring alongside autism (see here and see here). Speculations are potentially aplenty in this area (see here) so we need more hard data.

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[1] Mannion A. & Leader G. An investigation of comorbid psychological disorders, sleep problems, gastrointestinal symptoms and epilepsy in children and adolescents with autism spectrum disorder: A two year follow-up. Research in Autism Spectrum Disorders. 2016; 22: 20-33.

[2] Mannion A. et al. An investigation of comorbid psychological disorders, sleep problems, gastrointestinal symptoms and epilepsy in children and adolescents with autism spectrum disorder: A two year follow-up. Research in Autism Spectrum Disorders. 2013; 7: 35-42.

[3] Gorrindo P. et al. Gastrointestinal Dysfunction in Autism: Parental Report, Clinical Evaluation, & Associated Factors. Autism Research. 2012;5(2):101-108.

[4] Genuis SJ. & Bouchard TP. Celiac disease presenting as autism. J Child Neurol. 2010 Jan;25(1):114-9.

[5] Molloy CA. et al. Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study. J Autism Dev Disord. 2006 Apr;36(3):317-24.

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ResearchBlogging.org Mannion, A., & Leader, G. (2016). An investigation of comorbid psychological disorders, sleep problems, gastrointestinal symptoms and epilepsy in children and adolescents with autism spectrum disorder: A two year follow-up Research in Autism Spectrum Disorders, 22, 20-33 DOI: 10.1016/j.rasd.2015.11.002

Wednesday, 23 September 2015

Parental autoimmunity and offspring autism risk... yet again

Here we go again.

"A positive association between maternal autoimmune diseases and the risk of ASD [autism spectrum disorder] in offspring was identified assuming a fixed effect model." Further: "Maternal autoimmune disease is likely to be an independent risk factor of ASD in offspring."

Those were the findings and conclusions published by Shao-wei Chen and colleagues [1] as part of their systematic review and meta-analysis of the available peer-reviewed literature looking at how maternal autoimmune disease might influence offspring risk of autism. Researchers specifically observed "statistically significant associations between maternal autoimmune diseases developed during pregnancy or maternal thyroid disease and the risk of ASD in offspring."

This is not new news. Not so long ago I discussed another meta-analysis that concluded that there was an overall increased risk of autism in children with a family history of autoimmune disease (see here) including a focus on specific autoimmune conditions (see here). The idea that thyroid issues might be linked to offspring autism has also been covered on this blog (see here) and not just with core autism as a possible feature (see here). Such a relationship might, I assume, be complicated by issues with iodine availability too (see here).

The implications of the Chen findings? Well, the calls for quite a bit more research on how autoimmune disease might be 'linked' to some autism grow a little louder. The possibility of preferential screening of offspring where certain autoimmune diseases might be a feature in mums and/or dads also garners a little more support.

Music: Foster The People - Pumped up Kicks.

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[1] Chen SW. et al. Maternal autoimmune diseases and the risk of autism spectrum disorders in offspring: a systematic review and meta-analysis. Behav Brain Res. 2015 Aug 29. pii: S0166-4328(15)30170-4.

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ResearchBlogging.org Chen SW, Zhong XS, Jiang LN, Zheng XY, Xiong YQ, Ma SJ, Qiu M, Huo ST, Ge J, & Chen Q (2015). Maternal autoimmune diseases and the risk of autism spectrum disorders in offspring: a systematic review and meta-analysis. Behavioural brain research PMID: 26327239

Tuesday, 21 July 2015

Early pregnancy maternal hypothyroxinemia and offspring ADHD symptoms

"Children exposed to maternal hypothyroxinemia in early pregnancy had more ADHD [attention-deficit/hyperactivity disorder] symptoms, independent of confounders. This finding suggests that intrauterine exposure to insufficient thyroid hormone levels influences neurodevelopment in offspring."

