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The symptoms associated with BPH are related to bladder outlet obstruction, which is comprised of two underlying components: a static component and a dynamic component. The static component is a consequence of an increase in prostate size. Over time, the prostate will continue to enlarge. However, clinical studies have demonstrated that the size of the prostate does not correlate with the severity of BPH symptoms or the degree of urinary obstruction. The dynamic component is a function of an increase in smooth muscle tone in the prostate and bladder neck, leading to constriction of the bladder outlet. Smooth muscle tone is mediated by sympathetic nervous stimulation of alpha-l adrenoceptors, which are abundant in the prostate, prostatic capsule and bladder neck. The reduction in symptoms and improvement in urine flow rates following administration of terazosin is related to relaxation of smooth muscle produced by blockade of alpha-l adrenoceptors in the bladder neck and prostate. Because there are relatively few alpha-l adrenoceptors in the bladder body, terazosin is able to reduce the bladder outlet obstruction without affecting bladder contractility.

Terazosin has been studied in 1222 men with symptomatic BPH. In three placebo-controlled studies, symptom evaluation and uroflowmetric measurements were performed approximately 24 hours following dosing. Symptoms were quantified using the Boyarsky Index. The questionnaire evaluated both obstructive (hesitancy, intermittency, terminal dribbling, impairment of size and force of stream, sensation of incomplete bladder emptying) and irritative (nocturia, daytime frequency, urgency, dysuria) symptoms by rating each of the 9 symptoms from 0-3, for a total score of 27 points. Results from these studies indicated that terazosin statistically significantly improved symptoms and peak urine flow rates over placebo as follows:

Symptom Score (Range 0-27)

Peak Flow Rate (mL/sec)

N

Mean Baseline

Mean Change (%)

N

Mean Baseline

Mean Change (%)

Study 1 (10 mg)a

Titration to fixed dose (12 wks)

 

Placebo

55

9.7

-2.3 (24)

54

10.1

+1.0 (10)

 

Terazosin

54

10.1

-4.5 (45)*

52

8.8

+3.0 (34)*

Study 2 (2, 5, 10, 20 mg)b

Titration to response (24 wks)

 

Placebo

89

12.5

-3.8 (30)

88

8.8

+1.4 (16)

 

Terazosin

85

12.2

-5.3 (43)*

84

8.4

+2.9 (35)*

Study 3 (1, 2 , 5, 10 mg)c

Titration to response (24 wks)

 

Placebo

74

10.4

-1.1 (11)

74

8.8

+1.2 (14)

 

Terazosin

73

10.9

-4.6 (42)*

73

8.6

+2.6 (30)*

a Highest dose 10 mg shown.

b 23% of patients on 10 mg, 41%of patients on 20 mg.

c 67%of patients on 10 mg.

* Significantly (p<0.05) more improvement than placebo.