Vocca Cristina, Abrego-Guandique Diana Marisol, Cione Erika, Rania Vincenzo, Marcianò Gianmarco, Palleria Caterina, Catarisano Luca, Colosimo Manuela, La Cava Gregorio, Palumbo Italo Michele, De Sarro Giovambattista, Ceccato Tommaso, Botti Simone, Cai Tommaso, Palmieri Alessandro, Gallelli Luca
Operative Unit of Clinical Pharmacology and Pharmacovigilance, Department of Health Science, AOU Dulbecco, University Magna Graecia of Catanzaro, 88100 Catanzaro, Italy.
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Microorganisms. 2025 Jan 10;13(1):130. doi: 10.3390/microorganisms13010130.
Several studies have suggested that probiotics could play a role in the management of patients with chronic bacterial prostatitis (CBP). In this randomized, placebo-controlled clinical study, we evaluated the efficacy and safety of consumption of probiotics containing human DG as an add-on treatment in patients with clinical recurrences of CBP, through gut microbiota modification analysis. Enrolled patients with CBP were randomized to receive for 3 months probiotics containing human DG or placebo following 1 month treatment with ciprofloxacin. During the enrollment and follow-ups, urological examinations analyzed symptoms and quality of life, while microbiological tests analyzed gut and seminal microbiota. During the study, the development of adverse drug reactions was evaluated through the Naranjo scale. Twenty-four patients with CBP were recruited and treated for 3 months with placebo (n. 12) or with DG (n. 12). DG induced a significantly ( < 0.01) faster recovery of symptoms than placebo (2 days vs. 8 days) and an increased time free from symptoms (86 days vs. 42 days) without the occurrence of adverse events. In the probiotic group, the appearance of after 30 days (T1) was higher vs. the placebo group, and a significant reduction in , , , , and was also observed. These preliminary data suggest that in patients with CBP, the use of DG after an antimicrobial treatment improves the days free of symptoms and the quality of life, without the development of adverse drug reactions.
多项研究表明,益生菌可能在慢性细菌性前列腺炎(CBP)患者的管理中发挥作用。在这项随机、安慰剂对照的临床研究中,我们通过肠道微生物群修饰分析,评估了含人源DG的益生菌作为附加治疗对CBP临床复发患者的疗效和安全性。入选的CBP患者在接受1个月环丙沙星治疗后,随机接受含人源DG的益生菌或安慰剂治疗3个月。在入组和随访期间,泌尿外科检查分析症状和生活质量,而微生物学检测分析肠道和精液微生物群。在研究过程中,通过Naranjo量表评估药物不良反应的发生情况。招募了24例CBP患者,分别用安慰剂(n = 12)或DG(n = 12)治疗3个月。与安慰剂相比,DG使症状恢复显著更快(P < 0.01)(2天对8天),且无症状时间增加(86天对42天),未发生不良事件。在益生菌组中,30天(T1)后DG的出现率高于安慰剂组,同时还观察到[具体细菌名称1]、[具体细菌名称2]、[具体细菌名称3]、[具体细菌名称4]、[具体细菌名称5]和[具体细菌名称6]显著减少。这些初步数据表明,在CBP患者中,抗菌治疗后使用DG可改善无症状天数和生活质量,且不会发生药物不良反应。