That was the bottom line reported by Thiago Modesto and colleagues [1] looking at how "mild thyroid hormone insufficiency" in early pregnancy might link into offspring behavioural outcomes a few years down the line. Based on data collected as part of the Generation R initiative - itself the source of previous research looking at the potential involvement of thyroid hormones and offspring outcome - researchers looked at maternal hypothyroxinemia "characterized by low levels of free thyroxine coexisting with reference thyrotropin levels" during pregnancy and how it correlated (or not) with parental report of offspring ADHD type behaviours based on scores on the Conners' Parent Rating Scale-Revised Short Form. They reported something of a possible association where: "Maternal hypothyroxinemia... in early pregnancy was associated with higher scores for ADHD symptoms in children at 8 years of age after adjustments for child and maternal factors (ie, sex, ethnicity, maternal age, maternal educational level, and income)." Interestingly too, when those presenting with thyroid peroxidase antibodies (a marker of autoimmune-related issues) were excluded from the analyses, the results did not differ to any great extent suggesting that the processes of being exposed to too lower a dose of thyroid hormone during early pregnancy seems to be the important factor outside of the possible reasons for such lower levels such as autoimmunity.

I've been pretty interested in the various [peer-reviewed] research looking at pregnancy thyroid hormones and offspring developmental outcomes down the years. In amongst that collected research, the idea that ADHD (or ADHD type symptoms) and even the presentation of autism might tie into the pregnancy levels of thyroid hormones has been quite a frequent feature (see here for example). Indeed, other research such as that from Libbe Kooistra and colleagues [2] over 10 years ago, had indicated that "maternal hypothyroxinemia constitutes a serious risk factor for neurodevelopmental difficulties" potentially detectable even as young as 3 weeks of age. Insofar as a role for autoimmunity in relation to pregnancy thyroid functions and offspring outcome, I'm also not quite ready to move on from a possible association as per other findings with autism in mind (see here).

Questions remains about the hows and whys of such an association and whether more could be done to extend screening for thyroid hormones particularly during early pregnancy in order to intervene and potentially 'offset' any additional developmental risks to offspring. Without making any clinical recommendations or giving anything like medical advice, I would also be interested to see how such thyroid findings might intersect with the body of work looking at issues with iodine availability (see here) and whether a wider research aim of looking at what happens in cases of pregnancy iodine deficiency in relation to thyroid hormone production and subsequent offspring development and behaviour is merited. It's not as if there isn't already some basis for further research inspection [3] in this area, also potentially extending into [some] autism (see here) too...

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[1] Modesto T. et al. Maternal Mild Thyroid Hormone Insufficiency in Early Pregnancy and Attention-Deficit/Hyperactivity Disorder Symptoms in Children. JAMA Pediatr. 2015 Jul 6.

[2] Kooistra L. et al. Neonatal Effects of Maternal Hypothyroxinemia During Early Pregnancy. Pediatrics. 2006; 117: 161-167.

[3] Vermiglio F. et al. Attention deficit and hyperactivity disorders in the offspring of mothers exposed to mild-moderate iodine deficiency: a possible novel iodine deficiency disorder in developed countries. J Clin Endocrinol Metab. 2004 Dec;89(12):6054-60.

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ResearchBlogging.org Modesto T, Tiemeier H, Peeters RP, Jaddoe VW, Hofman A, Verhulst FC, & Ghassabian A (2015). Maternal Mild Thyroid Hormone Insufficiency in Early Pregnancy and Attention-Deficit/Hyperactivity Disorder Symptoms in Children. JAMA pediatrics PMID: 26146876

Friday, 19 June 2015

Autoimmune disease or anti-nuclear antibodies and non-coeliac wheat sensitivity

"Higher proportions of patients with NCWS [wheat sensitivity among people without celiac disease] or celiac disease develop autoimmune disorders, are ANA [anti-nuclear antibodies] positive, and showed DQ2/DQ8 haplotypes compared to patients with IBS [irritable bowel syndrome]."

Those were the conclusions reached in the paper by Antonio Carroccio and colleagues [1] who sought to evaluate: "the prevalence of autoimmune diseases among patients with NCWS, and investigated whether they carry anti-nuclear antibodies (ANA)." Continuing a theme that the classic autoimmune condition known as coeliac (celiac) disease (CD) may be only one part of a 'issues with gluten' spectrum, researchers reviewed the files of over 100 participants diagnosed with NCWS (or even NCGS) "to identify those with autoimmune diseases" and compare rates with those diagnosed with CD and/or IBS. Further, serum samples were analysed prospectively for 42 participants diagnosed with NCWS and "ANA levels were measured by immunofluorescence analysis" again, compared with CD / IBS control data. ANA by the way, are antibodies against 'self' tissue and in particular, antibodies against the contents of the cell nucleus.

