Lupus (systemic lupus erythematosus)

Lupus (systemic lupus erythematosus)

BioCertica Content Team

Systemic lupus erythematosus (SLE), commonly referred to just as lupus, is a chronic autoimmune disorder that can affect multiple organs and tissues throughout the body. Lupus arises when the immune system mistakenly attacks healthy cells and tissues, resulting in inflammation and damage to them.


The symptoms of lupus can vary widely but may include fatigue, joint pain and stiffness, skin rashes, fever, and sensitivity to sunlight. The condition can also affect the kidneys, lungs, heart, and other organs, leading to a range of symptoms depending on the extent and location of organ damage.


While the exact cause of lupus is not fully understood, research has shown that genetics can play a role in its development. Studies have identified several genes that may contribute to the development of lupus, although no single gene has been identified as the primary cause. 


The genetic factors involved in the development of lupus are complex and involve a combination of genetic variations that can increase or decrease an individual's risk of developing the condition. For example, certain variations in the interferon regulatory factor 5 (IRF5) gene have been shown to increase the risk of developing lupus, particularly in individuals of African ancestry.


It's important to note that while genetics can play a role in the development of lupus, the condition is not solely determined by genetics. Other factors, such as exposure to viruses or other environmental triggers, may also contribute to the development of the condition.


Stress is a significant trigger that can contribute to the development of lupus, especially in genetically predisposed individuals. Thus, for prevention, the most important consideration would be stress management. 


Although there is no cure for lupus, treatment is available to help manage symptoms and prevent extensive damage to the body’s organs. It can be a difficult condition to diagnose, which may impede treatment. Therefore, knowing your genetic predisposition may aid in early detection and intervention if symptoms arise. 

 

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