the prostate normally functions to close off the bladder neck during orgasm to prevent retrograde ejaculation into the bladder.
circulating testosterone is converted by type 2 5-alpha reductase in prostate stromal cells to dihydrotestosterone (DHT) which is a more potent and longer binding agent activating nuclear androgen receptors on both stromal and epithelial cells resulting in synthesis of growth factors and thus the resultant hyperplasia.
castrated males (ie, who are unable to make testosterone) do not develop BPH
there may be a role for hyperinsulinaemia to contribute to prostatic growth
BPH originates in the transition zone surrounding the urethra
in patients with BPH, the prostate usually weighs 60-100g
the combination of increased size of the prostate tissue, with smooth muscle mediated contraction of the prostate results in urethral obstruction.
patients experience increased urinary frequency, nocturia, difficulty in starting and stopping the stream of urine, overflow dribbling, and dysuria.
the symptoms are not only due to the bladder outlet obstruction itself, but are also due to the secondary hypertophic effects on the bladder wall which becomes thickened, trabeculated and irritable with increased sensitivity (detrusor over-activity) to even small bladder volumes resulting in urinary frequency.
increased resistance to flow results in bladder hypertrophy and distension with risk of sudden onset of
acute urinary retention.
inability to empty the bladder creates a reservoir of residual urine which is a common source of infection and
urinary tract infections (UTIs) / cystitis, and may result in bladder stones (3.4% of autopsies with BPH vs 0.4% in those without BPH).