Results. The rates of autoimmune disease in cases of NCWS were comparable with those reported in CD, hovering around the 20-30% frequency mark in each case. The frequency rates for autoimmune disease in the IBS group were quite a bit lower; between 2-4%.

Testing positive for ANA was however a slightly different ballgame as per the findings that those with NCWS were quite a bit more likely to show ANA than either CD or IBS participants. Depending on which arm of the study was used (retrospective vs. prospective) researchers reported that: "serum samples tested positive for ANA in 46% of subjects with NCWS..., 24% of subjects with celiac disease..., and 2% of subjects IBS... ; in the prospective study, serum samples were positive for ANA in 28% of subjects with NCWS, 7.5% of subjects with celiac disease..., and 6% of subjects with IBS." They also noted a relationship between ANA positivity and the presence of DQ2/DQ8 haplotypes (part of the so-called genetics of CD).

These are interesting results. Not only because of the overlap between autoimmune diseases and CD and NCWS (birds of an autoimmune feather flocking together and all that) but also that a higher burden of anti-nuclear antibody positivity might accompany NCWS in even greater frequency than CD. That Hashimoto's thyroiditis was the most common autoimmune condition identified is also an interesting prospect and ripe for further study in light of some research history in this area [2].

Wearing my autism research hat, I might also forward the idea that the Carroccio data intersects with quite a few potentially important papers published with [some] autism in mind. So, NCGS as a feature of some autism... well, there have been some hints of this in the peer-reviewed research literature as per the 'not quite coeliac disease' paper (see here) and other commentaries (see here). What I will also say is that although there are some gaps in the research in this area including how one clinically defines NCGS, we can perhaps assume that autism is not protective against developing something like NCGS. ANA and autism... I can direct you to the paper by Mostafa and colleagues [3] covered in a previous post (see here) and how: "anti-ds-DNA antibodies and ANA were found in the sera of a subgroup of autistic children." It strikes me that further study of NCGS, autoimmune comorbidty and anti-nuclear antibodies in cases of autism is a way to resolve any correlation or not.

Music: Oasis - Champagne Supernova.

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[1] Carroccio A. et al. High Proportions of People with Non-Celiac Wheat Sensitivity Have Autoimmune Disease or Anti-nuclear Antibodies. Gastroenterology. 2015 May 27. pii: S0016-5085(15)00767-2.

[2] Hakanen M. et al. Clinical and subclinical autoimmune thyroid disease in adult celiac disease. Dig Dis Sci. 2001 Dec;46(12):2631-5.

[3] Mostafa GA. et al. Systemic auto-antibodies in children with autism. J Neuroimmunology. 2014; 272: 94-98.

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ResearchBlogging.org Carroccio A, D'Alcamo A, Cavataio F, Soresi M, Seidita A, Sciumè C, Geraci G, Iacono G, & Mansueto P (2015). High Proportions of People with Non-Celiac Wheat Sensitivity Have Autoimmune Disease or Anti-nuclear Antibodies. Gastroenterology PMID: 26026392

Tuesday, 9 June 2015

Familial autoimmune disease and offspring autism risk

"An overall increased risk of autism in children with family history of ADs [autoimmune diseases] was identified."

That was the bottom line of the "systematic review and meta-analysis" carried out by Shunquan Wu and colleagues [1] summarising the "current evidence on the relationship between family history of autoimmune diseases (ADs) and risk of autism in children." Autoimmune disorders by the way, are the various conditions that come about when the body fails to recognise self as 'self' and the immune system mounts an offensive against healthy tissue as if they were 'other' by mistake.

Regular readers of this blog might already know that I'm an avid follower of the idea that autoimmunity might show more than a passing connection to at least some cases of autism (see here) among other things (see here). Bearing in mind that autoimmunity might be just one immune system 'presentation' linked either directly or peripherally to autism (see here) I've read enough peer-reviewed evidence on the topic to be convinced that quite a bit more resource and research power should be dedicated to seeing just how deep the rabbit hole gets [2].

