Literature DB >> 28672971

Effect of α-receptor blockers on lower urinary tract symptoms, sexual function and quality of life in young and middle-aged men with benign prostatic hyperplasia.

Tongqing Wang1, Lei Wang1, Yalin Liang2, Jiechang Ju3, Yi Cai1, Jie Zhang1, Hongtao Zhen1, Yaolei Liu1, Xiaolong Tang1, Jizheng Wang1, Jian Liu1.   

Abstract

The purpose of the present study was to compare the effectiveness of two common α1-receptor blockers, alfuzosin and tamsulosin, on lower urinary tract symptoms, sexual function, and quality of life in young and middle-aged people with benign prostatic hyperplasia. We recruited 80 young and middle-aged patients with benign prostatic hyperplasia and divided them into two groups that received either the non-selective α1-receptor blocker alfuzosin or the selective α1A-receptor blocker tamsulosin for 18 consecutive days. After intervention, maximum urinary flow, bladder compliance, maximum detrusor pressure, maximum urethral pressure, 72 h urination frequency and urination frequency at night, average urinary volume, residual urinary volume, urinary symptom distress score were significantly better in the tamsulosin group than in the alfuzosin group. Also, sperm density, sperm motility, sperm activity, and sperm DNA fragmentation index were significantly better in the tamsulosin group compared to the alfuzosin group. Finally, international index of erectile function-5 scores, increased libido and erection, retrograde ejaculation, and the quality of life were significantly better in the tamsulosin group compared to the alfuzosin group. Overall, tamsulosin effectively relieved the lower urinary tract symptoms, improved semen quality, and increased sexual life and quality of life in young and middle-aged patients with benign prostatic hyperplasia.

Entities:  

Keywords:  alfuzosin; benign prostatic hyperplasia; life quality; lower urinary tract symptoms; sexual function; tamsulosin

Year:  2017        PMID: 28672971      PMCID: PMC5488476          DOI: 10.3892/etm.2017.4518

Source DB:  PubMed          Journal:  Exp Ther Med        ISSN: 1792-0981            Impact factor:   2.447


Introduction

The development of medical technology has led to rapid improvements in endoscopic surgery. In particular, the use of endoscopy surgery has markedly reduced the proportion of open surgery for prostatic hyperplasia (1). Benign prostatic hyperplasia is mostly treated by minimally invasive procedures (2). Previous studies have confirmed that about 15% of the patients with normal sexual life before the onset of prostatic hyperplasia who received prostate surgery suffered erectile dysfunction (ED), especially young and middle-aged patients (3). Postoperative ED, retrograde ejaculation, and other surgical complications seriously affect sexual function. To improve the quality of life of patients, it is critical to protect the sexual and urinary functions (4). α1-Αdrenergic receptor blockers can effectively reduce the pressure on the bladder outlet and promote a smooth urinary flow. This relieves the clinical symptoms of benign prostatic hyperplasia and improves the lower urinary tract symptoms regardless of whether they receive surgery (5). At this time, a variety of selective α1-receptor blockers are available for clinical use (6). However, it is unclear which specific agents can improve lower urinary tract symptoms, male sexual function, and quality of life. Here, we investigated this question by comparing the benefits of alfuzosin and tamsulosin in a group of 80 young and middle-aged men suffering prostatic hyperplasia.

Patients and methods

Patient information

We recruited 80 young and middle-aged patients aged 30–60 years with benign prostatic hyperplasia admitted to Zhengzhou Central Hospital Affiliated to the Zhengzhou University from March 2013 to December 2015. Patients were diagnosed by clinical manifestations, urodynamic examination, and prostatic ultrasound. All patients signed the informed consent forms before enrollment. The study was approved by the Ethics Committee of the Zhengzhou Central Hospital Affiliated to the Zhengzhou University. Urinary function before onset was normal; after the onset, patients urinated immediately after the micturition desire, and it was difficult to control. Patients urinated more than 8 times per day and 3 times at night. Exclusion criteria: patients with serious cardiopulmonary and renal dysfunction, urinary dysfunction, urinary incontinence, clear urinary tract infection, coagulation dysfunction, severe cardiopulmonary, hepatic and renal dysfunction, mental illness, preoperative ED, reduced preoperative sperm quality, severe endocrine system diseases, and malignant tumors caused by other reasons. The 80 patients were equally divided into control and experimental groups according to the random number method.

