کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1918621 1047963 2007 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A study of 17β-estradiol-regulated genes in the vagina of postmenopausal women with vaginal atrophy
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی سالمندی
پیش نمایش صفحه اول مقاله
A study of 17β-estradiol-regulated genes in the vagina of postmenopausal women with vaginal atrophy
چکیده انگلیسی

BackgroundVaginal atrophy (VA) is a prevalent disorder in postmenopausal women that is characterized by decreased epithelial thickness, reduced vaginal maturation index (VMI) and increased vaginal pH. Current medical therapy consists of local or systemic replacement of estrogens.ObjectiveThe goal of this study was to understand, at a molecular level, the effect of estradiol (E2) on the vaginal epithelium.MethodsNineteen women were treated with E2 delivered through a skin patch at a dose of 0.05 mg/day for 12 weeks. The diagnosis of VA was confirmed by a VMI with ≤5% superficial cells and vaginal pH > 5.0. Vaginal biopsy samples were collected at baseline and after treatment. Differentially expressed mRNA transcripts in these biopsies were determined by microarray analysis.ResultsAll 19 subjects had increased VMI (>5%) and/or reduced pH (≤5) following treatment. Most subjects also had increased serum E2 levels and reduced serum FSH levels. Transcriptional profiling of vaginal biopsies identified over 3000 E2-regulated genes, including those involved in several key pathways known to regulate cell growth and proliferation, barrier function and pathogen defense.ConclusionsE2 controls a plethora of cellular pathways that are concordant with its profound effect on vaginal physiology. The data presented here are a useful step toward understanding the role of E2 in vaginal tissue and the development of novel therapeutics for the treatment of VA.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Maturitas - Volume 58, Issue 4, 20 December 2007, Pages 366–376
نویسندگان
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