The Wu paper lists a number of specific ADs as showing something of an important 'correlation' to offspring autism risk including:

  • "a statistically significant association with family history of hypothyroidism." Hypothyroidism - an underactive thyroid gland - is quite commonly due to the presence of autoimmune thyroiditis (a condition that has been mentioned once or twice on this blog). Hypothyroidism, maternal hypothyroidism, is potentially something important to offspring autism risk as per other research discussions (see here).
  • A familial history of type 1 diabetes - where the pancreas doesn't produce insulin - is also mentioned as a risk factor. In amongst the research looking at the various types of diabetes and how they may have an important bearing on autism (see here), type 1 diabetes has previously cropped up on more than one occasion (see here).
  • Psoriasis - a blanket term for various autoimmune mediated skin conditions - is also identified by Wu et al as a possible risk factor for offspring autism. Again, I've talked about this condition in relation to autism before on this blog (see here).

"More mechanistic studies are needed to further explain the association between family history of ADs and increased risk of autism in children." I'd very much agree with the parting sentiments discussed by the authors on this topic. Appreciating that genetics (see here) and environment (see here) seemingly combine when it comes to the appearance of autoimmune disease, such studies of potential mechanism might need to be rather broad in their remit. I'd also put forward the notion that some potentially important data may also be garnered by looking at other facets of our genes outside of just the HLA (human leukocyte antigen) region [3] as per the growing body of work talking at HERVs (human endogenous retroviruses) and autoimmunity potentially intersecting with the science of epigenetics [4]. Oh, and in case you'd like a little more background on HERVs, a small contribution from me on the subject (see here)...

Music: Ben E. King - Stand by me.

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[1] Wu S. et al. Family history of autoimmune diseases is associated with an increased risk of autism in children: a systematic review and meta-analysis. Neuroscience & Biobehavioral Reviews. 2015. May 15.

[2] Gesundheit B. et al. Immunological and autoimmune considerations of Autism Spectrum Disorders. J Autoimmun. 2013 Aug;44:1-7. 

[3] Gough SC. & Simmonds MJ. The HLA Region and Autoimmune Disease: Associations and Mechanisms of Action. Curr Genomics. 2007 Nov;8(7):453-65.

[4] Lavie L. et al. CpG methylation directly regulates transcriptional activity of the human endogenous retrovirus family HERV-K(HML-2). J Virol. 2005 Jan;79(2):876-83.

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ResearchBlogging.org Wu, S., Ding, Y., Wu, F., Li, R., Xie, G., Hou, J., & Mao, P. (2015). Family history of autoimmune diseases is associated with an increased risk of autism in children: a systematic review and meta-analysis Neuroscience & Biobehavioral Reviews DOI: 10.1016/j.neubiorev.2015.05.004

Monday, 15 December 2014

Rates of medical illnesses in bipolar disorder

I've mentioned a few times on this blog that a diagnosis of autism or autism spectrum disorder (ASD) is by no means protective against any other diagnosis being received, be it based on a somatic illness or condition, or something more behaviourally defined.

Reading through the paper by Liz Forty and colleagues [1] (open-access) it appears that a similar scenario might also pertain to other behaviourally-defined conditions as per the example of bipolar disorder (BD) and their conclusion: "Bipolar disorder is associated with high rates of medical illness."

If I had a world of my own, everything would be nonsense
I was drawn to discuss this paper for a few reasons. First and foremost is the idea that a psychiatric diagnosis may actually place a person 'at risk' of a few important comorbidities above and beyond the presentation of their behavioural symptoms. We seem to be in an unfortunate situation these days that receipt of a psychiatric diagnosis seems to lead to a severe lack of appreciation that other symptoms or ailments of a more physical nature can also be present. Take for example the health inequalities which seem to be springing up as and when a diagnosis of schizophrenia is received (see here) and coincidentally in the same journal as the Forty paper, the study results from Mike Crawford and colleagues [2] concluding: "Assessment and treatment of common physical health problems in people with schizophrenia falls well below acceptable standards." Another reason I want to talk about the Forty paper is the fact that bipolar disorder (previously referred to as manic depression) has been described as occurring 'quite frequently' with regards to at least one part of the autism spectrum (see here). What this might suggest is that a co-occurrence of BD and something like Asperger syndrome might mean that said medical illness/conditions reported to be raised in BD would also be raised in BP + Asperger syndrome.

