Chiang Bing-Juin, Kuo Hann-Chorng, Liao Chun-Hou
College of Medicine, Fu-Jen Catholic University, New Taipei City 24205, Taiwan.
Department of Urology, Cardinal Tien Hospital, New Taipei City 23148, Taiwan.
Toxins (Basel). 2019 Sep 19;11(9):547. doi: 10.3390/toxins11090547.
Patients with benign prostatic hyperplasia (BPH) can exhibit various lower urinary tract symptoms (LUTS) owing to bladder outlet obstruction (BOO), prostatic inflammation, and bladder response to BOO. The pathogenesis of BPH involves an imbalance of internal hormones and chronic prostatic inflammation, possibly triggered by prostatic infection, autoimmune responses, neurogenic inflammation, oxidative stress, and autonomic dysfunction. Botulinum toxin A (BoNT-A) is well recognized for its ability to block acetylcholine release at the neuromuscular junction by cleaving synaptosomal-associated proteins. Although current large clinical trials have shown no clinical benefits of BoNT-A for the management of LUTS due to BPH, BoNT-A has demonstrated beneficial effects in certain subsets of BPH patients with LUTS, especially in males with concomitant chronic prostatitis/chronic pelvic pain syndrome and smaller prostate. We conducted a review of published literature in Pubmed, using Botulinum toxin, BPH, BOO, inflammation, LUTS, and prostatitis as the key words. This article reviewed the mechanisms of BPH pathogenesis and anti-inflammatory effects of BoNT-A. The results suggested that to achieve effectiveness, the treatment of BPH with BoNT-A should be tailored according to more detailed clinical information and reliable biomarkers.
良性前列腺增生(BPH)患者由于膀胱出口梗阻(BOO)、前列腺炎症以及膀胱对BOO的反应,可表现出各种下尿路症状(LUTS)。BPH的发病机制涉及体内激素失衡和慢性前列腺炎症,可能由前列腺感染、自身免疫反应、神经源性炎症、氧化应激和自主神经功能障碍引发。肉毒杆菌毒素A(BoNT-A)因其能够通过裂解突触体相关蛋白来阻断神经肌肉接头处乙酰胆碱的释放而广为人知。尽管目前的大型临床试验表明BoNT-A对治疗BPH所致LUTS无临床益处,但BoNT-A已在某些患有LUTS的BPH患者亚组中显示出有益效果,尤其是伴有慢性前列腺炎/慢性盆腔疼痛综合征且前列腺较小的男性患者。我们在Pubmed上对已发表的文献进行了综述,使用肉毒杆菌毒素、BPH、BOO、炎症、LUTS和前列腺炎作为关键词。本文综述了BPH的发病机制及BoNT-A的抗炎作用。结果表明,为达到疗效,使用BoNT-A治疗BPH应根据更详细的临床信息和可靠的生物标志物进行个体化治疗。