Methods

Patients received symptomatic and supportive treatment, such as risk assessment, being alert to complications, and strengthening health education. The control group was treated with alfuzosin orally (NMPN H20010398; Shenyang Tianling Pharmaceutical Co., Ltd., Liaoning, China) (2.5 mg, 3 times per day), and the maximum daily dose was controlled within 10 mg. The experimental group received tamsulosin orally (NMPN J20140015; Astellas Pharma, Tokyo, Japan) (0.2 mg, 1 time per day). Patients in both groups were treated for 18 consecutive days.

Experimental indexes

We compared urodynamics after intervention, 72 h urination log record after intervention, urinary symptom distress scores before and after intervention, Semen production indexes after intervention, international index of erectile function-5 (IIEF-5) scores at different time points, indexes related to sexual function at 6 months after intervention, and quality of life scores before and after intervention.

Evaluation criteria

Urinary function

Postoperative urodynamics included the maximum flow, maximum detrusor systolic pressure, bladder compliance, and maximum urethral pressure of patients after surgery. Maximum urinary flow referred to the maximum amount of urine discharged from the urinary tract measured by chamber pot. The other indexes were measured with a bladder double-chamber piezometer tube combined with rectal piezometric tube as follows: normal saline was slowly and reversely injected into the bladder. The rectal tube was used to determine the changes in abdominal pressure, and the maximum pressure of detrusor under systolic pressure with the influences of abdominal pressure eliminated effectively, to understand bladder compliance, and determine the maximum urethral pressure.

Residual urinary volume

A Philips iU22 transabdominal B-ultrasound (Philips, Amsterdam, The Netherlands) was used for the measures. The residual urinary volume after the urination was recorded and each measurement was performed by the same ultrasound physician with more than 5 years of experience.

Urinary symptoms distress score

Assessment was by subjective perception to determine the degree of distress and tolerance to lower urinary tract symptoms. They were classified as happy, satisfied, generally satisfactory, generally unsatisfactory, and distressed or poor with 1–6 points (36 points in total). The higher the score, the more obvious the lower urinary tract discomfort symptoms were.

Urinary log

Clinically known as the urinary frequency table, mainly used to record urination habits under living conditions. Generally recommended to record for 72 h continuously, including the total intake of liquid, urination time, urinary volume each time, number of episodes of urinary incontinence and environment, urinary volume during urinary incontinence, 72 h urination frequency, urination frequency at night, and average urinary volume.

Erectile function

Erectile function was evaluated using IIEF-5 scores (24 points in total). Scores below 21 points suggested ED.

Retrograde ejaculation

Retrograde ejaculation referred to the existence of ejaculation feeling during sexual intercourse, but without semen ejection from the urethra and urine analysis after sexual intercourse showed sperms in the urine. The enhanced sexual desire meant that the requirement of sex was increased by more than 50% on average every month.

Examination of semen

Routine semen examination was conducted before the discharge. Semen was collected with masturbation or instrument. DNA fragmentation index (DFI) was detected using sperm DNA fragment detection kit (SCD method) and observed under a light microscope at ×40. The sperm aureole in semen was compared to evaluate sperm damage and DNA fragmentation.

Quality of life

Quality of life was evaluated using the Nottingham Health Survey Questionnaire, including energy, pain, emotional changes, sleep quality, adaptability to social life, and physical activity. The full score for each item was 100 points, with the higher scores indicating the worse quality of life.

Statistical analysis

SPSS 19 (IBM Corp., Armonk, NY, USA) was used for statistical processing. Measurement data were presented as mean ± standard deviation. t-test was used for the comparison of means between the two groups, chi-square test was used for the comparisons between the two groups, and analysis of variance (ANOVA) was used for comparing means within the group. P<0.05 indicates that the difference was statistically significant.

Results

Demographic and functional distribution of patients

Distribution by gender, age, disease course, maximum urinary flow, bladder compliance, maximum detrusor pressure, maximum urethral pressure, 72 h urination frequency, urination frequency at night, average urinary volume, residual urinary volume, urinary symptom distress scores, sperm density, sperm motility, sperm activity, sperm DFI, IIEF-5 scores, and quality of life scores in the two groups are shown in Table I. We found no statistically significant differences in any of the parameters between the groups.
Table I.

