EARLY DETECTION AND TREATMENT OF CROHN’S DISEASE
IBD Sensor
The IBD Sensor uses genetic analysis to determine the risk of Crohn’s disease.
The IBD Sensor uses genetic analysis to determine the risk of Crohn’s disease.
Crohn’s disease is an inflammatory bowel disease, which can cause both chronic and intermittent symptoms. Typical symptoms include abdominal pain, diarrhea, weight loss, and fatigue.
Crohn’s disease can also lead to a dangerous lack of nutrients and inflammation in other parts of the body, such as the joints. The course of the disease varies from patient to patient. In some cases, ulcers can also form in the intestine over time.
The exact causes of Crohn’s disease have not yet clear. In addition to an unhealthy lifestyle, genetic changes play a particularly important role in Crohn’s disease.
About half of all those affected have specific genetic defects that influence the immune system. For this reason, genetic analysis can help to assess the individual risk of Crohn’s disease and take appropriate preventive measures if necessary.
For our IBD Sensor, we analyze the submitted sample in our laboratory. We investigate the NOD2 gene for three genetic variations associated with Crohn’s disease. In addition, we assess the effect of 21 relevant drugs based on their genetic profile.
In this way, we can assess the risk of Crohn’s disease and whether concrete preventive measures should be taken.
Once the analysis has been successfully completed, we prepare a written report in which we present the results of our investigations and recommend any preventive measures that may be necessary.
In this way, our IBD Sensor enables reliable early detection and helps those affected to recognize symptoms in good time and alleviate them with an appropriate diet.
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