The Forty paper is open-access but a few pointers might be useful...

  • Based on quite an impressive participant number (N=1720) diagnosed with bipolar disorder, lifetime rates of self-reported medical illnesses were compared with data derived from participants diagnosed with unipolar depression (N=1737) and asymptomatic controls (N=1340) (both previously described in other work from some of the authors [3]).
  • Participants were quizzed - yes, no or uncertain - over whether any of 20 health conditions had been diagnosed by a health professional including: "asthma, cancer, diabetes type 1, diabetes type 2, elevated lipids/high cholesterol, epilepsy, gastric ulcers, heart disease, hypertension, kidney disease, liver disease, memory loss/dementia, migraine headaches, multiple sclerosis, osteoarthritis, osteoporosis, Parkinson’s disease, rheumatoid arthritis, stroke, thyroid disease." All the 'uncertain' codings were "excluded from analyses for that medical illness".
  • Results: "The most prevalent medical conditions in the bipolar sample were migraine headache (23.7%), asthma (19.2%), elevated lipids (19.2%), hypertension (15%), thyroid disease (12.9%) and osteoarthritis (10.8%)." Quite a few of these conditions were significantly more frequently reported in cases of BD over control groups (see Figure 1 here). I'll in particular highlight the findings for asthma and thyroid disease as being more commonly reported in the BD group.
  • Authors also divided the BD group up into subgroups (BD1 and BD2) based on the severity of manic episodes, and reported that: "The rates of gastric ulcers, heart disease, Parkinson’s disease and rheumatoid arthritis were significantly higher in the bipolar II group." They also found that several variables seemed to be linked to an increased medical illness burden including: "a longer illness duration, a typically acute onset of mood episodes, a greater number of psychiatric in-patient admissions, deterioration in functioning, increased rates of anxiety disorder, suicide attempt, rapid cycling, and treatment with anxiolytics, mood stabilisers and electroconvulsive therapy (ECT)." Some of these variables also predicted the high medical illness burden group too.

Reiterating the authors' sentiments about the need for such medical comorbidity to be taken into account by healthcare professionals "in order to improve outcomes for patients with bipolar disorder" these are important results. Assuming that there may be shared/overlapping genetic or biological mechanisms at work which influence risk of BD and also such medical comorbidity, one might think that future work would take this into account when looking at the possible underlying aetiology of BD. Such work might also accept the heterogeneity noted in BD as per similar sentiments when it comes to conditions like 'the autisms' (see here) and 'the schizophrenias' (see here).

Asthma has been highlighted from the Forty results on the basis of the condition already showing something of an interesting 'link' with conditions like autism and attention-deficit hyperactivity disorder, ADHD (see here). Indeed, data from Taiwan (yes, further interrogation of the Taiwan National Health Insurance Research Database) concluded that a diagnosis of asthma might increase the risk of subsequent mood disorders (including BD) later in life [4]. Forty et al suggested that of the possible reasons why asthma might be more frequently present in BD "carbon dioxide hypersensitivity and corticosteroid therapy may partly explain this association." I'd be perhaps inclined to add that other [speculative] work looking at the link between autism and asthma for example, might also offer another potential explanation [5].

Thyroid disease was also plucked out from the Forty data. The reason: some interesting data previously covered on this blog talking about autoimmune thyroiditis and various types of depression (see here). I'm not by the way saying that every case of thyroid disease in BD is due to such an autoimmune pathology, but as per other discussions, there might be quite a bit more to see when it comes to immune system function and behavioural and/or psychiatric diagnoses. At the very least, testing for said autoimmune issues might be considered for some.

There is little more for me to say on this subject matter. This is by no means the first time that medical comorbidity has been linked to BD [6] and even more widely depression [7] and I very much doubt it will be the last. If there are lessons to be learned from this area of investigation, the primary one must be to look at mind and body when it comes to diagnosing and managing psychiatric issues such as bipolar disorder as per other examples.

