







IMPORTANT!
THE PRICE OF THE TEST INCLUDES A DNA SAMPLE COLLECTION KIT.
The Apixmed Prism Digestive System Health and Microbiome genetic test covers 26 markers across six areas of digestive system function, including 22 complex markers and 4 individual genetic variants in 4 genes.
A DNA kit for collecting your saliva sample yourself is already included in the price of the test.
Genotyping of the sample in an accredited laboratory.
A report explaining 26 markers and genetic variants in plain language, with an interpretation of the results:
22 polygenic (complex) traits with an explanation of your individual result and what it means;
4 individual genetic variants with an explanation of their possible biological significance.
Context for every marker: genetics is not considered in isolation from lifestyle, age, environment and other factors.
Personalized recommendations on nutrition, physical activity, sleep, lifestyle and preventive approaches.
The option of a consultation with an Apixmed Prism specialist based on your report results.
Pointers to potentially relevant laboratory or clinical parameters that you can discuss with your doctor.
Data protection in line with ISO 27001, GDPR and HIPAA standards.
The Digestive System Health and Microbiome genetic test covers six areas, within which it analyzes 22 complex markers and 4 individual genetic variants in 4 genes: from the esophagus and stomach to bowel motility, inflammatory bowel conditions and the microbiome. It assesses how your genetic profile and individual genetic variants are associated with a relatively higher or lower predisposition for each marker compared with a reference population. The test does not diagnose any condition directly — instead it examines the stable genetic context that complements a gastroenterological examination rather than replacing it.
DNA sample collection is done using saliva. You receive the kit by post and collect your own DNA sample into a special tube — it takes just a few minutes and requires no preparation. The sample is then sent for analysis to an accredited laboratory, and you receive your result in digital format.
22 markers across six areas. Assessed using polygenic risk scores: tens and hundreds of variants together shape the contribution to a predisposition, and no single one of them determines the picture on its own.
Esophagus and reflux conditions: esophageal disease, gastroesophageal reflux disease, Barrett's esophagus, esophageal cancer
Stomach and peptic conditions: stomach disease, gastritis, peptic ulcer disease, stomach ulcer, duodenal ulcer, stomach polyp, nausea
Bowel motility and function: irritable bowel syndrome (IBS), stool frequency, constipation
Inflammatory bowel disease: Crohn's disease, ulcerative colitis
Immune-mediated and structural gut conditions: celiac disease, malabsorption syndrome, diverticular disease
Microbiome, microbial exposure and gut barrier: gut microbiome variability, gut permeability, Helicobacter pylori seropositivity
4 genetic variants in 4 genes. A mechanistic link to the trait is described for each, so they are interpreted individually and are not included in the complex markers.
MCM6: a gene whose variant regulates the activity of the lactase gene LCT, associated with lactase persistence — the ability to digest lactose in adulthood
NOD2: recognition of bacterial components in the gut; three variants are among the best-studied associations with Crohn's disease
FUT2: secretor status, associated with interaction with the gut microbiome
Discomfort after dairy products: genetic context on lactase persistence for a conversation with your doctor or dietitian.
Family history of inflammatory bowel disease or celiac disease: specific topics for a work-up instead of guesswork.
Chronic digestive symptoms: additional context for a conversation with a gastroenterologist, not a self-diagnosis.
When choosing supplements: a reason to discuss whether they are appropriate with your doctor, not grounds to change anything on your own.
The Digestive System Health and Microbiome test is not a diagnosis and does not replace consultation with a doctor.
The results assess probability rather than establishing a predetermined outcome. They are not a diagnosis, do not confirm a disease and do not determine treatment. The test does not replace endoscopy, stool tests or other gastroenterological investigations. Clinical decisions are made by a specialist, taking into account your history, symptoms, diet, age, medication and laboratory data.