• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

盆腔器官脱垂的遗传学:在泌尿妇科研究中跨越基础研究与临床应用之间的桥梁

Genetics of pelvic organ prolapse: crossing the bridge between bench and bedside in urogynecologic research.

作者信息

Bortolini Maria Augusta Tezelli, Rizk Diaa E E

机构信息

Division of Urogynecology and Reconstructive Pelvic Surgery, Department of Gynecology, Federal University of São Paulo, Borges Lagoa, 783 Cj. 31, 04038-031, São Paulo, SP, Brazil.

出版信息

Int Urogynecol J. 2011 Oct;22(10):1211-9. doi: 10.1007/s00192-011-1502-4. Epub 2011 Jul 26.

DOI:10.1007/s00192-011-1502-4
PMID:21789659
Abstract

An increasing number of scientists have studied the molecular and biochemical basis of pelvic organ prolapse (POP). The extracellular matrix content of the pelvic floor is the major focus of those investigations and pointed for potential molecular markers of the dysfunction. The identification of women predisposed to develop POP would help in the patients' management and care. This article includes a critical analysis of the literature up to now; discusses implications for future research and the role of the genetics in POP.

摘要

越来越多的科学家研究了盆腔器官脱垂(POP)的分子和生化基础。盆底的细胞外基质成分是这些研究的主要焦点,并指出了功能障碍的潜在分子标志物。识别易患POP的女性将有助于患者的管理和护理。本文对迄今为止的文献进行了批判性分析;讨论了对未来研究的影响以及遗传学在POP中的作用。

相似文献

1
Genetics of pelvic organ prolapse: crossing the bridge between bench and bedside in urogynecologic research.盆腔器官脱垂的遗传学:在泌尿妇科研究中跨越基础研究与临床应用之间的桥梁
Int Urogynecol J. 2011 Oct;22(10):1211-9. doi: 10.1007/s00192-011-1502-4. Epub 2011 Jul 26.
2
Genetics of pelvic organ prolapse: comment.
Int Urogynecol J. 2012 Apr;23(4):509-10; author reply 511-2. doi: 10.1007/s00192-011-1638-2.
3
Genetics of Female Pelvic Organ Prolapse: Up to Date.女性盆底器官脱垂遗传学研究进展。
Biomolecules. 2024 Sep 1;14(9):1097. doi: 10.3390/biom14091097.
4
[Association of polymorphism of 1800255 COL3A1 gene with pelvic organ prolapse and urinary incontinence in women: preliminary data].[1800255 COL3A1基因多态性与女性盆腔器官脱垂及尿失禁的相关性:初步数据]
Urologiia. 2017 Dec(6):30-33.
5
Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17.10号和17号染色体上存在盆腔器官脱垂易感基因的证据。
Am J Obstet Gynecol. 2015 Jun;212(6):771.e1-7. doi: 10.1016/j.ajog.2014.12.037. Epub 2014 Dec 31.
6
Assessment of Metalloproteinase Matrix 9 (MMP9) Gene Polymorphisms Risk Factors for Pelvic Organ Prolapse in the Brazilian Population.巴西人群中基质金属蛋白酶9(MMP9)基因多态性作为盆腔器官脱垂危险因素的评估
Rev Bras Ginecol Obstet. 2019 Mar;41(3):164-169. doi: 10.1055/s-0039-1681112. Epub 2019 Apr 2.
7
Pelvic floor disorders: linking genetic risk factors to biochemical changes.盆底功能障碍:将遗传风险因素与生化变化联系起来。
BJU Int. 2011 Oct;108(8):1240-7. doi: 10.1111/j.1464-410X.2011.10385.x. Epub 2011 Aug 26.
8
A systematic review of clinical studies on hereditary factors in pelvic organ prolapse.盆腔器官脱垂遗传因素的临床研究系统评价。
Int Urogynecol J. 2012 Oct;23(10):1327-36. doi: 10.1007/s00192-012-1704-4. Epub 2012 Mar 16.
9
Identification of pelvic organ prolapse risk susceptibility gene SNP locus in Xinjiang women.新疆女性盆腔器官脱垂风险易感性基因单核苷酸多态性位点的鉴定
Int Urogynecol J. 2020 Jan;31(1):123-130. doi: 10.1007/s00192-019-04039-z. Epub 2019 Jul 2.
10
Urogynecology digest : presented by J. Oliver Daly.
Int Urogynecol J. 2014 Apr;25(4):551-2. doi: 10.1007/s00192-013-2270-0. Epub 2013 Dec 7.

引用本文的文献

1
Quantification of senescence-associated secretory phenotype proteins in the vaginal secretions of pre- and postmenopausal women with and without prolapse.有或无子宫脱垂的绝经前和绝经后女性阴道分泌物中衰老相关分泌表型蛋白的定量分析
Aging Med (Milton). 2023 May 14;6(2):124-131. doi: 10.1002/agm2.12255. eCollection 2023 Jun.
2
Study of the polymorphism rs3025058 of the MMP-3 gene and risk of pelvic organ prolapse in Brazilian women.巴西女性中基质金属蛋白酶-3(MMP-3)基因多态性rs3025058与盆腔器官脱垂风险的研究。
Eur J Obstet Gynecol Reprod Biol X. 2019 Apr 30;3:100031. doi: 10.1016/j.eurox.2019.100031. eCollection 2019 Jul.
3

