Li Jinze, Peng Lei, Cao Dehong, Gou Haocheng, Li Yunxiang, Wei Qiang
Department of Urology, Nanchong Central Hospital, The Second Clinical Medical College, North Sichuan Medical College, Sichuan, China.
Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, China.
Aging Male. 2020 Dec;23(5):1388-1399. doi: 10.1080/13685538.2020.1771552. Epub 2020 Jun 2.
We performed this meta-analysis to assess the association between metabolic syndrome (MetS) and benign prostatic hyperplasia (BPH).
We conducted extensive searches on the PubMed, Science and Cochrane Library to identify all articles. Outcomes including annual prostate growth rate, prostate volume (PV), International Prostate Symptom Score (IPSS), IPSS sub-scores (voiding and storage), prostate- specific antigen (PSA), maximum urine flow rate (Qmax), post-void residual urine volume (PVR) and quality of life (QoL) were assessed.
21 studies with 15,317 patients were included. Patients with MetS had higher annual prostate growth rate [weighted mean difference (WMD) = 0.79; < .001], larger PV (WMD = 2.62; < .001), lower Qmax (WMD = -0.48; = .001) and more PVR (WMD = 8.28; < .001). However, no significant differences were found between two groups in IPSS (WMD = 0.20; = .37), IPSS-voiding (WMD = -0.05; = .78), IPSS-storage (WMD = -0.22; = .26), PSA (WMD = 0.04; = .43), and QoL (WMD = -0.01; = .70).
The study suggested that MetS may be one of the risk factors for the clinical progress of BPH. However, further study is warranted to support these results.
我们进行这项荟萃分析以评估代谢综合征(MetS)与良性前列腺增生(BPH)之间的关联。
我们在PubMed、科学网和考克兰图书馆进行了广泛检索以识别所有文章。对包括年前列腺生长率、前列腺体积(PV)、国际前列腺症状评分(IPSS)、IPSS子评分(排尿和储尿)、前列腺特异性抗原(PSA)、最大尿流率(Qmax)、排尿后残余尿量(PVR)和生活质量(QoL)等结果进行了评估。
纳入了21项研究,共15317例患者。患有MetS的患者年前列腺生长率更高[加权平均差(WMD)=0.79;P<0.001],PV更大(WMD = 2.62;P<0.001),Qmax更低(WMD = -0.48;P = 0.001),PVR更多(WMD = 8.28;P<0.001)。然而,两组在IPSS(WMD = 0.20;P = 0.37)、IPSS排尿(WMD = -`0.05;P = 0.78)、IPSS储尿(WMD = -0.22;P = 0.26)、PSA(WMD = 0.04;P = 0.43)和QoL(WMD = -0.01;P = 0.70)方面未发现显著差异。
该研究表明MetS可能是BPH临床进展的危险因素之一。然而,需要进一步研究来支持这些结果。