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P8.102 Patients with large prostate size show Higher
Prevalence of Androgenetic Alopecia
Chao-Chun Yang1, Tzong-Shin Tzai2, Meng-Chi
Wu1, WenChieh
Chen3
1Department of Dermatology and 2Urology, College of Medicine,
National Cheng Kung University, Tainan, Taiwan; * Department of Dermatology, Chang Gung
University, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan
Objectives: Androgenetic
alopecia (AGA) and benign prostatic hyperplasia (BPH) are both
androgen-dependent disorders, displaying in situ high level of
dihydrotestosterone with good therapeutic response to finasteride, a specific
type II 5-reductase inhibitor. The hair follicle and prostate share
similarities in embryological development with mesenchymal-epithelial
interaction, influenced by the expression of type II 5- reductase. The
present study aims to understand the association between the prostate size and
the prevalence and severity of AGA.
Methods: Ninety-seven
patients (Mean age 69.8 year-old) were retrospectively recruited from the
Urology clinic. BPH was defined and diagnosed by (1) prostate size > 20 cm3,
measured by transrectal ultrasound (2) maximal urine flow rate < 15 ml/sec
and mean urine flow rate < 10 ml/sec (3) PSA < 10 ng/ml. Included as
controls were patients with urogenital infection or urolithiasis. The presence
and severity of AGA were evaluated by dermatologists using a modified
Norwood/Hamilton classification. The difference of prevalence of AGA was
analyzed by Chi-square test. Correlation between severity of AGA and size of
prostate was estimated by Spearman’s rank correlation test. Comparison of mean
prostate size in AGA vs. non-AGA patients was analyzed by Student’s t-test.
Results: Patients with prostate size larger than
30 cm3 in volume have higher prevalence of AGA than patients with
smaller prostate (<30 cm3). (83.3 % vs. 61.3 %; p< 0.05). The
prostate size, however, does not correlate with the severity of AGA in either
group or in the whole patient group. The prevalence of AGA is not significantly
different in patients with or without BPH (85.7 % vs. 70.6 %). The mean
prostate size is slightly larger in patients with AGA than those without AGA
(42.7±17.4 cm3 vs. 35.4±14.9 cm3), but this is not
statistically significant. There is no significant correlation between the
onset age of AGA and the development of BPH.
Conclusions: Patients with
larger prostate size seem to have higher prevalence of AGA. It remains to see
if long-term use of finasteride in AGA patients could prophylactically lower
the incidence of BPH.
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