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|Title:||Men with Kennedy disease have a reduced risk of androgenetic alopecia.|
|Epworth Authors:||Sinclair, Rodney|
|Other Authors:||Greenland, K. J.|
van Egmond, Sylvia
Zajac, J. D.
Severity of Illness Index
Trinucleotide Repeat Expansion
Chair of Dermatology, Epworth HealthCare
Head & Neck Clinical Institute, Epworth HealthCare
|Citation:||Br J Dermatol. 2007 Aug;157(2):290-4|
|Abstract:||BACKGROUND: Spinal and bulbar muscular atrophy or Kennedy disease (KD) is an X-linked neurodegenerative disease caused by an expansion of a polymorphic tandem CAG repeat within the androgen receptor (AR) gene on chromosomal locus Xq11-q12. The CAG repeat region encodes a polyglutamine tract that, when expanded to above 40 in number, results in KD, a neurodegenerative disease primarily targeting lower motor neurones. KD is also associated with partial androgen insensitivity due to loss of receptor function. Degree of expansion of this repeat region, located in the first exon, is correlated with age at onset and disease severity. Androgenetic alopecia (AGA) is a polygenic trait also associated with functional polymorphism of the AR gene. OBJECTIVES: To test whether partial loss of function in the AR gene associated with CAG polymorphism reduces the risk of AGA in affected men. METHODS: Members of the Kennedy's Disease Association, an American-based support group, were invited to participate in an online survey to determine the age-related prevalence of AGA among men affected by KD. Data from 115 respondents with KD were compared with data from 654 white men of European descent in Maryborough, Australia. RESULTS: The mean AGA score for men with KD was 1.64 (95% confidence interval, CI 1.41-1.87). The mean score for men in Maryborough was 2.82 (95% CI 2.71-2.93). The difference between the means was highly significant (P < 0.001), indicating thicker hair among the KD cohort. Treating AGA score as a continuous variable we found age to be highly significantly related to AGA score in men from Maryborough (P < 0.001) but not among men affected by KD (P = 0.90). CONCLUSIONS: Men with KD have a reduced risk of AGA, likely to be due to a functional alteration in the AR caused by the polyglutamine expansion.|
|Journal Title:||British Journal of Dermatology|
|Affiliated Organisations:||Department of Dermatology, University of Melbourne, St Vincent's Hospital, Fitzroy, Victoria, Australia|
|Type of Clinical Study or Trial:||Survey|
|Appears in Collections:||Head & Neck|
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