Follicle-Stimulating Hormone and the Pituitary-Testicular-Prostate Axis at the Time of Initial Diagnosis of Prostate Cancer and Subsequent Cluster Selection of the Patient Population Undergoing Standard Radical Prostatectomy
Autor: | Claudio Cocco, Teodoro Sava, Claudio Ghimenton, Mario Romano, Antonio Benito Porcaro, Aldo Petrozziello, Emanuele Rubilotta, Beatrice Caruso, Vincenzo Lacola, Luigi Comunale, Filippo Migliorini, Stefano Zecchinini Antoniolli, Carmelo Monaco |
---|---|
Rok vydání: | 2012 |
Předmět: |
Male
medicine.medical_treatment Follicle-stimulating hormone Luteinizing hormone Total testosterone Free testosterone Estradiol hormone Prostate-specific antigen Prostate cancer Prostate Testis Cluster Analysis Testosterone Estradiol Prostatectomy Middle Aged medicine.anatomical_structure Pituitary Gland Follicle Stimulating Hormone Human Kallikreins hormones hormone substitutes and hormone antagonists Image-Guided Biopsy endocrine system medicine.medical_specialty Urology Decision Support Techniques Predictive Value of Tests Internal medicine medicine Humans Aged Retrospective Studies Analysis of Variance business.industry Patient Selection Prostatic Neoplasms Luteinizing Hormone Prostate-Specific Antigen medicine.disease Prolactin Endocrinology Linear Models Neoplasm Grading business Hormone |
Zdroj: | Urologia Internationalis. 90:45-55 |
ISSN: | 1423-0399 0042-1138 |
Popis: | Aim: A preceding exploratory analysis has shown that follicle-stimulating hormone (FSH) was significantly correlated to and predicted by prostate-specific antigen (PSA) in a prostate cancer population. The aim of the study was to evaluate FSH physiopathology along the pituitary-testicular-prostate (PTP) axis at the time of initial diagnosis of prostate cancer in an operated population clustered according to the FSH/PSA ratio. Patients and Methods: The study included 93 patients who underwent standard radical prostatectomy. Age, percentages of positive cores at transrectal ultrasound scan biopsy (TRUSB) (P+), biopsy Gleason score (bGS), pathology Gleason score (pGS), luteinizing hormone (LH), FSH, prolactin hormone (PRL), total testosterone (TT), free testosterone (FT), estradiol (ESR) and PSA were the continuous variables. Category variables were pT and biopsy/pathology Gleason pattern I/II (b/pGPI/II). The population was clustered according to the FSH/PSA ratio which was computed from empirical data and then ranked for clustering the population as groups A (range 0.13 ≤ FSH/PSA ≤ 0.20), B (range 0.20 < FSH/PSA ≤ 0.50), C (range 0.50 < FSH/PSA ≤ 0.75), D (range 0.75 < FSH/PSA ≤ 1.00), E (range 1.00 < FSH/PSA ≤ 1.25), F (range 1.25 < FSH/PSA ≤ 2.00), G (range 2.00 < FSH/PSA ≤ 2.25), H (range 2.25 < FSH/PSA ≤ 6.40) and I (range 6.40 < FSH/ PSA ≤ 19.40). The model was assessed by simple linear regression analysis and differences between the groups were investigated by analysis of variance (ANOVA) for continuous variables and by contingency tables for category variables. Results: FSH was significantly correlated to and predicted by PSA in groups A (p = 0.04), B (p < 0.0001), C (p < 0.0001), D (p < 0.0001), E (p < 0.0001), F (p < 0.0001), G (p < 0.0001), H (p = 0.0001) and I (p = 0.001). Also, clusters (A–I) differed significantly for mean values of FSH (p < 0.0001), LH (p < 0.0001), TT (p = 0.04), PSA (p < 0.0001), bGS (p = 0.005), pGS (p = 0.01) and PSA/FT ratio (p < 0.0001); moreover, the nine groups showed significant different frequency distributions of pGPI (p = 0.02), pGPII (p = 0.0002) and bGPI (p = 0.04). Conclusion: The ranking FSH/PSA ratio significantly clustered, along the PTP axis, an operated population diagnosed with prostate cancer. Also, the ranking FSH/PSA ratio selected prostate cancer clusters expressing different levels of hormonal disorder along the PTP axis and prognostic potential with different risks of progression. As a theory, in the current advancing world, the ranking FSH/PSA model might be considered as an interesting and effective tool for prostate cancer study as well as individualized, risk-adapted approaches of the disease. However, confirmatory studies are needed. |
Databáze: | OpenAIRE |
Externí odkaz: |