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首页> 外文期刊>International urogynecology journal and pelvic floor dysfunction >Polymorphism rs1800255 from COL3A1 gene and the risk for pelvic organ prolapse
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Polymorphism rs1800255 from COL3A1 gene and the risk for pelvic organ prolapse

机译:来自COL3A1基因的多态性RS1800255和盆腔器官脱垂的风险

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Introduction and hypothesis Genetic variations of type III collagen may compromise the supportive structures of the female pelvic floor and consequently favor pelvic organ prolapse. The single nucleotide polymorphism G/A rs1800255 located in the coding region for type III collagen (COL3A1) was evaluated as a risk factor for pelvic organ prolapse. Methods A single-center prospective cohort study including women with clinical diagnosis of stage III and IV prolapse (POP group) and prolapse stage 0 or I (control group). Sociodemographic, clinical data and obstetric history were retrieved by physician interview. DNA including the rs1800255 polymorphism was amplified by polymerase chain reaction from blood genomic cells and digested with AluI restriction enzyme for distinction of G and A variants. Qualitative variables were compared using the chi-square and Fisher's exact tests and unpaired t-test for quantitative variables. After stratification of the groups, risk factors for POP were estimated using odds ratios (ORs) from the binary logistic regression model. Results A total of 292 women were included, 112 in the POP group and 180 in the control group. There was no significant difference between groups regarding rs1800255. Age and home birth were the only significant risk factors for pelvic organ prolapse. Conclusion Polymorphism rs1800255 from COL3A1 gene was not a risk factor for pelvic organ prolapse.
机译:III型胶原蛋白的引言和假设遗传变化可能损害雌性骨盆地板的支撑结构,从而有利于骨盆器官脱垂。位于III型胶原(COL3A1)的编码区域中的单核苷酸多态性G / A RS1800255被评价为盆腔器官脱垂的危险因素。方法采用单中心前瞻性队列研究,包括患有临床诊断和IV阶段和IV脱垂(POP组)和脱垂阶段0或I(对照组)的妇女。医师采访检索社会渗目,临床数据和产科历史。通过从血液基因组细胞的聚合酶链反应扩增包括RS1800255多态性,并用alui限制酶消化,以区分G和变体。使用Chi-Square和Fisher的精确测试和定量变量的未配对T检验进行比较定性变量。在组分层后,使用来自二元逻辑回归模型的差异比率(或)估计流行危险因素。结果总共包括292名妇女,在流行集团和180名控制组中有112名。关于RS1800255的团体之间没有显着差异。年龄和家庭出生是盆腔器官脱垂的唯一显着的风险因素。结论来自COL3A1基因的多态性RS1800255不是盆腔器官脱垂的危险因素。

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