General biometric and clinical data.

GroupsExperimentalControlt-test or χ2P-value
Age (years)48.5±2.148.6±2.10.2130.832
Course of disease (months)3.2±0.33.3±0.31.4910.140
Maximum urinary flow (ml/sec)5.3±0.25.3±0.30.0001.000
Maximum detrusor pressure (cm H2O)8.1±0.38.2±0.31.4910.793
Maximum urethral pressure (cm H2O)20.4±1.520.5±1.50.2980.766
Urination frequency during 72 h (times)56.6±2.956.7±3.00.1520.880
Urination frequency at night (times)6.9±1.17.0±1.10.4070.686
Average urinary volume (ml)89.5±2.990.1±3.00.9090.366
Residual urinary volume (ml)115.8±11.3116.3±11.40.1970.844
Urinary symptom distress score (points)30.2±1.830.3±1.80.2480.804
Sperm density (109/l)36.1±2.336.2±2.40.1900.850
Sperm motility (%)61.1±10.560.9±10.60.0850.933
Sperm activity (%)78.2±10.077.3±10.10.4000.690
DFI (%)25.9 ± 5.226.0±5.10.0870.931
IIEF-5 score18.3±1.218.2±1.20.3730.710
Quality of life score81.5±2.381.6±2.30.1940.846

DFI, DNA fragmentation index; IIEF-5, international index of erectile function-5.

Urodynamics after treatment

After intervention, the maximum urinary flow, the bladder compliance, the maximum detrusor pressure, and the maximum urethral pressure in the experimental group was higher than in the control group (Table II).
Table II.

Urodynamics after intervention (mean ± standard deviation).

GroupsMaximum urinary flow (ml/sec)Bladder compliance (cm H2O)Maximum detrusor pressure (cm H2O)Maximum urethral pressure (cm H2O)
Experimental13.3±1.235.0±3.119.1±2.042.1±3.1
Control9.0±0.526.5±1.313.4±0.637.5±2.3
t-test20.92015.99217.2657.537
P-value<0.001<0.001<0.001<0.001

Urination log record after treatment

After intervention, the 72 h urination frequency, the urination frequency at night, the average urinary volume, and the residual urinary were lower in the experimental group than those in the control group (Table III).
Table III.

Frequency of urination after intervention during 72 h (mean ± standard deviation).

GroupsUrination frequency during 72 h (times)Urination frequency at night (times)Average urinary volume (ml)Residual urinary volume (ml)
Experimental23.5±1.92.5±0.3256.3±25.18.1±1.3
Control43.2±5.15.1±1.1118.9±16.366.5±4.9
t-test22.89315.36429.03672.858
P-value<0.001<0.001<0.001<0.001

Urinary symptom distress scores before and after treatment

The difference in urinary symptom distress between the two groups before the intervention was not statistically significant (Table IV). However, the urinary symptom distress after intervention was significantly higher in the experimental group than that in the control group (Table IV).
Table IV.

Urinary distress scores before and after intervention (mean ± standard deviation).

GroupsBefore interventionAfter interventiont-testP-value
Experimental30.2±1.85.9±0.384.220<0.001
Control30.3±1.820.4±1.228.943<0.001
t-test0.24874.140
P-value0.804<0.001

Semen indexes after intervention

Sperm density, sperm motility, and sperm activity after intervention were higher in the experimental group than those in the control group (Table V). DFI was lower in the experimental group than that in control group (Table V).
Table V.

Indexes related to semen after intervention (mean ± standard deviation).

GroupsSperm density (109/l)Motility (%)Activity (%)DFI (%)
Experimental45.1±2.381.1±11.578.2±10.08.9±1.3
Control24.2±1.458.9±9.155.6±8.131.0±5.1
t-test49.0929.57411.10726.557
P-value<0.001<0.001<0.001<0.001

DFI, DNA fragmentation index.

IIEF-5 scores at different time points

The difference in IIEF-5 scores between the two groups before intervention was not statistically significant (Table VI). After 3 and 6 months of intervention, IIEF-5 scores were higher in experimental group than those in the control group (Table VI).
Table VI.

IIEF-5 scores at different time points (mean ± standard deviation).

