Rył Aleksandra, Rotter Iwona, Grzywacz Anna, Małecka Iwona, Skonieczna-Żydecka Karolina, Grzesiak Katarzyna, Słojewski Marcin, Szylińska Aleksandra, Sipak-Szmigiel Olimpia, Piasecka Małgorzata, Walczakiewicz Kinga, Laszczyńska Maria
Department of Histology and Developmental Biology, Pomeranian Medical University, 70-210 Szczecin, Poland.
Department of Medical Rehabilitation and Clinical Physiotherapy, Pomeranian Medical University, 70-210 Szczecin, Poland.
Int J Environ Res Public Health. 2017 Oct 30;14(11):1318. doi: 10.3390/ijerph14111318.
: The etiology of benign prostatic hyperplasia (BPH) has not so far been fully explicated. However, it is assumed that changes in the levels of hormones associated with aging can contribute to the development of prostatic hyperplasia. Dihydrotestosterone combines with the androgen receptor (AR) proteins of the prostate gland. Enzyme activity is based on two isoenzymes: type 1 and type 2. 5α-reductase type 1 is encoded by the gene, and type 2 is encoded by the gene. The aim of our study was to determine the frequency of the (rs6884552, rs3797177) and (rs523349, rs12470143) genes' polymorphisms, and to assess the relationships between the genotypes of the tested mutations, and the levels of biochemical and hormonal parameters in patients with BPH. : The study involved 299 men with benign prostatic hyperplasia. We determined the serum levels of particular biochemical parameters-fasting plasma glucose (FPG), total cholesterol (TC), low-density lipoprotein (LDL), high-density lipoprotein (HDL) and triglycerides (TG)-by the spectrophotometric method, using ready reagent kits. The ELISA method was used to determine the levels of the following hormonal parameters and proteins: total testosterone (TT), free testosterone (FT), insulin (I), luteinizing hormone (LH), and sex hormone binding protein (SHBG). Metabolic syndrome was diagnosed. Genotyping was performed by real-time PCR. : We analyzed the relationships between the incidence of particular diseases and the genotypes of the and polymorphisms among patients with BPH. The BPH patients with the CC genotype of the rs523349 and rs12470143 polymorphisms were considerably less frequently diagnosed with metabolic syndrome (MetS) ( = 0.022 and = 0.023 respectively). Our analysis revealed that homozygotes with the CC of the rs12470143 polymorphism had visibly higher HDL levels than those with the TT and CT genotypes ( = 0.001). Additionally, we found that the patients with the CC genotype of the rs12470143 polymorphism had considerably higher FT levels ( = 0.001) than the heterozygotes with the CT and the homozygotes with the TT of the genetic variant analyzed in our study. Furthermore, the patients with at least one G allele of the rs523349 polymorphism had significantly lower SGBG levels ( = 0.022) compared with the homozygotes with the CC genotype. The presence of at least one A allele (AA + AG genotypes) of the rs3797177 polymorphism entailed notably lower serum insulin levels than those observed in homozygotes with the GG genotype ( = 0.033). : The study described in this article shows that selected and polymorphisms can alter the levels of metabolic and hormonal parameters in patients with BPH. Special attention should be paid to the rs12470143 polymorphism, which is associated with a change in lipid profile, as well as with the inheritance and incidence rate of MetS among these patients. An analysis of the frequency of this polymorphism among BPH patients could be useful in estimating the risk of getting ill, and planning therapies of concomitant diseases for BPH patients.
良性前列腺增生(BPH)的病因迄今尚未完全阐明。然而,据推测,与衰老相关的激素水平变化可能促使前列腺增生的发展。双氢睾酮与前列腺的雄激素受体(AR)蛋白结合。酶活性基于两种同工酶:1型和2型。1型5α-还原酶由 基因编码,2型由 基因编码。我们研究的目的是确定 (rs6884552,rs3797177)和 (rs523349,rs12470143)基因多态性的频率,并评估所检测突变的基因型与BPH患者生化和激素参数水平之间的关系。:该研究纳入了299名良性前列腺增生男性患者。我们使用现成的试剂盒,通过分光光度法测定了特定生化参数的血清水平——空腹血糖(FPG)、总胆固醇(TC)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)和甘油三酯(TG)。采用酶联免疫吸附测定(ELISA)法测定以下激素参数和蛋白质的水平:总睾酮(TT)、游离睾酮(FT)、胰岛素(I)、促黄体生成素(LH)和性激素结合球蛋白(SHBG)。诊断代谢综合征。通过实时聚合酶链反应(PCR)进行基因分型。:我们分析了BPH患者中特定疾病的发病率与 和 多态性的基因型之间的关系。rs523349和rs12470143多态性的CC基因型BPH患者被诊断为代谢综合征(MetS)的频率显著较低(分别为 = 0.022和 = 0.023)。我们的分析显示,rs12470143多态性的CC纯合子的HDL水平明显高于TT和CT基因型的个体( = 0.001)。此外,我们发现,rs12470143多态性的CC基因型患者的FT水平( = 0.001)明显高于我们研究中分析的该基因变体的CT杂合子和TT纯合子。此外,rs523349多态性至少有一个G等位基因(AA + AG基因型)的患者与CC基因型纯合子相比,SGBG水平显著较低( = 0.022)。rs3797177多态性至少有一个A等位基因(AA + AG基因型)的个体血清胰岛素水平明显低于GG基因型纯合子( = 0.033)。:本文所述研究表明,选定的 和 多态性可改变BPH患者的代谢和激素参数水平。应特别关注rs12470143多态性,其与血脂谱变化以及这些患者中MetS的遗传和发病率有关。分析BPH患者中这种多态性的频率可能有助于估计患病风险,并为BPH患者规划伴发疾病的治疗方案。