29 citations
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November 2018 in “Journal of The European Academy of Dermatology and Venereology” This study found that anxiety-related traits significantly predict the impact of hair loss on quality of life across different alopecia types, with variations observed based on gender.
8 citations
,
May 2025 in “British Journal of Dermatology” This study found that the psychosocial impact of AA is more strongly related to patients' illness perceptions and stigma than to the severity of the disease.
4 citations
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July 2021 in “International Journal of Environmental Research and Public Health” This study found that women with severe hair loss from childhood irradiation for tinea capitis were at a higher risk of developing psychosocial symptoms, including depression, compared to men.
4 citations
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November 2022 in “Frontiers in Medicine” This study found that people with alopecia areata have a higher likelihood of experiencing anxiety and depression, and a moderate negative impact on their quality of life compared to healthy individuals.
8 citations
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October 2018 in “Journal of Investigative Dermatology” This study observed that alopecia areata patients experience significant psychosocial issues, with a high prevalence of anxiety, depression, and impaired quality of life across symptoms, functioning, and emotions.