GroupsBefore intervention3 months after intervention6 months after interventionFP-value
Experimental18.3±1.221.3±0.422.3±0.518.569<0.001
Control18.2±1.219.4±1.220.6±0.423.361<0.001
t-test0.3739.50016.791
P-value0.7100.000<0.001

IIEF-5, international index of erectile function-5.

Sexual function 6 months after intervention

The increase in libido and erection function were higher in the experimental group than those in the control group (Table VII). In contrast, the rate of retrograde ejaculation was lower in the experimental group than that in the control group (Table VII).
Table VII.

Sexual function indexes 6 months after intervention (cases).

GroupsIncreased libidoEnhanced erection functionRetrograde ejaculation
Experimental19212
Control6911
χ28.3786.4535.878
P-value0.0040.0110.015

Quality of life scores before and after intervention

The difference in quality of life scores before intervention between the two groups was not statistically significant (Table VIII). The quality of life scores for both groups were superior after intervention compared to those before intervention (Table VIII), but the scores for experimental group were higher than that for the control group (Table VIII).
Table VIII.

Quality of life scores before and after intervention (points, mean ± standard deviation).

GroupsBefore interventionAfter interventiont-testP-value
Experimental81.5±2.335.3±1.1114.608<0.001
Control81.6±2.356.6±1.755.823<0.001
t-test0.19466.530
P-value0.846<0.001

Discussion

With the change of living and eating habits, the onset of benign prostatic hyperplasia has showed a younger trend (7). Benign prostatic hyperplasia has become the most common urinary disease in young and middle-aged men. This disease leads to urinary tract obstruction and lower urinary tract symptoms, such as frequent urination, urgent urination and dysuria. Longer disease course or acute obstructions also cause acute renal insufficiency, and patients complicated with severe cardiovascular disease may even suffer from acute myocardial infarction because of urination difficulty (8). Therefore, benign prostatic hyperplasia seriously reduces the quality of life and endangers the lives of patients (9). The preferred treatment is surgery, but the operation is not widely recommended due to the trauma and postoperative complications (10). Some patients, especially young and middle-aged patients with relatively mild symptoms, receive a conservative drug treatment (11). However, a dozen of selective α1-receptor blockers are used in the treatment of benign prostatic hyperplasia (12). The present study compared the effectiveness of two commonly-used selective α1-receptor blockers, alfuzosin and tamsulosin. Examining multiple parameters of urinary function, we found that the ultra-selective α1-receptor blocker tamsulosin improved the performance of alfuzosin in all parameters. Thus, tamsulosin treatment can effectively improve bladder compliance in young and middle-aged patients with benign prostatic hyperplasia. This may be possibly accomplished because tamsulosin can selectively act on the smooth muscles of the urinary tract system, relieve spasms (13), and reduce the aseptic inflammatory response in the prostate tissues, thus improving the urinary function of patients (14). Tamsulosin can also act on the sympathetic nervous system of the pelvic floor, promote the relaxation of the pelvic floor muscles, and alleviate pain and discomfort caused by muscle tension in the perineum, the urethra, and the pelvic floor (15,16). In addition, the comparisons of indexes for semen production and quality, sexual function and satisfaction, and overall quality of life showed that tamsulosin performed better than alfuzosin in all parameters. The semen quality after tamsulosin was better than that in patients treated with alfuzosin because the latter acted on all the α1-adrenergic receptors in the sympathetic nervous system of the sperm transport pathway. This leads to the contraction of smooth muscles in the reproductive system and inhibits the contraction of smooth muscles in seminal vesicle and ejaculatory duct (17), thus blocking sperm transport. Tamsulosin is an ultra-selective α1-adrenergic receptor blocker, which reduces the impact on the smooth muscles of the male reproductive system without affecting the transport and release of semen (18), and reduces the incidence of ejaculation pain. The improvement of quality of life after tamsulosin is due to the selective block of the spinal semen secretion center and ejaculatory center α1D-receptor, thereby reducing sexual excitability and increasing the ejaculation threshold (19). This activity also significantly relaxed the smooth muscles of the above structures via blocking α1A-receptors in the seminiferous duct, seminal vesicle, ejaculatory duct, and prostate to delay the ejaculation (20). The enhanced erectile function might be due to tamsulosin block of α1A-receptor, better regulating the contraction and relaxation of penile corpus cavernosum, and increasing blood flow into the corpus cavernosum under sexual excitement, thereby increasing the penis hardness and improving libido. Tamsulosin, also inhibited the α1-receptors in the bladder neck, posterior urethra, and prostate, thus eliminating the smooth muscle spasms in the urethra, reducing the pressure within the urethra, and slowing the reflux of prostatic fluid during ejaculation, reducing retrograde ejaculation. In conclusion, tamsulosin is more effective than alfuzosin in relieving the lower urinary tract symptoms, it improves the semen quality, sexual life, and quality of life in young and middle-aged patients with benign prostatic hyperplasia.
  20 in total

