Androgenetic alopecia risk in allergic rhinitis: A cohort study of immune and antihistamine effects.

BACKGROUND

Androgenetic alopecia (AGA), though traditionally attributed to androgens and genetics, is increasingly linked to immune and inflammatory pathways. Allergic rhinitis (AR) and AGA may share overlapping mechanisms, including prostaglandin signaling abnormalities. Second-generation H1-antihistamines (sgSH), used to treat AR, have anti-inflammatory and immunomodulatory properties and may influence hair follicle biology. This study aimed to determine the association between AR and the risk of AGA and to explore whether the use of sgSH impacts this risk.

METHODS

This retrospective cohort study used the Taiwan National Health Insurance Research Database (NHIRD) between 2000 and 2021. Totally, 539,397 patients diagnosed with AR were included and categorized into sgSH users and nonusers. AGA incidence was estimated using Cox proportional hazards models.

RESULTS

AR patients had a higher risk of AGA (adjusted hazard ratio [aHR]: 1.81, 95% confidence interval [CI]: 1.69-1.93, p < 0.001). Among AR patients, sgSHs users had a lower risk of AGA than nonusers (aHR: 0.23, 95% CI: 0.20-0.26), with a dose-dependent effect (p < 0.001). The strongest effect seen in patients <30 years old (aHR: 0.18, 95% CI: 0.15-0.21, p < 0.001).

CONCLUSIONS

This study observed that AR is associated with an increased risk of AGA and that sgSH use was statistically associated with a lower incidence of AGA, especially in younger individuals. However, the possibility that the observed associations reflect unmeasured confounding, rather than direct biological effects, cannot be ruled out. Future research should further clarify the complex relationship between allergic diseases and hair loss from multiple perspectives and assess the possibility of sgSH as a supplementary measure in the prevention or treatment of AGA. From a clinical perspective, our findings underscore the importance of heightened awareness of early hair loss in patients with chronic AR.