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1.
Int. braz. j. urol ; 41(5): 869-897, Sept.-Oct. 2015. tab, graf
Article in English | LILACS | ID: lil-767037

ABSTRACT

ABSTRACT We had investigated whether sequence variants within DKK3 gene are associated with the development of prostate cancer in a Korean study cohort. We evaluated the association between 53 single nucleotide polymorphisms (SNPs) in the DKK3 gene and prostate cancer risk as well as clinical characteristics (PSA, clinical stage, pathological stage and Gleason score) in Korean men (272 prostate cancer subjects and 173 benign prostate hyperplasia subjects) using unconditional logistic regression analysis. Of the 53 SNPs and 25 common haplotypes, 5 SNPs and 4 haplotypes were associated with prostate cancer risk (P=0.02–0.04); 3 SNPs and 2 haplotypes were significantly associated with susceptibility to prostate cancer, however 2 SNPs and 2 haplotypes exhibited a significant protective effect on prostate cancer. Logistic analyses of the DKK3 gene polymorphisms with several prostate cancer related factors showed that several SNPs were significant; three SNPs and two haplotypes to PSA level, three SNPs and two haplotypes to clinical stage, nine SNPs and two haplotype to pathological stage, one SNP and one haplotypes to Gleason score. To the author's knowledge, this is the first report documenting that DKK3 polymorphisms are not only associated with prostate cancer but also related to prostate cancer-related factors.


Subject(s)
Aged , Aged, 80 and over , Humans , Male , Disease Progression , Intercellular Signaling Peptides and Proteins/genetics , Polymorphism, Single Nucleotide/genetics , Prostatic Neoplasms/genetics , Case-Control Studies , Cohort Studies , Gene Frequency , Genetic Association Studies , Genetic Markers , Haplotypes , Logistic Models , Neoplasm Grading , Neoplasm Staging , Prostatic Neoplasms/pathology , Reference Values , Regression Analysis , Risk Factors , Seoul
2.
Int. braz. j. urol ; 40(3): 356-366, may-jun/2014. tab
Article in English | LILACS | ID: lil-718254

ABSTRACT

Purpose To evaluate the association between prostatic inflammation and lower urinary tract symptoms (LUTS), and to identify the effects of prostatic inflammation on the treatment with an alpha blocker. Materials and Methods 111 Participants who were aged ≥ 50 years, the presence of LUTS (maximal flow rate < 20 m/s, IPSS ≥ 11), and an elevated PSA level (3-20ng/mL) were treated with tamsulosin 0.2mg once daily for 3 months after prostate biopsies. Prostatic inflammation was scored as none (0), mild (I), moderate (II), or marked (III). LUTS parameters including urine flow rates, IPSS, PSA, and prostate volume were evaluated. Results Inflammation grading resulted in 25, 60, and 26 patients that were grade 0, I, and II, respectively. Lower grade inflammation was related to higher urine flow rate at baseline. Patients with higher inflammation grades had larger prostate volumes, larger total and transitional zone volumes, and higher PSA levels. Overall, urine flow rates and residual urine volume were improved after 3 months of alpha blocker therapy. Eighty percent of patients with grade 0 inflammation, 73% of patients with grade I inflammation, and 92.3% of patients with grade II inflammation showed improvement of LUTS after treatment. Longer duration of treatment was related to a decreased chance of improvement of LUTS. Patients with increased IPSS voiding subscales could be predictive of improvement of LUTS. Conclusions Patients with high grade inflammation had lower flow rates and higher prostatic volumes than patients with low grade inflammation. Inflammation grade did not affect the outcomes of alpha blocker treatment. .


Subject(s)
Aged , Humans , Male , Middle Aged , Adrenergic alpha-1 Receptor Antagonists/therapeutic use , Lower Urinary Tract Symptoms/drug therapy , Prostatic Hyperplasia/drug therapy , Prostatitis/drug therapy , Sulfonamides/therapeutic use , Biopsy , Disease Progression , Lower Urinary Tract Symptoms/pathology , Organ Size , Predictive Value of Tests , Prostate-Specific Antigen/blood , Prostatic Hyperplasia/pathology , Prostatitis/complications , Prostatitis/pathology , Severity of Illness Index , Statistics, Nonparametric , Treatment Outcome
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