What is Diacetoxyscirpenol (DAS)? And Why Does the Toxin Zoomer Test for It?

Trichothecene fungal mycotoxin
Diacetoxyscirpenol (DAS) is a trichothecene mycotoxin produced by Fusarium fungi that can interfere with cellular protein synthesis. Measuring urinary DAS helps detect recent environmental or food-based exposure and, when paired with detox genetics, gives clinicians context about potential toxic load and clearance capacity.
Diacetoxyscirpenol (DAS)
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About Diacetoxyscirpenol (DAS)
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Diacetoxyscirpenol (DAS) FAQs

What is Diacetoxyscirpenol (DAS) and why is it important?
DAS is a mold-derived trichothecene mycotoxin produced by certain Fusarium species. It is monitored because its presence indicates recent exposure to fungal contamination in food or environments. Knowing DAS levels helps clinicians see one part of a person’s total mycotoxin burden and how that exposure fits with other toxin and genetic data.
What does it mean if my Diacetoxyscirpenol (DAS) levels are low?
Low or non-detectable DAS usually suggests little recent exposure to Fusarium mycotoxins or that sampling did not capture the exposure window. It can also reflect rapid metabolic conversion or effective elimination. Low DAS is most informative when considered alongside other toxin markers and detoxification genetics to confirm a low mycotoxin burden.
What does it mean if my Diacetoxyscirpenol (DAS) levels are high?
Higher urinary DAS suggests recent contact with a Fusarium-related source, such as contaminated food or a moldy environment, or slower clearance due to individual factors. Elevated levels can flag increased mycotoxin load and potential contribution to inflammatory or metabolic stress in research observations. Accurate interpretation requires viewing DAS with other mycotoxin results, environmental chemical findings, and detox-genetic data.
Why is Diacetoxyscirpenol (DAS) measured on the Toxin Zoomer?
DAS provides a specific indicator of Fusarium mycotoxin exposure within the comprehensive Toxin Zoomer profile. Measuring DAS helps identify exposure sources, quantify part of the mycotoxin burden, and, when combined with detox genetics, supports a more personalized assessment of how environmental pressures may interact with an individual’s clearance capacity.

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