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. |
|