Factors Associated with Bothersome Lower Urinary Tract Symptoms in Middle-Aged Men Receiving Health Checkup

The prospective study is to investigate the associations between serum testosterone levels and LUTS among middle-aged men ≥40 years receiving health check-up. Lower urinary tract symptoms were evaluated by the self-administered International Prostate Symptom Score questionnaire. Serum prostate specific antigen and total testosterone level were checked in all subjects. A total of 1752 men were enrolled into the study. The mean age was 55.6 ± 9.7 years. All study subjects were stratified into low, medium and high testosterone levels by two cut-off, 3.0 and 4.11 ng/mL. We found that testosterone levels were significantly associated with metabolic syndrome and body fat components. Compared to those with low testosterone levels, subjects with high and medium testosterone had a significantly higher IPSS (5.84 ± 5.55 vs 6.71 ± 5.68 and 6.34 ± 5.66, p = 0.032) and storage score (2.76 ± 2.29 vs 3.20 ± 2.49 and 2.90 ± 2.49; p = 0.009), and a more moderate/severe LUTS (IPSS ≧ 8) (26.5% vs 35.7% and 29.9%; p = 0.002). Multivariate analyses showed that high vs low testosterone levels (OR, 1.76; 95% CI, 1.26–2.45) and prostate volume ≧25 vs <25 mL (OR, 1.38; 95% CI, 1.04–1.82) significantly associated with the presence of moderate/severe LUTS. Pearson correlation analyses showed significantly positive correlations between testosterone level and IPSS in whole study sample (Pearson correlation coefficient, 0.066; p < 0.01) and in the subgroup of moderate/severe LUTS (Pearson correlation coefficient, 0.038; p < 0.05). In conclusion, high testosterone and prostate volume adversely impacted LUTS in our target population.


Statistics.
For descriptive findings, the continuous variables were presented as mean and standard deviations (SD), and categorical variables as percentages. The total testosterone level below 3 ng/mL has been used in clinical practice as a cut-off for the diagnosis of low testosterone and testosterone deficiency. All study subjects were stratified into three subgroups based on serum total testosterone as low, medium, and high testosterone levels by using 3.0 and 4.11 ng/mL as cut-off points. In our study, the range of testosterone level in the low testosterone subgroup was 0.2-3.0 ng/mL. For subjects with serum testosterone level >3 ng/mL, we divided them into medium (range 3.1-4.1 ng/mL) and high (>4.1 ng/mL) testosterone subgroups for further analyses. Differences in baseline characteristics among the three groups were analyzed using one-way ANOVA and chi-squared tests. A p-value less than 0.05 was considered statistically significant. Multivariate analyses to evaluate the impact of the respective factors on LUTS were performed by logistic regression method. All potential risk factors for LUTS such as age, prostate volume, serum PSA level and the presence of metabolic syndrome were included in the analyses. To examine the correlations between testosterone level as continuous parameter and other parameters, we calculated Pearson correlation coefficients to measure the linear associations of testosterone level with IPSS, age, serum PSA and prostate volume. In addition, we divided the cohort into two groups, mild (IPSS < 8) and moderate/severe LUTS (IPSS ≥ 8). We analyzed the relationships of testosterone level with IPSS, age, serum PSA and prostate volume in subjects with moderate/severe LUTS. All analyses were performed with SPSS statistical software for Windows (SPSS, version 13.0; SPSS Inc., Chicago, IL).

