Background: The role of IGF-I in prostate development is currently under thorough investigation since it has been claimed that IGF-I is a positive predictor of prostate cancer. Objective: To investigate the effect of chronic GH and IGF-I deficiency alone or associated with testosterone deficiency on prostate pathophysiology in a series of patients with hypopituitarism. Design: Pituitary, androgen and prostate hormonal assessments and transrectal prostate ultrasonography (TRUS) were performed in 30 men with adulthood onset GH deficiency (GHD) and 30 age-matched healthy controls, free from previous or concomitant prostate disorders. Results: Plasma IGF-I levels were significantly lower in GHD patients than in controls (Pearson's coefficient P <0.0001). At study entry, 6 of the 13 hypogonadal patients and 7 of the 17 eugonadal patients had plasma IGF-I below the age- adjusted normal range. At study entry, testosterone levels were low in 13 patients (mean ± S.E.M., 3.8 ± 1.0 nmol/l) while they were normal in the remaining 17 (19.4 ± 1.4 nmol/l). No difference in prostate-specific antigen (PSA), and PSA density was found between GHD patients (either hypo- or eugonadal) and controls, while free PSA levels were significantly higher in eugonadal GHD than in controls (0.4 ± 0.04 vs 0.2 ± 0.03 μg/l; P <0.01). No difference in antero-posterior prostate diameter and transitional zone volume (TZV) was observed among groups, while both transverse and cranio-caudal diameters were significantly lower in hypogonadal (P <0.01) and eugonadal GHD patients (P <0.05) than in controls. Prostate volume (PV) was significantly lower in hypogonadal GHD patients (18.2 ± 3.0 ml) and eugonadal GHD patients (22.3 ± 1.6 ml), than in controls (25.7 ± 1.4, P <0.05). The prevalence of prostate hyperplasia (PV > 30 ml) was significantly lower in hypogonadal and eugonadal GHD patients, without any difference between them (15.3% and 5.8%), than in controls (43.3%) (χ2 = 6.90, P = 0.005). No difference was found in PV between patients with normal or deficient IGF-I levels both in the hypogonadal group (19.9 ± 4.7 vs 17.3 ± 4.0 ml) and in the eugonadal group (22.6 ± 2.3 vs 21.8 ± 2.5 ml). When controls and patients were divided according to age (<60 years and > 60 years). PV was significantly lower in hypogonadal GHD patients aged below 60 years than in age-matched controls (P <0.01) or eugonadal GHD patients (P <0.01), without any difference between controls and eugonadal GHD patients. Controls aged above 60 years had significantly higher PV than both hypogonadal and eugonadal GHD patients (P <0.01). Calcifications, cysts or nodules were found in 56.7% of patients and in 50% of controls (χ2 = 0.067, P = 0.79). In controls, but not in GHD patients, PV and TZV were correlated with age (r = 0.82, r = 0.46, P <0.0001 and P <0.01 respectively). PV was also correlated with GH (r = -0.52, P = 0.0026), IGF-I (r = -0.62, P = 0.0002) and IGF-binding protein 3 (IGFBP-3) levels (r = -0.39, P = 0.032) but neither with testosterone or dihydrotestosterone (DHT) levels. In GHD patients TZV but not PV was correlated with age (r = 0.58, P = 0.0007) and neither TZV nor PV were correlated with GH, IGF-I or IGFBP-3 levels. Conclusions: Chronic GH deficiency in adulthood causes a decrease in prostate size, mostly in patients with concomitant androgen deficiency and age below 60 years, without significant changes in the prevalence of structural prostate abnormalities.
|Number of pages||9|
|Journal||European Journal of Endocrinology|
|Publication status||Published - Jul 2000|
ASJC Scopus subject areas