首页> 外文期刊>The journal of obstetrics and gynaecology research >TT polymorphism in rs2165241 and rs1048661 region in lysyl oxidase like-1 gene may have a role in stress urinary incontinence physiopathology.
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TT polymorphism in rs2165241 and rs1048661 region in lysyl oxidase like-1 gene may have a role in stress urinary incontinence physiopathology.

机译:赖氨酰氧化酶样-1基因rs2165241和rs1048661区域的TT多态性可能与应激性尿失禁的生理病理有关。

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摘要

In experimental studies, lysyl oxidase like-1 (LOX-L1) (-/-) mice were shown to have similar pelvic floor dysfunction to female rats. LOX-L1 levels in endopelvic fascia decrease as a result of increasing births in women with pelvic prolapse. For these reasons, we investigated the LOX-L1 gene polymorphism, which has an important role in connective tissue and collagenous metabolism in stress urinary incontinence (SUI).A total of 87 women with SUI who underwent normal vaginal delivery and 87 controls were involved in the study. Single nucleotide gene polymorphisms in LOX-L1's rs1048661, G>T, pArg141Leu, Exon-1 SmaI; rs3825942, C>T, pGly153Asp, Hinf-1 and rs2165241, C>T, ?ntron-1 BsrI regions were searched. The results were statistically compared as alleles with 3×2 χ(2) -test. Results:? A total of 32 (34%) GG, 20 (21%) GT, 42 (45%) TT, 32 (37%) GG, 43 (39%) GT, 21 (24%) TT polymorphisms in rs1048661; 30 (36%) CC, 16 (19%) CT, 37 (45%) TT, 41 (59%) CC, 15 (22%) CT, 13 (19%) TT polymorphisms in rs2165241; and 63 (72%) CC, 21 (24%) CT, 3 (4%) TT; 48 (6%) CC, 22 (30%) CT, 3 (4%) TT polymorphisms in rs3825942 were found in patients and the control group, respectively. In patients, the TT polymorphism in the rs1048661 and rs2165241 region were found to be significant.The homozygote TT polymorphism in the rs1048661 and rs2165241 region of LOX-L1 gene may be responsible from SUI physiopathology.
机译:在实验研究中,Lysyl oxidase like-1(LOX-L1)(-/-)小鼠表现出与雌性大鼠相似的骨盆底功能障碍。由于盆腔脱垂妇女的出生增加,盆腔内筋膜的LOX-L1水平降低。基于这些原因,我们研究了LOX-L1基因多态性,该基因在应激性尿失禁(SUI)的结缔组织和胶原代谢中具有重要作用。总共87例经正常阴道分娩的SUI妇女和87名对照者参与其中。研究。 LOX-L1的rs1048661中的单核苷酸基因多态性,G> T,pArg141Leu,外显子1 SmaI;搜寻rs3825942,C> T,pGly153Asp,Hinf-1和rs2165241,C> T,?ntron-1 BsrI区。将结果作为等位基因进行3×2χ(2)-检验进行统计学比较。结果:? rs1048661中共有32(34%)GG,20(21%)GT,42(45%)TT,32(37%)GG,43(39%)GT,21(24%)TT多态性; rs2165241中的30(36%)CC,16(19%)CT,37(45%)TT,41(59%)CC,15(22%)CT,13(19%)TT多态性;和63(72%)CC,21(24%)CT,3(4%)TT; rs3825942患者和对照组分别发现48(6%)CC,22(30%)CT,3(4%)TT多态性。在患者中,发现rs1048661和rs2165241区域的TT多态性很显着.LOX-L1基因的rs1048661和rs2165241区域的纯合子TT多态性可能是SUI生理病理学的原因。

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