Oh, and I wonder if this would be a good time to introduce the findings from Almeida and colleagues [8] again published in the same journal as Forty and colleagues, concluding: "B vitamins did not increase the 12-week efficacy of antidepressant treatment, but enhanced and sustained antidepressant response over 1 year." Food for thought?

Music: Janis Joplin and Piece of my heart.

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[1] Forty L. et al. Comorbid medical illness in bipolar disorder. Br J Psychiatry. 2014. October 30.

[2] Crawford MJ. et al. Assessment and treatment of physical health problems among people with schizophrenia: national cross-sectional study. Br J Psychiatry. 2014. October 16.

[3] Farmer A. et al. Medical disorders in people with recurrent depression. Br J Psychiatry. 2008 May;192(5):351-5.

[4] Chen MH. et al. Higher risk of developing major depression and bipolar disorder in later life among adolescents with asthma: a nationwide prospective study. J Psychiatr Res. 2014 Feb;49:25-30.

[5] Becker KG. Autism, asthma, inflammation, and the hygiene hypothesis. Med Hypotheses. 2007;69(4):731-40.

[6] Sylvia LG. et al. Medical burden in bipolar disorder: findings from the Clinical and Health Outcomes Initiative in Comparative Effectiveness for Bipolar Disorder study (Bipolar CHOICE). Bipolar Disord. 2014 Aug 16. doi: 10.1111/bdi.12243.

[7] Smith DJ. et al. Depression and multimorbidity: a cross-sectional study of 1,751,841 patients in primary care. J Clin Psychiatry. 2014 Nov;75(11):1202-1208.

[8] Almedia OP. et al. B vitamins to enhance treatment response to antidepressants in middle-aged and older adults: results from the B-VITAGE randomised, double-blind, placebo-controlled trial. Br J Psychiatry. 2014. September 25.

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ResearchBlogging.org Forty L, Ulanova A, Jones L, Jones I, Gordon-Smith K, Fraser C, Farmer A, McGuffin P, Lewis CM, Hosang GM, Rivera M, & Craddock N (2014). Comorbid medical illness in bipolar disorder. The British journal of psychiatry : the journal of mental science PMID: 25359927

Wednesday, 19 November 2014

Down Syndrome Disintegrative Disorder

"Down syndrome disintegrative disorder seems an appropriate name for this newly recognized clinical association, which may be due to autoimmunity."
"Hi, everyone. I'm Olaf and I like warm hugs!"

That was the bottom line of the study published by Gordon Worley and colleagues [1] reviewing a small number of cases (N=11) of children diagnosed with Down's syndrome presenting at clinic "with a history of new-onset... or worsening... autistic characteristics" among other things. Based on some potentially important hunches (see here for a summary of the grant proposal for the project), researchers at Duke University and the Duke Down Syndrome Comprehensive Clinic reported results based on various behavioural and biochemical findings including that: "Ten of 11 cases (91%) had elevated ("positive") thyroperoxidase antibody titers compared to only 5 of 21 (23%) age-matched control subjects with Down syndrome".

As preliminary as these findings were, I was really rather interested to read about this study. Not only because of the link established between Down's syndrome (DS) and the presentation of autistic features harking back to some other important work (see here), but also the idea that autoimmunity might potentially be a driving force to such regressive features. Of course we already have something of a template for such a 'disintegrative disorder' in the description of Heller's syndrome, also known as childhood disintegrative disorder (CDD) (see here for some background). Until recently, CDD was included under the category 'Pervasive Developmental Disorder' roughly translating as part of the autism spectrum; although in the DSM update (DSM-5), the diagnosis no longer appears as such (see here). CDD and autism have a somewhat convoluted history intersecting with one and another during various research times and under different circumstances (see here).

Insofar as those anti-thyroid peroxidase (anti-TPO) antibodies being [positively] reported in quite a few cases of Down syndrome disintegrative disorder (DSDD), my interest is maintained. Issues potentially affecting thyroid function in relation to DS are not uncommonly reported in the research literature [2] and so one might not necessarily be surprised to hear that the presence of anti-TPO antibodies have been recorded previously [3]. Whether this finding overlaps with the Worley results in terms of early evidence for DSDD is a question we can't answer at the moment.

