Two research groups site the locus of risk for androgenetic alopecia, but the responsible mutation or gene is still being untangled.
Androgenetic alopecia (AGA) is probably the most common form of hair loss in both men and women. Although a genetic component is recognized in the condition’s appellation, the true genetic basis of this phenotype is unknown. In previous studies, AGA was associated with changes in the androgen receptor (AR) gene on the X chromosome. Two groups of investigators recently tackled this common phenotype at the genome level.
Hillmer and colleagues conducted a genome-wide association study in German subjects to identify predisposing genetic factors in AGA. The researchers genotyped 296 males with early-onset (age, <40) AGA, with a median Hamilton and Norwood hair-loss grade of VI (range, IV–VII) and 383 population-based controls (201 women; the mixe…
Reviewing Author
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)
DisclosuresConsultant / advisory board Lubax; WorldCare Clinical
EquityLubax
Grant / Research support NIH; Department of Defense; American Skin Association; Piramal
Editorial boardsBritish Journal of Dermatology; Journal of the American Academy of Dermatology; Journal of Investigative Dermatology
Leadership positions in professional societies American Academy of Dermatology (Chair, Skin Cancer and Melanoma Committee); American Board of Dermatology (Director)