Eczema is an inflammatory skin disease characterized by skin redness and intense itching. Very common, eczema is also the subject of several theories. Among all the ideas circulating about this condition, the one suggesting that eczema has a genetic origin stands out. Discover here if this disease is indeed hereditary.
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Eczema: Could it be Hereditary?
Summary
Published September 20, 2023,
updated on June 24, 2024,
by
Pauline, Chemical Engineer
—
4 min read
Eczema: Definition and Symptoms.
Theeczema is a chronic inflammatory skin disease, characterized by red and warm lesions, varying in extent on the body. These are accompanied by intense itching. It's worth noting that eczema can affect almost all parts of the face and body. At the site of the lesions, there is a thickening of the skin, known as lichenification. Small vesicles filled with clear fluid then appear at the site of the red lesions, and eventually burst due to scratching. A crust then forms, which heals to varying degrees afterwards.
Eczema is often persistent. Between flare-ups or outbreaks of eczema, there are periods of remission where the skin remains very dry (xerosis). However, eczema is considered a benign condition. Indeed, even though the itching it causes and its psychological impact cannot be overlooked, this disease does not pose a life-threatening risk to health. Moreover, appropriate management and following dermatological advice can limit its impact on the quality of life of those affected. Finally, it is important to emphasize that eczema is non-contagious.
Eczema: A Hereditary Dermatosis?
In some cases, eczema indeed has a hereditary component. According to several studies, 50 to 70% of children affected by eczema have a first-degree relative who has also been affected. This is referred to asatopic eczema, meaning that the individuals affected have a predisposition to develop common allergies to pollen, dust, or animal hair, for example. Several biological mechanisms play a role in this atopy.
One of the primary causes of atopic eczema is the mutation of the gene coding for filaggrin. In atopic individuals, this gene is often inactive. A study has indeed shown that a mutation of this gene in a pregnant woman results in a 50% increase in the risk of atopic dermatitis for the unborn child. Indeed, filaggrin is a protein of the stratum corneum that plays an essential role in the proper functioning of the skin barrier. It is notably incorporated into the lipid envelope and also interacts with keratin filaments. A lack of filaggrin in the stratum corneum is associated with greater transepidermal water loss (TEWL) and a higher capacity for allergens to penetrate the skin. This skin is generally more dry, more permeable, and less protected.
Furthermore, it is estimated that about 70 to 80% of people with atopic eczema naturally produce an abnormally high amount of immunoglobulin E (IgE), antibodies, in response to environmental allergens. When a person is sensitive to an allergen, their immune system produces specific IgE for that allergen. These IgE attach to receptors found on mast cells, immune cells primarily located in connective tissues. Consequently, any exposure to this allergen causes it to bind to the IgE and triggers the release of histamine, a chemical mediator, from the granules contained in the mast cells. This then leads to a cascade of reactions resulting in typical eczema inflammation, characterized by redness and itching.
Note : not all forms of eczema are hereditary, for instance, consider contact eczema. Furthermore, even if your eczema has a genetic component, if you decide to have a child, they may not necessarily be affected.
Sources
GOLDENBERG G. & al. Eczema. The Mount Sinai Journal of Medicine (2011).
LEE Y.-A. & al. The genetics of the skin barrier in eczema and other allergic disorders. Current Opinion in Allergy and Clinical Immunology (2015).
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