首页> 外文期刊>The journal of clinical endocrinology and metabolism >Polymorphism in Vitamin D-Binding Protein as a Genetic Risk Factor in the Pathogenesis of Endometriosis
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Polymorphism in Vitamin D-Binding Protein as a Genetic Risk Factor in the Pathogenesis of Endometriosis

机译:维生素D结合蛋白的多态性作为子宫内膜异位症发病机制中的遗传危险因素

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Context: Previous studies have implicated a deficiency in the inflammatory response in women who develop endometriosis. The specific immunological deficits have not been completely elucidated.Objective: Our objective was to identify differences in protein expression in serum that might shed light on the pathophysiology of endometriosis.Design and Setting: This cross-sectional study of women undergoing laparoscopy between 2003 and 2005 took place at a university medical center.Patients: Patients included consenting women age 18–49 yr undergoing surgery for pain and/or infertility or elective tubal ligation. Women with acute or chronic medical conditions were excluded.Intervention: Blood was collected preoperatively.Main Outcome Measure: Proteomic analysis of serum was done using two-dimensional difference gel electrophoresis.Results: We found 25 protein spots with a significant difference in abundance between women with endometriosis and controls, including acute-phase proteins and complement components. The abundance of vitamin D-binding protein was higher in all endometriosis pools by a factor of approximately 3 compared with the control pool ( P < 0.02). Analysis of specific allele products using nano-scale liquid chromatography-electrospray ionization-mass spectrometry indicated that it was the GC*2 allele product that was in greater concentration in serum pools, as well as in single validation samples, in women with endometriosis ( P = 0.006). In contrast to the GC*1 allele product, which is readily converted to a potent macrophage factor (Gc protein-derived macrophage-activating factor), the GC*2 allele product undergoes practically no such conversion.Conclusions: We speculate that the inability to sufficiently activate macrophages’ phagocytotic function in those carrying the GC*2 polymorphism (more prevalent in endometriosis) may allow endometriotic tissues to implant in the peritoneal cavity. Future studies evaluating specific vitamin D-binding protein polymorphisms as a risk factor for endometriosis in larger populations of women are warranted.
机译:背景:以前的研究表明,子宫内膜异位症妇女的炎症反应不足。具体的免疫缺陷尚未完全阐明。目的:我们的目标是鉴定血清中蛋白质表达的差异,这可能有助于阐明子宫内膜异位症的病理生理学。设计与背景:这项横断面研究是在2003年至2005年间对接受腹腔镜检查的女性进行的。患者:患者包括18-49岁的同意患者,她们因疼痛和/或不育症或选择性输卵管结扎术而接受手术。干预:术前采集血液。主要指标:使用二维差异凝胶电泳对血清进行蛋白质组学分析。结果:我们发现了25个蛋白斑点,女性之间的丰度差异显着。子宫内膜异位和控制,包括急性期蛋白和补体成分。与对照库相比,所有子宫内膜异位症库中维生素D结合蛋白的丰度高出约3倍(P <0.02)。使用纳米级液相色谱-电喷雾电离质谱技术对特定等位基因产物进行分析表明,子宫内膜异位症妇女的血清池以及单个验证样品中的GC * 2等位基因产物浓度较高(P = 0.006)。与GC * 1等位基因产物很容易转化为有效的巨噬细胞因子(Gc蛋白衍生的巨噬细胞激活因子)相反,GC * 2等位基因产物几乎没有这种转化。结论:我们推测无法在具有GC * 2多态性的子宫内膜中充分激活巨噬细胞的吞噬功能(在子宫内膜异位症中更为普遍)可能使子宫内膜异位组织植入腹膜腔。将来有必要评估特定的维生素D结合蛋白多态性作为更多妇女子宫内膜异位症的危险因素的研究。

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