BACKGROUND: Epidemiological data indicate that lower urinary tract symptoms (LUTS)/BPH can be associated with metabolic syndrome (MetS). Chronic inflammation has been proposed as a candidate mechanism at the crossroad between these two clinical entities. Aim of study is to examine the correlation among pre-operatory LUTS/BPH severity, MetS features and inflammatory infiltrates in prostatectomy specimens. METHODS: A total of 271 consecutive men treated with simple prostatectomy were retrospectively selected for this study in two tertiary referral centers for LUTS/BPH. Prostate diameters and volume were measured by transrectal ultrasound, LUTS scored by International Prostate Symptom Score (IPSS) and obstruction by uroflowmetry. The International Diabetes Federation and American Heart Association and the National Heart, Lung and Blood Institute was used to define MetS. The inflammatory infiltrate was investigated combining anatomic location, grade and extent of flogosis into the overall inflammatory score (IS); the glandular disruption (GD) was used as a further marker. RESULTS: Eighty-six (31.7%) men were affected by MetS. Prostatic volume and anterior-posterior (AP) diameter were positively associated to the number of MetS components. Among MetS determinants, only dyslipidaemia (increased serum triglycerides and reduced serum high-density lipoprotein) was associated with an increased risk of having a prostatic volume >60 cm(3) (hazard ratio (HR) = 3.268, P<0.001). A significant positive correlation between the presence of MetS and the IS was observed. MetS patients presented lower uroflowmetric parameters as compared with those without MetS (Maximum flow rate (Q(max)): 8.6 vs 10.1, P = 0.008 and average flow rate (Q(ave)): 4.6 vs 5.3, P = 0.033, respectively), and higher obstructive urinary symptoms score (P = 0.064). A positive correlation among both IS-GD and IPSS Score was also observed (adjusted r = 0.172, P = 0.008 and adjusted r = 0.128, P = 0.050). CONCLUSIONS: MetS is associated with prostate volume, prostatic AP diameter and intraprostatic IS. The significantly positive association between MetS and prostatic AP diameter could support the observation that MetS patients presented lower uroflowmetric parameters. In conclusion, MetS can be regarded as a new determinant of prostate inflammation and BPH progression. Prostate Cancer and Prostatic Disease (2013) 16, 100-105; doi:10.1038/pcan.2012.44; published online 20 November 2012

Metabolic syndrome and lower urinary tract symptoms: the role of inflammation / M., Gacci; L., Vignozzi; A., Sebastianelli; M., Salvi; C., Giannessi; Tubaro, Andrea; G., Corona; G., Rastrelli; R., Santi; G., Nesi; S., Serni; M., Carini; M., Maggi; DE NUNZIO, Cosimo. - In: PROSTATE CANCER AND PROSTATIC DISEASES. - ISSN 1365-7852. - STAMPA. - 16:1(2013), pp. 100-105. [10.1038/pcan.2012.44]

Metabolic syndrome and lower urinary tract symptoms: the role of inflammation

TUBARO, ANDREA;DE NUNZIO, Cosimo
2013

Abstract

BACKGROUND: Epidemiological data indicate that lower urinary tract symptoms (LUTS)/BPH can be associated with metabolic syndrome (MetS). Chronic inflammation has been proposed as a candidate mechanism at the crossroad between these two clinical entities. Aim of study is to examine the correlation among pre-operatory LUTS/BPH severity, MetS features and inflammatory infiltrates in prostatectomy specimens. METHODS: A total of 271 consecutive men treated with simple prostatectomy were retrospectively selected for this study in two tertiary referral centers for LUTS/BPH. Prostate diameters and volume were measured by transrectal ultrasound, LUTS scored by International Prostate Symptom Score (IPSS) and obstruction by uroflowmetry. The International Diabetes Federation and American Heart Association and the National Heart, Lung and Blood Institute was used to define MetS. The inflammatory infiltrate was investigated combining anatomic location, grade and extent of flogosis into the overall inflammatory score (IS); the glandular disruption (GD) was used as a further marker. RESULTS: Eighty-six (31.7%) men were affected by MetS. Prostatic volume and anterior-posterior (AP) diameter were positively associated to the number of MetS components. Among MetS determinants, only dyslipidaemia (increased serum triglycerides and reduced serum high-density lipoprotein) was associated with an increased risk of having a prostatic volume >60 cm(3) (hazard ratio (HR) = 3.268, P<0.001). A significant positive correlation between the presence of MetS and the IS was observed. MetS patients presented lower uroflowmetric parameters as compared with those without MetS (Maximum flow rate (Q(max)): 8.6 vs 10.1, P = 0.008 and average flow rate (Q(ave)): 4.6 vs 5.3, P = 0.033, respectively), and higher obstructive urinary symptoms score (P = 0.064). A positive correlation among both IS-GD and IPSS Score was also observed (adjusted r = 0.172, P = 0.008 and adjusted r = 0.128, P = 0.050). CONCLUSIONS: MetS is associated with prostate volume, prostatic AP diameter and intraprostatic IS. The significantly positive association between MetS and prostatic AP diameter could support the observation that MetS patients presented lower uroflowmetric parameters. In conclusion, MetS can be regarded as a new determinant of prostate inflammation and BPH progression. Prostate Cancer and Prostatic Disease (2013) 16, 100-105; doi:10.1038/pcan.2012.44; published online 20 November 2012
2013
complications/epidemiology; inflammation; male; metabolic syndrome x; bph; humans; lower urinary tract symptoms; prostatic hyperplasia; aged; prostate; complications; luts; metabolic syndrome; prostatectomy; complications/pathology/surgery; mets; retrospective studies
01 Pubblicazione su rivista::01a Articolo in rivista
Metabolic syndrome and lower urinary tract symptoms: the role of inflammation / M., Gacci; L., Vignozzi; A., Sebastianelli; M., Salvi; C., Giannessi; Tubaro, Andrea; G., Corona; G., Rastrelli; R., Santi; G., Nesi; S., Serni; M., Carini; M., Maggi; DE NUNZIO, Cosimo. - In: PROSTATE CANCER AND PROSTATIC DISEASES. - ISSN 1365-7852. - STAMPA. - 16:1(2013), pp. 100-105. [10.1038/pcan.2012.44]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/727070
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