Yoon Hana, Yoon Hyun Suk, Lee Yong Seong, Cho Sung Tae, Han Deok Hyun
Department of Urology, Ewha Womans University School of Medicine, Seoul, Republic of Korea.
Department of Urology, Ewha Womans University School of Medicine, Seoul, Republic of Korea.
Urology. 2016 Feb;88:135-42. doi: 10.1016/j.urology.2015.07.074. Epub 2015 Nov 4.
To investigate the efficacy of tamsulosin, a selective alpha-1 blocker, in lower urinary tract symptoms (LUTS) patients with metabolic syndrome (MS).
This prospective, multicenter clinical trial included men and women (20-75 years old) with LUTS, with or without MS. Patients were categorized as MS+ or MS-, respectively, and all of them were administered tamsulosin 0.2 mg per oral once daily for 24 weeks. Patients were assessed based on the International Prostate Symptom Score, King's Health Questionnaire (KHQ), Overactive Bladder Questionnaire, uroflowmetry with postvoid residuals, and MS factors (blood pressure, waist-to-hip ratio, and serum levels of fasting blood glucose, triglyceride, and high-density lipoprotein cholesterol) at baseline and at 4, 12, and 24 weeks of treatment.
Ninety-two patients were enrolled in this study (53/92 were MS- [57.6%]; 39/92 were MS+ [42.4%]). After 24 weeks of tamsulosin treatment, fasting blood glucose (P = .02) and triglyceride (P < .001) levels of changes were significantly greater in the MS+ group than in the MS- group. Total International Prostate Symptom Score, total Overactive Bladder Questionnaire score, and the scores of each question on the KHQ showed significant improvement after treatment without intergroup differences. In KHQ, although improvements in emotional status, sleep quality, fatigue, and personal distress were greater in the MS+ group (P = .05), the difference between the groups did not reach statistical significance.
Tamsulosin was effective in both LUTS patients with and without MS. Furthermore, tamsulosin had beneficial effects on some of the factors associated with MS.
探讨选择性α-1受体阻滞剂坦索罗辛对代谢综合征(MS)合并下尿路症状(LUTS)患者的疗效。
这项前瞻性、多中心临床试验纳入了患有或未患有MS的LUTS患者(年龄20 - 75岁),男女不限。患者分别被归类为MS+或MS-,所有患者均每日口服一次0.2mg坦索罗辛,持续24周。在基线以及治疗的第4、12和24周,根据国际前列腺症状评分、国王健康问卷(KHQ)、膀胱过度活动症问卷、排尿后残余尿量的尿流率测定以及MS相关因素(血压、腰臀比以及空腹血糖、甘油三酯和高密度脂蛋白胆固醇的血清水平)对患者进行评估。
本研究共纳入92例患者(53/92为MS- [57.6%];39/92为MS+ [42.4%])。坦索罗辛治疗24周后,MS+组空腹血糖(P = .02)和甘油三酯(P < .001)水平的变化显著大于MS-组。治疗后,国际前列腺症状总分、膀胱过度活动症问卷总分以及KHQ各问题得分均有显著改善,组间无差异。在KHQ中,虽然MS+组在情绪状态、睡眠质量、疲劳和个人困扰方面的改善更大(P = .05),但两组间差异未达到统计学意义。
坦索罗辛对患有和未患有MS的LUTS患者均有效。此外,坦索罗辛对一些与MS相关的因素有有益影响。