Rosacea is a widespread skin condition in France and around the world. Over the past few decades, several hypotheses have been proposed regarding the causes of this disease, and various sources attribute rosacea to a hereditary origin. Discover below if scientific literature truly mentions genetic predispositions to developing rosacea.
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Rosacea: Are there genetic predispositions to developing this dermatosis?
Summary
Published September 12, 2024,
updated on September 12, 2024,
by
Marie, Scientific Editor
—
5 min read
Topics:
Is Rosacea a Hereditary Condition?
Rosacea is an inflammatory and chronic dermatosis that predominantly affects the face, rosacea is characterized by a widespread and diffuse redness, sometimes accompanied by the dilation of small blood vessels, making them visible. Other symptoms often accompany this disease, such as hot flashes, skin hypersensitivity, or burning sensations. In some cases, rosacea can progress and lead to the appearance of pimples, significant skin thickening, or even affect the eyes.
While the causes of rosacea are still poorly understood and seem to be multifactorial, one hypothesis stands out in the scientific community: that of a genetic predisposition to develop this skin condition. This suspicion comes notably from the frequency of rosacea occurrence in individuals with very fair skin and eyes. It has indeed been observed that people from Northern Europe, who predominantly have phototypes I to III, are more affected by the disease than those with darker skin.
According to some epidemiological data, up to 30% of individuals with rosacea have a family history of this condition.
A study conducted by POPKIN in 2015 aimed to highlight the link between genetics and the development of rosacea. For this purpose, 233 pairs of monozygotic twins and 42 pairs of dizygotic twins, totaling 550 individuals, were surveyed to determine if they exhibited symptoms of rosacea. As a reminder, monozygotic twins share almost 100% of their genetic material, while dizygotic twins share about 50% of their genes. By observing the incidence of rosacea among the different twins, as well as their lifestyle habits, the researchers were able to establish a genetic correlation percentage, evaluated here at 46%. According to this study, rosacea appears to be attributable in equal parts to genetic factors and environmental factors, such as exposure to UV rays, alcohol consumption, or smoking.
Rosacea and Genetics: What are the Mechanisms Involved?
While it appears that rosacea may be partly due to genetic predispositions, the involved genes and underlying mechanisms are not yet fully understood. However, several genetic analyses have demonstrated the existence of a specific polymorphism, called rs763035, which would be associated with rosacea. This is located between the HLA-DRA and BTLN2 genes. As a reminder, polymorphism refers to the different forms a single gene can take. Based on these findings, it seems that rosacea is linked to three class II HLA alleles, the same ones involved in the development of type I diabetes retinopathy. This hypothesis aligns with other epidemiological observations showing an association of rosacea with certain autoimmune diseases.
A study conducted by OUSSEDIK in 2018 also delved into the genetics of rosacea to better understand its mechanisms. The researchers particularly studied the anti-microbial peptides secreted by keratinocytes and their role in the genetic predispositions of rosacea. Fundamentally, these peptides are found in the sebaceous glands and serve as an endogenous defense against external microorganisms. In addition to their antimicrobial function, some of these peptides, such as linear cationic α-helical peptides like LL-37, a human cathelicidin, can also increase the production of cytokines, thereby contributing to inflammation. LL-37 is also suspected to play a role in skin immunity, and its dysfunction could influence the pathogenesis of rosacea.
Indeed, the analysis of transcription in a murine model has established that the cathelicidin LL-37 was upregulated in the case of rosacea. Researchers have also shown that the overexpression of LL-37 was linked to an increase in the transcription of TRPV4 in mast cells. Now, TRPV4 partially ensures skin homeostasis and the maintenance of the skin barrier. A disruption in the expression of this gene could therefore also be implicated in the development of rosacea.
Even though some mechanisms are beginning to become clear, progress in understanding the genetic component of rosacea remains necessary in order to develop targeted therapies and improve disease management.
Sources
NOVAK P. & al. Clinical, cellular, and molecular aspects in the pathophysiology of rosacea. Journal of Investigative Dermatology Symposium Proceedings (2011).
LEYDEN J. & al. New insight into rosacea pathophysiology : A review of recent findings. Journal of the American Academy of Dermatology (2013).
POPKIN D. & al. Genetic vs environmental factors that correlate with rosacea: A cohort-based survey of twins. JAMA Dermatology (2015).
OUSSEDIK E. & al. Genetic Predisposition to Rosacea. Dermatologic Clinics (2018).
SARKAR R. & al. Rosacea in skin of color: A comprehensive review. Indian Journal of Dermatology, Venereology and Leprology (2020).
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