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  • 1
    In: Urologia Internationalis, S. Karger AG, Vol. 89, No. 1 ( 2012), p. 39-44
    Abstract: 〈 b 〉 〈 i 〉 Objectives: 〈 /i 〉 〈 /b 〉 To clarify the association of 〈 i 〉 kallikrein-related peptidase 3 (KLK3) 〈 /i 〉 rs2735839 G/A polymorphism with serum prostate-specific antigen (PSA) levels in Japanese men. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 Subjects were participants of the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study who visited the Seirei Preventive Health Care Center in Shizuoka, Japan. Among the 5,040 individuals aged 35–69 years who were enrolled in 2006–2007, serum PSA data were available for 2,323 male subjects without a past history of prostate cancer. The diagnostic criteria for PSA positivity was PSA ≥4.0 ng/ml. Genotyping of the 〈 i 〉 KLK3 〈 /i 〉 polymorphism was conducted by the polymerase chain reaction with the confronting two-pair primers (PCR-CTPP) method. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The mean ± SD of PSA levels (mg/dl) were 1.54 ± 1.73 for those with 〈 i 〉 KLK3 〈 /i 〉 rs2735839 〈 i 〉 G 〈 /i 〉 / 〈 i 〉 G 〈 /i 〉 genotype, 1.34 ± 1.33 for 〈 i 〉 G 〈 /i 〉 / 〈 i 〉 A 〈 /i 〉 , and 1.20 ± 1.23 for 〈 i 〉 A 〈 /i 〉 / 〈 i 〉 A 〈 /i 〉 , which was significantly different (p 〈 0.0001). The age-adjusted odds ratios of PSA test positivity were 0.62 (95% confidence interval 0.41–0.94) for those with 〈 i 〉 G 〈 /i 〉 / 〈 i 〉 A 〈 /i 〉 + 〈 i 〉 A 〈 /i 〉 / 〈 i 〉 A 〈 /i 〉 relative to those with 〈 i 〉 G 〈 /i 〉 / 〈 i 〉 G 〈 /i 〉 . 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 The present study revealed that the 〈 i 〉 KLK3 〈 /i 〉 rs2735839 〈 i 〉 G 〈 /i 〉 allele was significantly associated with higher serum PSA levels also in Japanese.
    Type of Medium: Online Resource
    ISSN: 0042-1138 , 1423-0399
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    Language: English
    Publisher: S. Karger AG
    Publication Date: 2012
    detail.hit.zdb_id: 1464417-4
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  • 2
    In: American Journal of Nephrology, S. Karger AG, Vol. 47, No. 5 ( 2018), p. 304-316
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Chronic kidney disease (CKD) is a rapidly growing, worldwide public health problem. Recent advances in genome-wide-association studies (GWAS) revealed several genetic loci associated with renal function traits worldwide. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 〈 i 〉 〈 /i 〉 We investigated the association of genetic factors with the levels of serum creatinine (SCr) and the estimated glomerular filtration rate (eGFR) in Japanese population-based cohorts analyzing the GWAS imputed data with 11,221 subjects and 12,617,569 variants, and replicated the findings with the 148,829 hospital-based Japanese subjects. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 In the discovery phase, 28 variants within 4 loci (chromosome [chr] 2 with 8 variants including rs3770636 in the 〈 i 〉 LDL receptor related protein 2 〈 /i 〉 gene locus, on chr 5 with 2 variants including rs270184, chr 17 with 15 variants including rs3785837 in the 〈 i 〉 BCAS3 〈 /i 〉 gene locus, and chr 18 with 3 variants including rs74183647 in the 〈 i 〉 nuclear factor of ­activated T-cells 1 〈 /i 〉 gene locus) reached the suggestive level of 〈 i 〉 p 〈 /i 〉 & #x3c; 1 × 10 〈 sup 〉 –6 〈 /sup 〉 in association with eGFR and SCr, and 2 variants on chr 4 (including rs78351985 in the 〈 i 〉 microsomal triglyceride transfer protein 〈 /i 〉 gene locus) fulfilled the suggestive level in association with the risk of CKD. In the replication phase, 25 variants within 3 loci (chr 2 with 7 variants, chr 17 with 15 variants and chr 18 with 3 variants) in association with eGFR and SCr, and 2 variants on chr 4 associated with the risk of CKD became nominally statistically significant after Bonferroni correction, among which 15 variants on chr 17 and 3 variants on chr 18 reached genome-wide significance of 〈 i 〉 p 〈 /i 〉 & #x3c; 5 × 10 〈 sup 〉 –8 〈 /sup 〉 in the combined study meta-analysis. The associations of the loci on chr 2 and 18 with eGFR and SCr as well as that on chr 4 with CKD risk have not been previously reported in the Japanese and East Asian populations. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Although the present GWAS of renal function traits included the largest sample of Japanese participants to date, we did not identify novel loci for renal traits. However, we identified the novel associations of the genetic loci on chr 2, 4, and 18 with renal function traits in the Japanese population, suggesting these are transethnic loci. Further investigations of these associations are expected to further validate our findings for the potential establishment of personalized prevention of renal disease in the Japanese and East Asian populations.
    Type of Medium: Online Resource
    ISSN: 0250-8095 , 1421-9670
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2018
    detail.hit.zdb_id: 1468523-1
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  • 3
    In: American Journal of Nephrology, S. Karger AG, Vol. 36, No. 5 ( 2012), p. 444-450
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 The aim of this study was to explore the associations between the prevalence of chronic kidney disease (CKD) and polymorphisms in the genes encoding matrix metalloproteinases (MMPs) and tissue inhibitor of matrix metalloproteinases (TIMPs). MMPs degrade extracellular matrix proteins in the glomerulus, and play important roles in kidney disease progression. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 DNA samples from 3,309 subjects aged 35–69 years were genotyped for 10 potentially functional polymorphisms in 〈 i 〉 MMP 〈 /i 〉 and 〈 i 〉 TIMP 〈 /i 〉 genes. The prevalence of CKD (estimated glomerular filtration rate 〈 60 ml/min/1.73 m 〈 sup 〉 2 〈 /sup 〉 ) was compared among the genotypes. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The prevalence of CKD decreased significantly with the number of minor alleles in 〈 i 〉 MMP9 〈 /i 〉 C–1562T (odds ratios (ORs) 0.77 for CT and 0.65 for TT compared with CC; p for trend = 0.023) and 〈 i 〉 MMP9 〈 /i 〉 R668Q (ORs, 0.79 for RQ and 0.64 for QQ compared with RR; p for trend = 0.024). The haplotype 〈 i 〉 MMP9 〈 /i 〉 –1562T/279R/668Q showed a reduced risk for CKD compared with the most common –1562C/279R/668R (OR 0.77, p = 0.008), and the genotype combination –1562TT/ 279RR/668QQ showed a halved risk for CKD compared with major allele homozygous –1562CC/279RR/668RR (OR 0.53, p = 0.091). 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 The potentially functional polymorphisms of 〈 i 〉 MMP9 〈 /i 〉 were associated with the prevalence of CKD in a large Japanese population. These genotypes have been reported to increase 〈 i 〉 MMP9 〈 /i 〉 expression, supporting the hypothesis that MMP-9 has a protective role in the progression of kidney diseases.
    Type of Medium: Online Resource
    ISSN: 0250-8095 , 1421-9670
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2012
    detail.hit.zdb_id: 1468523-1
    Location Call Number Limitation Availability
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