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Genetics of Erectile Dysfunction

机译:勃起功能障碍的遗传学

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Purpose: Erectile dysfunction affects 50% of men older than 40 years. Recently more attempts have been made to identify genetic predictors of this disease. We reviewed animal and human data on genes related to the development and increased risk of erectile dysfunction.Materials and Methods: A literature search was performed using the PubMed~R database. Articles addressing genes involved in erectile dysfunction were evaluated.Results: The majority of studies used a candidate gene approach to investigate genetic polymorphisms of known pathways mediating erection/detumes-cence. Studies in human and animal models are available. Human studies often compared the frequency of a specifically predetermined genetic polymorphism in men with erectile dysfunction to that in matched controls in whom few genes were persistently replicated. Several gene expression profiling studies are available that targeted specific erectile dysfunction models. Currently, there are few human genome wide association studies of erectile dysfunction.Conclusions: Studies investigating the genetics of erectile dysfunction are mostly derived from animal models and candidate gene approaches. Candidate gene studies omit the greater portion of the genome, a problem that can be solved using a genome wide association study approach. The lack of persistently replicated results of candidate gene studies may be related to different patient ethnic backgrounds, variations in erectile dysfunction etiology and small sample sizes. Using strict inclusion/exclusion criteria for erectile dysfunction etiology and ethnicity in human studies may lead to improved understanding of the genetics of erectile dysfunction in specific populations.
机译:目的:勃起功能障碍影响50%的40岁以上男性。最近,人们进行了更多尝试来确定这种疾病的遗传预测因子。我们回顾了动物和人类有关与勃起功能障碍的发展和风险增加相关的基因的数据。材料与方法:使用PubMed〜R数据库进行文献检索。结果:大多数研究使用候选基因方法研究介导勃起/脱发的已知途径的遗传多态性。现有关于人类和动物模型的研究。人体研究经常将勃起功能障碍的男性中特定预定的基因多态性的频率与持续复制很少基因的匹配对照组中的频率进行比较。有几种针对特定勃起功能障碍模型的基因表达谱研究。目前,关于人类勃起功能障碍的全基因组关联研究很少。结论:研究勃起功能障碍遗传学的研究主要来自动物模型和候选基因方法。候选基因研究忽略了基因组的大部分,可以使用全基因组关联研究方法解决该问题。候选基因研究结果缺乏持续重复的结果可能与不同的患者种族背景,勃起功能障碍病因学差异以及样本量少有关。在人类研究中对勃起功能障碍的病因学和种族使用严格的纳入/排除标准可能会导致对特定人群勃起功能障碍的遗传学有了更好的了解。

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