1.  Effectiveness of Solifenacin and Trospium for Managing of Severe Symptoms of Overactive Bladder in Patients With Benign Prostatic Hyperplasia.

Authors:  Kirill Vladimirovich Kosilov; Sergay A Loparev; Marina A Ivanovskaya; Liliya V Kosilova
Journal:  Am J Mens Health       Date:  2015-07-17

2.  Comparing Monotherapy with Tadalafil or Tamsulosin and Their Combination Therapy in Men with Benign Prostatic Hyperplasia: A Randomized Clinical Trial.

Authors:  Hossein Karami; Amin Hassanzadeh-Hadad; Morteza Fallah-Karkan
Journal:  Urol J       Date:  2016-12-08       Impact factor: 1.510

3.  Words of Wisdom: Re: A Randomized Controlled Study of the Efficacy of Tamsulosin Monotherapy and its Combination with Mirabegron for Overactive Bladder Induced by Benign Prostatic Obstruction.

Authors:  Martin C Michel
Journal:  Eur Urol       Date:  2016-01       Impact factor: 20.096

Review 4.  Serenoa repens, selenium and lycopene to manage lower urinary tract symptoms suggestive for benign prostatic hyperplasia.

Authors:  Andrea Russo; Paolo Capogrosso; Giovanni La Croce; Eugenio Ventimiglia; Luca Boeri; Alberto Briganti; Rocco Damiano; Francesco Montorsi; Andrea Salonia
Journal:  Expert Opin Drug Saf       Date:  2016-06-01       Impact factor: 4.250

5.  Discovery of ONO-7300243 from a Novel Class of Lysophosphatidic Acid Receptor 1 Antagonists: From Hit to Lead.

Authors:  Masahiko Terakado; Hidehiro Suzuki; Kazuya Hashimura; Motoyuki Tanaka; Hideyuki Ueda; Hiroshi Kohno; Taku Fujimoto; Hiroshi Saga; Shinji Nakade; Hiromu Habashita; Yoshikazu Takaoka; Takuya Seko
Journal:  ACS Med Chem Lett       Date:  2016-08-19       Impact factor: 4.345

6.  [Long-term outcomes of the use of α-blockers tamsulosin in men with lower urinary tract symptoms and benign prostatic hyperplasia].

Authors:  G G Krivoborodov; E I Tur
Journal:  Urologiia       Date:  2014 Nov-Dec

7.  Adverse Effects of Pharmacological Therapy of Benign Prostatic Hyperplasia on Sexual Function in Men.

Authors:  Nebojša Stojanović; Ivan Ignjatović; Nebojša Djenić; Dragan Bogdanović
Journal:  Srp Arh Celok Lek       Date:  2015 May-Jun       Impact factor: 0.207

8.  Effect of tamsulosin on the pharmacokinetics of dutasteride in Chinese male healthy volunteers.

Authors:  Huafang Li; Jiansong Yang; Hongxin Zhao; Michael J Fossler; Chunrong Wang
Journal:  Clin Pharmacol Drug Dev       Date:  2015-07-20

9.  Alpha blocker monotherapy versus combination therapy with antimuscarinics in men with persistent LUTS refractory to alpha-adrenergic treatment: patterns of persistence.

Authors:  Jack Barkin; Demitri Diles; Billy Franks; Todd Berner
Journal:  Can J Urol       Date:  2015-08       Impact factor: 1.344

10.  Effects of hexanic extract of Serenoa repens (Permixon® 160 mg) on inflammation biomarkers in the treatment of lower urinary tract symptoms related to benign prostatic hyperplasia.

Authors:  Alain Latil; Marie-Thérèse Pétrissans; Jérôme Rouquet; Grégoire Robert; Alexandre de la Taille
Journal:  Prostate       Date:  2015-08-26       Impact factor: 4.104

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.