本文引用的文献

1
Expression of Bone Morphogenetic Protein-1 in vaginal tissue of women with severe pelvic organ prolapse.骨形态发生蛋白-1 在重度盆腔器官脱垂女性阴道组织中的表达。
Am J Obstet Gynecol. 2011 Jun;204(6):544.e1-8. doi: 10.1016/j.ajog.2011.01.021. Epub 2011 Mar 11.
2
MicroRNA functions in stress responses.MicroRNA 在应激反应中的功能。
Mol Cell. 2010 Oct 22;40(2):205-15. doi: 10.1016/j.molcel.2010.09.027.
3
[MMP-1 and MMP-3 gene encoding polymorphism and the risk of the development of pelvic organ prolapse and stress urinary incontinence].
Association between col1a2 Polymorphism and the Occurrence of Pelvic Organ Prolapse in Brazilian Women.
巴西女性中col1a2基因多态性与盆腔器官脱垂发生之间的关联。
Rev Bras Ginecol Obstet. 2019 Jan;41(1):31-36. doi: 10.1055/s-0038-1676599. Epub 2019 Feb 4.
4
The increased of MMP-9 and MMP-2 with the decreased of TIMP-1 on the uterosacral ligament after childbirth.产后子宫骶韧带处基质金属蛋白酶-9(MMP-9)和基质金属蛋白酶-2(MMP-2)增加,而金属蛋白酶组织抑制因子-1(TIMP-1)减少。
Pan Afr Med J. 2018 Aug 23;30:283. doi: 10.11604/pamj.2018.30.283.9905. eCollection 2018.
5
Evaluation of COLIA1-1997 G/T polymorphism as a related factor to genital prolapse.评估COLIA1-1997 G/T多态性作为与生殖器脱垂相关因素的情况。
Int Urogynecol J. 2020 Jan;31(1):133-137. doi: 10.1007/s00192-018-3833-x. Epub 2018 Nov 27.
6
Differential gene expression of extracellular-matrix-related proteins in the vaginal apical compartment of women with pelvic organ prolapse.盆腔器官脱垂女性阴道顶端区域细胞外基质相关蛋白的差异基因表达
Int Urogynecol J. 2019 Mar;30(3):439-446. doi: 10.1007/s00192-018-3637-z. Epub 2018 Mar 29.
7
Collagen XVIII and LOXL-4 polymorphisms in women with and without advanced pelvic organ prolapse.患有和未患有晚期盆腔器官脱垂的女性中胶原蛋白 XVIII 和赖氨酰氧化酶样蛋白 4 基因多态性
Int Urogynecol J. 2018 Jun;29(6):893-898. doi: 10.1007/s00192-018-3597-3. Epub 2018 Mar 12.
8
Association between metabolic syndrome and pelvic organ prolapse severity.代谢综合征与盆腔器官脱垂严重程度之间的关联。
Int Urogynecol J. 2015 Apr;26(4):563-8. doi: 10.1007/s00192-014-2468-9. Epub 2014 Jul 22.
9
Genetics of pelvic organ prolapse: comment.
Int Urogynecol J. 2012 Apr;23(4):509-10; author reply 511-2. doi: 10.1007/s00192-011-1638-2.
[基质金属蛋白酶-1和基质金属蛋白酶-3基因编码多态性与盆腔器官脱垂及压力性尿失禁发生风险]
Ginekol Pol. 2010 Aug;81(8):594-9.
4
The genome-wide association study--a new era for common polygenic disorders.全基因组关联研究——常见多基因疾病的新纪元。
J Cardiovasc Transl Res. 2010 Jun;3(3):173-82. doi: 10.1007/s12265-010-9178-6. Epub 2010 Mar 27.
5
LOX family enzymes expression in vaginal tissue of premenopausal women with severe pelvic organ prolapse.严重盆腔器官脱垂的绝经前女性阴道组织中赖氨氧化酶家族酶的表达
Int Urogynecol J. 2010 Nov;21(11):1397-404. doi: 10.1007/s00192-010-1199-9. Epub 2010 Jun 18.
6
Genitourinary prolapse and joint hypermobility are associated with altered type I and III collagen metabolism.泌尿生殖系统脱垂和关节过度活动与 I 型和 III 型胶原代谢改变有关。
Arch Gynecol Obstet. 2011 May;283(5):1081-5. doi: 10.1007/s00404-010-1518-x. Epub 2010 May 26.
7
Vaginal delivery and pelvic floor dysfunction: current evidence and implications for future research.
Int Urogynecol J. 2010 Aug;21(8):1025-30. doi: 10.1007/s00192-010-1146-9. Epub 2010 May 6.
8
Genetics and the lower urinary tract.遗传与下尿路
Neurourol Urodyn. 2010 Apr;29(4):609-11. doi: 10.1002/nau.20908.
9
Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse?层粘连蛋白γ-1 是否是晚期盆腔器官脱垂的候选基因?
Am J Obstet Gynecol. 2010 May;202(5):505.e1-5. doi: 10.1016/j.ajog.2010.01.014. Epub 2010 Mar 12.
10
Changes of glycoprotein and collagen immunolocalization in the uterine artery wall of postmenopausal women with and without pelvic organ prolapse.绝经后伴或不伴盆腔器官脱垂女性子宫动脉壁中糖蛋白和胶原免疫定位的变化。
Acta Histochem. 2011 May;113(3):375-81. doi: 10.1016/j.acthis.2010.02.001. Epub 2010 Mar 1.