Results
Of the 2083 men who volunteered to undergo medical check-up during the study period, we excluded 331 subjects. Patients were excluded if any one of the exclusion criteria applied: the use of hormone replacement therapy (n = 13) or 5-alpha reductase inhibitors (n = 56) within the last 6 months, having a history of prostate cancer (n = 13) or prostate surgery (n = 36), or current use of anticholinergics (n = 97) or sympatholytics (n = 135). The remaining 1752 men were included in the study. Table 1 lists the baseline characteristics of all study subjects. The mean testosterone level was 3.76 ng/mL (SD 1.38). Overall, 138 (7.8%) of the study subjects had hypogonadism (testosterone level below 2.30 ng/mL). All study subjects were stratified into low, medium and high testosterone subgroup by cut-off of 3.0 and 4.11 ng/mL.
The mean age was 55.6 years (SD 9.7). Age, height, prostate volume and serum PSA did not differ significantly among the three groups. Contrastingly, weight (76.0 ± 12.3 vs. 72.2 ± 9.47 and70.2 ± 9.01 kg) and body mass index, (26.3 ± 3.60 vs. 25.0 ± 2.85and 24.2 ± 2.77 kg/m 2 ) of subjects in the low testosterone level group were significantly higher compared to those in the medium and high testosterone groups (p < 0.001 for both). Several metabolism-related blood chemistry profiles were significantly higher in the low testosterone group compared to the medium and high testosterone groups, including serum albumin (4.73 ± 0.25 vs. 4.68 ± 0.26 and 4.63 ± 0.24), glycated hemoglobin (5.92 ± 0.83 vs. 5.75 ± 0.66 and 5.70 ± 0.69) and uric acid (6.70 ± 1.40 vs. 6.49 ± 1.18 and 6.27 ± 1.23). Similarly, five MS associated medical conditions were more prevalent in the low testosterone group compared to the medium and high testosterone groups (all p < 0.001); these include an increase in waist circumference (59.7% vs. 46.8% and 37.7%), higher blood pressure (59.4% vs. 55.8% and 48.4%), higher fasting blood sugar (39.1% vs. 29.2% and 22.5%), higher triglyceride levels (46.7% vs. 31.1% and 20.9%) and higher high-density lipoprotein (HDL) levels (49.7% vs 39.6% and 29.2%). Additionally, 52.1%of subjects in the low testosterone group fit the diagnosis of MS compared to 37.4% and 23.2% in the medium and high testosterone groups, respectively (p < 0.001). Body mass indices such as body fat (%), fatness (kg), body fat mass (kg), lean body mass (kg), total body water (kg), basal metabolic rate, intracellular fluid (kg), extracellular fluid (kg), protein (kg), muscle (kg) and mineral (kg) were significantly different in the low testosterone group compared to the medium and high testosterone groups (all p < 0.05). Subjects with low testosterone levels had significantly In Table 2, we compared LUTS across the three groups. Subjects with low testosterone levels had lower IPSS scores than subjects with medium and high testosterone levels (5.84 ± 5.55 vs 6.34 ± 5.66 and 6.71 ± 5.68; p = 0.032). Moreover, subjects with low testosterone levels had significantly lower storage scores than subjects with medium and high testosterone levels (2.76 ± 2.29 vs 2.90 ± 2.49 and 3.20 ± 2.49; p = 0.009). Subjects with high testosterone levels had more severe symptoms of frequency and intermittency (p < 0.05). Overall, 35.7% of subjects in the high testosterone group had moderate/severe LUTS (IPSS ≧ 8), compared to 29.9% in the medium testosterone group and 26.5% in the low testosterone group.
We further subdivided subjects into three groups within age categories of 40-49, 50-59, and 60-69 years. We then compared the MS and LUTS among three groups. As shown in Table 3, subjects in older age categories had higher IPSS scores compared to those in younger group. There was no significantly difference for MS diagnosis among three groups; nevertheless, several MS associated medical conditions such as blood pressure, fasting blood sugar and serum triglyceride were significantly different among three groups (all p < 0.001). Several body mass indices such as lean body mass (kg), total body water (kg), basal metabolic rate, intracellular fluid (kg), extracellular fluid (kg), protein (kg), muscle (kg) and mineral (kg) were significantly different among three groups (all p < 0.001).  Table 5 shows the correlations between testosterone level as a continuous parameter and other parameters such as age, prostate volume, PSA and IPSS in all study subjects. The results showed there was significantly positive correlation between testosterone level and IPSS (Pearson correlation coefficient, 0.066; p < 0.01). We then divided the cohort into two groups, mild (IPSS < 8) and moderate/severe LUTS (IPSS ≥ 8). We analyzed the relationships of testosterone level with IPSS, age, serum PSA and prostate volume in subjects with moderate/ severe LUTS. As is shown in Table 6, testosterone level was positively correlated with LUTS (Pearson correlation coefficient, 0.038; p < 0.05) in subjects with moderate/severe LUTS.

