Our study is the first ever genome-wide association study into frontal fibrosing alopecia (FFA), a lichenoid inflammatory and scarring condition affecting almost exclusively women. We have identified causal variants conferring susceptibility to this increasingly common and highly distressing disease, whilst some of our work has highlighted potential new treatment targets. We are very grateful to all our referring clinicians in the UK and Spain, all clinical and research staff, our patients and the National Institute for Health Research, for financially supporting our work.Dr Christos Tziotzios, study lead, NIHR Academic Clinical Fellow in the Genetic Skin Disease Group, St John's Institute of Dermatology
08 March 2019
Scientists identify genetic locations implicated in development of frontal fibrosing alopecia
In a first ever genome wide association study into frontal fibrosing alopecia (FFA) scientists have shown that it is caused by a complex immune-inflammatory response.
A study involving 5,161 women in the United Kingdom and Spain was published by researchers from the Biomedical Research Centre and St John's Institute of Dermatology. The researchers identified four locations within the genome, where variations or mutations are believed to be strongly associated with the onset of Frontal fibrosing alopecia (FFA).
FFA is a distressing skin disorder, occurring predominantly in women, causing skin inflammation, scarring and irreversible hair loss. Since the disease was first described in 1994 there has been a significant increase in its incidence worldwide, leading scientists and clinicians to conclude that the disease may have both environmental and genetic causes.
The study identified a location within the HLA-B gene that is most strongly associated with the occurrence of FFA. HLA-B is an important immune recognition gene. Variation in immune recognition genes may cause a response that results in auto-immune inflammation which leads to the destruction of stem cells around the hair follicle, which in turn causes irreversible hair loss. The study also found that this mutation within the HLA-B gene may result in a five-fold increase in the risk of developing FFA.
It also identified what could potentially be an environmental basis for the disease in a second genetic location of importance, CYP1B1 – a gene that codes for a metabolic enzyme that is involved in xenobiotic and sex hormone degradation. The scientists now plan to investigate what role sex hormones and other environmental factors might have in putting women at risk of developing FFA.
These discoveries provide a potential way of identifying women at risk of FFA along with the potential for new therapies.
The study was published in Nature Communications and can be read here.