This test requires a blood draw, so please ensure you can refer to a phlebotomist in the clients area before you order this test.
Zonulin has been identified as a key biomarker for intestinal permeability, which has been associated with celiac disease, non-celiac gluten sensitivity (NCGS), and other GI and systemic conditions.
Circulating zonulin is a clinically useful marker of intestinal permeability. Zonulin is a protein, synthesized in intestinal and liver cells, that reversibly regulates intestinal permeability.
High levels of zonulin have been associated with increased intestinal permeability, as zonulin induces the breakdown of the tight junctions between intestinal epithelial cells. Several autoimmune, inflammatory, and neoplastic diseases have been associated with elevated levels of zonulin or evidence of increased intestinal permeability. These include celiac disease, type 1 diabetes, and juvenile nonalcoholic fatty liver disease. In addition, evidence is accumulating to support an association with multiple sclerosis, rheumatoid arthritis, asthma, and inflammatory bowel disease.
Zonulin levels may be higher in obese adults and in adults with glucose intolerance. Elevated serum levels of zonulin and increased permeability are commonly observed in patients at risk of developing Crohn’s disease or type 1 diabetes prior to the onset of symptoms. Zonulin levels may increase with corticosteroid use.
Cellular receptors for zonulin are present in the small and upper large intestines, the heart, and the brain. Zonulin release from the epithelium may be triggered by gliadin fragments or by the adherence of bacteria to the epithelial cell surface. Simple sugars, sodium, emulsifiers, the food additive microbial transglutaminase, and nanoparticles are known to disrupt intestinal barrier function.
Restoration of the gastrointestinal mucosal barrier may include dietary changes, treatment of dysbiosis, digestive supports, and anti-inflammatory therapies. These may include supplements such as quercetin, vitamin C, curcumin, gamma-linoleic acid, omega-3 fatty acids (EPA, DHA), and aloe vera. Other nutrients such as zinc, beta-carotene, pantothenic acid, and L-glutamine may provide some support for rejuvenation of the GI mucosa. Consider a Comprehensive Stool Analysis to further investigate potential causes of increased intestinal permeability.
Zonulin expression in the small intestine occurs when a chemokine receptor is stimulated by gliadin or chemokines and induces proinflammatory signaling pathways in gastrointestinal epithelial cells. The released zonulin activates the cell-signaling pathway via protease-activated receptor 2 and epidermal growth factor, which causes disassembly of the tight junctions between the GI epithelial cells. The loss of the tight junctions increases intestinal permeability and allows polypeptides and other macromolecules to pass between epithelial cells into the lamina propria layer of the gut wall. The macromolecules and polypeptides induce an antigen response and promote proinflammatory cytokine production in the enteric immune system.
Zonulin is a prehaptoglobulin—levels are modulated by the presence or absence of haptoglobin (HP) gene. When zonulin is cleaved by intestinal tryptase IV, it is converted into haptogloblulin, a protein with heme (iron)-binding and antimicrobial properties. HP-1-1 genotypes have zero (null) copies of the HP gene. HP-2-2 genotypes have two copies of the gene, and HP-1-2 genotypes have one copy of the gene. HP 1-1 (null) genotypes may have zonulin levels in the normal range, even if the presence of inflammatory or autoimmune disease is confirmed by other biomarkers. Zonulin levels may increase in nephrotic syndrome (Hp2-1 or 2-2 phenotypes).
This test is useful for:
Celiac disease
Non-celiac gluten sensitivity
Type I diabetes
Juvenile nonalcoholic fatty liver disease
Multiple sclerosis
Rhuematoid arthritis
Asthma
Inflammatory bowel disease
Adult glucose intolerance
Overview
Analytes Tested:
Zonulin; serum
Practical
Sample required:
Serum
This is a serum sample and requires a full blood draw
Turnaround Time:
Maximum of 21 days