Discussion
The significant association between MS and low testosterone levels has been well studied. Testosterone levels have been reported to be a valuable indicator of MS in middle-aged men 14 . Additionally, there is an inverse relationship between testosterone and body fat in men 15 . Our results confirmed the significant associations between testosterone levels and MS as well as body fat components in the present study.  LUTS are mostly attributed to BPE in middle-aged men and declining testosterone levels and the presence of MS are prevalent in middle-aged men 16,17 . These two important factors may also play a role in LUTS of middle-aged men. MS has been thought to be associated with prostate enlargement 18,19 . The correlations between severity of male LUTS and MS-related medical conditions have been reported [20][21][22][23] . Nevertheless, the exact relationship between MS and LTUS remains controversial. Some studies indicated a positive correlation between MS and LUTS 24,25 . Several studies from Asia papulation suggested no significant associations between MS and male LUTS [25][26][27] . In contrast, some studies indicated that men with MS had lower risk of developing moderate to severe LUTS compared to those without MS 28 . Eom et al. reported that MS and accompanying hyperinsulinemia may have a favorable impact on IPSS and voiding score 29 .
The relationship among testosterone, LUTS and MS is ambiguous. Cohan et al. introduced a hypogonadism-obesity-BPE-LUTS model and found that abdominal obesity and intra-abdominal pressure caused by the net positive caloric balance leads to reduced testosterone and elevated the estrogen levels. The continuous hypogonadism will enlarge the prostate and worsen LUTS 30 . An animal model showed that hypercholesterolemia and the associated pelvic ischemia can cause bladder fibrosis, smooth muscle atrophy, and decrease bladder compliance 31 . Long-term testosterone replacement in men with hypogonadism and erectile dysfunction can restore functions, reduce obesity parameters and improve metabolic syndrome and health-related quality of life 32 . Our results show that larger prostate volume and high testosterone levels were significantly associated with moderate/severe LUTS (IPSS ≧ 8) in our target male population. In contrast, age, metabolic syndrome and metabolic syndrome-associated medical conditions were not independent predictors of moderate/severe LUTS in our study sample.
Several studies also showed a negative correlation between testosterone levels and LUTS 33,34 . However, most of these study cohorts were composed of men with LUTS or erectile dysfunction seeking for help. Antunes et al. reported that higher testosterone levels are associated with a severe AUA score symptom index in obese patients 35 . The recommendations for testosterone replacement therapy made by the Endocrine Society were critically re-examined recently 36 ; it was suggested that men with large prostates should be treated with caution. Based on   the results of our study, testosterone replacement therapy should be approached cautiously in middle-aged men with severe LUTS. Recent studies reported that testosterone replacement therapy did not induce aggravation of LUTS 8,9,37 . Kohn et al. reviewed a series of randomized control trials and concluded the impacts of testosterone replacement therapy on LUTS were similar to placebo effect 9 . The results of this study was limited by the characteristics of study participants. The study did not include men with severe LUTS, who were the main concern in prescribing testosterone replacement 38 . Since the problem remains unsolved, patients with LUTS should be treated carefully regarding testosterone replacement therapy. Our study has several strengths. Firstly, all study subjects excluded those treated with BPE-related medications and diagnosed with prostate disease. Moreover, all study subjects were enrolled in a screening setting. The bias from BPE or prostate disease was minimized. Secondly, we collected comprehensive anthropometric measurements and evaluations on metabolic syndrome, LUTS, uroflowmetry, transrectal ultrasound and digital rectal examination, which allowed us to elucidate the said mutual relationships. This work is more difficult to achieve in a large-scale population-based study. This study provides a valuable link between metabolic disorders, testosterone levels and LUTS. The results provided important information on the pathogenesis of LUTS and therapeutic guidance of testosterone replacement therapy in such patients.
The present study has several limitations that must be considered when interpreting the results. Firstly, the present study is cross-sectional in nature and the effect of time was not considered. Several risk factors, such as the subjects' life styles and socioeconomic statuses, were not collected and analyzed 20,26,39,40 . Secondly, only ethnic Taiwanese individuals who attended the voluntary annual medical health check-up were enrolled into the study. Nevertheless, the prevalence was 29.6% (518/1752) for moderate/severe LUTS and 37.6% (659/1752) for metabolic syndrome. These results were comparable to those of the population-based study in Taiwan 41,42 . We should beware of the limitations when extrapolating the results to other populations. Third, the data of dihydrotestosterone levels were lacking in this study. The measurement of dihydrotestosterone may provide more information in this study, especially considering the effect of dihydrotestosterone on prostate enlargement. More evidence with larger samples and a long-term follow up is necessary to clarify the associations between LUTS with testosterone and metabolic syndrome in different male populations at various ages.

Conclusion
In the present study, we elucidated a significant impact of total serum testosterone levels and prostate volume on moderate/severe LUTS among middle-aged men receiving health checkup. Testosterone supplement therapy should be used cautiously in patients with moderate/severe LUTS and large prostates.