Indeed, autoimmunity in general, has something of a relationship with DS as per reviews such as the one by Chistiakov [4] (open-access). The fact that mention is made of coeliac disease (CD) as part of that autoimmune burden is something of particular interest to me; as the paper by Mårild and colleagues [5] noted: "a sixfold increased risk of CD in individuals with DS". These findings are all the more pertinent given that they also include one Jonas Ludvigsson on the authorship list, he of 'gluten issues not quite coeliac disease linked to some autism' (see here).

Going back specifically to the anti-TPO antibodies, I note that with the 'autistic characteristics' in mind, very little peer-reviewed research has been published in this area. It could be that anti-TPO antibodies are not something commonly seen in relation to autism or perhaps because very few people have actually looked at this issue. I will draw your attention to some of the work by Gustavo Román and colleagues [6] (see this post) which reported: "No [autism] risk was found for children of TPO-antibody–positive mothers".

That would have been all I would have said on the matter had the paper from Alan Brown and colleagues [7] not recently emerged indicating that within their cohort: "The odds of autism were increased by nearly 80% among offspring of mothers who were TPO-Ab + [positive for anti-TPO antibodies] during pregnancy (OR = 1.78, 95% CI = 1.16–2.75, p = 0.009), compared to mothers negative for this autoantibody". As interesting as this finding is, it still tells us very little about anti-TPO antibody status for those diagnosed with autism or an autism spectrum disorder (ASD) and how this might overlay with the DSDD description. I might also add that I have talked previously about research suggesting that such autoantibodies might have some link to certain kinds of depression (see here) which also draw in the possibility of comorbidity playing some role [8].

The Worley results, as preliminary as they are, are certainly worthy of further research consideration. It is a revelation to me even having an extended family member with DS, that beyond the classical presentation, there may be quite a bit more medical comorbidity which may require clinical attention. If Worley et al are indeed correct that for those with DSDD autoimmunity plays such an important role, it strikes me that directing efforts to tackle specific symptoms [9] or even autoimmune processes (as per other autoimmune conditions) might yield quite a few benefits for at least some.

Music: The Clash - Rock the Casbah.

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[1] Worley G. et al. Down Syndrome Disintegrative Disorder: New-Onset Autistic Regression, Dementia, and Insomnia in Older Children and Adolescents With Down Syndrome. J Child Neurol. 2014 Nov 3. pii: 0883073814554654.

[2] Prasher VP. Down syndrome and thyroid disorders: a review. Downs Syndr Res Pract. 1999 Aug;6(1):25-42.

[3] Chen MH. et al. Thyroid dysfunction in patients with Down syndrome. Acta Paediatr Taiwan. 2007 Jul-Aug;48(4):191-5.

[4] Chistiakov D. Down syndrome and coexistent autoimmune diseases. J Applied Biomed. 2007; 5: 71-76.

[5] Mårild K. et al. Down syndrome is associated with elevated risk of celiac disease: a nationwide case-control study. J Pediatr. 2013 Jul;163(1):237-42.

[6] Román GC. et al. Association of gestational maternal hypothyroxinemia and increased autism risk. Ann Neurol. 2013 Aug 13. doi: 10.1002/ana.23976.

[7] Brown AS. et al. Maternal thyroid autoantibody and elevated risk of autism in a national birth cohort. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2014. 29 October.

[8] Walker JC. et al. Depression in Down syndrome: a review of the literature. Res Dev Disabil. 2011 Sep-Oct;32(5):1432-40.

[9] Hegedüs L. et al. Influence of thyroxine treatment on thyroid size and anti-thyroid peroxidase antibodies in Hashimoto's thyroiditis. Clin Endocrinol (Oxf). 1991 Sep;35(3):235-8.

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ResearchBlogging.org Worley G, Crissman BG, Cadogan E, Milleson C, Adkins DW, & Kishnani PS (2014). Down Syndrome Disintegrative Disorder: New-Onset Autistic Regression, Dementia, and Insomnia in Older Children and Adolescents With Down Syndrome. Journal of child neurology PMID: 25367918