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首页> 外文期刊>Journal of the American Medical Directors Association >Reply to the letter to the editor by Dr. Wiwanitkit
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Reply to the letter to the editor by Dr. Wiwanitkit

机译:回复Wiwanitkit博士给编辑的信

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Port wine stains in the malar area of the face can develop thickening in early adult life. We began a study with a hypothesis that this thickening can be associated with elevation of low density lipoprotein. In a retrospective review, we divided 53 subjects with malar port wine stains into 4 groups, adults 25-39. years of age with thickening, that age group without thickening, adults 40+ years of age with thickening, and that age group without thickening. Low density lipoprotein levels in the subjects were compared to age and sex matched controls randomly selected from the general Dermatology clinic. The younger subjects with thickening demonstrated significantly higher low density lipoprotein levels than their controls (p .0082) and without thickening lower low density lipoprotein levels than their controls with great significance (p .00058). The subjects without thickening also consisted mainly of women. The low density lipoprotein levels in the older age groups, whether thickened or not, demonstrated no significant difference in low density lipoprotein levels between subjects and controls. This led to a new hypothesis that there is a factor in a subgroup of young adult women with malar port wine stains that suppresses thickening and delays the elevation of low density lipoprotein and that this factor might be estrogen. The implications of this hypothesis are that it could define a marker for a subset of the population that might be protected from the diseases associated with early elevation of low density lipoprotein and provide a source of cutaneous tissue for studying the basic science of this protection (although limited by cosmetic considerations). Future laboratory research to test the new hypothesis might include testing blood of women with malar port wine stains with or without thickening for estrogen and other sex hormones. It might also include skin biopsies to study receptors for estrogen, other sex hormones, and angiogenic factors in malar port wine stains with or without thickening. Future clinical research might include a long term prospective project to study the development of low density lipoprotein related diseases in women with malar port wine stains with or without thickening over years.
机译:在成年早期,面部黄斑区域的葡萄酒色斑会逐渐增厚。我们以一种假设开始研究,这种假设可能与低密度脂蛋白的升高有关。在回顾性回顾中,我们将53名患有黄斑部波特酒渍的受试者分为4组,每组25-39岁。年岁有增厚,该年龄段未增厚,成人40岁以上增厚,该年龄段无增厚。将受试者中的低密度脂蛋白水平与从普通皮肤科诊所随机选择的年龄和性别匹配的对照进行比较。具有增厚作用的年轻受试者表现出比其对照(p.0082)高得多的低密度脂蛋白水平,而没有比其对照组具有显着意义的低密度脂蛋白水平低(p.00058)。没有增厚的受试者也主要由女性组成。老年人群中的低密度脂蛋白水平,无论是否增厚,在受试者和对照组之间均未显示出低密度脂蛋白水平的显着差异。这导致了一个新的假设,即在患有成年苹果酒斑点的年轻成年女性亚组中有一个因素可以抑制增稠并延迟低密度脂蛋白的升高,并且该因素可能是雌激素。该假设的含义是,它可以为可能受到保护的人群的一部分定义一个标记物,以免与低密度脂蛋白的早期升高相关的疾病,并为研究这种保护的基础科学提供皮肤组织来源(尽管受化妆品方面的限制)。检验新假说的未来实验室研究可能包括测试患有或不伴有雌激素和其他性激素增稠作用的苹果酒带有苹果酒渍的妇女的血液。它也可能包括皮肤活检,以研究是否有增稠的苹果酸端口酒渍中的雌激素,其他性激素和血管生成因子的受体。未来的临床研究可能包括一个长期的前瞻性项目,以研究患有或不伴有增稠的苹果酸波尔多酒渍的妇女中低密度脂蛋白相关疾病的发展。

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