Leiomyoma: genetics, assisted reproduction, pregnancy and therapeutic advances

被引:50
作者
Levy, Gary [1 ,2 ]
Hill, Micah J. [1 ]
Beall, Stephanie [1 ]
Zarek, Shvetha M. [1 ]
Segars, James H. [1 ]
Catherino, William H. [2 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Reprod & Adult Endocrinol, NIH, Bethesda, MD USA
[2] Uniformed Serv Univ Hlth Sci, Dept Obstet & Gynecol, Bethesda, MD 20814 USA
关键词
Assisted reproductive technologies; Leiomyoma genetics; Leiomyoma; UTERINE-ARTERY EMBOLIZATION; ESTROGEN-RECEPTOR-ALPHA; LOW-DOSE MIFEPRISTONE; LAPAROSCOPIC MYOMECTOMY; EXTRACELLULAR-MATRIX; ABDOMINAL MYOMECTOMY; CYTOGENETIC ABNORMALITIES; CLINICAL-SIGNIFICANCE; FIBROID EMBOLIZATION; ULIPRISTAL ACETATE;
D O I
10.1007/s10815-012-9784-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Uterine leiomyomas are common, benign, reproductive tract tumors affecting a majority of reproductive aged women. They are associated with gynecologic morbidity and detrimentally affect reproductive potential. The etiology of leiomyomas is poorly understood and their diagnosis prior to treatment with Assisted Reproductive Technologies (ART) represents a management dilemma. The purpose of this paper is to review known genetic and molecular contributions to the etiologies of leiomyomas, describe their impact on ART outcomes and reproductive potential, and review alternative therapies and future directions in management. A critical review of the literature pertaining to genetic component of uterine leiomyomas, their impact on ART and pregnancy and leiomyoma therapeutics was performed. Uterine leiomyomas are characterized by complex molecular mechanisms. Their location and size determines their potential detriment to ART and reproductive function and novel therapeutic modalities are being developed. The high prevalence of uterine leiomyomas and their potential detrimental influence on ART and reproductive function warrants continued well-designed studies to ascertain their etiology, optimal treatment and novel less morbid therapies.
引用
收藏
页码:703 / 712
页数:10
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