Dietetics Predispositions

Caffeine is the most widely consumed psychoactive substance globally, found in coffee, tea, energy drinks, and some medications. The way your body processes caffeine depends largely on genetic factors, specifically how fast or slow caffeine is metabolized.

This test analyses specific genetic variations that affect how efficiently your body breaks down caffeine. People with certain genetic variations metabolize caffeine more slowly, leading to prolonged effects and potentially stronger stimulation. Slow metabolizers may also be at a higher risk for side effects like headaches, insomnia, and an increased risk of heart issues. Understanding your caffeine metabolism rate can help manage caffeine consumption for better health outcomes.

Cholesterol plays a vital role in heart health, but imbalances can lead to serious conditions like atherosclerosis, heart attacks, and strokes. High cholesterol is a major risk factor for cardiovascular diseases, which are the leading cause of death globally.

This test analyses genetic variations that affect how your body processes cholesterol. Identifying these variations can help understand your risk for high cholesterol and related health issues, providing insights into better managing your cardiovascular health.

Folic acid is essential for the proper functioning of the nervous, circulatory, and cardiovascular systems. This vitamin plays a key role in the metabolism of amino and nucleic acids, and deficiencies can lead to serious conditions like nervous system disorders and anaemia. It is also particularly important for women planning pregnancy, as folic acid is vital for foetal development.

This test analyses genetic variations that affect how efficiently your body converts folic acid. Changes in this gene can reduce folic acid absorption, increasing the risk of deficiency. Understanding your genetic predisposition can help manage folic acid levels for better health.

Lactose intolerance occurs when the body cannot properly digest lactose, a sugar found in dairy products, due to a lack of the lactase enzyme.

Our Lactose Intolerance Genetic Test analyses genetic variations that determine how well your body produces the enzyme needed to break down lactose. Identifying these variations helps determine your level of lactose tolerance, allowing you to manage symptoms and adjust your diet accordingly.

Peanut allergy is a serious condition that can trigger life-threatening reactions, such as anaphylaxis, after consuming peanuts.

This test analyses specific genetic variations that are associated with an increased susceptibility to the development of peanut allergies and play a key role in hereditary peanut allergy. Understanding your genetic predisposition can help manage the risk of severe allergic reactions, enabling better lifestyle choices and preventive measures.

Vitamin C is essential for immune function and overall health, acting as a powerful antioxidant. However, not everyone metabolizes vitamin C efficiently due to genetic factors.

This test analyses specific genetic variations that affect how your body processes vitamin C. Certain genetic deletions can reduce your ability to metabolize this vitamin, leading to lower levels despite similar dietary intake. Understanding your genetic predisposition can help ensure you meet your body's vitamin C needs through diet and supplementation.

Vitamin D is essential for maintaining healthy bones, muscles, and immune function. It is primarily produced in the skin through sun exposure, but genetic factors can affect how well your body metabolizes and transports this crucial nutrient.

This test analyses specific genetic variations that influence the efficiency of vitamin D metabolism. People with certain genetic changes may have a reduced ability to process vitamin D, leading to deficiency even with normal sun exposure or dietary intake. In the UAE, despite ample sunlight, vitamin D deficiency is widespread due to limited sun exposure and lifestyle factors. Understanding your genetic predisposition can help manage vitamin D levels to prevent associated health issues.

Vitamin E is a powerful antioxidant, essential for immune function, skin health, and proper nerve and muscle function. Vitamin E also contributes to the maintenance of the proper functions of the reproductive organs of men and women, while during pregnancy, an optimal amount aids in the development of the foetus. 

This test analyses specific genetic variations that affect how your body metabolizes fats, which are necessary for absorbing vitamin E. People with certain genetic changes may struggle to efficiently absorb vitamin E, leading to potential deficiencies. Understanding your genetic predisposition can help manage vitamin E levels, promoting overall health and vitality.

Fructose intolerance is a condition where the body cannot properly digest fructose, a sugar found in fruits, honey, and certain vegetables. This can lead to digestive issues such as bloating, abdominal pain, and diarrhoea, as well as more severe complications like liver problems and hypoglycaemia.

This test analyses specific genetic variations that affect how the body metabolizes fructose. People with certain changes in their genes may have reduced ability to process fructose, leading to intolerance. Understanding your genetic predisposition can help manage symptoms and prevent long-term health complications.

Iron is essential for oxygen transport, immune system function, and many other vital processes. Low iron levels can result in anaemia, causing symptoms like fatigue, weakness, and dizziness. While environmental factors can influence iron levels, genetic factors also play a significant role.

Our Iron Metabolism Genetic Test analyses variations in a key gene that helps regulate iron levels in the body. Certain genetic changes can predispose individuals to iron deficiency anaemia, making it harder to maintain healthy iron levels. Understanding your genetic predisposition can help identify the cause of chronic low iron and guide appropriate management.

Vitamin B12 is crucial for producing red blood cells, supporting the nervous system, and aiding various metabolic functions. Deficiencies can lead to symptoms like anaemia, dizziness, weakness, and neurological issues.

This test analyses specific genetic variations that affect the production of an enzyme involved in the absorption of vitamin B12 in the small intestine and its transport between the cells in the human body. People with an unfavourable genetic variant have a higher risk of vitamin B12 deficiency, related to the malabsorption of this vitamin. Understanding your genetic predisposition can help manage vitamin B12 levels to support overall health.

Coeliac disease (Gluten Intolerance) is an autoimmune condition where the body reacts negatively to gluten, causing inflammation and damage to the intestinal lining. This leads to malabsorption of nutrients, resulting in symptoms like abdominal pain, diarrhoea, and weight loss.

This test analyses specific genetic variations that affect the body’s immune response and tolerance to gluten. People with certain genetic variants are more likely to develop coeliac disease. Understanding your genetic predisposition can help identify gluten intolerance early, allowing for dietary adjustments to avoid long-term health complications.