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Wheat Found To Contribute To Rare Liver Disease In Children

Friday, November 25, 2016 11:19
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A study published in the Journal of Pediatric Gastroenterology and Nutrition implicates gluten-containing grains in the pathogenesis of two related pediatric liver conditions: cryptogenic hypertransaminasemia (HTS), marked by the elevation of liver enzymes (transaminases) with unknown cause, and autoimmune hepatitis (AIH), marked by the host immune system producing autoantibodies that attack the liver.  In fact, the relative risk of a positive diagnosis of autoimmune hepatitis in children with celiac disease was found to be 188.54 times higher than in those without celiac disease, indicating that the damage commonly associated with severe, immune-mediated intolerance to wheat proteins (i.e. celiac disease) extend “beyond the intestine” to the liver. It also opens the door for the therapeutic role of a gluten-free diet in certain pediatric liver diseases.

The researchers conducted a systematic review and meta-analysis of the biomedical literature, spanning from 1977 to May 2012, in order to evaluate the prevalence of celiac disease in children with the two aforementioned liver conditions.  Nine studies involving a total of 2046 patients were identified. The results were as follows:

  1. Pooled prevalences of celiac disease in children with mild, non-specific cryptogenic persistent HTS and HTS in children with celiac disease were 12.0% (95% CI 4.17-29.96) and 36.0% (95% CI 32.15-40.11), respectively.
  2. A gluten-free diet normalized transaminase levels in 77%-100% of celiac disease patients within 4-8 months.
  3. Pooled prevalences of celiac disease in children with AIH and AIH in children with celiac disease were 6.3% (95% CI 3.87-11.73) and 1.4% (95% CI 0.84-2.15), respectively.
  4. The relative risk (RR) of HTS in children with celiac disease versus the general population, and of celiac disease in children with HTS was 6.55 (95% CI 5.65-7.60) and 11.59 (95% CI 3.80-35.33) fold higher, respectively. The corresponding RRs of AIH in children with celiac disease were 188.54 (95% CI 92.23-385.43) fold higher. The RR of celiac disease in children with AIH was 6.63 (95% CI 3.86-11.40) higher.

Their Conclusion was as Follows

Celiac disease is associated with elevated transaminase levels in about one-third of newly diagnosed children. Cryptogenic persistent HTS may signal gluten-dependent non-specific mild hepatitis (12.0% of cases) or more rarely (6.3%) severe celiac disease-related autoimmune hepatopathy. Relative risks confirm these trends in the considered associations.


Wheat’s potential to cause immune-mediated liver damage has been observed in previous studies. For instance, in 2008, a study was published in the journal Liver International  that found celiac disease prevalence in a five-fold higher percentage of patients with end-stage autoimmune liver disease.[i]

Another study published in the Scandinavian Journal of Gastroentology in 2003 found that patients with chronic liver disease have a high prevalence of anti-tissue transglutaminase enazymes, similar to patients with celiac disease.[ii]

While these studies are illuminating, there is an 800 lb gluten-grain eating gorilla in the room, which is the weight of the biomedical literature itself when it comes to evidence describing the disease-promoting properties of wheat, and gluten containing grains in general. This research has found wheat has a wide range of modes of toxicity, from immunotoxic to neurotoxic, teratogenic to inflammatory, etc. We have painstakingly indexed over 200 adverse health effects and/or diseases associated with wheat consumption alone which can be viewed here: Wheat Toxicity Research. Moreover, there are over 23,000 distinct proteins produced by the gene-dense modern wheat plant (a hexaploid species, having six sets of chromosomes), any of which could induce an antigenic response in the human body, especially considering how difficult it is to digest disulfide-bonded proteins down to their non-immunogenic free amino acids.


The post Wheat Found To Contribute To Rare Liver Disease In Children appeared first on The Sleuth Journal.


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  • Fokofpoes

    Insane speculation, but, Gluten is not a functional protein, it is a chimeric agent for the promotion of spores and “culture”, if you know what I mean.

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